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Biomaterials

The effect of a Mn(III)tetrakis(4-benzoic acid)porphyrin (MnTBAP) coating on the chronic recording performance of planar silicon intracortical microelectrode arrays

04 November 2023
Hernandez-Reynoso, A. G., B. S. Sturgill, et al.

The effect of a Mn(III)tetrakis(4-benzoic acid)porphyrin (MnTBAP) coating on the chronic recording performance of planar silicon intracortical microelectrode arrays. Biomaterials 303: 122351. >> View Publication

Cell Reports

Cell type specializations of the vocal-motor cortex in songbirds

30 October 2023
Nevue, A. A., B. M. Zemel, et al.

Cell type specializations of the vocal-motor cortex in songbirds. Cell Reports 42(11). >> View Publication

eneuro

Microglia are dispensable for developmental dendrite pruning of mitral cells in mice

27 October 2023
Tetsushi, N., F. Satoshi, et al.

Microglia are dispensable for developmental dendrite pruning of mitral cells in mice. eneuro: ENEURO.0323-0323.2023. >> View Publication

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Hernandez-Reynoso, A. G., B. S. Sturgill, et al. (2023). "The effect of a Mn(III)tetrakis(4-benzoic acid)porphyrin (MnTBAP) coating on the chronic recording performance of planar silicon intracortical microelectrode arrays." Biomaterials 303: 122351. https://doi.org/10.1016/j.biomaterials.2023.122351

Nevue, A. A., B. M. Zemel, et al. (2023). "Cell type specializations of the vocal-motor cortex in songbirds." Cell Reports 42(11). https://doi.org/10.1016/j.celrep.2023.113344

Qin, Y., X.-Y. Zhang, et al. (2023). "Downregulation of mGluR1-mediated signaling underlying autistic-like core symptoms in Shank1 P1812L-knock-in mice." Translational Psychiatry 13(1): 329. https://doi.org/10.1038/s41398-023-02626-9

Tetsushi, N., F. Satoshi, et al. (2023). "Microglia are dispensable for developmental dendrite pruning of mitral cells in mice." eneuro: ENEURO.0323-0323.2023. https://doi.org/10.1523/ENEURO.0323-23.2023

Jeon, K.-I., A. Kumar, et al. (2023). "Blocking Mitochondrial Pyruvate Transport Alters Corneal Myofibroblast Phenotype: A New Target for Treating Fibrosis." Investigative Ophthalmology & Visual Science 64(13): 36-36. https://doi.org/10.1167/iovs.64.13.36

Timonidis, N., M. Rubio-Teves, et al. (2023). "Analyzing Thalamocortical Tract-Tracing Experiments in a Common Reference Space." Neuroinformatics. https://doi.org/10.1007/s12021-023-09644-4

Stallings, N. R., M. A. O’Neal, et al. (2023). "Long-term normalization of calcineurin activity in model mice rescues Pin1 and attenuates Alzheimer’s phenotypes without blocking peripheral T cell IL-2 response." Alzheimer's Research & Therapy 15(1): 179. https://doi.org/10.1186/s13195-023-01323-5

Ament, S. A., M. Cortes-Gutierrez, et al. "A single-cell genomic atlas for maturation of the human cerebellum during early childhood." Science Translational Medicine 0(0): eade1283. https://www.science.org/doi/full/10.1126/scitranslmed.ade1283

Gamage, R., I. Rossetti, et al. (2023). "Chronic neuroinflammation during aging leads to cholinergic neurodegeneration in the mouse medial septum." Journal of Neuroinflammation 20(1): 235. https://doi.org/10.1186/s12974-023-02897-5

Beers, D., D. Goniotaki, et al. (2023). "Barcodes distinguishing morphology of neuronal tauopathy." Physical Review Research 5(4): 043006. https://doi.org/10.1103/PhysRevResearch.5.043006

Massa, G., S. Camuso, et al. (2023). Investigating Cerebellar Abnormalities in a mouse model of lysosomal lipid storage disease: Implication for Social Behavior. https://www.researchgate.net/publication/374470148_Investigating_Cerebellar_Abnormalities_in_a_mouse_model_of_lysosomal_lipid_storage_disease_Implication_for_Social_Behavior

Pérez-Fernández, V., A. L. Thananjeyan, et al. (2023). "The effects of a highly bioavailable curcumin PhytosomeTM preparation on the retinal architecture and glial reactivity in the GFAP-IL6 mice." Frontiers in Ophthalmology 3. https://doi.org/10.3389/fopht.2023.1205542

Jongwon, L., C. Amanda, et al. (2023). "Structural and functional development of inhibitory connections from the medial nucleus of the trapezoid body to the superior paraolivary nucleus." The Journal of Neuroscience: JN-RM-0920-0923. https://doi.org/10.1523/JNEUROSCI.0920-23.2023

Sun, C., S. Zheng, et al. (2023). "Maternal diet during early gestation influences postnatal taste activity-dependent pruning by microglia." J Exp Med 220(12): 21. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512853/

Beola, L., N. Iturrioz-Rodríguez, et al. (2023). "Drug-Loaded Lipid Magnetic Nanoparticles for Combined Local Hyperthermia and Chemotherapy against Glioblastoma Multiforme." ACS Nano. https://doi.org/10.1021/acsnano.3c06085

Camp, C. R., A. Vlachos, et al. (2023). "Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons." Communications Biology 6(1): 952. https://doi.org/10.1038/s42003-023-05298-9

Natale, G., M. Colella, et al. (2023). "Astrocyte Responses Influence Local Effects of Whole-Brain Magnetic Stimulation in Parkinsonian Rats." Mov Disord 12(10): 29599. https://pubmed.ncbi.nlm.nih.gov/37700489/

Delestrée, N., E. Semizoglou, et al. (2023). "Serotonergic dysfunction impairs locomotor coordination in spinal muscular atrophy." Brain: awad221. https://doi.org/10.1093/brain/awad221

Kokkosis, A. G., M. M. Madeira, et al. (2023). "Chronic psychosocial stress triggers microglial-/macrophage-induced inflammatory responses leading to neuronal dysfunction and depressive-related behavior." Glia 7(10): 24464. https://pubmed.ncbi.nlm.nih.gov/37675659/

Li, X., S. Hao, et al. (2023). "Cortex-restricted deletion of Foxp1 impairs barrel formation and induces aberrant tactile responses in a mouse model of autism." Molecular Autism 14(1): 34. https://doi.org/10.1186/s13229-023-00567-0

Rasmussen, V. F., A. Schmeichel, et al. (2023). "Sweat gland nerve fiber density and association with sudomotor function, symptoms, and risk factors in adolescents with type 1 diabetes." Clinical Autonomic Research. https://doi.org/10.1007/s10286-023-00973-7

Dubey, V., A. Roy, et al. (2023). "Dendritic reorganization in the hippocampus, anterior temporal lobe, and frontal neocortex of lithium-pilocarpine induced Status Epilepticus (SE)." Journal of Chemical Neuroanatomy: 102329. https://doi.org/10.1016/j.jchemneu.2023.102329

Laricchiuta, D., J. Gimenez, et al. (2023). "Synaptic and transcriptomic features of cortical and amygdala pyramidal neurons predict inefficient fear extinction." Cell Rep 42(9): 113066. https://pubmed.ncbi.nlm.nih.gov/37656620/

Zhou, F., L. Ouyang, et al. (2023). "Co-exposure to low-dose lead, cadmium, and mercury promotes memory deficits in rats: Insights from the dynamics of dendritic spine pruning in brain development." Ecotoxicology and Environmental Safety 264: 115425. https://doi.org/10.1016/j.ecoenv.2023.115425

Wicke, K. D., L. Oppe, et al. (2023). "Neuronal morphology and synaptic input patterns of neurons in the intermediate nucleus of the lateral lemniscus of gerbils." Scientific Reports 13(1): 14182. https://doi.org/10.1038/s41598-023-41180-8

Collier, T. J., L. Begg, et al. (2023). "Quinpirole inhibits levodopa-induced dyskinesias at structural and behavioral levels: Efficacy negated by co-administration of isradipine." Experimental Neurology 369: 114522. https://doi.org/10.1016/j.expneurol.2023.114522

Nguyen, T., N. Nguyen, et al. (2023). "Repeated closed-head mild traumatic brain injury-induced inflammation is associated with nociceptive sensitization." Journal of Neuroinflammation 20(1): 196. https://doi.org/10.1186/s12974-023-02871-1

Han, R., X. Lan, et al. (2023). "Improving outcomes in intracerebral hemorrhage through microglia/macrophage-targeted IL-10 delivery with phosphatidylserine liposomes." Biomaterials 301: 122277. https://doi.org/10.1016/j.biomaterials.2023.122277

Sanchez-Molano, J., M. O. Blaya, et al. (2023). "Multimodal magnetic resonance imaging after experimental moderate and severe traumatic brain injury: A longitudinal correlative assessment of structural and cerebral blood flow changes." PLOS ONE 18(8): e0289786. https://doi.org/10.1371/journal.pone.0289786

Pfau, D. R., S. Baribeau, et al. (2023). "Loss of TRPC2 function in mice alters sex differences in brain regions regulating social behaviors." J Comp Neurol 27(10): 25528. https://pubmed.ncbi.nlm.nih.gov/37496437/

Schellino, R., D. Besusso, et al. (2023). "hESC-derived striatal progenitors grafted into a Huntington’s disease rat model support long-term functional motor recovery by differentiating, self-organizing and connecting into the lesioned striatum." Stem Cell Research & Therapy 14(1): 189. https://doi.org/10.1186/s13287-023-03422-4

Parmar, J., G. von Jonquieres, et al. (2023). "TRPC Channels Activated by G Protein-Coupled Receptors Drive Ca2+ Dysregulation Leading to Secondary Brain Injury in the Mouse Model." Translational Stroke Research. https://doi.org/10.1007/s12975-023-01173-1

Courtney, K. W., M. G. Kelsey, et al. (2023). "Cross-Platform Synaptic Network Analysis of Human Entorhinal Cortex Identifies TWF2 as a Modulator of Dendritic Spine Length." The Journal of Neuroscience 43(20): 3764. https://doi.org/10.1523/JNEUROSCI.2102-22.2023

Soad, E. and B. C. Peter (2023). "Vascularization in mTOR Mouse Mutants: An Effort Not in Vein." eneuro 10(7): ENEURO.0122-0123.2023. https://doi.org/10.1523/ENEURO.0122-23.2023

Doorn, N., E. J. H. van Hugte, et al. "An in silico and in vitro human neuronal network model reveals cellular mechanisms beyond NaV1.1 underlying Dravet syndrome." Stem Cell Reports. https://doi.org/10.1016/j.stemcr.2023.06.003

Marino, G., F. Campanelli, et al. (2023). "Intensive exercise ameliorates motor and cognitive symptoms in experimental Parkinson's disease restoring striatal synaptic plasticity." Science Advances 9(28): eadh1403. https://www.science.org/doi/10.1126/sciadv.adh1403

Shi, Y., H. Cui, et al. (2023). "Laminar and dorsoventral organization of layer 1 interneuronal microcircuitry in superficial layers of the medial entorhinal cortex." Cell Reports 42(7). https://doi.org/10.1016/j.celrep.2023.112782

Kim, H. S., H. G. Seo, et al. (2023). "Machine Learning-assisted Quantitative Mapping of Intracortical Axonal Plasticity Following a Focal Cortical Stroke in Rodents." Experimental Neurobiology 32(3): 170-180. https://doi.org/10.5607/en23016

McLaurin, K. A., H. Li, et al. (2023). "Constitutive expression of HIV-1 viral proteins induces progressive synaptodendritic alterations in medium spiny neurons: implications for substance use disorders." NeuroImmune Pharmacology and Therapeutics. https://doi.org/10.1515/nipt-2023-0008

Xia, Q.-q., A. K. Walker, et al. (2023). "Effects of heterozygous deletion of autism-related gene Cullin-3 in mice." PLOS ONE 18(7): e0283299. https://doi.org/10.1371/journal.pone.0283299

Mugnaini, M., D. Mehrotra, et al. (2023). "Supra-orbital whiskers act as wind-sensing antennae in rats." PLOS Biology 21(7): e3002168. https://doi.org/10.1371/journal.pbio.3002168

Reynolds, L. M., G. Hernandez, et al. (2023). "Amphetamine disrupts dopamine axon growth in adolescence by a sex-specific mechanism in mice." Nature Communications 14(1): 4035. https://doi.org/10.1038/s41467-023-39665-1

Hu, M., B. Bodnar, et al. Defective neurite elongation and branching in Nibp/Trappc9 deficient zebrafish and mice, Int J Biol Sci. 2023 Jun 19;19(10):3226-48. doi: 10.7150/ijbs.78489. eCollection 2023. doi: 10.7150/ijbs.78489

Di Mascolo, D., I. Guerriero, et al. (2023). "μMESH-Enabled Sustained Delivery of Molecular and Nanoformulated Drugs for Glioblastoma Treatment." ACS Nano. https://doi.org/10.1021/acsnano.3c01574

Ekaterina, P., V. Peter, et al. (2023). "SpineTool is an open-source software for analysis of morphology of dendritic spines." Scientific Reports 13(1): 10561. https://doi.org/10.1038/s41598-023-37406-4

Guo, Y., M. Shen, et al. (2023). "Elevated levels of FMRP-target MAP1B impair human and mouse neuronal development and mouse social behaviors via autophagy pathway." Nature Communications 14(1): 3801. https://doi.org/10.1038/s41467-023-39337-0

Li, K., E. C. Gonye, et al. (2023). "The astrocytic Na+-HCO3− exchanger NBCe1 is dispensable for respiratory chemosensitivity." The Journal of Physiology n/a(n/a). https://doi.org/10.1113/JP284960

Nowinski, W. L. (2023). Toward the Human Nanoscale Connectome: Neuronal Morphology Format, Modeling, and Storage Requirement Estimation. Computational Science – ICCS 2023, Cham, Springer Nature Switzerland. https://doi.org/10.1007/978-3-031-36021-3_66

Guaiquil, V. H., D. Lara-Newman, et al. (2023). "Role of EphrinB2 in corneal epithelium proliferation and neuronal growth." Investigative Ophthalmology & Visual Science 64(8): 3130-3130. 2023;64(8):3130.

Massoumi, H., E. Katz, et al. (2023). "Extracellular vesicles (EVs) from 3D cultured human bone marrow mesenchymal stem cells (hBM-MSC) demonstrated increased complexity and neurite elongation in an in-vivo corneal injury model." Investigative Ophthalmology & Visual Science 64(8): 2350-2350.

Pérez-Cervera, L., S. De Santis, et al. (2023). "Alcohol-induced damage to the fimbria/fornix reduces hippocampal-prefrontal cortex connection during early abstinence." Acta Neuropathologica Communications 11(1): 101. https://doi.org/10.1186/s40478-023-01597-8

Smith, M. A., S. Dewan, et al. (2023). "Assessment of non-image forming retinal pathways following traumatic brain injury." Investigative Ophthalmology & Visual Science 64(8): 5227-5227. 2023;64(8):5227.

Life, B., L. E. B. Bettio, et al. (2023). "Progranulin is an FMRP target that influences macroorchidism but not behaviour in a mouse model of Fragile X Syndrome." Current Research in Neurobiology: 100094. https://doi.org/10.1016/j.crneur.2023.100094

Lucarelli, M., S. Camuso, et al. (2023). "Reduced Cerebellar BDNF Availability Affects Postnatal Differentiation and Maturation of Granule Cells in a Mouse Model of Cholesterol Dyshomeostasis." Molecular Neurobiology. https://doi.org/10.1007/s12035-023-03435-3

Mishra, E. and M. K. Thakur (2023). "Mdivi-1 Rescues Memory Decline in Scopolamine-Induced Amnesic Male Mice by Ameliorating Mitochondrial Dynamics and Hippocampal Plasticity." Molecular Neurobiology. https://doi.org/10.1007/s12035-023-03397-6

Realinho, A. M., R. Boia, et al. (2023). "Maternal diabetes affects rat offspring retinal structure and function: Sex-specific vulnerabilities at infancy." Life Sciences 327: 121852. https://doi.org/10.1016/j.lfs.2023.121852

Deiringer, N., U. Schneeweiß, et al. (2023). "The functional anatomy of elephant trunk whiskers." Communications Biology 6(1): 591. https://doi.org/10.1038/s42003-023-04945-5

Fujimoto, S., M. N. Leiwe, et al. (2023). "Activity-dependent local protection and lateral inhibition control synaptic competition in developing mitral cells in mice." Developmental Cell. https://doi.org/10.1016/j.devcel.2023.05.004

Muller, S. Z., L. F. Abbott, et al. "A mechanism for differential control of axonal and dendritic spiking underlying learning in a cerebellum-like circuit." Current Biology. https://doi.org/10.1016/j.cub.2023.05.040

Obi-Nagata, K., N. Suzuki, et al. (2023). "Distorted neurocomputation by a small number of extra-large spines in psychiatric disorders." Science Advances 9(23): eade5973. DOI: 10.1126/sciadv.ade5973

Bonzano, S., E. Dallorto, et al. (2023). "Nr2f1 shapes mitochondria in the mouse brain unraveling new insights into the neurodevelopmental disorder BBSOAS." Disease Models & Mechanisms. https://doi.org/10.1242/dmm.049854

Forro, T. and T. Klausberger "Differential behavior-related activity of distinct hippocampal interneuron types during odor-associated spatial navigation." Neuron. https://doi.org/10.1016/j.neuron.2023.05.007

Lerchner, W., K. Dash, et al. (2023). "Efficient viral expression of a chemogenetic receptor in the old-world monkey amygdala." Current Research in Neurobiology 4: 100091. https://doi.org/10.1016/j.crneur.2023.100091

Ma, J., D. Nguyen, et al. (2023). "Topographical Distribution and Morphology of Calcitonin Gene-Related Peptide (CGRP) Nociceptive Afferent Axons in the Flat-Mounts of the Whole Stomach in Male and Female Mice: Tracing, Digitization, and 3D Scaffold." Physiology 38(S1): 5734053. https://doi.org/10.1152/physiol.2023.38.S1.5734053

Gullotta, G. S., D. De Feo, et al. (2023). "Age-induced alterations of granulopoiesis generate atypical neutrophils that aggravate stroke pathology." Nature Immunology. https://doi.org/10.1038/s41590-023-01505-1

Paranjape, N., Y.-H. T. Lin, et al. (2023). "A CRISPR-engineered isogenic model of the 22q11.2 A-B syndromic deletion." Scientific Reports 13(1): 7689. https://doi.org/10.1038/s41598-023-34325-2

Schafer, S. T., A. A. Mansour, et al. (2023). "An in vivo neuroimmune organoid model to study human microglia phenotypes." Cell 186(10): 2111-2126.e2120. https://doi.org/10.1016/j.cell.2023.04.022

Beebe, N. L., Y. N. Herrera, et al. (2023). "Characterization of three cholinergic inputs to the cochlear nucleus." Journal of Chemical Neuroanatomy 131: 102284. https://doi.org/10.1016/j.jchemneu.2023.102284

Keto, L. and T. Manninen (2023). "CellRemorph: A Toolkit for Transforming, Selecting, and Slicing 3D Cell Structures on the Road to Morphologically Detailed Astrocyte Simulations." Neuroinformatics. https://doi.org/10.1007/s12021-023-09627-5

Lavertu-Jolin, M., B. Chattopadhyaya, et al. (2023). "Acan downregulation in parvalbumin GABAergic cells reduces spontaneous recovery of fear memories." Molecular Psychiatry. https://doi.org/10.1038/s41380-023-02085-0

Panahi, M., Y. Hase, et al. (2023). "ER stress induced immunopathology involving complement in CADASIL: implications for therapeutics." Acta Neuropathologica Communications 11(1): 76. https://doi.org/10.1186/s40478-023-01558-1

Travis, M. R., V. G. Violet, et al. (2023). "Structural preservation does not ensure function at sensory Ia – motoneuron synapses following peripheral nerve injury and repair." The Journal of Neuroscience: JN-RM-0103-0123. https://doi.org/10.1523/JNEUROSCI.0103-23.2023

Wei, H., X. Wu, et al. (2023). "Glial progenitor heterogeneity and key regulators revealed by single-cell RNA sequencing provide insight to regeneration in spinal cord injury." Cell Reports 42(5): 112486. https://doi.org/10.1016/j.celrep.2023.112486

Liu, A., L. Yu, et al. (2023). "Celsr2‐mediated morphological polarization and functional phenotype of reactive astrocytes in neural repair." Glia. DOI:10.1002/glia.24378

Lv, J., S. Meng, et al. (2023). "Epigenetic landscape reveals MECOM as an endothelial lineage regulator." Nature Communications 14(1): 2390. https://doi.org/10.1038/s41467-023-38002-w

Mahoney-Rafferty, E. C., H. R. Tucker, et al. (2023). "Assessing the Location, Relative Expression and Subclass of Dopamine Receptors in the Cerebellum of Hemi-Parkinsonian Rats." Neuroscience. https://doi.org/10.1016/j.neuroscience.2023.03.020

McGregor, R., A. Matzeu, et al. (2023). "Sensitivity of hypocretin system to chronic alcohol exposure: A human and animal study." Neuroscience. https://doi.org/10.1016/j.neuroscience.2023.04.018

Schoenfeld, T. J., D. Rhee, et al. (2023). "Rewarded maze training increases approach behavior in rats through neurogenesis-dependent growth of ventral hippocampus-prelimbic circuits." Biological Psychiatry Global Open Science. https://doi.org/10.1016/j.bpsgos.2023.04.003

Garrett, L., M. Irmler, et al. (2023). "GPR101 loss promotes insulin resistance and diet-induced obesity risk." Neuroscience Applied: 101126. https://doi.org/10.1016/j.nsa.2023.101126

Abdessattar, K., J. Vidya, et al. (2023). "Syngap1 disruption induced by recombination between inverted loxP sites is associated with hippocampal interneuron dysfunction." eneuro: ENEURO.0475-0422.2023. https://doi.org/10.1523/ENEURO.0475-22.2023

Lazarczyk, M. J., B. A. Eyford, et al. (2023). "The intracellular domain of major histocompatibility class-I proteins is essential for maintaining excitatory spine density and synaptic ultrastructure in the brain." Scientific Reports 13(1): 6448. https://doi.org/10.1038/s41598-023-30054-8

Koehler, C. C., L. S. Almassri, et al. (2023). "Age-related changes of GAD1 mRNA expression in the central inferior colliculus." Translational Medicine of Aging. https://doi.org/10.1016/j.tma.2023.04.001

Liu, H., R. N. Caballero-Florán, et al. (2023). "DSCAM gene triplication causes excessive GABAergic synapses in the neocortex in Down syndrome mouse models." PLOS Biology 21(4): e3002078. https://doi.org/10.1371/journal.pbio.3002078

Williams, S. R., X. Zhou, et al. "Compartment-specific dendritic information processing in striatal cholinergic interneurons is reconfigured by peptide neuromodulation." Neuron. https://doi.org/10.1016/j.neuron.2023.03.038

Yang, L. and J. H. Martin "Effects of motor cortex neuromodulation on the specificity of corticospinal tract spinal axon outgrowth and targeting in rats." Brain Stimulation: Basic, Translational, and Clinical Research in Neuromodulation. https://doi.org/10.1016/j.brs.2023.04.014

Koehler, C. C., L. S. Almassri, et al. (2023). "Age-related changes of GAD1 mRNA expression in the central inferior colliculus." Translational Medicine of Aging. https://doi.org/10.1016/j.tma.2023.04.001

Courtney, K. W., M. G. Kelsey, et al. (2023). "Cross-Platform Synaptic Network Analysis of Human Entorhinal Cortex Identifies TWF2 as a Modulator of Dendritic Spine Length." The Journal of Neuroscience: JN-RM-2102-2122. https://doi.org/10.1523/JNEUROSCI.2102-22.2023

Balkaya, M., P. Dohare, et al. (2023). "Conditional deletion of LRRC8A in the brain reduces stroke damage independently of swelling-activated glutamate release." iScience: 106669. https://doi.org/10.1016/j.isci.2023.106669

Cheung, G., O. Chever, et al. (2023) "Astroglial Connexin 43 Regulates Synaptic Vesicle Release at Hippocampal Synapses." Cells 12 DOI: 10.3390/cells12081133. https://doi.org/10.3390/cells12081133

Courtney, K. W., M. G. Kelsey, et al. (2023). "Cross-Platform Synaptic Network Analysis of Human Entorhinal Cortex Identifies TWF2 as a Modulator of Dendritic Spine Length." The Journal of Neuroscience: JN-RM-2102-2122. https://doi.org/10.1523/JNEUROSCI.2102-22.2023

Quillet, R., A. C. Dickie, et al. (2023). "Characterisation of NPFF-expressing neurons in the superficial dorsal horn of the mouse spinal cord." Scientific Reports 13(1): 5891. https://doi.org/10.1038/s41598-023-32720-3

Roque, S., D. de Sá-Calçada, et al. (2023). "Chronic Mycobacterium avium infection differentially affects the cytokine expression profile of three mouse strains, but has no effect on behavior." Scientific Reports 13(1): 6199. https://doi.org/10.1038/s41598-023-33121-2

Ruskowitz, E. R., B. G. Munoz-Robles, et al. (2023). "Spatiotemporal functional assembly of split protein pairs through a light-activated SpyLigation." Nature Chemistry. https://doi.org/10.1038/s41557-023-01152-x

Hurst, C., D. A. Pugh, et al. (2023). "Integrated Proteomics to Understand the Role of Neuritin (NRN1) as a Mediator of Cognitive Resilience to Alzheimer’s Disease." Molecular & Cellular Proteomics: 100542. https://doi.org/10.1016/j.mcpro.2023.100542

Zhang, Y., A. Bizanti, et al. (2023). "Topographical mapping of catecholaminergic axon innervation in the flat-mounts of the mouse atria: a quantitative analysis." Scientific Reports 13(1): 4850. https://doi.org/10.1038/s41598-023-27727-9

Babb, J. A., A. Zuberer, et al. (2023). "Disturbances in fear extinction learning after mild traumatic brain injury in mice are accompanied by alterations in dendritic plasticity in the medial prefrontal cortex and basolateral nucleus of the amygdala." Brain Research Bulletin. https://doi.org/10.1016/j.brainresbull.2023.04.001

Prevot, T., A. Bernardo, et al. (2023). "Improvement of Cognitive Functions and Neurotrophic Effects Across Animal Models Mediated by A5-GABAA Receptor Positive Allosteric Modulation." Biological Psychiatry 93(9, Supplement): S5. https://doi.org/10.1016/j.biopsych.2023.02.033

Miranda, C. O., K. Hegedüs, et al. (2023) "Synaptic Targets of Glycinergic Neurons in Laminae I–III of the Spinal Dorsal Horn." International Journal of Molecular Sciences 24 DOI: 10.3390/ijms24086943. https://doi.org/10.3390/ijms24086943

Clarity, T., R. Mikofsky, et al. (2023). "Activity-Induced Reshaping of Hippocampal Input-Prefrontal Interneuron Interactions in Wildtype and 22q11.2 Deletion-Relevant Model Mice." Biological Psychiatry 93(9, Supplement): S4-S5. https://doi.org/10.1016/j.biopsych.2023.02.032

Ehlers, J. S., K. Bracke, et al. (2023). "Morphological and behavioral analysis of Slc35f1-deficient mice revealed no neurodevelopmental phenotype." Brain Structure and Function. https://doi.org/10.1007/s00429-023-02629-8

Fard, D., E. Testa, et al. (2023). "SEMA6C: a novel adhesion-independent FAK and YAP activator, required for cancer cell viability and growth." Cellular and Molecular Life Sciences 80(4): 111. https://doi.org/10.1007/s00018-023-04756-1

Gonzalez-Burgos, G., T. Miyamae, et al. (2023). "Mechanisms regulating the properties of inhibition-based gamma oscillations in primate prefrontal and parietal cortices." Cerebral Cortex: bhad077. https://doi.org/10.1093/cercor/bhad077

Meeuwissen, A. J. M., M. Möck, et al. (2023). "Normal connectivity of thalamorecipient networks in barrel equivalents of the reeler cortex." Cerebral Cortex. https://doi.org/10.1093/cercor/bhad072

Morairty, S. R., Y. Sun, et al. (2023). "Activation of the nociceptin/orphanin-FQ receptor promotes NREM sleep and EEG slow wave activity." Proceedings of the National Academy of Sciences 120(13): e2214171120. https://doi.org/10.1073/pnas.2214171120

Sobierajski, E., G. Lauer, et al. (2023). "Development of myelin in fetal and postnatal neocortex of the pig, the European wild boar Sus scrofa." Brain Structure and Function. https://doi.org/10.1007/s00429-023-02633-y

Lewis, V., E. M. Bonniwell, et al. (2023). "A non-hallucinogenic LSD analog with therapeutic potential for mood disorders." Cell Reports 42(3). https://doi.org/10.1016/j.celrep.2023.112203

Coolen, R. L., J. C. Cambier, et al. (2023). "Androgen receptors in the forebrain: a study in adult male cats." Journal of Morphology n/a(n/a). https://doi.org/10.1002/jmor.21553

Jaffey, D. M., J. McAdams, et al. "Vagal Preganglionic Axons Arborize in the Myenteric Plexus into Two Types: Nitrergic and Non-nitrergic Postganglionic Motor Pools?" American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 0(0): null. https://doi.org/10.1152/ajpregu.00260.2022

Marsan, E., D. Velmeshev, et al. (2023). "Astroglial toxicity promotes synaptic degeneration in the thalamocortical circuit in frontotemporal dementia with GRN mutations." The Journal of Clinical Investigation. 10.1172/JCI164919

Pellis, S. M., V. C. Pellis, et al. (2023). "Play fighting and the development of the social brain: The rat’s tale." Neuroscience & Biobehavioral Reviews 145: 105037. https://doi.org/10.1016/j.neubiorev.2023.105037

Fernandes, V., K. Preeti, et al. (2022). “Neuroepigenetic Changes in DNA Methylation Affecting Diabetes-Induced Cognitive Impairment.” Cellular and Molecular Neurobiology. https://doi.org/10.1007/s10571-022-01278-5

Polgár, E., A. C. Dickie, et al. (2022). “Grpr expression defines a population of superficial dorsal horn vertical cells that have a role in both itch and pain.” Pain 11(10): 0000000000002677. DOI: 10.1097/j.pain.0000000000002677

Hellysaz, A., L. Svensson, et al. (2022). “Rotavirus Downregulates Tyrosine Hydroxylase in the Noradrenergic Sympathetic Nervous System in Ileum, Early in Infection and Simultaneously with Increased Intestinal Transit and Altered Brain Activities.” mBio 12(10): 01387-01322. 10.1128/mbio.01387-22

Huang, W., Q. Xu, et al. (2022). “Linking transcriptomes with morphological and functional phenotypes in mammalian retinal ganglion cells.” Cell Reports 40(11): 111322. https://doi.org/10.1016/j.celrep.2022.111322

Ogata, S., Y. Miyamoto, et al. (2022). “The tail of the mouse striatum contains a novel large type of GABAergic neuron incorporated in a unique disinhibitory pathway that relays auditory signals to subcortical nuclei.” The Journal of Neuroscience: JN-RM-2236-2221. https://doi.org/10.1523/JNEUROSCI.2236-21.2022

Srivastava, M., C. Angel, et al. (2022). “Form, synapses and orientation topography of a new cell type in layer 6 of the cat’s primary visual cortex.” Scientific Reports 12(1): 15428. https://doi.org/10.1038/s41598-022-19746-9

Pullin, A. N., V. S. Farrar, et al. (2022). “Providing height to pullets does not influence hippocampal dendritic morphology or brain-derived neurotrophic factor at the end of the rearing period.” Poultry Science: 102161. https://doi.org/10.1016/j.psj.2022.102161

Benraiss, A., J. N. Mariani, et al. (2022). “A TCF7L2-responsive suppression of both homeostatic and compensatory remyelination in Huntington disease mice.” Cell Reports 40(9): 111291. https://doi.org/10.1016/j.celrep.2022.111291

Xu, X., R. O. Beleza, et al. (2022). “Adenosine A2A receptors control synaptic remodeling in the adult brain.” Scientific Reports 12(1): 14690. https://doi.org/10.1038/s41598-022-18884-4

Hatayama, M., K.-i. Katayama, et al. (2022). “SLITRK1-mediated noradrenergic projection suppression in the neonatal prefrontal cortex.” Communications Biology 5(1): 935. https://doi.org/10.1038/s42003-022-03891-y

Imado, E., S. Sun, et al. (2022). “Prenatal exposure to valproic acid causes allodynia associated with spinal microglial activation.” Neurochemistry International 160: 105415. https://doi.org/10.1016/j.neuint.2022.105415

Koukouli, F., M. Montmerle, et al. (2022). “Visual-area-specific tonic modulation of GABA release by endocannabinoids sets the activity and coordination of neocortical principal neurons.” Cell Reports 40(8): 111202. https://doi.org/10.1016/j.celrep.2022.111202

Jiang, S.-N., J.-W. Cao, et al. (2022). “Sncg, Mybpc1, and Parm1 Classify subpopulations of VIP-expressing interneurons in layers 2/3 of the somatosensory cortex.” Cerebral Cortex: bhac343. https://doi.org/10.1093/cercor/bhac343

Fisher, K. M., J. P. Garner, et al. (2022). “Small sensory spinal lesions that affect hand function in monkeys greatly alter primary afferent and motor neuron connections in the cord.” Journal of Comparative Neurology n/a(n/a). https://doi.org/10.1002/cne.25395

Schmidt, S., M. D. Luecken, et al. (2022). “Primary cilia and SHH signaling impairments in human and mouse models of Parkinson’s disease.” Nature Communications 13(1): 4819. https://doi.org/10.1038/s41467-022-32229-9

Kent, M. H., J. C. Jacob, et al. (2022). “Disrupted development from head to tail: Pervasive effects of postnatal restricted resources on neurobiological, behavioral, and morphometric outcomes.” Front Behav Neurosci 16(910056). doi: 10.3389/fnbeh.2022.910056

Jalilian, E., H. Massoumi, et al. (2022). “Bone marrow mesenchymal stromal cells in a 3D system produce higher concentration of extracellular vesicles (EVs) with increased complexity and enhanced neuronal growth properties.” Stem Cell Research & Therapy 13(1): 425. https://doi.org/10.1186/s13287-022-03128-z

Traxler, L., J. R. Herdy, et al. (2022). “Warburg-like metabolic transformation underlies neuronal degeneration in sporadic Alzheimer’s disease.” Cell Metabolism. https://doi.org/10.1016/j.cmet.2022.07.014

Ploppert, E., J. Jacob, et al. (2022). “Influence of Effort-based Reward Training on Neuroadaptive Cognitive Responses: Implications for Preclinical Behavioral Approaches for Depressive Symptoms.” Neuroscience. https://doi.org/10.1016/j.neuroscience.2022.08.002

Stern, S., S. Lau, et al. (2022). “Reduced synaptic activity and dysregulated extracellular matrix pathways in midbrain neurons from Parkinson’s disease patients.” npj Parkinson’s Disease 8(1): 103. https://doi.org/10.1038/s41531-022-00366-z

Fell, C. W., A. Hagelkruys, et al. (2022). “FIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorder.” EMBO Molecular Medicine n/a(n/a): e15829. https://doi.org/10.15252/emmm.202215829

Guimaraes, J. S., N. A. M. Lemos, et al. (2022). “Microelectrode implants, inflammatory response and long-lasting effects on NADPH diaphorase neurons in the rat frontal cortex.” Experimental Brain Research. https://doi.org/10.1007/s00221-022-06434-3

Kersten, Y., B. Friedrich-Müller, et al. (2022). “A brain atlas of the carrion crow (Corvus corone).” Journal of Comparative Neurology n/a(n/a). https://doi.org/10.1002/cne.25392

Hyer, M. M., S. K. Dyer, et al. (2022). “Fructose-Induced Cognitive Impairment Co-occurs with Morphological Changes in Dendrites and Microglia of Male Rats.” Psychoneuroimmunology Journal. DOI:10.32371/pnij/246142

Sohn, J., M. Suzuki, et al. (2022). “Presynaptic supervision of cortical spine dynamics in motor learning.” Science Advances 8(30): eabm0531. DOI: 10.1126/sciadv.abm0531

Mohr, M. A., N. S. Michael, et al. (2022). “Sex differences in proliferation and attrition of pubertally born cells in the rat posterior dorsal medial amygdala.” Developmental Cognitive Neuroscience 57: 101141. https://doi.org/10.1016/j.dcn.2022.101141

Madison, F. N., N. Palin, et al. (2022). “Sex-specific effects of neonatal paternal deprivation on microglial cell density in adult California mouse (Peromyscus californicus) dentate gyrus.” Brain, Behavior, and Immunity 106: 1-10. https://doi.org/10.1016/j.bbi.2022.07.161

Lin, X., T. Zhao, et al. (2022). “7,8-Dihydroxyflavone accelerates recovery of Brown-Sequard syndrome in adult female rats with spinal cord lateral hemisection.” Biomedicine & Pharmacotherapy 153: 113397. https://doi.org/10.1016/j.biopha.2022.113397


Amer, A. and J. H. Martin (2022). “Repeated motor cortex theta-burst stimulation produces persistent strengthening of corticospinal motor output and durable spinal cord structural changes in the rat.” Brain Stimulation. https://doi.org/10.1016/j.brs.2022.07.005


Amalyan, S., S. Tamboli, et al. (2022). “Enhanced motor cortex output and disinhibition in asymptomatic female mice with C9orf72 genetic expansion.” Cell Reports 40(1): 111043. https://doi.org/10.1016/j.celrep.2022.111043


Rahimian, R., K. Perlman, et al. (2022). “Targeting microglia–oligodendrocyte crosstalk in neurodegenerative and psychiatric disorders.” Drug Discovery Today. https://doi.org/10.1016/j.drudis.2022.06.015


Tu, X., X. Li, et al. (2022). “Unilateral cerebral ischemia induces morphological changes in the layer V projection neurons of the contralateral hemisphere.” Neuroscience Research. https://doi.org/10.1016/j.neures.2022.06.007


Jacob, J., S. Watanabe, et al. (2022). “Divergent neural and endocrine responses in wild-caught and laboratory-bred Rattus norvegicus.” Behavioural Brain Research 432: 113978. https://doi.org/10.1016/j.bbr.2022.113978


Taxier, L. R., S. M. Philippi, et al. (2022). “APOE4 homozygote females are resistant to the beneficial effects of 17β-estradiol on memory and CA1 dendritic spine density in the EFAD mouse model of Alzheimer’s disease.” Neurobiology of Aging. https://doi.org/10.1016/j.neurobiolaging.2022.06.005


Wang, M. Z., B. Y. Hayden, et al. (2022). “A structural and functional subdivision in central orbitofrontal cortex.” Nature Communications 13(1): 3623. https://doi.org/10.1038/s41467-022-31273-9


Zhou, J., S. Hormigo, et al. (2022). “Caution influences avoidance and approach behaviors differently.” The Journal of Neuroscience: JN-RM-1892-1821. https://doi.org/10.1523/JNEUROSCI.1892-21.2022


Coverdell, T. C., R.-J. Abraham-Fan, et al. (2022). “Genetic encoding of an esophageal motor circuit.” Cell Reports 39(11): 110962. https://doi.org/10.1016/j.celrep.2022.110962


Xiao, C., D. Lara, et al. (2022). “Netrin-4 modulates corneal wound healing by enhancing corneal epithelium and nerve regeneration in vitro and in vivo.” Investigative Ophthalmology & Visual Science 63(7): 3234 – A0269-3234 – A0269. https://iovs.arvojournals.org/article.aspx?articleid=2781095


Jalilian, E., B. Bigit, et al. (2022). “Exosomes from 3D cultures of Bone Marrow Mesenchymal Stem Cell (BM-MSCs) have higher neuro-regenerative potential than those generated from 2D conditions.” Investigative Ophthalmology & Visual Science 63(7): 1209 – A0209-1209 – A0209. https://iovs.arvojournals.org/article.aspx?articleid=2779796


Khokhar, S. K., M. Kambali, et al. “Role of an enriched environment in ameliorating early life stress-induced changes in structure and functions of hippocampus and amygdala in rats.” Indian Journal of Physiology and Pharmacology 66. doi:10.25259/IJPP_96_2022

Ramos-Prats, A., E. Paradiso, et al. (2022). “VIP-expressing interneurons in the anterior insular cortex contribute to sensory processing to regulate adaptive behavior.” Cell Reports 39(9): 110893. https://doi.org/10.1016/j.celrep.2022.110893


Hagena, H., M. Feldmann, et al. (2022). “Lifelong changes of neurotransmitter receptor expression and debilitation of hippocampal synaptic plasticity following early postnatal blindness.” Scientific Reports 12(1): 9142. https://doi.org/10.1038/s41598-022-13127-y


Kugler, E. C., A. Rampun, et al. (2022). “Analytical Approaches for the Segmentation of the Zebrafish Brain Vasculature.” Current Protocols 2(5): e443. https://doi.org/10.1002/cpz1.443


Puhahn-Schmeiser, B., T. Kleemann, et al. (2022). “Granule cell dispersion in two mouse models of temporal lobe epilepsy and reeler mice is associated with changes in dendritic orientation and spine distribution.” Hippocampus n/a(n/a). https://doi.org/10.1002/hipo.23447


Garcia-Hernandez, R., A. Cerdán Cerdá, et al. “Mapping microglia and astrocyte activation in vivo using diffusion MRI.” Science Advances 8(21): eabq2923. DOI: 10.1126/sciadv.abq2923

Zhou, F., P. Ebea, et al. (2022). “Small Extracellular Vesicles in Milk Cross the Blood-Brain Barrier in Murine Cerebral Cortex Endothelial Cells and Promote Dendritic Complexity in the Hippocampus and Brain Function in C57BL/6J Mice.” Frontiers in nutrition 9: 838543-838543. 10.3389/fnut.2022.838543

van Wageningen, T. A., E. Gerrits, et al. (2020). “Distinct gene expression profiles in leukocortical demyelinated white and grey matter areas of Multiple Sclerosis patients.” bioRxiv: 2020.2006.2003.131300. https://doi.org/10.1101/2020.06.03.131300


Zambon, A., L. C. Rico, et al. (2022). “Gestational immune activation disrupts hypothalamic neurocircuits of maternal care behavior.” Molecular Psychiatry. https://doi.org/10.1038/s41380-022-01602-x 


Nelson, D. W., D. L. Puhl, et al. (2022). “Multivariate analysis reveals topography dependent relationships amongst neurite morphological features from dorsal root ganglia neurons.” Journal of Neural Engineering. https://doi.org/10.1088/1741-2552/ac7078 


Anstötz, M., S. K. Lee, et al. (2022). “Glutamate released by Cajal-Retzius cells impacts specific hippocampal circuits and behaviors.” Cell Reports 39(7): 110822. https://doi.org/10.1016/j.celrep.2022.110822 


Guo, S., J. Xue, et al. (2022). “Smart imaging to empower brain-wide neuroscience at single-cell levels.” Brain Informatics 9(1): 10. https://doi.org/10.1186/s40708-022-00158-4


Ichise, M., K. Sakoori, et al. (2022). “Leucine-Rich Repeats and Transmembrane Domain 2 Controls Protein Sorting in the Striatal Projection System and Its Deficiency Causes Disturbances in Motor Responses and Monoamine Dynamics.” Frontiers in Molecular Neuroscience 15. https://doi.org/10.3389/fnmol.2022.856315


Zhou, L., G. Kong, et al. “Reversible CD8 T cell–neuron cross-talk causes aging-dependent neuronal regenerative decline.” Science 376(6594): eabd5926. DOI: 10.1126/science.abd5926

Huang, W., Q. Xu, et al. (2022). “Identification of TPBG-Expressing Amacrine Cells in DAT-tdTomato Mouse.” Investigative Ophthalmology & Visual Science 63(5): 13-13. https://doi.org/10.1167/iovs.63.5.13


Ma, J., D. Nguyen, et al. (2022). “Spinal Afferent Innervation of the Rat Stomach: Anterograde Tracing.” The FASEB Journal 36(S1). https://doi.org/10.1096/fasebj.2022.36.S1.R5454


Maloney, S. E., D. R. Tabachnick, et al. (2022). “Fluoxetine exposure throughout neurodevelopment differentially influences basilar dendritic morphology in the motor and prefrontal cortices.” Scientific Reports 12(1): 7605. https://doi.org/10.1038/s41598-022-11614-w


Papes, F., A. P. Camargo, et al. (2022). “Transcription Factor 4 loss-of-function is associated with deficits in progenitor proliferation and cortical neuron content.” Nature Communications 13(1): 2387. https://doi.org/10.1038/s41467-022-29942-w


Sun, W., X. Chen, et al. (2022). “Prelimbic proBDNF Facilitates Retrieval-Dependent Fear Memory Destabilization by Regulation of Synaptic and Neural Functions in Juvenile Rats.” Molecular Neurobiology. https://doi.org/10.1007/s12035-022-02849-9


Gegenhuber, B., M. V. Wu, et al. (2022). “Gene regulation by gonadal hormone receptors underlies brain sex differences.” Nature. https://doi.org/10.1038/s41586-022-04686-1


Ardizzone, A., V. Bova, et al. (2022). "SUN11602, a bFGF mimetic, modulated neuroinflammation, apoptosis and calcium-binding proteins in an in vivo model of MPTP-induced nigrostriatal degeneration." Journal of Neuroinflammation 19(1): 107. https://doi.org/10.1186/s12974-022-02457-3


Csabai, D., A. Sebők-Tornai, et al. (2022). "A Preliminary Quantitative Electron Microscopic Analysis Reveals Reduced Number of Mitochondria in the Infralimbic Cortex of Rats Exposed to Chronic Mild Stress." Frontiers in Behavioral Neuroscience 16. https://doi.org/10.3389/fnbeh.2022.885849


Maehata, K., K. Shimizu, et al. (2020). "Hippocampal 7α-Hydroxylated Neurosteroids Are Raised by Training and Bolster Remote Spatial Memory with Increase of the Spine Densities." iScience 23(10): 101559. https://doi.org/10.1016/j.isci.2020.101559


Prevot, T., A. Bernardo, et al. (2022). "P99. Role of α5-GABAA Receptor Positive Allosteric Modulation on Cognitive Functions and Neurotrophic Effects Across Animal Models." Biological Psychiatry 91(9): S127. https://doi.org/10.1016/j.biopsych.2022.02.333


Ali, Z., G. Sivakumar, et al. (2022). "A report on digitised neuronal tracing method to study neurons in their entirety." MethodsX: 101715. https://doi.org/10.1016/j.mex.2022.101715


Boda, E., M. Lorenzati, et al. (2022). "Molecular and functional heterogeneity in dorsal and ventral oligodendrocyte progenitor cells of the mouse forebrain in response to DNA damage." Nature Communications 13(1): 2331. https://doi.org/10.1038/s41467-022-30010-6


Saini, V., D. Lutz, et al. (2016). "The polysialic acid mimetics 5-nonyloxytryptamine and vinorelbine facilitate nervous system repair." Scientific Reports 6(1): 26927. https://doi.org/10.1038/srep26927


Costa, V. S., A. O. B. Suassuna, et al. (2022). Immediate Cortical and Spinal C-Fos Immunoreactivity After ICMS of the Primary Somatosensory Cortex in Rats. XXVII Brazilian Congress on Biomedical Engineering, Cham, Springer International Publishing. https://doi.org/10.1007/978-3-030-70601-2_330


Shotaro Tanaka and Fumio Nakamura, “Exploring the Bio-Functional Breaking Point of Living Tissue Subjected to External Physical Pressure,” J. Robot. Mechatron., Vol.34, No.2, pp. 319-321, 2022. doi: 10.20965/jrm.2022.p0319

Catale, C., L. Lo Iacono, et al. (2022). "Early Life Social Stress Causes Sex- and Region-Dependent Dopaminergic Changes that Are Prevented by Minocycline." Molecular Neurobiology. https://doi.org/10.1007/s12035-022-02830-6


El Khoueiry, C., C. Alba-Delgado, et al. (2022). "GABAA and Glycine Receptor-Mediated Inhibitory Synaptic Transmission onto Adult Rat Lamina IIi PKCγ-Interneurons: Pharmacological but Not Anatomical Specialization." Cells 11(8): 1356. https://doi.org/10.3390/cells11081356


Park, H. H., Y.-M. Kim, et al. (2022). "Dual-functional hydrogel system for spinal cord regeneration with sustained release of arylsulfatase B alleviates fibrotic microenvironment and promotes axonal regeneration." Biomaterials 284: 121526. https://doi.org/10.1016/j.biomaterials.2022.121526


Georgiou, C., V. Kehayas, et al. (2022). "A subpopulation of cortical VIP-expressing interneurons with highly dynamic spines." Communications Biology 5(1): 352. https://doi.org/10.1038/s42003-022-03278-z


Balsamo, G., E. Blanco-Hernández, et al. (2022). "Modular microcircuit organization of the presubicular head-direction map." Cell Reports 39(2): 110684. https://doi.org/10.1016/j.celrep.2022.110684


Dhar, S., S. Gadd, et al. (2022). "A tumor suppressor role for EZH2 in diffuse midline glioma pathogenesis." Acta Neuropathologica Communications 10(1): 47. https://doi.org/10.1186/s40478-022-01336-5


Hibbard, E. A. and D. R. Sengelaub (2022). "Intraneural Topography of Rat Sciatic Axons: Implications for Polyethylene Glycol Fusion Peripheral Nerve Repair." Frontiers in Cellular Neuroscience 16. https://doi.org/10.3389/fncel.2022.852933


Stables, J., E. K. Green, et al. (2022). "A kinase-dead Csf1r mutation associated with adult-onset leukoencephalopathy has a dominant inhibitory impact on CSF1R signalling." Development 149(8). https://doi.org/10.1242/dev.200237


Inagaki, M., K.-i. Inoue, et al. (2022). "Rapid processing of threatening faces in the amygdala of nonhuman primates: subcortical inputs and dual roles." Cerebral Cortex: bhac109. https://doi.org/10.1093/cercor/bhac109


Stella, T., K. Alexandros, et al. (2022). Research Square. 10.21203/rs.3.rs-882180/v1

Souza, G. M. P. R., R. L. Stornetta, et al. (2022). "Adrenergic C1 neurons monitor arterial blood pressure and determine the sympathetic response to hemorrhage." Cell Reports 38(10): 110480. https://doi.org/10.1016/j.celrep.2022.110480


McKinney, A., M. Hu, et al. (2022). "Cellular and Circuit Organization of the Locus Coeruleus of Adult Mice." bioRxiv: 2022.2003.2001.481656. https://doi.org/10.1101/2022.03.01.481656


Iavarone, E., J. Simko, et al. (2022). "Reconstruction and simulation of thalamoreticular microcircuitry." bioRxiv: 2022.2002.2028.482273. https://doi.org/10.1101/2022.02.28.482273


Inagaki, H. K., S. Chen, et al. (2022). "A midbrain-thalamus-cortex circuit reorganizes cortical dynamics to initiate movement." Cell. https://doi.org/10.1016/j.cell.2022.02.006


Murase, S., S. E. Robertson, et al. (2022). "Chronic Monocular Deprivation Reveals MMP9-Dependent and -Independent Aspects of Murine Visual System Plasticity." International Journal of Molecular Sciences 23(5). 10.3390/ijms23052438

Rusznák, K., Á. I. Horváth, et al. (2022). "Experimental Arthritis Inhibits Adult Hippocampal Neurogenesis in Mice." Cells 11(5). 10.3390/cells11050791

Chen, S., H. Xu, et al. (2022). "Morpho-Electric Properties and Diversity of Oxytocin Neurons in Paraventricular Nucleus of Hypothalamus in Female and Male Mice." The Journal of Neuroscience: JN-RM-2494-2421. 10.1523/jneurosci.2494-21.2022

Ivan, B., S. Dora, et al. (2022). Molecular Neurobiology. 10.21203/rs.3.rs-1351458/v1

Neubauer, F. B., R. Min, et al. (2022). "Presynaptic NMDA Receptors Influence Ca<sup>2+</sup> Dynamics by Interacting with Voltage-Dependent Calcium Channels during the Induction of Long-Term Depression." Neural Plasticity 2022: 2900875. https://doi.org/10.1155/2022/2900875


Rogers, D. J., B. P. Bergeron, et al. (2022). "3D printed chamber for live cell imaging on an upright epifluorescence microscope." Journal of Biological Education: 1-7. https://doi.org/10.1080/00219266.2022.2030389


Tanaka, S., K. Takizawa, et al. (2022). "One-step visualization of natural cell activities in non-labeled living spheroids." Scientific Reports 12(1): 1500. https://doi.org/10.1038/s41598-022-05347-z


Purkart, L., J. M. Tuff, et al. (2022). "Trigeminal ganglion and sensory nerves suggest tactile specialization of elephants." Current Biology. https://doi.org/10.1016/j.cub.2021.12.051


Chalif, J. I., M. d. L. Martínez-Silva, et al. (2022). "Control of mammalian locomotion by ventral spinocerebellar tract neurons." Cell 185(2): 328-344.e326. https://doi.org/10.1016/j.cell.2021.12.014


Vomero, M., F. Ciarpella, et al. (2022). "On the longevity of flexible neural interfaces: Establishing biostability of polyimide-based intracortical implants." Biomaterials 281: 121372. https://doi.org/10.1016/j.biomaterials.2022.121372


Perumal, M. B. and P. Sah (2022). "A protocol to investigate cellular and circuit mechanisms generating sharp wave ripple oscillations in rodent basolateral amygdala using ex vivo slices." STAR Protocols 3(1): 101085. https://doi.org/10.1016/j.xpro.2021.101085


Fernández-Pérez, A., A. Sanz-Magro, et al. (2022). "Restricting feeding to dark phase fails to entrain circadian activity and energy expenditure oscillations in Pitx3-mutant Aphakia mice." Cell Reports 38(2): 110241. https://doi.org/10.1016/j.celrep.2021.110241


Jakovcevski, I., D. von, et al. (2022). "Mice lacking perforin have improved regeneration of the injured femoral nerve." Neural Regeneration Research 17(8): 1802-1808. DOI: 10.4103/1673-5374.332152

Clabough, E., J. Ingersoll, et al. (2022). "Acute Ethanol Exposure during Synaptogenesis Rapidly Alters Medium Spiny Neuron Morphology and Synaptic Protein Expression in the Dorsal Striatum." International Journal of Molecular Sciences 23(1). https://doi.org/10.3390/ijms23010290


Goeke, C. M., X. Zhang, et al. (2022). "Astrocyte tissue plasminogen activator expression during brain development and its role in pyramidal neuron neurite outgrowth." Neuroscience Letters 769: 136422. https://doi.org/10.1016/j.neulet.2021.136422


Jenny, A. B. and P. D. Cheney (2022). "Monkey flexor and abductor pollicis brevis motoneuron pools: Proximal dendritic trees and small motoneurons." Neuroscience Letters 769: 136429. https://doi.org/10.1016/j.neulet.2021.136429


Spoleti, E., P. Krashia, et al. (2021). "Early derailment of firing properties in CA1 pyramidal cells of the ventral hippocampus in an Alzheimer's disease mouse model." Experimental Neurology: 113969. https://doi.org/10.1016/j.expneurol.2021.113969


Qiu, Y., X.-j. Xue, et al. (2021). "Perillaldehyde improves cognitive function in vivo and in vitro by inhibiting neuronal damage via blocking TRPM2/NMDAR pathway." Chinese Medicine 16(1): 136. https://doi.org/10.1186/s13020-021-00545-9


Barak, T., E. Ristori, et al. (2021). "PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans." Nature Medicine 27(12): 2165-2175. https://doi.org/10.1038/s41591-021-01572-7


Patel, A. V., S. A. Codeluppi, et al. (2021). "Developmental Age and Biological Sex Influence Muscarinic Receptor Function and Neuron Morphology within Layer VI of the Medial Prefrontal Cortex." Cerebral Cortex: bhab406. https://doi.org/10.1093/cercor/bhab406


Lebowitz, J. J., M. Trinkle, et al. (2021). "Subcellular localization of D2 receptors in the murine substantia nigra." Brain Structure and Function. https://doi.org/10.1007/s00429-021-02432-3


Sobierajski, E., G. Lauer, et al. (2021). "Development of microglia in fetal and postnatal neocortex of the pig, the European wild boar (Sus scrofa)." Journal of Comparative Neurology n/a(n/a). https://doi.org/10.1002/cne.25280


Gonzalez, S., T. L. M. McHugh, et al. (2022). "Small molecule modulation of TrkB and TrkC neurotrophin receptors prevents cholinergic neuron atrophy in an Alzheimer's disease mouse model at an advanced pathological stage." Neurobiology of Disease 162: 105563. https://doi.org/10.1016/j.nbd.2021.105563


Rotterman, T. M., D. I. Carrasco, et al. (2021). "Axon initial segment geometry in relation to motoneuron excitability." PLOS ONE 16(11): e0259918. https://doi.org/10.1371/journal.pone.0259918


Hogg, P. W., P. Coleman, et al. (2021). "Quantifying neuronal structural changes over time using dynamic morphometrics." Trends in Neurosciences. https://doi.org/10.1016/j.tins.2021.10.011


Prokop, S., P. Ábrányi-Balogh, et al. (2021). "PharmacoSTORM nanoscale pharmacology reveals cariprazine binding on Islands of Calleja granule cells." Nature Communications 12(1): 6505. https://doi.org/10.1038/s41467-021-26757-z


Natale, N. R., M. Kent, et al. (2021). "Neurobiological effects of a probiotic-supplemented diet in chronically stressed male Long-Evans rats: Evidence of enhanced resilience." IBRO Neuroscience Reports. https://doi.org/10.1016/j.ibneur.2021.10.004


Sheikh, A., X. Meng, et al. (2021). "Neonatal Hypoxia-Ischemia Causes Persistent Intracortical Circuit Changes in Layer 4 of Rat Auditory Cortex." Cerebral Cortex(bhab365). https://doi.org/10.1093/cercor/bhab365


Trujillo-Estrada, L., P. W. Vanderklish, et al. (2021). "SPG302 Reverses Synaptic and Cognitive Deficits Without Altering Amyloid or Tau Pathology in a Transgenic Model of Alzheimer’s Disease." Neurotherapeutics. https://doi.org/10.1007/s13311-021-01143-1


Yang, C., Y. Tian, et al. (2021). "Restoration of FMRP expression in adult V1 neurons rescues visual deficits in a mouse model of fragile X syndrome." Protein & Cell. https://doi.org/10.1007/s13238-021-00878-z


Oberto, V. J., C. J. Boucly, et al. (2021). "Distributed cell assemblies spanning prefrontal cortex and striatum." Current Biology. https://doi.org/10.1016/j.cub.2021.10.007


Liu, J., Z. Deng, et al. (2021). "The circRNA circ-Nbea participates in regulating diabetic encephalopathy." Brain Research: 147702. https://doi.org/10.1016/j.brainres.2021.147702


Bourel, J., V. Planche, et al. (2021). "Complement C3 mediates early hippocampal neurodegeneration and memory impairment in experimental multiple sclerosis." Neurobiology of Disease 160: 105533. https://doi.org/10.1016/j.nbd.2021.105533


Xie, S., H. Li, et al. (2021). "PUPIL enables mapping and stamping of transient electrical connectivity in developing nervous systems." Cell Reports 37(3): 109853. https://doi.org/10.1016/j.celrep.2021.109853


Kolk, S. M. and P. Rakic (2021). "Development of prefrontal cortex." Neuropsychopharmacology. https://doi.org/10.1038/s41386-021-01137-9


Morecraft, R. J., K. S. Stilwell-Morecraft, et al. (2021). "Lack of somatotopy among corticospinal tract fibers passing through the primate craniovertebral junction and cervical spinal cord: pathoanatomical substrate of central cord syndrome and cruciate paralysis." Journal of Neurosurgery: 1-15. https://doi.org/10.3171/2021.4.JNS202464


Matho, K. S., D. Huilgol, et al. (2021). "Genetic dissection of the glutamatergic neuron system in cerebral cortex." Nature 598(7879): 182-187. https://doi.org/10.1038/s41586-021-03955-9


Gentili, M., L. Hidalgo-Garcia, et al. (2021). "A recombinant glucocorticoid-induced leucine zipper protein ameliorates symptoms of dextran sulfate sodium-induced colitis by improving intestinal permeability." The FASEB Journal 35(11): e21950. https://doi.org/10.1096/fj.202100778RRRR


Lane, A. R., I. C. Cogdell, et al. (2021). "Genetic targeting of adult Renshaw cells using a Calbindin 1 destabilized Cre allele for intersection with Parvalbumin or Engrailed1." Scientific Reports 11(1): 19861. https://doi.org/10.1038/s41598-021-99333-6


Medalla, M., W. Chang, et al. (2021). "Layer-specific pyramidal neuron properties underlie diverse anterior cingulate cortical motor and limbic networks." Cerebral Cortex(bhab347). https://doi.org/10.1093/cercor/bhab347


Sarkar, D., M. Shariq, et al. (2021). "Adult brain neurons require continual expression of the schizophrenia-risk gene Tcf4 for structural and functional integrity." Translational Psychiatry 11(1): 494. https://doi.org/10.1038/s41398-021-01618-x


Yang, F.-C., L. B. Dokovna, et al. (2021). "Functional Differentiation of Dorsal and Ventral Posterior Parietal Cortex of the Rat: Implications for Controlled and Stimulus-Driven Attention." Cerebral Cortex(bhab308). https://doi.org/10.1093/cercor/bhab308


Heyer, D. B., R. Wilbers, et al. (2021). "Verbal and General IQ Associate with Supragranular Layer Thickness and Cell Properties of the Left Temporal Cortex." Cerebral Cortex(bhab330). https://doi.org/10.1093/cercor/bhab330


Noftz, W. A., N. L. Beebe, et al. (2021). "Dense cholinergic projections to auditory and multisensory nuclei of the intercollicular midbrain." Hearing Research 411: 108352. https://doi.org/10.1016/j.heares.2021.108352


Watanabe, S., T. Kurotani, et al. (2021). "Functional and molecular characterization of a non-human primate model of autism spectrum disorder shows similarity with the human disease." Nature Communications 12(1): 5388. https://doi.org/10.1038/s41467-021-25487-6


Masachs, N., V. Charrier, et al. (2021). "The temporal origin of dentate granule neurons dictates their role in spatial memory." Molecular Psychiatry. https://doi.org/10.1038/s41380-021-01276-x


Guzun, L., P. Fortier-Poisson, et al. (2021). "Tactile sensitivity in the rat: a correlation between receptor structure and function." Experimental Brain Research. https://doi.org/10.1007/s00221-021-06193-7


Abate, G., Colazingari, S., Accoto, A., Conversi, D., & Bevilacqua, A. (2018). Dendritic spine density and EphrinB2 levels of hippocampal and anterior cingulate cortex neurons increase sequentially during formation of recent and remote fear memory in the mouse. Behavioural Brain Research. doi. https://www.sciencedirect.com/science/article/pii/S0166432817313888


Abbasi, S., & Kumar, S. S. (2014). Regular-spiking cells in the presubiculum are hyperexcitable in a rat model of Temporal Lobe Epilepsy. Journal of Neurophysiology, jn. 00406.02014. doi. 

Abbasi, S., & Kumart, S. S. (2013). Electrophysiological and morphological characterization of cells in superficial layers of rat presubiculum. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23365. http://dx.doi.org/10.1002/cne.23365


Abbott, S. B., Kanbar, R., Bochorishvili, G., Coates, M. B., Stornetta, R. L., & Guyenet, P. G. (2012). C1 neurons excite locus coeruleus and A5 noradrenergic neurons along with sympathetic outflow in rats. Journal of Physiology. doi. 

Abbott, S. B. G., DePuy, S. D., Nguyen, T., Coates, M. B., Stornetta, R. L., & Guyenet, P. G. (2013). Selective Optogenetic Activation of Rostral Ventrolateral Medullary Catecholaminergic Neurons Produces Cardiorespiratory Stimulation in Conscious Mice. Journal of Neuroscience, 33(7), 3164-3177. doi: 10.1523/jneurosci.1046-12.2013. http://www.jneurosci.org/content/33/7/3164.abstract


Abbott, S. B. G., Holloway, B. B., Viar, K. E., & Guyenet, P. G. (2013). Vesicular glutamate transporter 2 is required for the respiratory and parasympathetic activation produced by optogenetic stimulation of catecholaminergic neurons in the rostral ventrolateral medulla of mice in vivo. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12421. http://dx.doi.org/10.1111/ejn.12421


Abbott, S. B. G., Stornetta, R. L., Coates, M. B., & Guyenet, P. G. (2011). Phox2b-Expressing Neurons of the Parafacial Region Regulate Breathing Rate, Inspiration, and Expiration in Conscious Rats. Journal of Neuroscience, 31(45), 16410-16422. doi: 10.1523/jneurosci.3280-11.2011. http://www.jneurosci.org/content/31/45/16410.abstract


Abbott, S. B. G., Stornetta, R. L., Fortuna, M. G., Depuy, S. D., West, G. H., Harris, T. E., & Guyenet, P. G. (2009). Photostimulation of Retrotrapezoid Nucleus Phox2b-Expressing Neurons In Vivo Produces Long-Lasting Activation of Breathing in Rats. Journal of Neuroscience, 29(18), 5806-5819. doi: 10.1523/jneurosci.1106-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/18/5806 


Abbott, S. B. G., Stornetta, R. L., Socolovsky, C. S., West, G. H., & Guyenet, P. G. (2009). Photostimulation of channelrhodopsin-2 expressing ventrolateral medullary neurons increases sympathetic nerve activity and blood pressure in rats. Journal of Physiology, 587(23), 5613-5631. doi. 

Abdellah, M., Hernando, J., Eilemann, S., Lapere, S., Antille, N., Markram, H., & Schürmann, F. (2018). NeuroMorphoVis: a collaborative framework for analysis and visualization of neuronal morphology skeletons reconstructed from microscopy stacks. Bioinformatics, 34(13), i574-i582. doi: 10.1093/bioinformatics/bty231. http://dx.doi.org/10.1093/bioinformatics/bty231


Abdel-Rahman, A., Rao, M. S., & Shetty, A. K. (2004). Nestin expression in hippocampal astrocytes after injury depends on the age of the hippocampus. Glia, 47(4), 299-313. doi. 

Abdolhoseini, M., Walker, F., & Johnson, S. (2016, 16-20 Aug. 2016). Automated tracing of microglia using multilevel thresholding and minimum spanning trees. Paper presented at the 2016 38th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC).

Abe, C., Inoue, T., Inglis, M. A., Viar, K. E., Huang, L., Ye, H., . . . Guyenet, P. G. (2017). C1 neurons mediate a stress-induced anti-inflammatory reflex in mice. [Article]. Nature Neuroscience, advance online publication. doi: 10.1038/nn.4526

http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.4526.html#suppl.... http://dx.doi.org/10.1038/nn.4526


Abel, P. L., O'Brien, B. J., & Olavarria, J. F. (2000). Organization of callosal linkages in visual area V2 of macaque monkey. Journal of Comparative Neurology, 428(2), 278-293. doi. 

Abel, T. W., & Rance, N. E. (1999). Proopiomelanocortin gene expression is decreased in the infundibular nucleus of postmenopausal women. Molecular Brain Research, 69(2), 202-208. doi. 

Abel, T. W., Voytko, M. L., & Rance, N. E. (1999). The effects of hormone replacement therapy on hypothalamic neuropeptide gene expression in a primate model of menopause. Journal of Clinical Endocrinology and Metabolism, 84(6), 2111-2118. doi. http://www.ncbi.nlm.nih.gov/pubmed/10372719


Abelson, J. F., Kwan, K. Y., O'Roak, B. J., Baek, D. Y., Stillman, A. A., Morgan, T. M., . . . State, M. W. (2005). Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome. Science, 310(5746), 317-320. doi: 10.1126/science.1116502. http://www.sciencemag.org/cgi/content/abstract/310/5746/317 


Ables, J. L., DeCarolis, N. A., Johnson, M. A., Rivera, P. D., Gao, Z., Cooper, D. C., . . . Eisch, A. J. (2010). Notch1 Is Required for Maintenance of the Reservoir of Adult Hippocampal Stem Cells. Journal of Neuroscience, 30(31), 10484-10492. doi: 10.1523/jneurosci.4721-09.2010. http://www.jneurosci.org/cgi/content/abstract/30/31/10484 


Ábrahám, H., & Lázár, G. (2000). Early microglial reaction following mild forebrain ischemia induced by common carotid artery occlusion in rats. Brain Research, 862(1-2), 63-73. doi. 

Abraham, H., & Meyer, G. (2003). Reelin-expressing neurons in the postnatal and adult human hippocampal formation. Hippocampus, 13(6), 715-727. doi. 

Abrahám, H., Orsi, G., & Seress, L. (2007). Ontogeny of cocaine-and amphetamine-regulated transcript (CART) peptide and calbindin immunoreactivity in granule cells of the dentate gyrus in the rat. International Journal of Developmental Neuroscience, 25(5), 265-274. doi. 

Ábrahám, H., Richter, Z., Gyimesi, C., Horváth, Z., Janszky, J., Dóczi, T., & Seress, L. (2011). Degree and pattern of calbindin immunoreactivity in granule cells of the dentate gyrus differ in mesial temporal sclerosis, cortical malformation-and tumor-related epilepsies. Brain Research. doi. 

Ábrahám, H., Somogyvari-Vigh, A., Maderdrut, J. L., Vigh, S., & Arimura, A. (2003). Rapidly activated microglial cells in the preoptic area may play a role in the generation of hyperthermia following occlusion of the middle cerebral artery in the rat. Experimental Brain Research, 153(1), 84-91. doi. 

Ábrahám, H., Tornóczky, T., Kosztolányi, G., & Seress, L. (2001). Cell formation in the cortical layers of the developing human cerebellum. International Journal of Developmental Neuroscience, 19(1), 53-62. doi. 

Ábrahám, H., Tornóczky, T., Kosztolányi, G., & Seress, L. (2004). Cell proliferation correlates with the postconceptual and not with the postnatal age in the hippocampal dentate gyrus, temporal neocortex and cerebellar cortex of preterm infants. Early Human Development, 78(1), 29-43. doi. 

Abraham, H., Tóth, Z., Bari, F., Domoki, F., & Seress, L. (2005). Novel calretinin and reelin expressing neuronal population includes Cajal-Retzius-type cells in the neocortex of adult pigs. Neuroscience, 136(1), 217-230. doi. 

Abulafia, D. P., de Rivero Vaccari, J. P., Lozano, J. D., Lotocki, G., Keane, R. W., & Dietrich, W. D. (2008). Inhibition of the inflammasome complex reduces the inflammatory response after thromboembolic stroke in mice. Journal of Cerebral Blood Flow Metabolism. doi. http://dx.doi.org/10.1038/jcbfm.2008.143 


Abulafia, R., Zalkind, V., & Devor, M. (2009). Cerebral Activity during the Anesthesia-Like State Induced by Mesopontine Microinjection of Pentobarbital. Journal of Neuroscience, 29(21), 7053-7064. doi: 10.1523/jneurosci.1357-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/21/7053 


Acabchuk, R., Briggs, D. I., Angoa-Pérez, M., Powers, M., Wolferz, R., Soloway, M., . . . Conover, J. C. (2016). Repeated mild traumatic brain injury causes focal response in lateral septum and hippocampus. Concussion. doi: 10.2217/cnc-2015-0001. http://dx.doi.org/10.2217/cnc-2015-0001


Acabchuk, R. L., Sun, Y., Wolferz, J. R., Eastman, M. B., Lennington, J. B., Shook, B. A., . . . Conover, J. C. (2015). 3D Modeling of the Lateral Ventricles and Histological Characterization of Periventricular Tissue in Humans and Mouse. JoVE, (99), e52328. doi: doi:10.3791/52328. http://www.jove.com/video/52328


Aceti, M., Vetere, G., Novembre, G., Restivo, L., & Ammassari-Teule, M. (2015). Progression of activity and structural changes in the anterior cingulate cortex during remote memory formation. Neurobiology of Learning and Memory, (0). doi: http://dx.doi.org/10.1016/j.nlm.2015.05.003. http://www.sciencedirect.com/science/article/pii/S1074742715000866


Aceves, M., Bancroft, E., Aceves, A. R., & Hook, M. (2016). NorBNI blocks the adverse effects of morphine following spinal cord injury. Journal of Neurotrauma. doi: 10.1089/neu.2016.4601. http://dx.doi.org/10.1089/neu.2016.4601


Aceves, M., Terminel, M. N., Okoreeh, A., Aceves, A. R., Ming Gong, Y., Polanco, A., . . . Hook, M. A. (2019). Morphine increases macrophages at the lesion site following spinal cord injury: Protective effects of minocycline. Brain, Behavior, and Immunity. doi: https://doi.org/10.1016/j.bbi.2019.01.023. http://www.sciencedirect.com/science/article/pii/S0889159119300790


Acker, C. D., & Antic, S. D. (2009). Quantitative assessment of the distributions of membrane conductances involved in action potential backpropagation along basal dendrites. Journal of Neurophysiology, 101(3), 1524-1541. doi. 

Ackermann, J., Ashton, G., Lyons, S., James, D., Hornung, J. P., Jones, N., & Breitwieser, W. (2011). Loss of ATF2 function leads to cranial motoneuron degeneration during embryonic mouse development. PLoS ONE, 6(4), e19090-e19090. doi. 

Ackley, M. A., Hurley, R. W., Virnich, D. E., & Hammond, D. L. (2001). A cellular mechanism for the antinociceptive effect of a< i> kappa</i> opioid receptor agonist. Pain, 91(3), 377-388. doi. 

Acsady, L., Kamondi, A., Sik, A., Freund, T., & Buzsaki, G. (1998). GABAergic Cells Are the Major Postsynaptic Targets of Mossy Fibers in the Rat Hippocampus. Journal of Neuroscience, 18(9), 3386-3403. doi. http://www.jneurosci.org/cgi/content/abstract/18/9/3386


Adachi, K., Fujita, S., Yoshida, A., Sakagami, H., Koshikawa, N., & Kobayashi, M. (2012). Anatomical and electrophysiological mechanisms for asymmetrical excitatory propagation in the rat insular cortex: in vivo optical imaging and whole-cell patch-clamp studies. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23246. http://dx.doi.org/10.1002/cne.23246


Adams, V. L., Goodman, R. L., Salm, A. K., Coolen, L. M., Karsch, F. J., & Lehman, M. N. (2006). Morphological Plasticity in the Neural Circuitry Responsible for Seasonal Breeding in the Ewe. Endocrinology, 147(10), 4843-4851. doi: 10.1210/en.2006-0408. http://endo.endojournals.org/cgi/content/abstract/147/10/4843 


Adar, E., Nottebohm, F., & Barnea, A. (2008). The Relationship between Nature of Social Change, Age, and Position of New Neurons and Their Survival in Adult Zebra Finch Brain. Journal of Neuroscience, 28(20), 5394-5400. doi: 10.1523/jneurosci.5706-07.2008. http://www.jneurosci.org/cgi/content/abstract/28/20/5394 


Adesnik, H., Li, G., During, M. J., Pleasure, S. J., & Nicoll, R. A. (2008). NMDA receptors inhibit synapse unsilencing during brain development. Proceedings of the National Academy of Sciences, 105(14), 5597-5602. doi: 10.1073/pnas.0800946105. http://www.pnas.org/cgi/content/abstract/105/14/5597 


Adkins, D. A. L., Bury, S. D., & Jones, T. A. (2002). Laminar-dependent dendritic spine alterations in the motor cortex of adult rats following callosal transection and forced forelimb use. Neurobiology of Learning and Memory, 78(1), 35-52. doi. 

Adkins, D. A. L., Campos, P., Quach, D., Borromeo, M., Schallert, K., & Jones, T. A. (2006). Epidural cortical stimulation enhances motor function after sensorimotor cortical infarcts in rats. Experimental Neurology, 200(2), 356-370. doi. 

Adkins, D. A. L., Hsu, J. E., & Jones, T. A. (2008). Motor cortical stimulation promotes synaptic plasticity and behavioral improvements following sensorimotor cortex lesions. Experimental Neurology, 212(1), 14-28. doi. 

Adkins, D. A. L., & Jones, T. A. (2005). D-amphetamine enhances skilled reaching after ischemic cortical lesions in rats. Neuroscience Letters, 380(3), 214-218. doi. 

Adler, S. M., Girotti, M., & Morilak, D. A. (2020). Optogenetically-induced long term depression in the rat orbitofrontal cortex ameliorates stress-induced reversal learning impairment. Neurobiology of Stress, 13, 100258. doi: https://doi.org/10.1016/j.ynstr.2020.100258. http://www.sciencedirect.com/science/article/pii/S2352289520300485


Adler, W. T., Platt, M. P., Mehlhorn, A. J., Haight, J. L., Currier, T. A., Etchegaray, M. A., . . . Rosen, G. D. (2013). Position of Neocortical Neurons Transfected at Different Gestational Ages with shRNA Targeted against Candidate Dyslexia Susceptibility Genes. PLoS ONE, 8(5), e65179. doi: 10.1371/journal.pone.0065179. http://dx.doi.org/10.1371%2Fjournal.pone.0065179


Adolf, A., Leondaritis, G., Rohrbeck, A., Eickholt, B. J., Just, I., Ahnert-Hilger, G., & Höltje, M. (2016). The intermediate filament protein vimentin is essential for axonotrophic effects of Clostridium botulinum C3 exoenzyme. Journal of Neurochemistry, n/a-n/a. doi: 10.1111/jnc.13739. http://dx.doi.org/10.1111/jnc.13739


Advani, A., Connelly, K. A., Yuen, D. A., Zhang, Y., Advani, S. L., Trogadis, J., . . . others. (2011). Fluorescent Microangiography Is a Novel and Widely Applicable Technique for Delineating the Renal Microvasculature. PLoS ONE, 6(10), e24695-e24695. doi. 

Afroz, S., Shen, H., & Smith, S. S. (2017). α4βδ GABAA receptors reduce dendritic spine density in CA1 hippocampus and impair relearning ability of adolescent female mice: Effects of a GABA agonist and a stress steroid. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2017.01.051. http://www.sciencedirect.com/science/article/pii/S0306452217300714


Agarwal, V. R., Sinton, C. M., Liang, C. L., Fisher, C., German, D. C., & Simpson, E. R. (2000). Upregulation of estrogen receptors in the forebrain of aromatase knockout (ArKO) mice. Molecular and Cellular Endocrinology, 162(1-2), 9-16. doi. 

Agasse, F., Benzakour, O., Berjeaud, J.-M., Roger, M., & Coronas, V. (2006). Endogenous factors derived from embryonic cortex regulate proliferation and neuronal differentiation of postnatal subventricular zone cell cultures. European Journal of Neuroscience, 23(8), 1970-1976. doi: doi:10.1111/j.1460-9568.2006.04739.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2006.04739.x 


Agasse, F., Mendez-David, I., Christaller, W., Carpentier, R., Braz, B. Y., David, D. J., . . . Humbert, S. (2020). Chronic Corticosterone Elevation Suppresses Adult Hippocampal Neurogenesis by Hyperphosphorylating Huntingtin. Cell Reports, 32(1), 107865. doi: https://doi.org/10.1016/j.celrep.2020.107865. http://www.sciencedirect.com/science/article/pii/S2211124720308469


Agasse, F., Nicoleau, C., Petit, J., Jaber, M., Roger, M., Benzakour, O., & Coronas, V. (2007). Evidence for a major role of endogenous fibroblast growth factor-2 in apoptotic cortex-induced subventricular zone cell proliferation. European Journal of Neuroscience, 26(11), 3036-3042. doi: doi:10.1111/j.1460-9568.2007.05915.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05915.x 


Agasse, F., Roger, M., & Coronas, V. (2004). Neurogenic and intact or apoptotic non-neurogenic areas of adult brain release diffusible molecules that differentially modulate the development of subventricular zone cell cultures. European Journal of Neuroscience, 19(6), 1459-1468. doi. http://www.blackwell-synergy.com/links/doi/10.1111/j.1460-9568.2004.0325...


Ago, Y., Hayata-Takano, A., Kawanai, T., Yamauchi, R., Takeuchi, S., Cushman, J. D., . . . Waschek, J. A. (2017). Impaired extinction of cued fear memory and abnormal dendritic morphology in the prelimbic and infralimbic cortices in VPAC2 receptor (VIPR2)-deficient mice. Neurobiology of Learning and Memory. doi: https://doi.org/10.1016/j.nlm.2017.10.010. http://www.sciencedirect.com/science/article/pii/S1074742717301624


Agster, K. L., & Burwell, R. D. (2013). Hippocampal and subicular efferents and afferents of the perirhinal, postrhinal, and entorhinal cortices of the rat. Behavioural Brain Research, (0). doi: http://dx.doi.org/10.1016/j.bbr.2013.07.005. http://www.sciencedirect.com/science/article/pii/S016643281300404X


Aguiar, P., Sousa, M., & Szucs, P. (2013). Versatile Morphometric Analysis and Visualization of the Three-Dimensional Structure of Neurons. Neuroinformatics, 1-11. doi: 10.1007/s12021-013-9188-z. http://dx.doi.org/10.1007/s12021-013-9188-z


Aguiar, P., & Szucs, P. (2011). Detailed visualization and morphometric analysis of reconstructed neurons using Blender and Python. BMC neuroscience, 12(Suppl 1), P323-P323. doi. 

Aguilar, J. R., & Castro-Alamancos, M. A. (2005). Spatiotemporal Gating of Sensory Inputs in Thalamus during Quiescent and Activated States. Journal of Neuroscience, 25, 10990-11002. doi. 

Aguilar-Arredondo, A., & Zepeda, A. (2018). Memory retrieval-induced activation of adult-born neurons generated in response to damage to the dentate gyrus. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-018-1664-7. https://doi.org/10.1007/s00429-018-1664-7


Ahlborn, P., Schachner, M., & Irintchev, A. (2007). One hour electrical stimulation accelerates functional recovery after femoral nerve repair. Experimental Neurology, 208(1), 137-144. doi. 

Ahlfeld, J., Mustari, M., & Horn, A. K. E. (2011). Sources of calretinin inputs to motoneurons of extraocular muscles involved in upgaze. Annals of the New York Academy of Sciences, 1233(1), 91-99. doi: 10.1111/j.1749-6632.2011.06168.x. http://dx.doi.org/10.1111/j.1749-6632.2011.06168.x


Ahmad, A., Momenan, R., van Gelderen, P., Moriguchi, T., Greiner, R. S., Salem, J. R., & others. (2004). Gray and white matter brain volume in aged rats raised on n-3 fatty acid deficient diets. Nutritional Neuroscience, 7(1), 13-20. doi. 

Ahmad, A., Moriguchi, T., & Salem, N. (2002). Decrease in neuron size in docosahexaenoic acid-deficient brain. Pediatric Neurology, 26(3), 210-218. doi. 

Ahmad, A., & Spear, P. D. (1993). Effects of aging on the size, density, and number of rhesus monkey lateral geniculate neurons. Journal of Comparative Neurology, 334(4), 631-643. doi. 

Ahmed, B., Cordery, P. M., McLelland, D., Bair, W., & Krug, K. (2012). Long-Range Clustered Connections within Extrastriate Visual Area V5/MT of the Rhesus Macaque. Cerebral Cortex, 22(1), 60-73. doi. 

Ahn, S., Kim, T.-G., Kim, K.-S., & Chung, S. (2015). Differentiation of human pluripotent stem cells into medial ganglionic eminence vs. caudal ganglionic eminence cells. Methods. doi: http://dx.doi.org/10.1016/j.ymeth.2015.09.009. http://www.sciencedirect.com/science/article/pii/S1046202315300815


Ahnert-Hilger, G., Höltje, M., Grosse, G., Pickert, G., Mucke, C., Nixdorf-Bergweiler, B., . . . Just, I. (2004). Differential effects of Rho GTPases on axonal and dendritic development in hippocampal neurones. Journal of Neurochemistry, 90(1), 9-18. doi. 

Ai, J., Epstein, P. N., Gozal, D., Yang, B., Wurster, R., & Cheng, Z. J. (2007). Morphology and topography of nucleus ambiguus projections to cardiac ganglia in rats and mice. Neuroscience, 149(4), 845-860. doi. 

Ai, J., Gozal, D., Li, L., Wead, W. B., Chapleau, M. W., Wurster, R., . . . Cheng, Z. (2007). Degeneration of vagal efferent axons and terminals in cardiac ganglia of aged rats. Journal of Comparative Neurology, 504(1), 74-88. doi. http://dx.doi.org/10.1002/cne.21431 


Ai, J., Wurster, R. D., Harden, S. W., & Cheng, Z. J. (2009). Vagal afferent innervation and remodeling in the aortic arch of young-adult fischer 344 rats following chronic intermittent hypoxia. Neuroscience, 164(2), 658-666. doi. 

Aihara, S., Fujimoto, S., Sakaguchi, R., & Imai, T. (2021). BMPR-2 gates activity-dependent stabilization of primary dendrites during mitral cell remodeling. Cell Reports, 35(12), 109276. doi: https://doi.org/10.1016/j.celrep.2021.109276. https://www.sciencedirect.com/science/article/pii/S2211124721006434


Airado, C., Gómez, C., Recio, J. S., Baltanás, F. C., Weruaga, E., & Alonso, J. R. (2008). Zincergic innervation from the anterior olfactory nucleus to the olfactory bulb displays plastic responses after mitral cell loss. Journal of Chemical Neuroanatomy, 36(3-4), 197-208. doi. 

Ajoy, R., Lo, Y.-C., Ho, M.-H., Chen, Y.-Y., Wang, Y., Chen, Y.-H., . . . Chou, S.-Y. (2021). CCL5 promotion of bioenergy metabolism is crucial for hippocampal synapse complex and memory formation. Molecular Psychiatry. doi: 10.1038/s41380-021-01103-3. https://doi.org/10.1038/s41380-021-01103-3


Akashi, K., Kakizaki, T., Kamiya, H., Fukaya, M., Yamasaki, M., Abe, M., . . . Sakimura, K. (2009). NMDA receptor GluN2B (GluRΣ2/NR2B) subunit is crucial for channel function, postsynaptic macromolecular organization, and actin cytoskeleton at hippocampal CA3 synapses. Journal of Neuroscience, 29(35), 10869-10882. doi. 

Akers, K. G., Martinez-Canabal, A., Restivo, L., Yiu, A. P., De Cristofaro, A., Hsiang, H.-L. L., . . . Shoji, H. (2014). Hippocampal Neurogenesis Regulates Forgetting During Adulthood and Infancy. Science, 344(6184), 598-602. doi. http://www.sciencemag.org/content/344/6184/598.short


Akgül, G., Abebe, D., Yuan, X. Q., Auville, K., & McBain, C. J. (2019). The Role of AMPARs in the Maturation and Integration of Caudal Ganglionic Eminence-Derived Interneurons into Developing Hippocampal Microcircuits. Scientific Reports, 9(1), 5435. doi: 10.1038/s41598-019-41920-9. https://doi.org/10.1038/s41598-019-41920-9


Akhtar, M. W., Sanz-Blasco, S., Dolatabadi, N., Parker, J., Chon, K., Lee, M. S., . . . Lipton, S. A. (2016). Elevated glucose and oligomeric [beta]-amyloid disrupt synapses via a common pathway of aberrant protein S-nitrosylation. [Article]. Nat Commun, 7. doi: 10.1038/ncomms10242. http://dx.doi.org/10.1038/ncomms10242


Akyüz, N., Rost, S., Mehanna, A., Bian, S., Loers, G., Oezen, I., . . . Schachner, M. (2013). Dermatan 4-O-sulfotransferase1 ablation accelerates peripheral nerve regeneration. Experimental Neurology, (0). doi: http://dx.doi.org/10.1016/j.expneurol.2013.01.025. http://www.sciencedirect.com/science/article/pii/S0014488613000381


Al Ghamdi, K. S., Polgár, E., & Todd, A. J. (2009). Soma size distinguishes projection neurons from neurokinin 1 receptor-expressing interneurons in lamina I of the rat lumbar spinal dorsal horn. Neuroscience, 164(4), 1794-1804. doi. 

Alam, M. N., Kumar, S., Bashir, T., Suntsova, N., Methippara, M. M., Szymusiak, R., & McGinty, D. (2005). GABA-mediated control of hypocretin- but not melanin-concentrating hormone-immunoreactive neurones during sleep in rats. Journal of Physiology, 563(2), 569-582. doi: 10.1113/jphysiol.2004.076927. http://jp.physoc.org/cgi/content/abstract/563/2/569 


Alberquilla, S., Gonzalez-Granillo, A., Martin, E. D., & Moratalla, R. (2019). Dopamine regulates spine density in striatal projection neurons in a concentration-dependent manner. Neurobiology of Disease, 104666. doi: https://doi.org/10.1016/j.nbd.2019.104666. http://www.sciencedirect.com/science/article/pii/S0969996119303419


Albrecht, P. J., Hines, S., Eisenberg, E., Pud, D., Finlay, D. R., Connolly, M. K., . . . Rice, F. L. (2006). Pathologic alterations of cutaneous innervation and vasculature in affected limbs from patients with complex regional pain syndrome. Pain, 120(3), 244-266. doi. 

Albrecht, P. J., Hou, Q., Argoff, C. E., Storey, J. R., Wymer, J. P., & Rice, F. L. (2013). Excessive Peptidergic Sensory Innervation of Cutaneous Arteriole–Venule Shunts (AVS) in the Palmar Glabrous Skin of Fibromyalgia Patients: Implications for Widespread Deep Tissue Pain and Fatigue. Pain Medicine, n/a-n/a. doi: 10.1111/pme.12139. http://dx.doi.org/10.1111/pme.12139


Alçada-Morais, S., Gonçalves, N., Moreno-Juan, V., Andres, B., Ferreira, S., Marques, J. M., . . . Rodrigues, R. J. (2021). Adenosine A2A Receptors Contribute to the Radial Migration of Cortical Projection Neurons through the Regulation of Neuronal Polarization and Axon Formation. Cerebral Cortex, (bhab188). doi: 10.1093/cercor/bhab188. https://doi.org/10.1093/cercor/bhab188


Aleksic, D., Aksić, M., Divac, N., Radonjić, V., Filipović, B., & Jakovčevski, I. (2014). Thermomineral water promotes axonal sprouting but does not reduce glial scar formation in a mouse model of spinal cord injury. Neural Regeneration Research, 9(24), 2174. doi. http://www.nrronline.org/citation.asp?issn=1673-5374;year=2014;volume=9;...


Alexander, T. C., Butcher, H., Krager, K., Kiffer, F., Groves, T., Wang, J., . . . Allen, A. R. (2018). Behavioral Effects of Focal Irradiation in a Juvenile Murine Model. Radiation Research, 0(0), null. doi: 10.1667/rr14847.1. http://www.rrjournal.org/doi/abs/10.1667/RR14847.1


Alexander, T. C., Kiffer, F., Groves, T., Anderson, J., Wang, J., Hayar, A., . . . Allen, A. R. (2019). Effects of thioTEPA chemotherapy on cognition and motor coordination. Synapse, 0(ja). doi: doi:10.1002/syn.22085. https://onlinelibrary.wiley.com/doi/abs/10.1002/syn.22085


Alexander, T. C., Simecka, C. M., Kiffer, F., Groves, T., Anderson, J., Carr, H., . . . Allen, A. R. (2017). Changes in cognition and dendritic complexity following intrathecal methotrexate and cytarabine treatment in a juvenile murine model. Behavioural Brain Research. doi: https://doi.org/10.1016/j.bbr.2017.12.008. https://www.sciencedirect.com/science/article/pii/S0166432817314122


Ali, A. B., Deuchars, J., Pawelzik, H., & Thomson, A. M. (1998). CA1 pyramidal to basket and bistratified cell EPSPs: dual intracellular recordings in rat hippocampal slices. Journal of Physiology, 507(1), 201-217. doi. http://jp.physoc.org/cgi/content/abstract/507/1/201 


Ali, A. B., Rossier, J., Staiger, J. F., & Audinat, E. (2001). Kainate receptors regulate unitary IPSCs elicited in pyramidal cells by fast-spiking interneurons in the neocortex. Journal of Neuroscience, 21(9), 2992-2992. doi. 

Al-Khater, K. M., Kerr, R., & Todd, A. J. (2008). A quantitative study of spinothalamic neurons in laminae I, III, and IV in lumbar and cervical segments of the rat spinal cord. Journal of Comparative Neurology, 511(1), 1-18. doi. 

Al-Khater, K. M., & Todd, A. J. (2009). Collateral projections of neurons in laminae I, III, and IV of rat spinal cord to thalamus, periaqueductal gray matter, and lateral parabrachial area. Journal of Comparative Neurology, 515(6), 629-646. doi. 

Al-Kofahi, K. A., Can, A., Lasek, S., Szarowski, D. H., Dowell-Mesfin, N., Shain, W., . . . Roysam, B. (2003). Median-based robust algorithms for tracing neurons from noisy confocal microscope images. Information Technology in Biomedicine, IEEE Transactions on, 7(4), 302-317. doi. 

Al-Kofahi, K. A., Lasek, S., Szarowski, D. H., Pace, C. J., Nagy, G., Turner, J. N., & Roysam, B. (2002). Rapid automated three-dimensional tracing of neurons from confocal image stacks. Information Technology in Biomedicine, IEEE Transactions on, 6(2), 171-187. doi. 

Al-Kofahi, O., Can, A., Lasek, S., Szarowski, D. H., Turner, J. N., & Roysam, B. (2003). Algorithms for accurate 3D registration of neuronal images acquired by confocal scanning laser microscopy. Journal of Microscopy, 211(1), 8-18. doi: doi:10.1046/j.1365-2818.2003.01196.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1365-2818.2003.01196.x 


Alkondon, M., & Albuquerque, E. X. (2001). Nicotinic acetylcholine receptor α7 and α4β2 subtypes differentially control GABAergic input to CA1 neurons in rat hippocampus. Journal of Neurophysiology, 86(6), 3043-3043. doi. 

Alkondon, M., & Albuquerque, E. X. (2004). The nicotinic acetylcholine receptor subtypes and their function in the hippocampus and cerebral cortex. Progress in Brain Research, 145, 109-120. doi. 

Alkondon, M., & Albuquerque, E. X. (2006). Subtype-Specific Inhibition of Nicotinic Acetylcholine Receptors by Choline: A Regulatory Pathway. Journal of Pharmacology and Experimental Therapeutics, 318(1), 268-275. doi: 10.1124/jpet.106.103135. http://jpet.aspetjournals.org/cgi/content/abstract/318/1/268 


Alkondon, M., Aracava, Y., Pereira, E. F. R., & Albuquerque, E. X. (2009). A Single in Vivo Application of Cholinesterase Inhibitors Has Neuron Type-Specific Effects on Nicotinic Receptor Activity in Guinea Pig Hippocampus. Journal of Pharmacology and Experimental Therapeutics, 328(1), 69-82. doi: 10.1124/jpet.108.146068. http://jpet.aspetjournals.org/cgi/content/abstract/328/1/69 


Alkondon, M., Braga, M. F. M., Pereira, E. F. R., Maelicke, A., & Albuquerque, E. X. (2000). Alpha-7 Nicotinic acetylcholine receptors and modulation of gabaergic synaptic transmission in the hippocampus. European Journal of Pharmacology, 393(1-3), 59-67. doi. 

Alkondon, M., Pereira, E. F. R., & Albuquerque, E. X. (2003). NMDA and AMPA Receptors Contribute to the Nicotinic Cholinergic Excitation of CA1 Interneurons in the Rat Hippocampus. Journal of Neurophysiology, 90(3), 1613-1625. doi: 10.1152/jn.00214.2003. http://jn.physiology.org/cgi/content/abstract/90/3/1613 


Alkondon, M., Pereira, E. F. R., & Albuquerque, E. X. (2007). Age-dependent changes in the functional expression of two nicotinic receptor subtypes in CA1 stratum radiatum interneurons in the rat hippocampus. Biochemical Pharmacology, 74(8), 1134-1144. doi. 

Alkondon, M., Pereira, E. F. R., Almeida, L. E. F., Randall, W. R., & Albuquerque, E. X. (2000). Nicotine at concentrations found in cigarette smokers activates and desensitizes nicotinic acetylcholine receptors in CA1 interneurons of rat hippocampus. Neuropharmacology, 39(13), 2726-2739. doi. 

Alkondon, M., Pereira, E. F. R., Eisenberg, H. M., & Albuquerque, E. X. (2000). Nicotinic Receptor Activation in Human Cerebral Cortical Interneurons: a Mechanism for Inhibition and Disinhibition of Neuronal Networks. Journal of Neuroscience, 20(1), 66-75. doi. http://www.jneurosci.org/cgi/content/abstract/20/1/66


Alkondon, M., Pereira, E. F. R., Eisenberg, H. M., Kajii, Y., Schwarcz, R., & Albuquerque, E. X. (2011). Age Dependency of Inhibition of α7 Nicotinic Receptors and Tonically Active N-Methyl-d-aspartate Receptors by Endogenously Produced Kynurenic Acid in the Brain. Journal of Pharmacology and Experimental Therapeutics, 337(3), 572-582. doi: 10.1124/jpet.110.177386. http://jpet.aspetjournals.org/content/337/3/572.abstract


Alkondon, M., Pereira, E. F. R., Potter, M. C., Kauffman, F. C., Schwarcz, R., & Albuquerque, E. X. (2007). Strain-Specific Nicotinic Modulation of Glutamatergic Transmission in the CA1 Field of the Rat Hippocampus: August Copenhagen Irish Versus Sprague-Dawley. Journal of Neurophysiology, 97(2), 1163-1170. doi: 10.1152/jn.01119.2006. http://jn.physiology.org/cgi/content/abstract/97/2/1163 


Alkondon, M., Pereira, E. F. R., Yu, P., Arruda, E. Z., Almeida, L. E. F., Guidetti, P., . . . Albuquerque, E. X. (2004). Targeted Deletion of the Kynurenine Aminotransferase II Gene Reveals a Critical Role of Endogenous Kynurenic Acid in the Regulation of Synaptic Transmission via α7 Nicotinic Receptors in the Hippocampus. Journal of Neuroscience, 24(19), 4635-4648. doi. http://www.jneurosci.org/cgi/content/abstract/24/19/4635


Allen, A. G., Worell, S. D., Nwaozo, G. C., Madrid, R., Dampier, W., Nonnemacher, M. R., & Wigdahl, B. (2019). Abstracts of the 16th International Symposium on NeuroVirology November 12-16, 2019 Atlanta, GA, USA. Journal of Neurovirology. doi: 10.1007/s13365-019-00807-1. https://doi.org/10.1007/s13365-019-00807-1


Allen, K., Potvin, O., Dore, F. Y., & Goulet, S. (2004). Modulation of the impairment of hippocampectomized rats on the radial-arm maze cue task by visual characteristics and subicular damage. Behavioral Neuroscience, 118(6), 1214-1214. doi. 

Allen, K., Potvin, O., Thibaudeau, G., Doré, F. Y., & Goulet, S. (2007). Processing idiothetic cues to remember visited locations: Hippocampal and vestibular contributions to radial-arm maze performance. Hippocampus, 17(8), 642-653. doi. 

Allene, C., Picardo, M. A., Becq, H., Miyoshi, G., Fishell, G., & Cossart, R. (2012). Dynamic Changes in Interneuron Morphophysiological Properties Mark the Maturation of Hippocampal Network Activity. Journal of Neuroscience, 32(19), 6688-6698. doi: 10.1523/jneurosci.0081-12.2012. http://www.jneurosci.org/content/32/19/6688.abstract


Allman, B. L., Bittencourt-Navarrete, R. E., Keniston, L. P., Medina, A. E., Wang, M. Y., & Meredith, M. A. (2008). Do Cross-Modal Projections Always Result in Multisensory Integration? Cerebral Cortex, bhm230. doi: 10.1093/cercor/bhm230. http://cercor.oxfordjournals.org/cgi/content/abstract/bhm230v1 


Allman, B. L., Keniston, L. P., & Meredith, M. A. (2009). Adult deafness induces somatosensory conversion of ferret auditory cortex. Proceedings of the National Academy of Sciences, 106(14), 5925-5930. doi: 10.1073/pnas.0809483106. http://www.pnas.org/content/106/14/5925.abstract 


Allred, R. P., Adkins, D. A. L., Woodlee, M. T., Husbands, L. C., Maldonado, M. A., Kane, J. R., . . . Jones, T. A. (2008). The vermicelli handling test: a simple quantitative measure of dexterous forepaw function in rats. Journal of Neuroscience Methods, 170(2), 229-244. doi. 

Allred, R. P., Cappellini, C. H., & Jones, T. A. (2010). The “good” limb makes the “bad” limb worse: Experience-dependent interhemispheric disruption of functional outcome after cortical infarcts in rats. Behavioral Neuroscience, 124(1), 124-124. doi. 

Allred, R. P., & Jones, T. A. (2004). Unilateral ischemic sensorimotor cortical damage in female rats: forelimb behavioral effects and dendritic structural plasticity in the contralateral homotopic cortex. Experimental Neurology, 190(2), 433-445. doi. 

Allred, R. P., & Jones, T. A. (2008). Maladaptive effects of learning with the less-affected forelimb after focal cortical infarcts in rats. Experimental Neurology, 210(1), 172-181. doi. 

Allred, R. P., Maldonado, M. A., & Jones, T. A. (2005). Training the" less-affected" forelimb after unilateral cortical infarcts interferes with functional recovery of the impaired forelimb in rats. Restorative Neurology and Neuroscience, 23(5), 297-302. doi. 

Almog, M., & Korngreen, A. (2014). A Quantitative Description of Dendritic Conductances and Its Application to Dendritic Excitation in Layer 5 Pyramidal Neurons. Journal of Neuroscience, 34(1), 182-196. doi. http://www.jneurosci.org/content/34/1/182.abstract


Al-Mosawie, A., Wilson, J. M., & Brownstone, R. M. (2007). Heterogeneity of V2-derived interneurons in the adult mouse spinal cord. European Journal of Neuroscience, 26(11), 3003-3015. doi: doi:10.1111/j.1460-9568.2007.05907.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05907.x 


Alonso, M., Medina, J. H., & Pozzo-Miller, L. (2004). ERK1/2 activation is necessary for BDNF to increase dendritic spine density in hippocampal CA1 pyramidal neurons. Learning and Memory, 11(2), 172-178. doi. 

Alp├ír, A., Ueberham, U., Bruckner, M. K., Seeger, G., Arendt, T., & Gartner, U. (2006). Different dendrite and dendritic spine alterations in basal and apical arbors in mutant human amyloid precursor protein transgenic mice. Brain Research, 1099(1), 189-198. doi. 

Alpár, A., Gärtner, U., Seeger, G., Härtig, W., Brauer, K., & Arendt, T. (2004). Constitutive expression of p21H-rasVal12 in pyramidal neurons results in reorganization of mouse neocortical afferents. Journal of Neurobiology, 60(3), 263-274. doi. 

Alpár, A., Künzle, H., Gärtner, U., Popkova, Y., Bauer, U., Grosche, J., . . . Härtig, W. (2010). Slow age-dependent decline of doublecortin expression and BrdU labeling in the forebrain from lesser hedgehog tenrecs. Brain Research, 1330, 9-19. doi. 

Alpár, A., Naumann, N., Arendt, T., & Gärtner, U. (2009). Constitutively enhanced p21Ras activity amplifies dendritic remodeling of hippocampal neurons during physical activity. International Journal of Developmental Neuroscience, 27(4), 407-411. doi. 

Alpar, A., Naumann, N., Härtig, W., Arendt, T., & Gärtner, U. (2008). Enhanced Ras activity preserves dendritic size and extension as well as synaptic contacts of neurons after functional deprivation in synRas mice. European Journal of Neuroscience, 27(12), 3083-3094. doi. 

Alpár, A., Naumann, N., Ueberham, U., Arendt, T., & Gärtner, U. (2009). Deprivation-induced dendritic shrinkage might be oppositely affected by the expression of wild-type and mutated human amyloid precursor protein. Journal of Neuroscience Research, 87(8), 1813-1822. doi. 

Alpar, A., Palm, K., Schierwagen, A., Arendt, T., & Gartner, U. (2003). Expression of constitutively active p21H-rasval12 in postmitotic pyramidal neurons results in increased dendritic size and complexity. Journal of Comparative Neurology, 467(1), 119-133. doi. 

Alpár, A., Ueberham, U., Brückner, M. K., Arendt, T., & Gärtner, U. (2006). The expression of wild-type human amyloid precursor protein affects the dendritic phenotype of neocortical pyramidal neurons in transgenic mice. International Journal of Developmental Neuroscience, 24(2), 133-140. doi. 

Alpár, A., Ueberham, U., Lendvai, D., Naumann, N., Rohn, S., Gáti, G., . . . Gartner, U. (2011). Activity-induced dendrite and dendritic spine development in human amyloid precursor protein transgenic mice. International Journal of Developmental Neuroscience. doi. 

Alpar, A., Ueberham, U., Seeger, G., Arendt, T., & Gartner, U. (2007). Effects of wild-type and mutant human amyloid precursor protein on cortical afferent network. NeuroReport, 18(12), 1247-1250. doi. 

Alqudah, S., Chertoff, M., Durham, D., Moskovitz, J., Staecker, H., & Peppi, M. (2018). Methionine Sulfoxide Reductase A Knockout Mice Show Progressive Hearing Loss and Sensitivity to Acoustic Trauma. Audiology and Neurotology, 23(1), 20-31. doi. https://www.karger.com/DOI/10.1159/000488276


Altemus, K. L., Lavenex, P., Ishizuka, N., & Amaral, D. G. (2005). Morphological characteristics and electrophysiological properties of CA1 pyramidal neurons in macaque monkeys. Neuroscience, 136(3), 741-756. doi. 

Alvandi, M. S., Bourmpoula, M., Homberg, J. R., & Fathollahi, Y. (2017). Association of contextual cues with morphine reward increases neural and synaptic plasticity in the ventral hippocampus of rats. Addiction Biology, n/a-n/a. doi: 10.1111/adb.12547. http://dx.doi.org/10.1111/adb.12547


Alvarado, J. A., Dhande, O. S., Prosseda, P. P., Kowal, T. J., Ning, K., Jabbehdari, S., . . . Sun, Y. (2020). Developmental Distribution of Primary Cilia in the Retinofugal Visual Pathway. Journal of Comparative Neurology, n/a(n/a). doi: 10.1002/cne.25029. https://doi.org/10.1002/cne.25029


Alvarado, J. C., Fuentes-Santamaria, V., Franklin, S. R., Brunso-Bechtold, J. K., & Henkel, C. K. (2005). Unilateral cochlear ablation in adult ferrets results in upregulation in calretinin immunostaining in the central nucleus of the inferior colliculus. Neuroscience, 136(3), 957-969. doi. 

Alvarado, J. C., Fuentes-Santamaria, V., Henkel, C. K., & Brunso-Bechtold, J. K. (2004). Alterations in calretinin immunostaining in the ferret superior olivary complex after cochlear ablation. Journal of Comparative Neurology, 470(1), 63-79. doi. 

Alvarez, F. J., Bullinger, K. L., Titus, H. E., Nardelli, P., & Cope, T. C. (2010). Permanent reorganization of Ia afferent synapses on motoneurons after peripheral nerve injuries. Annals of the New York Academy of Sciences, 1198(1), 231-241. doi. 

Alvarez, F. J., Titus-Mitchell, H. E., Bullinger, K. L., Kraszpulski, M., Nardelli, P., & Cope, T. C. (2011). Permanent central synaptic disconnection of proprioceptors after nerve injury and regeneration. I. Loss of VGLUT1/IA synapses on motoneurons. Journal of Neurophysiology, 106(5), 2450-2470. doi: 10.1152/jn.01095.2010. http://jn.physiology.org/content/106/5/2450.abstract


Alves, M. J., Goksel, M., Kaya, B., Mostafa, H., Gygli, P., Stephens, J., . . . Czeisler, C. M. (2018). CCNA2 Ablation in Aged Mice Results in Abnormal rRNA Granule Accumulation in Hippocampus. The American journal of pathology. doi: https://doi.org/10.1016/j.ajpath.2018.10.020. http://www.sciencedirect.com/science/article/pii/S000294401830381X


Amateau, S. K., & McCarthy, M. M. (2002). A Novel Mechanism of Dendritic Spine Plasticity Involving Estradiol Induction of Prostaglandin-E2. Journal of Neuroscience, 22, 8586-8596. doi. 

Amateau, S. K., & McCarthy, M. M. (2002). Sexual Differentiation of Astrocyte Morphology in the Developing Rat Preoptic Area,. Journal of Neuroendocrinology, 14(11), 904. doi. 

Amateau, S. K., & McCarthy, M. M. (2004). Induction of PGE2 by estradiol mediates developmental masculinization of sex behavior. Nature Neuroscience, 7, 643-650. doi. 

Ambalavanar, R., Tanaka, Y., Selbie, W. S., & Ludlow, C. L. (2004). Neuronal Activation in the Medulla Oblongata During Selective Elicitation of the Laryngeal Adductor Response. Journal of Neurophysiology, 92(5), 2920-2932. doi: 10.1152/jn.00064.2004. http://jn.physiology.org/cgi/content/abstract/92/5/2920 


Ambros-Ingerson, J., & Holmes, W. R. (2005). Analysis and comparison of morphological reconstructions of hippocampal field CA1 pyramidal cells. Hippocampus, 15(3), 302-315. doi. 

Ambrus, A., Kraftsik, R., & Barakat-Walter, I. (1998). Ontogeny of calretinin expression in rat dorsal root ganglia. Developmental Brain Research, 106(1-2), 101-108. doi. 

Amegandjin, C. A., Choudhury, M., Jadhav, V., Carriço, J. N., Quintal, A., Berryer, M., . . . Di Cristo, G. (2021). Sensitive period for rescuing parvalbumin interneurons connectivity and social behavior deficits caused by TSC1 loss. Nature Communications, 12(1), 3653. doi: 10.1038/s41467-021-23939-7. https://doi.org/10.1038/s41467-021-23939-7


Amendola, J., & Durand, J. (2008). Morphological differences between wild-type and transgenic superoxide dismutase 1 lumbar motoneurons in postnatal mice. Journal of Comparative Neurology, 511(3), 329-341. doi. 

Amendola, J., Gueritaud, J. P., Lamotte D'Incamps, B., Bories, C., Liabeuf, S., Allene, C., . . . Durand, J. (2007). Postnatal electrical and morphological abnormalities in lumbar motoneurons from transgenic mouse models of amyotrophic lateral sclerosis. Archives Italiennes de Biologie, 145(3), 311-323. doi. 

Amitai, Y., Gibson, J. R., Beierlein, M., Patrick, S. L., Ho, A. M., Connors, B. W., & Golomb, D. (2002). The Spatial Dimensions of Electrically Coupled Networks of Interneurons in the Neocortex. Journal of Neuroscience, 22(10), 4142-4152. doi. http://www.jneurosci.org/cgi/content/abstract/22/10/4142


Ammari, R., Lopez, C., Bioulac, B., Garcia, L., & Hammond, C. (2010). Subthalamic nucleus evokes similar long lasting glutamatergic excitations in pallidal, entopeduncular and nigral neurons in the basal ganglia slice. Neuroscience, 166(3), 808-818. doi. 

Amran, M. Y., Fujii, J., Suzuki, S. O., Kolling, G. L., Villanueva, S. Y. A. M., Kainuma, M., . . . Yoshida, S.-i. (2013). Investigation of Encephalopathy Caused by Shiga Toxin 2c-Producing <italic>Escherichia coli</italic> Infection in Mice. PLoS ONE, 8(3), e58959. doi: 10.1371/journal.pone.0058959. http://dx.doi.org/10.1371%2Fjournal.pone.0058959


An, J. J., Gharami, K., Liao, G. Y., Woo, N. H., Lau, A. G., Vanevski, F., . . . others. (2008). Distinct role of long 3′ UTR BDNF mRNA in spine morphology and synaptic plasticity in hippocampal neurons. Cell, 134(1), 175-187. doi. 

Anastassiou, C. A., Perin, R., Buzsaki, G., Markram, H., & Koch, C. (2015). Cell-type- and activity-dependent extracellular correlates of intracellular spiking. [10.1152/jn.00628.2014]. Journal of Neurophysiology. doi. http://jn.physiology.org/content/early/2015/05/14/jn.00628.2014.abstract


Andersen, B. (2019). Coupled Microglia Response in the Brainstem Following Lingual Nerve Transection in Sprague-Dawley Rats. doi. https://digitalcommons.unomaha.edu/srcaf/2019/Schedule/163/


Anderson, B. (1995). Dendrites and cognition: A negative pilot study in the rat. Intelligence, 20(3), 291-308. doi. 

Anderson, B., & Harvey, T. (1996). Alterations in cortical thickness and neuronal density in the frontal cortex of Albert Einstein. Neuroscience Letters, 210(3), 161-164. doi. 

Anderson, B., & Rutledge, V. (1996). Age and hemisphere effects on dendritic structure. Brain, 119(6), 1983-1990. doi. 

Anderson, J. E., Trujillo, M., McElroy, T., Groves, T., Alexander, T., Kiffer, F., & Allen, A. R. (2019). Early effects of Cyclophosphamide, Methotrexate, and 5-fluorouracil on neuronal morphology and hippocampal-dependent behavior in a murine model. Toxicological Sciences. doi: 10.1093/toxsci/kfz213. https://doi.org/10.1093/toxsci/kfz213


Anderson, K., Bones, B., Robinson, B., Hass, C., Lee, H., Ford, K., . . . Jacobs, B. (2009). The morphology of supragranular pyramidal neurons in the human insular cortex: a quantitative Golgi study. Cerebral Cortex, 19(9), 2131-2144. doi. 

Anderson, K., Bones, B., Robinson, B., Hass, C., Lee, H., Ford, K., . . . Jacobs, B. (2009). The Morphology of Supragranular Pyramidal Neurons in the Human Insular Cortex: A Quantitative Golgi Study. Cerebral Cortex, bhn234. doi: 10.1093/cercor/bhn234. http://cercor.oxfordjournals.org/cgi/content/abstract/bhn234v1 


Anderson, K., Yamamoto, E., Kaplan, J., Hannan, M., & Jacobs, B. (2010). Neurolucida Lucivid versus Neurolucida camera: A quantitative and qualitative comparison of three-dimensional neuronal reconstructions. Journal of Neuroscience Methods, 186(2), 209-214. doi. 

Anderson, L. A., Malmierca, M. S., Wallace, M. N., & Palmer, A. R. (2006). Evidence for a direct, short latency projection from the dorsal cochlear nucleus to the auditory thalamus in the guinea pig. European Journal of Neuroscience, 24(2), 491-498. doi: doi:10.1111/j.1460-9568.2006.04930.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2006.04930.x 


Anderson, L. A., Wallace, M. N., & Palmer, A. R. (2007). Identification of subdivisions in the medial geniculate body of the guinea pig. Hearing Research, 228(1), 156-167. doi. 

Anderson, M. A., Burda, J. E., Ren, Y., Ao, Y., O’Shea, T. M., Kawaguchi, R., . . . Sofroniew, M. V. (2016). Astrocyte scar formation aids central nervous system axon regeneration. [Article]. Nature, advance online publication. doi: 10.1038/nature17623

http://www.nature.com/nature/journal/vaop/ncurrent/abs/nature17623.html#.... http://dx.doi.org/10.1038/nature17623


Anderson, M. A., O’Shea, T. M., Burda, J. E., Ao, Y., Barlatey, S. L., Bernstein, A. M., . . . Sofroniew, M. V. (2018). Required growth facilitators propel axon regeneration across complete spinal cord injury. Nature. doi: 10.1038/s41586-018-0467-6. https://doi.org/10.1038/s41586-018-0467-6


Anderson, R. M., Birnie, A. K., Koblesky, N. K., Romig-Martin, S. A., & Radley, J. J. (2014). Adrenocortical Status Predicts the Degree of Age-Related Deficits in Prefrontal Structural Plasticity and Working Memory. The Journal of Neuroscience, 34(25), 8387-8397. doi. http://www.jneurosci.org/content/34/25/8387.short


Anderson, R. M., Glanz, R. M., Johnson, S. B., Miller, M. M., Romig-Martin, S., & Radley, J. J. (2016). Prolonged corticosterone exposure induces dendritic spine remodeling and attrition in the rat medial prefrontal cortex. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24019. http://dx.doi.org/10.1002/cne.24019


Anderson, R. M., Johnson, S. B., Lingg, R. T., Hinz, D. C., Romig-Martin, S. A., & Radley, J. J. (2019). Evidence for Similar Prefrontal Structural and Functional Alterations in Male and Female Rats Following Chronic Stress or Glucocorticoid Exposure. Cerebral Cortex. doi: 10.1093/cercor/bhz092. https://doi.org/10.1093/cercor/bhz092


Anderson, W., Newson, P., Skeri, M., Janssen, N., Milne, S., Yip, J., . . . Chahl, L. A. (2011). Effect of subchronic administration of tachykinin antagonists on response of guinea-pigs to mild and severe stress. Regulatory Peptides. doi. 

Andersson, C., Rajala, T., & Särkkä, A. (2017). Hierarchical models for epidermal nerve fiber data. Statistics in Medicine, n/a-n/a. doi: 10.1002/sim.7516. http://dx.doi.org/10.1002/sim.7516


Andersson, E. R., Prakash, N., Cajanek, L., Minina, E., Bryja, V., Bryjova, L., . . . Arenas, E. (2008). Wnt5a regulates ventral midbrain morphogenesis and the development of A9–A10 dopaminergic cells in vivo. PLoS ONE, 3(10), e3517-e3517. doi. 

ANDEZ, L. Z. D. B., & EIDEN, L. (2017). SUBCORTICAL HOMEOSTATIC CIRCUITRY MODULATES BRAIN WAVES AND BEHAVIORAL ADAPTATION: RELEVANCE FOR THE EMERGING MULTIDISCIPLINE OF SOCIAL NEUROSCIENCE. Mathematical Biology and Biological Physics, 204. doi. https://books.google.com/books?hl=en&lr=lang_en&id=vIcvDwAAQBAJ&oi=fnd&p...


Andiman, S. E., Haynes, R. L., Trachtenberg, F. L., Billiards, S. S., Folkerth, R. D., Volpe, J. J., & Kinney, H. C. (2010). The cerebral cortex overlying periventricular leukomalacia: analysis of pyramidal neurons. Brain Pathology, 20(4), 803-814. doi. 

Andjelic, S., Gallopin, T., Cauli, B., Hill, E. L., Roux, L., Badr, S., . . . Lambolez, B. (2008). Glutamatergic non-pyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons. Journal of Neurophysiology, 91094.92008. doi: 10.1152/jn.91094.2008. http://jn.physiology.org/cgi/content/abstract/91094.2008v1 


Andjelkovic, A., Nikolic, B., Pachter, J., & Zecevic, N. (1998). Macrophages/microglial cells in human central nervous system during development: an immunohistochemical study. Brain Research, 814, 13 - 25. doi. 

Andjus, P. R., Zhu, L., Cesa, R., Carulli, D., & Strata, P. (2003). A change in the pattern of activity affects the developmental regression of the Purkinje cell polyinnervation by climbing fibers in the rat cerebellum. Neuroscience, 121(3), 563-572. doi. 

Ando, K., Laborde, Q., Brion, J.-P., & Duyckaerts, C. (2018). Chapter 21 - 3D imaging in the postmortem human brain with CLARITY and CUBIC. In I. Huitinga & M. J. Webster (Eds.), Handbook of Clinical Neurology (Vol. 150, pp. 303-317): Elsevier.

Andolina, D., Di Segni, M., Bisicchia, E., D'Alessandro, F., Cestari, V., Ventura, A., . . . Ventura, R. (2016). Effects of lack of microRNA-34 on the neural circuitry underlying the stress response and anxiety. Neuropharmacology. doi: http://dx.doi.org/10.1016/j.neuropharm.2016.03.044. http://www.sciencedirect.com/science/article/pii/S0028390816301162


Andorfer, C., Acker, C. M., Kress, Y., Hof, P. R., Duff, K., & Davies, P. (2005). Cell-Cycle Reentry and Cell Death in Transgenic Mice Expressing Nonmutant Human Tau Isoforms. Journal of Neuroscience, 25(22), 5446-5454. doi: 10.1523/jneurosci.4637-04.2005. http://www.jneurosci.org/cgi/content/abstract/25/22/5446 


André, C., Guzman-Quevedo, O., Rey, C., Rémus-Borel, J., Clark, S., Castellanos-Jankiewicz, A., . . . Cota, D. (2016). Inhibiting Microglia Expansion Prevents Diet-induced Hypothalamic and Peripheral Inflammation. [10.2337/db16-0586]. Diabetes. doi. http://diabetes.diabetesjournals.org/content/early/2016/11/30/db16-0586....


Andreassen, O. A., Ferrante, R. J., Hughes, D. B., Klivenyi, P., Dedeoglu, A., Ona, V. O., . . . Beal, M. F. (2000). Malonate and 3-Nitropropionic Acid Neurotoxicity Are Reduced in Transgenic Mice Expressing a Caspase-1 Dominant-Negative Mutant. Journal of Neurochemistry, 75(2), 847-852. doi. http://www.jneurochem.org/cgi/content/abstract/75/2/847


Andressoo, J. O., Mitchell, J. R., de Wit, J., Hoogstraten, D., Volker, M., Toussaint, W., . . . others. (2006). An< i> Xpd</i> mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria. Cancer Cell, 10(2), 121-132. doi. 

Andrew, R. G., Changiz, G., & Sultan, D. (2018). The Cholinergic System in the Basal Forebrain of the Atlantic White‐Sided Dolphin (Lagenorhynchus acutus). Journal of Comparative Neurology, 0(ja). doi: doi:10.1002/cne.24460. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24460


Andrey, P., & Maurin, Y. (2005). Free-D: an integrated environment for three-dimensional reconstruction from serial sections. Journal of Neuroscience Methods, 145(1-2), 233-244. doi. 

Andrioli, A., Alonso-Nanclares, L., Arellano, J. I., & DeFelipe, J. (2007). Quantitative analysis of parvalbumin-immunoreactive cells in the human epileptic hippocampus. Neuroscience, 149(1), 131-143. doi. 

ANGELUCCI, G. S. F. F. A. (2018). Scaling Big Data Neuroscience: From Interactive Analytics to HPC Platforms. Big Data and HPC: Ecosystem and Convergence, 33, 53. doi. https://books.google.com/books?hl=en&lr=lang_en&id=Yo1xDwAAQBAJ&oi=fnd&p...


Angiari, C., Ferrarini, M., Taioli, F., Cavallaro, T., Fabrizi, G. M., & Rizzuto, N. (2004). Charcot-marie-tooth disease type 1: novel cases and novel mutations detected by DHPLC. Journal of the Peripheral Nervous System, 9(2), 122-122. doi. 

Angulo, M. C., Staiger, J. F., Rossier, J., & Audinat, E. (2003). Distinct Local Circuits Between Neocortical Pyramidal Cells and Fast-Spiking Interneurons in Young Adult Rats. Journal of Neurophysiology, 89(2), 943-953. doi: 10.1152/jn.00750.2002. http://jn.physiology.org/cgi/content/abstract/89/2/943 


Anilkumar, S., Patel, D., de Boer, S. F., Chattarji, S., & Buwalda, B. (2021). Decreased dendritic spine density in posterodorsal medial amygdala neurons of proactive coping rats. Behavioural Brain Research, 397, 112940. doi: https://doi.org/10.1016/j.bbr.2020.112940. http://www.sciencedirect.com/science/article/pii/S0166432820306392


Annamneedi, A., Caliskan, G., Müller, S., Montag, D., Budinger, E., Angenstein, F., . . . Stork, O. (2018). Ablation of the presynaptic organizer Bassoon in excitatory neurons retards dentate gyrus maturation and enhances learning performance. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-018-1692-3. https://doi.org/10.1007/s00429-018-1692-3


Anselmi, L., Bove, C., Coleman, F. H., Le, K., Subramanian, M. P., Venkiteswaran, K., . . . Travagli, R. A. (2018). Ingestion of subthreshold doses of environmental toxins induces ascending Parkinsonism in the rat. npj Parkinson's Disease, 4(1), 30. doi: 10.1038/s41531-018-0066-0. https://doi.org/10.1038/s41531-018-0066-0


Anselmi, L., Toti, L., Bove, C., Hampton, J., & Travagli, R. A. (2017). A Nigro-Vagal Pathway Controls Gastric Motility and is Affected in a Rat Model of Parkinsonism. Gastroenterology. doi: https://doi.org/10.1053/j.gastro.2017.08.069. http://www.sciencedirect.com/science/article/pii/S0016508517361383


Anselmi, L., Toti, L., Bove, C., Hampton, J., & Travagli, R. A. (2017). A Nigro−Vagal Pathway Controls Gastric Motility and Is Affected in a Rat Model of Parkinsonism. Gastroenterology, 153(6), 1581-1593. doi: https://doi.org/10.1053/j.gastro.2017.08.069. http://www.sciencedirect.com/science/article/pii/S0016508517361383


Ansorge, J., Humanes-Valera, D., Pauzin, F. P., Schwarz, M. K., & Krieger, P. (2020). Cortical layer 6 control of sensory responses in higher-order thalamus. The Journal of Physiology, n/a(n/a). doi: 10.1113/jp279915. https://physoc.onlinelibrary.wiley.com/doi/abs/10.1113/JP279915


Anstötz, M., Cosgrove, K., Hack, I., Mugnaini, E., Maccaferri, G., & Lübke, J. R. (2013). Morphology, input–output relations and synaptic connectivity of Cajal–Retzius cells in layer 1 of the developing neocortex of CXCR4-EGFP mice. Brain Structure and Function, 1-21. doi: 10.1007/s00429-013-0627-2. http://dx.doi.org/10.1007/s00429-013-0627-2


Anstötz, M., Fiske, M. P., & Maccaferri, G. (2021). Impaired KCC2 Function Triggers Interictal-Like Activity Driven by Parvalbumin-Expressing Interneurons in the Isolated Subiculum In Vitro. Cerebral Cortex, (bhab115). doi: 10.1093/cercor/bhab115. https://doi.org/10.1093/cercor/bhab115


Anstötz, M., Huang, H., Marchionni, I., Haumann, I., Maccaferri, G., & Lübke, J. H. R. (2015). Developmental Profile, Morphology, and Synaptic Connectivity of Cajal–Retzius Cells in the Postnatal Mouse Hippocampus. Cerebral Cortex. doi: 10.1093/cercor/bhv271. http://cercor.oxfordjournals.org/content/early/2015/11/18/cercor.bhv271....


Anstötz, M., Karsak, M., & Rune, G. M. (2018). Integrity of Cajal-Retzius cells in the reeler-mouse hippocampus. Hippocampus, 0(ja). doi: doi:10.1002/hipo.23049. https://onlinelibrary.wiley.com/doi/abs/10.1002/hipo.23049


Anstötz, M., Lee, S. K., Neblett, T. I., Rune, G. M., & Maccaferri, G. (2017). Experience-Dependent Regulation of Cajal–Retzius Cell Networks in the Developing and Adult Mouse Hippocampus. Cerebral Cortex, 1-16. doi. https://academic.oup.com/cercor/article-abstract/doi/10.1093/cercor/bhx1...


Antal, M., Eyre, M., Finklea, B., & Nusser, Z. (2006). External tufted cells in the main olfactory bulb form two distinct subpopulations. European Journal of Neuroscience, 24(4), 1124-1136. doi: doi:10.1111/j.1460-9568.2006.04988.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2006.04988.x 


Antic, S. D. (2003). Action potentials in basal and oblique dendrites of rat neocortical pyramidal neurons. Journal of Physiology, 550(1), 35-50. doi: 10.1113/jphysiol.2002.033746. http://jp.physoc.org/cgi/content/abstract/550/1/35 


Anton-Sanchez, L., Bielza, C., Larrañaga, P., & DeFelipe, J. (2016). Wiring Economy of Pyramidal Cells in the Juvenile Rat Somatosensory Cortex. PLoS ONE, 11(11), e0165915. doi: 10.1371/journal.pone.0165915. http://dx.doi.org/10.1371%2Fjournal.pone.0165915


Antonucci, F., Cerri, C., Vetencourt, J. F., & Caleo, M. (2010). Acute neuroprotection by the synaptic blocker botulinum neurotoxin E in a rat model of focal cerebral ischaemia. Neuroscience, 169(1), 395-401. doi. 

Antzoulatos, E., Jakowec, M. W., Petzinger, G. M., & Wood, R. I. (2011). MPTP Neurotoxicity and Testosterone Induce Dendritic Remodeling of Striatal Medium Spiny Neurons in the C57Bl/6 Mouse. Parkinson's Disease, 2011. doi. 

Anwar, H., Hepburn, I., Nedelescu, H., Chen, W., & De Schutter, E. (2013). Stochastic Calcium Mechanisms Cause Dendritic Calcium Spike Variability. Journal of Neuroscience, 33(40), 15848-15867. doi: 10.1523/jneurosci.1722-13.2013. http://www.jneurosci.org/content/33/40/15848.abstract


Aoki, C. (2016). Synaptic changes in the hippocampus of adolescent female rodents associated with resilience to anxiety and suppression of food restriction-evoked hyperactivity in an animal model for anorexia nervosa. Brain Research. doi: http://dx.doi.org/10.1016/j.brainres.2016.01.019. http://www.sciencedirect.com/science/article/pii/S0006899316000329


Aoki, S., Coulon, P., & Ruigrok, T. J. H. (2017). Multizonal Cerebellar Influence Over Sensorimotor Areas of the Rat Cerebral Cortex. Cerebral Cortex. doi: 10.1093/cercor/bhx343. http://dx.doi.org/10.1093/cercor/bhx343


Apa, K. L. (2017). Foliate Taste Bud Volume Following Chorda Tympani Nerve Injury in Rats. doi. http://digitalcommons.unomaha.edu/srcaf/2017/schedule/79/


Apicella, A. J., Wickersham, I. R., Seung, H. S., & Shepherd, G. M. G. (2012). Laminarly Orthogonal Excitation of Fast-Spiking and Low-Threshold-Spiking Interneurons in Mouse Motor Cortex. Journal of Neuroscience, 32(20), 7021-7033. doi: 10.1523/jneurosci.0011-12.2012. http://www.jneurosci.org/content/32/20/7021.abstract


Apolloni, S., Amadio, S., Montilli, C., Volonté, C., & D'Ambrosi, N. (2013). Ablation of P2X7 receptor exacerbates gliosis and motoneuron death in the SOD1-G93A mouse model of amyotrophic lateral sclerosis. Human Molecular Genetics. doi: 10.1093/hmg/ddt259. http://hmg.oxfordjournals.org/content/early/2013/06/03/hmg.ddt259.abstract


Apolloni, S., Fabbrizio, P., Amadio, S., & Volonté, C. (2016). Actions of the antihistaminergic clemastine on presymptomatic SOD1-G93A mice ameliorate ALS disease progression. [journal article]. Journal of Neuroinflammation, 13(1), 1-15. doi: 10.1186/s12974-016-0658-8. http://dx.doi.org/10.1186/s12974-016-0658-8


Apolloni, S., Fabbrizio, P., Parisi, C., Amadio, S., & Volonté, C. (2014). Clemastine Confers Neuroprotection and Induces an Anti-Inflammatory Phenotype in SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis. Molecular Neurobiology, 1-14. doi: 10.1007/s12035-014-9019-8. http://dx.doi.org/10.1007/s12035-014-9019-8


Apostolova, I., Irintchev, A., & Schachner, M. (2006). Tenascin-R Restricts Posttraumatic Remodeling of Motoneuron Innervation and Functional Recovery after Spinal Cord Injury in Adult Mice. Journal of Neuroscience, 26(30), 7849-7859. doi: 10.1523/jneurosci.1526-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/30/7849 


Aprile, I., Stalberg, E., Caliandro, P., Pazzaglia, C., Tonali, P., Foschini, M., . . . Padua, L. (2004). New neurophysiological findings on skin receptors or intradermal nerve endings after repetitive capsaicin application. Journal of the Peripheral Nervous System, 9(2), 109-110. doi: doi:10.1111/j.1085-9489.2004.009209s.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Arango, V., Underwood, M. D., & Mann, J. J. (1996). Fewer pigmented locus coeruleus neurons in suicide victims: preliminary results. Biological Psychiatry, 39(2), 112-120. doi. 

Arango, V., Underwood, M. D., Pauler, D. K., Kass, R. E., & Mann, J. J. (1996). Differential Age-Related Loss of Pigmented Locus Coeruleus Neurons in Suicides, Alcoholics, and Alcoholic Suicides. Alcoholism: Clinical and Experimental Research, 20(7), 1141-1148. doi. 

Araya-Callís, C., Hiemke, C., Abumaria, N., & Flugge, G. (2012). Chronic psychosocial stress and citalopram modulate the expression of the glial proteins GFAP and NDRG2 in the hippocampus. Psychopharmacology, 1-14. doi. 

Ardeshirpour, F., Hurliman, E., Wendelschafer-Crabb, G., & et al. (2017). Comparison of neurovascular characteristics of facial skin in patients after primary and revision rhytidectomies. JAMA Facial Plastic Surgery. doi: 10.1001/jamafacial.2017.0007. http://dx.doi.org/10.1001/jamafacial.2017.0007


Arellano, J. I., Benavides-Piccione, R., DeFelipe, J., & Yuste, R. (2007). Ultrastructure of dendritic spines: correlation between synaptic and spine morphologies. Frontiers in Neuroscience, 1(1), 131-131. doi. 

Arellano, J. I., Espinosa, A., Fairén, A., Yuste, R., & DeFelipe, J. (2007). Non-synaptic dendritic spines in neocortex. Neuroscience, 145(2), 464-469. doi. 

Arendt, T., Bender, K. J., Rangel, J., & Feldman, D. E. (2003). Development of Columnar Topography in the Excitatory Layer 4 to Layer 2/3 Projection in Rat Barrel Cortex. Journal of Neuroscience, 23(25), 8759-8770 * 8759. doi. 

Arévalo-Serrano, J., Sanz-Anquela, J. M., & Gonzalo-Ruiz, A. (2008). Beta-amyloid peptide-induced modifications in α7 nicotinic acetylcholine receptor immunoreactivity in the hippocampus of the rat: Relationship with GABAergic and calcium-binding proteins perikarya. Brain Research Bulletin, 75(5), 533-544. doi. 

Argue, K. J., VanRyzin, J. W., Falvo, D. J., Whitaker, A. R., Yu, S. J., & McCarthy, M. M. (2017). Activation of both CB1 and CB2 endocannabinoid receptors are critical for masculinization of the developing medial amygdala and juvenile social play behavior. [10.1523/ENEURO.0344-16.2017]. eneuro. doi. http://eneuro.org/content/early/2017/01/16/ENEURO.0344-16.2017.abstract


Ariatti, A., Cappelli, G., Suozzi, R., & Galassi, G. (2004). Neuromuscular complications of jejunoileal shunt for morbid obesity: case report and literature review. Journal of the Peripheral Nervous System, 9(2), 116-117. doi: doi:10.1111/j.1085-9489.2004.009209ao.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Ariel, M., Ward, K. C., & Tolbert, D. L. (2009). Topography of Purkinje Cells and Other Calbindin-Immunoreactive Cells Within Adult and Hatchling Turtle Cerebellum. The Cerebellum. doi. 

Arisi, G. M., & Garcia-Cairasco, N. (2006). Hippocampal doublecortin-positive granular neurons have abnormal dendritic morphology in the temporal lobe epilepsy pilocarpine model. Journal of Epilepsy and Clinical Neurophysiology, 12(3), 135-138. doi. 

Arisi, G. M., & Garcia-Cairasco, N. (2006). A proliferação de neurônios granulares hipocampais aumenta e os dendritos dos novos neurônios são anormais no modelo experimental de ELT induzida por pilocarpina. Journal of Epilepsy and Clinical Neurophysiology, 12(3), 135-138. doi. 

Arisi, G. M., & Garcia-Cairasco, N. (2007). Doublecortin-positive newly born granule cells of hippocampus have abnormal apical dendritic morphology in the pilocarpine model of temporal lobe epilepsy. Brain Research, 1165, 126-134. doi. 

Arisi, G. M., Ruch, M., Foresti, M. L., Mukherjee, S., Ribak, C. E., & Shapiro, L. A. (2011). Astrocyte Alterations in the Hippocampus Following Pilocarpine-induced Seizures in Aged Rats. Aging and Disease, 2(4), 294-300. doi. 

Ariza, J., Hurtado, J., Rogers, H., Ikeda, R., Dill, M., Steward, C., . . . Martínez-Cerdeño, V. (2017). Maternal autoimmune antibodies alter the dendritic arbor and spine numbers in the infragranular layers of the cortex. PLoS ONE, 12(8), e0183443. doi. https://www.ncbi.nlm.nih.gov/pubmed/28820892


Ariza, J., Rogers, H., Hashemi, E., Noctor, S. C., & Martínez-Cerdeño, V. (2016). The Number of Chandelier and Basket Cells Are Differentially Decreased in Prefrontal Cortex in Autism. Cerebral Cortex. doi: 10.1093/cercor/bhw349. http://cercor.oxfordjournals.org/content/early/2016/11/23/cercor.bhw349....


Armañanzas, R., & Ascoli, G. A. (2015). Towards the automatic classification of neurons. Trends in Neurosciences, (0). doi: http://dx.doi.org/10.1016/j.tins.2015.02.004. http://www.sciencedirect.com/science/article/pii/S016622361500034X


Armelle, R., Jeanne, L., Quentin, P., Hélène, G., Isabelle, F., Tania, V., & Jean, R. (2010). Degenerative abnormalities in transgenic neocortical neuropeptide Y interneurons expressing tau-green fluorescent protein. Journal of Neuroscience Research, 88(3), 487-499. doi. http://dx.doi.org/10.1002/jnr.22234 


Arnott, R. H., Wallace, M. N., Shackleton, T. M., & Palmer, A. R. (2004). Onset neurones in the anteroventral cochlear nucleus project to the dorsal cochlear nucleus. Jaro-Journal of the Association for Research in Otolaryngology, 5, 153-170. doi. 

Aroniadou, V. A., & Keller, A. (1993). The patterns and synaptic properties of horizontal intracortical connections in the rat motor cortex. Journal of Neurophysiology, 70(4), 1553-1569. doi. 

Aroniadou-Anderjaska, V., & Keller, A. (1996). Intrinsic inhibitory pathways in mouse barrel cortex. NeuroReport, 7, 2363-2368. doi. 

Arrant, A. E., Filiano, A. J., Warmus, B. A., Hall, A. M., & Roberson, E. D. (2016). Progranulin haploinsufficiency causes biphasic social dominance abnormalities in the tube test. Genes, Brain and Behavior, n/a-n/a. doi: 10.1111/gbb.12300. http://dx.doi.org/10.1111/gbb.12300


Arruda-Carvalho, M., Restivo, L., Guskjolen, A., Epp, J. R., Elgersma, Y., Josselyn, S. A., & Frankland, P. W. (2014). Conditional Deletion of α-CaMKII Impairs Integration of Adult-Generated Granule Cells into Dentate Gyrus Circuits and Hippocampus-Dependent Learning. The Journal of Neuroscience, 34(36), 11919-11928. doi. http://www.jneurosci.org/content/34/36/11919.short


Arslan, E., Garip, I. C., Gulseren, G., Tekinay, A. B., & Guler, M. O. (2014). Bioactive Supramolecular Peptide Nanofibers for Regenerative Medicine. Advanced Healthcare Materials, n/a-n/a. doi: 10.1002/adhm.201300491. http://dx.doi.org/10.1002/adhm.201300491


Arsznov, B. M., Lundrigan, B. L., Holekamp, K. E., & Sakai, S. T. (2010). Sex and the frontal cortex: a developmental CT study in the spotted hyena. Brain, Behavior and Evolution, 76(3-4), 185-197. doi. 

Arszovszki, A., Borhegyi, Z., & Klausberger, T. (2014). Three axonal projection routes of individual pyramidal cells in the ventral CA1 hippocampus. [Original Research]. Frontiers in Neuroanatomy, 8. doi: 10.3389/fnana.2014.00053. http://www.frontiersin.org/Journal/Abstract.aspx?s=742&name=neuroanatomy...


Artinian, J., Peret, A., Mircheva, Y., Marti, G., & Crépel, V. (2015). Impaired neuronal operation through aberrant intrinsic plasticity in epilepsy. Annals of Neurology, n/a-n/a. doi: 10.1002/ana.24348. http://dx.doi.org/10.1002/ana.24348


Arvola, O., Kaidonis, G., Xu, L., Griffiths, B., & Stary, C. M. (2019). Hippocampal sub-regional differences in the microRNA response to forebrain ischemia. Molecular and Cellular Neuroscience. doi: https://doi.org/10.1016/j.mcn.2019.05.003. http://www.sciencedirect.com/science/article/pii/S1044743118304032


Arzt, M., Sakmann, B., & Meyer, H. S. (2017). Anatomical Correlates of Local, Translaminar, and Transcolumnar Inhibition by Layer 6 GABAergic Interneurons in Somatosensory Cortex. Cerebral Cortex, 1(12). doi. https://academic.oup.com/cercor/article-abstract/doi/10.1093/cercor/bhx1...


Asai, H., Ozaki, N., Shinoda, M., Nagamine, K., Tohnai, I., Ueda, M., & Sugiura, Y. (2005). Heat and mechanical hyperalgesia in mice model of cancer pain. Pain, 117(1-2), 19-29. doi. 

Asante, C. O., & Martin, J. H. (2013). Differential Joint-Specific Corticospinal Tract Projections within the Cervical Enlargement. PLoS ONE, 8(9), e74454. doi: 10.1371/journal.pone.0074454. http://dx.doi.org/10.1371%2Fjournal.pone.0074454


Asboth, L., Friedli, L., Beauparlant, J., Martinez-Gonzalez, C., Anil, S., Rey, E., . . . Courtine, G. (2018). Cortico–reticulo–spinal circuit reorganization enables functional recovery after severe spinal cord contusion. Nature Neuroscience, 21(4), 576-588. doi: 10.1038/s41593-018-0093-5. https://doi.org/10.1038/s41593-018-0093-5


Aschenbeck, K. A., Hordinsky, M. K., Kennedy, W. R., Wendelschafer-Crabb, G., Ericson, M. E., Kavand, S., . . . Panoutsopoulou, I. G. (2018). Neuromodulatory treatment of recalcitrant plaque psoriasis with onabotulinumtoxinA. Journal of the American Academy of Dermatology, 79(6), 1156-1159. doi: 10.1016/j.jaad.2018.07.058. https://doi.org/10.1016/j.jaad.2018.07.058


Ascoli, G. A. (1999). Progress and perspectives in computational neuroanatomy. The Anatomical Record, 257(6), 195-207. doi. 

Ascoli, G. A. (2002). Neuroanatomical algorithms for dendritic modelling. Network: Computation in Neural Systems, 13(3), 247-260. doi. 

Ascoli, G. A. (2006). Mobilizing the base of neuroscience data: the case of neuronal morphologies. Nature Reviews Neuroscience, 7, 318-324. doi. 

Ascoli, G. A. (2007). Successes and rewards in sharing digital reconstructions of neuronal morphology. Neuroinformatics, 5(3), 154-160. doi. 

Ascoli, G. A., Brown, K. M., Calixto, E., Card, J. P., Galvan, E. J., Perez-Rosello, T., & Barrionuevo, G. (2009). Quantitative morphometry of electrophysiologically identified CA3b interneurons reveals robust local geometry and distinct cell classes. Journal of Comparative Neurology, 515(6), 677-695. doi. 

Ascoli, G. A., Donohue, D. E., & Halavi, M. (2007). NeuroMorpho.Org: A Central Resource for Neuronal Morphologies. Journal of Neuroscience, 27(35), 9247-9251. doi: 10.1523/jneurosci.2055-07.2007. http://www.jneurosci.org 


Ascoli, G. A., & Krichmar, J. L. (2000). L-Neuron: a modeling tool for the efficient generation and parsimonious description of dendritic morphology. Neurocomputing, 32, 1003-1011. doi. 

Ascoli, G. A., Krichmar, J. L., Nasuto, S. J., & Senft, S. L. (2001). Generation, description and storage of dendritic morphology data. Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences, 356(1412), 1131-1145. doi. 

Ascoli, G. A., & Scorcioni, R. (2006). Neuron and network modeling. Neuroanatomical Tract-Tracing 3, 604-630. doi. 

Ashaber, M., Pálfi, E., Friedman, R. M., Palmer, C., Jákli, B., Chen, L. M., . . . Négyessy, L. (2013). Connectivity of somatosensory cortical area 1 form an anatomical substrate for the emergence of multifinger receptive fields and complex feature selectivity in the squirrel monkey (Saimiri sciureus). Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23499. http://dx.doi.org/10.1002/cne.23499


Atherton, J. F., Wokosin, D. L., Ramanathan, S., & Bevan, M. D. (2008). Autonomous initiation and propagation of action potentials in neurons of the subthalamic nucleus. Journal of Physiology, jphysiol.2008.155861. doi: 10.1113/jphysiol.2008.155861. http://jp.physoc.org/cgi/content/abstract/jphysiol.2008.155861v1 


Atkins, C. M., Cepero, M. L., Kang, Y., Liebl, D. J., & Dietrich, W. D. (2012). Effects of rolipram on histopathological outcome after controlled cortical impact injury in mice. Neuroscience Letters, (0). doi: 10.1016/j.neulet.2012.10.019. http://www.sciencedirect.com/science/article/pii/S0304394012013766


Atkins, C. M., Kang, Y., Furones, C., Truettner, J. S., Alonso, O. F., & Dietrich, W. D. (2012). Postinjury treatment with rolipram increases hemorrhage after traumatic brain injury. Journal of Neuroscience Research, n/a-n/a. doi: 10.1002/jnr.23069. http://dx.doi.org/10.1002/jnr.23069


Atkins, C. M., Oliva, A. A., Alonso, O. F., Chen, S., Bramlett, H. M., Hu, B.-R., & Dietrich, W. D. (2007). Hypothermia treatment potentiates ERK1/2 activation after traumatic brain injury. European Journal of Neuroscience, 26(4), 810-819. doi: doi:10.1111/j.1460-9568.2007.05720.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05720.x 


Atkins, C. M., Oliva Jr, A. A., Alonso, O. F., Pearse, D. D., Bramlett, H. M., & Dietrich, W. D. (2007). Modulation of the cAMP signaling pathway after traumatic brain injury. Experimental Neurology, 208(1), 145-158. doi. 

Atkins, C. M., Truettner, J. S., Lotocki, G., Sanchez-Molano, J., Kang, Y., Alonso, O. F., . . . Bramlett, H. M. (2010). Post-traumatic seizure susceptibility is attenuated by hypothermia therapy. European Journal of Neuroscience, no-no. doi: 10.1111/j.1460-9568.2010.07467.x. http://dx.doi.org/10.1111/j.1460-9568.2010.07467.x


Atkinson, R. A. K., Fair, H. L., Wilson, R., Vickers, J. C., & King, A. E. (2021). Effects of TDP-43 overexpression on neuron proteome and morphology in vitro. Molecular and Cellular Neuroscience, 114, 103627. doi: https://doi.org/10.1016/j.mcn.2021.103627. https://www.sciencedirect.com/science/article/pii/S1044743121000403


Au - Economides, G., Au - Falk, S., & Au - Mercer, A. (2018). Biocytin Recovery and 3D Reconstructions of Filled Hippocampal CA2 Interneurons. JoVE, (141), e58592. doi: doi:10.3791/58592. https://www.jove.com/video/58592


Aubrecht, T. G., Weil, Z. M., & Nelson, R. J. (2014). Melatonin treatment during early life interacts with restraint to alter neuronal morphology and provoke depressive-like responses. Behavioural Brain Research, (0). doi: http://dx.doi.org/10.1016/j.bbr.2014.01.025. http://www.sciencedirect.com/science/article/pii/S0166432814000394


Aungst, J. L., Heyward, P. M., Puche, A. C., Karnup, S. V., Hayar, A., Szabo, G., & Shipley, M. T. (2003). Centre–surround inhibition among olfactory bulb glomeruli. Nature, 426, 323-329. doi. 

Ausdenmoore, B. D., Markwell, Z. A., & Ladle, D. R. (2011). Localization of presynaptic inputs on dendrites of individually labeled neurons in three dimensional space using a center distance algorithm. Journal of Neuroscience Methods. doi. 

Austgen, J. R., Fong, A. Y., Foley, C. M., Mueller, P. J., Kline, D. D., Heesch, C. M., & Hasser, E. M. (2009). Expression of group I metabotropic glutamate receptors on phenotypically different cells within the nucleus of the solitary tract in the rat. Neuroscience, 159(2), 701-716. doi. 

Austin, J. E., & Buckmaster, P. S. (2004). Recurrent excitation of granule cells with basal dendrites and low interneuron density and inhibitory postsynaptic current frequency in the dentate gyrus of macaque monkeys. Journal of Comparative Neurology, 476(3), 205-218. doi. 

Austin, M. C., Rice, P. M., Mann, J. J., & Arango, V. (1995). Localization of corticotropin-releasing hormone in the human locus coeruleus and pedunculopontine tegmental nucleus: an immunocytochemical and in situ hybridization study. Neuroscience, 64(3), 713-727. doi. 

Avallone, J., Gashi, E., Magrys, B., & Friedman, L. K. (2006). Distinct regulation of metabotropic glutamate receptor (mGluR1 alpha) in the developing limbic system following multiple early-life seizures. Experimental Neurology, 202(1), 100-111. doi. 

Averaimo, S., Gritti, M., Barini, E., Gasparini, L., & Mazzanti, M. (2014). CLIC1 functional expression is required for cAMP-induced neurite elongation in postnatal mouse retinal ganglion cells. Journal of Neurochemistry, n/a-n/a. doi: 10.1111/jnc.12832. http://dx.doi.org/10.1111/jnc.12832


Averbeck, B. B., Lehman, J., Jacobson, M., & Haber, S. N. (2014). Estimates of Projection Overlap and Zones of Convergence within Frontal-Striatal Circuits. The Journal of Neuroscience, 34(29), 9497-9505. doi. http://www.jneurosci.org/content/34/29/9497.short


Avermann, M., Tomm, C., Mateo, C., Gerstner, W., & Petersen, C. C. H. (2012). Microcircuits of excitatory and inhibitory neurons in layer 2/3 of mouse barrel cortex. Journal of Neurophysiology. doi: 10.1152/jn.00917.2011. http://jn.physiology.org/content/early/2012/03/02/jn.00917.2011.abstract


Avior, Y., Ron, S., Kroitorou, D., Albeldas, C., Lerner, V., Corneo, B., . . . Cohen Solal, T. (2021). Depression patient-derived cortical neurons reveal potential biomarkers for antidepressant response. Translational Psychiatry, 11(1), 201. doi: 10.1038/s41398-021-01319-5. https://doi.org/10.1038/s41398-021-01319-5


Avramescu, S., Nita, D. A., & Timofeev, I. (2009). Neocortical post-traumatic epileptogenesis is associated with loss of GABAergic neurons. Journal of Neurotrauma, 26(5), 799-812. doi. 

Awad, P. N., Amegandjin, C. A., Szczurkowska, J., Carriço, J. N., Fernandes do Nascimento, A. S., Baho, E., . . . Di Cristo, G. (2018). KCC2 Regulates Dendritic Spine Formation in a Brain-Region Specific and BDNF Dependent Manner. Cerebral Cortex, bhy198-bhy198. doi: 10.1093/cercor/bhy198. http://dx.doi.org/10.1093/cercor/bhy198


Awad, P. N., Sanon, N. T., Chattopadhyaya, B., Carriço, J. N., Ouardouz, M., Gagné, J., . . . Di Cristo, G. (2016). Reducing premature KCC2 expression rescues seizure susceptibility and spine morphology in atypical febrile seizures. Neurobiology of Disease. doi: http://dx.doi.org/10.1016/j.nbd.2016.02.014. http://www.sciencedirect.com/science/article/pii/S0969996116300353


Awasaki, T., & Ito, K. (2004). Engulfing Action of Glial Cells Is Required for Programmed Axon Pruning during< i> Drosophila</i> Metamorphosis. Current Biology, 14(8), 668-677. doi. 

Axelrod, C. J., Laberge, F., & Robinson, B. W. (2018). Intraspecific brain size variation between coexisting sunfish ecotypes. [10.1098/rspb.2018.1971]. Proceedings of the Royal Society B: Biological Sciences, 285(1890). doi. http://rspb.royalsocietypublishing.org/content/285/1890/20181971.abstract


Ayata, P., Badimon, A., Strasburger, H. J., Duff, M. K., Montgomery, S. E., Loh, Y.-H. E., . . . Schaefer, A. (2018). Epigenetic regulation of brain region-specific microglia clearance activity. Nature Neuroscience, 21(8), 1049-1060. doi: 10.1038/s41593-018-0192-3. https://doi.org/10.1038/s41593-018-0192-3


Ayoub, A. E., & Salm, A. K. (2003). Increased Morphological Diversity of Microglia in the Activated Hypothalamic Supraoptic Nucleus. Journal of Neuroscience, 23(21), 7759-7766. doi. http://www.jneurosci.org/cgi/content/abstract/23/21/7759 


Aytan, N., Choi, J.-K., Carreras, I., Crabtree, L., Nguyen, B., Lehar, M., . . . Dedeoglu, A. (2018). Protective effects of 7,8-dihydroxyflavone on neuropathological and neurochemical changes in a mouse model of Alzheimer's disease. European Journal of Pharmacology. doi: https://doi.org/10.1016/j.ejphar.2018.02.045. https://www.sciencedirect.com/science/article/pii/S0014299918301304


Azan, G., Low, W. C., Wendelschafer-Crabb, G., Ikramuddin, S., & Kennedy, W. R. (2011). Evidence for neural progenitor cells in the human adult enteric nervous system. Cell and Tissue Research, 1-9. doi. 

Azim, K., Fiorelli, R., Zweifel, S., Hurtado-Chong, A., Yoshikawa, K., Slomianka, L., & Raineteau, O. (2012). 3-Dimensional Examination of the Adult Mouse Subventricular Zone Reveals Lineage-Specific Microdomains. PLoS ONE, 7(11), e49087. doi: 10.1371/journal.pone.0049087. http://dx.doi.org/10.1371%2Fjournal.pone.0049087


Azim, K., Zweifel, S., Klaus, F., Yoshikawa, K., Amrein, I., & Raineteau, O. (2012). Early Decline in Progenitor Diversity in the Marmoset Lateral Ventricle. Cerebral Cortex. doi: 10.1093/cercor/bhs085. http://cercor.oxfordjournals.org/content/early/2012/04/03/cercor.bhs085....


Ba, Q., Cui, C., Wen, L., Feng, S., Zhou, J., & Yang, K. (2015). Schisandrin B shows neuroprotective effect in 6-OHDA-induced Parkinson’s disease via inhibiting the negative modulation of miR-34a on Nrf2 pathway. Biomedicine and Pharmacotherapy. doi: http://dx.doi.org/10.1016/j.biopha.2015.07.034. http://www.sciencedirect.com/science/article/pii/S075333221500178X


Babic, T., Bhagat, R., Wan, S., Browning, K. N., Snyder, M., Fortna, S. R., & Travagli, R. A. (2012). Role of the vagus in the reduced pancreatic exocrine function in copper-deficient rats. American Journal of Physiology-Gastrointestinal and Liver Physiology, 304(4), G437-G448. doi. https://www.physiology.org/doi/full/10.1152/ajpgi.00402.2012


Bacci, A., Rudolph, U., Huguenard, J. R., & Prince, D. A. (2003). Major Differences in Inhibitory Synaptic Transmission onto Two Neocortical Interneuron Subclasses. Journal of Neuroscience, 23(29), 9664-9674. doi. http://www.jneurosci.org/cgi/content/abstract/23/29/9664 


Bachmann, C., Nguyen, H., Rosenbusch, J., Pham, L., Rabe, T., Patwa, M., . . . Tuoc, T. (2016). mSWI/SNF (BAF) Complexes Are Indispensable for the Neurogenesis and Development of Embryonic Olfactory Epithelium. PLoS Genet, 12(9), e1006274. doi: 10.1371/journal.pgen.1006274. http://dx.doi.org/10.1371%2Fjournal.pgen.1006274


Bachmann, L. C., Lindau, N. T., Felder, P., & Schwab, M. E. (2014). Sprouting of Brainstem–Spinal Tracts in Response to Unilateral Motor Cortex Stroke in Mice. The Journal of Neuroscience, 34(9), 3378-3389. doi. http://www.jneurosci.org/content/34/9/3378.short


Bacigaluppi, M., Russo, G. L., Peruzzotti-Jametti, L., Rossi, S., Sandrone, S., Butti, E., . . . Martino, G. (2016). Neural Stem Cell Transplantation Induces Stroke Recovery by Upregulating Glutamate Transporter GLT-1 in Astrocytes. [10.1523/JNEUROSCI.1643-16.2016]. The Journal of Neuroscience, 36(41), 10529. doi. http://www.jneurosci.org/content/36/41/10529.abstract


Badura, A., Schonewille, M., Voges, K., Galliano, E., Renier, N., Gao, Z., . . . De Zeeuw, Chris I. (2013). Climbing Fiber Input Shapes Reciprocity of Purkinje Cell Firing. Neuron, (0). doi: http://dx.doi.org/10.1016/j.neuron.2013.03.018. http://www.sciencedirect.com/science/article/pii/S0896627313002651


Bae, M. H., Bissonette, G. B., Mars, W. M., Michalopoulos, G. K., Achim, C. L., Depireux, D. A., & Powell, E. M. (2010). Hepatocyte growth factor (HGF) modulates GABAergic inhibition and seizure susceptibility. Experimental Neurology, 221(1), 129-135. doi. 

Bagley, J., LaRocca, G., Jimenez, D., & Urban, N. (2007). Adult neurogenesis and specific replacement of interneuron subtypes in the mouse main olfactory bulb. BMC Neuroscience, 8(1), 92. doi. http://www.biomedcentral.com/1471-2202/8/92 


Bagnall, M. W., Bushong, E. A., Ellisman, M. H., Scanziani, M., & others. (2011). Multiple clusters of release sites formed by individual thalamic afferents onto cortical interneurons ensure reliable transmission. Neuron, 71(1), 180-194. doi. 

Bagnall, M. W., Zingg, B., Sakatos, A., Moghadam, S. H., Zeilhofer, H. U., & Lac, S. d. (2009). Glycinergic Projection Neurons of the Cerebellum. Journal of Neuroscience, 29(32), 10104-10110. doi: 10.1523/jneurosci.2087-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/32/10104 


Baharnoori, M., Brake, W. G., & Srivastava, L. K. (2009). Prenatal immune challenge induces developmental changes in the morphology of pyramidal neurons of the prefrontal cortex and hippocampus in rats. Schizophrenia Research, 107(1), 99-109. doi. 

Bahia, C. P., Houzel, J. C., Picanço-Diniz, C. W., & Pereira Jr, A. (2008). Spatiotemporal distribution of proteoglycans in the developing rat's barrel field and the effects of early deafferentation. Journal of Comparative Neurology, 510(2), 145-157. doi. 

Bahia, C. P., Vianna-Barbosa, R. J., Tovar-Moll, F., & Lent, R. (2018). Terminal Arbors of Callosal Axons Undergo Plastic Changes in Early-Amputated Rats. Cerebral Cortex. doi: 10.1093/cercor/bhy043. http://dx.doi.org/10.1093/cercor/bhy043


Bähner, F., Weiss, E. K., Birke, G., Maier, N., Schmitz, D., Rudolph, U., . . . Draguhn, A. (2011). Cellular correlate of assembly formation in oscillating hippocampal networks in vitro. Proceedings of the National Academy of Sciences, 108(35), E607–E616. doi: 10.1073/pnas.1103546108. http://www.pnas.org/content/108/35/E607.abstract


Bailey, C. D. C., Alves, N. C., Nashmi, R., De Biasi, M., & Lambe, E. K. (2011). Nicotinic α5 Subunits Drive Developmental Changes in the Activation and Morphology of Prefrontal Cortex Layer VI Neurons. Biological Psychiatry. doi. 

Bailey, C. D. C., Tian, M. K., Kang, L., O'Reilly, R., & Lambe, E. K. (2013). Chrna5 genotype determines the long-lasting effects of developmental in vivo nicotine exposure on prefrontal attention circuitry. Neuropharmacology, (0). doi: http://dx.doi.org/10.1016/j.neuropharm.2013.09.003. http://www.sciencedirect.com/science/article/pii/S0028390813004103


Bailey, D. J., Wade, J., & Saldanha, C. J. (2009). Hippocampal lesions impair spatial memory performance, but not song—a developmental study of independent memory systems in the zebra finch. Developmental Neurobiology, 69(8), 491-504. doi. 

Bailey, T. W., Hermes, S. M., Whittier, K. L., Aicher, S. A., & Andresen, M. C. (2007). A-type potassium channels differentially tune afferent pathways from rat solitary tract nucleus to caudal ventrolateral medulla or paraventricular hypothalamus. Journal of Physiology, 582(2), 613-628. doi: 10.1113/jphysiol.2007.132365. http://jp.physoc.org/cgi/content/abstract/582/2/613 


Bajic, D. (2016). Combining Anterograde Tracing and Immunohistochemistry to Define Neuronal Synaptic Circuits. doi. http://link.springer.com/protocol/10.1007/7657_2015_81


Bajic, D., & Proudfit, H. K. (2013). Projections from the rat cuneiform nucleus to the A7, A6 (locus coeruleus), and A5 pontine noradrenergic cell groups. Journal of Chemical Neuroanatomy, (0). doi: http://dx.doi.org/10.1016/j.jchemneu.2013.03.001. http://www.sciencedirect.com/science/article/pii/S0891061813000276


Bajic, D., Van Bockstaele, E. J., & Proudfit, H. K. (2012). Ultrastructural analysis of rat ventrolateral periaqueductal gray projections to the a5 cell group. Neuroscience, (0). doi: 10.1016/j.neuroscience.2012.08.021. http://www.sciencedirect.com/science/article/pii/S0306452212008482?v=s5


Bajic, D., VanManh Hoang, Q., Nakajima, S., & Nakajima, Y. (2004). Dissociated histaminergic neuron cultures from the tuberomammillary nucleus of rats: culture methods and ghrelin effects. Journal of Neuroscience Methods, 132(2), 177-184. doi. 

Bajo, V. M., Leach, N. D., Cordery, P. M., Nodal, F. R., & King, A. J. (2014). The cholinergic basal forebrain in the ferret and its inputs to the auditory cortex. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12653. http://dx.doi.org/10.1111/ejn.12653


Bajo, V. M., & Moore, D. R. (2005). Descending projections from the auditory cortex to the inferior colliculus in the gerbil, Meriones unguiculatus. Journal of Comparative Neurology, 486(2), 101-116. doi. 

Bajo, V. M., Nodal, F. R., Bizley, J. K., & King, A. J. (2010). The non-lemniscal auditory cortex in ferrets: convergence of corticotectal inputs in the superior colliculus. Frontal Neuroanatomy, 21(4), 18. doi. 

Bajo, V. M., Nodal, F. R., Bizley, J. K., Moore, D. R., & King, A. J. (2007). The ferret auditory cortex: descending projections to the inferior colliculus. Cerebral Cortex, 17(2), 475-491. doi. 

Bajo, V. M., Nodal, F. R., Moore, D. R., & King, A. J. (2010). The descending corticocollicular pathway mediates learning-induced auditory plasticity. Nature Neuroscience, 13(2), 253-260. doi. 

Baker, C. A., Bolton, M. M., & Parra, A. (2019). Regional Specialization of Pyramidal Neuron Morphology and Physiology in the Tree Shrew Neocortex. doi: 10.1093/cercor/bhy326. https://dx.doi.org/10.1093/cercor/bhy326


Baker, F. C., Shah, S., Stewart, D., Angara, C., Gong, H., Szymusiak, R., . . . McGinty, D. (2005). Interleukin 1β enhances non-rapid eye movement sleep and increases c-Fos protein expression in the median preoptic nucleus of the hypothalamus. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 288(4), R998–R1005-R1998–R1005. doi. 

Bakken, G. S., Colayori, S. E., & Duong, T. (2012). Analytical methods for the geometric optics of thermal vision illustrated with four species of pitvipers. Journal of Experimental Biology, 215(15), 2621-2629. doi: 10.1242/jeb.063495. http://jeb.biologists.org/content/215/15/2621.abstract


Bakken, T. E., & Stevens, C. F. (2012). Visual system scaling in teleost fish. Journal of Comparative Neurology, 520(1), 142-153. doi: 10.1002/cne.22704. http://dx.doi.org/10.1002/cne.22704


Bakker, R., & Tiesinga, P. H. E. (2016). Web-based neuron morphology viewer as an aid to develop new standards for neuron morphology file formats. [Abstract]. Frontiers in neuroinformatics. doi: 10.3389/conf.fninf.2016.20.00079. http://www.frontiersin.org/Journal/FullText.aspx?s=752&name=neuroinforma...


Baksa, B., Kovács, A., Bayasgalan, T., Szentesi, P., Kőszeghy, Á., Szücs, P., & Pál, B. (2019). Characterization of functional subgroups among genetically identified cholinergic neurons in the pedunculopontine nucleus. [journal article]. Cellular and Molecular Life Sciences. doi: 10.1007/s00018-019-03025-4. https://doi.org/10.1007/s00018-019-03025-4


Bal, R., Green, G. G. R., Rees, A., & Sanders, D. J. (2002). Firing patterns of inferior colliculus neurons-histology and mechanism to change firing patterns in rat brain slices. Neuroscience Letters, 317(1), 42-46. doi. 

Balakrishnan, B., Dai, H., Janisse, J., Romero, R., & Kannan, S. (2013). Maternal Endotoxin Exposure Results in Abnormal Neuronal Architecture in the Newborn Rabbit. Developmental Neuroscience. doi. 

Balan, I. S., Fiskum, G., & Kristian, T. (2010). Visualization and quantification of NAD (H) in brain sections by a novel histo-enzymatic nitrotetrazolium blue staining technique. Brain Research, 1316, 112-119. doi. 

Balaram, P., Hackett, T. A., & Kaas, J. H. (2013). Differential expression of vesicular glutamate transporters 1 and 2 may identify distinct modes of glutamatergic transmission in the macaque visual system. Journal of Chemical Neuroanatomy, (0). doi: http://dx.doi.org/10.1016/j.jchemneu.2013.02.007. http://www.sciencedirect.com/science/article/pii/S0891061813000185


Balaram, P., Isaamullah, M., Petry, H. M., Bickford, M. E., & Kaas, J. H. (2014). Distributions of vesicular glutamate transporters 1 and 2 in the visual system of tree shrews (Tupaia belangeri). Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23727. http://dx.doi.org/10.1002/cne.23727


Baldi, A., Calia, E., Ciampini, A., Riccio, M., Vetuschi, A., Persico, A. M., & Keller, F. (2000). Deafferentation-induced apoptosis of neurons in thalamic somatosensory nuclei of the newborn rat: critical period and rescue from cell death by peripherally applied neurotrophins. European Journal of Neuroscience, 12(7), 2281. doi. 

Baldwin, M. K. L., Balaram, P., & Kaas, J. H. (2012). Projectionsof the superior colliculus to the pulvinar in prosimian galagos(Otolemur garnettii) and VGLUT2 staining of the visual pulvinar. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23252. http://dx.doi.org/10.1002/cne.23252


Baldwin, M. K. L., & Kaas, J. H. (2011). Cortical projections to the superior colliculus in prosimian galagos (Otolemur garnetti). Journal of Comparative Neurology. doi. 

Baldwin, M. K. L., Kaskan, P. M., Zhang, B., Chino, Y. M., & Kaas, J. H. (2012). Cortical and subcortical connections of V1 and V2 in early postnatal macaque monkeys. Journal of Comparative Neurology, 520(3), 544-569. doi: 10.1002/cne.22732. http://dx.doi.org/10.1002/cne.22732


Baldwin, M. K. L., Wong, P., Reed, J. L., & Kaas, J. H. (2011). Superior colliculus connections with visual thalamus in gray squirrels (Sciurus carolinensis): Evidence for four subdivisions within the pulvinar complex. Journal of Comparative Neurology, 519(6), 1071-1094. doi: 10.1002/cne.22552. http://dx.doi.org/10.1002/cne.22552


Balemans, M. C. M., Kasri, N. N., Kopanitsa, M. V., Afinowi, N. O., Ramakers, G., Peters, T. A., . . . Van der Zee, C. E. E. M. (2012). Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome. Human Molecular Genetics. doi: 10.1093/hmg/dds490. http://hmg.oxfordjournals.org/content/early/2012/11/21/hmg.dds490.abstract


Bálint, E., Kitka, T., Zachar, G., Ádám, Á., Hemmings, H. C., & Csillag, A. (2004). Abundance and location of DARPP-32 in striato-tegmental circuits of domestic chicks. Journal of Chemical Neuroanatomy, 28(1), 27-36. doi. 

Balka, L., Hägerrotha, P.-Å., Åkermana, G., Hansona, M., Tjärnlunda, U., Hanssona, T., . . . Sundberga, H. (2009). Wild birds of declining European species are dying from a thiamine deficiency syndrome. Proceedings of the National Academy of Sciences, 106(29), 12001-12006. doi: 10.1073/pnas.0902903106. http://www.pnas.org/content/106/29/12001.abstract 


Ball, K. T., Wellman, C. L., Fortenberry, E., & Rebec, G. V. (2009). Sensitizing regimens of ($\pm$) 3, 4-methylenedioxymethamphetamine (ecstasy) elicit enduring and differential structural alterations in the brain motive circuit of the rat. Neuroscience, 160(2), 264-274. doi. 

Ball, K. T., Wellman, C. L., Fortenberry, E., & Rebec, G. V. (2009). Sensitizing regimens of MDMA (ecstasy) elicit enduring and differential structural alterations in the brain motive circuit of the rat. Neuroscience, 160(2), 264-264. doi. 

Ball, K. T., Wellman, C. L., Miller, B. R., & Rebec, G. V. (2010). Electrophysiological and structural alterations in striatum associated with behavioral sensitization to ($\pm$) 3, 4-methylenedioxymethamphetamine (ecstasy) in rats: role of drug context. Neuroscience, 171(3), 794-811. doi. 

Ballesteros-Yanez, I., Ambrosio, E., Benavides-Piccione, R., Perez, J., Torres, I., Miguens, M., . . . DeFelipe, J. (2007). The effects of morphine self-administration on cortical pyramidal cell structure in addiction-prone Lewis rats. Cerebral Cortex, 17(1), 238-249. doi. 

Ballesteros-Yanez, I., Ambrosio, E., Pérez, J., Torres, I., Miguéns, M., García-Lecumberri, C., & Defelipe, J. (2008). Morphine self-administration effects on the structure of cortical pyramidal cells in addiction-resistant rats. Brain Research. doi. 

Ballesteros-Yanez, I., Benavides-Piccione, R., Bourgeois, J.-P., Changeux, J.-P., & DeFelipe, J. (2010). Alterations of cortical pyramidal neurons in mice lacking high-affinity nicotinic receptors. Proceedings of the National Academy of Sciences, 107(25), 11567-11572. doi: 10.1073/pnas.1006269107. http://www.pnas.org/content/107/25/11567.abstract 


Ballesteros-Yanez, I., Benavides-Piccione, R., Elston, G. N., Yuste, R., & DeFelipe, J. (2006). Density and morphology of dendritic spines in mouse neocortex. Neuroscience, 138(2), 403-409. doi. 

Ballesteros-Yáñez, I., Valverde, O., Ledent, C., Maldonado, R., & DeFelipe, J. (2007). Chronic cocaine treatment alters dendritic arborization in the adult motor cortex through a CB< sub> 1</sub> cannabinoid receptor–dependent mechanism. Neuroscience, 146(4), 1536-1545. doi. 

Ballester-Rosado, C. J., Albright, M. J., Wu, C.-S., Liao, C.-C., Zhu, J., Xu, J., . . . Lu, H.-C. (2010). mGluR5 in Cortical Excitatory Neurons Exerts Both Cell-Autonomous and -Nonautonomous Influences on Cortical Somatosensory Circuit Formation. Journal of Neuroscience, 30(50), 16896-16909. doi: 10.1523/jneurosci.2462-10.2010. http://www.jneurosci.org/cgi/content/abstract/30/50/16896


Ballester-Rosado, C. J., Sun, H., Huang, J.-Y., & Lu, H.-C. (2016). mGluR5 Exerts Cell-Autonomous Influences on the Functional and Anatomical Development of Layer IV Cortical Neurons in the Mouse Primary Somatosensory Cortex. The Journal of Neuroscience, 36(34), 8802-8814. doi. http://www.jneurosci.org/content/36/34/8802.short


Ballou, E. W., Smith, W. B., Anelli, R., & Heckman, C. J. (2006). Measuring dendritic distribution of membrane proteins. Journal of Neuroscience Methods, 156(1-2), 257-266. doi. 

Balsara, R. D., Ferreira, A. N., Donahue, D. L., Castellino, F. J., & Sheets, P. L. (2014). Probing NMDA receptor GluN2A and GluN2B subunit expression and distribution in cortical neurons. Neuropharmacology, (0). doi: http://dx.doi.org/10.1016/j.neuropharm.2014.01.005. http://www.sciencedirect.com/science/article/pii/S0028390814000124


Baltussen, L. L., Negraes, P. D., Silvestre, M., Claxton, S., Moeskops, M., Christodoulou, E., . . . Ultanir, S. K. (2018). Chemical genetic identification of CDKL5 substrates reveals its role in neuronal microtubule dynamics. [10.15252/embj.201899763]. The EMBO journal. doi. http://emboj.embopress.org/content/early/2018/09/28/embj.201899763.abstract


Balu, D. T., Basu, A. C., Corradi, J. P., Cacace, A. M., & Coyle, J. T. (2011). The NMDA receptor co-agonists, d-serine and glycine, regulate neuronal dendritic architecture in the somatosensory cortex. Neurobiology of Disease. doi. 

Balu, D. T., & Coyle, J. T. (2012). Neuronal d-serine regulates dendritic architecture in the somatosensory cortex. Neuroscience Letters, 517(2), 77-81. doi: 10.1016/j.neulet.2012.04.020. http://www.sciencedirect.com/science/article/pii/S0304394012005289


Balu, D. T., & Coyle, J. T. (2014). Chronic D-serine reverses arc expression and partially rescues dendritic abnormalities in a mouse model of NMDA receptor hypofunction. Neurochemistry International, (0). doi: http://dx.doi.org/10.1016/j.neuint.2014.05.015. http://www.sciencedirect.com/science/article/pii/S0197018614001375


Balu, D. T., Li, Y., Puhl, M. D., Benneyworth, M. A., Basu, A. C., Takagi, S., . . . Coyle, J. T. (2013). Multiple risk pathways for schizophrenia converge in serine racemase knockout mice, a mouse model of NMDA receptor hypofunction. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1304308110. http://www.pnas.org/content/early/2013/05/30/1304308110.abstract


Bamber, N. I., Li, H., Lu, X., Oudega, M., Aebischer, P., & Xu, X. M. (2001). Neurotrophins BDNF and NT-3 promote axonal re-entry into the distal host spinal cord through Schwann cell-seeded mini-channels. European Journal of Neuroscience, 13(2), 257. doi. 

Bamberl, N. I., Li, H., & Xu, M. (1999). into Hemisected Adult Rat Spinal Cords. Neural Plasticity, 6(4). doi. 

Bang, P. I., Sewell, W. F., & Malicki, J. J. (2001). Morphology and cell type heterogeneities of the inner ear epithelia in adult and juvenile zebrafish (Danio rerio). Journal of Comparative Neurology, 438(2), 173-190. doi. 

Bang, S. J., & Brown, T. H. (2009). Perirhinal cortex supports acquired fear of auditory objects. Neurobiology of Learning and Memory, 92(1), 53-62. doi. 

Bangasser, D., Zhang, X., Garachh, V., Hanhauser, E., & Valentino, R. (2011). Sexual dimorphism in locus coeruleus dendritic morphology: a structural basis for sex differences in emotional arousal. Physiology and Behavior. doi. 

Bangasser, D. A., Reyes, B. A. S., Piel, D., Garachh, V., Zhang, X. Y., Plona, Z. M., . . . Valentino, R. J. (2012). Increased vulnerability of the brain norepinephrine system of females to corticotropin-releasing factor overexpression. Molecular Psychiatry. doi. 

Banke, T. G., & McBain, C. J. (2006). GABAergic Input onto CA3 Hippocampal Interneurons Remains Shunting throughout Development. Journal of Neuroscience, 26(45), 11720-11725. doi: 10.1523/jneurosci.2887-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/45/11720 


Banks, G. T., Haas, M. A., Line, S., Shepherd, H. L., AlQatari, M., Stewart, S., . . . Fisher, E. M. C. (2011). Behavioral and Other Phenotypes in a Cytoplasmic Dynein Light Intermediate Chain 1 Mutant Mouse. Journal of Neuroscience, 31(14), 5483-5494. doi: 10.1523/jneurosci.5244-10.2011. http://www.jneurosci.org/content/31/14/5483.abstract


Bannatyne, B. A., Liu, T. T., Hammar, I., Stecina, K., Jankowska, E., & Maxwell, D. J. (2009). Excitatory and inhibitory intermediate zone interneurons in pathways from feline group I and II afferents: differences in axonal projections and input. Journal of Physiology, 587(2), 379-399. doi: 10.1113/jphysiol.2008.159129. http://jp.physoc.org/cgi/content/abstract/587/2/379 


Banno, R., Arima, H., Hayashi, M., Goto, M., Watanabe, M., Sato, I., . . . Oiso, Y. (2007). Central administration of melanocortin agonist increased insulin sensitivity in diet-induced obese rats. FEBS Letters, 581(6), 1131-1136. doi. 

Banno, T., Ichinohe, N., Rockland, K. S., & Komatsu, H. (2011). Reciprocal Connectivity of Identified Color-Processing Modules in the Monkey Inferior Temporal Cortex. Cerebral Cortex, 21(6), 1295-1310. doi. 

Banovac, I., Sedmak, D., Džaja, D., Jalšovec, D., Jovanov Milošević, N., Rašin, M. R., & Petanjek, Z. (2019). Somato-dendritic morphology and axon origin site specify von Economo neurons as a subclass of modified pyramidal neurons in the human anterior cingulate cortex. Journal of Anatomy, 235(3), 651-669. doi: 10.1111/joa.13068. https://onlinelibrary.wiley.com/doi/abs/10.1111/joa.13068


Bantle, C. M., Phillips, A. T., Smeyne, R. J., Rocha, S. M., Olson, K. E., & Tjalkens, R. B. (2019). Infection with mosquito-borne alphavirus induces selective loss of dopaminergic neurons, neuroinflammation and widespread protein aggregation. npj Parkinson's Disease, 5(1), 20. doi: 10.1038/s41531-019-0090-8. https://doi.org/10.1038/s41531-019-0090-8


Bao, Y., Bramlett, H. M., Atkins, C. M., Truettner, J. S., Lotocki, G., Alonso, O. F., & Dietrich, W. D. (2011). Post-traumatic seizures exacerbate histopathological damage after fluid-percussion brain injury. Journal of Neurotrauma, 28(1), 35-42. doi. 

Bao, Y., Hua, B., Hou, W., Shi, Z., Li, W., Li, C., . . . Qin, Y. (2013). Involvement of Protease-Activated Receptor 2 in Nociceptive Behavior in a Rat Model of Bone Cancer. Journal of Molecular Neuroscience, 1-11. doi: 10.1007/s12031-013-0112-7. http://dx.doi.org/10.1007/s12031-013-0112-7


Baptista, S., Lourenço, J., Milhazes, N., Borges, F., Paula Silva, A., & Bacci, A. (2016). Chronic treatment with low doses of methamphetamine promotes neuronal differentiation and strengthens long-term potentiation of glutamatergic synapses onto dentate granule neurons. [10.1523/ENEURO.0141-16.2016]. eneuro. doi. http://eneuro.org/content/early/2016/06/22/ENEURO.0141-16.2016.abstract


Baptista, V., Zheng, Z. L., Coleman, F. H., Rogers, R. C., & Travagli, R. A. (2005). Characterization of neurons of the nucleus tractus solitarius pars centralis. Brain Research, 1052(2), 139-146. doi. 

Baptista, V., Zheng, Z. L., Coleman, F. H., Rogers, R. C., & Travagli, R. A. (2005). Cholecystokinin Octapeptide Increases Spontaneous Glutamatergic Synaptic Transmission to Neurons of the Nucleus Tractus Solitarius Centralis. Journal of Neurophysiology, 94(4), 2763-2771. doi: 10.1152/jn.00351.2005. http://jn.physiology.org/cgi/content/abstract/94/4/2763 


Baquet, Z. C., Bickford, P. C., & Jones, K. R. (2005). Brain-Derived Neurotrophic Factor Is Required for the Establishment of the Proper Number of Dopaminergic Neurons in the Substantia Nigra Pars Compacta. Journal of Neuroscience, 25(26), 6251-6259. doi: 10.1523/jneurosci.4601-04.2005. http://www.jneurosci.org/cgi/content/abstract/25/26/6251 


Baquet, Z. C., Gorski, J. A., & Jones, K. R. (2004). Early Striatal Dendrite Deficits followed by Neuron Loss with Advanced Age in the Absence of Anterograde Cortical Brain-Derived Neurotrophic Factor. Journal of Neuroscience, 24(17), 4250-4258. doi: 10.1523/jneurosci.3920-03.2004. http://www.jneurosci.org/cgi/content/abstract/24/17/4250 


Baraban, S. C., Stornetta, R. L., & Guyenet, P. G. (1995). Effects of morphine and morphine withdrawal on adrenergic neurons of the rat rostral ventrolateral medulla. Brain Research, 676(2), 245-257. doi. 

Barakat-Walter, I., Kraftsik, R., Kuntzer, T., Bogousslavsky, J., & Magistretti, P. (2000). Differential effect of thyroid hormone deficiency on the growth of calretinin–expressing neurons in rat spinal cord and dorsal root ganglia. Journal of Comparative Neurology, 426(4), 519-533. doi. 

Barakat-Walter, I., Kraftsik, R., Schenker, M., & Kuntzer, T. (2007). Thyroid hormone in biodegradable nerve guides stimulates sciatic nerve regeneration: a potential therapeutic approach for human peripheral nerve injuries. Journal of Neurotrauma, 24(3), 567-577. doi. 

Baranova, O., Miranda, L. F., Pichiule, P., Dragatsis, I., Johnson, R. S., & Chavez, J. C. (2007). Neuron-Specific Inactivation of the Hypoxia Inducible Factor 1α Increases Brain Injury in a Mouse Model of Transient Focal Cerebral Ischemia. Journal of Neuroscience, 27(23), 6320-6332. doi: 10.1523/jneurosci.0449-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/23/6320 


Barapatre, N., Haeussner, E., Grynspan, D., Schmitz, C., Edler von Koch, F., & Frank, H.-G. (2019). The Density of Cell Nuclei at the Materno-Fetal Exchange Barrier is Sexually Dimorphic in Normal Placentas, but not in IUGR. Scientific Reports, 9(1), 2359. doi: 10.1038/s41598-019-38739-9. https://doi.org/10.1038/s41598-019-38739-9


Barapatre, N., Kampfer, C., Henschen, S., Schmitz, C., Edler von Koch, F., & Frank, H.-G. (2021). Growth restricted placentas show severely reduced volume of villous components with perivascular myofibroblasts. Placenta, 109, 19-27. doi: https://doi.org/10.1016/j.placenta.2021.04.006. https://www.sciencedirect.com/science/article/pii/S0143400421001211


Barbas, H., Medalla, M., Alade, O., Suski, J., Zikopoulos, B., & Lera, P. (2005). Relationship of prefrontal connections to inhibitory systems in superior temporal areas in the rhesus monkey. Cerebral Cortex, 15(9), 1356-1356. doi. 

Barbas, H., Saha, S., Rempel-Clower, N., & Ghashghaei, T. (2003). Serial pathways from primate prefrontal cortex to autonomic areas may influence emotional expression. BMC Neuroscience, 4(1), 25. doi. http://www.biomedcentral.com/1471-2202/4/25 


Barbour, D. L., & Callaway, E. M. (2008). Excitatory Local Connections of Superficial Neurons in Rat Auditory Cortex. Journal of Neuroscience, 28(44), 11174-11185. doi: 10.1523/jneurosci.2093-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/44/11174 


Bardi, M., True, M., Franssen, C. L., Kaufman, C., Rzucidlo, A., & Lambert, K. G. (2012). Effort-Based Reward (EBR) training enhances neurobiological efficiency in a problem-solving task: Insights for depression therapies. Brain Research, (0). doi: 10.1016/j.brainres.2012.10.027. http://www.sciencedirect.com/science/article/pii/S0006899312016733


Bardy, C., van den Hurk, M., Kakaradov, B., Erwin, J. A., Jaeger, B. N., Hernandez, R. V., . . . Gage, F. H. (2016). Predicting the functional states of human iPSC-derived neurons with single-cell RNA-seq and electrophysiology. [Original Article]. Molecular Psychiatry. doi: 10.1038/mp.2016.158. http://dx.doi.org/10.1038/mp.2016.158


Barhwal, K., Das, S. K., Kumar, A., Hota, S. K., Srivastava, R. B., & Kumar, B. (2015). Insulin Receptor A and Sirtuin 1 synergistically improve learning and spatial memory following chronic salidroside treatment during hypoxia. Journal of Neurochemistry, n/a-n/a. doi: 10.1111/jnc.13225. http://dx.doi.org/10.1111/jnc.13225


Bari, B. A., Ollerenshaw, D. R., Millard, D. C., Wang, Q., & Stanley, G. B. (2013). Behavioral and Electrophysiological Effects of Cortical Microstimulation Parameters. PLoS ONE, 8(12), e82170. doi: 10.1371/journal.pone.0082170. http://dx.doi.org/10.1371%2Fjournal.pone.0082170


Barini, E., Antico, O., Zhao, Y., Asta, F., Tucci, V., Catelani, T., . . . Gasparini, L. (2016). Metformin promotes tau aggregation and exacerbates abnormal behavior in a mouse model of tauopathy. [journal article]. Molecular Neurodegeneration, 11(1), 1-20. doi: 10.1186/s13024-016-0082-7. http://dx.doi.org/10.1186/s13024-016-0082-7


Barkan, S., Ayali, A., Nottebohm, F., & Barnea, A. (2007). Neuronal recruitment in adult zebra finch brain during a reproductive cycle. Developmental Neurobiology, 67(6), 687-701. doi. 

Barkat, T. R., Polley, D. B., & Hensch, T. K. (2011). A critical period for auditory thalamocortical connectivity. Nature Neuroscience, 14(9), 1189-1194. doi. 

Barna, B. F., Takakura, A. C., & Moreira, T. S. (2012). Pontomedullary and hypothalamic distribution of Fos-like immunoreactive neurons after acute exercise in rats. Neuroscience, 212(0), 120-130. doi: 10.1016/j.neuroscience.2012.03.039. http://www.sciencedirect.com/science/article/pii/S030645221200303X


Barnea, A., Mishal, A., & Nottebohm, F. (2006). Social and spatial changes induce multiple survival regimes for new neurons in two regions of the adult brain: An anatomical representation of time? Behavioural Brain Research, 167(1), 63-74. doi. 

Baron, J., Blex, C., Rohrbeck, A., Rachakonda, S. K., Birnbaumer, L., Ahnert-Hilger, G., & Brunk, I. (2012). The α-subunit of the trimeric GTPase Go2 regulates axonal growth. Journal of Neurochemistry, n/a-n/a. doi: 10.1111/jnc.12123. http://dx.doi.org/10.1111/jnc.12123


Baron, M. S., Noonan, J. B., & Mewes, K. (2006). Restricted ablative lesions in motor portions of GPi in primates produce extensive loss of motor-related neurons and degeneration of the lenticular fasciculus. Experimental Neurology, 202(1), 67-75. doi. 

Baroody, F. M., Cheng, C. C., Moylan, B., deTineo, M., Haney, L., Reed, K. D., . . . others. (2001). Absence of nasal mucosal atrophy with fluticasone aqueous nasal spray. Archives of Otolaryngology- Head and Neck Surgery, 127(2), 193-193. doi. 

Barr, T. P., Albrecht, P. J., Hou, Q., Mongin, A. A., Strichartz, G. R., & Rice, F. L. (2013). Air-Stimulated ATP Release from Keratinocytes Occurs through Connexin Hemichannels. PLoS ONE, 8(2), e56744. doi: 10.1371/journal.pone.0056744. http://dx.doi.org/10.1371%2Fjournal.pone.0056744


Barrera, K., Chu, P., Abramowitz, J., Steger, R., Ramos, R. L., & Brumberg, J. C. (2012). Organization of myelin in the mouse somatosensory barrel cortex and the effects of sensory deprivation. Developmental Neurobiology, n/a-n/a. doi: 10.1002/dneu.22060. http://dx.doi.org/10.1002/dneu.22060


Barthas, F., Sellmeijer, J., Hugel, S., Waltisperger, E., Barrot, M., & Yalcin, I. (2014). The Anterior Cingulate Cortex is a Critical Hub for Pain-Induced Depression. Biological Psychiatry. doi: 10.1016/j.biopsych.2014.08.004. http://www.biologicalpsychiatryjournal.com/article/S0006-3223(14)00597-6/abstract

Bartho, P., Slezia, A., Varga, V., Bokor, H., Pinault, D., Buzsaki, G., & Acsady, L. (2007). Cortical Control of Zona Incerta. Journal of Neuroscience, 27(7), 1670-1681. doi: 10.1523/jneurosci.3768-06.2007. http://www.jneurosci.org/cgi/content/abstract/27/7/1670 


Bartkowska, K., Aniszewska, A., Turlejski, K., & Djavadian, R. L. (2014). Distribution and function of TrkB receptors in the developing brain of the opossum Monodelphis domestica. Developmental Neurobiology, n/a-n/a. doi: 10.1002/dneu.22165. http://dx.doi.org/10.1002/dneu.22165


Bartkowska, K., Gajerska, M., Turlejski, K., & Djavadian, R. L. (2013). Expression of TrkC Receptors in the Developing Brain of the <italic>Monodelphis</italic><italic> opossum</italic> and Its Effect on the Development of Cortical Cells. Plos one, 8(9), e74346. doi: 10.1371/journal.pone.0074346. http://dx.doi.org/10.1371%2Fjournal.pone.0074346


Bartkowska, K., Swiatek, I., Aniszewska, A., Jurewicz, E., Turlejski, K., Filipek, A., & Djavadian, R. L. (2017). Stress-Dependent Changes in the CacyBP/SIP Interacting Protein S100A6 in the Mouse Brain. PLoS ONE, 12(1), e0169760. doi: 10.1371/journal.pone.0169760. http://dx.doi.org/10.1371%2Fjournal.pone.0169760


Bartkowska, K., Turlejski, K., Grabiec, M., Ghazaryan, A., Yavruoyan, E., & Djavadian, R. L. (2010). Adult neurogenesis in the hedgehog (Erinaceus concolor) and mole (Talpa europaea). Brain, Behavior and Evolution, 76(2), 128-143. doi. 

Bartlett, E. L., & Smith, P. H. (1999). Anatomic, Intrinsic, and Synaptic Properties of Dorsal and Ventral Division Neurons in Rat Medial Geniculate Body. Journal of Neurophysiology, 81(5), 1999-2016. doi. http://jn.physiology.org/cgi/content/abstract/81/5/1999 


Bartolini, A., Vigliani, M. C., Magrassi, L., Vercelli, A., & Rossi, F. (2011). G-CSF administration to adult mice stimulates the proliferation of microglia but does not modify the outcome of ischemic injury. Neurobiology of Disease, 41(3), 640-649. doi. 

Bartos, M., Vida, I., Frotscher, M., Geiger, J. R. P., & Jonas, P. (2001). Rapid Signaling at Inhibitory Synapses in a Dentate Gyrus Interneuron Network. Journal of Neuroscience, 21(8), 2687-2698. doi. http://www.jneurosci.org/cgi/content/abstract/21/8/2687


Bartus, R. T., Baumann, T. L., Brown, L., Kruegel, B. R., Ostrove, J. M., & Herzog, C. D. (2012). Advancing neurotrophic factors as treatments for age-related neurodegenerative diseases: developing and demonstrating “clinical proof-of-concept” for AAV-neurturin (CERE-120) in Parkinson's disease. Neurobiology of Aging, (0). doi: 10.1016/j.neurobiolaging.2012.07.018. http://www.sciencedirect.com/science/article/pii/S0197458012004216


Bar-Yehuda, D., & Korngreen, A. (2008). Space-Clamp Problems When Voltage Clamping Neurons Expressing Voltage-Gated Conductances. Journal of Neurophysiology, 99(3), 1127-1136. doi: 10.1152/jn.01232.2007. http://jn.physiology.org/cgi/content/abstract/99/3/1127 


Basaldella, E., Takeoka, A., Sigrist, M., & Arber, S. (2015). Multisensory Signaling Shapes Vestibulo-Motor Circuit Specificity. Cell, 163(2), 301-312. doi: http://dx.doi.org/10.1016/j.cell.2015.09.023. http://www.sciencedirect.com/science/article/pii/S0092867415011848


Baseer, N., Polgár, E., Watanabe, M., Furuta, T., Kaneko, T., & Todd, A. J. (2012). Projection Neurons in Lamina III of the Rat Spinal Cord Are Selectively Innervated by Local Dynorphin-Containing Excitatory Neurons. Journal of Neuroscience, 32(34), 11854-11863. doi: 10.1523/jneurosci.2707-12.2012. http://www.jneurosci.org/content/32/34/11854.abstract


Bashir, K., Elble, R. J., Ghobrial, M., & Struble, R. G. (1998). Hemianopsia in Dementia With Lewy Bodies. Archives of Neurology, 55(8), 1132-1135. doi: 10.1001/archneur.55.8.1132. http://archneur.ama-assn.org/cgi/content/abstract/55/8/1132 


Bashir, S., Kaeser, M., Wyss, A., Hamadjida, A., Liu, Y., Bloch, J., . . . Rouiller, E. M. (2012). Short-term effects of unilateral lesion of the primary motor cortex (M1) on ipsilesional hand dexterity in adult macaque monkeys. Brain Structure and Function, 1-17. doi. 

Bast, T., Wilson, I. A., Witter, M. P., & Morris, R. G. M. (2009). From rapid place learning to behavioral performance: a key role for the intermediate hippocampus. PLoS Biology, 7(4), e1000089-e1000089. doi. 

Bast, T., Zhang, W. N., & Feldon, J. (2003). Dorsal hippocampus and classical fear conditioning to tone and context in rats: Effects of local NMDA-receptor blockade and stimulation. Hippocampus, 13(6), 657-675. doi. 

Bastidas, J., Athauda, G., De La Cruz, G., Chan, W.-M., Golshani, R., Berrocal, Y., . . . Pearse, D. D. (2017). Human schwann cells exhibit long-term cell survival, are not tumorigenic and promote repair when transplanted into the contused spinal cord. Glia, n/a-n/a. doi: 10.1002/glia.23161. http://dx.doi.org/10.1002/glia.23161


bastien Jouhanneau, J.-S., Kremkow, J., Dorrn, A. L., & Poulet, J. F. (2015). In Vivo Monosynaptic Excitatory Transmission between Layer 2 Cortical Pyramidal Neurons. doi. http://www.cell.com/cell-reports/pdf/S2211-1247(15)01311-X.pdf

Basting, T. M., Abe, C., Viar, K. E., Stornetta, R. L., & Guyenet, P. G. (2016). Is plasticity within the retrotrapezoid nucleus responsible for the recovery of the PCO2 set-point after carotid body denervation in rats? The Journal of Physiology, n/a-n/a. doi: 10.1113/jp272046. http://dx.doi.org/10.1113/JP272046


Basting, T. M., Burke, P. G., Kanbar, R., Viar, K. E., Stornetta, D. S., Stornetta, R. L., & Guyenet, P. G. (2015). Hypoxia Silences Retrotrapezoid Nucleus Respiratory Chemoreceptors via Alkalosis. The Journal of Neuroscience, 35(2), 527-543. doi. http://www.jneurosci.org/content/35/2/527.short


Basu, J., Srinivas, Kalyan V., Cheung, Stephanie K., Taniguchi, H., Huang, Z. J., & Siegelbaum, Steven A. (2013). A Cortico-Hippocampal Learning Rule Shapes Inhibitory Microcircuit Activity to Enhance Hippocampal Information Flow. Neuron, 79(6), 1208-1221. doi: http://dx.doi.org/10.1016/j.neuron.2013.07.001. http://www.sciencedirect.com/science/article/pii/S0896627313005667


Basu, J., Zaremba, J. D., Cheung, S. K., Hitti, F. L., Zemelman, B. V., Losonczy, A., & Siegelbaum, S. A. (2016). Gating of hippocampal activity, plasticity, and memory by entorhinal cortex long-range inhibition. [10.1126/science.aaa5694]. Science, 351(6269). doi. http://science.sciencemag.org/content/351/6269/aaa5694.abstract


Batalha, V. L., Pego, J. M., Fontinha, B. M., Costenla, A. R., Valadas, J. S., Baqi, Y., . . . Lopes, L. V. (2012). Adenosine A2A receptor blockade reverts hippocampal stress-induced deficits and restores corticosterone circadian oscillation. Molecular Psychiatry. doi. 

Bathellier, B., Margrie, T. W., & Larkum, M. E. (2009). Properties of Piriform Cortex Pyramidal Cell Dendrites: Implications for Olfactory Circuit Design. Journal of Neuroscience, 29(40), 12641-12652. doi: 10.1523/jneurosci.1124-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/40/12641 


Batista-Brito, R., Rossignol, E., Hjerling-Leffler, J., Denaxa, M., Wegner, M., Lefebvre, V., . . . Fishell, G. (2009). The Cell-Intrinsic Requirement of< i> Sox6</i> for Cortical Interneuron Development. Neuron, 63(4), 466-481. doi. 

Batra, R., & Fitzpatrick, D. C. (1997). Neurons Sensitive to Interaural Temporal Disparities in the Medial Part of the Ventral Nucleus of the Lateral Lemniscus. Journal of Neurophysiology, 78(1), 511-515. doi. http://jn.physiology.org/cgi/content/abstract/78/1/511 


Batra, R., & Fitzpatrick, D. C. (1999). Discharge Patterns of Neurons in the Ventral Nucleus of the Lateral Lemniscus of the Unanesthetized Rabbit. Journal of Neurophysiology, 82(3), 1097-1113. doi. http://jn.physiology.org/cgi/content/abstract/82/3/1097 


Baufreton, J., Kirkham, E., Atherton, J. F., Menard, A., Magill, P. J., Bolam, J. P., & Bevan, M. D. (2009). Sparse but selective and potent synaptic transmission from the globus pallidus to the subthalamic nucleus. Journal of Neurophysiology, 00305.02009. doi: 10.1152/jn.00305.2009. http://jn.physiology.org/cgi/content/abstract/00305.2009v1 


Baulch, J. E., Acharya, M. M., Allen, B. D., Ru, N., Chmielewski, N. N., Martirosian, V., . . . Limoli, C. L. (2016). Cranial grafting of stem cell-derived microvesicles improves cognition and reduces neuropathology in the irradiated brain. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1521668113. http://www.pnas.org/content/early/2016/03/30/1521668113.abstract


Baum, P., Vogt, M. A., Gass, P., Unsicker, K., & von Bohlen und Halbach, O. (2016). FGF-2 deficiency causes dysregulation of Arhgef6 and downstream targets in the cerebral cortex accompanied by altered neurite outgrowth and dendritic spine morphology. International Journal of Developmental Neuroscience. doi: http://dx.doi.org/10.1016/j.ijdevneu.2016.03.002. http://www.sciencedirect.com/science/article/pii/S0736574816300259


Bäurle, J., Frischmuth, S., & Kranda, K. (2004). TRAIL-related death receptors in normal,< i> Lurcher</i> and< i> weaver</i> mutant mouse brain. Neuroscience Letters, 372(1), 46-51. doi. 

Bausch, S. B., He, S., Petrova, Y., Wang, X.-M., & McNamara, J. O. (2006). Plasticity of Both Excitatory and Inhibitory Synapses Is Associated With Seizures Induced by Removal of Chronic Blockade of Activity in Cultured Hippocampus. Journal of Neurophysiology, 96(4), 2151-2167. doi: 10.1152/jn.00355.2006. http://jn.physiology.org/cgi/content/abstract/96/4/2151 


Bayraktar, T., Welker, E., Freund, T. F., Zilles, K., & Staiger, J. F. (2000). Neurons immunoreactive for vasoactive intestinal polypeptide in the rat primary somatosensory cortex: Morphology and spatial relationship to barrel-related columns. Journal of Comparative Neurology, 420(3), 291-304. doi. 

Bazelot, M., Dinocourt, C., Cohen, I., & Miles, R. (2010). Unitary inhibitory field potentials in the CA3 region of rat hippocampus. Journal of Physiology, 588(12), 2077-2090. doi. 

Bazelot, M., Simonnet, J., Dinocourt, C., Bruel-Jungerman, E., Miles, R., Fricker, D., & Francis, F. (2012). Cellular anatomy, physiology and epileptiform activity in the CA3 region of Dcx knockout mice: a neuronal lamination defect and its consequences. European Journal of Neuroscience, 35(2), 244-256. doi. 

Bearden, S. E. (2006). Effect of aging on the structure and function of skeletal muscle microvascular networks. Microcirculation, 13(4), 279-288. doi. 

Bearden, S. E., Payne, G. W., Chisty, A., & Segal, S. S. (2004). Arteriolar network architecture and vasomotor function with ageing in mouse gluteus maximus muscle. Journal of Physiology, 561(2), 535-545. doi: 10.1113/jphysiol.2004.068262. http://jp.physoc.org/cgi/content/abstract/561/2/535 


Bearden, S. E., & Segal, S. S. (2005). Neurovascular Alignment in Adult Mouse Skeletal Muscles. Microcirculation, 12, 161-167. doi. 

Beare, J. E., Morehouse, J. R., DeVries, W. H., Enzmann, G. U., Burke, D. A., Magnuson, D. S. K., & Whittemore, S. R. (2009). Gait analysis in normal and spinal contused mice using the TreadScan system. Journal of Neurotrauma, 26(11), 2045-2056. doi. 

Beare, R., Richards, K., Murphy, S., Petrou, S., & Reutens, D. (2008). An assessment of methods for aligning two-dimensional microscope sections to create image volumes. Journal of Neuroscience Methods, 170(2), 332-344. doi. 

Beau, A. D., Shrestha, S. S., Anne Bannatyne, B., Jalicy, S. M., Linnen, S., & Maxwell, D. J. (2012). Neurotransmitter Phenotypes of Descending Systems in the Rat Lumbar Spinal Cord. Neuroscience, (0). doi: 10.1016/j.neuroscience.2012.09.037. http://www.sciencedirect.com/science/article/pii/S0306452212009578?v=s5


Beaud, M. L., Rouiller, E. M., Bloch, J., Mir, A., Schwab, M. E., Wannier, T., & Schmidlin, E. (2012). Invasion of lesion territory by regenerating fibers after spinal cord injury in adult macaque monkeys. Neuroscience, (0). doi: 10.1016/j.neuroscience.2012.09.052. http://www.sciencedirect.com/science/article/pii/S0306452212009724?v=s5


Beauparlant, J., van den Brand, R., Barraud, Q., Friedli, L., Musienko, P., Dietz, V., & Courtine, G. (2013). Undirected compensatory plasticity contributes to neuronal dysfunction after severe spinal cord injury. Brain. doi: 10.1093/brain/awt204. http://brain.oxfordjournals.org/content/early/2013/09/28/brain.awt204.ab...


Beaver, C. J., Cannon, R. C., & Turner, D. A. (2005). Cellular Morphology. Databasing the brain: from data to knowledge (neuroinformatics), 251-251. doi. 

Beck, L. A., & Wade, J. (2009). Morphology and estrogen receptor α mRNA expression in the developing green anole forebrain. Journal of Experimental Zoology Part A: Ecological Genetics and Physiology, 311(3), 162-171. doi. 

Becker, C. G., & Becker, T. (2000). Gradients of ephrin-A2 and ephrin-A5b mRNA during retinotopic regeneration of the optic projection in adult zebrafish. Journal of Comparative Neurology, 427(3), 469-483. doi. 

Becker, C. G., & Becker, T. (2002). Repellent Guidance of Regenerating Optic Axons by Chondroitin Sulfate Glycosaminoglycans in Zebrafish. Journal of Neuroscience, 22(3), 842-853. doi. http://www.jneurosci.org/cgi/content/abstract/22/3/842


Becker, K., Abraham, A., Kindler, J., Helmeke, C., & Braun, K. (2007). Exposure to neonatal separation stress alters exploratory behavior and corticotropin releasing factor expression in neurons in the amygdala and hippocampus. Developmental Neurobiology, 67(5), 617-629. doi. 

Becker, T., & Becker, C. G. (2001). Regenerating descending axons preferentially reroute to the gray matter in the presence of a general macrophage/microglial reaction caudal to a spinal transection in adult zebrafish. Journal of Comparative Neurology, 433(1), 131-147. doi. 

Becker, T., Becker, C. G., Schachner, M., & Bernhardt, R. R. (2001). Antibody to the HNK-1 glycoepitope affects fasciculation and axonal pathfinding in the developing posterior lateral line nerve of embryonic zebrafish. Mechanisms of Development, 109(1), 37-49. doi. 

Beckius, G. E., Batra, R., & Oliver, D. L. (1999). Axons from Anteroventral Cochlear Nucleus that Terminate in Medial Superior Olive of Cat: Observations Related to Delay Lines. Journal of Neuroscience, 19(8), 3146-3161. doi. http://www.jneurosci.org/cgi/content/abstract/19/8/3146


Becknell, B., Carpenter, A. R., Allen, J. L., Wilhide, M. E., Ingraham, S. E., Hains, D. S., & McHugh, K. M. (2013). Molecular Basis of Renal Adaptation in a Murine Model of Congenital Obstructive Nephropathy. PLoS ONE, 8(9), e72762. doi: 10.1371/journal.pone.0072762. http://dx.doi.org/10.1371%2Fjournal.pone.0072762


Becq, H., Jorquera, I., Ben-Ari, Y., Weiss, S., & Represa, A. (2005). Differential properties of dentate gyrus and CA1 neural precursors. Journal of Neurobiology, 62(2), 243-261. doi. 

Bedard, A., Gravel, C., & Parent, A. (2006). Chemical characterization of newly generated neurons in the striatum of adult primates. Experimental Brain Research, 170(4), 501-512. doi. 

Bedrosian, T. A., Fonken, L. K., Walton, J. C., Haim, A., & Nelson, R. J. (2011). Dim light at night provokes depression-like behaviors and reduces CA1 dendritic spine density in female hamsters. Psychoneuroendocrinology. doi. 

Bedrosian, T. A., Weil, Z. M., & Nelson, R. J. (2012). Chronic Citalopram Treatment Ameliorates Depressive Behavior Associated With Light at Night. Behavioral Neuroscience. doi: 10.1037/a0029699. 

Bedrosian, T. A., Weil, Z. M., & Nelson, R. J. (2012). Chronic dim light at night provokes reversible depression-like phenotype: possible role for TNF. Molecular Psychiatry. doi. http://dx.doi.org/10.1038/mp.2012.96


Beebe, N. L., & Schofield, B. R. (2018). Perineuronal nets in subcortical auditory nuclei of four rodent species with differing hearing ranges. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24383. http://dx.doi.org/10.1002/cne.24383


Beebe, N. L., Young, J. W., Mellott, J. G., & Schofield, B. R. (2016). Extracellular Molecular Markers and Soma Size of Inhibitory Neurons: Evidence for Four Subtypes of GABAergic Cells in the Inferior Colliculus. The Journal of Neuroscience, 36(14), 3988-3999. doi. http://www.jneurosci.org/content/36/14/3988.short


Beed, P., Bendels, M. H. K., Wiegand, H. F., Leibold, C., Johenning, F. W., & Schmitz, D. (2010). Analysis of excitatory microcircuitry in the medial entorhinal cortex reveals cell-type-specific differences. Neuron, 68(6), 1059-1066. doi. 

Beed, P., Gundlfinger, A., Schneiderbauer, S., Song, J., Böhm, C., Burgalossi, A., . . . Schmitz, D. (2013). Inhibitory Gradient along the Dorsoventral Axis in the Medial Entorhinal Cortex. Neuron, 79(6), 1197-1207. doi: http://dx.doi.org/10.1016/j.neuron.2013.06.038. http://www.sciencedirect.com/science/article/pii/S0896627313005540


Beed, P., Ray, S., Velasquez, L. M., Stumpf, A., Parthier, D., Swaminathan, A., . . . Schmitz, D. (2020). Species-specific differences in synaptic transmission and plasticity. Scientific Reports, 10(1), 16557. doi: 10.1038/s41598-020-73547-6. https://doi.org/10.1038/s41598-020-73547-6


Beers, D. R., Ho, B.-K., Sikl, L., Alexianu, M. E., Mosier, D. R., Mohamed, A. H., . . . Appel, S. H. (2001). Parvalbumin overexpression alters immune-mediated increases in intracellular calcium, and delays disease onset in a transgenic model of familial amyotrophic lateral sclerosis. Journal of Neurochemistry, 79(3), 499. doi. 

Beguin, S., Crépel, V., Aniksztejn, L., Becq, H., Pelosi, B., Pallesi-Pocachard, E., . . . Represa, A. (2012). An Epilepsy-Related ARX Polyalanine Expansion Modifies Glutamatergic Neurons Excitability and Morphology Without Affecting GABAergic Neurons Development. Cerebral Cortex. doi: 10.1093/cercor/bhs138. http://cercor.oxfordjournals.org/content/early/2012/05/24/cercor.bhs138....


Behan, M., Steinhacker, K., Jeffrey-Borger, S., & Meredith, M. A. (2002). Chemoarchitecture of GABAergic neurons in the ferret superior colliculus. Journal of Comparative Neurology, 452(4), 334-359. doi. 

Behnke, J., Cheedalla, A., Bhatt, V., Bhat, M., Teng, S., Palmieri, A., . . . Alder, J. (2017). Neuropeptide VGF Promotes Maturation of Hippocampal Dendrites That Is Reduced by Single Nucleotide Polymorphisms. International Journal of Molecular Sciences, 18(3), 612. doi. http://www.mdpi.com/1422-0067/18/3/612


Bekirov, I. H., Nagy, V., Svoronos, A., Huntley, G. W., & Benson, D. L. (2008). Cadherin-8 and N-cadherin differentially regulate pre-and postsynaptic development of the hippocampal mossy fiber pathway. Hippocampus, 18(4), 349-363. doi. 

Belanger, A. M., Przybylska, M., Gefteas, E., Furgerson, M., Geller, S., Kloss, A., . . . Yew, N. S. (2018). Inhibiting neutral amino acid transport for the treatment of phenylketonuria. JCI Insight, 3(14). doi: 10.1172/jci.insight.121762. https://doi.org/10.1172/jci.insight.121762


Belevych, N., Buchanan, K., Chen, Q., Bailey, M., & Quan, N. (2010). Location-specific activation of the paraventricular nucleus of the hypothalamus by localized inflammation. Brain, Behavior, and Immunity, 24(7), 1137-1147. doi. 

Bell, J. A., Wolke, M. L., Ortez, R. C., Jones, T. A., & Kerr, A. L. (2014). Training Intensity Affects Motor Rehabilitation Efficacy Following Unilateral Ischemic Insult of the Sensorimotor Cortex in C57BL/6 Mice. Neurorehabilitation and neural repair. doi: 10.1177/1545968314553031. http://nnr.sagepub.com/content/early/2014/10/08/1545968314553031.abstract


Bell, L. A., Bell, K. A., & McQuiston, A. R. (2013). Synaptic muscarinic response types in hippocampal CA1 interneurons depend on different levels of presynaptic activity and different muscarinic receptor subtypes. Neuropharmacology, (0). doi: http://dx.doi.org/10.1016/j.neuropharm.2013.05.026. http://www.sciencedirect.com/science/article/pii/S0028390813002402


Bell, L. A., Bell, K. A., & McQuiston, A. R. (2014). Muscarinic receptor activation by optogenetically released acetylcholine in hippocampal CA1 depolarizes VIP-expressing but has varying effects on PV-expressing perisomatic interneurons. The Journal of Physiology, n/a-n/a. doi: 10.1113/jphysiol.2014.277814. http://dx.doi.org/10.1113/jphysiol.2014.277814


Bell, M. R., De Lorme, K. C., Figueira, R. J., Kashy, D. A., & Sisk, C. L. (2012). Adolescent gain in positive valence of a socially relevant stimulus: engagement of the mesocorticolimbic reward circuitry. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12058. http://dx.doi.org/10.1111/ejn.12058


Bell, M. R., Meerts, S. H., & Sisk, C. L. (2013). Adolescent brain maturation is necessary for adult-typical mesocorticolimbic responses to a rewarding social cue. Developmental Neurobiology, n/a-n/a. doi: 10.1002/dneu.22106. http://dx.doi.org/10.1002/dneu.22106


Bell, S., Rousseau, J., Peng, H., Aouabed, Z., Priam, P., Theroux, J.-F., . . . Campeau, P. M. (2019). Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. The American Journal of Human Genetics, 104(5), 815-834. doi: https://doi.org/10.1016/j.ajhg.2019.03.022. http://www.sciencedirect.com/science/article/pii/S0002929719301181


Bell, Z. W., Lovell, P., Mello, C. V., Yip, P. K., George, J. M., & Clayton, D. F. (2019). Urotensin-related gene transcripts mark developmental emergence of the male forebrain vocal control system in songbirds. Scientific Reports, 9(1), 816. doi: 10.1038/s41598-018-37057-w. https://doi.org/10.1038/s41598-018-37057-w


Bellavance, M.-A., Takatoh, J., Lu, J., Demers, M., Kleinfeld, D., Wang, F., & Deschênes, M. (2017). Parallel Inhibitory and Excitatory Trigemino-Facial Feedback Circuitry for Reflexive Vibrissa Movement. Neuron. doi: https://doi.org/10.1016/j.neuron.2017.06.045. http://www.sciencedirect.com/science/article/pii/S0896627317305974


Belloli, S., Brioschi, A., Politi, L. S., Ronchetti, F., Calderoni, S., Raccagni, I., . . . Moresco, R. M. (2013). Characterization of biological features of a rat F98 GBM model: A PET-MRI study with [18F]FAZA and [18F]FDG. Nuclear Medicine and Biology, 40(6), 831-840. doi: http://dx.doi.org/10.1016/j.nucmedbio.2013.05.004. http://www.sciencedirect.com/science/article/pii/S0969805113001054


Bellone, E., Balestra, P., Di Maria, E., Pigullo, S., Gulli, R., Ajmar, F., & Mandich, P. (2004). Screening for mutations in the lipopolysaccharide-induced tumor necrosis factor-alpha factor (litaf) gene in italian patients with charcot-marie-tooth disease. Journal of the Peripheral Nervous System, 9(2), 112-112. doi. 

Belmer, A., Patkar, O. L., Lanoue, V., & Bartlett, S. E. (2018). 5-HT1A receptor-dependent modulation of emotional and neurogenic deficits elicited by prolonged consumption of alcohol. Scientific Reports, 8(1), 2099. doi: 10.1038/s41598-018-20504-z. https://doi.org/10.1038/s41598-018-20504-z


Belnoue, L., Malvaut, S., Ladevèze, E., Abrous, D. N., & Koehl, M. (2016). Plasticity in the olfactory bulb of the maternal mouse is prevented by gestational stress. [Article]. Scientific Reports, 6, 37615. doi: 10.1038/srep37615. http://dx.doi.org/10.1038/srep37615


Beloate, L. N., Omrani, A., Adan, R. A., Webb, I. C., & Coolen, L. M. (2016). Ventral Tegmental Area Dopamine Cell Activation during Male Rat Sexual Behavior Regulates Neuroplasticity and d-Amphetamine Cross-Sensitization following Sex Abstinence. The Journal of Neuroscience, 36(38), 9949-9961. doi. http://www.jneurosci.org/content/36/38/9949.short


Beltramo, R., D'Urso, G., Dal Maschio, M., Farisello, P., Bovetti, S., Clovis, Y., . . . Fellin, T. (2013). Layer-specific excitatory circuits differentially control recurrent network dynamics in the neocortex. Nature Medicine. doi. 

beltWillis, K. L., McCormick, C. A., & Carr, C. E. (2012). Hindbrain auditory circuits of turtles. [Abstract]. Frontiers in Behavioral Neuroscience. doi: 10.3389/conf.fnbeh.2012.27.00034. 

Ben Hamed, S., Duhamel, J. R., Bremmer, F., & Graf, W. (2001). Representation of the visual field in the lateral intraparietal area of macaque monkeys: a quantitative receptive field analysis. Experimental Brain Research, 140(2), 127-144. doi. 

Ben M'Barek, K., Pla, P., Orvoen, S., Benstaali, C., Godin, J. D., Gardier, A. M., . . . Humbert, S. (2013). Huntingtin Mediates Anxiety/Depression-Related Behaviors and Hippocampal Neurogenesis. Journal of Neuroscience, 33(20), 8608-8620. doi: 10.1523/jneurosci.5110-12.2013. http://www.jneurosci.org/content/33/20/8608.abstract


Benali, A., Trippe, J., Weiler, E., Mix, A., Petrasch-Parwez, E., Girzalsky, W., . . . Funke, K. (2011). Theta-Burst Transcranial Magnetic Stimulation Alters Cortical Inhibition. Journal of Neuroscience, 31(4), 1193-1203. doi: 10.1523/jneurosci.1379-10.2011. http://www.jneurosci.org/cgi/content/abstract/31/4/1193


Ben-Ari, Y., & Cossart, R. (2000). Kainate, a double agent that generates seizures: two decades of progress. Trends in Neurosciences, 23(11), 580-587. doi. 

Benavides-Piccione, R., Arellano, J. I., & DeFelipe, J. (2005). Catecholaminergic Innervation of Pyramidal Neurons in the Human Temporal Cortex. Cerebral Cortex, 15(doi:10.1093/cercor/bhi036), 1584-1591. doi. 

Benavides-Piccione, R., & DeFelipe, J. (2007). Distribution of neurons expressing tyrosine hydroxylase in the human cerebral cortex. Journal of Anatomy, 211(2), 212-222. doi: doi:10.1111/j.1469-7580.2007.00760.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1469-7580.2007.00760.x 


Benavides-Piccione, R., Hamzei-Sichani, F., Ballesteros-Yanez, I., DeFelipe, J., & Yuste, R. (2006). Dendritic size of pyramidal neurons differs among mouse cortical regions. Cerebral Cortex, 16(7), 990-990. doi. 

Benavides-Piccione, R., Regalado-Reyes, M., Fernaud-Espinosa, I., Kastanauskaite, A., Tapia-González, S., León-Espinosa, G., . . . DeFelipe, J. (2019). Differential Structure of Hippocampal CA1 Pyramidal Neurons in the Human and Mouse. Cerebral Cortex. doi: 10.1093/cercor/bhz122. https://doi.org/10.1093/cercor/bhz122


Benavides-Piccione, R., Rojo, C., Kastanauskaite, A., & DeFelipe, J. (2021). Variation in Pyramidal Cell Morphology Across the Human Anterior Temporal Lobe. Cerebral Cortex, (bhab034). doi: 10.1093/cercor/bhab034. https://doi.org/10.1093/cercor/bhab034


Bendels, M. H. K., Beed, P., Leibold, C., Schmitz, D., & Johenning, F. W. (2008). A novel control software that improves the experimental workflow of scanning photostimulation experiments. Journal of Neuroscience Methods, 175(1), 44-57. doi. 

Bender, K., Deshmukh, S., & Feldman, D. (2006). LTD as a Mechanism for Map Plasticity in Rat Barrel Cortex. Development and Plasticity in Sensory Thalamus and Cortex, 271-287. doi. 

Benedetti, L., Zuccarino, R., Grandis, M., Fiocchi, I., Beronio, A., Ghiglione, E., . . . Schenone, A. (2004). Is clinical variability in CMT1A related to epigenetic factors? Journal of the Peripheral Nervous System, 9(2), 111-111. doi: doi:10.1111/j.1085-9489.2004.009209w.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Benedetti, S., Previtali, S., Toniolo, D., Iannaccone, S., Sferrazza, B., Comi, G., . . . Bertini, E. (2004). Dominant lamin A/C gene mutations can be associated with muscular dystrophy and peripheral neuropathy. Journal of the Peripheral Nervous System, 9(2), 113-113. doi: doi:10.1111/j.1085-9489.2004.009209ad.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Bengochea, M., Berón de Astrada, M., Tomsic, D., & Sztarker, J. (2017). A crustacean lobula plate: morphology, connections and retinotopic organization. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24322. http://dx.doi.org/10.1002/cne.24322


Bengtsson Gonzales, C., Hunt, S., Munoz-Manchado, A. B., McBain, C. J., & Hjerling-Leffler, J. (2020). Intrinsic electrophysiological properties predict variability in morphology and connectivity among striatal Parvalbumin-expressing Pthlh-cells. Scientific Reports, 10(1), 15680. doi: 10.1038/s41598-020-72588-1. https://doi.org/10.1038/s41598-020-72588-1


Benito-Gonzalez, A., & Alvarez, F. J. (2012). Renshaw Cells and Ia Inhibitory Interneurons Are Generated at Different Times from p1 Progenitors and Differentiate Shortly after Exiting the Cell Cycle. Journal of Neuroscience, 32(4), 1156-1170. doi: 10.1523/jneurosci.3630-12.2012. http://www.jneurosci.org/content/32/4/1156.abstract


Benneyworth, M. A., & Coyle, J. T. (2012). Altered Acquisition and Extinction of Amphetamine-Paired Context Conditioning in Genetic Mouse Models of Altered NMDA Receptor Function. Neuropsychopharmacology. doi. http://dx.doi.org/10.1038/npp.2012.108


Bennur, S., Rao, S., Pawlak, R., Strickland, S., McEwen, B. S., & Chattarji, S. (2007). Stress-induced spine loss in the medial amygdala is mediated by tissue-plasminogen activator. Neuroscience, 144(1), 8-16. doi. 

Benson, C. G., & Cant, N. B. (2008). The ventral nucleus of the lateral lemniscus of the gerbil (Meriones unguiculatus): organization of connections with the cochlear nucleus and the inferior colliculus. Journal of Comparative Neurology, 510(6), 673-690. doi. 

Benton, R. L., & Whittemore, S. R. (2003). VEGF 165 therapy exacerbates secondary damage following spinal cord injury. Neurochemical Research, 28(11), 1693-1703. doi. 

Benton, R. L., Woock, J. P., Gozal, E., Hetman, M., & Whittemore, S. R. (2005). Intraspinal application of endothelin results in focal ischemic injury of spinal gray matter and restricts the differentiation of engrafted neural stem cells. Neurochemical Research, 30(6), 809-823. doi. 

Bento-Torres, J., Sobral, L. L., Reis, R. R., de Oliveira, R. B., Anthony, D. C., Vasconcelos, P. F. C., . . . o Diniz, C. W. (2017). Age and Environment Influences on Mouse Prion Disease Progression: Behavioral Changes and Morphometry and Stereology of Hippocampal Astrocytes. Oxidative Medicine and Cellular Longevity, 2017, 18. doi: 10.1155/2017/4504925. https://doi.org/10.1155/2017/4504925


Berezovskii, V. K., & Born, R. T. (2000). Specificity of Projections from Wide-Field and Local Motion-Processing Regions within the Middle Temporal Visual Area of the Owl Monkey. Journal of Neuroscience, 20(3), 1157-1169. doi. http://www.jneurosci.org/cgi/content/abstract/20/3/1157


Berezovskii, V. K., Nassi, J. J., & Born, R. T. (2011). Segregation of feedforward and feedback projections in mouse visual cortex. Journal of Comparative Neurology, 519(18), 3672-3683. doi: 10.1002/cne.22675. http://dx.doi.org/10.1002/cne.22675


Berg, A. P., & Bayliss, D. A. (2007). Striatal Cholinergic Interneurons Express a Receptor-Insensitive Homomeric TASK-3-Like Background K+ Current. Journal of Neurophysiology, 97(2), 1546-1552. doi: 10.1152/jn.01090.2006. http://jn.physiology.org/cgi/content/abstract/97/2/1546 


Berger, T., Larkum, M. E., & Luscher, H.-R. (2001). High Ih Channel Density in the Distal Apical Dendrite of Layer V Pyramidal Cells Increases Bidirectional Attenuation of EPSPs. Journal of Neurophysiology, 85(2), 855-868. doi. http://jn.physiology.org/cgi/content/abstract/85/2/855 


Berger, T. K., Silberberg, G., Perin, R., & Markram, H. (2010). Brief bursts self-inhibit and correlate the pyramidal network. PLoS Biology, 8(9), e1000473-e1000473. doi. 

Berggren, K., Ezerman, E. B., McCaffery, P., & Forehand, C. J. (2001). Expression and regulation of the retinoic acid synthetic enzyme RALDH-2 in the embryonic chicken wing. Developmental Dynamics, 222(1), 1-16. doi. 

Bergstrom, H., McDonald, C., Dey, S., Tang, H., Selwyn, R., & Johnson, L. (2012). The structure of Pavlovian fear conditioning in the amygdala. Brain Structure and Function, 1-21. doi: 10.1007/s00429-012-0478-2. http://dx.doi.org/10.1007/s00429-012-0478-2


Bergstrom, H. C., & Johnson, L. R. (2014). An organization of visual and auditory fear conditioning in the lateral amygdala. Neurobiology of Learning and Memory, (0). doi: http://dx.doi.org/10.1016/j.nlm.2014.07.008. http://www.sciencedirect.com/science/article/pii/S107474271400135X


Bergstrom, H. C., McDonald, C. G., French, H. T., & Smith, R. F. (2008). Continuous nicotine administration produces selective, age-dependent structural alteration of pyramidal neurons from prelimbic cortex. Synapse, 62(1), 31-39. doi. 

Bergstrom, H. C., McDonald, C. G., & Johnson, L. R. (2011). Pavlovian fear conditioning activates a common pattern of neurons in the lateral amygdala of individual brains. PLoS ONE, 6(1), e15698-e15698. doi. 

Bergstrom, H. C., Smith, R. F., Mollinedo, N. S., & McDonald, C. G. (2010). Chronic nicotine exposure produces lateralized, age-dependent dendritic remodeling in the rodent basolateral amygdala. Synapse, 64(10), 754-764. doi. 

Bergwell, H. R. (2017). Chronic Capsaicin Does Not Induce Microglia Response in Adult Rat. doi. http://digitalcommons.unomaha.edu/srcaf/2017/schedule/1/


Berkley, K. J., Dmitrieva, N., Curtis, K. S., & Papka, R. E. (2004). Innervation of ectopic endometrium in a rat model of endometriosis. Proceedings of the National Academy of Sciences, 101(30), 11094-11098. doi: 10.1073/pnas.0403663101. http://www.pnas.org/cgi/content/abstract/101/30/11094 


Berlanga, M. L., Price, D. L., Phung, B. S., Giuly, R., Terada, M., Yamada, N., . . . others. (2011). Multiscale imaging characterization of dopamine transporter knockout mice reveals regional alterations in spine density of medium spiny neurons. Brain Research. doi. 

Berman, R. F., Murray, K. D., Arque, G., Hunsaker, M. R., & Wenzel, H. J. (2012). Abnormal dendrite and spine morphology in primary visual cortex in the CGG knock-in mouse model of the fragile X premutation. Epilepsia, 53, 150-160. doi: 10.1111/j.1528-1167.2012.03486.x. http://dx.doi.org/10.1111/j.1528-1167.2012.03486.x


Berman, R. F., Schwartzer, J. J., & Hunsaker, M. R. (2015). Mouse Models of the Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) and the Fragile X Premutation. doi. http://mrhunsaker.github.io/CGGKIMotor/


Bernácer, J., Prensa, L., & Giménez-Amaya, J. M. (2007). Cholinergic interneurons are differentially distributed in the human striatum. PLoS ONE, 2(11), e1174-e1174. doi. 

Bernard, R., & Veh, R. W. (2012). Individual neurons in the rat lateral habenular complex mostly project to either the dopaminergic ventral tegmental area or to the serotonergic raphe nuclei. Journal of Comparative Neurology. doi. 

Bernreuther, C., Dihne, M., Johann, V., Schiefer, J., Cui, Y., Hargus, G., . . . Schachner, M. (2006). Neural Cell Adhesion Molecule L1-Transfected Embryonic Stem Cells Promote Functional Recovery after Excitotoxic Lesion of the Mouse Striatum. Journal of Neuroscience, 26(45), 11532-11539. doi: 10.1523/jneurosci.2688-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/45/11532 


Bernstein, S. L., Guo, Y., Slater, B. J., Puche, A., & Kelman, S. E. (2007). Neuron stress and loss following rodent anterior ischemic optic neuropathy in double-reporter transgenic mice. Investigative Ophthalmology and Visual Science, 48(5), 2304-2310. doi. 

Bernstock, J. D., Peruzzotti-Jametti, L., Leonardi, T., Vicario, N., Ye, D., Lee, Y.-j., . . . Pluchino, S. (2019). SUMOylation promotes survival and integration of neural stem cell grafts in ischemic stroke. EBioMedicine. doi: https://doi.org/10.1016/j.ebiom.2019.03.035. http://www.sciencedirect.com/science/article/pii/S2352396419301756


Berryer, M. H., Chattopadhyaya, B., Xing, P., Riebe, I., Bosoi, C., Sanon, N., . . . Di Cristo, G. (2016). Decrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function. [Article]. Nature Communications, 7, 13340. doi: 10.1038/ncomms13340

http://www.nature.com/articles/ncomms13340#supplementary-information. http://dx.doi.org/10.1038/ncomms13340


Bersano, A., Allaria, S., & Nobile-Orazio, E. (2004). 14-3-3 protein in the CSF of inflammatory peripheral neuropathies. Journal of the Peripheral Nervous System, 9(2), 108-108. doi. 

Berson, D. M., Stein, J. J., & others. (1995). Retinotopic organization of the superior colliculus in relation to the retinal distribution of afferent ganglion cells. Visual Neuroscience, 12, 671-671. doi. 

Berthet, A., Margolis, E. B., Zhang, J., Hsieh, I., Zhang, J., Hnasko, T. S., . . . Huang, E. J. (2014). Loss of Mitochondrial Fission Depletes Axonal Mitochondria in Midbrain Dopamine Neurons. The Journal of Neuroscience, 34(43), 14304-14317. doi. http://www.jneurosci.org/content/34/43/14304.short


Bertram, J., Koschützke, L., Pfannmöller, J. P., Esche, J., van Diepen, L., Kuss, A. W., . . . von Bohlen und Halbach, O. (2016). Morphological and behavioral characterization of adult mice deficient for SrGAP3. [journal article]. Cell and Tissue Research, 1-11. doi: 10.1007/s00441-016-2413-y. http://dx.doi.org/10.1007/s00441-016-2413-y


Berzhanskaya, J., & Ascoli, G. (2008). Computational neuroanatomy. Scholarpedia, 3(3), 1313-1313. doi. 

Bessa, J., Morais, M., Marques, F., Pinto, L., Palha, J., Almeida, O., & Sousa, N. (2013). Stress-induced anhedonia is associated with hypertrophy of medium spiny neurons of the nucleus accumbens. Translational Psychiatry, 3(6), e266. doi. http://www.nature.com/tp/journal/v3/n6/abs/tp201339a.html


Bessa, J. M., Ferreira, D., Melo, I., Marques, F., Cerqueira, J. J., Palha, J. A., . . . Sousa, N. (2008). The mood-improving actions of antidepressants do not depend on neurogenesis but are associated with neuronal remodeling. Molecular Psychiatry. doi. 

Bethea, C. L., Coleman, K., Phu, K., Reddy, A. P., & Phu, A. (2014). Relationships between androgens, serotonin gene expression and innervation in male macaques. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2014.05.056. http://www.sciencedirect.com/science/article/pii/S0306452214004643


Beutler, L. R., Eldred, K. C., Quintana, A., Keene, C. D., Rose, S. E., Postupna, N., . . . Palmiter, R. D. (2011). Severely Impaired Learning and Altered Neuronal Morphology in Mice Lacking NMDA Receptors in Medium Spiny Neurons. PLoS ONE, 6(11), e28168-e28168. doi. 

Beynon, S. B., & Walker, F. R. (2012). Microglial activation in the injured and healthy brain: what are we really talking about? Practical and theoretical issues associated with the measurement of changes in microglial morphology. Neuroscience, (0). doi: 10.1016/j.neuroscience.2012.07.029. http://www.sciencedirect.com/science/article/pii/S0306452212007543?v=s5


Bezchlibnyk, Y. B., Stone, S. S. D., Hamani, C., & Lozano, A. M. (2016). High frequency stimulation of the infralimbic cortex induces morphological changes in rat hippocampal neurons. Brain Stimulation. doi: http://dx.doi.org/10.1016/j.brs.2016.11.013. http://www.sciencedirect.com/science/article/pii/S1935861X1630314X


Bezgin, G., Reid, A. T., Schubert, D., & Kötter, R. (2009). Matching spatial with ontological brain regions using Java tools for visualization, database access, and integrated data analysis. Neuroinformatics, 7(1), 7-22. doi. 

Bhagat, R., Fortna, S. R., & Browning, K. N. (2014). Exposure to a high fat diet during the perinatal period alters vagal motoneurone excitability, even in the absence of obesity. The Journal of Physiology, n/a-n/a. doi: 10.1113/jphysiol.2014.282806. http://dx.doi.org/10.1113/jphysiol.2014.282806


Bhagwandin, A., Gravett, N., Hemingway, J., Oosthuizen, M. K., Bennett, N. C., Siegel, J. M., & Manger, P. R. (2011). Orexinergic neuron numbers in three species of African mole rats with rhythmic and arrhythmic chronotypes. Neuroscience. doi. 

Bhalala, U., Lee, E. J., Armstrong, J., Parikh, M., Lee, J., Kannan, S., . . . Koehler, R. (2014). 581: NEUROINFLAMMATION PERSISTS BEYOND ACUTE INJURY AFTER PEDIATRIC HYPOXIC-ASPHYXIC CARDIAC ARREST. Critical Care Medicine, 42(12), A1499-A1500 1410.1097/1401.ccm.0000458078.0000447859.0000458070a. doi. http://journals.lww.com/ccmjournal/Fulltext/2014/12001/581___NEUROINFLAM...


Bhumbra, G. S., Bannatyne, B. A., Watanabe, M., Todd, A. J., Maxwell, D. J., & Beato, M. (2014). The Recurrent Case for the Renshaw Cell. The Journal of Neuroscience, 34(38), 12919-12932. doi. http://www.jneurosci.org/content/34/38/12919.full


Biamonte, F., Assenza, G., Marino, R., D'Amelio, M., Panteri, R., Caruso, D., . . . others. (2009). Interactions between neuroactive steroids and reelin haploinsufficiency in Purkinje cell survival. Neurobiology of Disease, 36(1), 103-115. doi. 

Bian, S., Akyüz, N., Bernreuther, C., Loers, G., Laczynska, E., Jakovcevski, I., & Schachner, M. (2011). Dermatan sulfotransferase Chst14/D4st1, but not chondroitin sulfotransferase Chst11/C4st1, regulates proliferation and neurogenesis of neural progenitor cells. Journal of Cell Science, 124(23), 4051-4063. doi: 10.1242/jcs.088120. http://jcs.biologists.org/content/124/23/4051.abstract


Bianchi, S., Bauernfeind, A. L., Gupta, K., Stimpson, C. D., Spocter, M. A., Bonar, C. J., . . . Sherwood, C. C. (2011). Neocortical neuron morphology in Afrotheria: comparing the rock hyrax with the African elephant. Annals of the New York Academy of Sciences, 1225(1), 37-46. doi. 

Bianchi, S., Stimpson, C. D., Bauernfeind, A. L., Schapiro, S. J., Baze, W. B., McArthur, M. J., . . . Sherwood, C. C. (2012). Dendritic Morphology of Pyramidal Neurons in the Chimpanzee Neocortex: Regional Specializations and Comparison to Humans. Cerebral Cortex. doi: 10.1093/cercor/bhs239. http://cercor.oxfordjournals.org/content/early/2012/08/08/cercor.bhs239....


Bianchi, S., Stimpson, C. D., Duka, T., Larsen, M. D., Janssen, W. G. M., Collins, Z., . . . Sherwood, C. C. (2013). Synaptogenesis and development of pyramidal neuron dendritic morphology in the chimpanzee neocortex resembles humans. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1301224110. http://www.pnas.org/content/early/2013/06/04/1301224110.abstract


Biasiotta, A. (2012). Neuropathic pain in neuropathy: A combined clinical, neurophysiological and morphological study. doi. 

Bicanic, I., Hladnik, A., & Petanjek, Z. (2017). A Quantitative Golgi Study of Dendritic Morphology in the Mice Striatal Medium Spiny Neurons. [Original Research]. Frontiers in Neuroanatomy, 11(37). doi: 10.3389/fnana.2017.00037. http://journal.frontiersin.org/article/10.3389/fnana.2017.00037


Bickford, M. E., Zhou, N., Krahe, T. E., Govindaiah, G., & Guido, W. (2015). Retinal and Tectal “Driver-Like” Inputs Converge in the Shell of the Mouse Dorsal Lateral Geniculate Nucleus. The Journal of Neuroscience, 35(29), 10523-10534. doi. http://www.jneurosci.org/content/35/29/10523.short


Bielza, C., Benavides-Piccione, R., López-Cruz, P., Larrañaga, P., & DeFelipe, J. (2014). Branching angles of pyramidal cell dendrites follow common geometrical design principles in different cortical areas. Scientific Reports, 4. doi. http://www.nature.com/srep/2014/140801/srep05909/full/srep05909.html


Bienvenu, T. C., Busti, D., Micklem, B. R., Mansouri, M., Magill, P. J., Ferraguti, F., & Capogna, M. (2015). Large Intercalated Neurons of Amygdala Relay Noxious Sensory Information. The Journal of Neuroscience, 35(5), 2044-2057. doi. http://www.jneurosci.org/content/35/5/2044.short


Biering-Sørensen, F., Biering-Sørensen, T., Liu, N., Malmqvist, L., Wecht, J. M., & Krassioukov, A. (2017). Alterations in cardiac autonomic control in spinal cord injury. Autonomic Neuroscience. doi. http://www.autonomicneuroscience.com/article/S1566-0702(17)30044-9/abstract

Biernaskie, J., Chernenko, G., & Corbett, D. (2004). Efficacy of Rehabilitative Experience Declines with Time after Focal Ischemic Brain Injury. Journal of Neuroscience, 24(5), 1245-1254. doi: 10.1523/jneurosci.3834-03.2004. http://www.jneurosci.org/cgi/content/abstract/24/5/1245 


Biernaskie, J., & Corbett, D. (2001). Enriched Rehabilitative Training Promotes Improved Forelimb Motor Function and Enhanced Dendritic Growth after Focal Ischemic Injury. Journal of Neuroscience, 21(14), 5272-5280. doi. http://www.jneurosci.org/cgi/content/abstract/21/14/5272


Biffiger, K., Bartsch, S., Montag, D., Aguzzi, A., Schachner, M., & Bartsch, U. (2000). Severe Hypomyelination of the Murine CNS in the Absence of Myelin-Associated Glycoprotein and Fyn Tyrosine Kinase. Journal of Neuroscience, 20(19), 7430-7437. doi. http://www.jneurosci.org/cgi/content/abstract/20/19/7430


Bigbee, J. W., Sharma, K. V., Chan, E. L. P., & Bögler, O. (2000). Evidence for the direct role of acetylcholinesterase in neurite outgrowth in primary dorsal root ganglion neurons. Brain Research, 861(2), 354-362. doi. 

Biggs, B. T., Tang, T., & Krimm, R. F. (2016). Insulin-Like Growth Factors Are Expressed in the Taste System, but Do Not Maintain Adult Taste Buds. PLoS ONE, 11(2), e0148315. doi: 10.1371/journal.pone.0148315. http://dx.doi.org/10.1371%2Fjournal.pone.0148315


Bilgen, M., Dancause, N., Al-Hafez, B., He, Y. Y., & Malone, T. M. (2005). Manganese-enhanced MRI of rat spinal cord injury. Magnetic Resonance Imaging, 23(7), 829-832. doi. 

Billeci, L., Pioggia, G., Vaglini, F., & Ahluwalia, A. (2010). Automated extraction and classification of dynamic metrical features of morphological development in dissociated Purkinje neurons. Journal of Neuroscience Methods, 185(2), 315-324. doi. 

Billiards, S. S., Haynes, R. L., Folkerth, R. D., Borenstein, N. S., Trachtenberg, F. L., Rowitch, D. H., . . . Kinney, H. C. (2008). Myelin Abnormalities without Oligodendrocyte Loss in Periventricular Leukomalacia. Brain Pathology. doi: doi:10.1111/j.1750-3639.2007.00107.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1750-3639.2007.00107.x 


Billiards, S. S., Haynes, R. L., Folkerth, R. D., Trachtenberg, F. L., Liu, L. G., Volpe, J. J., & Kinney, H. C. (2006). Development of microglia in the cerebral white matter of the human fetus and infant. Journal of Comparative Neurology, 497(2), 199-208. doi. 

Bindu, B., Alladi, P. A., Mansooralikhan, B. M., Srikumar, B. N., Raju, T. R., & Kutty, B. M. (2007). Short-term exposure to an enriched environment enhances dendritic branching but not brain-derived neurotrophic factor expression in the hippocampus of rats with ventral subicular lesions. Neuroscience, 144(2), 412-423. doi. 

Binley, K. E., Ng, W. S., Tribble, J. R., Song, B., & Morgan, J. E. (2014). Sholl analysis: A quantitative comparison of semi-automated methods. Journal of Neuroscience Methods, (0). doi: http://dx.doi.org/10.1016/j.jneumeth.2014.01.017. http://www.sciencedirect.com/science/article/pii/S0165027014000284


Binneboese, A., & Morecraft, R. J. (2015). Localization of Orofacial Motor Representation in the Corona Radiata, Internal Capsule, and Cerebral Peduncle in the Non-Human Primate. South Dakota Medicine, 68(9). doi. http://web.a.ebscohost.com/abstract?direct=true&profile=ehost&scope=site...


Biran, V., Heine, V. M., Verney, C., Sheldon, R., Spadafora, R., Vexler, Z. S., . . . Ferriero, D. M. (2011). Cerebellar abnormalities following hypoxia alone compared to hypoxic–ischemic forebrain injury in the developing rat brain. Neurobiology of Disease, 41(1), 138-146. doi. 

Bird, C. W., Gardiner, A. S., Bolognani, F., Tanner, D. C., Chen, C.-Y., Lin, W.-J., . . . Perrone- Bizzozero, N. (2013). KSRP Modulation of GAP-43 mRNA Stability Restricts Axonal Outgrowth in Embryonic Hippocampal Neurons. PLoS ONE, 8(11), e79255. doi: 10.1371/journal.pone.0079255. http://dx.doi.org/10.1371%2Fjournal.pone.0079255


Birinyi, A., Rácz, N., Kecskes, S., Matesz, C., & Kovalecz, G. (2017). Neural circuits underlying jaw movements for the prey-catching behavior in frog: distribution of vestibular afferent terminals on motoneurons supplying the jaw. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-017-1581-1. https://doi.org/10.1007/s00429-017-1581-1


Biró, Á. A., Brémaud, A., Falck, J., & Ruiz, A. J. (2018). A-type K+ channels impede supralinear summation of clustered glutamatergic inputs in layer 3 neocortical pyramidal neurons. Neuropharmacology. doi: https://doi.org/10.1016/j.neuropharm.2018.07.005. http://www.sciencedirect.com/science/article/pii/S0028390818303605


Biro, A. A., Holderith, N. B., & Nusser, Z. (2005). Quantal Size Is Independent of the Release Probability at Hippocampal Excitatory Synapses. Journal of Neuroscience, 25(1), 223-232. doi. http://www.jneurosci.org/cgi/content/abstract/25/1/223


Biro, A. A., Holderith, N. B., & Nusser, Z. (2006). Release Probability-Dependent Scaling of the Postsynaptic Responses at Single Hippocampal GABAergic Synapses. Journal of Neuroscience, 26(48), 12487-12496. doi: 10.1523/jneurosci.3106-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/48/12487 


Bisicchia, E., Sasso, V., Catanzaro, G., Leuti, A., Besharat, Z. M., Chiacchiarini, M., . . . Chiurchiù, V. (2018). Resolvin D1 Halts Remote Neuroinflammation and Improves Functional Recovery after Focal Brain Damage Via ALX/FPR2 Receptor-Regulated MicroRNAs. [journal article]. Molecular Neurobiology. doi: 10.1007/s12035-018-0889-z. https://doi.org/10.1007/s12035-018-0889-z


Bissonette, G. B., Bae, M. H., Suresh, T., Jaffe, D. E., & Powell, E. M. (2010). Astrocyte-Mediated Hepatocyte Growth Factor/Scatter Factor Supplementation Restores GABAergic Interneurons and Corrects Reversal Learning Deficits in Mice. Journal of Neuroscience, 30(8), 2918-2923. doi: 10.1523/jneurosci.5268-09.2010. http://www.jneurosci.org/cgi/content/abstract/30/8/2918 


Bissonette, G. B., Bae, M. H., Suresh, T., Jaffe, D. E., & Powell, E. M. (2013). Prefrontal cognitive deficits in mice with altered cerebral cortical GABAergic interneurons. Behavioural Brain Research, (0). doi: http://dx.doi.org/10.1016/j.bbr.2013.10.051. http://www.sciencedirect.com/science/article/pii/S0166432813006761


Bittner, G., Sengelaub, D., & Ghergherehchi, C. (2018). Conundrums and confusions regarding how polyethylene glycol-fusion produces excellent behavioral recovery after peripheral nerve injuries. [Invited Review]. Neural Regeneration Research, 13(1), 53-57. doi: 10.4103/1673-5374.224363. http://www.nrronline.org/article.asp?issn=1673-5374;year=2018;volume=13;...


Bizley, J. K., Bajo, V. M., Nodal, F. R., & King, A. J. (2015). Cortico-cortical connectivity within ferret auditory cortex. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23784. http://dx.doi.org/10.1002/cne.23784


Bizon, J. L., & Gallagher, M. (2003). Production of new cells in the rat dentate gyrus over the lifespan: relation to cognitive decline. European Journal of Neuroscience, 18(1), 215-219. doi: doi:10.1046/j.1460-9568.2003.02733.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.2003.02733.x 


Bizon, J. L., Helm, K. A., Han, J. S., Chun, H. J., Pucilowska, J., Lund, P. K., & Gallagher, M. (2001). Hypothalamic–pituitary–adrenal axis function and corticosterone receptor expression in behaviourally characterized young and aged Long–Evans rats. European Journal of Neuroscience, 14(10), 1739-1751. doi. 

Bizon, J. L., Helm, K. A., Han, J.-S., Chun, H.-J., Pucilowska, J., Lund, P. K., & Gallagher, M. (2001). Hypothalamic-pituitary-adrenal axis function and corticosterone receptor expression in behaviourally characterized young and aged Long-Evans rats. European Journal of Neuroscience, 14(10), 1739-1751. doi: doi:10.1046/j.0953-816x.2001.01781.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.0953-816x.2001.01781.x 


Bizon, J. L., Lee, H. J., & Gallagher, M. (2004). Neurogenesis in a rat model of age-related cognitive decline. Aging Cell, 3(4), 227-234. doi. http://www.blackwell-synergy.com/links/doi/10.1111/j.1474-9728.2004.0009...


Bjaalie, J. G. (2002). Localization in the brain: new solutions emerging. Nature Reviews Neuroscience, 3, 322-325. doi. 

Bjaalie, J. G., & Leergaard, T. B. (2006). Three-dimensional computerized reconstruction from serial sections: cell populations, regions, and whole brain. Neuroanatomical Tract-Tracing 3, 530-565. doi. 

Bjaalie, J. G., Leergaard, T. B., & Pettersen, C. (2006). Micro3D: computer program for three-dimensional reconstruction visualization, and analysis of neuronal populations and barin regions. International Journal of Neuroscience, 116(4), 515-540. doi. 

Bjornsson, C. S., Lin, G., Al-Kofahi, Y., Narayanaswamy, A., Smith, K. L., Shain, W., & Roysam, B. (2008). Associative image analysis: a method for automated quantification of 3D multi-parameter images of brain tissue. Journal of Neuroscience Methods, 170(1), 165-178. doi. 

Black, C., Resau, J., West, R., Grever, W., Hlady, V., & McAllister, J. (2009). Are we implanting catheters that facilitate shunt failure? Cerebrospinal Fluid Research, 6(Suppl 1), S42. doi. http://www.cerebrospinalfluidresearch.com/content/6/S1/S42 


Blackman, A. V., Grabuschnig, S., Legenstein, R., & Sjöström, P. J. (2014). A Comparison of Manual Neuronal Reconstruction from Biocytin Histology or 2-Photon Imaging: Morphometry and Computer Modeling. Frontiers in Neuroanatomy, 8, 65. doi. http://journal.frontiersin.org/Journal/10.3389/fnana.2014.00065/abstract


Blackmore, E. M., Miranda Dos Santos, F., Krajewski-Hall, S. J., Rance, N. E., & McMullen, N. T. (2019). Glutamatergic Neurokinin 3 receptor neurons in the median preoptic nucleus modulate heat-defense pathways in female mice. doi: 10.1210/en.2018-00934. https://dx.doi.org/10.1210/en.2018-00934


Blackmore, M. G., Moore, D. L., Smith, R. P., Goldberg, J. L., Bixby, J. L., & Lemmon, V. P. (2010). High content screening of cortical neurons identifies novel regulators of axon growth. Molecular and Cellular Neuroscience, 44(1), 43-54. doi. 

Blakely, B. D., Bye, C. R., Fernando, C., Prasad, A., Pasterkamp, J., Macheda, M. L., . . . Parish, C. (2013). Ryk, a receptor regulating Wnt5a-mediated neurogenesis and axon morphogenesis of ventral midbrain dopaminergic neurons. Stem Cells and Development, (ja). doi. 

Blanchet, J., Longpré, F., Bureau, G., Morissette, M., DiPaolo, T., Bronchti, G., & Martinoli, M. G. (2008). Resveratrol, a red wine polyphenol, protects dopaminergic neurons in MPTP-treated mice. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 32(5), 1243-1250. doi. 

Bland, K. M., Aharon, A., Widener, E. L., Song, M. I., Casey, Z. O., Zuo, Y., & Vidal, G. S. (2021). FMRP regulates the subcellular distribution of cortical dendritic spine density in a non-cell-autonomous manner. Neurobiology of Disease, 150, 105253. doi: https://doi.org/10.1016/j.nbd.2021.105253. https://www.sciencedirect.com/science/article/pii/S0969996121000024


Blaszczyk, W. M., Telkes, I., & Distler, C. (2004). GABA-immunoreactive starburst amacrine cells in pigmented and albino rats. European Journal of Neuroscience, 20(11), 3195-3198. doi: doi:10.1111/j.1460-9568.2004.03761.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2004.03761.x 


Blatow, M., Rozov, A., Katona, I., Hormuzdi, S. G., Meyer, A. H., Whittington, M. A., . . . Monyer, H. (2003). A novel network of multipolar bursting interneurons generates theta frequency oscillations in neocortex. Neuron, 38(5), 805-817. doi. 

Blaya, M. O., Bramlett, H., Nadoo, J., Pieper, A. A., & Dietrich III, W. D. (2013). Neuroprotective efficacy of a proneurogenic compound after traumatic brain injury. Journal of Neurotrauma, (ja). doi. http://online.liebertpub.com/doi/abs/10.1089/neu.2013.3135


Blaya, M. O., Tsoulfas, P., Bramlett, H. M., & Dietrich, W. D. (2014). Neural progenitor cell transplantation promotes neuroprotection, enhances hippocampal neurogenesis, and improves cognitive outcomes after traumatic brain injury. Experimental Neurology, (0). doi: http://dx.doi.org/10.1016/j.expneurol.2014.11.014. http://www.sciencedirect.com/science/article/pii/S0014488614003847


Blazquez-Llorca, L., Garcia-Marin, V., & DeFelipe, J. (2010). Frontiers: Pericellular innervation of neurons expressing abnormally hyperphosphorylated tau in the hippocampal formation of Alzheimer's disease patients. Frontiers in Neuroanatomy, 4. doi. 

Blazquez-Llorca, L., Garcia-Marin, V., & DeFelipe, J. (2010). Pericellular Innervation of Neurons Expressing Abnormally Hyperphosphorylated Tau in the Hippocampal Formation of Alzheimer's Disease Patients. Frontiers in Neuroanatomy, 4. doi. 

Blazquez-Llorca, L., García-Marín, V., & DeFelipe, J. (2010). GABAergic complex basket formations in the human neocortex. Journal of Comparative Neurology, 518(24), 4917-4937. doi: 10.1002/cne.22496. http://dx.doi.org/10.1002/cne.22496


Blazquez-Llorca, L., Garcia-Marin, V., Merino-Serrais, P., Ávila, J., & DeFelipe, J. (2011). Abnormal Tau Phosphorylation in the Thorny Excrescences of CA3 Hippocampal Neurons in Patients with Alzheimer's Disease. Journal of Alzheimer's Disease, 26(4), 683-698. doi. 

Bloch, S. L., & Friis, M. (2011). Objective measurement of the human endolymphatic sac dimensions in Ménière's disease. Otology & Neurotology, 32(8), 1364-1364. doi. 

Blöchlinger, S., Weinmann, O., Schwab, M. E., & Thallmair, M. (2001). Neuronal plasticity and formation of new synaptic contacts follow pyramidal lesions and neutralization of Nogo-A: A light and electron microscopic study in the pontine nuclei of adult rats. Journal of Comparative Neurology, 433(3), 426-436. doi. 

Blondel, O., Collin, C., McCarran, W. J., Zhu, S., Zamostiano, R., Gozes, I., . . . McKay, R. D. G. (2000). A Glia-Derived Signal Regulating Neuronal Differentiation. Journal of Neuroscience, 20(21), 8012-8020. doi. http://www.jneurosci.org/cgi/content/abstract/20/21/8012


Bloss, E. B., Janssen, W. G., McEwen, B. S., & Morrison, J. H. (2010). Interactive Effects of Stress and Aging on Structural Plasticity in the Prefrontal Cortex. Journal of Neuroscience 30(19), 6726-6731. doi: 10.1523/jneurosci.0759-10.2010. http://www.jneurosci.org/cgi/content/abstract/30/19/6726 


Blouin, A. M., Thannickal, T. C., Worley, P. F., Baraban, J. M., Reti, I. M., & Siegel, J. M. (2005). Narp immunostaining of human hypocretin (orexin) neurons: Loss in narcolepsy. Neurology, 65(8), 1189-1192. doi: 10.1212/01.wnl.0000175219.01544.c8. http://www.neurology.org/cgi/content/abstract/65/8/1189 


Blume, S. R., Freedberg, M., Vantrease, J. E., Chan, R., Padival, M., Record, M. J., . . . Rosenkranz, J. A. (2017). Sex- and estrus-dependent differences in rat basolateral amygdala. [10.1523/JNEUROSCI.0758-17.2017]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2017/09/27/JNEUROSCI.0758-17.2017...


Blume, S. R., Padival, M., Urban, J. H., & Rosenkranz, J. A. (2019). Disruptive effects of repeated stress on basolateral amygdala neurons and fear behavior across the estrous cycle in rats. Scientific Reports, 9(1), 12292. doi: 10.1038/s41598-019-48683-3. https://doi.org/10.1038/s41598-019-48683-3


Blutstein, T., Baab, P. J., Zielke, H. R., & Mong, J. A. (2009). Hormonal modulation of amino acid neurotransmitter metabolism in the arcuate nucleus of the adult female rat: A novel action of estradiol. Endocrinology, en.2008-1701. doi: 10.1210/en.2008-1701. http://endo.endojournals.org/cgi/content/abstract/en.2008-1701v1 


Blythe, S. N., Wokosin, D., Atherton, J. F., & Bevan, M. D. (2009). Cellular Mechanisms Underlying Burst Firing in Substantia Nigra Dopamine Neurons. Journal of Neuroscience, 29(49), 15531-15541. doi: 10.1523/jneurosci.2961-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/49/15531 


Boato, F., Hendrix, S., Huelsenbeck, S. C., Hofmann, F., Gro\sse, G., Djalali, S., . . . others. (2010). C3 peptide enhances recovery from spinal cord injury by improved regenerative growth of descending fiber tracts. Journal of Cell Science, 123(10), 1652-1662. doi. 

Boccazzi, M., Rolando, C., Abbracchio, M. P., Buffo, A., & Ceruti, S. (2013). Purines regulate adult brain subventricular zone cell functions: Contribution of reactive astrocytes. Glia, n/a-n/a. doi: 10.1002/glia.22614. http://dx.doi.org/10.1002/glia.22614


Bocchio, M., Fisher, S. P., Unal, G., Ellender, T. J., Vyazovskiy, V. V., & Capogna, M. (2016). Sleep and serotonin modulate paracapsular nitric oxide synthase expressing neurons of the amygdale. [10.1523/ENEURO.0177-16.2016]. eneuro. doi. http://eneuro.sfn.org/content/early/2016/09/26/ENEURO.0177-16.2016.abstract


Bochorishvili, G., Nguyen, T., Coates, M. B., Viar, K. E., Stornetta, R. L., & Guyenet, P. G. (2014). The orexinergic neurons receive synaptic input from C1 cells in rats. Journal of Comparative Neurology. doi. http://onlinelibrary.wiley.com/doi/10.1002/cne.23643/abstract


Bock, A. S., Kroenke, C. D., Taber, E. N., & Olavarria, J. F. (2012). Retinal input influences the size and corticocortical connectivity of visual cortex during postnatal development in the ferret. Journal of Comparative Neurology, 520(5), 914-932. doi: 10.1002/cne.22738. http://dx.doi.org/10.1002/cne.22738


Bock, A. S., & Olavarria, J. F. (2011). Neonatal enucleation during a critical period reduces the precision of cortico-cortical projections in visual cortex. Neuroscience Letters. doi. 

Bock, J., & Braun, K. (1999). Blockade of N-methyl-d-aspartate receptor activation suppresses learning-induced synaptic elimination. Proceedings of the National Academy of Sciences, 96(5), 2485-2490. doi. 

Bock, J., & Braun, K. (1999). Filial imprinting in domestic chicks is associated with spine pruning in the associative area, dorsocaudal neostriatum. European Journal of Neuroscience, 11(7), 2566. doi. 

Bock, J., Gruss, M., Becker, S., & Braun, K. (2005). Experience-induced changes of dendritic spine densities in the prefrontal and sensory cortex: correlation with developmental time windows. Cerebral Cortex, 15(6), 802-808. doi. 

Bock, J., Murmu, M. S., Biala, Y., Weinstock, M., & Braun, K. (2011). Prenatal stress and neonatal handling induce sex-specific changes in dendritic complexity and dendritic spine density in hippocampal subregions of prepubertal rats. Neuroscience. doi. 

Bock, J., Poeschel, J., Schindler, J., Börner, F., Shachar-Dadon, A., Ferdman, N., . . . Poeggel, G. (2014). Transgenerational sex-specific impact of preconception stress on the development of dendritic spines and dendritic length in the medial prefrontal cortex. Brain Structure and Function, 1-9. doi: 10.1007/s00429-014-0940-4. http://dx.doi.org/10.1007/s00429-014-0940-4


Boda, E., Di Maria, S., Rosa, P., Taylor, V., Abbracchio, M. P., & Buffo, A. (2014). Early phenotypic asymmetry of sister oligodendrocyte progenitor cells after mitosis and its modulation by aging and extrinsic factors. Glia, n/a-n/a. doi: 10.1002/glia.22750. http://dx.doi.org/10.1002/glia.22750


Boda, E., Viganò, F., Rosa, P., Fumagalli, M., Labat-Gest, V., Tempia, F., . . . Buffo, A. (2011). The GPR17 receptor in NG2 expressing cells: Focus on in vivocell maturation and participation in acute trauma and chronic damage. Glia, 59(12), 1958-1973. doi: 10.1002/glia.21237. http://dx.doi.org/10.1002/glia.21237


Bódi, I., Minkó, K., Molnár, D., Nagy, N., & Oláh, I. (2014). A novel aspect of the structure of the avian thymic medulla. Cell and Tissue Research, 1-13. doi: 10.1007/s00441-014-2027-1. http://dx.doi.org/10.1007/s00441-014-2027-1


Boeckler, F., Leng, A., Mura, A., Bettinetti, L., Feldon, J., Gmeiner, P., & Ferger, B. (2003). Attenuation of 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP) neurotoxicity by the novel selective dopamine D3-receptor partial agonist FAUC 329 predominantly in the nucleus accumbens of mice. Biochemical Pharmacology, 66(6), 1025-1032. doi. 

Boele, H.-J., Koekkoek, S. K., De Zeeuw, C. I., & Ruigrok, T. J. (2013). Axonal Sprouting and Formation of Terminals in the Adult Cerebellum during Associative Motor Learning. Journal of Neuroscience, 33(45), 17897-17907. doi. http://www.jneurosci.org/content/33/45/17897.abstract


Boerma, M., Singh, P., Sridharan, V., Tripathi, P., Sharma, S., & Singh, S. P. (2015). Effects of Local Heart Irradiation in a Glutathione S-Transferase Alpha 4-Null Mouse Model. Radiation Research, 183(6), 610-619. doi: doi:10.1667/RR13979.1. http://www.rrjournal.org/doi/abs/10.1667/RR13979.1


Boers, J., Gerrits, P. O., Meijer, E., & Holstege, G. (1999). Estrogen receptor-α-immunoreactive neurons in the mesencephalon, pons and medulla oblongata of the female golden hamster. Neuroscience Letters, 267(1), 17-20. doi. 

Boers, J., Hulshoff, A. C., de Weerd, H., Mouton, L. J., Kuipers, R., & Holstege, G. (2005). Afferent projections to pharynx and soft palate motoneurons: A light and electron microscopical tracing study in the cat. Journal of Comparative Neurology, 486(1), 18-38. doi. 

Bogdanov, M. B., Ferrante, R. J., Kuemmerle, S., Klivenyi, P., & Beal, M. F. (1998). Increased Vulnerability to 3-Nitropropionic Acid in an Animal Model of Huntington's Disease. Journal of Neurochemistry, 71, 2642-2644. doi. 

Boger, H. A., Middaugh, L. D., Patrick, K. S., Ramamoorthy, S., Denehy, E. D., Zhu, H., . . . McGinty, J. F. (2007). Long-Term Consequences of Methamphetamine Exposure in Young Adults Are Exacerbated in Glial Cell Line-Derived Neurotrophic Factor Heterozygous Mice. Journal of Neuroscience, 27(33), 8816-8825. doi: 10.1523/jneurosci.1067-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/33/8816 


Böhm, C., Pangalos, M., Schmitz, D., & Winterer, J. (2015). Serotonin Attenuates Feedback Excitation onto O-LM Interneurons. Cerebral Cortex. doi: 10.1093/cercor/bhv098. http://cercor.oxfordjournals.org/content/early/2015/05/28/cercor.bhv098....


Böhm, C., Peng, Y., Maier, N., Winterer, J., Poulet, J. F., Geiger, J. R., & Schmitz, D. (2015). Functional Diversity of Subicular Principal Cells during Hippocampal Ripples. The Journal of Neuroscience, 35(40), 13608-13618. doi. https://www.jneurosci.org/content/35/40/13608.full#


Bohn, M. C., Choi-Lundberg, D. L., Davidson, B. L., Leranth, C., Kozlowski, D. A., Smith, J. C., . . . Redmond, D. E. (1999). Adenovirus-mediated transgene expression in nonhuman primate brain. Human Gene Therapy, 10(7), 1175-1184. doi. 

Boido, M., Garbossa, D., Fontanella, M., Ducati, A., & Vercelli, A. (2012). Mesenchymal stem cell transplantation reduces glial cyst and improves functional outcome following spinal cord compression. World Neurosurgery, (0). doi: 10.1016/j.wneu.2012.08.014. http://www.sciencedirect.com/science/article/pii/S1878875012009084?v=s5


Boido, M., Garbossa, D., & Vercelli, A. (2011). Early graft of neural precursors in spinal cord compression reduces glial cyst and improves function. Journal of Neurosurgery: Spine, 15(1), 97-106. doi. 

Boillot, M., Lee, C.-Y., Allene, C., Leguern, E., Baulac, S., & Rouach, N. (2016). LGI1 acts presynaptically to regulate excitatory synaptic transmission during early postnatal development. [Article]. Scientific Reports, 6, 21769. doi: 10.1038/srep21769

http://www.nature.com/articles/srep21769#supplementary-information. http://dx.doi.org/10.1038/srep21769


Boitard, M., Bocchi, R., Egervari, K., Petrenko, V., Viale, B., Gremaud, S., . . . Kiss, Jozsef Z. (2015). Wnt Signaling Regulates Multipolar-to-Bipolar Transition of Migrating Neurons in the Cerebral Cortex. Cell Reports, 10(8), 1349-1361. doi: http://dx.doi.org/10.1016/j.celrep.2015.01.061. http://www.sciencedirect.com/science/article/pii/S2211124715001035


Bokor, H., Acsady, L., & Deschenes, M. (2008). Vibrissal Responses of Thalamic Cells That Project to the Septal Columns of the Barrel Cortex and to the Second Somatosensory Area. Journal of Neuroscience, 28(20), 5169-5177. doi: 10.1523/jneurosci.0490-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/20/5169 


Bolat, D. (2017). Three-dimensional reconstruction of the spinal cord of thoroughbred. Eurasian Journal of Veterinary Sciences, 33(2), 127-129. doi. https://www.cabdirect.org/cabdirect/abstract/20173212610


Boley, A. M., Perez, S. M., & Lodge, D. J. (2014). A fundamental role for hippocampal parvalbumin in the dopamine hyperfunction associated with schizophrenia. Schizophrenia Research, (0). doi: http://dx.doi.org/10.1016/j.schres.2014.05.005. http://www.sciencedirect.com/science/article/pii/S0920996414002345


Bolis, A., Previtali, S., Bussini, S., Dina, G., Dati, G., Feltri, M. L., . . . Bolino, A. (2004). Unravelling the molecular basis of CMT4B pathology. Journal of the Peripheral Nervous System, 9(2), 125-125. doi: doi:10.1111/j.1085-9489.2004.009209bq.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Bomer, K., Brichta, A., Baroody, F., Boonlayangoor, S., Li, X., & Naclerio, R. M. (1998). A mouse model of acute bacterial rhinosinusitis. Archives of Otolaryngology- Head and Neck Surgery, 124(11), 1227-1227. doi. 

Bonifazi, P., Goldin, M., Picardo, M. A., Jorquera, I., Cattani, A., Bianconi, G., . . . Cossart, R. (2009). GABAergic Hub Neurons Orchestrate Synchrony in Developing Hippocampal Networks. Science, 326(5958), 1419-1424. doi: 10.1126/science.1175509. http://www.sciencemag.org/cgi/content/abstract/326/5958/1419 


Bonn, M., Schmitt, A., Lesch, K. P., Van Bockstaele, E. J., & Asan, E. (2012). Serotonergic innervation and serotonin receptor expression of NPY-producing neurons in the rat lateral and basolateral amygdaloid nuclei. Brain Structure and Function, 1-15. doi. 

Bonthius, D., Mahoney, J., Buchmeier, M., Karacay, B., & Taggard, D. (2002). Critical Role for Glial Cells in the Propagation and Spread of Lymphocytic Choriomeningitis Virus in the Developing Rat Brain. Journal of Virology, 76(13), 6618-6635. doi. 

Bony, G., Szczurkowska, J., Tamagno, I., Shelly, M., Contestabile, A., & Cancedda, L. (2013). Non-hyperpolarizing GABAB receptor activation regulates neuronal migration and neurite growth and specification by cAMP/LKB1. Nature Communications, 4, 1800. doi. 

Bonzano, S., Bovetti, S., Fasolo, A., Peretto, P., & De Marchis, S. (2014). Odour enrichment increases adult-born dopaminergic neurons in the mouse olfactory bulb. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12724. http://dx.doi.org/10.1111/ejn.12724


Booker, S. A., Gross, A., Althof, D., Shigemoto, R., Bettler, B., Frotscher, M., . . . Vida, I. (2013). Differential GABAB-Receptor-Mediated Effects in Perisomatic- and Dendrite-Targeting Parvalbumin Interneurons. Journal of Neuroscience, 33(18), 7961-7974. doi: 10.1523/jneurosci.1186-12.2013. http://www.jneurosci.org/content/33/18/7961.abstract


Bordt, A. S., Hoshi, H., Yamada, E. S., Perryman-Stout, W. C., & Marshak, D. W. (2006). Synaptic input to OFF parasol ganglion cells in macaque retina. Journal of Comparative Neurology, 498(1), 46-57. doi. 

Borgesius, N. Z., de Waard, M. C., van der Pluijm, I., Omrani, A., Zondag, G. C. M., van der Horst, G. T. J., . . . Elgersma, Y. (2011). Accelerated Age-Related Cognitive Decline and Neurodegeneration, Caused by Deficient DNA Repair. Journal of Neuroscience, 31(35), 12543-12553. doi: 10.1523/jneurosci.1589-11.2011. http://www.jneurosci.org/content/31/35/12543.abstract


Borgna, M., Lombardi, R., Lauria, G., Grezzi, P., Savino, C., Bianchi, R., . . . Cavaletti, G. (2004). Intraepidermal innervation and tail nerve conduction velocity in neurotoxicity models: results of a correlation study in normal and pathological conditions. Journal of the Peripheral Nervous System, 9(2), 104-105. doi: doi:10.1111/j.1085-9489.2004.009209c.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Bories, C., Husson, Z., Guitton, M. J., & De Koninck, Y. (2013). Differential Balance of Prefrontal Synaptic Activity in Successful versus Unsuccessful Cognitive Aging. Journal of Neuroscience, 33(4), 1344-1356. doi: 10.1523/jneurosci.3258-12.2013. http://www.jneurosci.org/content/33/4/1344.abstract


Borin, M., Saraceno, C., Catania, M., Lorenzetto, E., Pontelli, V., Paterlini, A., . . . Bolognin, S. (2018). Rac1 activation links tau hyperphosphorylation and Aβ dysmetabolism in Alzheimer’s disease. [journal article]. Acta Neuropathologica Communications, 6(1), 61. doi: 10.1186/s40478-018-0567-4. https://doi.org/10.1186/s40478-018-0567-4


Borniger, J. C., Walker Ii, W. H., Surbhi, Emmer, K. M., Zhang, N., Zalenski, A. A., . . . DeVries, A. C. (2018). A Role for Hypocretin/Orexin in Metabolic and Sleep Abnormalities in a Mouse Model of Non-metastatic Breast Cancer. Cell Metabolism. doi: https://doi.org/10.1016/j.cmet.2018.04.021. http://www.sciencedirect.com/science/article/pii/S155041311830305X


Boros, B. D., Greathouse, K. M., Gearing, M., & Herskowitz, J. H. (2018). Dendritic spine remodeling accompanies Alzheimer’s disease pathology and genetic susceptibility in cognitively normal aging. Neurobiology of Aging. doi: https://doi.org/10.1016/j.neurobiolaging.2018.09.003. http://www.sciencedirect.com/science/article/pii/S0197458018303269


Boros, B. D., Greathouse, K. M., Gentry, E. G., Curtis, K. A., Birchall, E. L., Gearing, M., & Herskowitz, J. H. (2017). Dendritic spines provide cognitive resilience against Alzheimer's disease. Annals of Neurology, n/a-n/a. doi: 10.1002/ana.25049. http://dx.doi.org/10.1002/ana.25049


Borowska, J., Jones, C. T., Zhang, H., Blacklaws, J., Goulding, M., & Zhang, Y. (2013). Functional Subpopulations of V3 Interneurons in the Mature Mouse Spinal Cord. Journal of Neuroscience, 33(47), 18553-18565. doi. http://www.jneurosci.org/content/33/47/18553.short


Borra, E., Ichinohe, N., Sato, T., Tanifuji, M., & Rockland, K. S. (2010). Cortical connections to area TE in monkey: hybrid modular and distributed organization. Cerebral Cortex, 20(2), 257-270. doi. 

Borreca, A., Latina, V., Corsetti, V., Middei, S., Piccinin, S., Della Valle, F., . . . Amadoro, G. (2018). AD-Related N-Terminal Truncated Tau Is Sufficient to Recapitulate In Vivo the Early Perturbations of Human Neuropathology: Implications for Immunotherapy. [journal article]. Molecular Neurobiology. doi: 10.1007/s12035-018-0974-3. https://doi.org/10.1007/s12035-018-0974-3


Borrell, V., & Callaway, E. M. (2002). Reorganization of Exuberant Axonal Arbors Contributes to the Development of Laminar Specificity in Ferret Visual Cortex. Journal of Neuroscience, 22(15), 6682-6695. doi. http://www.jneurosci.org/cgi/content/abstract/22/15/6682


Borrell, V., Kaspar, B. K., Gage, F. H., & Callaway, E. M. (2006). In vivo evidence for radial migration of neurons by long-distance somal translocation in the developing ferret visual cortex. Cerebral Cortex, 16(11), 1571-1583. doi. 

Borrett, S., & Hughes, L. (2016). Reporting methods for processing and analysis of data from serial block face scanning electron microscopy. Journal of Microscopy, n/a-n/a. doi: 10.1111/jmi.12377. http://dx.doi.org/10.1111/jmi.12377


Borsello, T., Clarke, P. G. H., Hirt, L., Vercelli, A., Repici, M., Schorderet, D. F., . . . Bonny, C. (2003). A peptide inhibitor of c-Jun N-terminal kinase protects against excitotoxicity and cerebral ischemia. Nature of Medicine, 9, 1180-1186. doi. 

Bortolato, M., Chen, K., Godar, S. C., Chen, G., Wu, W., Rebrin, I., . . . Shih, J. C. (2011). Social Deficits and Perseverative Behaviors, but not Overt Aggression, in MAO-A Hypomorphic Mice. Neuropsychopharmacology. doi. 

Bortolato, M., Godar, S. C., Alzghoul, L., Zhang, J., Darling, R. D., Simpson, K. L., . . . Shih, J. C. (2012). Monoamine oxidase A and A/B knockout mice display autistic-like features. International Journal of Neuropsychopharmacology, FirstView, 1-20. doi: doi:10.1017/S1461145712000715. http://dx.doi.org/10.1017/S1461145712000715


Bortone, Dante S., Olsen, Shawn R., & Scanziani, M. (2014). Translaminar Inhibitory Cells Recruited by Layer 6 Corticothalamic Neurons Suppress Visual Cortex. Neuron, (0). doi: http://dx.doi.org/10.1016/j.neuron.2014.02.021. http://www.sciencedirect.com/science/article/pii/S0896627314001524


Bosch, C., Degos, B., Deniau, J.-M., & Venance, L. (2011). Subthalamic nucleus high-frequency stimulation generates a concomitant synaptic excitation–inhibition in substantia nigra pars reticulata. Journal of Physiology, 589(17), 4189-4207. doi: 10.1113/jphysiol.2011.211367. http://dx.doi.org/10.1113/jphysiol.2011.211367


Bosch, D., & Ehrlich, I. (2015). Postnatal maturation of GABAergic modulation of sensory inputs onto lateral amygdala principal neurons. The Journal of Physiology, n/a-n/a. doi: 10.1113/jp270645. http://dx.doi.org/10.1113/JP270645


Boschen, K. E., McKeown, S. E., Roth, T. L., & Klintsova, A. Y. (2016). Impact of exercise and a complex environment on hippocampal dendritic morphology, Bdnf gene expression, and DNA methylation in male rat pups neonatally exposed to alcohol. Developmental Neurobiology, n/a-n/a. doi: 10.1002/dneu.22448. http://dx.doi.org/10.1002/dneu.22448


Boschen, K. E., Ruggiero, M. J., & Klintsova, A. Y. (2016). Neonatal binge alcohol exposure increases microglial activation in the developing rat hippocampus. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2016.03.033. http://www.sciencedirect.com/science/article/pii/S0306452216300033


Bosking, W. H., Kretz, R., Pucak, M. L., & Fitzpatrick, D. (2000). Functional Specificity of Callosal Connections in Tree Shrew Striate Cortex. Journal of Neuroscience, 20(6), 2346-2359. doi. http://www.jneurosci.org/cgi/content/abstract/20/6/2346


Bosking, W. H., Zhang, Y., Schofield, B., & Fitzpatrick, D. (1997). Orientation Selectivity and the Arrangement of Horizontal Connections in Tree Shrew Striate Cortex. Journal of Neuroscience, 17(6), 2112-2127. doi. http://www.jneurosci.org/cgi/content/abstract/17/6/2112


Bossolasco, P., Cova, L., Levandis, G., Diana, V., Cerri, S., Deliliers, G. L., . . . Armentero, M. T. (2012). Noninvasive near-infrared live imaging of human adult mesenchymal stem cells transplanted in a rodent model of Parkinson’s disease. International Journal of Nanomedicine, 7, 435-435. doi. 

Bota, M., & Arbib, M. A. (2002). The NeuroHomology Database: an online KMS for handling and evaluation of the neurobiological information. Neuroscience Databases: A practical guide, 203-220. doi. 

Both, M., Bähner, F., von Bohlen und Halbach, O., & Draguhn, A. (2008). Propagation of specific network patterns through the mouse hippocampus. Hippocampus, 18(9), 899-908. doi. 

Bothwell, S., Meredith, G. E., Phillips, J., Staunton, H., Doherty, C., Grigorenko, E., . . . Farrell, M. (2001). Neuronal Hypertrophy in the Neocortex of Patients with Temporal Lobe Epilepsy. Journal of Neuroscience, 21(13), 4789-4800. doi. http://www.jneurosci.org/cgi/content/abstract/21/13/4789 


Bottjer, S. W., Alderete, T. L., & Chang, D. (2010). Conjunction of vocal production and perception regulates expression of the immediate early gene ZENK in a novel cortical region of songbirds. Journal of Neurophysiology, 103(4), 1833-1842. doi. 

Bottjer, S. W., & To, M. (2012). Afferents from Vocal Motor and Respiratory Effectors Are Recruited during Vocal Production in Juvenile Songbirds. Journal of Neuroscience, 32(32), 10895-10906. doi: 10.1523/jneurosci.0990-12.2012. http://www.jneurosci.org/content/32/32/10895.abstract


Boucetta, S., Cissé, Y., Mainville, L., Morales, M., & Jones, B. E. (2014). Discharge Profiles across the Sleep–Waking Cycle of Identified Cholinergic, GABAergic, and Glutamatergic Neurons in the Pontomesencephalic Tegmentum of the Rat. The Journal of Neuroscience. doi. 

Boucetta, S., & Jones, B. E. (2009). Activity Profiles of Cholinergic and Intermingled GABAergic and Putative Glutamatergic Neurons in the Pontomesencephalic Tegmentum of Urethane-Anesthetized Rats. Journal of Neuroscience, 29(14), 4664-4674. doi: 10.1523/jneurosci.5502-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/14/4664 


Boudrias, M.-H., McPherson, R. L., Frost, S. B., & Cheney, P. D. (2009). Output Properties and Organization of the Forelimb Representation of Motor Areas on the Lateral Aspect of the Hemisphere in Rhesus Macaques. Cerebral Cortex, bhp084. doi: 10.1093/cercor/bhp084. http://cercor.oxfordjournals.org/cgi/content/abstract/bhp084v1 


Bouley, D. M., Alarcón, C. N., Hildebrandt, T., & O’Connell-Rodwell, C. E. (2007). The distribution, density and three-dimensional histomorphology of Pacinian corpuscles in the foot of the Asian elephant (Elephas maximus) and their potential role in seismic communication. Journal of Anatomy, 211(4), 428-435. doi. 

Bourgeois, J. R., & Ferland, R. J. (2019). Loss of the neurodevelopmental Joubert syndrome causing protein, Ahi1, causes motor and muscle development delays independent of central nervous system involvement. Developmental Biology. doi: https://doi.org/10.1016/j.ydbio.2019.01.014. http://www.sciencedirect.com/science/article/pii/S0012160618304238


Bouslama, M., Renaud, J., Olivier, P., Fontaine, R. H., Matrot, B., Gressens, P., & Gallego, J. (2007). Melatonin prevents learning disorders in brain-lesioned newborn mice. Neuroscience, 150(3), 712-719. doi. 

Bousquet, M., St-Amour, I., Vandal, M., Julien, P., Cicchetti, F., & Calon, F. (2011). High-fat diet exacerbates MPTP-induced dopaminergic degeneration in mice. Neurobiology of Disease. doi. 

Boussaoud, D., Tanné-Gariépy, J., Wannier, T., & Rouiller, E. (2005). Callosal connections of dorsal versus ventral premotor areas in the macaque monkey: a multiple retrograde tracing study. BMC Neuroscience, 6(1), 67. doi. http://www.biomedcentral.com/1471-2202/6/67 


Boutte, R. W., Merlin, S., Yona, G., Griffiths, B., Angelucci, A., Kahn, I., . . . Blair, S. (2017). Utah optrode array customization using stereotactic brain atlases and 3-D CAD modeling for optogenetic neocortical interrogation in small rodents and nonhuman primates. Neurophotonics, 4(4), 041502-041502. doi: 10.1117/1.NPh.4.4.041502. http://dx.doi.org/10.1117/1.NPh.4.4.041502


Bove, C., Coleman, F. H., & Travagli, R. A. (2019). Characterization of the Basic Membrane Properties of Neurons of the Rat Dorsal Motor Nucleus of the Vagus in Paraquat-Induced Models of Parkinsonism. Neuroscience, 418, 122-132. doi: https://doi.org/10.1016/j.neuroscience.2019.08.048. http://www.sciencedirect.com/science/article/pii/S030645221930630X


Bovetti, S., Bonzano, S., Garzotto, D., Giannelli, S. G., Iannielli, A., Armentano, M., . . . De Marchis, S. (2013). COUP-TFI controls activity-dependent tyrosine hydroxylase expression in adult dopaminergic olfactory bulb interneurons. Development. doi: 10.1242/dev.089961. http://dev.biologists.org/content/early/2013/11/12/dev.089961.abstract


Bovetti, S., Hsieh, Y.-C., Bovolin, P., Perroteau, I., Kazunori, T., & Puche, A. C. (2007). Blood Vessels Form a Scaffold for Neuroblast Migration in the Adult Olfactory Bulb. Journal of Neuroscience, 27(22), 5976-5980. doi: 10.1523/jneurosci.0678-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/22/5976 


Bovetti, S., Veyrac, A., Peretto, P., Fasolo, A., & De Marchis, S. (2009). Olfactory enrichment influences adult neurogenesis modulating GAD67 and plasticity-related molecules expression in newborn cells of the olfactory bulb. PLoS ONE, 4(7), e6359-e6359. doi. 

Boy, J., Leergaard, T. B., Schmidt, T., Odeh, F., Bichelmeier, U., Nuber, S., . . . others. (2006). Expression mapping of tetracycline-responsive prion protein promoter: digital atlasing for generating cell-specific disease models. Neuroimage, 33(2), 449-462. doi. 

Boyd, Alison M., Sturgill, James F., Poo, C., & Isaacson, Jeffry S. (2012). Cortical Feedback Control of Olfactory Bulb Circuits. Neuron, 76(6), 1161-1174. doi: http://dx.doi.org/10.1016/j.neuron.2012.10.020. http://www.sciencedirect.com/science/article/pii/S0896627312009403


Boyett, J. M., & Buckmaster, P. S. (2001). Somatostatin-immunoreactive interneurons contribute to lateral inhibitory circuits in the dentate gyrus of control and epileptic rats. Hippocampus, 11(4), 418-422. doi. 

Boyette-Davis, J. A., Cata, J. P., Zhang, H., Driver, L. C., Wendelschafer-Crabb, G., Kennedy, W. R., & Dougherty, P. M. (2011). Follow-Up Psychophysical Studies in Bortezomib-Related Chemoneuropathy Patients. Journal of Pain. doi. 

Boyle, K. A., Gutierrez-Mecinas, M., Polgár, E., Mooney, N., O'Connor, E., Furuta, T., . . . Todd, A. J. (2017). A quantitative study of neurochemically defined populations of inhibitory interneurons in the superficial dorsal horn of the mouse spinal cord. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2017.08.044. http://www.sciencedirect.com/science/article/pii/S0306452217306206


Boyle, R., Ehsanian, R., Mofrad, A., Popova, Y., & Varelas, J. (2018). Morphology of the Utricular Otolith Organ in the Toadfish, Opsanus tau. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24429. http://dx.doi.org/10.1002/cne.24429


Bozdagi, O., Valcin, M., Poskanzer, K., Tanaka, H., & Benson, D. L. (2004). Temporally distinct demands for classic cadherins in synapse formation and maturation. Molecular and Cellular Neuroscience, 27(4), 509-521. doi. 

Bozis, A., & Moschovakis, A. K. (1998). Neural network simulations of the primate oculomotor system III. An one-dimensional, one-directional model of the superior colliculus. Biological Cybernetics, 79(3), 215-230. doi. 

Braas, K. M., Rossignol, T. M., Girard, B. M., May, V., & Parsons, R. L. (2004). Pituitary adenylate cyclase activating polypeptide (PACAP) decreases neuronal somatostatin immunoreactivity in cultured guinea-pig parasympathetic cardiac ganglia. Neuroscience, 126(2), 335-346. doi. 

Bracke, A., Domanska, G., Bracke, K., Harzsch, S., van den Brandt, J., Bröker, B., & von Bohlen und Halbach, O. (2019). Obesity Impairs Mobility and Adult Hippocampal Neurogenesis. Journal of Experimental Neuroscience, 13, 1179069519883580. doi: 10.1177/1179069519883580. https://doi.org/10.1177/1179069519883580


Bracke, A., Schäfer, S., von Bohlen und Halbach, V., Klempin, F., Bente, K., Bracke, K., . . . von Bohlen und Halbach, O. (2018). ATP6AP2 over-expression causes morphological alterations in the hippocampus and in hippocampus-related behaviour. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-018-1633-1. https://doi.org/10.1007/s00429-018-1633-1


Bragg, E. M., & Briggs, F. (2017). Large-scale Reconstructions and Independent, Unbiased Clustering Based on Morphological Metrics to Classify Neurons in Selective Populations. (120), e55133. doi: doi:10.3791/55133. https://www.jove.com/video/55133


Brambilla, R., Bracchi-Ricard, V., Hu, W. H., Frydel, B., Bramwell, A., Karmally, S., . . . Bethea, J. R. (2005). Inhibition of astroglial nuclear factor KB reduces inflammation and improves functional recovery after spinal cord injury. Journal of Experimental Medicine, 202(1), 145-156. doi. 

Branchereau, P., Cattaert, D., Delpy, A., Allain, A.-E., Martin, E., & Meyrand, P. (2016). Depolarizing GABA/glycine synaptic events switch from excitation to inhibition during frequency increases. [Article]. Scientific Reports, 6, 21753. doi: 10.1038/srep21753

http://www.nature.com/articles/srep21753#supplementary-information. http://dx.doi.org/10.1038/srep21753


Branco, T., Clark, B. A., & Häusser, M. (2010). Dendritic Discrimination of Temporal Input Sequences in Cortical Neurons. Science 329(5999), 1671-1675. doi. 

Branco, T., & Häusser, M. (2011). Synaptic integration gradients in single cortical pyramidal cell dendrites. Neuron, 69(5), 885-892. doi. 

Brandt, N., Löffler, T., Fester, L., & Rune, G. M. (2020). Sex-specific features of spine densities in the hippocampus. Scientific Reports, 10(1), 11405. doi: 10.1038/s41598-020-68371-x. https://doi.org/10.1038/s41598-020-68371-x


Braun, K., Antemano, R., Helmeke, C., Büchner, M., & Poeggel, G. (2009). Juvenile separation stress induces rapid region-and layer-specific changes in S100\ss-and glial fibrillary acidic protein-immunoreactivity in astrocytes of the rodent medial prefrontal cortex. Neuroscience, 160(3), 629-638. doi. 

Braun, K., & Hofmann, H. (1995). Slice cultures of the imprinting-relevant forebrain area MNH of the domestic chick: quantitative characterization of neuronal morphology. Developmental Brain Research, 86, 286-296. doi. 

Braun, K., & Segal, M. (2000). FMRP involvement in formation of synapses among cultured hippocampal neurons. Cerebral Cortex, 10(10), 1045-1052. doi. 

Brauth, S. E., Liang, W., Amateau, S. K., & Robert, T. F. (2005). Sexual dimorphism of vocal control nuclei in budgerigars (Melopsittacus undulatus) revealed with Nissl and NADPH-d staining. Journal of Comparative Neurology, 484(1), 15-27. doi. 

Bravin, M., Morando, L., Vercelli, A., Rossi, F., & Strata, P. (1999). Control of spine formation by electrical activity in the adult rat cerebellum. Proceedings of the National Academy of Sciences, 96(4), 1704-1709. doi. 

Bravin, M., Rossi, F., & Strata, P. (1995). Different climbing fibres innervate separate dendritic regions of the same purkinje cell in hypogranular cerebellum. Journal of Comparative Neurology, 357(3), 395-407. doi. http://dx.doi.org/10.1002/cne.903570306 


Breach, M. R., Moench, K. M., & Wellman, C. L. (2019). Social instability in adolescence differentially alters dendritic morphology in the medial prefrontal cortex and its response to stress in adult male and female rats. Developmental Neurobiology, 0(0). doi: 10.1002/dneu.22723. https://onlinelibrary.wiley.com/doi/abs/10.1002/dneu.22723


Brecht, M., Roth, A., & Sakmann, B. (2003). Dynamic receptive fields of reconstructed pyramidal cells in layers 3 and 2 of rat somatosensory barrel cortex. Journal of Physiology, 553(1), 243-265. doi: 10.1113/jphysiol.2003.044222. http://jp.physoc.org/cgi/content/abstract/553/1/243 


Brecht, M., & Sakmann, B. (2002). Dynamic representation of whisker deflection by synaptic potentials in spiny stellate and pyramidal cells in the barrels and septa of layer 4 rat somatosensory cortex. Journal of Physiology, 543(1), 49-70. doi: 10.1113/jphysiol.2002.018465. http://jp.physoc.org/cgi/content/abstract/543/1/49 


Brecht, M., & Sakmann, B. (2002). Whisker maps of neuronal subclasses of the rat ventral posterior medial thalamus, identified by whole-cell voltage recording and morphological reconstruction. Journal of Physiology, 538(2), 495-515. doi: 10.1113/jphysiol.2001.012334. http://jp.physoc.org/cgi/content/abstract/538/2/495 


Brecht, M., Schneider, M., Sakmann, B., & Margrie, T. W. (2003). Whisker movements evoked by stimulation of single pyramidal cells in rat motor cortex. Nature, 427, 704-710. doi. 

Bregy, A., Nixon, R., Lotocki, G., Alonso, O. F., Atkins, C. M., Tsoulfas, P., . . . Dietrich, W. D. (2011). Posttraumatic hypothermia increases doublecortin expressing neurons in the dentate gyrus after traumatic brain injury in the rat. Experimental Neurology. doi. 

Bremen, P., & Joris, P. X. (2013). Axonal Recordings from Medial Superior Olive Neurons Obtained from the Lateral Lemniscus of the Chinchilla (Chinchilla laniger). The Journal of Neuroscience, 33(44), 17506-17518. doi. http://www.jneurosci.org/content/33/44/17506.short


Bremmer, F., Duhamel, J.-R., Ben Hamed, S., & Graf, W. (2002). Heading encoding in the macaque ventral intraparietal area (VIP). European Journal of Neuroscience, 16(8), 1554-1568. doi: doi:10.1046/j.1460-9568.2002.02207.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.2002.02207.x 


Bremmer, F., Klam, F., Duhamel, J.-R., Ben Hamed, S., & Graf, W. (2002). Visual-vestibular interactive responses in the macaque ventral intraparietal area (VIP). European Journal of Neuroscience, 16(8), 1569-1586. doi: doi:10.1046/j.1460-9568.2002.02206.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.2002.02206.x 


Brennaman, L. H., & Maness, P. F. (2008). Developmental regulation of GABAergic interneuron branching and synaptic development in the prefrontal cortex by soluble neural cell adhesion molecule. Molecular and Cellular Neuroscience, 37(4), 781-793. doi. 

Brennaman, L. H., Zhang, X., Guan, H., Triplett, J. W., Brown, A., Demyanenko, G. P., . . . Maness, P. F. (2012). Polysialylated NCAM and EphrinA/EphA Regulate Synaptic Development of GABAergic Interneurons in Prefrontal Cortex. Cerebral Cortex, bhr392. doi: 10.1093/cercor/bhr392. http://cercor.oxfordjournals.org/cgi/content/abstract/bhr392v1


Brennan, A. R., Yuan, P., Dickstein, D. L., Rocher, A. B., Hof, P. R., Manji, H., & Arnsten, A. F. T. (2009). Protein kinase C activity is associated with prefrontal cortical decline in aging. Neurobiology of Aging, 30(5), 782-792. doi. 

Brennan, C., Rivas-Plata, K., & Landis, S. C. (1999). The p75 neurotrophin receptor influences NT-3 responsiveness of sympathetic neurons in vivo. Nature Neuroscience, 2, 699-705. doi. 

Bressoud, R., & Innocenti, G. M. (1999). Typology, early differentiation, and exuberant growth of a set of cortical axons. Journal of Comparative Neurology, 406(1), 87-108. doi. http://dx.doi.org/10.1002/(SICI)1096-9861(19990329)406:1<87::AID-CNE6>3.0.CO;2-S 

Breton, J. M., Charbit, A. R., Snyder, B. J., Fong, P. T. K., Dias, E. V., Himmels, P., . . . Margolis, E. B. (2018). Relative Contributions and Mapping of Ventral Tegmental Area Dopamine and GABA Neurons by Projection Target in the Rat. Journal of Comparative Neurology, 0(ja). doi: doi:10.1002/cne.24572. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24572

Brette, R., Rudolph, M., Carnevale, T., Hines, M., Beeman, D., Bower, J. M., . . . others. (2007). Simulation of networks of spiking neurons: a review of tools and strategies. Journal of Computational Neuroscience, 23(3), 349-398. doi. 

Brett-Green, B., Fifková, E., Larue, D. T., Winer, J. A., & Barth, D. S. (2003). A multisensory zone in rat parietotemporal cortex: Intra-and extracellular physiology and thalamocortical connections. Journal of Comparative Neurology, 460(2), 223-237. doi. 

Brettle, M., Suchowerska, A. K., Chua, S. W., Ittner, L. M., & Fath, T. (2015). Amyotrophic lateral sclerosis-associated mutant profilin 1 increases dendritic arborisation and spine formation in primary hippocampal neurons. Neuroscience Letters. doi: http://dx.doi.org/10.1016/j.neulet.2015.09.034. http://www.sciencedirect.com/science/article/pii/S0304394015301609


Breunig, J. J., Silbereis, J., Vaccarino, F. M., Sestan, N., & Rakic, P. (2007). Notch regulates cell fate and dendrite morphology of newborn neurons in the postnatal dentate gyrus. Proceedings of the National Academy of Sciences, 104(51), 20558-20563. doi: 10.1073/pnas.0710156104. http://www.pnas.org/cgi/content/abstract/104/51/20558 


Brevik, A., Leergaard, T. B., Svanevik, M., & Bjaalie, J. G. (2001). Three-dimensional computerised atlas of the rat brain stem precerebellar system: approaches for mapping, visualization, and comparison of spatial distribution data. Anatomy and Embryology, 204(4), 319-332. doi. 

Brewer, G. J., Espinosa, J. A., & Struble, R. G. (2003). Effect of Neuregen nutrient medium on survival of cortical neurons after aspiration lesion in rats. Journal of Neurosurgery, 98(6), 1291-1298. doi. 

Brewer, K. L., Lee, J. W., Downs, H., Oaklander, A. L., & Yezierski, R. P. (2008). Dermatomal scratching after intramedullary quisqualate injection: correlation with cutaneous denervation. Journal of Pain, 9(11), 999-1005. doi. 

Brewster, A. L., Lugo, J. N., Patil, V. V., Lee, W. L., Qian, Y., Vanegas, F., & Anderson, A. E. (2013). Rapamycin Reverses Status Epilepticus-Induced Memory Deficits and Dendritic Damage. PLoS ONE, 8(3), e57808. doi: 10.1371/journal.pone.0057808. http://dx.doi.org/10.1371%2Fjournal.pone.0057808


Briani, C., Zara, G., Bernardinello, L., Cavalletto, L., Ermani, M., & Chemello, L. (2004). Pegylated alpha-interferons peripheral neurotoxicity: prospective study in chronic hepatitis C. Journal of the Peripheral Nervous System, 9(2), 110-111. doi. 

Bribián, A., Barallobre, M. J., Soussi-Yanicostas, N., & de Castro, F. (2006). Anosmin-1 modulates the FGF-2-dependent migration of oligodendrocyte precursors in the developing optic nerve. Molecular and Cellular Neuroscience, 33(1), 2-14. doi. 

Bridges, N., Slais, K., & Syková, E. (2008). The effects of chronic corticosterone on hippocampal astrocyte numbers: A comparison of male and female Wistar rats. Acta Neurobiologiae Experimentalis, 68(2), 131-131. doi. 

Briffaud, V., Williams, P., Courty, J., & Broberger, C. (2015). Excitation of Tuberoinfundibular Dopamine Neurons by Oxytocin: Crosstalk in the Control of Lactation. The Journal of Neuroscience, 35(10), 4229-4237. doi. http://www.jneurosci.org/content/35/10/4229.short


Briggs, F., & Callaway, E. M. (2005). Laminar patterns of local excitatory input to layer 5 neurons in macaque primary visual cortex. Cerebral Cortex, 15(5), 479-488. doi. 

Briggs, F., Kiley, Caitlin W., Callaway, Edward M., & Usrey, W. M. (2016). Morphological Substrates for Parallel Streams of Corticogeniculate Feedback Originating in Both V1 and V2 of the Macaque Monkey. Neuron. doi: http://dx.doi.org/10.1016/j.neuron.2016.02.038. http://www.sciencedirect.com/science/article/pii/S0896627316001756


Bright, F. M., Byard, R. W., Vink, R., & Paterson, D. S. (2017). Medullary Serotonin Neuron Abnormalities in an Australian Cohort of Sudden Infant Death Syndrome. Journal of Neuropathology and Experimental Neurology. doi. https://academic.oup.com/jnen/article-abstract/doi/10.1093/jnen/nlx071/4...


Brill, M. S., Ninkovic, J., Winpenny, E., Hodge, R. D., Ozen, I., Yang, R., . . . others. (2009). Adult generation of glutamatergic olfactory bulb interneurons. Nature Neuroscience, 12(12), 1524-1533. doi. 

Brilliant, M. J., Elble, R. J., Ghobrial, M., & Struble, R. G. (1997). The distribution of amyloid β protein deposition in the corpus striatum of patients with Alzheimer's disease. Neuropathology and Applied Neurobiology, 23(4), 322-325. doi. 

Brindani, F., Gemignani, F., Zinno, L., & Marbini, A. (2004). Aquadynia. a manifestation of small fiber sensory neuropathy? Journal of the Peripheral Nervous System, 9(2), 119-119. doi: doi:10.1111/j.1085-9489.2004.009209av.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Briner, A., De Roo, M., Dayer, A., Muller, D., Habre, W., & Vutskits, L. (2010). Volatile anesthetics rapidly increase dendritic spine density in the rat medial prefrontal cortex during synaptogenesis. Anesthesiology, 112(3), 546-546. doi. 

Briner, A., Nikonenko, I., De Roo, M., Dayer, A., Muller, D., & Vutskits, L. (2011). Developmental stage-dependent persistent impact of propofol anesthesia on dendritic spines in the rat medial prefrontal cortex. Anesthesiology, 115(2), 282-282. doi. 

Brinkmann, B. G., Agarwal, A., Sereda, M. W., Garratt, A. N., Müller, T., Wende, H., . . . others. (2008). Neuregulin-1/ErbB signaling serves distinct functions in myelination of the peripheral and central nervous system. Neuron, 59(4), 581-595. doi. 

Briska, A. M., Uhlrich, D. J., & Lytton, W. W. (2000). Independent dendritic domains in the thalamic circuit. Neurocomputing, 32, 299-305. doi. 

Briska, A. M., Uhlrich, D. J., & Lytton, W. W. (2003). Computer model of passive signal integration based on whole-cell in vitro studies of rat lateral geniculate nucleus. European Journal of Neuroscience, 17(8), 1531-1541. doi: doi:10.1046/j.1460-9568.2003.02579.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.2003.02579.x 


Brizuela, M., Blizzard, C. A., Chuckowree, J. A., Pitman, K. A., Young, K. M., & Dickson, T. (2017). Mild traumatic brain injury leads to decreased inhibition and a differential response of calretinin positive interneurons in the injured cortex. Journal of Neurotrauma. doi: 10.1089/neu.2017.4977. http://dx.doi.org/10.1089/neu.2017.4977


Broadbelt, K. G., Paterson, D. S., Rivera, K. D., L Trachtenberg, F., & Kinney, H. C. (2010). Neuroanatomic relationships between the GABAergic and serotonergic systems in the developing human medulla. Autonomic Neuroscience, 154(1-2), 30-41. doi. 

Broadbelt, K. G., Rivera, K. D., Paterson, D. S., Duncan, J. R., Trachtenberg, F. L., Paulo, J. A., . . . others. (2012). Brainstem deficiency of the 14-3-3 regulator of serotonin synthesis: a proteomics analysis in the sudden infant death syndrome. Molecular & Cellular Proteomics, 11(1). doi. 

Brockett, E. G., Seenan, P. G., Anne Bannatyne, B., & Maxwell, D. J. (2013). Ascending and descending propriospinal pathways between lumbar and cervical segments in the rat: evidence for a substantial ascending excitatory pathway. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2013.02.039. http://www.sciencedirect.com/science/article/pii/S0306452213001735


Brohlin, M., Kingham, P. J., Novikova, L. N., Novikov, L. N., & Wiberg, M. (2012). Aging Effect on Neurotrophic Activity of Human Mesenchymal Stem Cells. PLoS ONE, 7(9), e45052. doi: 10.1371/journal.pone.0045052. http://dx.doi.org/10.1371%2Fjournal.pone.0045052


Brombas, A., Fletcher, L. N., & Williams, S. R. (2014). Activity-Dependent Modulation of Layer 1 Inhibitory Neocortical Circuits by Acetylcholine. The Journal of Neuroscience, 34(5), 1932-1941. doi. http://www.jneurosci.org/content/34/5/1932.short


Broser, P. J., Erdogan, S., Grinevich, V., Osten, P., Sakmann, B., & Wallace, D. J. (2008). Automated axon length quantification for populations of labelled neurons. Journal of Neuroscience Methods, 169(1), 43-54. doi. 

Brown, E. C. Z., Steadman, C. J., Lee, T. M., Padmanabhan, V., Lehman, M. N., & Coolen, L. M. (2015). Sex differences and effects of prenatal exposure to excess testosterone on ventral tegmental area dopamine neurons in adult sheep. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12871. http://dx.doi.org/10.1111/ejn.12871


Brown, J., Cooper-Kuhn, C. M., Kempermann, G., Praag, H. V., Winkler, J., Gage, F. H., & Kuhn, H. G. (2003). Enriched environment and physical activity stimulate hippocampal but not olfactory bulb neurogenesis. European Journal of Neuroscience, 17(10), 2042. doi. 

Brown, K. M., Barrionuevo, G., Canty, A. J., De Paola, V., Hirsch, J. A., Jefferis, G. S. X. E., . . . Ascoli, G. A. (2011). The DIADEM data sets: Representative light microscopy images of neuronal morphology to advance automation of digital reconstructions. Neuroinformatics, 1-15. doi. 

Brown, K. M., Donohue, D. E., D'Alessandro, G., & Ascoli, G. A. (2005). A cross-platform freeware tool for digital reconstruction of neuronal arborizations from image stacks. Neuroinformatics, 3(4), 343-360. doi. 

Brown, K. M., Sugihara, I., Shinoda, Y., & Ascoli, G. A. (2012). Digital Morphometry of Rat Cerebellar Climbing Fibers Reveals Distinct Branch and Bouton Types. Journal of Neuroscience, 32(42), 14670-14684. doi: 10.1523/jneurosci.2018-12.2012. http://www.jneurosci.org/content/32/42/14670.abstract


Brown, M. E., Martin, J. R., Rosenbluth, J., & Ariel, M. (2011). A novel path for rapid transverse communication of vestibular signals in turtle cerebellum. Journal of Neurophysiology, 105(3), 1071-1088. doi: 10.1152/jn.00986.2009. http://jn.physiology.org/content/105/3/1071.abstract


Brown, P. B., Millecchia, R., Lawson, J. J., Brown, A. G., Koerber, H. R., Culberson, J., & Stephens, S. (2005). From innervation density to tactile acuity 2:: Embryonic and adult pre-and postsynaptic somatotopy in the dorsal horn. Brain Research, 1055(1), 36-59. doi. 

Brown, R. E., McKenna, J. T., Winston, S., Basheer, R., Yanagawa, Y., Thakkar, M. M., & McCarley, R. W. (2008). Characterization of GABAergic neurons in rapid-eye-movement sleep controlling regions of the brainstem reticular formation in GAD67-green fluorescent protein knock-in mice. European Journal of Neuroscience, 27(2), 352-363. doi: doi:10.1111/j.1460-9568.2008.06024.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2008.06024.x 


Brown, S. M., Henning, S., & Wellman, C. L. (2005). Mild, short-term stress alters dendritic morphology in rat medial prefrontal cortex. Cerebral Cortex, 15(11), 1714-1722. doi. 

Brown, S. P., & Hestrin, S. (2009). Intracortical circuits of pyramidal neurons reflect their long-range axonal targets. Nature. doi. http://dx.doi.org/10.1038/nature07658

http://www.nature.com/nature/journal/vaop/ncurrent/suppinfo/nature07658_...


Browning, K. N., Babic, T., Holmes, G. M., Swartz, E. M., & Travagli, R. A. (2013). A critical re-evaluation of the specificity of action of perivagal capsaicin. Journal of Physiology. doi: 10.1113/jphysiol.2012.246827. http://jp.physoc.org/content/early/2013/01/07/jphysiol.2012.246827.abstract


Browning, K. N., Babic, T., Toti, L., Holmes, G. M., Coleman, F. H., & Travagli, R. A. (2014). Plasticity in the brainstem vagal circuits controlling gastric motor function triggered by corticotropin releasing factor. The Journal of Physiology, 592(20), 4591-4605. doi: doi:10.1113/jphysiol.2014.278192. https://physoc.onlinelibrary.wiley.com/doi/abs/10.1113/jphysiol.2014.278192


Browning, K. N., Coleman, F. H., & Travagli, R. A. (2005). Characterization of pancreas-projecting rat dorsal motor nucleus of vagus neurons. American Journal of Physiology - Gastrointestinal Liver Physiology, 288(5), G950-955. doi: 10.1152/ajpgi.00549.2004. http://ajpgi.physiology.org/cgi/content/abstract/288/5/G950 


Browning, K. N., Coleman, F. H., & Travagli, R. A. (2005). Effects of pancreatic polypeptide on pancreas-projecting rat dorsal motor nucleus of the vagus neurons. American Journal of Physiol - Gastrointest Liver Physiology, 289(2), G209-219. doi: 10.1152/ajpgi.00560.2004. http://ajpgi.physiology.org/cgi/content/abstract/289/2/G209 


Browning, K. N., Travagli, R. A., & others. (2004). Morphological differences between planes of section do not influence the electrophysiological properties of identified rat dorsal motor nucleus of the vagus neurons. Brain Research, 1003(1), 54-60. doi. 

Brownstone, R. M., & Wilson, J. M. (2008). Strategies for delineating spinal locomotor rhythm-generating networks and the possible role of Hb9 interneurones in rhythmogenesis. Brain Research Reviews, 57(1), 64-76. doi. 

Brozoski, T., Brozoski, D., Wisner, K., & Bauer, C. (2017). Chronic tinnitus and unipolar brush cell alterations in the cerebellum and dorsal cochlear nucleus. Hearing Research, 350, 139-151. doi: https://doi.org/10.1016/j.heares.2017.04.016. http://www.sciencedirect.com/science/article/pii/S037859551730059X


Brückner, G., Morawski, M., & Arendt, T. (2008). Aggrecan-based extracellular matrix is an integral part of the human basal ganglia circuit. Neuroscience, 151(2), 489-504. doi. 

Brudvig, J. J., Cain, J. T., Schmidt-Grimminger, G. G., Stumpo, D. J., Roux, K. J., Blackshear, P. J., & Weimer, J. M. (2018). MARCKS Is Necessary for Netrin-DCC Signaling and Corpus Callosum Formation. [journal article]. Molecular Neurobiology. doi: 10.1007/s12035-018-0990-3. https://doi.org/10.1007/s12035-018-0990-3


Brumberg, J. C., Hamzei-Sichani, F., & Yuste, R. (2003). Morphological and Physiological Characterization of Layer VI Corticofugal Neurons of Mouse Primary Visual Cortex. Journal of Neurophysiology, 89(5), 2854-2867. doi: 10.1152/jn.01051.2002. http://jn.physiology.org/cgi/content/abstract/89/5/2854 


Brüne, M., Schöbel, A., Karau, R., Benali, A., Faustmann, P. M., Juckel, G., & Petrasch-Parwez, E. (2010). Von Economo neuron density in the anterior cingulate cortex is reduced in early onset schizophrenia. Acta Neuropathologica, 119(6), 771-778. doi. 

Brunjes, P. C. (2021). Pyramidal Cells in Olfactory Cortex. Chemical Senses, (bjab002). doi: 10.1093/chemse/bjab002. https://doi.org/10.1093/chemse/bjab002


Brunjes, P. C., Kay, R. B., & Arrivillaga, J. P. (2011). The mouse olfactory peduncle. Journal of Comparative Neurology, 519(14), 2870-2886. doi: 10.1002/cne.22662. http://dx.doi.org/10.1002/cne.22662


Brunjes, P. C., & Kenerson, M. C. (2010). The anterior olfactory nucleus: quantitative study of dendritic morphology. Journal of Comparative Neurology, 518(9), 1603-1616. doi. 

Bruno, R. M., Hahn, T. T. G., Wallace, D. J., de Kock, C. P. J., & Sakmann, B. (2009). Sensory Experience Alters Specific Branches of Individual Corticocortical Axons during Development. Journal of Neuroscience, 29(10), 3172-3181. doi: 10.1523/jneurosci.5911-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/10/3172 


Brus-Ramer, M., Carmel, J. B., Chakrabarty, S., & Martin, J. H. (2007). Electrical Stimulation of Spared Corticospinal Axons Augments Connections with Ipsilateral Spinal Motor Circuits after Injury. Journal of Neuroscience, 27(50), 13793-13801. doi: 10.1523/jneurosci.3489-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/50/13793 


Brzozowska, N. I., Smith, K. L., Zhou, C., Waters, P. M., Cavalcante, L. M., Abelev, S. V., . . . Arnold, J. C. (2017). Genetic deletion of P-glycoprotein alters stress responsivity and increases depression-like behavior, social withdrawal and microglial activation in the hippocampus of female mice. Brain, Behavior, and Immunity. doi: https://doi.org/10.1016/j.bbi.2017.05.008. http://www.sciencedirect.com/science/article/pii/S088915911730154X


Bu, Q., Wang, A., Hamzah, H., Waldman, A., Jiang, K., Dong, Q., . . . Chang, Q. (2017). CREB signaling is involved in Rett syndrome pathogenesis. [10.1523/JNEUROSCI.3735-16.2017]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2017/03/07/JNEUROSCI.3735-16.2017...


Bubser, M., Fadel, J. R., Jackson, L. L., Meador-Woodruff, J. H., Jing, D., & Deutch, A. Y. (2005). Dopaminergic regulation of orexin neurons. European Journal of Neuroscience, 21(11), 2993-3001. doi: doi:10.1111/j.1460-9568.2005.04121.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2005.04121.x 


Buchanan, Katherine A., Blackman, Arne V., Moreau, Alexandre W., Elgar, D., Costa, Rui P., Lalanne, T., . . . Sjöström, P. J. (2012). Target-Specific Expression of Presynaptic NMDA Receptors in Neocortical Microcircuits. Neuron, 75(3), 451-466. doi: 10.1016/j.neuron.2012.06.017. http://www.sciencedirect.com/science/article/pii/S089662731200579X


Buchser, W. J., Slepak, T. I., Gutierrez-Arenas, O., Bixby, J. L., & Lemmon, V. P. (2010). Kinase/phosphatase overexpression reveals pathways regulating hippocampal neuron morphology. Molecular systems biology, 6(1). doi. 

Buckiova, D., Popelar, J., & Syka, J. (2006). Collagen changes in the cochlea of aged Fischer 344 rats. Experimental Gerontology, 41(3), 296-302. doi. 

Buckiova, D., Popelar, J., & Syka, J. (2007). Aging cochleas in the F344 rat: morphological and functional changes. Experimental Gerontology, 42(7), 629-638. doi. 

Buckmaster, C. A., Eichenbaum, H., Amaral, D. G., Suzuki, W. A., & Rapp, P. R. (2004). Entorhinal Cortex Lesions Disrupt the Relational Organization of Memory in Monkeys. Journal of Neuroscience, 24(44), 9811-9825. doi: 10.1523/jneurosci.1532-04.2004. http://www.jneurosci.org/cgi/content/abstract/24/44/9811 


Buckmaster, P. S. (2004). Prolonged Infusion of Tetrodotoxin Does Not Block Mossy Fiber Sprouting in Pilocarpine-treated Rats. Epilepsia, 45(5), 452-458. doi: doi:10.1111/j.0013-9580.2004.67103.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.0013-9580.2004.67103.x 


Buckmaster, P. S. (2012). Mossy cell dendritic structure quantified and compared with other hippocampal neurons labeled in rats in vivo. Epilepsia, 53, 9-17. doi: 10.1111/j.1528-1167.2012.03470.x. http://dx.doi.org/10.1111/j.1528-1167.2012.03470.x


Buckmaster, P. S., Abrams, E., & Wen, X. (2017). Seizure frequency correlates with loss of dentate gyrus GABAergic neurons in a mouse model of temporal lobe epilepsy. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24226. http://dx.doi.org/10.1002/cne.24226


Buckmaster, P. S., Alonso, A., Canfield, D. R., & Amaral, D. G. (2004). Dendritic morphology, local circuitry, and intrinsic electrophysiology of principal neurons in the entorhinal cortex of macaque monkeys. Journal of Comparative Neurology, 470(3), 317-329. doi. 

Buckmaster, P. S., & Amaral, D. G. (2001). Intracellular recording and labeling of mossy cells and proximal CA3 pyramidal cells in macaque monkeys. Journal of Comparative Neurology, 430(2), 264-281. doi. 

Buckmaster, P. S., & Dudek, F. E. (1997). Network Properties of the Dentate Gyrus in Epileptic Rats With Hilar Neuron Loss and Granule Cell Axon Reorganization. Journal of Neurophysiology, 77(5), 2685-2696. doi. http://jn.physiology.org/cgi/content/abstract/77/5/2685 


Buckmaster, P. S., & Dudek, F. E. (1999). In Vivo Intracellular Analysis of Granule Cell Axon Reorganization in Epileptic Rats. Journal of Neurophysiology, 81(2), 712-721. doi. http://jn.physiology.org/cgi/content/abstract/81/2/712 


Buckmaster, P. S., Ingram, E. A., & Wen, X. (2009). Inhibition of the Mammalian Target of Rapamycin Signaling Pathway Suppresses Dentate Granule Cell Axon Sprouting in a Rodent Model of Temporal Lobe Epilepsy. Journal of Neuroscience, 29(25), 8259-8269. doi: 10.1523/jneurosci.4179-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/25/8259 


Buckmaster, P. S., & Jongen-Relo, A. L. (1999). Highly Specific Neuron Loss Preserves Lateral Inhibitory Circuits in the Dentate Gyrus of Kainate-Induced Epileptic Rats. Journal of Neuroscience, 19(21), 9519-9529. doi. http://www.jneurosci.org/cgi/content/abstract/19/21/9519


Buckmaster, P. S., & Wen, X. (2011). Rapamycin suppresses axon sprouting by somatostatin interneurons in a mouse model of temporal lobe epilepsy. Epilepsia, 52(11), 2057-2064. doi: 10.1111/j.1528-1167.2011.03253.x. http://dx.doi.org/10.1111/j.1528-1167.2011.03253.x


Buckmaster, P. S., Yamawaki, R., & Thind, K. (2016). More Docked Vesicles and Larger Active Zones at Basket Cell-to-Granule Cell Synapses in a Rat Model of Temporal Lobe Epilepsy. The Journal of Neuroscience, 36(11), 3295-3308. doi. http://www.jneurosci.org/content/36/11/3295.short


Buckmaster, P. S., Yamawaki, R., & Zhang, G. F. (2002). Axon arbors and synaptic connections of a vulnerable population of interneurons in the dentate gyrus in vivo. Journal of Comparative Neurology, 445(4), 360-373. doi. 

Buckmaster, P. S., Zhang, G. F., & Yamawaki, R. (2002). Axon Sprouting in a Model of Temporal Lobe Epilepsy Creates a Predominantly Excitatory Feedback Circuit. Journal of Neuroscience, 22(15), 6650-6658. doi. http://www.jneurosci.org/cgi/content/abstract/22/15/6650


Buckwalter, J. A., Parvizi, J., Morecraft, R. J., & van Hoesen, G. W. (2008). Thalamic projections to the posteromedial cortex in the macaque. Journal of Comparative Neurology, 507(5), 1709-1733. doi. 

Buckwalter, J. A., Schumann, C. M., & Van Hoesen, G. W. (2008). Evidence for direct projections from the basal nucleus of the amygdala to retrosplenial cortex in the Macaque monkey. Experimental Brain Research, 186(1), 47-57. doi. 

Budd, J. M. L., Kovács, K., Ferecskó, A. S., Buzás, P., Eysel, U. T., & Kisvárday, Z. F. (2010). Neocortical axon arbors trade-off material and conduction delay conservation. PLoS computational biology, 6(3), e1000711-e1000711. doi. 

Budzynski, C. A., Gagliardo, A., Ioal&eacute;, P., & Bingman, V. P. (2002). Participation of the homing pigeon thalamofugal visual pathway in sun-compass associative learning. European Journal of Neuroscience, 15(1), 197. doi. 

Buetler, T. M., Renard, M., Offord, E. A., Schneider, H., & Ruegg, U. T. (2002). Green tea extract decreases muscle necrosis in mdx mice and protects against reactive oxygen species. American Journal of Clinical Nutrition, 75(4), 749-753. doi. 

Buffo, A., Carulli, D., Rossi, F., & Strata, P. (2003). Extrinsic regulation of injury/growth-related gene expression in the inferior olive of the adult rat. European Journal of Neuroscience, 18(8), 2146-2158. doi: doi:10.1046/j.1460-9568.2003.02940.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.2003.02940.x 


Buffo, A., Rite, I., Tripathi, P., Lepier, A., Colak, D., Horn, A.-P., . . . Gotz, M. (2008). Origin and progeny of reactive gliosis: A source of multipotent cells in the injured brain. Proceedings of the National Academy of Sciences, 105(9), 3581-3586. doi: 10.1073/pnas.0709002105. http://www.pnas.org/cgi/content/abstract/105/9/3581 


Buffo, A., Vosko, M. R., Erturk, D., Hamann, G. F., Jucker, M., Rowitch, D., & Gotz, M. (2005). Expression pattern of the transcription factor Olig2 in response to brain injuries: Implications for neuronal repair. Proceedings of the National Academy of Sciences, 102(50), 18183-18188. doi: 10.1073/pnas.0506535102. http://www.pnas.org/cgi/content/abstract/102/50/18183 


Buffo, A., Zagrebelsky, M., Huber, A. B., Skerra, A., Schwab, M. E., Strata, P., & Rossi, F. (2000). Application of Neutralizing Antibodies against NI-35/250 Myelin-Associated Neurite Growth Inhibitory Proteins to the Adult Rat Cerebellum Induces Sprouting of Uninjured Purkinje Cell Axons. Journal of Neuroscience, 20(6), 2275-2286. doi. http://www.jneurosci.org/cgi/content/abstract/20/6/2275


Bugaysen, J., Bar-Gad, I., & Korngreen, A. (2013). Continuous Modulation of Action Potential Firing by a Unitary GABAergic Connection in the Globus Pallidus In Vitro. Journal of Neuroscience, 33(31), 12805-12809. doi: 10.1523/jneurosci.1970-13.2013. http://www.jneurosci.org/content/33/31/12805.abstract


Buhler, A. V., Choi, J., Proudfit, H. K., & Gebhart, G. F. (2005). Neurotensin activation of the NTR1 on spinally-projecting serotonergic neurons in the rostral ventromedial medulla is antinociceptive. Pain, 114(1), 285-294. doi. 

Buhler, A. V., Proudfit, H. K., & Gebhart, G. F. (2004). Separate populations of neurons in the rostral ventromedial medulla project to the spinal cord and to the dorsolateral pons in the rat. Brain Research, 1016(1), 12-19. doi. 

Buhler, A. V. K., Tachibana, S., Zhang, Y., & Quock, R. M. (2018). nNOS immunoreactivity co-localizes with GABAergic and cholinergic neurons, and associates with β-endorphinergic and met-enkephalinergic opioidergic fibers in rostral ventromedial medulla and A5 of the mouse. Brain Research, 1698, 170-178. doi: https://doi.org/10.1016/j.brainres.2018.08.003. http://www.sciencedirect.com/science/article/pii/S0006899318304189


Bui Quoc, E., Quenech'Du, N., & Milleret, C. (2005). Plasticity of Visual Interhemispheric Transfer to Areas 17 and 18 in Cats With Convergent Unilateral Early Strabismus. Investigative Ophtalmology and Visual Science, 46(5), 2958-2958. doi. 

Bullmann, T., Seeger, G., Stieler, J., Hanics, J., Reimann, K., Petra Kretzschmann, T., . . . Arendt, T. (2015). Tau phosphorylation associated spine regression does not impair hippocampal dependent memory in hibernating Golden hamsters. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22522. http://dx.doi.org/10.1002/hipo.22522


Bunce, J. G., Zikopoulos, B., Feinberg, M., & Barbas, H. (2013). Parallel prefrontal pathways reach distinct excitatory and inhibitory systems in memory-related rhinal cortices. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23413. http://dx.doi.org/10.1002/cne.23413


Burbridge, T. J., Wang, Y., Volz, A. J., Peschansky, V. J., Lisann, L., Galaburda, A. M., . . . Rosen, G. D. (2008). Postnatal analysis of the effect of embryonic knockdown and overexpression of candidate dyslexia susceptibility gene homolog Dcdc2 in the rat. Neuroscience, 152(3), 723-733. doi. 

Bureau, I., Shepherd, G. M. G., & Svoboda, K. (2004). Precise development of functional and anatomical columns in the neocortex. Neuron, 42(5), 789-801. doi. 

Bureau, I., Shepherd, G. M. G., & Svoboda, K. (2008). Circuit and Plasticity Defects in the Developing Somatosensory Cortex of Fmr1 Knock-Out Mice. Journal of Neuroscience, 28(20), 5178-5188. doi: 10.1523/jneurosci.1076-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/20/5178 


Bureau, I., von Saint Paul, F., & Svoboda, K. (2006). Interdigitated Paralemniscal and Lemniscal Pathways in the Mouse Barrel Cortex. PLoS Biology, 4(12), e382. doi. http://dx.doi.org/10.1371%2Fjournal.pbio.0040382 


Burianova, J., Ouda, L., Profant, O., & Syka, J. (2009). Age-related changes in GAD levels in the central auditory system of the rat. Experimental Gerontology, 44(3), 161-169. doi. 

Burke, M. C., Letts, P. A., Krajewski, S. J., & Rance, N. E. (2006). Coexpression of dynorphin and neurokinin B immunoreactivity in the rat hypothalamus: morphologic evidence of interrelated function within the arcuate nucleus. Journal of Comparative Neurology, 498(5), 712-726. doi. 

Burke, M. R., Adkins-Regan, E., & Wade, J. (2007). Laterality in syrinx muscle morphology of the Japanese quail (< i> Coturnix japonica</i>). Physiology and Behavior, 90(4), 682-686. doi. 

Burke, P. G. R., Abbott, S. B. G., Coates, M. B., Viar, K. E., Stornetta, R. L., & Guyenet, P. G. (2014). Optogenetic Stimulation of Adrenergic C1 Neurons Causes Sleep State Dependent Cardiorespiratory Stimulation and Arousal with Sighs in Rats. American Journal of Respiratory and Critical Care Medicine. doi: 10.1164/rccm.201407-1262OC. http://dx.doi.org/10.1164/rccm.201407-1262OC


Burke, P. G. R., Kanbar, R., Basting, T. M., Hodges, W. M., Viar, K. E., Stornetta, R. L., & Guyenet, P. G. (2015). State-dependent control of breathing by the retrotrapezoid nucleus. The Journal of Physiology, n/a-n/a. doi: 10.1113/jp270053. http://dx.doi.org/10.1113/JP270053


Burke, P. G. R., Kanbar, R., Viar, K. E., Stornetta, R. L., & Guyenet, P. G. (2015). Selective optogenetic stimulation of the retrotrapezoid nucleus in sleeping rats activates breathing without changing blood pressure or causing arousal or sighs. [10.1152/japplphysiol.00164.2015]. Journal of Applied Physiology. doi. http://jap.physiology.org/content/early/2015/04/07/japplphysiol.00164.20...


Burkhalter, J., Fiumelli, H., Erickson, J. D., & Martin, J.-L. (2007). A Critical Role for System A Amino Acid Transport in the Regulation of Dendritic Development by Brain-derived Neurotrophic Factor (BDNF). Journal of Biological Chemistry, 282(8), 5152-5159. doi: 10.1074/jbc.M608548200. http://www.jbc.org/cgi/content/abstract/282/8/5152 


Burleson, A., Nusstein, J., Reader, A., & Beck, M. (2007). The In Vivo Evaluation of Hand/Rotary/Ultrasound Instrumentation in Necrotic, Human Mandibular Molars. Journal of Endodontics, 33(7), 782-787. doi. 

Burnett, L. R., Stein, B. E., Chaponis, D., & Wallace, M. T. (2004). Superior colliculus lesions preferentially disrupt multisensory orientation. Neuroscience, 124(3), 535-547. doi. 

Burnett, L. R., Stein, B. E., Perrault, T. J., & Wallace, M. T. (2007). Excitotoxic lesions of the superior colliculus preferentially impact multisensory neurons and multisensory integration. Experimental Brain Research, 179(2), 325-338. doi. 

Burton, S. D., & Urban, N. N. (2015). Rapid Feedforward Inhibition and Asynchronous Excitation Regulate Granule Cell Activity in the Mammalian Main Olfactory Bulb. The Journal of Neuroscience, 35(42), 14103-14122. doi. http://www.jneurosci.org/content/35/42/14103.short


Bush, A. L., & Hyson, R. L. (2006). Lithium increases BCL-2 expression in chick cochlear nucleus and protects against deafferentation-induced cell death. Neuroscience, 138(4), 1341-1349. doi. 

Buskila, Y., Bellot-Saez, A., Kékesi, O., Cameron, M., & Morley, J. (2019). Extending the Life Span of Acute Neuronal Tissue for Imaging and Electrophysiological Studies. In N. J. D. Wright (Ed.), Basic Neurobiology Techniques (pp. 235-259). New York, NY: Springer US.

Busti, D., Bienvenu, T., Micklem, B., Magill, P., Shigemoto, R., Capogna, M., & Ferraguti, F. (2011). Morphological characterization of large intercalated neurons provides novel insight on intrinsic networks of the amygdala. BMC Pharmacology, 11(Suppl 2), A9-A9. doi. 

Busto, G. U., Guven-Ozkan, T., Chakraborty, M., & Davis, R. L. (2016). Developmental inhibition of miR-iab8-3p disrupts mushroom body neuron structure and adult learning ability. Developmental Biology. doi: http://dx.doi.org/10.1016/j.ydbio.2016.09.010. http://www.sciencedirect.com/science/article/pii/S0012160616303141


Butler, A. K., Dantzker, J. L., Shah, R. B., & Callaway, E. M. (2001). Development of visual cortical axons: Layer-specific effects of extrinsic influences and activity blockade. Journal of Comparative Neurology, 430(3), 321-331. doi. 

Butler, B. E., Chabot, N., Kral, A., & Lomber, S. G. (2016). Origins of thalamic and cortical projections to the posterior auditory field in congenitally deaf cats. Hearing Research. doi: http://dx.doi.org/10.1016/j.heares.2016.06.003. http://www.sciencedirect.com/science/article/pii/S0378595516301319


Butler, B. E., Chabot, N., & Lomber, S. G. (2016). Quantifying and comparing the pattern of thalamic and cortical projections to the posterior auditory field in hearing and deaf cats. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24005. http://dx.doi.org/10.1002/cne.24005


Butler, B. E., Chabot, N., & Lomber, S. G. (2016). A quantitative comparison of the hemispheric, areal, and laminar origins of sensory and motor cortical projections to the superior colliculus of the cat. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23980. http://dx.doi.org/10.1002/cne.23980


Butler, B. E., de la Rua, A., Ward-Able, T., & Lomber, S. G. (2017). Cortical and thalamic connectivity to the second auditory cortex of the cat is resilient to the onset of deafness. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-017-1523-y. https://doi.org/10.1007/s00429-017-1523-y


Butler, B. E., Sunstrum, J. K., & Lomber, S. G. (2018). Modified origins of cortical projections to the superior colliculus in the deaf: Dispersion of auditory efferents. [10.1523/JNEUROSCI.2858-17.2018]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2018/04/02/JNEUROSCI.2858-17.2018...


Butler, R. K., Oliver, E. M., Sharko, A. C., Parilla-Carrero, J., Kaigler, K. F., Fadel, J. R., & Wilson, M. A. (2016). Activation of corticotropin releasing factor-containing neurons in the rat central amygdala and bed nucleus of the stria terminalis following exposure to two different anxiogenic stressors. Behavioural Brain Research. doi: http://dx.doi.org/10.1016/j.bbr.2016.01.051. http://www.sciencedirect.com/science/article/pii/S0166432816300493


Butler, R. K., White, L. C., Frederick-Duus, D., Kaigler, K. F., Fadel, J. R., & Wilson, M. A. (2012). Comparison of the activation of somatostatin- and neuropeptide Y-containing neuronal populations of the rat amygdala following two different anxiogenic stressors. Experimental Neurology, (0). doi: 10.1016/j.expneurol.2012.08.002. http://www.sciencedirect.com/science/article/pii/S0014488612003111


Butovsky, O., Ziv, Y., Schwartz, A., Landa, G., Talpalar, A., Pluchino, S., . . . Schwartz, M. (2006). Microglia activated by IL-4 or IFN-gamma differentially induce neurogenesis and oligodendrogenesis from adult stem/progenitor cells. Molecular and Cellular Neurosciences, 31, 149 - 160. doi. 

Butti, C., Janeway, C., Townshend, C., Wicinski, B., Reidenberg, J., Ridgway, S., . . . Jacobs, B. (2014). The neocortex of cetartiodactyls: I. A comparative Golgi analysis of neuronal morphology in the bottlenose dolphin (Tursiops truncatus), the minke whale (Balaenoptera acutorostrata), and the humpback whale (Megaptera novaeangliae). Brain Structure and Function, 1-30. doi: 10.1007/s00429-014-0860-3. http://dx.doi.org/10.1007/s00429-014-0860-3


Buzas, P., Eysel, U., & Kisvarday, Z. (1998). Functional topography of single cortical cells: an intracellular approach combined with optical imaging. Brain Research Protocols, 3(2), 199-208. doi. 

Buzás, P., Eysel, U. T., Adorján, P., & Kisvárday, Z. F. (2001). Axonal topography of cortical basket cells in relation to orientation, direction, and ocular dominance maps. Journal of Comparative Neurology, 437(3), 259-285. doi. 

Buzás, P., Kovács, K., Ferecskó, A. S., Budd, J. M. L., Eysel, U. T., & Kisvárday, Z. F. (2006). Model-based analysis of excitatory lateral connections in the visual cortex. Journal of Comparative Neurology, 499(6), 861-881. doi. 

Byers, J. S., Huguenard, A. L., Kuruppu, D., Liu, N. K., Xu, X. M., & Sengelaub, D. R. (2012). Neuroprotective effects of testosterone on motoneuron and muscle morphology following spinal cord injury. Journal of Comparative Neurology. doi. 

C., G. K., Lu, L., Praveen, C., P., W. J., C., W. M., & Anna, C. L. (2018). Genetic inactivation of synaptosomal-associated protein 25 (SNAP-25) in adult hippocampal neural progenitors impairs pattern discrimination learning but not survival or structural maturation of newborn dentate granule cells. Hippocampus, 0(ja). doi: doi:10.1002/hipo.23008. https://onlinelibrary.wiley.com/doi/abs/10.1002/hipo.23008


Cabañero, D., Irie, T., Celorrio, M., Trousdale, C., Owens, D. M., Virley, D., . . . Morón, J. A. (2016). Identification of an epidermal keratinocyte AMPA glutamate receptor involved in dermatopathies associated with sensory abnormalities. PAIN Reports, 1(3), e573. doi: 10.1097/pr9.0000000000000573. http://journals.lww.com/painrpts/Fulltext/2016/09000/Identification_of_a...


Cabungcal, J. H., Nicolas, D., Kraftsik, R., Cuénod, M., Do, K. Q., & Hornung, J. P. (2006). Glutathione deficit during development induces anomalies in the rat anterior cingulate GABAergic neurons: relevance to schizophrenia. Neurobiology of Disease, 22(3), 624-637. doi. 

Caetano, L., Pinheiro, H., Patricio, P., Mateus-Pinheiro, A., Alves, N. D., Coimbra, B., . . . Gomes, C. A. (2016). Adenosine A2A receptor regulation of microglia morphological remodeling-gender bias in physiology and in a model of chronic anxiety. [Original Article]. Molecular Psychiatry. doi: 10.1038/mp.2016.173. http://dx.doi.org/10.1038/mp.2016.173


Cafforio, G., D’Avino, C., Calabrese, R., & Siciliano, G. (2004). Clinical open-label study for evaluation of efficacy and tolerability of oxcarbazepine in the treatment of neuropathic pain. Journal of the Peripheral Nervous System, 9(2), 120-120. doi. 

Cagalinec, M., Liiv, M., Hodurova, Z., Hickey, M. A., Vaarmann, A., Mandel, M., . . . Kaasik, A. (2016). Role of Mitochondrial Dynamics in Neuronal Development: Mechanism for Wolfram Syndrome. PLoS Biol, 14(7), e1002511. doi: 10.1371/journal.pbio.1002511. http://dx.doi.org/10.1371%2Fjournal.pbio.1002511


Cahill, S. P., Hatchard, T., Abizaid, A., & Holahan, M. R. (2014). An examination of early neural and cognitive alterations in hippocampal-spatial function of ghrelin receptor-deficient rats. Behavioural Brain Research, (0). doi: http://dx.doi.org/10.1016/j.bbr.2014.02.004. http://www.sciencedirect.com/science/article/pii/S0166432814000710


Cai, Y., Chew, C., Muñoz, F., & Sengelaub, D. R. (2016). Neuroprotective effects of testosterone metabolites and dependency on receptor action on the morphology of somatic motoneurons following the death of neighboring motoneurons. Developmental Neurobiology, n/a-n/a. doi: 10.1002/dneu.22445. http://dx.doi.org/10.1002/dneu.22445


Cain, D. M., Wacnik, P. W., Turner, M., Wendelschafer-Crabb, G., Kennedy, W. R., Wilcox, G. L., & Simone, D. A. (2001). Functional Interactions between Tumor and Peripheral Nerve: Changes in Excitability and Morphology of Primary Afferent Fibers in a Murine Model of Cancer Pain. Journal of Neuroscience, 21(23), 9367-9376. doi. http://www.jneurosci.org/cgi/content/abstract/21/23/9367


Caldwell, A. S. L., Eid, S., Kay, C. R., Jimenez, M., McMahon, A. C., Desai, R., . . . Walters, K. A. (2015). Haplosufficient genomic androgen receptor signaling is adequate to protect female mice from induction of polycystic ovary syndrome features by prenatal hyperandrogenization. Endocrinology, 0(0), en.2014-1887. doi: doi:10.1210/en.2014-1887. http://press.endocrine.org/doi/abs/10.1210/en.2014-1887


Calella, A., Nerlov, C., Lopez, R., Sciarretta, C., von Bohlen und Halbach, O., Bereshchenko, O., & Minichiello, L. (2007). Neurotrophin/Trk receptor signaling mediates C/EBPa, -ß and NeuroD recruitment to immediate-early gene promoters in neuronal cells and requires C/EBPs to induce immediate-early gene transcription. Neural Development, 2(1), 4. doi. http://www.neuraldevelopment.com/content/2/1/4 


Caleo, M., Cenni, M. C., Costa, M., Menna, E., Zentilin, L., Giadrossi, S., . . . Maffei, L. (2002). Expression of BCL-2 via adeno-associated virus vectors rescues thalamic neurons after visual cortex lesion in the adult rat. European Journal of Neuroscience, 15(8), 1271. doi. 

Caleo, M., Medini, P., von Bartheld, C. S., & Maffei, L. (2003). Provision of Brain-Derived Neurotrophic Factor via Anterograde Transport from the Eye Preserves the Physiological Responses of Axotomized Geniculate Neurons,. Journal of Neuroscience, 23, 287-296. doi. 

Caleo, M., Tropea, D., Rossi, C., Gianfranceschi, L., & Maffei, L. (2009). Environmental enrichment promotes fiber sprouting after deafferentation of the superior colliculus in the adult rat brain. Experimental Neurology, 216(2), 515-519. doi. 

Caliandro, P., Mondelli, M., Aprile, I., Pazzaglia, C., Sabatelli, M., Tonali, P., & Padua, L. (2004). Is carpal tunnel syndrome surgery useful in patients with diabetes or autoimmune polyneuropathies? Journal of the Peripheral Nervous System, 9(2), 109-109. doi: doi:10.1111/j.1085-9489.2004.009209r.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Calixto, E., Galván, E. J., Card, J. P., & Barrionuevo, G. (2008). Coincidence detection of convergent perforant path and mossy fibre inputs by CA3 interneurons. Journal of Physiology, 586(11), 2695-2712. doi. 

Calizo, L. H., Ma, X., Pan, Y., Lemos, J., Craige, C., Heemstra, L., & Beck, S. G. (2011). Raphe serotonin neurons are not homogenous: electrophysiological, morphological and neurochemical evidence. Neuropharmacology. doi. 

Callaway, E. M., & Borrell, V. (2011). Developmental Sculpting of Dendritic Morphology of Layer 4 Neurons in Visual Cortex: Influence of Retinal Input. Journal of Neuroscience, 31(20), 7456-7470. doi: 10.1523/jneurosci.5222-10.2011. http://www.jneurosci.org/content/31/20/7456.abstract


Callio, J., Oury, T. D., & Chu, C. T. (2005). Manganese Superoxide Dismutase Protects against 6-Hydroxydopamine Injury in Mouse Brains. Journal of Biological Chemistry, 280(18), 18536-18542. doi: 10.1074/jbc.M413224200. http://www.jbc.org/cgi/content/abstract/280/18/18536 


Calzavara, R., Mailly, P., & Haber, S. N. (2007). Relationship between the corticostriatal terminals from areas 9 and 46, and those from area 8A, dorsal and rostral premotor cortex and area 24c: an anatomical substrate for cognition to action. European Journal of Neuroscience, 26(7), 2005-2024. doi. 

Cambiaghi, M., Cherchi, L., Masin, L., Infortuna, C., Briski, N., Caviasco, C., . . . Battaglia, F. (2021). High-frequency repetitive transcranial magnetic stimulation enhances layer II/III morphological dendritic plasticity in mouse primary motor cortex. Behavioural Brain Research, 410, 113352. doi: https://doi.org/10.1016/j.bbr.2021.113352. https://www.sciencedirect.com/science/article/pii/S0166432821002400


Camelo, S., Iglesias, A. H., Hwang, D., Due, B., Ryu, H., Smith, K., . . . others. (2005). Transcriptional therapy with the histone deacetylase inhibitor trichostatin A ameliorates experimental autoimmune encephalomyelitis. Journal of Neuroimmunology, 164(1), 10-21. doi. 

Cameron, D., Gutierrez-Mecinas, M., Gomez-Lima, M., Watanabe, M., Polgár, E., & Todd, A. J. (2015). The organisation of spinoparabrachial neurons in the mouse. Pain, Publish Ahead of Print. doi: 10.1097/j.pain.0000000000000270. http://journals.lww.com/pain/Fulltext/publishahead/The_organisation_of_s...


Cameron, M. C., Zhan, R. Z., & Nadler, J. V. (2011). Morphologic integration of hilar ectopic granule cells into dentate gyrus circuitry in the pilocarpine model of temporal lobe epilepsy. Journal of Comparative Neurology, 519(11), 2175-2192. doi. 

Cameron, M. C., Zhan, R.-Z., & Nadler, J. V. (2011). Morphologic integration of hilar ectopic granule cells into dentate gyrus circuitry in the pilocarpine model of temporal lobe epilepsy. Journal of Comparative Neurology, 519(11), 2175-2192. doi: 10.1002/cne.22623. http://dx.doi.org/10.1002/cne.22623


Caminiti, R., Carducci, F., Piervincenzi, C., Battaglia-Mayer, A., Confalone, G., Visco-Comandini, F., . . . Innocenti, G. M. (2013). Diameter, Length, Speed, and Conduction Delay of Callosal Axons in Macaque Monkeys and Humans: Comparing Data from Histology and Magnetic Resonance Imaging Diffusion Tractography. Journal of Neuroscience, 33(36), 14501-14511. doi: 10.1523/jneurosci.0761-13.2013. http://www.jneurosci.org/content/33/36/14501.abstract


Caminiti, R., Ghaziri, H., Galuske, R., Hof, P. R., & Innocenti, G. M. (2009). Evolution amplified processing with temporally dispersed slow neuronal connectivity in primates. Proceedings of the National Academy of Sciences, 106(46), 19551-19556. doi: 10.1073/pnas.0907655106. http://www.pnas.org/content/106/46/19551.abstract 


Camiré, O., & Topolnik, L. (2012). Functional compartmentalisation and regulation of postsynaptic Ca< sup> 2+</sup> transients in inhibitory interneurons. Cell Calcium. doi. 

Camiré, O., & Topolnik, L. (2014). Dendritic Calcium Nonlinearities Switch the Direction of Synaptic Plasticity in Fast-Spiking Interneurons. The Journal of Neuroscience, 34(11), 3864-3877. doi. http://www.jneurosci.org/content/34/11/3864.short


Camp, M. C., MacPherson, K. P., Lederle, L., Graybeal, C., Gaburro, S., DeBrouse, L. M., . . . others. (2012). Genetic Strain Differences in Learned Fear Inhibition Associated with Variation in Neuroendocrine, Autonomic, and Amygdala Dendritic Phenotypes. Neuropsychopharmacology. doi. 

Campbell, H. R., Meek, J., Zhang, J., & Bell, C. C. (2007). Anatomy of the posterior caudal lobe of the cerebellum and the eminentia granularis posterior in a mormyrid fish. Journal of Comparative Neurology, 502(5), 714-735. doi. 

Campbell, J. C., Jeyamohan, S. B., Cruz, P. D. L., Chen, N., Shin, D., & Pilitsis, J. G. (2014). Place conditioning to apomorphine in rat models of Parkinson's disease: Differences by dose and side-effect expression. Behavioural Brain Research, (0). doi: http://dx.doi.org/10.1016/j.bbr.2014.09.002. http://www.sciencedirect.com/science/article/pii/S0166432814005853


Campbell, J. N., Churn, S. B., & Register, D. (2012). Traumatic brain injury causes an FK506-sensitive loss and an overgrowth of dendritic spines in rat forebrain. Journal of Neurotrauma, (ja). doi. 

Campbell, T., Lin, S., DeVries, C., & Lambert, K. (2003). Coping strategies in male and female rats exposed to multiple stressors. Physiology and Behavior, 78(3), 495-504. doi. 

Campeau, S., & Watson Jr, S. J. (2000). Connections of some auditory-responsive posterior thalamic nuclei putatively involved in activation of the hypothalamo–pituitary–adrenocortical axis in response to audiogenic stress in rats: An anterograde and retrograde tract tracing study combined with fos expression. Journal of Comparative Neurology, 423(3), 474-491. doi. 

Canese, R., Zoratto, F., Altabella, L., Porcari, P., Mercurio, L., de Pasquale, F., . . . Adriani, W. (2014). Persistent modification of forebrain networks and metabolism in rats following adolescent exposure to a 5-HT7 receptor agonist. Psychopharmacology, 1-15. doi: 10.1007/s00213-014-3639-6. http://dx.doi.org/10.1007/s00213-014-3639-6


Canh, M. Y., Serpe, C. J., Sanders, V., & Jones, K. J. (2006). CD4< sup>+</sup> T cell-mediated facial motoneuron survival after injury: Distribution pattern of cell death and rescue throughout the extent of the facial motor nucleus. Journal of Neuroimmunology, 181(1), 93-99. doi. 

Cannon, K. E., Chazot, P. L., Hann, V., Shenton, F., Hough, L. B., & Rice, F. L. (2007). Immunohistochemical localization of histamine H< sub> 3</sub> receptors in rodent skin, dorsal root ganglia, superior cervical ganglia, and spinal cord: Potential antinociceptive targets. Pain, 129(1), 76-92. doi. 

Cannon, R. C., Howell, F. W., Goddard, N. H., & De Schutter, E. (2002). Non-curated distributed databases for experimental data and models in neuroscience. Network: Computation in Neural Systems, 13(3), 415-428. doi. 

Cannon, R. C., O'Donnell, C., & Nolan, M. F. (2010). Stochastic ion channel gating in dendritic neurons: morphology dependence and probabilistic synaptic activation of dendritic spikes. PLoS computational biology, 6(8), e1000886-e1000886. doi. 

Cannon, R. C., Turner, D. A., Pyapali, G. K., & Wheal, H. V. (1998). An on-line archive of reconstructed hippocampal neurons. Journal of Neuroscience Methods, 84(1-2), 49-54. doi. 

Cannon, R. C., Wheal, H. V., & Turner, D. A. (1999). Dendrites of classes of hippocampal neurons differ in structural complexity and branching patterns. Journal of Comparative Neurology, 413. doi. 

Canta, A., Lanzani, F., Galbiati, S., Frigeni, B., Giussani, G., Marmiroli, P., . . . Cavaletti, G. (2004). RAT in vivo models of taxanes' peripheral neurotoxicity following chronic intravenous administration. Journal of the Peripheral Nervous System, 9(2), 104-104. doi: doi:10.1111/j.1085-9489.2004.009209b.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Canto, C. B., Koganezawa, N., Lagartos, M. J. D., Reilly, K. C., Mansvelder, H. D., & Witter, M. P. (2019). Postnatal development of functional projections from para- and presubiculum to medial entorhinal cortex in the rat. The Journal of Neuroscience, 1623-1619. doi: 10.1523/jneurosci.1623-19.2019. http://www.jneurosci.org/content/early/2019/09/11/JNEUROSCI.1623-19.2019...


Canto, C. B., Witter, L., & De Zeeuw, C. I. (2016). Whole-Cell Properties of Cerebellar Nuclei Neurons In Vivo. PLoS ONE, 11(11), e0165887. doi: 10.1371/journal.pone.0165887. http://dx.doi.org/10.1371%2Fjournal.pone.0165887


Canto, C. B., & Witter, M. P. (2011). Cellular properties of principal neurons in the rat entorhinal cortex. I. The lateral entorhinal cortex. Hippocampus. doi. 

Canto, C. B., & Witter, M. P. (2011). Cellular properties of principal neurons in the rat entorhinal cortex. II. The medial entorhinal cortex. Hippocampus. doi. 

Cantone, G., Xiao, J., McFarlane, N., & Levitt, J. B. (2005). Feedback connections to ferret striate cortex: direct evidence for visuotopic convergence of feedback inputs. Journal of Comparative Neurology, 487(3), 312-331. doi. 

Cantone, G., Xiao, J. U. N., & Levitt, J. B. (2006). Retinotopic organization of ferret suprasylvian cortex. Visual Neuroscience, 23(01), 61-77. doi. 

Canty, A. J., & De Paola, V. (2011). Axonal reconstructions going live. Neuroinformatics, 1-3. doi. 

Canty, A. J., Teles-Grilo Ruivo, L. M., Nesarajah, C., Song, S., Jackson, J. S., Little, G. E., & De Paola, V. (2013). Synaptic Elimination and Protection after Minimal Injury Depend on Cell Type and Their Prelesion Structural Dynamics in the Adult Cerebral Cortex. Journal of Neuroscience, 33(25), 10374-10383. doi: 10.1523/jneurosci.0254-13.2013. http://www.jneurosci.org/content/33/25/10374.abstract


Cao, Q., Xu, X.-M., DeVries, W. H., Enzmann, G. U., Ping, P., Tsoulfas, P., . . . Whittemore, S. R. (2005). Functional Recovery in Traumatic Spinal Cord Injury after Transplantation of Multineurotrophin-Expressing Glial-Restricted Precursor Cells. Journal of Neuroscience, 25(30), 6947-6957. doi. http://www.jneurosci.org/cgi/content/abstract/25/30/6947


Cao, Q., Zhang, Y. P., Iannotti, C., DeVries, W. H., Xu, X. M., Shields, C. B., & Whittemore, S. R. (2005). Functional and electrophysiological changes after graded traumatic spinal cord injury in adult rat. Experimental Neurology, 191, S3–S16-S13–S16. doi. 

Cao, X. C., Pappalardo, L. W., Waxman, S. G., & Tan, A. M. (2017). Dendritic spine dysgenesis in superficial dorsal horn sensory neurons after spinal cord injury. Molecular Pain, 13, 1744806916688016. doi: 10.1177/1744806916688016. http://dx.doi.org/10.1177/1744806916688016


Cao, Y., Matsuyama, K., Fujito, Y., & Aoki, M. (2006). Involvement of medullary GABAergic and serotonergic raphe neurons in respiratory control: electrophysiological and immunohistochemical studies in rats. Neuroscience Research, 56(3), 322-331. doi. 

Capasso, M., Caporale, C. M., De Angelis, M. V., Cantarella, C., Di Muzio, A., Lugaresi, A., & Uncini, A. (2004). Demyelinating motor guillain-barré syndrome following rubella. Journal of the Peripheral Nervous System, 9(2), 115-115. doi. 

Capito, R. M., Mata, A., & Stupp, S. I. (2009). Self-Assembling Peptide-Based Nanostructures for Regenerative Medicine. Nanotechnology. doi. 

Capogrosso, M., Milekovic, T., Borton, D., Wagner, F., Moraud, E. M., Mignardot, J.-B., . . . Courtine, G. (2016). A brain–spine interface alleviating gait deficits after spinal cord injury in primates. [Letter]. Nature, 539(7628), 284-288. doi: 10.1038/nature20118

http://www.nature.com/nature/journal/v539/n7628/abs/nature20118.html#sup.... http://dx.doi.org/10.1038/nature20118


Caporale, C. M., Capasso, M., Lucani, M., Gandolfi, P., De Angelis, M. V., Di Muzio, A., . . . Uncini, A. (2004). Experimental axonopathy induced by immunization with campylobacter jejuni lipopolysaccharide from a patient with guillain-barré syndrome. Journal of the Peripheral Nervous System, 9(2), 114-115. doi. 

Cappe, C., Morel, A., & Rouiller, E. M. (2007). Thalamocortical and the dual pattern of corticothalamic projections of the posterior parietal cortex in macaque monkeys. Neuroscience, 146(3), 1371-1387. doi. 

Cappello, S., Attardo, A., Wu, X., Iwasato, T., Itohara, S., Wilsch-Bräuninger, M., . . . Götz, M. (2006). The Rho-GTPase cdc42 regulates neural progenitor fate at the apical surface. Nature of Neuroscience, 9, 1099-1107. doi. 

Cappello, S., Böhringer, Christian R. J., Bergami, M., Conzelmann, K.-K., Ghanem, A., Tomassy, Giulio S., . . . Götz, M. (2012). A Radial Glia-Specific Role of RhoA in Double Cortex Formation. Neuron, 73(5), 911-924. doi: 10.1016/j.neuron.2011.12.030. http://www.sciencedirect.com/science/article/pii/S0896627312000803


Capshaw, G., Soares, D., & Carr, C. E. (2019). Bony labyrinth morphometry reveals hidden diversity in lungless salamanders (Family Plethodontidae): Structural correlates of ecology, development, and vision in the inner ear. Evolution, 0(ja). doi: 10.1111/evo.13837. https://onlinelibrary.wiley.com/doi/abs/10.1111/evo.13837


Caputi, A., Rozov, A., Blatow, M., & Monyer, H. (2009). Two calretinin-positive GABAergic cell types in layer 2/3 of the mouse neocortex provide different forms of inhibition. Cerebral Cortex, 19(6), 1345-1359. doi. 

Carballosa Gonzalez, M. M., Blaya, M. O., Alonso, O. F., Bramlett, H. M., & Hentall, I. D. (2012). Midbrain raphe stimulation improves behavioral and anatomical recovery from fluid-percussion brain injury. Journal of Neurotrauma, (ja). doi. 

Carbone, D. L., Zuloaga, D. G., Lacagnina, A. F., & Handa, R. J. (2012). Prepro-thyrotropin releasing hormone expressing neurons in the juxtaparaventricular region of the lateral hypothalamus are activated by leptin and altered by prenatal glucocorticoid exposure. Brain Research, (0). doi: 10.1016/j.brainres.2012.08.020. http://www.sciencedirect.com/science/article/pii/S0006899312013534


Carbone, D. L., Zuloaga, D. G., Lacagnina, A. F., McGivern, R. F., & Handa, R. J. (2012). Exposure to dexamethasone during late gestation causes female-specific decreases in core body temperature and prepro-thyrotropin-releasing hormone expression in the paraventricular nucleus of the hypothalamus in rats. Physiology &amp; Behavior, (0). doi: 10.1016/j.physbeh.2012.07.010. http://www.sciencedirect.com/science/article/pii/S0031938412002739


Carcea, I., Ma'ayan, A., Mesias, R., Sepulveda, B., Salton, S. R., & Benson, D. L. (2010). Flotillin-Mediated Endocytic Events Dictate Cell Type-Specific Responses to Semaphorin 3A. Journal of Neuroscience, 30(45), 15317-15329. doi: 10.1523/jneurosci.1821-10.2010. http://www.jneurosci.org/cgi/content/abstract/30/45/15317


Carcea, I., Patil, S. B., Robison, A. J., Mesias, R., Huntsman, M. M., Froemke, R. C., . . . Benson, D. L. (2014). Maturation of cortical circuits requires Semaphorin 7A. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1408680111. http://www.pnas.org/content/early/2014/09/03/1408680111.abstract


Cárdenas, A., Villalba, A., de Juan Romero, C., Picó, E., Kyrousi, C., Tzika, A. C., . . . Borrell, V. (2018). Evolution of Cortical Neurogenesis in Amniotes Controlled by Robo Signaling Levels. Cell. doi: https://doi.org/10.1016/j.cell.2018.06.007. http://www.sciencedirect.com/science/article/pii/S0092867418307323


Cardinale, A., Paldino, E., Giampà, C., Bernardi, G., & Fusco, F. R. (2015). PARP-1 Inhibition Is Neuroprotective in the R6/2 Mouse Model of Huntington’s Disease. PLoS ONE, 10(8), e0134482. doi: 10.1371/journal.pone.0134482. http://dx.doi.org/10.1371%2Fjournal.pone.0134482


Cardona, A., Saalfeld, S., Schindelin, J., Arganda-Carreras, I., Preibisch, S., Longair, M., . . . Douglas, R. J. (2012). TrakEM2 Software for Neural Circuit Reconstruction. PLoS ONE, 7(6), e38011. doi: 10.1371/journal.pone.0038011. http://dx.doi.org/10.1371%2Fjournal.pone.0038011


Cardoso, H. D., Santos Junior, E. F., de Santana, D. F., Gonçalves-Pimentel, C., Angelim, M. K., Isaac, A. R., . . . da Silveira Andrade-da-Costa, B. L. (2013). Omega-3 deficiency and neurodegeneration in the substantia nigra: Involvement of increased nitric oxide production and reduced BDNF expression. Biochimica et Biophysica Acta (BBA) - General Subjects, (0). doi: http://dx.doi.org/10.1016/j.bbagen.2013.12.023. http://www.sciencedirect.com/science/article/pii/S0304416513005515


Carim-Todd, L., Bath, K. G., Fulgenzi, G., Yanpallewar, S., Jing, D., Barrick, C. A., . . . others. (2009). Endogenous truncated TrkB. T1 receptor regulates neuronal complexity and TrkB kinase receptor function in vivo. Journal of Neuroscience, 29(3), 678-685. doi. 

Carim-Todd, L., Bath, K. G., Fulgenzi, G., Yanpallewar, S., Jing, D., Barrick, C. A., . . . Tessarollo, L. (2009). Endogenous Truncated TrkB.T1 Receptor Regulates Neuronal Complexity and TrkB Kinase Receptor Function In Vivo. Journal of Neuroscience, 29(3), 678-685. doi: 10.1523/jneurosci.5060-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/3/678 


Carletti, B., Grimaldi, P., Magrassi, L., & Rossi, F. (2002). Specification of Cerebellar Progenitors After Heterotopic-Heterochronic Transplantation to the Embryonic CNS In Vivo and In Vitro. Journal of Neuroscience, 22(16), 7132-7146. doi. http://www.jneurosci.org/cgi/content/abstract/22/16/7132


Carletti, B., Grimaldi, P., Magrassi, L., & Rossi, F. (2004). Engraftment and differentiation of neocortical progenitor cells transplanted to the embryonic brain in utero. Journal of Neurocytology, 33(3), 309-319. doi. 

Carletti, B., & Rossi, F. (2005). Selective rather than inductive mechanisms favour specific replacement of Purkinje cells by embryonic cerebellar cells transplanted to the cerebellum of adult Purkinje cell degeneration (pcd) mutant mice. European Journal of Neuroscience, 22(5), 1001-1012. doi: doi:10.1111/j.1460-9568.2005.04314.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2005.04314.x 


Carletti, B., Williams, I. M., Leto, K., Nakajima, K., Magrassi, L., & Rossi, F. (2008). Time constraints and positional cues in the developing cerebellum regulate Purkinje cell placement in the cortical architecture. Developmental Biology, 317(1), 147-160. doi. 

Carlin, K. P., Jiang, Z., & Brownstone, R. M. (2000). Characterization of calcium currents in functionally mature mouse spinal motoneurons. European Journal of Neuroscience, 12(5), 1624. doi. 

Carlo, C. N., Stefanacci, L., Semendeferi, K., & Stevens, C. F. (2010). Comparative analyses of the neuron numbers and volumes of the amygdaloid complex in old and new world primates. Journal of Comparative Neurology, 518(8), 1176-1198. doi. 

Carlo, C. N., & Stevens, C. F. (2011). Analysis of differential shrinkage in frozen brain sections and its implications for the use of guard zones in stereology. Journal of Comparative Neurology, 519(14), 2803-2810. doi: 10.1002/cne.22652. http://dx.doi.org/10.1002/cne.22652


Carlo, C. N., & Stevens, C. F. (2013). Structural uniformity of neocortex, revisited. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1221398110. http://www.pnas.org/content/early/2013/01/02/1221398110.abstract


Carlson, G. C., Shipley, M. T., & Keller, A. (2000). Long-Lasting Depolarizations in Mitral Cells of the Rat Olfactory Bulb. Journal of Neuroscience, 20(5), 2011-2021. doi. http://www.jneurosci.org/cgi/content/abstract/20/5/2011


Carlsson, Y., Schwendimann, L., Vontell, R., Rousset, C. I., Wang, X., Lebon, S., . . . others. (2011). Genetic inhibition of caspase-2 reduces hypoxic-ischemic and excitotoxic neonatal brain injury. Annals of Neurology. doi. 

Carmel, J. B., Kimura, H., Berrol, L. J., & Martin, J. H. (2013). Motor cortex electrical stimulation promotes axon outgrowth to brain stem and spinal targets that control the forelimb impaired by unilateral corticospinal injury. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12119. http://dx.doi.org/10.1111/ejn.12119


Carnevale, N. T., & Hines, M. (2008). The NEURON Simulation Environment in Epilepsy Research. Computational Neuroscience in Epilepsy, 18-18. doi. 

Carnevale, T. (2007). Neuron simulation environment. Scholarpedia, 2(6), 1378-1378. doi. 

Carpenter, A., Paulus, A., Robinson, M., Bates, C. M., Robinson, M. L., Hains, D., . . . McHugh, K. M. (2012). 3-dimensional morphometric analysis of murine bladder development and dysmorphogenesis. Developmental Dynamics, 241(3), 522-533. doi: 10.1002/dvdy.23744. http://dx.doi.org/10.1002/dvdy.23744


Carpo, M., Scarlato, M., Bardella, M. T., Terrani, C., Peracchi, M., Allaria, S., . . . Bresolin, N. (2004). Painful sensory neuropathy and dysimmunity: is there a relation? Journal of the Peripheral Nervous System, 9(2), 121-121. doi: doi:10.1111/j.1085-9489.2004.009209bc.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Carr, C. E., Shah, S., McColgan, T., Ashida, G., Kuokkanen, P. T., Brill, S., . . . Wagner, H. (2015). Maps of interaural delay in the owl's nucleus laminaris. [10.1152/jn.00644.2015]. Journal of Neurophysiology. doi. http://jn.physiology.org/content/early/2015/07/27/jn.00644.2015.abstract


Carr, H., Alexander, T. C., Groves, T., Kiffer, F., Wang, J., Price, E., . . . Allen, A. R. (2018). Early effects of 16O radiation on Neuronal Morphology and Cognition in a Murine Model. Life Sciences in Space Research. doi: https://doi.org/10.1016/j.lssr.2018.03.001. http://www.sciencedirect.com/science/article/pii/S2214552417301323


Carrascal, L., Nieto-Gonzalez, J. L., Torres, B., & Nunez-Abades, P. (2009). Changes in somatodendritic morphometry of rat oculomotor nucleus motoneurons during postnatal development. Journal of Comparative Neurology, 514(2), 189-202. doi. 

Carrascal, L., Nieto-González, J. L., Torres, B., & Nunez-Abades, P. (2011). Diminution of Voltage Threshold Plays a Key Role in Determining Recruitment of Oculomotor Nucleus Motoneurons during Postnatal Development. PLoS ONE, 6(12), e28748-e28748. doi. 

Carrasco, A., Brown, T. A., Kok, M. A., Chabot, N., Kral, A., & Lomber, S. G. (2013). Influence of Core Auditory Cortical Areas on Acoustically Evoked Activity in Contralateral Primary Auditory Cortex. Journal of Neuroscience, 33(2), 776-789. doi: 10.1523/jneurosci.1784-12.2013. http://www.jneurosci.org/content/33/2/776.abstract


Carrasco, A., & Lomber, S. G. (2013). Influence of inter-field communication on neuronal response synchrony across auditory cortex. Hearing Research, (0). doi: http://dx.doi.org/10.1016/j.heares.2013.05.012. http://www.sciencedirect.com/science/article/pii/S0378595513001421


Carrasco, M. M., Mao, Y.-T., Balmer, T. S., & Pallas, S. L. (2011). Inhibitory plasticity underlies visual deprivation-induced loss of receptive field refinement in the adult superior colliculus. European Journal of Neuroscience, 33(1), 58-68. doi: 10.1111/j.1460-9568.2010.07478.x. http://dx.doi.org/10.1111/j.1460-9568.2010.07478.x


Carrigan, I. D., Croll, R. P., & Wyeth, R. C. (2015). Morphology, innervation and peripheral sensory cells of the siphon of Aplysia californica. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23795. http://dx.doi.org/10.1002/cne.23795


Carter, M. A. (2017). Examination of Taste Bud Volumes on the Side of the Tongue Opposite to Nerve Injury in Young and Adult Rats. doi. http://digitalcommons.unomaha.edu/srcaf/2017/schedule/152/


Carulli, D., Buffo, A., Botta, C., Altruda, F., & Strata, P. (2002). Regenerative and survival capabilities of Purkinje cells overexpressing c-Jun. European Journal of Neuroscience, 16(1), 105. doi. 

Carulli, D., Foscarin, S., Faralli, A., Pajaj, E., & Rossi, F. (2013). Modulation of semaphorin3A in perineuronal nets during structural plasticity in the adult cerebellum. Molecular and Cellular Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.mcn.2013.08.003. http://www.sciencedirect.com/science/article/pii/S104474311300081X


Carulli, D., Pizzorusso, T., Kwok, J. C. F., Putignano, E., Poli, A., Forostyak, S., . . . Fawcett, J. W. (2010). Animals lacking link protein have attenuated perineuronal nets and persistent plasticity. Brain, awq145. doi: 10.1093/brain/awq145. http://brain.oxfordjournals.org/cgi/content/abstract/awq145v1 


Carvell, G. E., & Simons, D. J. (2017). Effect of Whisker Geometry on Contact Force Produced by Vibrissae Moving at Different Velocities. [10.1152/jn.00046.2017]. Journal of Neurophysiology. doi. http://jn.physiology.org/content/early/2017/06/26/jn.00046.2017.abstract


Casanova, J. R., Nishimura, M., Le, J., Lam, T. T., & Swann, J. W. (2013). Rapid hippocampal network adaptation to recurring synchronous activity – a role for calcineurin. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12315. http://dx.doi.org/10.1111/ejn.12315


Casanova, J. R., Nishimura, M., Owens, J. W., & Swann, J. W. (2012). Impact of seizures on developing dendrites: Implications for intellectual developmental disabilities. Epilepsia, 53, 116-124. doi: 10.1111/j.1528-1167.2012.03482.x. http://dx.doi.org/10.1111/j.1528-1167.2012.03482.x


Casas, C. E., Herrera, L. P., Prusmack, C., Ruenes, G., Marcillo, A., & Guest, J. D. (2005). Effects of epidural hypothermic saline infusion on locomotor outcome and tissue preservation after moderate thoracic spinal cord contusion in rats. Journal of Neurosurgery: Spine, 2(3), 308-318. doi. 

Case, L., & Broberger, C. (2017). Neurotensin Broadly Recruits Inhibition via White Matter Neurons in the Mouse Cerebral Cortex: Synaptic Mechanisms for Decorrelation. Cerebral Cortex, 1-14. doi. https://academic.oup.com/cercor/article-abstract/doi/10.1093/cercor/bhx1...


Casella, E., Thomas, T., Vanino, D., Fellows-Mayle, W., Lifshitz, J., Card, J. P., & Adelson, P. D. (2014). Traumatic brain injury alters long-term hippocampal neuron morphology in juvenile, but not immature, rats. Child's Nervous System, 1-10. doi: 10.1007/s00381-014-2446-z. http://dx.doi.org/10.1007/s00381-014-2446-z


Casella, G. T. B., Almeida, V. W., Grumbles, R. M., Liu, Y., & Thomas, C. K. (2010). Neurotrophic factors improve muscle reinnervation from embryonic neurons. Muscle and Nerve, 42(5), 788-797. doi: 10.1002/mus.21757. http://dx.doi.org/10.1002/mus.21757


Casellato, C., Di Troia, A., Terenghi, F., & Nobile-Orazio, E. (2004). Peripheral nervous system involvement as presenting symptom of systemic B-cell lymphoma. Journal of the Peripheral Nervous System, 9(2), 108-109. doi. 

Casoni, F., Malone, S. A., Belle, M., Luzzati, F., Collier, F., Allet, C., . . . Giacobini, P. (2016). Development of the neurons controlling fertility in humans: new insights from 3D imaging and transparent fetal brains. [10.1242/dev.139444]. Development, 143(21), 3969. doi. http://dev.biologists.org/content/143/21/3969.abstract


Casta├▒eda, M. T., Sanabria, E. R. G., Hernandez, S., Ayala, A., Reyna, T. A., Wu, J. Y., & Colom, L. V. (2005). Glutamic acid decarboxylase isoforms are differentially distributed in the septal region of the rat. Neuroscience Research, 52(1), 107-119. doi. 

Castellanos, D. A., Tsoulfas, P., Frydel, B. R., Gajavelli, S., Bes, J.-C., & Sagen, J. (2002). TrkC Overexpression enhances Survival and Migration of Neural Stem Cell Transplants in the Rat spinal cord. Cell Transplantation, 11, 297-307. doi. 

Castren, M., Tervonen, T., Karkkainen, V., Heinonen, S., Castren, E., Larsson, K., . . . Akerman, K. (2005). Altered differentiation of neural stem cells in fragile X syndrome. Proceedings of the National Academy of Sciences, 102(49), 17834-17839. doi: 10.1073/pnas.0508995102. http://www.pnas.org/cgi/content/abstract/102/49/17834 


Castro-Alamancos, M. A., & Tawara-Hirata, Y. (2007). Area-Specific Resonance of Excitatory Networks in Neocortex: Control by Outward Currents. Epilepsia, 48(8), 1572-1584. doi: doi:10.1111/j.1528-1167.2007.01113.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1528-1167.2007.01113.x 


Castro-Gomes, V., Bergstrom, H. C., McGuire, J. L., Parker, C. C., Coyner, J., Landeira-Fernandez, J., . . . Johnson, L. R. (2015). A dendritic organization of lateral amygdala neurons in fear susceptible and resistant mice. Neurobiology of Learning and Memory. doi: http://dx.doi.org/10.1016/j.nlm.2015.11.010. http://www.sciencedirect.com/science/article/pii/S1074742715002191


Cataldo, G., Lovric, J., Chen, C. C., Pytte, C. L., & Bodnar, R. J. (2010). Ventromedial and medial preoptic hypothalamic ibotenic acid lesions potentiate systemic morphine analgesia in female, but not male rats. Behavioural Brain Research, 214(2), 301-316. doi. 

Cattaert, D., Libersat, F., & El Manira, A. (2001). Presynaptic Inhibition and Antidromic Spikes in Primary Afferents of the Crayfish: A Computational and Experimental Analysis. Journal of Neuroscience, 21(3), 1007-1021. doi. http://www.jneurosci.org/cgi/content/abstract/21/3/1007


Catuara-Solarz, S., Espinosa-Carrasco, J., Erb, I., Langohr, K., Gonzalez, J. R., Notredame, C., & Dierssen, M. (2016). Combined treatment With environmental enrichment And (-)-epigallocatechin-3-gallate ameliorates learning deficits And hippocampal alterations In A mouse model Of Down syndrome. [10.1523/ENEURO.0103-16.2016]. eneuro. doi. http://eneuro.org/content/early/2016/10/19/ENEURO.0103-16.2016.abstract


Caudle, W. M., Kitsou, E., Li, J., Bradner, J., & Zhang, J. (2009). A role for a novel protein, nucleolin, in Parkinson's disease. Neuroscience Letters, 459(1), 11-15. doi. 

Cavaletti, G., Beronio, A., Reni, L., Ghiglione, E., Schenone, A., Briani, C., . . . Carpo, M. (2004). THalidomide sensory neurotoxicity: results of a collaborative clinical and neurophysiolgical study. Journal of the Peripheral Nervous System, 9(2), 105-105. doi: doi:10.1111/j.1085-9489.2004.009209e.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Cavallaro, T., Fabrizi, G. M., Angiari, C., Lus, G., Cabrini, I., Cotrufo, R., & Rizzuto, N. (2004). Are giant axons a pathological marker of charcot-marie-tooth neuropathy type 2E? Journal of the Peripheral Nervous System, 9(2), 124-124. doi. 

Cavarretta, F., Burton, S. D., Igarashi, K. M., Shepherd, G. M., Hines, M. L., & Migliore, M. (2018). Parallel odor processing by mitral and middle tufted cells in the olfactory bulb. Scientific Reports, 8(1), 7625. doi: 10.1038/s41598-018-25740-x. https://doi.org/10.1038/s41598-018-25740-x


Cazorla, M., de Carvalho, Fernanda D., Chohan, Muhammad O., Shegda, M., Chuhma, N., Rayport, S., . . . Kellendonk, C. (2014). Dopamine D2 Receptors Regulate the Anatomical and Functional Balance of Basal Ganglia Circuitry. Neuron, 81(1), 153-164. doi: http://dx.doi.org/10.1016/j.neuron.2013.10.041. http://www.sciencedirect.com/science/article/pii/S0896627313009938


Cazorla, M., Shegda, M., Ramesh, B., Harrison, N. L., & Kellendonk, C. (2012). Striatal D2 Receptors Regulate Dendritic Morphology of Medium Spiny Neurons via Kir2 Channels. Journal of Neuroscience, 32(7), 2398-2409. doi: 10.1523/jneurosci.6056-11.2012. http://www.jneurosci.org/content/32/7/2398.abstract


Cea-del Rio, C. A., Lawrence, J. J., Erdelyi, F., Szabo, G., & McBain, C. J. (2011). Cholinergic modulation amplifies the intrinsic oscillatory properties of CA1 hippocampal cholecystokinin-positive interneurons. Journal of Physiology, 589(3), 609-627. doi: 10.1113/jphysiol.2010.199422. http://dx.doi.org/10.1113/jphysiol.2010.199422


Cejková, J., Ardan, T., Simonová, Z., Cejka, C., Malec, J., Jirsová, K., . . . Brunová, B. (2007). Nitric oxide synthase induction and cytotoxic nitrogen-related oxidant formation in conjunctival epithelium of dry eye (Sjögren [] s syndrome). Nitric Oxide, 17(1), 10-17. doi. 

Ceredig, R. A., Pierre, F., Doridot, S., Alduntzin, U., Salvat, E., Yalcin, I., . . . Massotte, D. (2018). Peripheral Delta Opioid Receptors Mediate Duloxetine Anti-allodynic Effect in a Mouse Model of Neuropathic Pain. European Journal of Neuroscience, 0(ja). doi: doi:10.1111/ejn.14093. https://onlinelibrary.wiley.com/doi/abs/10.1111/ejn.14093


Cerkevich, C. M., Qi, H.-X., & Kaas, J. H. (2013). Corticocortical projections to representations of the teeth, tongue, and face in somatosensory area 3b of macaque monkeys. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23426. http://dx.doi.org/10.1002/cne.23426


Cerkevich, C. M., Qi, H.-X., & Kaas, J. H. (2013). Thalamic input to representations of the teeth, tongue, and face in somatosensory area 3b of macaque monkeys. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23386. http://dx.doi.org/10.1002/cne.23386


Cernea, M., Phillips, R., Padmanabhan, V., Coolen, L. M., & Lehman, M. N. (2016). Prenatal Testosterone Exposure Decreases Colocalization of Insulin Receptors in Kisspeptin/Neurokinin B/Dynorphin (KNDy) and Agouti-Related Peptide (AgRP) Neurons of the Adult Ewe. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.13373. http://dx.doi.org/10.1111/ejn.13373


Cerqueira, J. J., Mailliet, F., Almeida, O. F. X., Jay, T. M., & Sousa, N. (2007). The Prefrontal Cortex as a Key Target of the Maladaptive Response to Stress. Journal of Neuroscience, 27(11), 2781-2787. doi: 10.1523/jneurosci.4372-06.2007. http://www.jneurosci.org/cgi/content/abstract/27/11/2781 


Cerqueira, J. J., Pego, J. M., Taipa, R., Bessa, J. M., Almeida, O. F. X., & Sousa, N. (2005). Morphological Correlates of Corticosteroid-Induced Changes in Prefrontal Cortex-Dependent Behaviors. Journal of Neuroscience, 25(34), 7792-7800. doi: 10.1523/jneurosci.1598-05.2005. http://www.jneurosci.org/cgi/content/abstract/25/34/7792 


Cerqueira, J. J., Taipa, R., Uylings, H. B. M., Almeida, O. F. X., & Sousa, N. (2007). Specific configuration of dendritic degeneration in pyramidal neurons of the medial prefrontal cortex induced by differing corticosteroid regimens. Cerebral Cortex, 17(9), 1998-2006. doi. 

Cerrato, V., Parmigiani, E., Figueres-Oñate, M., Betizeau, M., Aprato, J., Nanavaty, I., . . . Buffo, A. (2018). Multiple origins and modularity in the spatiotemporal emergence of cerebellar astrocyte heterogeneity. PLoS Biology, 16(9), e2005513. doi: 10.1371/journal.pbio.2005513. https://doi.org/10.1371/journal.pbio.2005513


Cerri, S., Levandis, G., Ambrosi, G., Montepeloso, E., Antoninetti, G. F., Franco, R., . . . Pinna, A. (2014). Neuroprotective Potential of Adenosine A2A and Cannabinoid CB1 Receptor Antagonists in an Animal Model of Parkinson Disease. Journal of Neuropathology and Experimental Neurology. doi. 

Cerri, S., Levandis, G., Ambrosi, G., Montepeloso, E., Antoninetti, G. F., Franco, R., . . . Pinna, A. (2014). Neuroprotective Potential of Adenosine A2A and Cannabinoid CB1 Receptor Antagonists in an Animal Model of Parkinson Disease. Journal of Neuropathology and Experimental Neurology. doi. http://www.nature.com/ncomms/2014/140408/ncomms4602/full/ncomms4602.html


Cetas, J. S., De Venecia, R. K., & McMullen, N. T. (1999). Thalamocortical afferents of Lorente de No: medial geniculate axons that project to primary auditory cortex have collateral branches to layer I. Brain Research, 830(1), 203-208. doi. 

Cetas, J. S., Price, R. O., Velenovsky, D. S., Crowe, J. J., & McMullen, N. T. (2003). Dendritic Orientation and Laminar Architecture in the Rabbit Auditory Thalamus. Journal of Comparative Neurology, 458, 307-317. doi. 

Cetas, J. S., Price, R. O., Velenovsky, D. S., Crowe, J. J., Sinex, D. G., & McMullen, N. T. (2002). Cell Types and Response Properties of Neurons in the Ventral Division of the Medial Geniculate Body of the Rabbit. Journal of Comparative Neurology, 445, 78-96. doi. 

Cetas, J. S., Price, R. O., Velenovsky, D. S., Sinex, D. G., & McMullen, N. T. (2001). Frequency organization and cellular lamination in the medial geniculate body of the rabbit. Hearing Research, 155(1-2), 113-123. doi. 

Cha, M., Um, S. W., Kwon, M., Nam, T. S., & Lee, B. H. (2017). Repetitive motor cortex stimulation reinforces the pain modulation circuits of peripheral neuropathic pain. Scientific Reports, 7, 7986. doi: 10.1038/s41598-017-08208-2. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554204/


Chaaya, N., Jacques, A., Belmer, A., Richard, D. J., Bartlett, S. E., Battle, A. R., & Johnson, L. R. (2018). Localization of Contextual and Context Removed Auditory Fear Memory within the Basolateral Amygdala Complex. Neuroscience. doi: https://doi.org/10.1016/j.neuroscience.2018.12.004. http://www.sciencedirect.com/science/article/pii/S030645221830798X


Chabot, N., Butler, B. E., & Lomber, S. G. (2015). Differential modification of cortical and thalamic projections to cat primary auditory cortex following early- and late-onset deafness. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23790. http://dx.doi.org/10.1002/cne.23790


Chabot, N., Mellott, J. G., Hall, A. J., Tichenoff, E. L., & Lomber, S. G. (2013). Cerebral origins of the auditory projection to the superior colliculus of the cat. Hearing Research, (0). doi: http://dx.doi.org/10.1016/j.heares.2013.02.008. http://www.sciencedirect.com/science/article/pii/S0378595513000671


Chabot, N., Robert, S., Tremblay, R., Miceli, D., Boire, D., & Bronchti, G. (2007). Audition differently activates the visual system in neonatally enucleated mice compared with anophthalmic mutants. European Journal of Neuroscience, 26(8), 2334-2348. doi: doi:10.1111/j.1460-9568.2007.05854.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05854.x 


Chabrol, F. P., Eglen, S. J., & Sernagor, E. (2012). GABAergic control of retinal ganglion cell dendritic development. Neuroscience, (0). doi: 10.1016/j.neuroscience.2012.09.040. http://www.sciencedirect.com/science/article/pii/S0306452212009608?v=s5


Chailangkarn, T., Trujillo, C. A., Freitas, B. C., Hrvoj-Mihic, B., Herai, R. H., Yu, D. X., . . . Muotri, A. R. (2016). A human neurodevelopmental model for Williams syndrome. [Letter]. Nature, 536(7616), 338-343. doi: 10.1038/nature19067

http://www.nature.com/nature/journal/v536/n7616/abs/nature19067.html#sup.... http://dx.doi.org/10.1038/nature19067


Chakrabarty, A., Emerson, M. R., & LeVine, S. M. (2003). Hemeoxygenase-1 in SJL mice with experimental allergic encephalomyelitis. Multiple Sclerosis, 9(4), 372-381. doi. 

Chakrabarty, S., & Martin, J. (2011). Postnatal refinement of proprioceptive afferents in the cat cervical spinal cord. European Journal of Neuroscience. doi. 

Chakrabarty, S., Shulman, B., & Martin, J. H. (2009). Activity-Dependent Codevelopment of the Corticospinal System and Target Interneurons in the Cervical Spinal Cord. Journal of Neuroscience, 29(27), 8816-8827. doi: 10.1523/jneurosci.0735-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/27/8816 


Chakraborty, P., & Chattarji, S. (2018). Timing is everything: differential effects of chronic stress on fear extinction. [journal article]. Psychopharmacology. doi: 10.1007/s00213-018-5053-y. https://doi.org/10.1007/s00213-018-5053-y


Chakraborty, P., & Chattarji, S. (2019). Interventions after acute stress prevent its delayed effects on the amygdala. Neurobiology of Stress, 10, 100168. doi: https://doi.org/10.1016/j.ynstr.2019.100168. http://www.sciencedirect.com/science/article/pii/S2352289518301036


Chakravarty, S., Chikkatur, A., de Coninck, H., Pacala, S., Socolow, R., & Tavoni, M. (2009). Sharing global CO2 emission reductions among one billion high emitters. Proceedings of the National Academy of Sciences, 106(29), 11884-11888. doi: 10.1073/pnas.0905232106. http://www.pnas.org/content/106/29/11884.abstract 


Chalfin, B. P., Cheung, D. T., Muniz, J. A. P. C., de Lima Silveira, L. C., & Finlay, B. L. (2007). Scaling of neuron number and volume of the pulvinar complex in New World primates: comparisons with humans, other primates, and mammals. Journal of Comparative Neurology, 504(3), 265-274. doi. 

Chamberland, S., Salesse, C., Topolnik, D., & Topolnik, L. (2010). Synapse-specific inhibitory control of hippocampal feedback inhibitory circuit. Frontiers in Cellular Neuroscience, 4. doi. 

Chan, C.-F., Kuo, T.-W., Weng, J.-Y., Lin, Y.-C., Chen, T.-Y., Cheng, J.-K., & Lien, C.-C. (2013). Ba2+- and bupivacaine-sensitive background K+ conductances mediate rapid EPSP attenuation in oligodendrocyte precursor cells. Journal of Physiology, no-no. doi: 10.1113/jphysiol.2013.257113. http://dx.doi.org/10.1113/jphysiol.2013.257113


Chan, C. Y., Yoo, J. E., & Travers, S. P. (2004). Diverse bitter stimuli elicit highly similar patterns of Fos-like immunoreactivity in the nucleus of the solitary tract. Chemical Senses, 29(7), 573-581. doi. 

Chancey, J. H., Adlaf, E. W., Sapp, M. C., Pugh, P. C., Wadiche, J. I., & Overstreet-Wadiche, L. S. (2013). GABA Depolarization Is Required for Experience-Dependent Synapse Unsilencing in Adult-Born Neurons. Journal of Neuroscience, 33(15), 6614-6622. doi: 10.1523/jneurosci.0781-13.2013. http://www.jneurosci.org/content/33/15/6614.abstract


Chand, P., & Jain, N. (2015). Intracortical and Thalamocortical Connections of the Hand and Face Representations in Somatosensory Area 3b of Macaque Monkeys and Effects of Chronic Spinal Cord Injuries. The Journal of Neuroscience, 35(39), 13475-13486. doi. http://www.jneurosci.org/content/35/39/13475.abstract


Chang, E. H., Volpe, B. T., Mackay, M., Aranow, C., Watson, P., Kowal, C., . . . Diamond, B. (2015). Selective Impairment of Spatial Cognition Caused by Autoantibodies to the N-Methyl-d-Aspartate Receptor. EBioMedicine, (0). doi: http://dx.doi.org/10.1016/j.ebiom.2015.05.027. http://www.sciencedirect.com/science/article/pii/S2352396415300293


Chang, J. C., Leung, M., Gokozan, H. N., Gygli, P. E., Catacutan, F. P., Czeisler, C., & Otero, J. J. (2015). Mitotic Events in Cerebellar Granule Progenitor Cells That Expand Cerebellar Surface Area Are Critical for Normal Cerebellar Cortical Lamination in Mice. Journal of Neuropathology and Experimental Neurology, 74(3), 261-272. doi. http://journals.lww.com/jneuropath/Abstract/2015/03000/Mitotic_Events_in...


Chang, L. (2015). Quantitative analysis tools and correlative imaging applications for N-STORM. [Application Note]. Nat Meth, 12(11). doi: 10.1038/nmeth.f.385. http://dx.doi.org/10.1038/nmeth.f.385


Chang, Y.-M., & Luebke, J. I. (2007). Electrophysiological Diversity of Layer 5 Pyramidal Cells in the Prefrontal Cortex of the Rhesus Monkey: In Vitro Slice Studies. Journal of Neurophysiology, 98(5), 2622-2632. doi: 10.1152/jn.00585.2007. http://jn.physiology.org/cgi/content/abstract/98/5/2622 


Chang, Y. S., Mu, D., Wendland, M., Sheldon, R. A., Vexler, Z. S., McQuillen, P. S., & Ferriero, D. M. (2005). Erythropoietin Improves Functional and Histological Outcome in Neonatal Stroke. Pediatric Research, 58(1), 106-111. doi. 

Chang-Mu, C., Jen-Kun, L., Shing-Hwa, L., & Shoei-Yn, L. S. (2010). Characterization of neurotoxic effects of NMDA and the novel neuroprotection by phytopolyphenols in mice. Behavioral Neuroscience, 124(4), 541-541. doi. 

Chao, T. K., Burgess, B. J., Eddington, D. K., & Nadol, J. B. (2002). Morphometric changes in the cochlear nucleus in patients who had undergone cochlear implantation for bilateral profound deafness. Hearing Research, 174(1-2), 196-205. doi. 

Chapleau, C. A., Calfa, G. D., Lane, M. C., Albertson, A. J., Larimore, J. L., Kudo, S., . . . Pozzo-Miller, L. (2009). Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations. Neurobiology of Disease, 35(2), 219-233. doi. 

Chapman, M. A., & Zahm, D. S. (1996). Altered Fos-like immunoreactivity in terminal regions of the mesotelencephalic dopamine system is associated with reappearance of tyrosine hydroxylase immunoreactivity at the sites of focal 6-hydroxydopamine lesions in the nucleus accumbens. Brain Research, 736(1-2), 270-279. doi. 

Charbonneau, V., Laramée, M.-E., Boucher, V., Bronchti, G., & Boire, D. (2012). Cortical and subcortical projections to primary visual cortex in anophthalmic, enucleated and sighted mice. European Journal of Neuroscience, no-no. doi: 10.1111/j.1460-9568.2012.08215.x. http://dx.doi.org/10.1111/j.1460-9568.2012.08215.x


Charvet, C. J., Cahalane, D. J., & Finlay, B. L. (2013). Systematic, Cross-Cortex Variation in Neuron Numbers in Rodents and Primates. Cerebral Cortex. doi: 10.1093/cercor/bht214. http://cercor.oxfordjournals.org/content/early/2013/08/17/cercor.bht214....


Charvet, C. J., Reep, R. L., & Finlay, B. L. (2015). Evolution of cytoarchitectural landscapes in the mammalian isocortex: Sirenians (Trichechus manatus) in comparison with other mammals. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23864. http://dx.doi.org/10.1002/cne.23864


Chattopadhyaya, B., Baho, E., Huang, Z. J., Schachner, M., & Di Cristo, G. (2013). Neural Cell Adhesion Molecule-Mediated Fyn Activation Promotes GABAergic Synapse Maturation in Postnatal Mouse Cortex. Journal of Neuroscience, 33(14), 5957-5968. doi: 10.1523/jneurosci.1306-12.2013. http://www.jneurosci.org/content/33/14/5957.abstract


Chattopadhyaya, B., Cristo, G. D., Wu, C. Z., Knott, G., Kuhlman, S., Fu, Y., . . . Huang, Z. J. (2007). GAD67-mediated GABA synthesis and signaling regulate inhibitory synaptic innervation in the visual cortex. Neuron, 54(6), 889-903. doi. 

Chau, L. S., Prakapenka, A. V., Zendeli, L., Davis, A. S., & Galvez, R. (2014). Training-Dependent Associative Learning Induced Neocortical Structural Plasticity: A Trace Eyeblink Conditioning Analysis. PLoS ONE, 9(4), e95317. doi: 10.1371/journal.pone.0095317. http://dx.doi.org/10.1371%2Fjournal.pone.0095317


Chaudhary, P., Das-Earl, P., & Schreihofer, A. M. (2021). Preserved glycemic control and baroreflex efficacy in young adult hypertensive female obese Zucker rats. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. doi: 10.1152/ajpregu.00341.2020. https://doi.org/10.1152/ajpregu.00341.2020


Chaudhary, P., & Schreihofer, A. M. (2018). Improved glucose homeostasis in male obese Zucker rats coincides with enhanced baroreflexes and activation of the nucleus tractus solitarius. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 0(0), null. doi: 10.1152/ajpregu.00195.2018. https://www.physiology.org/doi/abs/10.1152/ajpregu.00195.2018


Chaudhuri, A. D., Dastgheyb, R. M., Yoo, S.-W., Trout, A., Talbot Jr, C. C., Hao, H., . . . Haughey, N. J. (2018). TNFα and IL-1β modify the miRNA cargo of astrocyte shed extracellular vesicles to regulate neurotrophic signaling in neurons. Cell Death & Disease, 9(3), 363. doi: 10.1038/s41419-018-0369-4. https://doi.org/10.1038/s41419-018-0369-4


Chauvette, S., Volgushev, M., & Timofeev, I. (2010). Origin of Active States in Local Neocortical Networks during Slow Sleep Oscillation. Cerebral Cortex, bhq009. doi: 10.1093/cercor/bhq009. http://cercor.oxfordjournals.org/cgi/content/abstract/bhq009v1 


Che, A., Babij, R., Iannone, A. F., Fetcho, R. N., Ferrer, M., Liston, C., . . . De Marco García, N. V. (2018). Layer I Interneurons Sharpen Sensory Maps during Neonatal Development. Neuron. doi: https://doi.org/10.1016/j.neuron.2018.06.002. http://www.sciencedirect.com/science/article/pii/S0896627318304707


Cheadle, L., Tzeng, C. P., Kalish, B. T., Harmin, D. A., Rivera, S., Ling, E., . . . Greenberg, M. E. (2018). Visual Experience-Dependent Expression of Fn14 Is Required for Retinogeniculate Refinement. Neuron. doi: https://doi.org/10.1016/j.neuron.2018.06.036. http://www.sciencedirect.com/science/article/pii/S0896627318305324


Chen, A. I., de Nooij, J. C., & Jessell, T. M. (2006). Graded activity of transcription factor Runx3 specifies the laminar termination pattern of sensory axons in the developing spinal cord. Neuron, 49(3), 395-408. doi. 

Chen, B., He, J., Yang, H., Zhang, Q., Zhang, L., Zhang, X., . . . Hao, D. (2015). Repair of spinal cord injury by implantation of bFGF-incorporated HEMA-MOETACL hydrogel in rats. [Article]. Sci. Rep., 5. doi: 10.1038/srep09017. http://dx.doi.org/10.1038/srep09017


Chen, B. K., Madigan, N. N., Hakim, J. S., Dadsetan, M., McMahon, S. S., Yaszemski, M. J., & Windebank, A. J. (2017). GDNF Schwann cells in hydrogel scaffolds promote regional axon regeneration, remyelination and functional improvement after spinal cord transection in rats. Journal of Tissue Engineering and Regenerative Medicine, n/a-n/a. doi: 10.1002/term.2431. http://dx.doi.org/10.1002/term.2431


Chen, C., Cheng, M., Ito, T., & Song, S. (2018). Neuronal organization in the inferior colliculus revisited with cell-type-dependent monosynaptic tracing. [10.1523/JNEUROSCI.2173-17.2018]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2018/02/26/JNEUROSCI.2173-17.2018...


Chen, C. C., Abrams, S., Pinhas, A., & Brumberg, J. C. (1988). Morphological heterogeneity of layer VI neurons in mouse barrel cortex. Journal of Comparative Neurology, 512(6), 511-519. doi. 

Chen, C. C., Tam, D., & Brumberg, J. C. (2011). Sensory deprivation differentially impacts the dendritic development of pyramidal versus non-pyramidal neurons in layer 6 of mouse barrel cortex. Brain Structure and Function, 1-12. doi. 

Chen, C.-C., Abrams, S., Pinhas, A., & Brumberg, J. C. (2009). Morphological heterogeneity of layer VI neurons in mouse barrel cortex. Journal of Comparative Neurology, 512(6), 726-746. doi. http://dx.doi.org/10.1002/cne.21926 


Chen, C.-C., Bajnath, A., & Brumberg, J. C. (2014). The Impact of Development and Sensory Deprivation on Dendritic Protrusions in the Mouse Barrel Cortex. Cerebral Cortex. doi: 10.1093/cercor/bht415. http://cercor.oxfordjournals.org/content/early/2014/01/08/cercor.bht415....


Chen, C.-C., Chu, P., & Brumberg, J. C. (2015). Experience-dependent regulation of tissue-type plasminogen activator in the mouse barrel cortex. Neuroscience Letters, 599(0), 152-157. doi: http://dx.doi.org/10.1016/j.neulet.2015.05.050. http://www.sciencedirect.com/science/article/pii/S0304394015004152


Chen, C.-C., Lu, H.-C., & Brumberg, J. C. (2012). mGluR5 knockout mice display increased dendritic spine densities. Neuroscience Letters, (0). doi: 10.1016/j.neulet.2012.07.014. http://www.sciencedirect.com/science/article/pii/S0304394012009378


Chen, C.-M., Orefice, L. L., Chiu, S.-L., LeGates, T. A., Hattar, S., Huganir, R. L., . . . Kuruvilla, R. (2017). Wnt5a is essential for hippocampal dendritic maintenance and spatial learning and memory in adult mice. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1615792114. http://www.pnas.org/content/early/2017/01/03/1615792114.abstract


Chen, F., Becker, A. J., & LoTurco, J. J. (2014). Contribution of Tumor Heterogeneity in a New Animal Model of CNS Tumors. Molecular Cancer Research. doi: 10.1158/1541-7786.mcr-13-0531. http://mcr.aacrjournals.org/content/early/2014/02/05/1541-7786.MCR-13-05...


Chen, F., & LoTurco, J. (2012). A method for stable transgenesis of radial glia lineage in rat neocortex by piggyBac mediated transposition. Journal of Neuroscience Methods, 207(2), 172-180. doi: 10.1016/j.jneumeth.2012.03.016. http://www.sciencedirect.com/science/article/pii/S0165027012001112


Chen, G., Jin, M., & Yuan, X.-b. (2015). Using in utero electroporation to investigate the role of semaphorin-3A in radial migration of cortical neurons. doi. https://www.scientificprotocols.org/protocols/using-in-utero-electropora...


Chen, G., Sima, J., Jin, M., Wang, K.-y., Xue, X.-j., Zheng, W., . . . Yuan, X.-b. (2007). Semaphorin-3A guides radial migration of cortical neurons during development. Nature Neuroscience. doi. 

Chen, H., Qian, K., Chen, W., Hu, B., Blackbourn, L. W. I. V., Du, Z., . . . Zhang, S.-C. (2015). Human-derived neural progenitors functionally replace astrocytes in adult mice. The Journal of clinical investigation, 125(3), 0-0. doi: 10.1172/jci69097. http://www.jci.org/articles/view/69097


Chen, H., Xiao, H., Liu, T., & Peng, H. (2015). SmartTracing: self-learning-based Neuron reconstruction. Brain Informatics, 1-10. doi. http://link.springer.com/article/10.1007/s40708-015-0018-y/fulltext.html


Chen, I., Limb, C. J., & Ryugo, D. K. (2010). The effect of cochlear-implant-mediated electrical stimulation on spiral ganglion cells in congenitally deaf white cats. Jaro-Journal of the Association for Research in Otolaryngology, 11(4), 587-603. doi. 

Chen, J., Hanna, P., Ardell, J. L., Hoover, D. B., Vadigepalli, R., Schwaber, J., . . . Cheng, Z. J. (2019). Intrinsic Cardiac Ganglionic Neurons Projecting to the SA node in the Rat and Pig Hearts: Retrograde Labeling and Neurolucida 3-D Reconstruction. The FASEB journal, 33(1_supplement), 773.772-773.772. doi: 10.1096/fasebj.2019.33.1_supplement.773.2. https://www.fasebj.org/doi/abs/10.1096/fasebj.2019.33.1_supplement.773.2


Chen, J., Lee, H. J., Jakovcevski, I., Shah, R., Bhagat, N., Loers, G., . . . others. (2010). The extracellular matrix glycoprotein tenascin-C is beneficial for spinal cord regeneration. Molecular Therapy, 18(10), 1769-1777. doi. 

Chen, J.-G., Rasin, M.-R., Kwan, K. Y., & Sestan, N. (2005). Zfp312 is required for subcortical axonal projections and dendritic morphology of deep-layer pyramidal neurons of the cerebral cortex. Proceedings of the National Academy of Sciences, 102(49), 17792-17797. doi: 10.1073/pnas.0509032102. http://www.pnas.org/cgi/content/abstract/102/49/17792 


Chen, J. L., Flanders, G. H., Lee, W.-C. A., Lin, W. C., & Nedivi, E. (2011). Inhibitory Dendrite Dynamics as a General Feature of the Adult Cortical Microcircuit. Journal of Neuroscience, 31(35), 12437-12443. doi: 10.1523/jneurosci.0420-11.2011. http://www.jneurosci.org/content/31/35/12437.abstract


Chen, J. L., Lin, W. C., Cha, J. W., So, P. T., Kubota, Y., & Nedivi, E. (2011). Structural basis for the role of inhibition in facilitating adult brain plasticity. Nature Neuroscience, 14(5), 587-594. doi. 

Chen, Jerry L., Villa, Katherine L., Cha, Jae W., So, Peter T. C., Kubota, Y., & Nedivi, E. (2012). Clustered Dynamics of Inhibitory Synapses and Dendritic Spines in the Adult Neocortex. Neuron, 74(2), 361-373. doi: 10.1016/j.neuron.2012.02.030. http://www.sciencedirect.com/science/article/pii/S089662731200267X


Chen, J. R., Wang, T. J., Wang, Y. J., & Tseng, G. F. (2010). The immediate large-scale dendritic plasticity of cortical pyramidal neurons subjected to acute epidural compression. Neuroscience, 167(2), 414-427. doi. 

Chen, J.-R., Tseng, G.-F., Wang, Y.-J., & Wang, T.-J. (2014). Exogenous dehydroisoandrosterone sulfate reverses the dendritic changes of the central neurons in aging male rats. Experimental Gerontology, 57(0), 191-202. doi: http://dx.doi.org/10.1016/j.exger.2014.06.010. http://www.sciencedirect.com/science/article/pii/S0531556514001892


Chen, J.-R., Wang, B.-N., Tseng, G.-F., Wang, Y.-J., Huang, Y.-S., & Wang, T.-J. (2014). Morphological changes of cortical pyramidal neurons in hepatic encephalopathy. BMC Neuroscience, 15(1), 15. doi. http://www.biomedcentral.com/1471-2202/15/15/


Chen, J.-R., Yan, Y.-T., Wang, T.-J., Chen, L.-J., Wang, Y.-J., & Tseng, G.-F. (2009). Gonadal Hormones Modulate the Dendritic Spine Densities of Primary Cortical Pyramidal Neurons in Adult Female Rat. Cerebral Cortex, bhp048. doi: 10.1093/cercor/bhp048. http://cercor.oxfordjournals.org/cgi/content/abstract/bhp048v1 


Chen, K., Godfrey, D. A., Ilyas, O., Xu, J., & Preston, T. W. (2009). Cerebellum-Related Characteristics of Scn8a-Mutant Mice. Cerebellum, 8(3), 192-201. doi. 

Chen, K., Henry, R. A., Hughes, S. M., & Connor, B. (2007). Creating a neurogenic environment: the role of BDNF and FGF2. Molecular and Cellular Neuroscience, 36(1), 108-120. doi. 

Chen, L.-H., Advani, S. L., Thai, K., Kabir, M. G., Sood, M. M., Gibson, I. W., . . . Advani, A. (2014). SDF-1/CXCR4 Signaling Preserves Microvascular Integrity and Renal Function in Chronic Kidney Disease. PLoS ONE, 9(3), e92227. doi: 10.1371/journal.pone.0092227. http://dx.doi.org/10.1371%2Fjournal.pone.0092227


Chen, L.-J., Wang, Y.-J., Chen, J.-R., & Tseng, G.-F. (2016). Hydrocephalus compacted cortex and hippocampus and altered their output neurons in association with spatial learning and memory deficits in rats. Brain Pathology, n/a-n/a. doi: 10.1111/bpa.12414. http://dx.doi.org/10.1111/bpa.12414


Chen, L.-J., Wang, Y.-J., & Tseng, G.-F. (2017). Cortical compression rapidly trimmed transcallosal projections and altered axonal anterograde transport machinery. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2017.08.020. http://www.sciencedirect.com/science/article/pii/S0306452217305869


Chen, N., Sugihara, H., Kim, J., Fu, Z., Barak, B., Sur, M., . . . Han, W. (2016). Direct modulation of GFAP-expressing glia in the arcuate nucleus bi-directionally regulates feeding. [JOUR]. eLife, 5, e18716. doi: 10.7554/eLife.18716. https://dx.doi.org/10.7554/eLife.18716


Chen, P., Zhang, T., Yuan, Z., Shen, B., & Chen, L. (2019). Expression of the RNA methyltransferase Nsun5 is essential for developing cerebral cortex. Molecular Brain, 12(1), 74. doi: 10.1186/s13041-019-0496-6. https://doi.org/10.1186/s13041-019-0496-6


Chen, Q., Jiang, L., Li, C., Hu, D., Bu, J.-w., Cai, D., & Du, J.-l. (2012). Haemodynamics-Driven Developmental Pruning of Brain Vasculature in Zebrafish. PLoS Biol, 10(8), e1001374. doi: 10.1371/journal.pbio.1001374. http://dx.doi.org/10.1371%2Fjournal.pbio.1001374


Chen, Q., Zhu, Y.-C., Yu, J., Miao, S., Zheng, J., Xu, L., . . . Xiong, Z.-Q. (2010). CDKL5, a Protein Associated with Rett Syndrome, Regulates Neuronal Morphogenesis via Rac1 Signaling. Journal of Neuroscience, 30(38), 12777-12786. doi: 10.1523/jneurosci.1102-10.2010. http://www.jneurosci.org/cgi/content/abstract/30/38/12777


Chen, S., Bennet, L., & McGregor, A. L. (2017). Delayed Varenicline Administration Reduces Inflammation and Improves Forelimb Use Following Experimental Stroke. Journal of Stroke and Cerebrovascular Diseases. doi: http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2017.06.051. http://www.sciencedirect.com/science/article/pii/S1052305717303476


Chen, S., & Buckmaster, P. S. (2005). Stereological analysis of forebrain regions in kainate-treated epileptic rats. Brain Research, 1057(1-2), 141-152. doi. 

Chen, S., Fujita, S., Koshikawa, N., & Kobayashi, M. (2010). Pilocarpine-induced status epilepticus causes acute interneuron loss and hyper-excitatory propagation in rat insular cortex. Neuroscience, 166(1), 341-353. doi. 

Chen, S., Kobayashi, M., Honda, Y., Kakuta, S., Sato, F., & Kishi, K. (2007). Preferential neuron loss in the rat piriform cortex following pilocarpine-induced status epilepticus. Epilepsy Research, 74(1), 1-18. doi. 

Chen, S. X., Tari, P. K., She, K., & Haas, K. (2010). Neurexin-neuroligin cell adhesion complexes contribute to synaptotropic dendritogenesis via growth stabilization mechanisms in vivo. Neuron, 67(6), 967-983. doi. 

Chen, W., & De Schutter, E. (2017). Time to Bring Single Neuron Modeling into 3D. [journal article]. Neuroinformatics, 1-3. doi: 10.1007/s12021-016-9321-x. http://dx.doi.org/10.1007/s12021-016-9321-x


Chen, W., Prithviraj, R., Mahnke, A. H., McGloin, K. E., Tan, J. W., Gooch, A. K., & Inglis, F. M. (2009). AMPA glutamate receptor subunits 1 and 2 regulate dendrite complexity and spine motility in neurons of the developing neocortex. Neuroscience, 159(1), 172-182. doi. 

Chen, W. J., Lin, Y., Xiong, Z. Q., Wei, W., Ni, W., Tan, G. H., . . . others. (2011). Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia. Nature Genetics, 43(12), 1252-1255. doi. 

Chen, X., Han, X., Blanchi, B., Guan, W., Ge, W., Yu, Y.-C., & Sun, Y. E. (2020). Graded and pan-neural disease phenotypes of Rett Syndrome linked with dosage of functional MeCP2. Protein & Cell. doi: 10.1007/s13238-020-00773-z. https://doi.org/10.1007/s13238-020-00773-z


Chen, X., Rochefort, Nathalie L., Sakmann, B., & Konnerth, A. (2013). Reactivation of the Same Synapses during Spontaneous Up States and Sensory Stimuli. Cell Reports, (0). doi: http://dx.doi.org/10.1016/j.celrep.2013.05.042. http://www.sciencedirect.com/science/article/pii/S2211124713002751


Chen, X., Shu, S., Kennedy, D. P., Willcox, S. C., & Bayliss, D. A. (2008). Subunit-Specific Effects of Isoflurane On Neuronal lh In HCN1 Knockout Mice. Journal of Neurophysiology, 01352.02007. doi: 10.1152/jn.01352.2007. http://jn.physiology.org/cgi/content/abstract/01352.2007v1 


Chen, X., Zhang, K., Zhou, L., Gao, X., Wang, J., Yao, Y., . . . Li, S. (2016). Coupled electrophysiological recording and single cell transcriptome analyses revealed molecular mechanisms underlying neuronal maturation. Protein & Cell, 1-12. doi. http://link.springer.com/article/10.1007/s13238-016-0247-8/fulltext.html


Chen, Y., Rex, C. S., Rice, C. J., Dubé, C. M., Gall, C. M., Lynch, G., & Baram, T. Z. (2010). Correlated memory defects and hippocampal dendritic spine loss after acute stress involve corticotropin-releasing hormone signaling. Proceedings of the National Academy of Sciences, 107(29), 13123-13128. doi: 10.1073/pnas.1003825107. http://www.pnas.org/content/107/29/13123.abstract 


Chen, Y., Wang, F., Long, H., Chen, Y., Wu, Z., & Ma, L. (2011). GRK5 promotes F-actin bundling and targets bundles to membrane structures to control neuronal morphogenesis. Journal of Cell Biology, 194(6), 905-920. doi: 10.1083/jcb.201104114. http://jcb.rupress.org/content/194/6/905.abstract


Chen, Y.-J. J., Johnson, M. A., Lieberman, M. D., Goodchild, R. E., Schobel, S., Lewandowski, N., . . . Role, L. W. (2008). Type III Neuregulin-1 Is Required for Normal Sensorimotor Gating, Memory-Related Behaviors, and Corticostriatal Circuit Components. Journal of Neuroscience, 28(27), 6872-6883. doi: 10.1523/jneurosci.1815-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/27/6872 


Chen, Y. M., Wang, Q. J., Hu, H. S., Yu, P. C., Zhu, J., Drewes, G., . . . Luo, Z. G. (2006). Microtubule affinity-regulating kinase 2 functions downstream of the PAR-3/PAR-6/atypical PKC complex in regulating hippocampal neuronal polarity. PNAS, 103(22), 8534-8539. doi: 10.1073/pnas.0509955103. http://www.pnas.org/cgi/content/abstract/103/22/8534 


Chen, Y.-P., & Chiao, C.-C. (2014). Spatial Distribution of Excitatory Synapses on the Dendrites of Ganglion Cells in the Mouse Retina. Plos one, 9(1), e86159. doi: 10.1371/journal.pone.0086159. http://dx.doi.org/10.1371%2Fjournal.pone.0086159


Chen, Z., Peppi, M., Kujawa, S. G., & Sewell, W. F. (2009). Regulated Expression of Surface AMPA Receptors Reduces Excitotoxicity in Auditory Neurons. Journal of Neurophysiology, 00288.02009. doi: 10.1152/jn.00288.2009. http://jn.physiology.org/cgi/content/abstract/00288.2009v1 


Cheng, J. X., Scala, F., Blanco, F. A., Niu, S., Firozi, K., Keehan, L., . . . Tolias, K. F. (2020). The Rac-GEF Tiam1 Promotes Dendrite and Synapse Stabilization of Dentate Granule Cells and Restricts Hippocampal-Dependent Memory Functions. The Journal of Neuroscience, JN-RM-3271-3217. doi: 10.1523/jneurosci.3271-17.2020. https://www.jneurosci.org/content/jneuro/early/2020/12/14/JNEUROSCI.3271...


Cheng, L., Itoh, K., & Lemmon, V. (2005). L1-Mediated Branching Is Regulated by Two Ezrin-Radixin-Moesin (ERM)-Binding Sites, the RSLE Region and a Novel Juxtamembrane ERM-Binding Region. Journal of Neuroscience, 25(2), 395-403. doi. http://www.jneurosci.org/cgi/content/abstract/25/2/395


Cheng, L., Lemmon, S., & Lemmon, V. (2005). RanBPM is an L1-interacting protein that regulates L1-mediated mitogen-activated protein kinase activation. Journal of Neurochemistry, 94(4), 1102-1110. doi: doi:10.1111/j.1471-4159.2005.03254.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1471-4159.2005.03254.x 


Cheng, L., & Lemmon, V. (2004). Pathological missense mutations of neural cell adhesion molecule L1 affect neurite outgrowth and branching on an L1 substrate. Molecular and Cellular Neuroscience, 27(4), 522-530. doi. 

Cheng, T.-L., Wang, Z., Liao, Q., Zhu, Y., Zhou, W.-H., Xu, W., & Qiu, Z. (2014). MeCP2 Suppresses Nuclear MicroRNA Processing and Dendritic Growth by Regulating the DGCR8/Drosha Complex. Developmental cell, 28(5), 547-560. doi: http://dx.doi.org/10.1016/j.devcel.2014.01.032. http://www.sciencedirect.com/science/article/pii/S1534580714000732


Cheng, X., Li, Y., Huang, Y., Feng, X., Feng, G., & Xiong, Z. Q. (2010). Pulse labeling and long-term tracing of newborn neurons in the adult subgranular zone. Cell Research, 21(2), 338-349. doi. 

Cheng, Z. (2016). Vagal cardiac efferent innervation in F344 rats: Effects of chronic intermittent hypoxia. Autonomic Neuroscience: Basic and Clinical. doi: 10.1016/j.autneu.2016.10.005. http://dx.doi.org/10.1016/j.autneu.2016.10.005


Chernock, M. L., Larue, D. T., & Winer, J. A. (2004). A periodic network of neurochemical modules in the inferior colliculus. Hearing Research, 188(1-2), 12-20. doi. 

Cheung, A. F. P., Kondo, S., Abdel-Mannan, O., Chodroff, R. A., Sirey, T. M., Bluy, L. E., . . . Molnar, Z. (2009). The Subventricular Zone Is the Developmental Milestone of a 6-Layered Neocortex: Comparisons in Metatherian and Eutherian Mammals. Cerebral Cortex, bhp168. doi: 10.1093/cercor/bhp168. http://cercor.oxfordjournals.org/cgi/content/abstract/bhp168v1 


Cheung, A. F. P., Pollen, A. A., Tavare, A., DeProto, J., & Molnar, Z. (2007). Comparative aspects of cortical neurogenesis in vertebrates. Journal of Anatomy, 211(2), 164-176. doi: doi:10.1111/j.1469-7580.2007.00769.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1469-7580.2007.00769.x 


Cheung, A. W. S., Lam, J. S. Y., & Chan, S. O. (2005). Selective inhibition of ventral temporal but not dorsal nasal neurites from mouse retinal explants during contact with chondroitin sulphate. Cell and Tissue Research, 321(1), 9-19. doi. 

Cheung, K. K., Chan, W. Y., & Burnstock, G. (2005). Expression of P2X purinoceptors during rat brain development and their inhibitory role on motor axon outgrowth in neural tube explant cultures. Neuroscience, 133(4), 937-945. doi. 

Chévere-Torres, I., Kaphzan, H., Bhattacharya, A., Kang, A., Maki, J. M., Gambello, M. J., . . . Klann, E. (2011). Metabotropic glutamate receptor-dependent long-term depression is impaired due to elevated ERK signaling in the ΔRG mouse model of tuberous sclerosis complex. Neurobiology of Disease. doi. 

Chew, C., Kiley, B. J., & Sengelaub, D. R. (2018). Neuroprotective effects on the morphology of somatic motoneurons following the death of neighboring motoneurons: A role for microglia? Developmental Neurobiology, 0(ja). doi: doi:10.1002/dneu.22652. https://onlinelibrary.wiley.com/doi/abs/10.1002/dneu.22652


Chew, C., & Sengelaub, D. R. (2020). Exercise is neuroprotective on the morphology of somatic motoneurons following the death of neighboring motoneurons via androgen action at the target muscle. [https://doi.org/10.1002/dneu.22794]. Developmental Neurobiology, n/a(n/a). doi: https://doi.org/10.1002/dneu.22794. https://doi.org/10.1002/dneu.22794


Chiang, E., & Strowbridge, B. W. (2007). Diversity of Neural Signals Mediated by Multiple, Burst-Firing Mechanisms in Rat Olfactory Tubercle Neurons. Journal of Neurophysiology, 98(5), 2716-2728. doi: 10.1152/jn.00807.2007. http://jn.physiology.org/cgi/content/abstract/98/5/2716 


Chidambaram, S. B., Rathipriya, A. G., Bolla, S. R., Bhat, A., Ray, B., Mahalakshmi, A. M., . . . Sakharkar, M. K. (2019). Dendritic spines: Revisiting the physiological role. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 92, 161-193. doi: https://doi.org/10.1016/j.pnpbp.2019.01.005. http://www.sciencedirect.com/science/article/pii/S0278584618306079


Chiesa, N., Barlow, C., Wynshaw-Boris, A., Strata, P., & Tempia, F. (2000). Atm-deficient mice Purkinje cells show age-dependent defects in calcium spike bursts and calcium currents. Neuroscience, 96(3), 575-583. doi. 

Chinta, S. J., Kumar, M. J., Hsu, M., Rajagopalan, S., Kaur, D., Rane, A., . . . Andersen, J. K. (2007). Inducible Alterations of Glutathione Levels in Adult Dopaminergic Midbrain Neurons Result in Nigrostriatal Degeneration. Journal of Neuroscience, 27(51), 13997-14006. doi: 10.1523/jneurosci.3885-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/51/13997 


Chiola, S., Napan, K. L., Wang, Y., Lazarenko, R. M., Armstrong, C. J., Cui, J., & Shcheglovitov, A. (2021). Defective AMPA-mediated synaptic transmission and morphology in human neurons with hemizygous SHANK3 deletion engrafted in mouse prefrontal cortex. Molecular Psychiatry. doi: 10.1038/s41380-021-01023-2. https://doi.org/10.1038/s41380-021-01023-2


Chirila, F. V., Rowland, K. C., Thompson, J. M., & Spirou, G. A. (2007). Development of gerbil medial superior olive: integration of temporally delayed excitation and inhibition at physiological temperature. Journal of Physiology, 584(1), 167-190. doi: 10.1113/jphysiol.2007.137976. http://jp.physoc.org/cgi/content/abstract/584/1/167 


Chitravanshi, V. C., Bhatt, S., & Sapru, H. N. (2009). Microinjections of alpha-melanocyte stimulating hormone into the nucleus ambiguus of the rat elicit vagally mediated bradycardia. Journal of Physiology - Regulatory, Integrative and Comparative Physiology, 90978.92008. doi: 10.1152/ajpregu.90978.2008. http://ajpregu.physiology.org/cgi/content/abstract/90978.2008v1 


Chitravanshi, V. C., Bhatt, S., & Sapru, H. N. (2009). Microinjections of α-melanocyte stimulating hormone into the nucleus ambiguus of the rat elicit vagally mediated bradycardia. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 296(5), R1402–R1411-R1402–R1411. doi. 

Chitravanshi, V. C., Kawabe, K., & Sapru, H. N. (2016). Stimulation of the hypothalamic arcuate nucleus increases brown adipose tissue nerve activity via hypothalamic paraventricular and dorsomedial nuclei. [10.1152/ajpheart.00176.2016]. American Journal of Physiology - Heart and Circulatory Physiology. doi. http://ajpheart.physiology.org/content/early/2016/07/06/ajpheart.00176.2...


Chittajallu, R., Craig, M. T., McFarland, A., Yuan, X., Gerfen, S., Tricoire, L., . . . Liang, B. J. (2013). Dual origins of functionally distinct O-LM interneurons revealed by differential 5-HT3AR expression. Nature Neuroscience. doi. http://www.nature.com/neuro/journal/vaop/ncurrent/full/nn.3538.html


Chiu, K. B., Lee, K. M., Robillard, K. N., & MacLean, A. G. (2019). A Method to Investigate Astrocyte and Microglial Morphological Changes in the Aging Brain of the Rhesus Macaque. In B. Di Benedetto (Ed.), Astrocytes: Methods and Protocols (pp. 265-276). New York, NY: Springer New York.

Chklovskii, D. B., Vitaladevuni, S., & Scheffer, L. K. (2010). Semi-automated reconstruction of neural circuits using electron microscopy. Current Opinion in Neurobiology, 20(5), 667-675. doi. 

Chmielewski, N. N., Caressi, C., Giedzinski, E., Parihar, V. K., & Limoli, C. L. (2016). Contrasting the effects of proton irradiation on dendritic complexity of subiculum neurons in wild type and MCAT mice. Environmental and Molecular Mutagenesis, n/a-n/a. doi: 10.1002/em.22006. http://dx.doi.org/10.1002/em.22006


Cho, Y. T., Ernst, M., & Fudge, J. L. (2013). Cortico–Amygdala–Striatal Circuits Are Organized as Hierarchical Subsystems through the Primate Amygdala. Journal of Neuroscience, 33(35), 14017-14030. doi: 10.1523/jneurosci.0170-13.2013. http://www.jneurosci.org/content/33/35/14017.abstract


Cho, Y. T., & Fudge, J. L. (2010). Heterogeneous dopamine populations project to specific subregions of the primate amygdala. Neuroscience, 165(4), 1501-1518. doi. 

Chocyk, A., Bobula, B., Dudys, D., Przyborowska, A., Majcher-Maślanka, I., Hess, G., & Wędzony, K. (2013). Early-life stress affects the structural and functional plasticity of the medial prefrontal cortex in adolescent rats. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12208. http://dx.doi.org/10.1111/ejn.12208


Choi, D.-J., Eun, J.-H., Kim, B. G., Jou, I., Park, S. M., & Joe, E.-H. (2017). AParkinson's disease gene, DJ-1, repairs brain injury through Sox9 stabilization and astrogliosis. Glia, n/a-n/a. doi: 10.1002/glia.23258. http://dx.doi.org/10.1002/glia.23258


Choi, E. Y., Tanimura, Y., Vage, P. R., Yates, E. H., & Haber, S. N. (2016). Convergence of prefrontal and parietal anatomical projections in a connectional hub in the striatum. Neuroimage. doi: http://dx.doi.org/10.1016/j.neuroimage.2016.09.037. http://www.sciencedirect.com/science/article/pii/S1053811916305146


Choi, J. K., Jenkins, B. G., Carreras, I., Kaymakcalan, S., Cormier, K., Kowall, N. W., & Dedeoglu, A. (2010). Anti-inflammatory treatment in AD mice protects against neuronal pathology. Experimental Neurology, 223(2), 377-384. doi. 

Choi, J. Y., Cui, Y., Chowdhury, S. T., & Kim, B. G. (2017). High-mobility group box-1 as an autocrine trophic factor in white matter stroke. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1702035114. http://www.pnas.org/content/early/2017/05/31/1702035114.abstract


Choi, J. Y., Kang, Y. M., Kim, J. H., Kim, J.-H., Lee, S. J., & Kim, B. G. (2014). Role of Toll-like receptor 2 in ischemic demyelination and oligodendrocyte death. Neurobiology of Aging, (0). doi: http://dx.doi.org/10.1016/j.neurobiolaging.2014.01.146. http://www.sciencedirect.com/science/article/pii/S0197458014001687


Cholanian, M., Krajewski-Hall, S. J., Levine, R. B., McMullen, N. T., & Rance, N. E. (2014). Electrophysiology of Arcuate Neurokinin B Neurons in Female Tac2-EGFP Transgenic Mice. Endocrinology, 0(0), en.2014-1065. doi: doi:10.1210/en.2014-1065. http://press.endocrine.org/doi/abs/10.1210/en.2014-1065


Cholanian, M., Krajewski-Hall, S. J., McMullen, N. T., & Rance, N. E. (2015). Oestradiol reduces the dendritic spine density of KNDy neurones in the arcuate nucleus of ovariectomized Tac2-EGFP transgenic mice. Journal of Neuroendocrinology, n/a-n/a. doi: 10.1111/jne.12263. http://dx.doi.org/10.1111/jne.12263


Chomsung, R. D., Petry, H. M., & Bickford, M. E. (2008). Ultrastructural examination of diffuse and specific tectopulvinar projections in the tree shrew. Journal of Comparative Neurology, 510(1), 24-46. doi. 

Chomsung, R. D., Wei, H., Day-Brown, J. D., Petry, H. M., & Bickford, M. E. (2010). Synaptic organization of connections between the temporal cortex and pulvinar nucleus of the tree shrew. Cerebral Cortex, 20(4), 997-1011. doi. 

Chong, C. H., Li, Q., Mak, P. H. S., Ng, C. C. P., Leung, E. H. W., Tan, V. H., . . . Chan, S. Y. (2019). Lrrc7 mutant mice model developmental emotional dysregulation that can be alleviated by mGluR5 allosteric modulation. Translational Psychiatry, 9(1), 244. doi: 10.1038/s41398-019-0580-9. https://doi.org/10.1038/s41398-019-0580-9


Chorev, E., & Brecht, M. (2012). In vivo dual intra and extracellular recordings suggest bi-directional coupling between CA1 pyramidal neurons. Journal of Neurophysiology. doi: 10.1152/jn.01115.2011. http://jn.physiology.org/content/early/2012/06/13/jn.01115.2011.abstract


Chowdhury, S. S., Lecomte, V., Erlich, J. H., Maloney, C. A., & Morris, M. J. (2016). Paternal High Fat Diet in Rats Leads to Renal Accumulation of Lipid and Tubular Changes in Adult Offspring. Nutrients, 8(9), 521. doi. http://www.mdpi.com/2072-6643/8/9/521/htm


Chowdhury, T., Barbarich-Marsteller, N., Chan, T., & Aoki, C. (2013). Activity-based anorexia has differential effects on apical dendritic branching in dorsal and ventral hippocampal CA1. Brain Structure and Function, 1-11. doi: 10.1007/s00429-013-0612-9. http://dx.doi.org/10.1007/s00429-013-0612-9


Chowdhury, T. G., Jimenez, J. C., Bomar, J. M., Cruz-Martin, A., Cantle, J. P., & Portera-Cailliau, C. (2010). Fate of Cajal–Retzius neurons in the postnatal mouse neocortex. Frontiers in Neuroanatomy, 4. doi. 

Chowdhury, T. G., Ríos, M. B., Chan, T. E., Barbarich-Marsteller, N. C., & Aoki, C. (2014). Activity-based anorexia during adolescence disrupts normal development of the CA1 pyramidal cells in the ventral hippocampus of female rats. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22320. http://dx.doi.org/10.1002/hipo.22320


Choy, J. M. C., Suzuki, N., Shima, Y., Budisantoso, T., Nelson, S. B., & Bekkers, J. M. (2015). Optogenetic Mapping of Intracortical Circuits Originating from Semilunar Cells in the Piriform Cortex. Cerebral Cortex. doi: 10.1093/cercor/bhv258. http://cercor.oxfordjournals.org/content/early/2015/10/25/cercor.bhv258....


Christensen, A., Dewing, P., & Micevych, P. (2011). Membrane-Initiated Estradiol Signaling Induces Spinogenesis Required for Female Sexual Receptivity. Journal of Neuroscience, 31(48), 17583-17589. doi: 10.1523/jneurosci.3030-11.2011. http://www.jneurosci.org/content/31/48/17583.abstract


Christensen-Dalsgaard, J., Brandt, C., Willis, K. L., Christensen, C. B., Ketten, D., Edds-Walton, P., . . . Carr, C. E. (2012). Specialization for underwater hearing by the tympanic middle ear of the turtle, Trachemys scripta elegans. Proceedings of the Royal Society B: Biological Sciences. doi: 10.1098/rspb.2012.0290. http://rspb.royalsocietypublishing.org/content/early/2012/03/16/rspb.201...


Christensen-Dalsgaard, J., Tang, Y., & Carr, C. E. (2011). Binaural processing by the gecko auditory periphery. Journal of Neurophysiology, 105(5), 1992-2004. doi: 10.1152/jn.00004.2011. http://jn.physiology.org/content/105/5/1992.abstract


Christian, K. M., Miracle, A. D., Wellman, C. L., & Nakazawa, K. (2011). Chronic stress-induced hippocampal dendritic retraction requires CA3 NMDA receptors. Neuroscience, 174, 26-36. doi. 

Christianson, J. A., Riekhof, J. T., & Wright, D. E. (2003). Restorative effects of neurotrophin treatment on diabetes-induced cutaneous axon loss in mice. Experimental Neurology, 179(2), 188-199. doi. 

Christophe, E., Roebuck, A., Staiger, J. F., Lavery, D. J., Charpak, S., & Audinat, E. (2002). Two Types of Nicotinic Receptors Mediate an Excitation of Neocortical Layer I Interneurons. Journal of Neurophysiology, 88(3), 1318-1327. doi. http://jn.physiology.org/cgi/content/abstract/88/3/1318 


Chu, H.-Y., McIver, E. L., Kovaleski, R. F., Atherton, J. F., & Bevan, M. D. (2017). Loss of Hyperdirect Pathway Cortico-Subthalamic Inputs Following Degeneration of Midbrain Dopamine Neurons. Neuron, 95(6), 1306-1318.e1305. doi: https://doi.org/10.1016/j.neuron.2017.08.038. http://www.sciencedirect.com/science/article/pii/S089662731730781X


Chu, P., Abraham, R., Budhu, K., Khan, U., De Marco Garcia, N., & Brumberg, J. C. (2018). The Impact of Perineuronal Net Digestion Using Chondroitinase ABC on the Intrinsic Physiology of Cortical Neurons. Neuroscience. doi: https://doi.org/10.1016/j.neuroscience.2018.07.004. http://www.sciencedirect.com/science/article/pii/S030645221830472X


Chu, Y.-F., Yen, C.-T., & Lee, L.-J. (2012). Neonatal whisker clipping alters behavior, neuronal structure and neural activity in adult rats. Behavioural Brain Research, (0). doi: 10.1016/j.bbr.2012.10.022. http://www.sciencedirect.com/science/article/pii/S0166432812006729


Chu, Z., Galarreta, M., & Hestrin, S. (2003). Synaptic Interactions of Late-Spiking Neocortical Neurons in Layer 1. Journal of Neuroscience, 23, 96-102. doi. 

Chung, B. Y. T., Bignell, W., Jacklin, D. L., Winters, B. D., & Bailey, C. D. C. (2016). Postsynaptic nicotinic acetylcholine receptors facilitate excitation of developing CA1 pyramidal neurons. [10.1152/jn.00370.2016]. Journal of Neurophysiology. doi. http://jn.physiology.org/content/early/2016/07/29/jn.00370.2016.abstract


Chung, C. G., Kwon, M. J., Jeon, K. H., Hyeon, D. Y., Han, M. H., Park, J. H., . . . Lee, S. B. (2017). Golgi Outpost Synthesis Impaired by Toxic Polyglutamine Proteins Contributes to Dendritic Pathology in Neurons. Cell Reports, 20(2), 356-369. doi: https://doi.org/10.1016/j.celrep.2017.06.059. http://www.sciencedirect.com/science/article/pii/S2211124717308902


Chung, H. S., Louis, J. M., & Eaton, W. A. (2009). Experimental determination of upper bound for transition path times in protein folding from single-molecule photon-by-photon trajectories. Proceedings of the National Academy of Sciences, 106(29), 11837-11844. doi: 10.1073/pnas.0901178106. http://www.pnas.org/content/106/29/11837.abstract 


Chung, J. R., Sung, C., Mayerich, D., Kwon, J., Miller, D. E., Huffman, T., . . . Choe, Y. (2011). Multiscale exploration of mouse brain microstructures using the knife-edge scanning microscope brain atlas. Frontiers in neuroinformatics, 5. doi. 

Chung, S., Picones, A., & Korenbrot, J. I. (2003). Developmental Maturation of Passive Electrical Properties of Retinal Ganglion Cells. Investigative Ophtalmology and Visual Science, 44(5), 1656-1656. doi. 

Churchill, J., Tharp, J., Wellman, C., Sengelaub, D., & Garraghty, P. (2004). Morphological correlates of injury-induced reorganization in primate somatosensory cortex. BMC Neuroscience, 5(1), 43. doi. http://www.biomedcentral.com/1471-2202/5/43 


Ciaramitaro, P., Poglio, F., Tavella, A., Rota, E., Prolasso, I., Isoardo, G., . . . Cocito, D. (2004). Phrenic nerve conduction study in CIDP. Journal of the Peripheral Nervous System, 9(2), 107-107. doi: doi:10.1111/j.1085-9489.2004.009209j.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Cicchetti, F., Gould, P. V., & Parent, A. (1996). Sparing of striatal neurons coexpressing calretinin and substance P (NK1) receptor in Huntington's disease. Brain Research, 730(1-2), 232-237. doi. 

Cicchetti, F., & Parent, A. (1996). Striatal interneurons in Huntington's disease: Selective increase in the density of calretinin-immunoreactive medium-sized neurons. Movement Disorders, 11(6), 619-626. doi. 

Cicchetti, F., Saporta, S., Hauser, R. A., Parent, M., Saint-Pierre, M., Sanberg, P. R., . . . Freeman, T. B. (2009). Neural transplants in patients with Huntington's disease undergo disease-like neuronal degeneration. Proceedings of the National Academy of Sciences, 106(30), 12483-12488. doi: 10.1073/pnas.0904239106. http://www.pnas.org/content/106/30/12483.abstract 


Ciceri, G., Dehorter, N., Sols, I., Huang, J. Z., Maravall, M., & Marín, O. (2013). Lineage-specific laminar organization of cortical GABAergic interneurons. Nature Neuroscience. doi. http://www.nature.com/neuro/journal/vaop/ncurrent/full/nn.3485.html


Cicvaric, A., Yang, J., Bulat, T., Zambon, A., Dominguez-Rodriguez, M., Kühn, R., . . . Monje, F. J. (2018). Enhanced synaptic plasticity and spatial memory in female but not male FLRT2-haplodeficient mice. Scientific Reports, 8(1), 3703. doi: 10.1038/s41598-018-22030-4. https://doi.org/10.1038/s41598-018-22030-4


Cid, E., Santos-Ledo, A., Parrilla-Monge, M., Lillo, C., Arévalo, R., Lara, J. M., . . . Velasco, A. (2010). Prox1 expression in rod precursors and Müller cells. Experimental Eye Research, 90(2), 267-276. doi. 

Cina, C., & Hochman, S. (2000). Diffuse distribution of sulforhodamine-labeled neurons during serotonin-evoked locomotion in the neonatal rat thoracolumbar spinal cord. Journal of Comparative Neurology, 423(4), 590-602. doi. 

Ciocchi, S., Herry, C., Grenier, F., Wolff, S. B. E., Letzkus, J. J., Vlachos, I., . . . others. (2010). Encoding of conditioned fear in central amygdala inhibitory circuits. Nature, 468(7321), 277-282. doi. 

Cipolloni, P. B., Kimerer, L., Weintraub, N. D., Smith, D. V., & Keller, A. (1998). Distribution of inhibitory synapses on the somata of pyramidal neurons in cat motor cortex. Somatosensory and Motor Research, 15(4), 276-286. doi. 

Cisbani, G., Drouin-Ouellet, J., Gibrat, C., Saint-Pierre, M., Lagacé, M., Badrinarayanan, S., . . . Cicchetti, F. (2015). Cystamine/cysteamine rescue the dopaminergic system and show neurorestorative properties in an animal model of Parkinson’s disease. Neurobiology of Disease. doi: http://dx.doi.org/10.1016/j.nbd.2015.07.012. http://www.sciencedirect.com/science/article/pii/S0969996115300152


Clancy, B., Silva-Filho, M., & Friedlander, M. J. (2001). Structure and projections of white matter neurons in the postnatal rat visual cortex. Journal of Comparative Neurology, 434(2), 233-252. doi. 

Clancy, B., Teague-Ross, T. J., & Nagarajan, R. (2009). Cross-species analyses of the cortical GABAergic and subplate neural populations. Frontiers in Neuroanatomy, 3. doi. 

Clark, C. G., Hasser, E. M., Kunze, D. L., Katz, D. M., & Kline, D. D. (2011). Endogenous Brain-Derived Neurotrophic Factor in the Nucleus Tractus Solitarius Tonically Regulates Synaptic and Autonomic Function. Journal of Neuroscience, 31(34), 12318-12329. doi: 10.1523/jneurosci.0746-11.2011. http://www.jneurosci.org/content/31/34/12318.abstract


Clark, D. P. Q., Perreau, V. M., Shultz, S. R., Brady, R. D., Lei, E., Dixit, S., . . . Boon, W. C. (2019). Inflammation in Traumatic Brain Injury: Roles for Toxic A1 Astrocytes and Microglial–Astrocytic Crosstalk. [journal article]. Neurochemical Research. doi: 10.1007/s11064-019-02721-8. https://doi.org/10.1007/s11064-019-02721-8


Clark, R. M., Blizzard, C. A., Young, K. M., King, A. E., & Dickson, T. C. (2017). Calretinin and Neuropeptide Y interneurons are differentially altered in the motor cortex of the SOD1G93A mouse model of ALS. [Article]. Scientific Reports, 7, 44461. doi: 10.1038/srep44461. http://dx.doi.org/10.1038/srep44461


Clark, T. A., Sullender, C., Kazmi, S. M., Speetles, B. L., Williamson, M. R., Palmberg, D. M., . . . Jones, T. A. (2019). Artery targeted photothrombosis widens the vascular penumbra, instigates peri-infarct neovascularization and models forelimb impairments. Scientific Reports, 9(1), 2323. doi: 10.1038/s41598-019-39092-7. https://doi.org/10.1038/s41598-019-39092-7


Clarke, J., Mala, H., Windle, V., Chernenko, G., & Corbett, D. (2009). The effects of repeated rehabilitation “tune-ups” on functional recovery after focal ischemia in rats. Neurorehabilitation and neural repair, 23(9), 886-894. doi. 

Clarkson, C., Juíz, J. M., & Merchán, M. A. (2010). Transient down-regulation of sound-induced c-Fos protein expression in the inferior colliculus after ablation of the auditory cortex. Frontiers in Neuroanatomy, 4. doi. 

Clarkson, C., Juíz, J. M., & Merchán, M. Á. (2010). Long-term regulation in calretinin staining in the rat inferior colliculus after unilateral auditory cortical ablation. Journal of Comparative Neurology, 518(20), 4261-4276. doi. 

Claus, C. P., Tsuru-Aoyagi, K., Adwanikar, H., Walker, B., Whetstone, W., & Noble-Haeusslein, L. J. (2010). Age is a determinant of leukocyte infiltration and loss of cortical volume after traumatic brain injury. Developmental Neuroscience, 32(5-6), 454-465. doi. 

Clause, A., Kim, G., Sonntag, M., Weisz, Catherine J. C., Vetter, Douglas E., Rűbsamen, R., & Kandler, K. (2014). The Precise Temporal Pattern of Prehearing Spontaneous Activity Is Necessary for Tonotopic Map Refinement. Neuron, 82(4), 822-835. doi: 10.1016/j.neuron.2014.04.001. http://www.cell.com/neuron/abstract/S0896-6273(14)00291-8

Clemens, A. M., Wang, H., & Brecht, M. (2020). The lateral septum mediates kinship behavior in the rat. Nature Communications, 11(1), 3161. doi: 10.1038/s41467-020-16489-x. https://doi.org/10.1038/s41467-020-16489-x


Clemens, S., Sawchuk, M. A., & Hochman, S. (2005). Reversal of the circadian expression of tyrosine-hydroxylase but not nitric oxide synthase levels in the spinal cord of dopamine D3 receptor knockout mice. Neuroscience, 133(2), 353-357. doi. 

Clement, James P., Aceti, M., Creson, Thomas K., Ozkan, Emin D., Shi, Y., Reish, Nicholas J., . . . Rumbaugh, G. (2012). Pathogenic SYNGAP1 Mutations Impair Cognitive Development by Disrupting Maturation of Dendritic Spine Synapses. Cell, 151(4), 709-723. doi: 10.1016/j.cell.2012.08.045. http://www.sciencedirect.com/science/article/pii/S0092867412012408


Clemente, D., Porteros, A., Arenzana, F. J., Aijon, J., Parrilla, M., Santos-Ledo, A., & Arevalo, R. (2008). Characterization of NADPH-diaphorase-positive glial cells of the tench optic nerve after axotomy. Archives Italiennes de Biologie, 146(1), 35-52. doi. 

Clements, I. P., Kim, Y., English, A. W., Lu, X., Chung, A., & Bellamkonda, R. V. (2009). Thin-film enhanced nerve guidance channels for peripheral nerve repair. Biomaterials, 30(23), 3834-3846. doi. 

Clemo, H. R., Allman, B. L., Donlan, M. A., & Meredith, M. A. (2007). Sensory and multisensory representations within the cat rostral suprasylvian cortex. Journal of Comparative Neurology, 503(1), 110-127. doi. 

Clemo, H. R., Lomber, S. G., & Meredith, M. A. (2014). Synaptic Basis for Cross-modal Plasticity: Enhanced Supragranular Dendritic Spine Density in Anterior Ectosylvian Auditory Cortex of the Early Deaf Cat. Cerebral Cortex. doi: 10.1093/cercor/bhu225. http://cercor.oxfordjournals.org/content/early/2014/10/01/cercor.bhu225....


Clemo, H. R., Lomber, S. G., & Meredith, M. A. (2017). Synaptic distribution and plasticity in primary auditory cortex (A1) exhibits laminar and cell-specific changes in the deaf. Hearing Research. doi: https://doi.org/10.1016/j.heares.2017.06.009. http://www.sciencedirect.com/science/article/pii/S037859551730165X


Cliburn, R. A., Dunn, A. R., Stout, K. A., Hoffman, C. A., Lohr, K. M., Bernstein, A. I., . . . Miller, G. W. (2016). Immunochemical localization of vesicular monoamine transporter 2 (VMAT2) in mouse brain. Journal of Chemical Neuroanatomy. doi: http://dx.doi.org/10.1016/j.jchemneu.2016.11.003. http://www.sciencedirect.com/science/article/pii/S0891061816300953


Codd, L. N., Blackmore, D. G., Vukovic, J., & Bartlett, P. F. (2020). Exercise reverses learning deficits induced by hippocampal injury by promoting neurogenesis. Scientific Reports, 10(1), 19269. doi: 10.1038/s41598-020-76176-1. https://doi.org/10.1038/s41598-020-76176-1


Coddington, Luke T., Rudolph, S., Vande Lune, P., Overstreet-Wadiche, L., & Wadiche, Jacques I. (2013). Spillover-Mediated Feedforward Inhibition Functionally Segregates Interneuron Activity. Neuron. doi. http://linkinghub.elsevier.com/retrieve/pii/S0896627313003218


Coe, C. L., Kramer, M., Czéh, B., Gould, E., Reeves, A. J., Kirschbaum, C., & Fuchs, E. (2003). Prenatal stress diminishes neurogenesis in the dentate gyrus of juvenile rhesus monkeys. Biological Psychiatry, 54(10), 1025-1034. doi. 

Cohen, A. S., Pfister, B. J., Schwarzbach, E., Sean Grady, M., Goforth, P. B., & Satin, L. S. (2007). Injury-induced alterations in CNS electrophysiology. Progress in Brain Research, 161, 143-169. doi. 

Cohen, J. D., & Castro-Alamancos, M. A. (2007). Early Sensory Pathways for Detection of Fearful Conditioned Stimuli: Tectal and Thalamic Relays. Journal of Neuroscience, 27(29), 7762-7776. doi: 10.1523/jneurosci.1124-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/29/7762 


Cohen, J. D., Hirata, A., & Castro-Alamancos, M. A. (2008). Vibrissa Sensation in Superior Colliculus: Wide-Field Sensitivity and State-Dependent Cortical Feedback. Journal of Neuroscience, 28(44), 11205-11220. doi: 10.1523/jneurosci.2999-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/44/11205 


Cohen, S., Gabel, H. W., Hemberg, M., Hutchinson, A. N., Sadacca, L. A., Ebert, D. H., . . . others. (2011). Genome-Wide Activity-Dependent MeCP2 Phosphorylation Regulates Nervous System Development and Function. Neuron, 72(1), 72-85. doi. 

Cohen, S. M., Suutari, B., He, X., Wang, Y., Sanchez, S., Tirko, N. N., . . . Ma, H. (2018). Calmodulin shuttling mediates cytonuclear signaling to trigger experience-dependent transcription and memory. Nature Communications, 9(1), 2451. doi: 10.1038/s41467-018-04705-8. https://doi.org/10.1038/s41467-018-04705-8


Coimbra, J. P., Trévia, N., Videira Marceliano, M. L., da Silveira Andrade-Da-Costa, B. L., Picanço-Diniz, C. W., & Yamada, E. S. (2009). Number and distribution of neurons in the retinal ganglion cell layer in relation to foraging behaviors of tyrant flycatchers. Journal of Comparative Neurology, 514(1), 66-73. doi. 

Colak, D., Mori, T., Brill, M. S., Pfeifer, A., Falk, S., Deng, C., . . . Gotz, M. (2008). Adult Neurogenesis Requires Smad4-Mediated Bone Morphogenic Protein Signaling in Stem Cells. Journal of Neuroscience, 28(2), 434-446. doi: 10.1523/jneurosci.4374-07.2008. http://www.jneurosci.org/cgi/content/abstract/28/2/434 


Colavito, V., Tognoli, C., Tiberio, L., Bentivoglio, M., Grassi-Zucconi, G., & Bertini, G. (2011). Neonatal treatment with clomipramine induces morphological and cellular changes in the adult rat brain. Italian Journal of Anatomy and Embryology, 116(2), 47-47. doi. 

Colbert, C. M., & Pan, E. (2002). Ion channel properties underlying axonal action potential initiation in pyramidal neurons. Nature Neuroscience, 5, 533-538. doi. 

Colciaghi, F., Finardi, A., Nobili, P., Locatelli, D., Spigolon, G., & Battaglia, G. S. (2014). Progressive Brain Damage, Synaptic Reorganization and NMDA Activation in a Model of Epileptogenic Cortical Dysplasia. PLoS ONE, 9(2), e89898. doi: 10.1371/journal.pone.0089898. http://dx.doi.org/10.1371%2Fjournal.pone.0089898


Colciaghi, F., Nobili, P., Cipelletti, B., Cagnoli, C., Zambon, S., Locatelli, D., . . . Battaglia, G. S. (2019). Targeting PSD95-nNOS interaction by Tat-N-dimer peptide during status epilepticus is neuroprotective in MAM-pilocarpine rat model. Neuropharmacology, 153, 82-97. doi: https://doi.org/10.1016/j.neuropharm.2019.04.028. http://www.sciencedirect.com/science/article/pii/S0028390819301431


Coldren, K. M., Brown, R., Hasser, E. M., & Heesch, C. M. (2015). Relaxin increases sympathetic nerve activity and activates spinally-projecting neurons in the paraventricular nucleus of nonpregnant, but not pregnant, rats. [10.1152/ajpregu.00186.2015]. American Journal of Physiology - Regulatory, Integrative and Comparative Physiology. doi. http://ajpregu.physiology.org/content/early/2015/09/23/ajpregu.00186.201...


Cole, C. J., Mercaldo, V., Restivo, L., Yiu, A. P., Sekeres, M. J., Han, J.-H., . . . Josselyn, S. A. (2012). MEF2 negatively regulates learning-induced structural plasticity and memory formation. [10.1038/nn.3189]. Nature Neuroscience, advance online publication. doi: http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.3189.html#suppl.... http://dx.doi.org/10.1038/nn.3189


Coletta, S., Zeraati, R., Nasr, K., Preston-Ferrer, P., & Burgalossi, A. (2018). Interspike Interval Analysis and Spikelets in Presubicular Head-Direction Cells. Journal of Neurophysiology, 0(0), null. doi: 10.1152/jn.00019.2018. https://www.physiology.org/doi/abs/10.1152/jn.00019.2018


Colicos, M. A., Firth, S. I., Bosze, J., Goldstein, J., & Feller, M. B. (2004). Emergence of Realistic Retinal Networks in Culture Promoted by the Superior Colliculus. Developmental Neuroscience, 26(5-6), 406-416. doi. http://www.karger.com/DOI/10.1159/000082283 


Colin-Le Brun, I., Ferrand, N., Caillard, O., Tosetti, P., Ben-Ari, Y., & Gaiarsa, J.-L. (2004). Spontaneous synaptic activity is required for the formation of functional GABAergic synapses in the developing rat hippocampus. Journal of Physiology, 559(1), 129-139. doi: 10.1113/jphysiol.2004.065060. http://jp.physoc.org/cgi/content/abstract/559/1/129 


Collier, T. J., O'Malley, J., Rademacher, D. J., Stancati, J. A., Sisson, K. A., Sortwell, C. E., . . . Steece-Collier, K. (2015). Interrogating the aged striatum: Robust survival of grafted dopamine neurons in aging rats produces inferior behavioral recovery and evidence of impaired integration. Neurobiology of Disease, (0). doi: http://dx.doi.org/10.1016/j.nbd.2015.03.005. http://www.sciencedirect.com/science/article/pii/S0969996115000674


Collin, C., Vicario-Abejon, C., Rubio, M. E., Wenthold, R. J., McKay, R. D. G., & Segal, M. (2001). Neurotrophins act at presynaptic terminals to activate synapses among cultured hippocampal neurons. European Journal of Neuroscience, 13(7), 1273. doi. 

Collins, D. P., Anastasiades, P. G., Marlin, J. J., & Carter, A. G. (2018). Reciprocal Circuits Linking the Prefrontal Cortex with Dorsal and Ventral Thalamic Nuclei. Neuron. doi: https://doi.org/10.1016/j.neuron.2018.03.024. https://www.sciencedirect.com/science/article/pii/S0896627318302307


Combs, H. L., Jones, T. A., Kozlowski, D. A., & Adkins, D. L. (2015). Combinatorial Motor Training Results In Functional Reorganization Of Remaining Motor Cortex After Controlled Cortical Impact In Rats. Journal of Neurotrauma. doi: 10.1089/neu.2015.4136. http://dx.doi.org/10.1089/neu.2015.4136


Comi, A. M., Weisz, C. J. C., Highet, B. H., Skolasky, R. L., Pardo, C. A., & Hess, E. J. (2005). Sturge-Weber syndrome: altered blood vessel fibronectin expression and morphology. Journal of Child Neurology, 20(7), 572-577. doi. 

Conde, D., & Komisaruk, B. R. (2012). A neuroanatomical correlate of sensorimotor recovery in response to repeated vaginocervical stimulation in rats. Frontiers in Physiology, 3. doi. 

Conde-Sousa, E., Szücs, P., Peng, H., & Aguiar, P. (2016). N3DFix: an Algorithm for Automatic Removal of Swelling Artifacts in Neuronal Reconstructions. [journal article]. Neuroinformatics, 1-8. doi: 10.1007/s12021-016-9308-7. http://dx.doi.org/10.1007/s12021-016-9308-7


Conforti, F. L., Muglia, M., Mazzei, R., Valentino, P., Patitucci, A., Bono, F., . . . others. (2004). A splice-junction mutation in SBF2 gene causes autosomal recessive charcot-marie-tooth disease (CMT4B2) in a family from southern italy. Journal of the Peripheral Nervous System, 9(2), 124-124. doi. 

Connelly, C. J., Ryugo, D. K., & Muniak, M. A. (2016). The effect of progressive hearing loss on the morphology of endbulbs of Held and bushy cells. Hearing Research. doi: http://dx.doi.org/10.1016/j.heares.2016.07.004. http://www.sciencedirect.com/science/article/pii/S0378595516301472


Connelly, W. M., Crunelli, V., & Errington, A. C. (2015). The Global Spike: Conserved Dendritic Properties Enable Unique Ca2+ Spike Generation in Low-Threshold Spiking Neurons. The Journal of Neuroscience, 35(47), 15505-15522. doi. http://www.jneurosci.org/content/35/47/15505.full


Conner, K. R., Forbes, M. E., Lee, W. H., Lee, Y. W., & Riddle, D. (2011). AT1 receptor antagonism does not influence early radiation-induced changes in microglial activation or neurogenesis in the normal rat brain. Radiation Research. doi. 

Conner, K. R., Payne, V. S., Forbes, M. E., Robbins, M. E., & Riddle, D. R. (2010). Effects of the AT1 receptor antagonist L-158,809 on microglia and neurogenesis after fractionated whole-brain irradiation. Radiation Research, 173(1), 49-49. doi. 

Connolly, J. D., Hashemi-Nezhad, M., & Lyon, D. C. (2012). Parallel feedback pathways in visual cortex of cats revealed through a modified rabies virus. Journal of Comparative Neurology, 520(5), 988-1004. doi: 10.1002/cne.22748. http://dx.doi.org/10.1002/cne.22748


Connor, B., Kozlowski, D. A., Schallert, T., Tillerson, J. L., Davidson, B. L., & Bohn, M. C. (1999). Differential effects of glial cell line-derived neurotrophic factor (GDNF) in the striatum and substantia nigra of the aged Parkinsonian rat. Gene Therapy, 6, 1936-1951. doi. 

Conte, D., Legg, E. D., McCourt, A. C., Silajdzic, E., Nagy, G. G., & Maxwell, D. J. (2005). Transmitter content, origins and connections of axons in the spinal cord that possess the serotonin (5-hydroxytryptamine) 3 receptor. Neuroscience, 134(1), 165-173. doi. 

Contestabile, A., Colangiulo, R., Lucchini, M., Gindrat, A. D., Hamadjida, A., Kaeser, M., . . . Schmidlin, E. (2018). Asymmetric and distant effects of a unilateral lesion of the primary motor cortex on the bilateral supplementary motor areas in adult macaque monkeys. [10.1523/JNEUROSCI.0904-18.2018]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2018/10/24/JNEUROSCI.0904-18.2018...


Conti, G., Baron, P. L., Scarpini, E., Bresolin, E., & De Pol, A. (2004). Pro-inflammatory cytokines induce differentiation in cultured schwann cells. Journal of the Peripheral Nervous System, 9(2), 106-106. doi: doi:10.1111/j.1085-9489.2004.009209g.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Conti, V., Pazzaglia, C., Aprile, I., Caliandro, P., Tonali, P., & Padua, L. (2004). The self-care approach as a new tool in modern health care. carpal tunnel syndrome, an ideal model to evaluate the efficacy of an instructional video. Journal of the Peripheral Nervous System, 9(2), 110-110. doi. 

Cook, P. M., Prusky, G., Ramoa, A. S., & others. (1999). The role of spontaneous retinal activity before eye opening in the maturation of form and function in the retinogeniculate pathway of the ferret. Visual Neuroscience, 16(3), 491-501. doi. 

Cook, S. C., & Wellman, C. L. (2004). Chronic stress alters dendritic morphology in rat medial prefrontal cortex. Journal of Neurobiology, 60(2), 236-248. doi. 

Cooke, B. M., Stokas, M. R., & Woolley, C. S. (2007). Morphological sex differences and laterality in the prepubertal medial amygdala. Journal of Comparative Neurology, 501(6), 904-915. doi. 

Cooke, B. M., & Woolley, C. S. (2009). Effects of prepubertal gonadectomy on a male-typical behavior and excitatory synaptic transmission in the amygdala. Developmental Neurobiology, 69(2-3), 141-152. doi. 

Coolen, L. M., Olivier, B., Peters, H. J. P. W., & Veening, J. G. (1997). Demonstration of Ejaculation-Induced Neural Activity in the Male Rat Brain Using 5-HT< sub> 1A</sub> Agonist 8-OH-DPAT. Physiology and Behavior, 62(4), 881-891. doi. 

Coomber, B., Edwards, D., Jones, S., Shackleton, T., Goldschmidt, J., Wallace, M., & Palmer, A. (2011). Frontiers: Cortical Inactivation by Cooling in Small Animals. Frontiers in Systems Neuroscience, 5. doi. 

Coombs, J., Van Der List, D., Wang, G. Y., & Chalupa, L. M. (2006). Morphological properties of mouse retinal ganglion cells. Neuroscience, 140(1), 123-136. doi. 

Coombs, J. L., Van Der List, D., & Chalupa, L. M. (2007). Morphological properties of mouse retinal ganglion cells during postnatal development. Journal of Comparative Neurology, 503(6), 803-814. doi. 

Coomes, D. L., & Schofield, B. R. (2004). Projections from the auditory cortex to the superior olivary complex in guinea pigs. European Journal of Neuroscience, 19(8), 2188-2200. doi. http://www.blackwell-synergy.com/links/doi/10.1111/j.0953-816X.2004.0331...


Coomes, D. L., & Schofield, B. R. (2004). Separate projections from the inferior colliculus to the cochlear nucleus and thalamus in guinea pigs. Hearing Research, 191(1-2), 67-78. doi. 

Coomes, D. L., Schofield, R. M., & Schofield, B. R. (2005). Unilateral and bilateral projections from cortical cells to the inferior colliculus in guinea pigs. Brain Research, 1042(1), 62-72. doi. 

Coomes Peterson, D., & Schofield, B. R. (2007). Projections from auditory cortex contact ascending pathways that originate in the superior olive and inferior colliculus. Hearing Research, 232(1-2), 67-77. doi. 

Cooper, D. C., Moore, S. J., Staff, N. P., & Spruston, N. (2003). Psychostimulant-Induced Plasticity of Intrinsic Neuronal Excitability in Ventral Subiculum. Journal of Neuroscience, 23(30), 9937-9946. doi. http://www.jneurosci.org/cgi/content/abstract/23/30/9937 


Cooper, O., & Isacson, O. (2004). Intrastriatal Transforming Growth Factor α Delivery to a Model of Parkinson's Disease Induces Proliferation and Migration of Endogenous Adult Neural Progenitor Cells without Differentiation into Dopaminergic Neurons. Journal of Neuroscience, 24(41), 8924-8931. doi: 10.1523/jneurosci.2344-04.2004. http://www.jneurosci.org/cgi/content/abstract/24/41/8924 


Copf, T. (2014). Developmental shaping of dendritic arbors in drosophila relies on tightly regulated intra-neuronal activity of protein kinase A (PKA). Developmental Biology, (0). doi: http://dx.doi.org/10.1016/j.ydbio.2014.07.002. http://www.sciencedirect.com/science/article/pii/S0012160614003364


Corbett, D., Giles, T., Evans, S., McLean, J., & Biernaskie, J. (2006). Dynamic changes in CA1 dendritic spines associated with ischemic tolerance. Experimental Neurology, 202(1), 133-138. doi. 

Corbett, N. J., Gabbott, P. L., Klementiev, B., Davies, H. A., Colyer, F. M., Novikova, T., & Stewart, M. G. (2013). Amyloid-Beta Induced CA1 Pyramidal Cell Loss in Young Adult Rats Is Alleviated by Systemic Treatment with FGL, a Neural Cell Adhesion Molecule-Derived Mimetic Peptide. PLoS ONE, 8(8), e71479. doi: 10.1371/journal.pone.0071479. http://dx.doi.org/10.1371%2Fjournal.pone.0071479


Cordeau, P., Jr., Lalancette-Hebert, M., Weng, Y. C., & Kriz, J. (2008). Live Imaging of Neuroinflammation Reveals Sex and Estrogen Effects on Astrocyte Response to Ischemic Injury. Stroke, 39(3), 935-942. doi: 10.1161/strokeaha.107.501460. http://stroke.ahajournals.org/cgi/content/abstract/39/3/935 


Cornbrooks, E. B., Pouliot, W. A., & Mawe, G. M. (1992). Structure of neurons and ganglia of the guinea pig gallbladder: Light and electron microscopic studies. Journal of Comparative Neurology, 317(1), 31-44. doi. 

Coronas, V., Arnault, P., & Roger, M. (2002). Cortical diffusible factors increase MAP-2 immunoreactive neuronal population in thalamic cultures. Neuroscience Research, 43(1), 57-67. doi. 

Coronas, V., Bantubungi, K., Fombonne, J., Krantic, S., Schiffmann, S. N., & Roger, M. (2004). Dopamine D3 receptor stimulation promotes the proliferation of cells derived from the post-natal subventricular zone. Journal of Neurochemistry, 91(6), 1292-1301. doi: doi:10.1111/j.1471-4159.2004.02823.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1471-4159.2004.02823.x 


Correa, D., & Segal, S. S. (2012). Neurovascular proximity in the diaphragm muscle of adult mice. Microcirculation. doi. 

Correia, S. S., Bassani, S., Brown, T. C., Lisé, M. F., Backos, D. S., El-Husseini, A., . . . Esteban, J. A. (2008). Motor protein–dependent transport of AMPA receptors into spines during long-term potentiation. Nature Neuroscience, 11(4), 457-466. doi. 

Corson, J. A., & Erisir, A. (2013). Monosynaptic convergence of chorda tympani and glossopharyngeal afferents onto ascending relay neurons in the nucleus of the solitary tract: A high-resolution confocal and correlative electron microscopy approach. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23357. http://dx.doi.org/10.1002/cne.23357


Corty, M. M., Tam, J., & Grueber, W. B. (2016). Dendritic diversification through transcription factor-mediated suppression of alternative morphologies. [10.1242/dev.130906]. Development, 143(8), 1351-1362. doi. http://dev.biologists.org/content/143/8/1351.abstract


Corvetti, L., & Rossi, F. (2005). Degradation of Chondroitin Sulfate Proteoglycans Induces Sprouting of Intact Purkinje Axons in the Cerebellum of the Adult Rat. Journal of Neuroscience, 25(31), 7150-7158. doi. http://www.jneurosci.org/cgi/content/abstract/25/31/7150


Cory-Slechta, D. A., Sobolewski, M., Marvin, E., Conrad, K., Merrill, A., Anderson, T., . . . Oberdorster, G. (2019). The Impact of Inhaled Ambient Ultrafine Particulate Matter on Developing Brain: Potential Importance of Elemental Contaminants. Toxicologic Pathology, 0192623319878400. doi: 10.1177/0192623319878400. https://doi.org/10.1177/0192623319878400


Cosgrove, K. E., Galván, E. J., Meriney, S. D., & Barrionuevo, G. (2010). Area CA3 interneurons receive two spatially segregated mossy fiber inputs. Hippocampus, 20(9), 1003-1009. doi. 

Cosgrove, K. E., & Maccaferri, G. (2012). mGlu1α-dependent recruitment of excitatory GABAergic input to neocortical Cajal-Retzius cells. Neuropharmacology, (0). doi: 10.1016/j.neuropharm.2012.04.025. http://www.sciencedirect.com/science/article/pii/S002839081200161X


Cosme, R., Lublin, D., Takafuji, V., Lynch, K., & Roche, J. K. (2000). Prostanoids in human colonic mucosa: effects of inflammation on PGE2 receptor expression. Human Immunology, 61(7), 684-696. doi. 

Cosme, R., & Roche, J. K. (2001). Immunohistochemical Detection and Quantitation of Cell Surface Receptors for Prostanoids. Colorectal cancer: methods and protocols, 50, 231-231. doi. 

Cossart, R. (2014). Operational hub cells: a morpho-physiologically diverse class of GABAergic neurons united by a common function. Current Opinion in Neurobiology, 26(0), 51-56. doi: http://dx.doi.org/10.1016/j.conb.2013.12.002. http://www.sciencedirect.com/science/article/pii/S0959438813002262


Cossart, R., Bernard, C., & Ben-Ari, Y. (2005). Multiple facets of GABAergic neurons and synapses: multiple fates of GABA signalling in epilepsies. Trends in Neurosciences, 28(2), 108-115. doi. 

Cossart, R., Dinocourt, C., Hirsch, J. C., Merchan-Perez, A., Felipe, J. D., Ben-Ari, Y., . . . Bernard, C. (2001). Dendritic but not somatic GABAergic inhibition is decreased in experimental epilepsy. Nature Neuroscience, 4, 52-62. doi. 

Cossart, R., Esclapez, M., Hirsch, J. C., Bernard, C., & Ben-Ari, Y. (1998). GluR5 kainate receptor activation in interneurons increases tonic inhibition of pyramidal cells. Nature Neuroscience, 1, 470-478. doi. 

Cossart, R., Petanjek, Z., Dumitriu, D., Hirsch, J. C., Ben-Ari, Y., Esclapez, M., & Bernard, C. (2006). Interneurons targeting similar layers receive synaptic inputs with similar kinetics. Hippocampus. doi. 

Cossette, M., Lecomte, F., & Parent, A. (2005). Morphology and distribution of dopaminergic neurons intrinsic to the human striatum. Journal of Chemical Neuroanatomy, 29(1), 1-11. doi. 

Costentin, C., Robert, M., Savéant, J.-M., & Teillout, A.-L. (2009). Concerted proton-coupled electron transfers in aquo/hydroxo/oxo metal complexes: Electrochemistry of [OsII(bpy)2py(OH2)]2+ in water. Proceedings of the National Academy of Sciences, 106(29), 11829-11836. doi: 10.1073/pnas.0905020106. http://www.pnas.org/content/106/29/11829.abstract 


Cotel, F., Fletcher, L. N., Kalita-de Croft, S., Apergis-Schoute, J., & Williams, S. R. (2017). Cell Class-Dependent Intracortical Connectivity and Output Dynamics of Layer 6 Projection Neurons of the Rat Primary Visual Cortex. Cerebral Cortex, 1-11. doi. https://academic.oup.com/cercor/article-abstract/doi/10.1093/cercor/bhx1...


Couch, B. A., DeMarco, G. J., Gourley, S. L., & Koleske, A. J. (2010). Increased dendrite branching in AβPP/PS1 mice and elongation of dendrite arbors by fasudil administration. Journal of Alzheimer's Disease, 20(4), 1003-1008. doi. 

Couchman, K., Grothe, B., & Felmy, F. (2010). Medial Superior Olivary Neurons Receive Surprisingly Few Excitatory and Inhibitory Inputs with Balanced Strength and Short-Term Dynamics. Journal of Neuroscience, 30(50), 17111-17121. doi: 10.1523/jneurosci.1760-10.2010. http://www.jneurosci.org/cgi/content/abstract/30/50/17111


Courtine, G., Song, B., Roy, R. R., Zhong, H., Herrmann, J. E., Ao, Y., . . . Sofroniew, M. V. (2008). Recovery of supraspinal control of stepping via indirect propriospinal relay connections after spinal cord injury. Nature Medicine, 14(1), 69-74. doi. 

Cova, L., Gelosa, P., Mura, E., Mauro, A., Stramba-Badiale, M., Michailidis, G., . . . Zanchetti, A. (2013). Vascular and parenchymal lesions along with enhanced neurogenesis characterize the brain of asymptomatic stroke-prone spontaneous hypertensive rats. Journal of Hypertension, Publish Ahead of Print, 10.1097/HJH.1090b1013e3283619d3283617f. doi. http://journals.lww.com/jhypertension/Fulltext/publishahead/Vascular_and...


Cox, S. J., & Raol, J. H. (2004). Recovering the passive properties of tapered dendrites from single and dual potential recordings. Mathematical Biosciences, 190(1), 9-37. doi. 

Craig, M. T., & McBain, C. J. (2015). Fast Gamma Oscillations Are Generated Intrinsically in CA1 without the Involvement of Fast-Spiking Basket Cells. The Journal of Neuroscience, 35(8), 3616-3624. doi. http://www.jneurosci.org/content/35/8/3616.short


Craig, M. T., & McBain, C. J. (2015). Navigating the circuitry of the brain's GPS system: Future challenges for neurophysiologists. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22456. http://dx.doi.org/10.1002/hipo.22456


Craver, B. M., Acharya, M. M., Allen, B. D., Benke, S. N., Hultgren, N. W., Baulch, J. E., & Limoli, C. L. (2016). 3D surface analysis of hippocampal microvasculature in the irradiated brain. Environmental and Molecular Mutagenesis, n/a-n/a. doi: 10.1002/em.22015. http://dx.doi.org/10.1002/em.22015


Crawford, L. K., Craige, C. P., & Beck, S. G. (2011). Glutamatergic input is selectively increased in dorsal raphe subfield 5-HT neurons: role of morphology, topography and selective innervation. European Journal of Neuroscience, 34(11), 1794-1806. doi: 10.1111/j.1460-9568.2011.07882.x. http://dx.doi.org/10.1111/j.1460-9568.2011.07882.x


Crépel, V., & Mulle, C. (2015). Physiopathology of kainate receptors in epilepsy. Current Opinion in Pharmacology, 20(0), 83-88. doi: http://dx.doi.org/10.1016/j.coph.2014.11.012. http://www.sciencedirect.com/science/article/pii/S1471489214001672


Creutz, L. M., & Kritzer, M. F. (2004). Mesostriatal and mesolimbic projections of midbrain neurons immunoreactive for estrogen receptor beta or androgen receptors in rats. Journal of Comparative Neurology, 476(4), 348-362. doi. 

Crimins, J., Rocher, A., & Luebke, J. (2012). Electrophysiological changes precede morphological changes to frontal cortical pyramidal neurons in the rTg4510 mouse model of progressive tauopathy. Acta Neuropathologica, 1-19. doi: 10.1007/s00401-012-1038-9. http://dx.doi.org/10.1007/s00401-012-1038-9


Criscuolo, C., Fontebasso, V., Middei, S., Stazi, M., Ammassari-Teule, M., Yan, S. S., & Origlia, N. (2017). Entorhinal Cortex dysfunction can be rescued by inhibition of microglial RAGE in an Alzheimer’s disease mouse model. Scientific Reports, 7, 42370. doi. 

Crochet, S., Chauvette, S., Boucetta, S., & Timofeev, I. (2005). Modulation of synaptic transmission in neocortex by network activities. European Journal of Neuroscience, 21(4), 1030-1044. doi: doi:10.1111/j.1460-9568.2005.03932.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2005.03932.x 


Crochet, S., Poulet, J. F. A., Kremer, Y., & Petersen, C. C. H. (2011). Synaptic mechanisms underlying sparse coding of active touch. Neuron, 69(6), 1160-1175. doi. 

Croci, L., Chung, S.-H., Masserdotti, G., Gianola, S., Bizzoca, A., Gennarini, G., . . . Consalez, G. G. (2006). A key role for the HLH transcription factor EBF2COE2,O/E-3 in Purkinje neuron migration and cerebellar cortical topography. Development, 133(14), 2719-2729. doi: 10.1242/dev.02437. http://dev.biologists.org/cgi/content/abstract/133/14/2719 


Crociara, P., Chieppa, M. N., Vallino Costassa, E., Berrone, E., Gallo, M., Lo Faro, M., . . . Corona, C. (2019). Motor neuron degeneration, severe myopathy and TDP-43 increase in a transgenic pig model of SOD1-linked familiar ALS. Neurobiology of Disease, 124, 263-275. doi: https://doi.org/10.1016/j.nbd.2018.11.021. http://www.sciencedirect.com/science/article/pii/S0969996118307526


Crociara, P., Parolisi, R., Conte, D., Fumagalli, M., & Bonfanti, L. (2013). Cellular and Molecular Characterization of Multipolar Map5-Expressing Cells: A Subset of Newly Generated, Stage-Specific Parenchymal Cells in the Mammalian Central Nervous System. PLoS ONE, 8(5), e63258. doi: 10.1371/journal.pone.0063258. http://dx.doi.org/10.1371%2Fjournal.pone.0063258


Crocker, A., Espana, R. A., Papadopoulou, M., Saper, C. B., Faraco, J., Sakurai, T., . . . Scammell, T. E. (2005). Concomitant loss of dynorphin, NARP, and orexin in narcolepsy. Neurology, 65(8), 1184-1188. doi: 10.1212/01.WNL.0000168173.71940.ab. http://www.neurology.org/cgi/content/abstract/65/8/1184 


Croisier, E., Moran, L., Dexter, D., Pearce, R., & Graeber, M. (2005). Microglial inflammation in the parkinsonian substantia nigra: relationship to alpha-synuclein deposition. J Neuroinflammation, 2, 14. doi. 

Crombe, A., Planche, V., Raffard, G., Bourel, J., Dubourdieu, N., Panatier, A., . . . Tourdias, T. (2018). Deciphering the microstructure of hippocampal subfields with in vivo DTI and NODDI: Applications to experimental multiple sclerosis. Neuroimage, 172, 357-368. doi: https://doi.org/10.1016/j.neuroimage.2018.01.061. https://www.sciencedirect.com/science/article/pii/S1053811918300612


Crook, J. M., Kisvarday, Z. F., & Eysel, U. T. (1998). Evidence for a contribution of lateral inhibition to orientation tuning and direction selectivity in cat visual cortex: reversible inactivation of functionally characterized sites combined with neuroanatomical tracing techniques. European Journal of Neuroscience, 10(6), 2056-2075. doi: doi:10.1046/j.1460-9568.1998.00218.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.1998.00218.x 


Crook, S., Gleeson, P., Howell, F., Svitak, J., & Silver, R. A. (2007). MorphML: level 1 of the NeuroML standards for neuronal morphology data and model specification. Neuroinformatics, 5(2), 96-104. doi. 

Croquelois, A., Bronchti, G., & Welker, E. (2005). Cortical origin of functional recovery in the somatosensory cortex of the adult mouse after thalamic lesion. European Journal of Neuroscience, 21(7), 1798-1806. doi: doi:10.1111/j.1460-9568.2005.03994.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2005.03994.x 


Croquelois, A., Giuliani, F., Savary, C., Kielar, M., Amiot, C., Schenk, F., & Welker, E. (2008). Characterization of the HeCo Mutant Mouse: A New Model of Subcortical Band Heterotopia Associated with Seizures and Behavioral Deficits. Cerebral Cortex, bhn106. doi: 10.1093/cercor/bhn106. http://cercor.oxfordjournals.org/cgi/content/abstract/bhn106v1 


Cross, D. J., & Cavazos, J. E. (2007). Synaptic reorganization in subiculum and CA3 after early-life status epilepticus in the kainic acid rat model. Epilepsy Research, 73(2), 156-165. doi. 

Crupi, R., Cambiaghi, M., Deckelbaum, R., Hansen, I., Mindes, J., Spina, E., & Battaglia, F. (2011). n-3 fatty acids prevent impairment of neurogenesis and synaptic plasticity in B-cell activating factor (BAFF) transgenic mice. Preventive Medicine. doi. 

Crupi, R., Cambiaghi, M., Spatz, L., Hen, R., Thorn, M., Friedman, E., . . . Battaglia, F. (2010). Reduced adult neurogenesis and altered emotional behaviors in autoimmune-prone B-cell activating factor transgenic mice. Biological Psychiatry, 67(6), 558-566. doi. 

Crutcher, E., Pal, R., Naini, F., Zhang, P., Laugsch, M., Kim, J., . . . Schaaf, C. P. (2019). mTOR and autophagy pathways are dysregulated in murine and human models of Schaaf-Yang syndrome. Scientific Reports, 9(1), 15935. doi: 10.1038/s41598-019-52287-2. https://doi.org/10.1038/s41598-019-52287-2


Cruz, D. A., Eggan, S. M., Azmitia, E. C., & Lewis, D. A. (2004). Serotonin1A receptors at the axon initial segment of prefrontal pyramidal neurons in schizophrenia. American Journal of Psychiatry, 161(4), 739-742. doi. 

Cruz, D. A., Eggan, S. M., & Lewis, D. A. (2003). Postnatal development of pre-and postsynaptic GABA markers at chandelier cell connections with pyramidal neurons in monkey prefrontal cortex. Journal of Comparative Neurology, 465(3), 385-400. doi. 

Cruz, D. A., Lovallo, E. M., Stockton, S., Rasband, M., & Lewis, D. A. (2009). Postnatal development of synaptic structure proteins in pyramidal neuron axon initial segments in monkey prefrontal cortex. Journal of Comparative Neurology, 514(4), 353-367. doi. 

Cruz, D. A., Weaver, C. L., Lovallo, E. M., Melchitzky, D. S., & Lewis, D. A. (2009). Selective alterations in postsynaptic markers of chandelier cell inputs to cortical pyramidal neurons in subjects with schizophrenia. Neuropsychopharmacology, 34(9), 2112-2124. doi. 

Cruz-Martin, A., & Portera-Cailliau, C. (2014). In Vivo Imaging of Axonal and Dendritic Structures in Neonatal Mouse Cortex. Cold Spring Harbor Protocols, 2014(1), pdb.prot080150. doi: 10.1101/pdb.prot080150. http://cshprotocols.cshlp.org/content/2014/1/pdb.prot080150.abstract


Csabai, D., Csekő, K., Szaiff, L., Varga, Z., Miseta, A., Helyes, Z., & Czéh, B. (2016). Low intensity, long term exposure to tobacco smoke inhibits hippocampal neurogenesis in adult mice. Behavioural Brain Research, 302, 44-52. doi: http://dx.doi.org/10.1016/j.bbr.2016.01.022. http://www.sciencedirect.com/science/article/pii/S0166432816300195


Csabai, D., Seress, L., Varga, Z., Ábrahám, H., Miseta, A., Wiborg, O., & Czéh, B. (2016). Electron microscopic analysis of hippocampal axo-somatic synapses in a chronic stress model for depression. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22650. http://dx.doi.org/10.1002/hipo.22650


Csajbók, É. A., Kocsis, Á. K., Faragó, N., Furdan, S., Kovács, B., Lovas, S., . . . Tamás, G. (2019). Expression of GLP-1 receptors in insulin-containing interneurons of rat cerebral cortex. [journal article]. Diabetologia. doi: 10.1007/s00125-018-4803-z. https://doi.org/10.1007/s00125-018-4803-z


Cuccioli, V., Bueno, C., Belvindrah, R., Lledo, P. M., & Martinez, S. (2014). Attractive action of FGF-signaling contributes to the postnatal developing hippocampus. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22386. http://dx.doi.org/10.1002/hipo.22386


Cui, D., Dougherty, K. J., Machacek, D. W., Sawchuk, M., Hochman, S., & Baro, D. J. (2006). Divergence between motoneurons: gene expression profiling provides a molecular characterization of functionally discrete somatic and autonomic motoneurons. Physiological Genomicss, 24(3), 276-289. doi: 10.1152/physiolgenomics.00109.2005. http://physiolgenomics.physiology.org/cgi/content/abstract/24/3/276 


Cui, R.-Z., Wang, L., Qiao, S.-N., Wang, Y.-C., Wang, X., Yuan, F., . . . Zhong, Y.-M. (2019). ON-Type Retinal Ganglion Cells are Preferentially Affected in STZ-Induced Diabetic MiceChanges of Retinal Ganglion Cells in Diabetic Mice. Investigative Ophthalmology and Visual Science, 60(5), 1644-1656. doi: 10.1167/iovs.18-26359. https://doi.org/10.1167/iovs.18-26359


Cui, Y.-F., Hargus, G., Xu, J.-C., Schmid, J. S., Shen, Y.-Q., Glatzel, M., . . . Bernreuther, C. (2010). Embryonic stem cell-derived L1 overexpressing neural aggregates enhance recovery in Parkinsonian mice. Brain, 133(1), 189-204. doi: 10.1093/brain/awp290. http://brain.oxfordjournals.org/cgi/content/abstract/133/1/189 


Cullen, C. L., Burne, T. H. J., Lavidis, N. A., & Moritz, K. M. (2013). Low Dose Prenatal Ethanol Exposure Induces Anxiety-Like Behaviour and Alters Dendritic Morphology in the Basolateral Amygdala of Rat Offspring. PLoS ONE, 8(1), e54924. doi: 10.1371/journal.pone.0054924. http://dx.doi.org/10.1371%2Fjournal.pone.0054924


Cullen, C. L., Burne, T. H. J., Lavidis, N. A., & Moritz, K. M. (2014). Low Dose Prenatal Alcohol Exposure Does Not Impair Spatial Learning and Memory in Two Tests in Adult and Aged Rats. PLoS ONE, 9(6), e101482. doi: 10.1371/journal.pone.0101482. http://dx.doi.org/10.1371%2Fjournal.pone.0101482


Cunningham, C. L., Martínez-Cerdeño, V., & Noctor, S. C. (2013). Microglia regulate the number of neural precursor cells in the developing cerebral cortex. Journal of Neuroscience, 33(10), 4216-4233. doi. https://search.proquest.com/openview/70a939d69a1cb77bdd1067296217c884/1....


Cunningham, J. T., Knight, W. D., Mifflin, S. W., & Nestler, E. J. (2012). An Essential Role for ΔFosB in the Median Preoptic Nucleus in the Sustained Hypertensive Effects of Chronic Intermittent Hypoxia. Hypertension. doi: 10.1161/hypertensionaha.112.193789. http://hyper.ahajournals.org/content/early/2012/06/11/HYPERTENSIONAHA.11...


Cunningham, M., Cho, J.-H., Leung, A., Savvidis, G., Ahn, S., Moon, M., . . . Chung, S. (2014). hPSC-Derived Maturing GABAergic Interneurons Ameliorate Seizures and Abnormal Behavior in Epileptic Mice. Cell Stem Cell, 15(5), 559-573. doi: 10.1016/j.stem.2014.10.006. http://www.cell.com/cell-stem-cell/abstract/S1934-5909(14)00457-3

Cunningham, M. O., Pervouchine, D. D., Racca, C., Kopell, N. J., Davies, C. H., Jones, R. S. G., . . . Whittington, M. A. (2006). Neuronal metabolism governs cortical network response state. PNAS, 0600604103. doi: 10.1073/pnas.0600604103. http://www.pnas.org/cgi/content/abstract/0600604103v1 


Curcio, C., Asheld, J. J., Chabla, J. M., Ayubcha, D., Hallas, B. H., Horowitz, J. M., & Torres, G. (2006). Expression profile of Bag 1 in the postmortem brain. Journal of Chemical Neuroanatomy, 32(2), 191-195. doi. 

Currier, T. A., Etchegaray, M. A., Haight, J. L., Galaburda, A. M., & Rosen, G. D. (2011). The effects of embryonic knockdown of the candidate dyslexia susceptibility gene homologue< i> Dyx1c1</i> on the distribution of GABAergic neurons in the cerebral cortex. Neuroscience, 172, 535-546. doi. 

Curtetti, R., Garbossa, D., & Vercelli, A. (2002). Development of dendritic bundles of pyramidal neurons in the rat visual cortex. Mechanisms of Ageing and Development, 123(5), 473-479. doi. 

Curto, G. G., Nieto-Estévez, V., Hurtado-Chong, A., Valero, J., Gómez, C., Alonso, J. R., . . . Vicario-Abejón, C. (2014). Pax6 is essential for the maintenance and multi-lineage differentiation of neural stem cells, and for neuronal incorporation into the adult olfactory bulb. Stem Cells and Development, (ja). doi. http://online.liebertpub.com/doi/abs/10.1089/scd.2014.0058


Cusimano, M., Biziato, D., Brambilla, E., Donegà, M., Alfaro-Cervello, C., Snider, S., . . . others. (2012). Transplanted neural stem/precursor cells instruct phagocytes and reduce secondary tissue damage in the injured spinal cord. Brain, 135(2), 447-460. doi. 

Cusimano, M., Brambilla, E., Capotondo, A., De Feo, D., Tomasso, A., Comi, G., . . . Martino, G. (2018). Selective killing of spinal cord neural stem cells impairs locomotor recovery in a mouse model of spinal cord injury. [journal article]. Journal of Neuroinflammation, 15(1), 58. doi: 10.1186/s12974-018-1085-9. https://doi.org/10.1186/s12974-018-1085-9


Cusmano, D. M., Hadjimarkou, M. M., & Mong, J. A. (2013). Gonadal Steroid Modulation of Sleep and Wakefulness in Male and Female Rats Is Sexually Differentiated and Neonatally Organized by Steroid Exposure. Endocrinology. doi: 10.1210/en.2013-1624. http://endo.endojournals.org/content/early/2013/11/01/en.2013-1624.abstract


Cutrer, F. M., Sandroni, P., & Wendelschafer-Crabb, G. (2010). Botulinum toxin treatment of cephalalgia alopecia increases substance P and calcitonin gene-related peptide-containing cutaneous nerves in scalp. Cephalalgia, 30(8), 1000-1006. doi. 

Cutuli, D., Rossi, S., Burello, L., Laricchiuta, D., De Chiara, V., Foti, F., . . . others. (2011). Before or after does it matter? Different protocols of environmental enrichment differently influence motor, synaptic and structural deficits of cerebellar origin. Neurobiology of Disease, 42(1), 9-20. doi. 

Czajkowski, R., Sugar, J., Zhang, S.-J., Couey, J. J., Ye, J., & Witter, M. P. (2013). Superficially Projecting Principal Neurons in Layer V of Medial Entorhinal Cortex in the Rat Receive Excitatory Retrosplenial Input. Journal of Neuroscience, 33(40), 15779-15792. doi: 10.1523/jneurosci.2646-13.2013. http://www.jneurosci.org/content/33/40/15779.abstract


Czaniecki, C., Ryan, T., Stykel, M. G., Drolet, J., Heide, J., Hallam, R., . . . Ryan, S. D. (2019). Axonal pathology in hPSC-based models of Parkinson’s disease results from loss of Nrf2 transcriptional activity at the Map1b gene locus. Proceedings of the National Academy of Sciences, 201900576. doi: 10.1073/pnas.1900576116. http://www.pnas.org/content/early/2019/06/21/1900576116.abstract


Czéh, B., Ábrahám, H., Tahtakran, S., Houser, C. R., & Seress, L. (2013). Number and regional distribution of GAD65 mRNA-expressing interneurons in the rat hippocampal formation. Acta Biologica Hungarica, 64(4), 395-413. doi. http://www.akademiai.com/content/5n72830655238p75/


Czéh, B., Abumaria, N., Rygula, R., & Fuchs, E. (2010). Quantitative changes in hippocampal microvasculature of chronically stressed rats: no effect of fluoxetine treatment. Hippocampus, 20(1), 174-185. doi. 

Czéh, B., Michaelis, T., Watanabe, T., Frahm, J., de Biurrun, G., van Kampen, M., . . . Fuchs, E. (2001). Stress-induced changes in cerebral metabolites, hippocampal volume, and cell proliferation are prevented by antidepressant treatment with tianeptine. Proceedings of the National Academy of Sciences, 98(22), 12796-12801. doi: 10.1073/pnas.211427898. http://www.pnas.org/cgi/content/abstract/98/22/12796 


Czéh, B., Pudovkina, O., van der Hart, M. G. C., Simon, M., Heilbronner, U., Michaelis, T., . . . Fuchs, E. (2005). Examining SLV-323, a novel NK 1 receptor antagonist, in a chronic psychosocial stress model for depression. Psychopharmacology, 180(3), 548-557. doi. 

Czéh, B., Varga, Z. K. K., Henningsen, K., Kovács, G. L., Miseta, A., & Wiborg, O. (2014). Chronic stress reduces the number of GABAergic interneurons in the adult rat hippocampus, dorsal-ventral and region-specific differences. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22382. http://dx.doi.org/10.1002/hipo.22382


Czéh, B., Welt, T., Fischer, A. K., Erhardt, A., Schmitt, W., Müller, M. B., . . . Keck, M. E. (2002). Chronic psychosocial stress and concomitant repetitive transcranial magnetic stimulation: effects on stress hormone levels and adult hippocampal neurogenesis. Biological Psychiatry, 52(11), 1057-1065. doi. 

Czurko, A., Czeh, B., Seress, L., Nadel, L., & Bures, J. (1997). Severe spatial navigation deficit in the Morris water maze after single high dose of neonatal x-ray irradiation in the rat. Proceedings of the National Academy of Sciences, 94(6), 2766-2771. doi: 10.1073/pnas.94.6.2766. http://www.pnas.org/cgi/content/abstract/94/6/2766 


D’Amato, A. R., Puhl, D. L., Ellman, S. A. T., Balouch, B., Gilbert, R. J., & Palermo, E. F. (2019). Vastly extended drug release from poly(pro-17β-estradiol) materials facilitates in vitro neurotrophism and neuroprotection. Nature Communications, 10(1), 4830. doi: 10.1038/s41467-019-12835-w. https://doi.org/10.1038/s41467-019-12835-w


D’Amato, A. R., Puhl, D. L., Ziemba, A. M., Johnson, C. D. L., Doedee, J., Bao, J., & Gilbert, R. J. (2019). Exploring the effects of electrospun fiber surface nanotopography on neurite outgrowth and branching in neuron cultures. PLoS ONE, 14(2), e0211731. doi: 10.1371/journal.pone.0211731. https://doi.org/10.1371/journal.pone.0211731


d’Errico, P., Boido, M., Piras, A., Valsecchi, V., De Amicis, E., Locatelli, D., . . . Battaglia, G. (2013). Selective Vulnerability of Spinal and Cortical Motor Neuron Subpopulations in delta7 SMA Mice. PLoS ONE, 8(12), e82654. doi: 10.1371/journal.pone.0082654. http://dx.doi.org/10.1371%2Fjournal.pone.0082654


D’Souza, R. D., Bista, P., Meier, A. M., Ji, W., & Burkhalter, A. (2019). Spatial Clustering of Inhibition in Mouse Primary Visual Cortex. Neuron. doi: https://doi.org/10.1016/j.neuron.2019.09.020. http://www.sciencedirect.com/science/article/pii/S0896627319307937


da Costa, N. M., & Martin, K. A. C. (2009). Selective Targeting of the Dendrites of Corticothalamic Cells by Thalamic Afferents in Area 17 of the Cat. Journal of Neuroscience, 29(44), 13919-13928. doi: 10.1523/jneurosci.2785-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/44/13919 


da Fontoura Costa, L., & Manoel, E. T. M. (2003). A percolation approach to neural morphometry and connectivity. Neuroinformatics, 1(1), 65-80. doi. 

da Rocha, E. G., Freire, M. A. M., Bahia, C. P., Pereira, A., Sosthenes, M. C. K., Silveira, L. C. L., . . . Picanço-Diniz, C. W. (2012). Dendritic structure varies as a function of eccentricity in V1: a quantitative study of NADPH diaphorase neurons in the diurnal South American rodent agouti,< i> Dasyprocta prymnolopha</i>. Neuroscience. doi. 

Da Silva, A. V., Houzel, J. C., Targas Yacubian, E. M., Carrete, H., Sakamoto, A. C., Priel, M. R., . . . others. (2006). Dysmorphic neurons in patients with temporal lobe epilepsy. Brain Research, 1072(1), 200-207. doi. 

da Silva, M. P., Moraes, D. J. A., Bonagamba, L. G. H., Mecawi, A. d. S., Varanda, W. A., & Machado, B. H. (2019). Hyperexcitability and plasticity induced by sustained hypoxia on rectus abdominis motoneurons. The Journal of Physiology, 0(ja). doi: doi:10.1113/JP277030. https://physoc.onlinelibrary.wiley.com/doi/abs/10.1113/JP277030


da Silva, S., Hasegawa, H., Scott, A., Zhou, X., Wagner, A. K., Han, B.-X., & Wang, F. (2011). Proper formation of whisker barrelettes requires periphery-derived Smad4-dependent TGF-β signaling. Proceedings of the National Academy of Sciences, 108(8), 3395-3400. doi: 10.1073/pnas.1014411108. http://www.pnas.org/content/108/8/3395.abstract


Daamen, W. F., Nillesen, S. T. M., Wismans, R. G., Reinhardt, D. P., Hafmans, T., Veerkamp, J. H., & van Kuppevelt, T. H. (2008). A biomaterial composed of collagen and solubilized elastin enhances angiogenesis and elastic fiber formation without calcification. Tissue Engineering Part A, 14(3), 349-360. doi. 

Dabrowska, J., & Rainnie, D. G. (2010). Expression and distribution of Kv4 potassium channel subunits and potassium channel interacting proteins in subpopulations of interneurons in the basolateral amygdala. Neuroscience, 171(3), 721-733. doi. 

Dacks, P. A., Krajewski, S. J., & Rance, N. E. (2011). Activation of Neurokinin 3 Receptors in the Median Preoptic Nucleus Decreases Core Temperature in the Rat. Endocrinology, 152(12), 4894-4905. doi. 

Dacks, P. A., Krajewski, S. J., & Rance, N. E. (2011). Ambient Temperature and 17β -Estradiol Modify Fos Immunoreactivity in the Median Preoptic Nucleus, a Putative Regulator of Skin Vasomotion. Endocrinology, 152(7), 2750-2759. doi. 

Dahlen, J. E., Jimenez, D. A., Gerkin, R. C., & Urban, N. N. (2011). Morphological analysis of activity-reduced adult-born neurons in the mouse olfactory bulb. [Original Research]. Frontiers in Neuroscience, 5. doi: 10.3389/fnins.2011.00066. http://www.frontiersin.org/Journal/Abstract.aspx?s=748&name=neurogenesis...


Dahme, M., Bartsch, U., Martini, R., Anliker, B., Schachner, M., & Mantei, N. (1997). Disruption of the mouse L1 gene leads to malformations of the nervous system. Nature Genetics, 17, 346-349. doi. 

Dajas-Bailador, F., Bonev, B., Garcez, P., Stanley, P., Guillemot, F., & Papalopulu, N. (2012). microRNA-9 regulates axon extension and branching by targeting Map1b in mouse cortical neurons. [10.1038/nn.3082]. Nature Neuroscience, 15(5), 697-699. doi: http://www.nature.com/neuro/journal/v15/n5/abs/nn.3082.html#supplementar.... http://dx.doi.org/10.1038/nn.3082


Dalrymple-Alford, J. C., Harland, B., Loukavenko, E. A., Perry, B., Mercer, S., Collings, D. A., . . . Wolff, M. (2015). Anterior thalamic nuclei lesions and recovery of function: Relevance to cognitive thalamus. Neuroscience and Biobehavioral Reviews, (0). doi: http://dx.doi.org/10.1016/j.neubiorev.2014.12.007. http://www.sciencedirect.com/science/article/pii/S0149763414003443


Daly, D. T., & Ariel, M. (2018). A Novel Cerebellar Commissure and Other Myelinated Axons in the Purkinje Cell Layer of a Pond Turtle (Trachemys Scripta Elegans). Journal of Comparative Neurology, 0(ja). doi: doi:10.1002/cne.24528. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24528


D'Amato, F. R., Zanettini, C., Sgobio, C., Sarli, C., Carone, V., Moles, A., & Ammassari-Teule, M. (2011). Intensification of maternal care by double-mothering boosts cognitive function and hippocampal morphology in the adult offspring. Hippocampus, 21(3), 298-308. doi: 10.1002/hipo.20750. http://dx.doi.org/10.1002/hipo.20750


D'Amelio, M., Cavallucci, V., Middei, S., Marchetti, C., Pacioni, S., Ferri, A., . . . others. (2010). Caspase-3 triggers early synaptic dysfunction in a mouse model of Alzheimer's disease. Nature Neuroscience, 14(1), 69-76. doi. 

Damiani, D., Novelli, E., Mazzoni, F., & Strettoi, E. (2011). Undersized dendritic arborizations in retinal ganglion cells of the rd1 mutant mouse, a paradigm of early-onset photoreceptor degeneration. Journal of Comparative Neurology. doi. 

Dancause, N., Barbay, S., Frost, S. B., Mahnken, J. D., & Nudo, R. J. (2007). Interhemispheric connections of the ventral premotor cortex in a new world primate. Journal of Comparative Neurology, 505(6), 701-715. doi. 

Dancause, N., Barbay, S., Frost, S. B., Plautz, E. J., Chen, D., Zoubina, E. V., . . . Nudo, R. J. (2005). Extensive Cortical Rewiring after Brain Injury. Journal of Neuroscience, 25, 10167-10179. doi. 

Dancause, N., Barbay, S., Frost, S. B., Plautz, E. J., Popescu, M., Dixon, P. M., . . . Nudo, R. J. (2006). Topographically divergent and convergent connectivity between premotor and primary motor cortex. Cerebral Cortex, 16(8), 1057-1057. doi. 

Dancause, N., Barbay, S., Frost, S. B., Plautz, E. J., Stowe, A. M., Friel, K. M., & Nudo, R. J. (2006). Ipsilateral connections of the ventral premotor cortex in a new world primate. Journal of Comparative Neurology, 495(4), 374-390. doi. 

Dancause, N., Duric, V., Barbay, S., Frost, S. B., Stylianou, A., & Nudo, R. J. (2008). An Additional Motor-Related Field in the Lateral Frontal Cortex of Squirrel Monkeys. Cerebral Cortex, 18, 2719 - 2728. doi: 10.1093/cercor/bhn050. http://cercor.oxfordjournals.org/cgi/content/abstract/bhn050v1 


D'Andrea, M. R., Saban, M. R., Gerard, N. P., Wershil, B. K., & Saban, R. (2005). Lack of neurokinin-1 receptor expression affects tissue mast cell numbers but not their spatial relationship with nerves. Journal of Physiology - Regulatory, Integrative and Comparative Physiology, 288(2), R491-500. doi: 10.1152/ajpregu.00452.2004. http://ajpregu.physiology.org/cgi/content/abstract/288/2/R491 


Dang, M. T., Yokoi, F., Yin, H. H., Lovinger, D. M., Wang, Y., & Li, Y. (2006). Disrupted motor learning and long-term synaptic plasticity in mice lacking NMDAR1 in the striatum. Proceedings of the National Academy of Sciences, 103(41), 15254-15259. doi. 

Dang, M. T., Yokoi, F., Yin, H. H., Lovinger, D. M., Wang, Y., & Li, Y. (2006). From the Cover: Disrupted motor learning and long-term synaptic plasticity in mice lacking NMDAR1 in the striatum. PNAS, 103(41), 15254-15259. doi: 10.1073/pnas.0601758103. http://www.pnas.org/cgi/content/abstract/103/41/15254 


Dang, V., Medina, B., Das, D., Moghadam, S., Martin, K. J., Lin, B., . . . Salehi, A. (2013). Formoterol, a Long-Acting β2 Adrenergic Agonist, Improves Cognitive Function and Promotes Dendritic Complexity in a Mouse Model of Down Syndrome. Biological Psychiatry, (0). doi: http://dx.doi.org/10.1016/j.biopsych.2013.05.024. http://www.sciencedirect.com/science/article/pii/S0006322313004988


Daniel Michael, V., Marissa, P., Emily, A., & Abigail, K. (2018). Enhanced total neurite outgrowth and secondary branching in dorsal root ganglion neurons elicited by low intensity pulsed ultrasound. Journal of neural engineering. doi. http://iopscience.iop.org/10.1088/1741-2552/aabeba


Daniel, S. E., Guo, J., & Rainnie, D. G. (2017). A Comparative Analysis of the Physiological Properties of Neurons in the Anterolateral Bed Nucleus of the Stria Terminalis in the Mus musculus, Rattus norvegicus, and Macaca mulatta. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24202. http://dx.doi.org/10.1002/cne.24202


Danton, G. H., Prado, R., Watson, B. D., & Dietrich, W. D. (2002). Temporal Profile of Enhanced Vulnerability of the Postthrombotic Brain to Secondary Embolic Events. Stroke, 33(4), 1113-1119. doi: 10.1161/hs0402.105554. http://stroke.ahajournals.org/cgi/content/abstract/33/4/1113 


Danzer, S., Price, O., McMullen, N. T., & Rance, N. E. (1999). Sex steroid modulation of neurokinin B gene expression in the arcuate nucleus of adult male rats. Molecular Brain Research. doi. 

Danzer, S. C., Crooks, K. R. C., Lo, D. C., & McNamara, J. O. (2002). Increased Expression of Brain-Derived Neurotrophic Factor Induces Formation of Basal Dendrites and Axonal Branching in Dentate Granule Cells in Hippocampal Explant Cultures. Journal of Neuroscience, 22(22), 9754-9763. doi. http://www.jneurosci.org/cgi/content/abstract/22/22/9754 


Danzer, S. C., He, X., Loepke, A. W., & McNamara, J. O. (2010). Structural plasticity of dentate granule cell mossy fibers during the development of limbic epilepsy. Hippocampus, 20(1), 113-124. doi. 

Danzer, S. C., Kotloski, R. J., Walter, C., Hughes, M., & McNamara, J. O. (2008). Altered morphology of hippocampal dentate granule cell presynaptic and postsynaptic terminals following conditional deletion of TrkB. Hippocampus, 18(7), 668-678. doi. 

Danzer, S. C., McMullen, N. T., & Rance, N. E. (1998). Dendritic growth of arcuate neuroendocrine neurons following orchidectomy in adult rats. Journal Comparative Neurology, 390, 234-246. doi. 

Danzer, S. C., McMullen, N. T., & Rance, N. E. (2001). Testosterone modulates the dendritic architecture of arcuate neuroendocrine neurons in adult male rats. Brain Research, 890(1), 78-85. doi. 

Daoud, R., Mies, G., Smialowska, A., Olah, L., Hossmann, K.-A., & Stamm, S. (2002). Ischemia Induces a Translocation of the Splicing Factor tra2-beta 1 and Changes Alternative Splicing Patterns in the Brain. Journal of Neuroscience, 22(14), 5889-5899. doi. http://www.jneurosci.org/cgi/content/abstract/22/14/5889


Darian-Smith, C., Lilak, A., Garner, J., & Irvine, K.-A. (2014). Corticospinal Sprouting Differs According to Spinal Injury Location and Cortical Origin in Macaque Monkeys. The Journal of Neuroscience, 34(37), 12267-12279. doi. http://www.jneurosci.org/content/34/37/12267.short


Darling, W., Morecraft, R., Rotella, D., Pizzimenti, M., Ge, J., Stilwell-Morecraft, K., . . . Cheney, P. (2014). Recovery of precision grasping after motor cortex lesion does not require forced use of the impaired hand in macaca mulatta. Experimental Brain Research, 1-10. doi: 10.1007/s00221-014-4068-9. http://dx.doi.org/10.1007/s00221-014-4068-9


Darling, W. G., Ge, J., Stilwell-Morecraft, K. S., Rotella, D. L., Pizzimenti, M. A., & Morecraft, R. J. (2018). Hand Motor Recovery following Extensive Frontoparietal Cortical Injury is accompanied by Upregulated Corticoreticular Projections in the Monkey. [10.1523/JNEUROSCI.0403-18.2018]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2018/06/13/JNEUROSCI.0403-18.2018...


Darmopil, S., Muneton-Gomez, V. C., de Ceballos, M. L., Bernson, M., & Moratalla, R. (2008). Tyrosine hydroxylase cells appearing in the mouse striatum after dopamine denervation are likely to be projection neurones regulated by l-DOPA. European Journal of Neuroscience, 27(3), 580-592. doi: doi:10.1111/j.1460-9568.2008.06040.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2008.06040.x 


Darmopil, S., Petanjek, Z., Mohammed, A. H., & Bogdanović, N. (2009). Environmental enrichment alters dentate granule cell morphology in oldest-old rat. Journal of Cellular and Molecular Medicine, 13(8b), 1845-1856. doi. 

Darnall, R. A., Schneider, R. W., Tobia, C. M., & Zemel, B. M. (2012). Arousal from sleep in response to intermittent hypoxia in rat pups is modulated by medullary raphe GABAergic mechanisms. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 302(5), R551–R560-R551–R560. doi. 

Das, G., Yu, Q., Hui, R., Reuhl, K., Gale, N. W., & Zhou, R. (2016). EphA5 and EphA6: regulation of neuronal and spine morphology. [journal article]. Cell & Bioscience, 6(1), 1-12. doi: 10.1186/s13578-016-0115-5. http://dx.doi.org/10.1186/s13578-016-0115-5


Das, I., Sparrow, J. R., Lin, M. I., Shih, E., Mikawa, T., & Hempstead, B. L. (2000). Trk C Signaling Is Required for Retinal Progenitor Cell Proliferation. Journal of Neuroscience, 20(8), 2887-2895. doi. http://www.jneurosci.org/cgi/content/abstract/20/8/2887


Das, M. M., Godoy, M., Chen, S., Moser, V. A., Avalos, P., Roxas, K. M., . . . Goodridge, H. S. (2019). Young bone marrow transplantation preserves learning and memory in old mice. Communications Biology, 2(1), 73. doi: 10.1038/s42003-019-0298-5. https://doi.org/10.1038/s42003-019-0298-5


Das, S., Nalini, A., Laxmi, T. R., & Raju, T. R. (2020). ALS-CSF-induced structural changes in spinal motor neurons of rat pups cause deficits in motor behaviour. Experimental Brain Research. doi: 10.1007/s00221-020-05969-7. https://doi.org/10.1007/s00221-020-05969-7


Das, S. K., Baitharu, I., Barhwal, K., Hota, S. K., & Singh, S. B. (2016). Early mood behavioral changes following exposure to monotonous environment during isolation stress is associated with altered hippocampal synaptic plasticity in male rats. Neuroscience Letters, 612, 231-237. doi: http://dx.doi.org/10.1016/j.neulet.2015.12.038. http://www.sciencedirect.com/science/article/pii/S0304394015303335


Dash, P. K., Tian, L.-M., & Moore, A. N. (1998). Sequestration of cAMP response element-binding proteins by transcription factor decoys causes collateral elaboration of regenerating Aplysia motor neuron axons. Proceedings of the National Academy of Sciences, 95(14), 8339-8344. doi: 10.1073/pnas.95.14.8339. http://www.pnas.org/cgi/content/abstract/95/14/8339 


Dautan, D., Souza, A. S., Huerta-Ocampo, I., Valencia, M., Assous, M., Witten, I. B., . . . Mena-Segovia, J. (2016). Segregated cholinergic transmission modulates dopamine neurons integrated in distinct functional circuits. [Article]. Nature Neuroscience, advance online publication. doi: 10.1038/nn.4335

http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.4335.html#suppl.... http://dx.doi.org/10.1038/nn.4335


Davenport, E. C., Szulc, B. R., Drew, J., Taylor, J., Morgan, T., Higgs, N. F., . . . Kittler, J. T. (2019). Autism and Schizophrenia-Associated CYFIP1 Regulates the Balance of Synaptic Excitation and Inhibition. Cell Reports, 26(8), 2037-2051.e2036. doi: https://doi.org/10.1016/j.celrep.2019.01.092. http://www.sciencedirect.com/science/article/pii/S2211124719301299


David, C., Schleicher, A., Zuschratter, W., & Staiger, J. F. (2007). The innervation of parvalbumin-containing interneurons by VIP-immunopositive interneurons in the primary somatosensory cortex of the adult rat. European Journal of Neuroscience, 25(8), 2329-2340. doi: doi:10.1111/j.1460-9568.2007.05496.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05496.x 


David, S., Stegenga, S. L., Hu, P., Xiong, G., Kerr, E., Becker, K. B., . . . Kalb, R. G. (2005). Expression of Serum- and Glucocorticoid-Inducible Kinase Is Regulated in an Experience-Dependent Manner and Can Cause Dendrite Growth. Journal of Neuroscience, 25(30), 7048-7053. doi. http://www.jneurosci.org/cgi/content/abstract/25/30/7048


Davis, S. F., Williams, K. W., Xu, W., Glatzer, N. R., & Smith, B. N. (2003). Selective Enhancement of Synaptic Inhibition by Hypocretin (Orexin) in Rat Vagal Motor Neurons: Implications for Autonomic Regulation. Journal of Neuroscience, 23, 3844-3854. doi. 

Davison, A. P., Hines, M. L., & Muller, E. (2009). Trends in programming languages for neuroscience simulations. Frontiers in Neuroscience, 3(3), 374-374. doi. 

Daw, M. I., Tricoire, L., Erdelyi, F., Szabo, G., & McBain, C. J. (2009). Asynchronous Transmitter Release from Cholecystokinin-Containing Inhibitory Interneurons Is Widespread and Target-Cell Independent. Journal of Neuroscience, 29(36), 11112-11122. doi: 10.1523/jneurosci.5760-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/36/11112 


Dawson, M. R. L., Polito, A., Levine, J. M., & Reynolds, R. (2003). NG2-expressing glial progenitor cells: an abundant and widespread population of cycling cells in the adult rat CNS. Molecular and Cellular Neuroscience, 24(2), 476-488. doi. 

Day-Brown, J. D., Wei, H., Chomsung, R. D., Petry, H. M., & Bickford, M. E. (2010). Frontiers: Pulvinar Projections to the Striatum and Amygdala in the Tree Shrew. Frontiers in Neuroanatomy, 4. doi. 

Day-Brown, J. D., Wei, H., Chomsung, R. D., Petry, H. M., & Bickford, M. E. (2010). Pulvinar projections to the striatum and amygdala in the tree shrew. Frontiers in Neuroanatomy, 4. doi. 

De Angelis, M. V., Capasso, M., Anghiari, C., Cavallaro, T., Di Muzio, A., Fabrizi, G. M., & Uncini, A. (2004). Myelin thickenings in val 102/fs null mutation of MPZ gene. Journal of the Peripheral Nervous System, 9(2), 121-121. doi: doi:10.1111/j.1085-9489.2004.009209bd.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


de Araújo Júnior, R. F., Leitão Oliveira, A. L. C., de Melo Silveira, R. F., de Oliveira Rocha, H. A., de França Cavalcanti, P., & de Araújo, A. A. (2014). Telmisartan induces apoptosis and regulates Bcl-2 in human renal cancer cells. Experimental Biology and Medicine. doi: 10.1177/1535370214546267. http://ebm.sagepub.com/content/early/2014/08/13/1535370214546267.abstract


De Bartolo, P., Gelfo, F., Burello, L., De Giorgio, A., Petrosini, L., & Granato, A. (2011). Plastic Changes in Striatal Fast-Spiking Interneurons Following Hemicerebellectomy and Environmental Enrichment. The Cerebellum, 1-9. doi. 

De Diego, I. R., Mellstrom, B., Vallejo, M., Naranjo, J. R., & Moratalla, R. (2014). Activation of DREAM, a calcium-binding protein, reduces L-DOPA-induced dyskinesias in mice. Biological Psychiatry, (0). doi: http://dx.doi.org/10.1016/j.biopsych.2014.03.023. http://www.sciencedirect.com/science/article/pii/S0006322314002248


De Guzman, R. M., Saulsbery, A. I., & Workman, J. L. (2018). High nursing demand reduces depression-like behavior despite increasing glucocorticoid concentrations and reducing hippocampal neurogenesis in late postpartum rats. Behavioural Brain Research, 353, 143-153. doi: https://doi.org/10.1016/j.bbr.2018.07.012. http://www.sciencedirect.com/science/article/pii/S0166432818304674


De Jong, T. R., Pattij, T., Veening, J. G., Dederen, P., Waldinger, M. D., Cools, A. R., & Olivier, B. (2005). Effects of chronic paroxetine pretreatment on ($\pm$)-8-hydroxy-2-(di-n-propyl-amino) tetralin induced c-fos expression following sexual behavior. Neuroscience, 134(4), 1351-1361. doi. 

de Kock, C. P. (2016). Juxtasomal Loose-Patch Recordings in Awake, Head-Fixed Rats to Study the Link Between Structure and Function of Individual Neurons. Advanced Patch-Clamp Analysis for Neuroscientists, 21-35. doi. http://link.springer.com/protocol/10.1007/978-1-4939-3411-9_2


de Kock, C. P. J., Bruno, R. M., Spors, H., & Sakmann, B. (2007). Layer- and cell-type-specific suprathreshold stimulus representation in rat primary somatosensory cortex. Journal of Physiology, 581(1), 139-154. doi: 10.1113/jphysiol.2006.124321. http://jp.physoc.org/cgi/content/abstract/581/1/139 


de Kock, C. P. J., Pie, J., Pieneman, A. W., Mease, R. A., Bast, A., Guest, J. M., . . . Sakmann, B. (2021). High-frequency burst spiking in layer 5 thick-tufted pyramids of rat primary somatosensory cortex encodes exploratory touch. Communications Biology, 4(1), 709. doi: 10.1038/s42003-021-02241-8. https://doi.org/10.1038/s42003-021-02241-8


De Kock, C. P. J., & Sakmann, B. (2008). High frequency action potential bursts (≥ 100 Hz) in L2/3 and L5B thick tufted neurons in anaesthetized and awake rat primary somatosensory cortex. Journal of Physiology, 586(14), 3353-3364. doi. 

de Kock, C. P. J., & Sakmann, B. (2009). Spiking in primary somatosensory cortex during natural whisking in awake head-restrained rats is cell-type specific. Proceedings of the National Academy of Sciences, 106(38), 16446-16450. doi: 10.1073/pnas.0904143106. http://www.pnas.org/content/106/38/16446.abstract 


de la Mothe, L. A., Blumell, S., Kajikawa, Y., & Hackett, T. A. (2006). Cortical connections of the auditory cortex in marmoset monkeys: core and medial belt regions. Journal of Comparative Neurology, 496(1), 27-71. doi. 

De La Mothe, L. A., Blumell, S., Kajikawa, Y., & Hackett, T. A. (2006). Thalamic connections of the auditory cortex in marmoset monkeys: core and medial belt regions. Journal of Comparative Neurology, 496(1), 72-96. doi. 

De la Rossa, A., Bellone, C., Golding, B., Vitali, I., Moss, J., Toni, N., . . . Jabaudon, D. (2013). In vivo reprogramming of circuit connectivity in postmitotic neocortical neurons. Nature Neuroscience. doi. 

De La Roza, C., Martínez-Mena, J., Sánchez-Valle, M. E., & Reinoso-Suárez, F. (2004). Projections from the cat posterior lateral hypothalamus to the ventral part of the oral pontine reticular nucleus contain a GABAergic component. Brain Research, 1020(1-2), 118-129. doi. 

De Lella Ezcurra, A. L., Chertoff, M., Ferrari, C., Graciarena, M., & Pitossi, F. (2010). Chronic expression of low levels of tumor necrosis factor-α in the substantia nigra elicits progressive neurodegeneration, delayed motor symptoms and microglia/macrophage activation. Neurobiology of Disease, 37(3), 630-640. doi. 

De Lorme, K. C., Schulz, K. M., Salas-Ramirez, K. Y., & Sisk, C. L. (2012). Pubertal testosterone organizes regional volume and neuronal number within the medial amygdala of adult male Syrian hamsters. Brain Research, 1460(0), 33-40. doi: 10.1016/j.brainres.2012.04.035. http://www.sciencedirect.com/science/article/pii/S0006899312007512


De Lorme, K. C., & Sisk, C. L. (2013). Pubertal testosterone programs context-appropriate agonistic behavior and associated neural activation patterns in male Syrian hamsters. Physiology and Behavior, (0). doi: http://dx.doi.org/10.1016/j.physbeh.2013.02.003. http://www.sciencedirect.com/science/article/pii/S0031938413000322


De Luca, A., Vassallo, S., Benitez-Temino, B., Menichetti, G., Rossi, F., & Buffo, A. (2009). Distinct Modes of Neuritic Growth in Purkinje Neurons at Different Developmental Stages: Axonal Morphogenesis and Cellular Regulatory Mechanisms. PLoS ONE, 4(8), e6848-e6848. doi. 

De Marchis, S., Temoney, S., Erdelyi, F., Bovetti, S., Bovolin, P., Szabo, G., & Puche, A. C. (2004). GABAergic phenotypic differentiation of a subpopulation of subventricular derived migrating progenitors. European Journal of Neuroscience, 20(5), 1307-1317. doi. http://www.blackwell-synergy.com/links/doi/10.1111/j.1460-9568.2004.0358...


De Marco Garcia, N. V., & Jessell, T. M. (2008). Early motor neuron pool identity and muscle nerve trajectory defined by postmitotic restrictions in Nkx6. 1 activity. Neuron, 57(2), 217-231. doi. 

de Novellis, V., Siniscalco, D., Galderisi, U., Fuccio, C., Nolano, M., Santoro, L., . . . Maione, S. (2004). Blockade of glutamate mGlu5 receptors in a rat model of neuropathic pain prevents early over-expression of pro-apoptotic genes and morphological changes in dorsal horn lamina II. Neuropharmacology, 46(4), 468-479. doi. 

de Oliveira, A. M., Nascimento Silva, M. L., Keher, N. B., Bittencourt Navarrete, R. E., Gattass, R., & da Franca, J. G. (2015). Architectonic mapping of somatosensory areas involved in skilled forelimb movements and tool use. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23916. http://dx.doi.org/10.1002/cne.23916


de Oliveira, R. B., Gomes Leal, W., Picanço-Diniz, D. L. W., Torres Neto, J. B., Lins, N., Malm, O., & Picanço-Diniz, C. W. (2008). Three dimensional morphometric analyses of axon terminals early changes induced by methylmercury intoxication in the adult cat striate cortex. Brain Research, 1244, 155-163. doi. 

de Oliveira, T. C. G., Carvalho-Paulo, D., de Lima, C. M., de Oliveira, R. B., Santos Filho, C., Diniz, D. G., . . . Picanço-Diniz, C. W. (2020). Long-term environmental enrichment reduces microglia morphological diversity of the molecular layer of dentate gyrus. European Journal of Neuroscience, n/a(n/a). doi: 10.1111/ejn.14920. https://onlinelibrary.wiley.com/doi/abs/10.1111/ejn.14920


De Paola, V., Holtmaat, A., Knott, G., Song, S., Wilbrecht, L., Caroni, P., & Svoboda, K. (2006). Cell type-specific structural plasticity of axonal branches and boutons in the adult neocortex. Neuron, 49(6), 861-875. doi. 

de Rivero Vaccari, J. P., Bastien, D., Yurcisin, G., Pineau, I., Dietrich, W. D., De Koninck, Y., . . . Lacroix, S. (2012). P2X4 Receptors Influence Inflammasome Activation after Spinal Cord Injury. Journal of Neuroscience, 32(9), 3058-3066. doi: 10.1523/jneurosci.4930-11.2012. http://www.jneurosci.org/content/32/9/3058.abstract


de Rivero Vaccari, J. P., Lotocki, G., Alonso, O. F., Bramlett, H. M., Dietrich, W. D., & Keane, R. W. (2009). Therapeutic neutralization of the NLRP1 inflammasome reduces the innate immune response and improves histopathology after traumatic brain injury. Journal of Cerebral Blood Flow and Metabolism, 29(7), 1251-1261. doi. 

de Rivero Vaccari, J. P., Lotocki, G., Marcillo, A. E., Dietrich, W. D., & Keane, R. W. (2008). A Molecular Platform in Neurons Regulates Inflammation after Spinal Cord Injury. Journal of Neuroscience, 28(13), 3404-3414. doi: 10.1523/jneurosci.0157-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/13/3404 


de Schultz, T., Bock, J., & Braun, K. (2020). Paternal Deprivation and Female Biparental Family Rearing Induce Dendritic and Synaptic Changes in Octodon degus: I. Medial Prefrontal Cortex. Frontiers in synaptic neuroscience, 12, 38-38. doi: 10.3389/fnsyn.2020.00038. https://pubmed.ncbi.nlm.nih.gov/33013347

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7498658/


de Sousa, A. A., dos Reis, R. R., de Lima, C. M., de Oliveira, M. A., Fernandes, T. N., Gomes, G. F., . . . Diniz, C. W. P. (2015). Three-dimensional morphometric analysis of microglial changes in a mouse model of virus encephalitis: age and environmental influences. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12951. http://dx.doi.org/10.1111/ejn.12951


de Vellis, J., Ghiani, C. A., Wanner, I. B., & Cole, R. (2009). Preparation of Normal and Reactive Astrocyte Cultures. Protocols for Neural Cell Culture, 193-216. doi. 

de Venecia, R. K., & McMullen, N. T. (1994). Single thalamocortical axons diverge to multiple patches in neonatal auditory cortex. Developmental Brain Research, 81, 135-142. doi. 

de Villers-Sidani, E., Tahvildari, B., & Alonso, A. (2004). Synaptic activation patterns of the perirhinal-entorhinal inter-connections. Neuroscience, 129(1), 255-265. doi. 

Dea, M., Hamadjida, A., Elgbeili, G., Quessy, S., & Dancause, N. (2016). Different Patterns of Cortical Inputs to Subregions of the Primary Motor Cortex Hand Representation in Cebus apella. Cerebral Cortex. doi: 10.1093/cercor/bhv324. http://cercor.oxfordjournals.org/content/early/2016/01/10/cercor.bhv324....


Dean, S. L., Knutson, J. F., Krebs-Kraft, D. L., & McCarthy, M. M. (2012). Prostaglandin E2 is an endogenous modulator of cerebellar development and complex behavior during a sensitive postnatal period. European Journal of Neuroscience, 35(8), 1218-1229. doi: 10.1111/j.1460-9568.2012.08032.x. http://dx.doi.org/10.1111/j.1460-9568.2012.08032.x


deazevedo, L. C., Hedin-Pereira, C., & Lent, R. (2002). Diaphorase-positive neurons in the cingulate cortex of human fetuses during the second half of gestation. Anatomy and Embryology, 205(1), 29-35. doi. 

DeBoer, E. M., Azevedo, R., Vega, T. A., Brodkin, J., Akamatsu, W., Okano, H., . . . Rasin, M.-R. (2014). Prenatal Deletion of the RNA-Binding Protein HuD Disrupts Postnatal Cortical Circuit Maturation and Behavior. The Journal of Neuroscience, 34(10), 3674-3686. doi. http://www.jneurosci.org/content/34/10/3674.short


deCampo, D. M., & Fudge, J. L. (2013). Amygdala projections to the lateral bed nucleus of the stria terminalis in the macaque: Comparison with ventral striatal afferents. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23340. http://dx.doi.org/10.1002/cne.23340


Decker, Y., Müller, A., Németh, E., Schulz-Schaeffer, W. J., Fatar, M., Menger, M. D., . . . Fassbender, K. (2017). Analysis of the vasculature by immunohistochemistry in paraffin-embedded brains. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-017-1595-8. https://doi.org/10.1007/s00429-017-1595-8


Dedeoglu, A., Kubilus, J. K., Jeitner, T. M., Matson, S. A., Bogdanov, M., Kowall, N. W., . . . Ferrante, R. J. (2002). Therapeutic Effects of Cystamine in a Murine Model of Huntington's Disease. Journal of Neuroscience, 22, 8942-8950. doi. 

Dedeoglu, A., Kubilus, J. K., Yang, L., Ferrante, K. L., Hersch, S. M., Beal, M. F., & Ferrante, a. R. J. (2003). Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice. Journal of Neurochemistry, 85(6), 1359-1367. doi: doi:10.1046/j.1471-4159.2003.01706.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1471-4159.2003.01706.x 


Dee, F. (2004). Grant Abstract: Database of Virtual Cervical Cytology  Retrieved January 25, 2005, from http://crisp.cit.nih.gov/crisp/CRISP_LIB.getdoc?textkey=6761930&p_grant_...

DeFelipe, J., López-Cruz, P. L., Benavides-Piccione, R., Bielza, C., Larrañaga, P., Anderson, S., . . . Feldmeyer, D. (2013). New insights into the classification and nomenclature of cortical GABAergic interneurons. Nature Reviews Neuroscience. doi. 

Dégenètais, E., Thierry, A. M., Glowinski, J., & Gioanni, Y. (2002). Electrophysiological properties of pyramidal neurons in the rat prefrontal cortex: an in vivo intracellular recording study. Cerebral Cortex, 12(1), 1-16. doi. 

Degos, B., Deniau, J. M., Le Cam, J., Mailly, P., & Maurice, N. (2008). Evidence for a direct subthalamo-cortical loop circuit in the rat. European Journal of Neuroscience, 27(10), 2599-2610. doi. 

Dehner, L. R., Keniston, L. P., Clemo, H. R., & Meredith, M. A. (2004). Cross-modal Circuitry Between Auditory and Somatosensory Areas of the Cat Anterior Ectosylvian Sulcal Cortex: A 'New' Inhibitory Form of Multisensory Convergence. Cerebral Cortex, 14(4), 387-403. doi: 10.1093/cercor/bhg135. http://cercor.oxfordjournals.org/cgi/content/abstract/14/4/387 


Dehorter, N., Guigoni, C., Lopez, C., Hirsch, J., Eusebio, A., Ben-Ari, Y., & Hammond, C. (2009). Dopamine-Deprived Striatal GABAergic Interneurons Burst and Generate Repetitive Gigantic IPSCs in Medium Spiny Neurons. Journal of Neuroscience, 29(24), 7776-7787. doi: 10.1523/jneurosci.1527-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/24/7776 


Dehorter, N., Lozovaya, N., Mdzomba, B. J., Michel, F. J., Lopez, C., Tsintsadze, V., . . . Hammond, C. (2012). Subthalamic Lesion or Levodopa Treatment Rescues Giant GABAergic Currents of PINK1-Deficient Striatum. Journal of Neuroscience, 32(50), 18047-18053. doi: 10.1523/jneurosci.2474-12.2012. http://www.jneurosci.org/content/32/50/18047.abstract


Dehorter, N., Michel, F. J., Marissal, T., Rotrou, Y., Matrot, B., Lopez, C., . . . Hammond, C. (2011). Frontiers: Onset of Pup Locomotion Coincides with Loss of NR2C/D-Mediated Cortico-Striatal EPSCs and Dampening of Striatal Network Immature Activity. Frontiers in cellular neuroscience, 5. doi. 

Dehorter, N., Michel, F. J., Marissal, T., Rotrou, Y., Matrot, B., Lopez, C., . . . Hammond, C. (2011). Onset of Pup Locomotion Coincides with Loss of NR2C/D-Mediated Cortico-Striatal EPSCs and Dampening of Striatal Network Immature Activity. Frontiers in cellular neuroscience, 5. doi. 

Deitcher, Y., Eyal, G., Kanari, L., Verhoog, M. B., Kahou, A., Antoine, G., . . . Segev, I. (2017). Comprehensive Morpho-Electrotonic Analysis Shows 2 Distinct Classes of L2 and L3 Pyramidal Neurons in Human Temporal Cortex. Cerebral Cortex, 1-17. doi. https://academic.oup.com/cercor/article/doi/10.1093/cercor/bhx226/415921...


del Blanco, B., Guiretti, D., Tomasoni, R., Lopez-Cascales, M. T., Muñoz-Viana, R., Lipinski, M., . . . Barco, A. (2019). CBP and SRF co-regulate dendritic growth and synaptic maturation. Cell Death and Differentiation. doi: 10.1038/s41418-019-0285-x. https://doi.org/10.1038/s41418-019-0285-x


Del Carro, U., Biffi, A., Baldoli, C., Gerevini, S., Amadio, S., Fumagalli, F., . . . Sessa, M. (2004). Clinical history and new prognostic indicators in metachromatic leukodystrophy. Journal of the Peripheral Nervous System, 9(2), 112-112. doi: doi:10.1111/j.1085-9489.2004.009209ab.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


del Pino, I., Brotons-Mas, J. R., Marques-Smith, A., Marighetto, A., Frick, A., Marin, O., & Rico, B. (2017). Abnormal wiring of CCK+ basket cells disrupts spatial information coding. [Article]. Nature Neuroscience, advance online publication. doi: 10.1038/nn.4544

http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.4544.html#suppl.... http://dx.doi.org/10.1038/nn.4544


Dela Cruz, J. A. D., Coke, T., & Bodnar, R. J. (2016). Simultaneous Detection of c-Fos Activation from Mesolimbic and Mesocortical Dopamine Reward Sites Following Naive Sugar and Fat Ingestion in Rats. (114), e53897. doi: doi:10.3791/53897. http://www.jove.com/video/53897


Delaloye, S., Kraftsik, R., Kuntzer, T., & Barakat-Walter, I. (2009). Does the physical disector method provide an accurate estimation

of sensory neuron number in rat dorsal root ganglia? Journal of Neuroscience Methods, 176, 290-297. doi. 

Delatour, B., & Witter, M. P. (2002). Projections from the parahippocampal region to the prefrontal cortex in the rat: evidence of multiple pathways. European Journal of Neuroscience, 15(8), 1400. doi. 

Delatour, L. C., Yeh, P. W., & Yeh, H. H. (2018). Ethanol Exposure In Utero Disrupts Radial Migration and Pyramidal Cell Development in the Somatosensory Cortex. Cerebral Cortex, bhy094-bhy094. doi: 10.1093/cercor/bhy094. http://dx.doi.org/10.1093/cercor/bhy094


Delatour, L. C., Yeh, P. W. L., & Yeh, H. H. (2019). Prenatal Exposure to Ethanol Alters Synaptic Activity in Layer V/VI Pyramidal Neurons of the Somatosensory Cortex. Cerebral Cortex. doi: 10.1093/cercor/bhz199. https://doi.org/10.1093/cercor/bhz199


Deleuze, C., & Huguenard, J. R. (2006). Distinct Electrical and Chemical Connectivity Maps in the Thalamic Reticular Nucleus: Potential Roles in Synchronization and Sensation. Journal of Neuroscience, 26(33), 8633-8645. doi: 10.1523/jneurosci.2333-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/33/8633 


Dell, L.-A., Patzke, N., Bhagwandin, A., Bux, F., Fuxe, K., Barber, G., . . . Manger, P. R. (2012). Organization and number of orexinergic neurons in the hypothalamus of two species of Cetartiodactyla: A comparison of giraffe (Giraffa camelopardalis) and harbour porpoise (Phocoena phocoena). Journal of Chemical Neuroanatomy, (0). doi: 10.1016/j.jchemneu.2012.06.001. http://www.sciencedirect.com/science/article/pii/S0891061812000336


Dellacasa-Lindberg, I., Fuks, J., Arrighi, R., Lambert, H., Wallin, R., Chambers, B., & Barragan, A. (2011). Migratory activation of primary cortical microglia upon infection with Toxoplasma gondii. Infection and Immunity, 79, 3046 - 3052. doi. 

Dellen, A., Welch, J., Dixon, R. M., Cordery, P., York, D., Styles, P., . . . Hannan, A. J. (2000). N-Acetylaspartate and DARPP-32 levels decrease in the corpus striatum of Huntington's disease mice. Neuroreport, 11(17), 3751-3751. doi. 

Dellen, A. v., Blakemore, C., Deacon, R., York, D., & Hannan, A. J. (2002). Delaying the onset of Huntington's in mice. Nature, 404, 721-722. doi. 

DeMarch, Z., Giampà, C., Patassini, S., Bernardi, G., & Fusco, F. R. (2008). Beneficial effects of rolipram in the R6/2 mouse model of Huntington's disease. Neurobiology of Disease, 30(3), 375-387. doi. 

De-May, C. L., & Ali, A. B. (2012). Cell-type specific regulation of inhibition via cannabinoid type 1 receptors in rat neocortex. Journal of Neurophysiology. doi: 10.1152/jn.00272.2012. http://jn.physiology.org/content/early/2012/10/05/jn.00272.2012.abstract


Dembrow, N. C., Chitwood, R. A., & Johnston, D. (2010). Projection-Specific Neuromodulation of Medial Prefrontal Cortex Neurons. Journal of Neuroscience, 30(50), 16922-16937. doi: 10.1523/jneurosci.3644-10.2010. http://www.jneurosci.org/cgi/content/abstract/30/50/16922


Demyanenko, G. P., Halberstadt, A. I., Rao, R. S., & Maness, P. F. (2010). CHL1 cooperates with PAK1-3 to regulate morphological differentiation of embryonic cortical neurons. Neuroscience, 165(1), 107-115. doi. 

Demyanenko, G. P., Mohan, V., Zhang, X., Brennaman, L. H., Dharbal, K. E., Tran, T. S., . . . Maness, P. F. (2014). Neural Cell Adhesion Molecule NrCAM Regulates Semaphorin 3F-Induced Dendritic Spine Remodeling. The Journal of Neuroscience, 34(34), 11274-11287. doi. http://www.jneurosci.org/content/34/34/11274.short


Demyanenko, G. P., Schachner, M., Anton, E., Schmid, R., Feng, G., Sanes, J., & Maness, P. F. (2004). Close homolog of L1 modulates area-specific neuronal positioning and dendrite orientation in the cerebral cortex. Neuron, 44(3), 423-437. doi. 

Dénes, V., Wilhelm, M., NÉMeth, A., & GÁBriel, R. (2009). Interactions of Serotoninergic, Cholinergic, and Tachykinin-Containing Nerve Elements in the Rabbit Small Intestine. Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology, 292(10), 1548-1558. doi. 

Deng, C.-Y., Lei, W.-L., Xu, X.-H., Ju, X.-C., Liu, Y., & Luo, Z.-G. (2014). JIP1 Mediates Anterograde Transport of Rab10 Cargos during Neuronal Polarization. The Journal of Neuroscience, 34(5), 1710-1723. doi. http://www.jneurosci.org/content/34/5/1710.short


Deng, L., Ruan, Y., Chen, C., Frye, C. C., Xiong, W., Jin, X., . . . Xu, X.-M. (2016). Characterization of dendritic morphology and neurotransmitter phenotype of thoracic descending propriospinal neurons after complete spinal cord transection and GDNF treatment. Experimental Neurology, 277, 103-114. doi: http://dx.doi.org/10.1016/j.expneurol.2015.12.018. http://www.sciencedirect.com/science/article/pii/S0014488615301461


Deng, L.-X., Liu, N.-K., Wen, R., Yang, S.-N., Wen, X., & Xu, X.-M. (2021). Laminin-coated multifilament entubulation, combined with Schwann cells and glial cell line-derived neurotrophic factor, promotes unidirectional axonal regeneration in a rat model of thoracic spinal cord hemisection. [Research Article]. Neural Regeneration Research, 16(1), 186-191. doi: 10.4103/1673-5374.289436. http://www.nrronline.org/article.asp?issn=1673-5374;year=2021;volume=16;...


Deng, M., Hofacer, R. D., Jiang, C., Joseph, B., Hughes, E. A., Jia, B., . . . Loepke, A. W. (2014). Brain regional vulnerability to anaesthesia-induced neuroapoptosis shifts with age at exposure and extends into adulthood for some regions. British Journal of Anaesthesia. doi: 10.1093/bja/aet469. http://bja.oxfordjournals.org/content/early/2014/01/14/bja.aet469.abstract


Deng, R., Kao, J. P. Y., & Kanold, P. O. (2017). Distinct Translaminar Glutamatergic Circuits to GABAergic Interneurons in the Neonatal Auditory Cortex. Cell Reports, 19(6), 1141-1150. doi: https://doi.org/10.1016/j.celrep.2017.04.044. http://www.sciencedirect.com/science/article/pii/S2211124717305387


Dent, G. W., Rule, B. L., Zhan, Y., & Grzanna, R. (2001). The acetylcholine release enhancer linopirdine induces Fos in neocortex of aged rats. Neurobiology of Aging, 22(3), 485-494. doi. 

DePuy, S. D., Kanbar, R., Coates, M. B., Stornetta, R. L., & Guyenet, P. G. (2011). Control of Breathing by Raphe Obscurus Serotonergic Neurons in Mice. Journal of Neuroscience, 31(6), 1981-1990. doi: 10.1523/jneurosci.4639-10.2011. http://www.jneurosci.org/content/31/6/1981.abstract


Dequen, F., Bomont, P., Gowing, G., Cleveland, D. W., & Julien, J. P. (2008). Modest loss of peripheral axons, muscle atrophy and formation of brain inclusions in mice with targeted deletion of gigaxonin exon 1. Journal of Neurochemistry, 107(1), 253-264. doi. 

Dercksen, V. J., Oberlaender, M., Sakmann, B., & Hege, H. C. (2012). Interactive Visualization–a Key Prerequisite for Reconstruction and Analysis of Anatomically Realistic Neural Networks. Visualization in Medicine and Life Sciences II, 27-44. doi. 

Derugin, N., Dingman, A., Wendland, M. F., Fox, C., Bollen, A., & Vexler, Z. S. (2005). Magnetic resonance imaging as a surrogate measure for histological sub-chronic endpoint in a neonatal rat stroke model. Brain Research, 1066(1), 49-56. doi. 

Deshmukh, S., Onozuka, K., Bender, K. J., Bender, V. A., Lutz, B., Mackie, K., & Feldman, D. E. (2007). Postnatal development of cannabinoid receptor type 1 expression in rodent somatosensory cortex. Neuroscience, 145(1), 279-287. doi. 

Deshpande, A., Dombrowski, S. M., Leichliter, A., Krajcir, N., Zingales, N., Inoue, M., . . . Luciano, M. G. (2009). Dissociation between vascular endothelial growth factor receptor-2 and blood vessel density in the caudate nucleus after chronic hydrocephalus. Journal of Cerebral Blood Flow and Metabolism, 29(11), 1806-1815. doi. 

Dessem, D., Moritani, M., & Ambalavanar, R. (2007). Nociceptive Craniofacial Muscle Primary Afferent Neurons Synapse in Both the Rostral and Caudal Brain Stem. Journal of Neurophysiology, 98(1), 214-223. doi: 10.1152/jn.00990.2006. http://jn.physiology.org/cgi/content/abstract/98/1/214 


Destot-Wong, K. D., Liang, K., Gupta, S. K., Favrais, G., Schwendimann, L., Pansiot, J., . . . others. (2009). The AMPA receptor positive allosteric modulator, S18986, is neuroprotective against neonatal excitotoxic and inflammatory brain damage through BDNF synthesis. Neuropharmacology, 57(3), 277-286. doi. 

Detrez, J. R., Verstraelen, P., Gebuis, T., Verschuuren, M., Kuijlaars, J., Langlois, X., . . . De Vos, W. H. (2016). Image Informatics Strategies for Deciphering Neuronal Network Connectivity. In H. W. De Vos, S. Munck & J.-P. Timmermans (Eds.), Focus on Bio-Image Informatics (pp. 123-148). Cham: Springer International Publishing.

Devanathan, V., Jakovcevski, I., Santuccione, A., Li, S., Lee, H. J., Peles, E., . . . Schachner, M. (2010). Cellular form of prion protein inhibits reelin-mediated shedding of Caspr from the neuronal cell surface to potentiate Caspr-mediated inhibition of neurite outgrowth. Journal of Neuroscience, 30(27), 9292-9305. doi. 

Devanathan, V., Jakovcevski, I., Santuccione, A., Li, S., Lee, H. J., Peles, E., . . . Schachner, M. (2010). Cellular Form of Prion Protein Inhibits Reelin-Mediated Shedding of Caspr from the Neuronal Cell Surface to Potentiate Caspr-Mediated Inhibition of Neurite Outgrowth. Journal of Neuroscience, 30(27), 9292-9305. doi: 10.1523/jneurosci.5657-09.2010. http://www.jneurosci.org/cgi/content/abstract/30/27/9292 


DeVito, L. M., Balu, D. T., Kanter, B. R., Lykken, C., Basu, A. C., Coyle, J. T., & Eichenbaum, H. (2010). Serine racemase deletion disrupts memory for order and alters cortical dendritic morphology. Genes, Brain and Behavior, no-no. doi: 10.1111/j.1601-183X.2010.00656.x. http://dx.doi.org/10.1111/j.1601-183X.2010.00656.x


Devor, A., & Yarom, Y. (2002). Electrotonic Coupling in the Inferior Olivary Nucleus Revealed by Simultaneous Double Patch Recordings. Journal of Neurophysiology, 87(6), 3048-3058. doi. http://jn.physiology.org/cgi/content/abstract/87/6/3048 


Devor, M., Zalkind, V., Fishman, Y., & Minert, A. (2016). Model of anesthetic induction by unilateral intracerebral microinjection of GABAergic agonists. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.13186. http://dx.doi.org/10.1111/ejn.13186


Dewitt, D. D., Kaszuba, S. N., Thompson, D. M., & Stegemann, J. P. (2009). Collagen I-matrigel scaffolds for enhanced Schwann cell survival and control of three-dimensional cell morphology. Tissue Engineering Part A, 15(10), 2785-2793. doi. 

DeWulf, V., & Bottjer, S. W. (2005). Neurogenesis within the juvenile zebra finch telencephalic ventricular zone: a map of proliferative activity. Journal of Comparative Neurology, 481(1), 70-83. doi. 

Dhande, O. S., Bhatt, S., Anishchenko, A., Elstrott, J., Iwasato, T., Swindell, E. C., . . . others. (2011). Role of adenylate cyclase 1 in retinofugal map development. Journal of Comparative Neurology. doi. 

Dhande, O. S., Estevez, M. E., Quattrochi, L. E., El-Danaf, R. N., Nguyen, P. L., Berson, D. M., & Huberman, A. D. (2013). Genetic Dissection of Retinal Inputs to Brainstem Nuclei Controlling Image Stabilization. Journal of Neuroscience, 33(45), 17797-17813. doi. http://www.jneurosci.org/content/33/45/17797.abstract


Dhande, O. S., Hua, E. W., Guh, E., Yeh, J., Bhatt, S., Zhang, Y., . . . Crair, M. C. (2011). Development of Single Retinofugal Axon Arbors in Normal and β2 Knock-Out Mice. Journal of Neuroscience, 31(9), 3384-3399. doi: 10.1523/jneurosci.4899-10.2011. http://www.jneurosci.org/content/31/9/3384.abstract


Dhande, O. S., Stafford, B. K., Franke, K., El-Danaf, R., Percival, K. A., Phan, A. H., . . . Huberman, A. D. (2018). Molecular fingerprinting of On-Off direction selective retinal ganglion cells across species and relevance to primate visual circuits. [10.1523/JNEUROSCI.1784-18.2018]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2018/10/29/JNEUROSCI.1784-18.2018...


Dhar, P., Das, S. K., Barhwal, K., Hota, S. K., Mishra, K. P., & Singh, S. B. (2019). Trans-Himalayan Phytococktail Confers Protection Against Hypobaric Hypoxia-Induced Hippocampal Neurodegeneration and Memory Impairment in Male Sprague Dawley Rats. High Altitude Medicine & Biology, 20(3), 279-292. doi: 10.1089/ham.2019.0011. https://doi.org/10.1089/ham.2019.0011


Di Cunto, F., Ferrara, L., Curtetti, R., Imarisio, S., Guazzone, S., Broccoli, V., . . . Silengo, L. (2003). Role of citron kinase in dendritic morphogenesis of cortical neurons. Brain Research Bulletin, 60(4), 319-327. doi. 

Di Rocco, F., Giannetti, S., Gaglini, P., Di Rocco, C., & Granato, A. (2001). Dendritic Anomalies in a Freezing Model of Microgyria: A Parametric Study. Pediatric Neurosurgery, 34(2), 57-62. doi. http://www.karger.com/DOI/10.1159/000055996 


Di Rocco, F., Giannetti, S., Gaglini, P., Di Rocco, C., & Granato, A. (2002). Dendritic architecture of corticothalamic neurons in a rat model of microgyria. Child's Nervous System, 18(12), 690-693. doi. 

Di Segni, M., Andolina, D., Coassin, A., Accoto, A., Luchetti, A., Pascucci, T., . . . Ventura, R. (2017). Sensitivity to cocaine in adult mice is due to interplay between genetic makeup, early environment and later experience. Neuropharmacology, 125, 87-98. doi: https://doi.org/10.1016/j.neuropharm.2017.07.014. http://www.sciencedirect.com/science/article/pii/S0028390817303428


Dias, C. M., Punetha, J., Zheng, C., Mazaheri, N., Rad, A., Efthymiou, S., . . . Maroofian, R. (2019). Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. The American Journal of Human Genetics. doi: https://doi.org/10.1016/j.ajhg.2019.09.025. http://www.sciencedirect.com/science/article/pii/S0002929719303866


Dias, I. A., Bahia, C. P., Franca, J. G., Houzel, J. C., Lent, R., Mayer, A. O., . . . Pereira, A. (2014). Topography and architecture of visual and somatosensory areas of the agouti. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23550. http://dx.doi.org/10.1002/cne.23550


Díaz, D., del Pilar, C., Carretero, J., Alonso, J. R., & Weruaga, E. (2019). Daily bone marrow cell transplantations for the management of fast neurodegenerative processes. Journal of Tissue Engineering and Regenerative Medicine, 0(ja). doi: 10.1002/term.2925. https://onlinelibrary.wiley.com/doi/abs/10.1002/term.2925


Díaz, D., Lepousez, G., Gheusi, G., Alonso, J. R., Lledo, P.-M., & Weruaga, E. (2012). Bone Marrow Cell Transplantation Restores Olfaction in the Degenerated Olfactory Bulb. Journal of Neuroscience, 32(26), 9053-9058. doi: 10.1523/jneurosci.0260-12.2012. http://www.jneurosci.org/content/32/26/9053.abstract


Díaz, D., Piquer-Gil, M., Recio, J. S., Martínez-Losa, M. M., Alonso, J. R., Weruaga, E., & Álvarez-Dolado, M. (2017). Bone marrow transplantation improves motor activity in a mouse model of ataxia. Journal of Tissue Engineering and Regenerative Medicine, n/a-n/a. doi: 10.1002/term.2626. http://dx.doi.org/10.1002/term.2626


Díaz, E., Bravo, D., Rojas, X., & Concha, M. L. (2011). Morphologic and immunohistochemical organization of the human habenular complex. Journal of Comparative Neurology, 519(18), 3727-3747. doi: 10.1002/cne.22687. http://dx.doi.org/10.1002/cne.22687


Diaz, H. S., Andrade, D. C., Toledo, C., Pereyra, K. V., Schwarz, K. G., Díaz-Jara, E., . . . Rio, R. D. (2019). Episodic stimulation of central chemoreceptor neurons elicits disordered breathing and autonomic dysfunction in volume overload heart failure. American Journal of Physiology-Lung Cellular and Molecular Physiology, 0(0), null. doi: 10.1152/ajplung.00007.2019. https://www.physiology.org/doi/abs/10.1152/ajplung.00007.2019


Diaz Vera, D., Soucy, J. R., Lee, A., Koppes, R. A., & Koppes, A. N. (2021). Light irradiation of peripheral nerve cells: Wavelength impacts primary sensory neuron outgrowth in vitro. Journal of Photochemistry and Photobiology B: Biology, 215, 112105. doi: https://doi.org/10.1016/j.jphotobiol.2020.112105. http://www.sciencedirect.com/science/article/pii/S1011134420305558


Dibaj, P., Steffens, H., Nadrigny, F., Neusch, C., Kirchhoff, F., & Schomburg, E. (2010). Long-lasting post-mortem activity of spinal microglia in situ in mice. Journal of Neuroscience Research, 88, 2431 - 2440. doi. 

DiBona, V. L., Shah, M. K., Krause, K. J., Zhu, W., Voglewede, M. M., Smith, D. M., . . . Zhang, H. (2021). Metformin reduces neuroinflammation and improves cognitive functions after traumatic brain injury. Neuroscience Research. doi: https://doi.org/10.1016/j.neures.2021.05.007. https://www.sciencedirect.com/science/article/pii/S016801022100105X


DiBona, V. L., Zhu, W., Shah, M. K., Rafalia, A., Ben Cheikh, H., Crockett, D. P., & Zhang, H. (2019). Loss of Par1b/MARK2 primes microglia during brain development and enhances their sensitivity to injury. [journal article]. Journal of Neuroinflammation, 16(1), 11. doi: 10.1186/s12974-018-1390-3. https://doi.org/10.1186/s12974-018-1390-3


DiCarlo, J. J., & Johnson, K. O. (2000). Spatial and Temporal Structure of Receptive Fields in Primate Somatosensory Area 3b: Effects of Stimulus Scanning Direction and Orientation. Journal of Neuroscience, 20(1), 495-510. doi. http://www.jneurosci.org/cgi/content/abstract/20/1/495


DiCarlo, J. J., Johnson, K. O., & Hsiao, S. S. (1998). Structure of Receptive Fields in Area 3b of Primary Somatosensory Cortex in the Alert Monkey. Journal of Neuroscience, 18(7), 2626-2645. doi. http://www.jneurosci.org/cgi/content/abstract/18/7/2626


Dick, J., G.C., B. F., Bin, W., Subramanian, V., Jan, V., Dies, M., . . . I., D. Z. C. (2018). The basal interstitial nucleus (BIN) of the cerebellum provides diffuse ascending inhibitory input to the floccular granule cell layer. Journal of Comparative Neurology, 0(ja). doi: doi:10.1002/cne.24479. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24479


Dickman, J. D., Huss, D., & Lowe, M. (2004). Morphometry of otoconia in the utricle and saccule of developing Japanese quail. Hearing Research, 188(1-2), 89-103. doi. 

Dickson, C. T., Magistretti, J., Shalinsky, M., Hamam, B., & Alonso, A. (2000). Oscillatory Activity in Entorhinal Neurons and Circuits: Mechanisms and Function. Annals of the New York Academy of Sciences, 911(1), 127-150. doi: doi:10.1111/j.1749-6632.2000.tb06723.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1749-6632.2000.tb0672...


Dickson, T. C., Mintz, C. D., Benson, D. L., & Salton, S. R. J. (2002). Functional binding interaction identified between the axonal CAM L1 and members of the ERM family. Journal of Cell Biology, 157(7), 1105-1112. doi: 10.1083/jcb.200111076. http://www.jcb.org/cgi/content/abstract/157/7/1105 


Dickstein, D. L., Brautigam, H., Stockton, S. D., Schmeidler, J., & Hof, P. R. (2010). Changes in dendritic complexity and spine morphology in transgenic mice expressing human wild-type tau. Brain Structure and Function, 214(2), 161-179. doi. 

Dickstein, D. L., Dickstein, D. R., Janssen, W. G. M., Hof, P. R., Glaser, J. R., Rodriguez, A., . . . Tappan, S. J. (2001). Automatic Dendritic Spine Quantification from Confocal Data with Neurolucida 360 Current Protocols in Neuroscience: John Wiley & Sons, Inc.

Dickstein, D. L., Talty, R., Bresnahan, E., Varghese, M., Perry, B., Janssen, W. G. M., . . . Limoli, C. L. (2018). Alterations in synaptic density and myelination in response to exposure to high-energy charged particles. Journal of Comparative Neurology, 0(ja). doi: doi:10.1002/cne.24530. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24530


Diederich, K., Sevimli, S., Dorr, H., Kosters, E., Hoppen, M., Lewejohann, L., . . . Schabitz, W.-R. (2009). The Role of Granulocyte-Colony Stimulating Factor (G-CSF) in the Healthy Brain: A Characterization of G-CSF-Deficient Mice. Journal of Neuroscience, 29(37), 11572-11581. doi: 10.1523/jneurosci.0453-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/37/11572 


Dieni, C. V., Nietz, A. K., Panichi, R., Wadiche, J. I., & Overstreet-Wadiche, L. (2013). Distinct Determinants of Sparse Activation during Granule Cell Maturation. Journal of Neuroscience, 33(49), 19131-19142. doi. http://www.jneurosci.org/content/33/49/19131.short


Dieni, C. V., Panichi, R., Aimone, J. B., Kuo, C. T., Wadiche, J. I., & Overstreet-Wadiche, L. (2016). Low excitatory innervation balances high intrinsic excitability of immature dentate neurons. [Article]. Nat Commun, 7. doi: 10.1038/ncomms11313. http://dx.doi.org/10.1038/ncomms11313


DiGiovanna, J., Dominici, N., Friedli, L., Rigosa, J., Duis, S., Kreider, J., . . . Micera, S. (2016). Engagement of the Rat Hindlimb Motor Cortex across Natural Locomotor Behaviors. The Journal of Neuroscience, 36(40), 10440-10455. doi. http://www.jneurosci.org/content/36/40/10440.short


Dihne, M., Bernreuther, C., Hagel, C., Wesche, K. O., & Schachner, M. (2006). Embryonic Stem Cell-Derived Neuronally Committed Precursor Cells with Reduced Teratoma Formation After Transplantation into the Lesioned Adult Mouse Brain. Stem Cells, 24(6), 1458-1466. doi: 10.1634/stemcells.2005-0413. http://stemcells.alphamedpress.org/cgi/content/abstract/24/6/1458 


Dillingham, C. H., Gay, S. M., Behrooz, R., & Gabriele, M. L. (2017). Modular-extramodular organization in developing multisensory shell regions of the mouse inferior colliculus. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24300. http://dx.doi.org/10.1002/cne.24300


Dima, A., Scholz, M., & Obermayer, K. (2002). Automatic segmentation and skeletonization of neurons from confocal microscopy images based on the 3-D wavelet transform. Image Processing, IEEE Transactions on, 11(7), 790-801. doi. 

Dima, A., Scholz, M., & Obermayer, K. (2003). Automatic three-dimensional graph construction of nerve cells from confocal microscopy scans. Journal of Electronic Imaging, 12, 134-134. doi. 

DiNardo, L. A., & Travers, J. B. (1997). Distribution of Fos-Like Immunoreactivity in the Medullary Reticular Formation of the Rat after Gustatory Elicited Ingestion and Rejection Behaviors. Journal of Neuroscience, 17(10), 3826-3839. doi. http://www.jneurosci.org/cgi/content/abstract/17/10/3826


Ding, L., Chen, H., Diamantaki, M., Coletta, S., Preston-Ferrer, P., & Burgalossi, A. (2020). Structural correlates of CA2 and CA3 pyramidal cell activity in freely-moving mice. The Journal of Neuroscience, JN-RM-0099-0020. doi: 10.1523/jneurosci.0099-20.2020. http://www.jneurosci.org/content/early/2020/06/18/JNEUROSCI.0099-20.2020...


Ding, S. L., & Van Hoesen, G. W. (2010). Borders, extent, and topography of human perirhinal cortex as revealed using multiple modern neuroanatomical and pathological markers. Human Brain Mapping, 31(9), 1359-1379. doi. 

Ding, T., Zhou, X., Kouadir, M., Shi, F., Yang, Y., Liu, J., . . . Zhao, D. (2013). Cellular prion protein participates in the regulation of inflammatory response and apoptosis in BV2 Microglia during infection with mycobacterium bovis. Journal of Molecular Neuroscience, 51(1), 118 - 126. doi. 

Ding, X.-F., Gao, X., Ding, X.-C., Fan, M., & Chen, J. (2016). Postnatal dysregulation of Notch signal disrupts dendrite development of adult-born neurons in the hippocampus and contributes to memory impairment. [Article]. Scientific Reports, 6, 25780. doi: 10.1038/srep25780

http://www.nature.com/articles/srep25780#supplementary-information. http://dx.doi.org/10.1038/srep25780


Ding, Y., Li, J., Luan, X., Ding, Y. H., Lai, Q., Rafols, J. A., . . . Diaz, F. G. (2004). Exercise pre-conditioning reduces brain damage in ischemic rats that may be associated with regional angiogenesis and cellular overexpression of neurotrophin. Neuroscience, 124(3), 583-591. doi. 

Ding, Y. H., Li, J., Yao, W. X., Rafols, J. A., Clark, J. C., & Ding, Y. (2006). Exercise preconditioning upregulates cerebral integrins and enhances cerebrovascular integrity in ischemic rats. Acta Neuropathologica, 112(1), 74-84. doi. 

Dingman, A., Lee, S. Y., Derugin, N., Wendland, M. F., & Vexler, Z. S. (2006). Aminoguanidine inhibits caspase-3 and calpain activation without affecting microglial activation following neonatal transient cerebral ischemia. Journal of Neurochemistry, 96(5), 1467-1479. doi: doi:10.1111/j.1471-4159.2006.03672.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1471-4159.2006.03672.x 


Diniz, G. B., Candido, P. L., Klein, M. O., Alvisi, R. D., Presse, F., Nahon, J.-L., . . . Bittencourt, J. C. (2018). The weaning period promotes alterations in the orexin neuronal population of rats in a suckling-dependent manner. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-018-1723-0. https://doi.org/10.1007/s00429-018-1723-0


Dinocourt, C., Aungst, S., Yang, K., & Thompson, S. M. (2011). Homeostatic increase in excitability in area CA1 after Schaffer collateral transection in vivo. Epilepsia, 52(9), 1656-1665. doi: 10.1111/j.1528-1167.2011.03113.x. http://dx.doi.org/10.1111/j.1528-1167.2011.03113.x


Dinocourt, C., Petanjek, Z., Freund, T. F., Ben-Ari, Y., & Esclapez, M. (2003). Loss of interneurons innervating pyramidal cell dendrites and axon initial segments in the CA1 region of the hippocampus following pilocarpine-induced seizures. Journal of Comparative Neurology, 459, 407-425. doi. 

Disma, N., Mondardini, M. C., Terrando, N., Absalom, A. R., & Bilotta, F. (2015). A systematic review of methodology applied during preclinical anesthetic neurotoxicity studies: important issues and lessons relevant to the design of future clinical research. Pediatric Anesthesia, n/a-n/a. doi: 10.1111/pan.12786. http://dx.doi.org/10.1111/pan.12786


Dissen, G. A., Lomniczi, A., Heger, S., Neff, T. L., & Ojeda, S. R. (2012). Hypothalamic EAP1 (enhanced at puberty 1) is required for menstrual cyclicity in nonhuman primates. Endocrinology, 153(1), 350-361. doi. 

Distler, C., Korbmacher, H., & Hoffmann, K. P. (2009). Retinal projections to the accessory optic system in pigmented and albino ferrets (Mustela putorius furo). Experimental Brain Research, 199(3), 333-343. doi. 

Dittgen, T., Nimmerjahn, A., Komai, S., Licznerski, P., Waters, J., Margrie, T. W., . . . Osten, P. (2004). Lentivirus-based genetic manipulations of cortical neurons and their optical and electrophysiological monitoring in vivo. PNAS, 101(52), 18206-18211. doi. http://www.pnas.org/cgi/content/abstract/101/52/18206


Dixon, K. J., Theus, M. H., Nelersa, C. M., Mier, J., Travieso, L. G., Yu, T.-S., . . . Liebl, D. J. (2014). Endogenous neural stem/progenitor cells stabilize the cortical microenvironment following traumatic brain injury. Journal of Neurotrauma. doi: 10.1089/neu.2014.3390. http://dx.doi.org/10.1089/neu.2014.3390


Dizon, M. L. V., Shin, L., Sundholm-Peters, N. L., Kang, E., & Szele, F. G. (2006). Subventricular zone cells remain stable in vitro after brain injury. Neuroscience, 142(3), 717-725. doi. 

Djalali, S., Holtje, M., Grosse, G., Rothe, T., Stroh, T., Grosse, J., . . . Ahnert-Hilger, G. (2005). Effects of brain-derived neurotrophic factor (BDNF) on glial cells and serotonergic neurones during development. Journal of Neurochemistry, 92(3), 616-627. doi: doi:10.1111/j.1471-4159.2004.02911.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1471-4159.2004.02911.x 


Djogo, N., Jakovcevski, I., Müller, C., Lee, H. J., Xu, J.-C., Jakovcevski, M., . . . Schachner, M. (2013). Adhesion molecule L1 binds to amyloid beta and reduces Alzheimer's disease pathology in mice. Neurobiology of Disease, (0). doi: http://dx.doi.org/10.1016/j.nbd.2013.04.014. http://www.sciencedirect.com/science/article/pii/S0969996113001289


Djurisic, M., Popovic, M., Carnevale, N., & Zecevic, D. (2008). Functional Structure of the Mitral Cell Dendritic Tuft in the Rat Olfactory Bulb. Journal of Neuroscience, 28(15), 4057-4068. doi: 10.1523/jneurosci.5296-07.2008. http://www.jneurosci.org/cgi/content/abstract/28/15/4057 


Dmitrieva, N., Nagabukuro, H., Resuehr, D., Zhang, G., McAllister, S. L., McGinty, K. A., . . . Berkley, K. J. (2010). Endocannabinoid involvement in endometriosis. Pain, 151(3), 703-710. doi. 

Dmitrieva, N., Zhang, G., & Nagabukuro, H. (2008). Increased α1D adrenergic receptor activity and protein expression in the urinary bladder of aged rats. World Journal of Urology, 26(6), 649-655. doi. 

Doan, T. P., Lagartos-Donate, M. J., Nilssen, E. S., Ohara, S., & Witter, M. P. (2019). Convergent Projections from Perirhinal and Postrhinal Cortices Suggest a Multisensory Nature of Lateral, but Not Medial, Entorhinal Cortex. Cell Reports, 29(3), 617-627.e617. doi: https://doi.org/10.1016/j.celrep.2019.09.005. http://www.sciencedirect.com/science/article/pii/S2211124719311738


Dobrović, B., Ćurić, G., Petanjek, Z., & Heffer, M. (2011). Dendritic morphology and spine density is not altered in motor cortex and dentate granular cells in mice lacking the ganglioside biosynthetic gene B4galnt1–a quantitative Golgi Cox study. Collegium Antropologicum, 35(Suppl.), 25-30. doi. 

Doche, I., Wilcox, G. L., Ericson, M., Valente, N. S., Romiti, R., McAdams, B. D., & Hordinsky, M. K. (2018). Evidence for neurogenic inflammation in lichen planopilaris and frontal fibrosing alopecia pathogenic mechanism. Experimental Dermatology, 0(ja). doi: doi:10.1111/exd.13835. https://onlinelibrary.wiley.com/doi/abs/10.1111/exd.13835


Doig, N. M., Magill, P. J., Apicella, P., Bolam, J. P., & Sharott, A. (2014). Cortical and Thalamic Excitation Mediate the Multiphasic Responses of Striatal Cholinergic Interneurons to Motivationally Salient Stimuli. The Journal of Neuroscience, 34(8), 3101-3117. doi. http://www.jneurosci.org/content/34/8/3101.short


Doischer, D., Aurel Hosp, J., Yanagawa, Y., Obata, K., Jonas, P., Vida, I., & Bartos, M. (2008). Postnatal Differentiation of Basket Cells from Slow to Fast Signaling Devices. Journal of Neuroscience, 28(48), 12956-12968. doi: 10.1523/jneurosci.2890-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/48/12956 


Dokter, M., Busch, R., Poser, R., Vogt, M. A., von Bohlen und Halbach, V., Gass, P., . . . von Bohlen und Halbach, O. (2014). Implications of p75NTR for dentate gyrus morphology and hippocampus-related behavior revisited. Brain Structure and Function, 1-14. doi: 10.1007/s00429-014-0737-5. http://dx.doi.org/10.1007/s00429-014-0737-5


Domonkos, A., Ledri, L. N., Laszlovszky, T., Cserép, C., Borhegyi, Z., Papp, E., . . . Varga, V. (2016). Divergent in vivo activity of non‐serotonergic and serotonergic VGluT3‐neurones in the median raphe region. The Journal of Physiology. doi. http://onlinelibrary.wiley.com/doi/10.1113/JP272036/full


DonCarlos, L. L., Garcia-Ovejero, D., Sarkey, S., Garcia-Segura, L. M., & Azcoitia, I. (2003). Androgen Receptor Immunoreactivity in Forebrain Axons and Dendrites in the Rat. Endocrinology, 144(8), 3632-3638. doi: 10.1210/en.2002-0105. http://endo.endojournals.org/cgi/content/abstract/144/8/3632 


DonCarlos, L. L., Sarkey, S., Lorenz, B., Azcoitia, I., Garcia-Ovejero, D., Huppenbauer, C., & Garcia-Segura, L. M. (2006). Novel cellular phenotypes and subcellular sites for androgen action in the forebrain. Neuroscience, 138(3), 801-807. doi. 

Donega, V., Marcy, G., Lo Giudice, Q., Zweifel, S., Angonin, D., Fiorelli, R., . . . Raineteau, O. (2018). Transcriptional Dysregulation in Postnatal Glutamatergic Progenitors Contributes to Closure of the Cortical Neurogenic Period. Cell Reports, 22(10), 2567-2574. doi: https://doi.org/10.1016/j.celrep.2018.02.030. https://www.sciencedirect.com/science/article/pii/S2211124718301980


Donegan, M., Kernisant, M., Cua, C., Jasmin, L., & Ohara, P. T. (2013). Satellite glial cell proliferation in the trigeminal ganglia after chronic constriction injury of the infraorbital nerve. Glia, n/a-n/a. doi: 10.1002/glia.22571. http://dx.doi.org/10.1002/glia.22571


Dong, H., Wang, Q., Valkova, K., Gonchar, Y., & Burkhalter, A. (2004). Experience-dependent development of feedforward and feedback circuits between lower and higher areas of mouse visual cortex. Vision Research, 44(28), 3389-3400. doi. 

Dong, Z., Ferger, B., Paterna, J.-C., Vogel, D., Furler, S., Osinde, M., . . . Bueler, H. (2003). Dopamine-dependent neurodegeneration in rats induced by viral vector-mediated overexpression of the parkin target protein, CDCrel-1. Proceedings of the National Academy of Sciences, 100(21), 12438-12443. doi: 10.1073/pnas.2132992100. http://www.pnas.org/cgi/content/abstract/100/21/12438 


Dong, Z., Wolfer, D. P., Lipp, H.-P., & Büeler, H. (2004). Hsp70 Gene Transfer by Adeno-associated Virus Inhibits MPTP-Induced Nigrostriatal Degeneration in the Mouse Model of Parkinson Disease. Molecular Therapy, 11, 80-88. doi. 

Donnelly, C. J., Willis, D. E., Xu, M., Tep, C., Jiang, C., Yoo, S., . . . others. (2011). Limited availability of ZBP1 restricts axonal mRNA localization and nerve regeneration capacity. EMBO journal, 30(22), 4665-4677. doi. 

Donohue, D. E., & Ascoli, G. A. (2011). Automated reconstruction of neuronal morphology: An overview. Brain research reviews, 67(1), 94-102. doi. 

Donohue, D. E., Scorcioni, R., & Ascoli, G. A. (2002). Generation and Description of Neuronal Morphology Using L-Neuron. Computational Neuroanatomy: Principles and Methods, 49-49. doi. 

Doobin, D. J. (2011). Unilateral primary afferent nerve cut causes altered pruning of dendrites in the developing central taste system. doi. 

Doron, G., von Heimendahl, M., Schlattmann, P., Houweling, Arthur R., & Brecht, M. (2014). Spiking Irregularity and Frequency Modulate the Behavioral Report of Single-Neuron Stimulation. Neuron, 81(3), 653-663. doi: http://dx.doi.org/10.1016/j.neuron.2013.11.032. http://www.sciencedirect.com/science/article/pii/S089662731301129X


Dostes, S., Dubreucq, S., Ladevèze, E., Marsicano, G., Abrous, D. N., Chaouloff, F., & Koehl, M. (2015). Running per se stimulates the dendritic arbor of newborn dentate granule cells in mouse hippocampus in a duration-dependent manner. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22551. http://dx.doi.org/10.1002/hipo.22551


Doubell, T. P., Skaliora, I., Baron, J., & King, A. J. (2003). Functional Connectivity between the Superficial and Deeper Layers of the Superior Colliculus: An Anatomical Substrate for Sensorimotor Integration. Journal of Neuroscience, 23, 6596-6607. doi. 

Doucet, J. R., Lenihan, N. M., & May, B. J. (2009). Commissural neurons in the rat ventral cochlear nucleus. Jaro-Journal of the Association for Research in Otolaryngology, 10(2), 269-280. doi. 

Doucet, J. R., & Ryugo, D. K. (2003). Axonal pathways to the lateral superior olive labeled with biotinylated dextran amine injections in the dorsal cochlear nucleus of rats. Journal of Comparative Neurology, 461(4), 452-465. doi. 

Dougherty, J. D., Garcia, A. D. R., Nakano, I., Livingstone, M., Norris, B., Polakiewicz, R., . . . Geschwind, D. H. (2005). PBK/TOPK, a Proliferating Neural Progenitor-Specific Mitogen-Activated Protein Kinase Kinase. Journal of Neuroscience, 25(46), 10773-10785. doi: 10.1523/jneurosci.3207-05.2005. http://www.jneurosci.org/cgi/content/abstract/25/46/10773 


Dougherty, K. A., Islam, T., & Johnston, D. (2012). Intrinsic excitability of CA1 pyramidal neurones from the rat dorsal and ventral hippocampus. Journal of Physiology, no-no. doi: 10.1113/jphysiol.2012.242693. http://dx.doi.org/10.1113/jphysiol.2012.242693


Dougherty, K. J., Bannatyne, B. A., Jankowska, E., Krutki, P., & Maxwell, D. J. (2005). Membrane Receptors Involved in Modulation of Responses of Spinal Dorsal Horn Interneurons Evoked by Feline Group II Muscle Afferents. Journal of Neuroscience, 25(3), 584-593. doi. http://www.jneurosci.org/cgi/content/abstract/25/3/584


Dougherty, K. J., & Hochman, S. (2008). Spinal Cord Injury Causes Plasticity in a Subpopulation of Lamina I GABAergic Interneurons. Journal of Neurophysiology, 100(1), 212-223. doi: 10.1152/jn.01104.2007. http://jn.physiology.org/cgi/content/abstract/100/1/212 


Dougherty, K. J., Sawchuk, M. A., & Hochman, S. (2005). Properties of Mouse Spinal Lamina I GABAergic Interneurons. Journal of Neurophysiology, 94(5), 3221-3227. doi: 10.1152/jn.00184.2005. http://jn.physiology.org/cgi/content/abstract/94/5/3221 


Dougherty, K. J., Sawchuk, M. A., & Hochman, S. (2009). Phenotypic diversity and expression of GABAergic inhibitory interneurons during postnatal development in lumbar spinal cord of glutamic acid decarboxylase 67-green fluorescent protein mice. Neuroscience, 163(3), 909-919. doi. 

Dougherty, S. E., Bartley, A. F., Lucas, E. K., Hablitz, J. J., Dobrunz, L. E., & Cowell, R. M. (2014). Mice lacking the transcriptional coactivator PGC-1α exhibit alterations in inhibitory synaptic transmission in the motor cortex. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2014.04.023. http://www.sciencedirect.com/science/article/pii/S030645221400325X


Downes, C. E., Wong, C. H. Y., Henley, K. J., Guio-Aguilar, P. L., Zhang, M., Ates, R., . . . Crack, P. J. (2013). MyD88 Is a Critical Regulator of Hematopoietic Cell-Mediated Neuroprotection Seen after Stroke. PLoS ONE, 8(3), e57948. doi: 10.1371/journal.pone.0057948. http://dx.doi.org/10.1371%2Fjournal.pone.0057948


Dragatsis, I., Dietrich, P., Ren, H., Deng, Y. P., Del Mar, N., Wang, H. B., . . . Reiner, A. (2018). Effect of early embryonic deletion of huntingtin from pyramidal neurons on the development and long-term survival of neurons in cerebral cortex and striatum. Neurobiology of Disease, 111, 102-117. doi: https://doi.org/10.1016/j.nbd.2017.12.015. https://www.sciencedirect.com/science/article/pii/S0969996117302991


Drago, I., & Davis, Ronald L. (2016). Inhibiting the Mitochondrial Calcium Uniporter during Development Impairs Memory in Adult <em>Drosophila</em>. Cell Reports. doi: 10.1016/j.celrep.2016.08.017. http://dx.doi.org/10.1016/j.celrep.2016.08.017


Drake, C. T., De Oliveira, A. X., Harris, J. A., Connor, D. M., Winkler, C. W., & Aicher, S. A. (2007). Kappa opioid receptors in the rostral ventromedial medulla of male and female rats. Journal of Comparative Neurology, 500(3), 465-476. doi. 

Drapeau, E., Montaron, M.-F., Aguerre, S., & Abrous, D. N. (2007). Learning-Induced Survival of New Neurons Depends on the Cognitive Status of Aged Rats. Journal of Neuroscience, 27(22), 6037-6044. doi: 10.1523/jneurosci.1031-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/22/6037 


Drissi, I., Deschamps, C., Alary, R., Robert, A., Dubreuil, V., Le Mouël, A., . . . Pierrefiche, O. (2020). Role of heat shock transcription factor 2 in the NMDA-dependent neuroplasticity induced by chronic ethanol intake in mouse hippocampus. Addiction Biology, n/a(n/a), e12939. doi: 10.1111/adb.12939. https://onlinelibrary.wiley.com/doi/abs/10.1111/adb.12939


Drouin-Ouellet, J., Brownell, A.-L., Saint-Pierre, M., Fasano, C., Emond, V., Trudeau, L.-E., . . . Cicchetti, F. (2011). Neuroinflammation is associated with changes in glial mGluR5 expression and the development of neonatal excitotoxic lesions. Glia, 59(2), 188-199. doi: 10.1002/glia.21086. http://dx.doi.org/10.1002/glia.21086


Druart, M., Groszer, M., & Le Magueresse, C. (2020). An etiological Foxp2 mutation impairs neuronal gain in layer VI cortico-thalamic cells through increased GABA&lt;sub&gt;B&lt;/sub&gt;/GIRK signaling. The Journal of Neuroscience, JN-RM-2615-2619. doi: 10.1523/jneurosci.2615-19.2020. http://www.jneurosci.org/content/early/2020/10/05/JNEUROSCI.2615-19.2020...


Dryanovski, D. I., Guzman, J. N., Xie, Z., Galteri, D. J., Volpicelli-Daley, L. A., Lee, V. M.-Y., . . . Surmeier, D. J. (2013). Calcium Entry and α-Synuclein Inclusions Elevate Dendritic Mitochondrial Oxidant Stress in Dopaminergic Neurons. Journal of Neuroscience, 33(24), 10154-10164. doi: 10.1523/jneurosci.5311-12.2013. http://www.jneurosci.org/content/33/24/10154.abstract


Du, F., Williamson, J., Bertram, E., Lothman, E., Okuno, E., & ., R. S. (1993). Kynurenien pathway enzymes in a rat model of chronic epilepsy: Immunohistochemical Study of activated Glial cells. Neuroscience, 55, 975-989. doi. 

Du, J., & Hull, E. M. (1999). Effects of testosterone on neuronal nitric oxide synthase and tyrosine hydroxylase. Brain Research, 836(1-2), 90-98. doi. 

Duan, X., Gleason, R. C., Li, F., Hosur, K. B., Huang, D., Wang, H., . . . Liang, S. (2015). Sex dimorphism in periodontitis in animal models. Journal of Periodontal Research, n/a-n/a. doi: 10.1111/jre.12298. http://dx.doi.org/10.1111/jre.12298


Duarte, J., Gaspar, R., Caetano, L., Patrício, P., Cunha, C., Mateus-Pinheiro, A., . . . Gomes, C. (2018). Brain region-specific control of microglia by adenosine A2A-adenosine receptors: uncoupling anxiety and cognition in female rodents. European Neuropsychopharmacology, 28, S35-S36. doi: 10.1016/j.euroneuro.2017.12.058. http://dx.doi.org/10.1016/j.euroneuro.2017.12.058


Duarte, J. M., Gaspar, R., Caetano, L., Patrício, P., Soares-Cunha, C., Mateus-Pinheiro, A., . . . Gomes, C. A. (2018). Region-specific control of microglia by adenosine A2A receptors: uncoupling anxiety and associated cognitive deficits in female rats. Glia, 0(0). doi: doi:10.1002/glia.23476. https://onlinelibrary.wiley.com/doi/abs/10.1002/glia.23476


Dubey, M., Bugiani, M., Ridder, M. C., Postma, N. L., Brouwers, E., Polder, E., . . . van der Knaap, M. S. (2014). Mice with Megalencephalic Leukoencephalopathy with Cysts: A developmental angle. Annals of Neurology, n/a-n/a. doi: 10.1002/ana.24307. http://dx.doi.org/10.1002/ana.24307


Dubourget, R., Sangare, A., Geoffroy, H., Gallopin, T., & Rancillac, A. (2016). Multiparametric characterization of neuronal subpopulations in the ventrolateral preoptic nucleus. [journal article]. Brain Structure and Function, 1-15. doi: 10.1007/s00429-016-1265-2. http://dx.doi.org/10.1007/s00429-016-1265-2


Dubovyk, V., & Manahan-Vaughan, D. (2017). Less means more: The magnitude of synaptic plasticity along the hippocampal dorso-ventral axis is inversely related to the expression levels of plasticity-related neurotransmitter receptors. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22816. http://dx.doi.org/10.1002/hipo.22816


Dubovyk, V., & Manahan-Vaughan, D. (2019). Distinct Time-Course of Alterations of Groups I and II Metabotropic Glutamate Receptor and GABAergic Receptor Expression Along the Dorsoventral Hippocampal Axis in an Animal Model of Psychosis. Frontiers in Behavioral Neuroscience, 13, 98-98. doi: 10.3389/fnbeh.2019.00098. https://www.ncbi.nlm.nih.gov/pubmed/31139061

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519509/


Dudanova, I., Tabuchi, K., Rohlmann, A., Südhof, T. C., & Missler, M. (2007). Deletion of α-neurexins does not cause a major impairment of axonal pathfinding or synapse formation. Journal of Comparative Neurology, 502(2), 261-274. doi. 

Dudok, B., Barna, L., Ledri, M., Szabo, S. I., Szabadits, E., Pinter, B., . . . Katona, I. (2014). Cell-specific STORM super-resolution imaging reveals nanoscale organization of cannabinoid signaling. [Article]. Nature Neuroscience, advance online publication. doi: 10.1038/nn.3892

http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.3892.html#suppl.... http://dx.doi.org/10.1038/nn.3892


Duffy, K. R., & Livingstone, M. S. (2003). Distribution of non-phosphorylated neurofilament in squirrel monkey V1 is complementary to the pattern of cytochrome-oxidase blobs. Cerebral Cortex, 13(7), 722-727. doi. 

Duffy, K. R., & Livingstone, M. S. (2005). Loss of neurofilament labeling in the primary visual cortex of monocularly deprived monkeys. Cerebral Cortex, 15(8), 1146-1154. doi. 

Dugladze, T., Schmitz, D., Whittington, M. A., Vida, I., & Gloveli, T. (2012). Segregation of Axonal and Somatic Activity During Fast Network Oscillations. Science, 336(6087), 1458-1461. doi: 10.1126/science.1222017. http://www.sciencemag.org/content/336/6087/1458.abstract


Dugladze, T., Vida, I., Tort, A. B., Gross, A., Otahal, J., Heinemann, U., . . . Gloveli, T. (2007). Impaired hippocampal rhythmogenesis in a mouse model of mesial temporal lobe epilepsy. Proceedings of the National Academy of Sciences, 104(44), 17530-17535. doi: 10.1073/pnas.0708301104. http://www.pnas.org/cgi/content/abstract/104/44/17530 


Dumanis, S. B., Cha, H. J., Song, J. M., Trotter, J. H., Spitzer, M., Lee, J. Y., . . . others. (2011). ApoE receptor 2 regulates synapse and dendritic spine formation. PLoS ONE, 6(2), e17203-e17203. doi. 

Dumanis, S. B., Tesoriero, J. A., Babus, L. W., Nguyen, M. T., Trotter, J. H., Ladu, M. J., . . . Hoe, H.-S. (2009). ApoE4 Decreases Spine Density and Dendritic Complexity in Cortical Neurons In Vivo. Journal of Neuroscience, 29(48), 15317-15322. doi: 10.1523/jneurosci.4026-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/48/15317 


Dumitriu, D., Cossart, R., Huang, J., & Yuste, R. (2007). Correlation between axonal morphologies and synaptic input kinetics of interneurons from mouse visual cortex. Cerebral Cortex, 17(1), 81-91. doi. 

Dumitriu, D., Rodriguez, A., & Morrison, J. H. (2011). High-throughput, detailed, cell-specific neuroanatomy of dendritic spines using microinjection and confocal microscopy. Nature Protocols, 6(9), 1391-1411. doi. 

Duong, A. T. H., Reitz, C. J., Louth, E. L., Creighton, S. D., Rasouli, M., Zwaiman, A., . . . Martino, T. A. (2019). The Clock Mechanism Influences Neurobiology and Adaptations to Heart Failure in Clock∆19/∆19 Mice With Implications for Circadian Medicine. Scientific Reports, 9(1), 4994. doi: 10.1038/s41598-019-41469-7. https://doi.org/10.1038/s41598-019-41469-7


Duque, A., Coman, D., Carlyle, B. C., Bordner, K. A., George, E. D., Papademetris, X., . . . Simen, A. A. (2011). Neuroanatomical changes in a mouse model of early life neglect. Brain Structure and Function, 1-14. doi. 

Duque, A., Gazula, V.-R., & Kaczmarek, L. K. (2013). Expression of Kv1.3 potassium channels regulates density of cortical interneurons. Developmental Neurobiology, n/a-n/a. doi: 10.1002/dneu.22105. http://dx.doi.org/10.1002/dneu.22105


Duque, A., & McCormick, D. A. (2010). Circuit-based Localization of Ferret Prefrontal Cortex. Cerebral Cortex, 20(5), 1020-1036. doi. 

Duque, A., & Rakic, P. (2011). Different Effects of Bromodeoxyuridine and [3H]Thymidine Incorporation into DNA on Cell Proliferation, Position, and Fate. Journal of Neuroscience, 31(42), 15205-15217. doi: 10.1523/jneurosci.3092-11.2011. http://www.jneurosci.org/content/31/42/15205.abstract


Duque, A., Tepper, J. M., Detari, L., Ascoli, G. A., & Zaborszky, L. (2007). Morphological characterization of electrophysiologically and immunohistochemically identified basal forebrain cholinergic and neuropeptide Y-containing neurons. Brain Structure and Function, 212(1), 55-73. doi. 

Durig, J., & Hornung, J. P. (2000). Neonatal serotonin depletion affects developing and mature mouse cortical neurons. Neuroreport, 11(4), 833-833. doi. 

Dursun, I., Jakubowska-Doğru, E., van der List, D., Liets, L. C., Coombs, J. L., & Berman, R. F. (2011). Effects of Early Postnatal Exposure to Ethanol on Retinal Ganglion Cell Morphology and Numbers of Neurons in the Dorsolateral Geniculate in Mice. Alcoholism: Clinical and Experimental Research. doi. 

Dutschmann, M., Waki, H., Manzke, T., Simms, A. E., Pickering, A. E., Richter, D. W., & Paton, J. F. R. (2009). The potency of different serotonergic agonists in counteracting opioid evoked cardiorespiratory disturbances. Philosophical Transactions of the Royal Society B: Biological Sciences, 364(1529), 2611-2623. doi. 

Dwivedy, A., Gertler, F. B., Miller, J., Holt, C. E., & Lebrand, C. (2007). Ena/VASP function in retinal axons is required for terminal arborization but not pathway navigation. Development, 134(11), 2137-2146. doi: 10.1242/dev.002345. http://dev.biologists.org/cgi/content/abstract/134/11/2137 


Dyhrfjeld-Johnsen, J., Maier, J., Schubert, D., Staiger, J., Luhmann, H. J., Stephan, K. E., & Kötter, R. (2005). CoCoDat: a database system for organizing and selecting quantitative data on single neurons and neuronal microcircuitry. Journal of Neuroscience Methods, 141(2), 291-308. doi. 

Dzirasa, K., Coque, L., Sidor, M. M., Kumar, S., Dancy, E. A., Takahashi, J. S., . . . Nicolelis, M. A. L. (2010). Lithium Ameliorates Nucleus Accumbens Phase-Signaling Dysfunction in a Genetic Mouse Model of Mania. Journal of Neuroscience, 30(48), 16314-16323. doi: 10.1523/jneurosci.4289-10.2010. http://www.jneurosci.org/cgi/content/abstract/30/48/16314


Eales, K. L., Palygin, O., O’Loughlin, T., Rasooli-Nejad, S., Gaestel, M., Müller, J., . . . Corrêa, S. A. (2014). The MK2/3 cascade regulates AMPAR trafficking and cognitive flexibility. Nature Communications, 5. doi. http://www.nature.com/ncomms/2014/140819/ncomms5701/full/ncomms5701.html


Eastwood, B. S., Hooks, B. M., Paletzki, R. F., O'Connor, N. J., Glaser, J. R., & Gerfen, C. R. (2018). Whole Mouse Brain Reconstruction and Registration to a Reference Atlas with Standard Histochemical Processing of Coronal Sections. Journal of Comparative Neurology, 0(ja), e24602. doi: doi:10.1002/cne.24602. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24602


Eaton, M. J., Gudehithlu, K. P., Quach, T., Silvia, C. P., Hadjiconstantinou, M., & Neff, N. H. (1993). Distribution of aromatic L-amino acid decarboxylase mRNA in mouse brain by in situ hybridization histology. Journal of Comparative Neurology, 337(4), 640-654. doi. 

Ebert, A. D., Chen, F., He, X., Cryns, V. L., & Bohn, M. C. (2005). A tetracycline-regulated adenovirus encoding dominant-negative caspase-9 is regulated in rat brain and protects against neurotoxin-induced cell death in vitro, but not in vivo. Experimental Neurology, 191, S80–S94-S80–S94. doi. 

Ebert, A. D., Hann, H. J., & Bohn, M. C. (2008). Progressive degeneration of dopamine neurons in 6-hydroxydopamine rat model of parkinson's disease does not involve activation of caspase-9 and caspase-3. Journal of Neuroscience Research, 86(2), 317-325. doi. 

Ebrahimi, M., Yamamoto, Y., Sharifi, K., Kida, H., Kagawa, Y., Yasumoto, Y., . . . Owada, Y. (2015). Astrocyte-expressed FABP7 regulates dendritic morphology and excitatory synaptic function of cortical neurons. Glia, n/a-n/a. doi: 10.1002/glia.22902. http://dx.doi.org/10.1002/glia.22902


Eckle, V.-S., Shcheglovitov, A., Vitko, I., Dey, D., Yap, C. C., Winckler, B., & Perez-Reyes, E. (2013). Mechanisms by which a CACNA1H mutation found in epilepsy patients increase seizure susceptibility. The Journal of Physiology. doi: 10.1113/jphysiol.2013.264176. http://jp.physoc.org/content/early/2013/11/22/jphysiol.2013.264176.abstract


Edfawy, M., Guedes, J. R., Pereira, M. I., Laranjo, M., Carvalho, M. J., Gao, X., . . . Peça, J. (2019). Abnormal mGluR-mediated synaptic plasticity and autism-like behaviours in Gprasp2 mutant mice. Nature Communications, 10(1), 1431. doi: 10.1038/s41467-019-09382-9. https://doi.org/10.1038/s41467-019-09382-9


Edlow, B. L., Haynes, R. L., Takahashi, E., Klein, J. P., Cummings, P., Benner, T., . . . Folkerth, R. D. (2013). Disconnection of the Ascending Arousal System in Traumatic Coma. Journal of Neuropathology and Experimental Neurology, Publish Ahead of Print, 10.1097/NEN.1090b1013e3182945bf3182946. doi. http://journals.lww.com/jneuropath/Fulltext/publishahead/Disconnection_o...


Edmunds, N. B., McCann, K. S., & Laberge, F. (2016). Food Web Structure Shapes the Morphology of Teleost Fish Brains. Brain, Behavior and Evolution, 0(0), 128-138. doi. http://www.karger.com/DOI/10.1159/000445973


Efimova, E. V., Kozlova, A. A., Razenkova, V., Katolikova, N. V., Antonova, K. A., Sotnikova, T. D., . . . Gainetdinov, R. R. (2021). Increased dopamine transmission and adult neurogenesis in trace amine-associated receptor 5 (TAAR5) knockout mice. Neuropharmacology, 182, 108373. doi: https://doi.org/10.1016/j.neuropharm.2020.108373. http://www.sciencedirect.com/science/article/pii/S002839082030441X


Egami, K., Yitta, S., Kasim, S., Lewers, J. C., Roberts, R. C., Lehar, M., & Jinnah, H. A. (2007). Basal ganglia dopamine loss due to defect in purine recycling. Neurobiology of Disease, 26, 396-407. doi. 

Egashira, Y., Tanaka, T., Soni, P., Sakuragi, S., Tominaga-Yoshino, K., & Ogura, A. (2010). Involvement of the p75NTR signaling pathway in persistent synaptic suppression coupled with synapse elimination following repeated long-term depression induction. Journal of Neuroscience Research, 88(16), 3433-3446. doi: 10.1002/jnr.22505. http://dx.doi.org/10.1002/jnr.22505


Egawa, R., & Yawo, H. (2019). Analysis of Neuro-Neuronal Synapses Using Embryonic Chick Ciliary Ganglion via Single-Axon Tracing, Electrophysiology, and Optogenetic Techniques. Current Protocols in Neuroscience, 0(0), e64. doi: doi:10.1002/cpns.64. https://currentprotocols.onlinelibrary.wiley.com/doi/abs/10.1002/cpns.64


Eggan, S. M., & Lewis, D. A. (2007). Immunocytochemical distribution of the cannabinoid CB1 receptor in the primate neocortex: a regional and laminar analysis. Cerebral Cortex, 17(1), 175-191. doi. 

Eggan, S. M., Mizoguchi, Y., Stoyak, S. R., & Lewis, D. A. (2010). Development of cannabinoid 1 receptor protein and messenger RNA in monkey dorsolateral prefrontal cortex. Cerebral Cortex, 20(5), 1164-1174. doi. 

Egger, R., Narayanan, R. T., Helmstaedter, M., de Kock, C. P. J., & Oberlaender, M. (2012). 3D Reconstruction and Standardization of the Rat Vibrissal Cortex for Precise Registration of Single Neuron Morphology. PLoS Comput Biol, 8(12), e1002837. doi: 10.1371/journal.pcbi.1002837. http://dx.doi.org/10.1371%2Fjournal.pcbi.1002837


Egger, V., Nevian, T., & Bruno, R. M. (2008). Subcolumnar Dendritic and Axonal Organization of Spiny Stellate and Star Pyramid Neurons within a Barrel in Rat Somatosensory Cortex. Cerebral Cortex, 18(4), 876-889. doi: 10.1093/cercor/bhm126. http://cercor.oxfordjournals.org/cgi/content/abstract/18/4/876 


Eggermann, E., & Feldmeyer, D. (2009). Cholinergic filtering in the recurrent excitatory microcircuit of cortical layer 4. Proceedings of the National Academy of Sciences, 106(28), 11753-11758. doi. 

Egusa, S. F., Inoue, Y. U., Asami, J., Terakawa, Y. W., Hoshino, M., & Inoue, T. (2015). Classic cadherin expressions balance postnatal neuronal positioning and dendrite dynamics to elaborate the specific cytoarchitecture of the mouse cortical area. Neuroscience Research. doi: http://dx.doi.org/10.1016/j.neures.2015.09.006. http://www.sciencedirect.com/science/article/pii/S0168010215002308


Ehlinger, D. G., Bergstrom, H. C., Burke, J. C., Fernandez, G. M., McDonald, C. G., & Smith, R. F. (2014). Adolescent nicotine-induced dendrite remodeling in the nucleus accumbens is rapid, persistent, and D1-dopamine receptor dependent. Brain Structure and Function, 1-13. doi: 10.1007/s00429-014-0897-3. http://dx.doi.org/10.1007/s00429-014-0897-3


Ehlinger, D. G., Bergstrom, H. C., McDonald, C. G., & Smith, R. F. (2012). Nicotine-induced dendritic remodeling in the insular cortex. Neuroscience Letters, (0). doi: 10.1016/j.neulet.2012.03.064. http://www.sciencedirect.com/science/article/pii/S030439401200448X


Ehlinger, D. G., Burke, J. C., McDonald, C. G., Smith, R. F., & Bergstrom, H. C. Nicotine-induced and D1-receptor-dependent dendritic remodeling in a subset of dorsolateral striatum medium spiny neurons. Neuroscience. doi: https://doi.org/10.1016/j.neuroscience.2017.05.036. http://www.sciencedirect.com/science/article/pii/S0306452217303706


Eid, T., Lee, T.-S. W., Thomas, M. J., Amiry-Moghaddam, M., Bjornsen, L. P., Spencer, D. D., . . . de Lanerolle, N. C. (2005). Loss of perivascular aquaporin 4 may underlie deficient water and K+ homeostasis in the human epileptogenic hippocampus. PNAS, 102(4), 1193-1198. doi. http://www.pnas.org/cgi/content/abstract/102/4/1193


Eisenstein, M. (2009). Neural circuits: Putting neurons on the map. Nature, 461(7267), 1149-1152. doi. 

Ekstrand, J. J., Domroese, M. E., Feig, S. L., Illig, K. R., & Haberly, L. B. (2001). Immunocytochemical analysis of basket cells in rat piriform cortex. Journal of Comparative Neurology, 434(3), 308-328. doi. 

ElBasiouny, S. M., Amendola, J., Durand, J., & Heckman, C. J. (2010). Evidence from Computer Simulations for Alterations in the Membrane Biophysical Properties and Dendritic Processing of Synaptic Inputs in Mutant Superoxide Dismutase-1 Motoneurons. Journal of Neuroscience, 30(16), 5544-5558. doi: 10.1523/jneurosci.0434-10.2010. http://www.jneurosci.org/cgi/content/abstract/30/16/5544 


El-Danaf, R. N., & Huberman, A. D. (2015). Characteristic Patterns of Dendritic Remodeling in Early-Stage Glaucoma: Evidence from Genetically Identified Retinal Ganglion Cell Types. The Journal of Neuroscience, 35(6), 2329-2343. doi. http://www.jneurosci.org/content/35/6/2329.short


Eldridge, M. A. G., Lerchner, W., Saunders, R. C., Kaneko, H., Krausz, K. W., Gonzalez, F. J., . . . Richmond, B. J. (2015). Chemogenetic disconnection of monkey orbitofrontal and rhinal cortex reversibly disrupts reward value. [Brief Communication]. Nature Neuroscience, advance online publication. doi: 10.1038/nn.4192

http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.4192.html#suppl.... http://dx.doi.org/10.1038/nn.4192


El-Gohary, Y., Tulachan, S., Guo, P., Welsh, C., Wiersch, J., Prasadan, K., . . . Gittes, G. (2013). Smad signaling pathways regulate pancreatic endocrine development. Developmental Biology, (0). doi: http://dx.doi.org/10.1016/j.ydbio.2013.04.003. http://www.sciencedirect.com/science/article/pii/S0012160613001723


El-Gohary, Y., Tulachan, S., Wiersch, J., Guo, P., Welsh, C., Prasadan, K., . . . Gittes, G. (2013). A smad signaling network regulates islet cell proliferation. Diabetes. doi: 10.2337/db13-0432. http://diabetes.diabetesjournals.org/content/early/2013/09/23/db13-0432....


Eliasieh, K., Liets, L. C., & Chalupa, L. M. (2007). Cellular reorganization in the human retina during normal aging. Investigative Ophthalmology and Visual Science, 48(6), 2824-2830. doi. 

Elibol-Can, B., Kilic, E., Yuruker, S., & Jakubowska-Dogru, E. (2013). Investigation into the effects of prenatal alcohol exposure on postnatal spine development and expression of synaptophysin and PSD95 in rat hippocampus. International Journal of Developmental Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.ijdevneu.2013.12.003. http://www.sciencedirect.com/science/article/pii/S0736574813001767


Ellender, T. J., Nissen, W., Colgin, L. L., Mann, E. O., & Paulsen, O. (2010). Priming of Hippocampal Population Bursts by Individual Perisomatic-Targeting Interneurons. Journal of Neuroscience Methods, 30(17), 5979-5991. doi: 10.1523/jneurosci.3962-09.2010. http://www.jneurosci.org/cgi/content/abstract/30/17/5979 


Elliott, K. C., Wu, W., Bertram, R., Hyson, R. L., & Johnson, F. (2017). Orthogonal Topography In The Parallel Input Architecture Of Songbird HVC. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24189. http://dx.doi.org/10.1002/cne.24189


Elliott, K. C., Wu, W., Bertram, R., & Johnson, F. (2013). Disconnection of a basal ganglia circuit in juvenile songbirds attenuates THE SPECTRAL differentiation of SONG syllables. Developmental Neurobiology, n/a-n/a. doi: 10.1002/dneu.22151. http://dx.doi.org/10.1002/dneu.22151


Elson, A. E. T., Dotson, C. D., Egan, J. M., & Munger, S. D. (2010). Glucagon signaling modulates sweet taste responsiveness. The FASEB journal, 24(10), 3960-3969. doi. 

Elste, A. M., & Benson, D. L. (2006). Structural basis for developmentally regulated changes in cadherin function at synapses. Journal of Comparative Neurology, 495(3), 324-335. doi. 

Elston, G. N., Oga, T., & Fujita, I. (2009). Spinogenesis and Pruning Scales across Functional Hierarchies. Journal of Neuroscience, 29(10), 3271-3275. doi: 10.1523/jneurosci.5216-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/10/3271 


Elston, G. N., Oga, T., Okamoto, T., & Fujita, I. (2010). Spinogenesis and pruning from early visual onset to adulthood: an intracellular injection study of layer III pyramidal cells in the ventral visual cortical pathway of the macaque monkey. Cerebral Cortex, 20(6), 1398-1408. doi. 

Elston, G. N., Oga, T., Okamoto, T., & Fujita, I. (2011). Spinogenesis and pruning in the anterior ventral inferotemporal cortex of the macaque monkey: an intracellular injection study of layer III pyramidal cells. Frontiers in Neuroanatomy, 5. doi. 

Elston, G. N., Okamoto, T., Oga, T., Dornan, D., & Fujita, I. (2010). Spinogenesis and pruning in the primary auditory cortex of the macaque monkey (Macaca fascicularis): An intracellular injection study of layer III pyramidal cells. Brain Research, 1316, 35-42. doi. 

Éltes, T., Kirizs, T., Nusser, Z., & Holderith, N. (2017). Target cell type-dependent differences in Ca&lt;sup&gt;2+&lt;/sup&gt; channel function underlie distinct release probabilities at hippocampal glutamatergic terminals. [10.1523/JNEUROSCI.2024-16.2017]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2017/01/23/JNEUROSCI.2024-16.2017...


Emmenegger, V., Qi, G., Wang, H., & Feldmeyer, D. (2018). Morphological and Functional Characterization of Non-fast-Spiking GABAergic Interneurons in Layer 4 Microcircuitry of Rat Barrel Cortex. Cerebral Cortex. doi: 10.1093/cercor/bhx352. http://dx.doi.org/10.1093/cercor/bhx352


Engelmann, J., Bacelo, J., van den Burg, E., & Grant, K. (2006). Sensory and Motor Effects of Etomidate Anesthesia. Journal of Neurophysiology, 95(2), 1231-1243. doi: 10.1152/jn.00405.2005. http://jn.physiology.org/cgi/content/abstract/95/2/1231 


Engle, M. P., Merrill, M. A., de Prado, B. M., & Hammond, D. L. (2011). Spinal nerve ligation decreases $\gamma$-aminobutyric acidB receptors on specific populations of immunohistochemically-identified neurons in L5 dorsal root ganglion of the rat. Journal of Comparative Neurology. doi. 

Enomoto, M., Bunge, M. B., & Tsoulfas, P. (2013). A multifunctional neurotrophin with reduced affinity to p75NTR enhances transplanted Schwann cell survival and axon growth after spinal cord injury. Experimental Neurology, (0). doi: http://dx.doi.org/10.1016/j.expneurol.2013.06.013. http://www.sciencedirect.com/science/article/pii/S0014488613001866


Enriquez-Barreto, L., Palazzetti, C., Brennaman, L. H., Maness, P. F., & Fairén, A. (2012). Neural cell adhesion molecule, NCAM, regulates thalamocortical axon pathfinding and the organization of the cortical somatosensory representation in mouse. Frontiers in Molecular Neuroscience, 5. doi. 

Eom, T. Y., & Jope, R. S. (2009). Blocked inhibitory serine-phosphorylation of glycogen synthase kinase-3α/β impairs in vivo neural precursor cell proliferation. Biological Psychiatry, 66(5), 494-502. doi. 

Erbel-Sieler, C., Dudley, C., Zhou, Y., Wu, X., Estill, S. J., Han, T., . . . McKnight, S. L. (2004). Behavioral and regulatory abnormalities in mice deficient in the NPAS1 and NPAS3 transcription factors. PNAS, 101(37), 13648-13653. doi. http://www.pnas.org/cgi/content/abstract/101/37/13648


Erekat, N. S. (2016). Cerebellar Purkinje Cells Die by Apoptosis in the Shaker Mutant Rat. Brain Research. doi: http://dx.doi.org/10.1016/j.brainres.2016.12.025. http://www.sciencedirect.com/science/article/pii/S0006899316308460


Erekat, N. S. (2018). Active caspase-3 upregulation is augmented in at-risk cerebellar Purkinje cells following inferior olive chemoablation in the shaker mutant rat: an immunofluorescence study. Neurological Research, 1-8. doi: 10.1080/01616412.2018.1548792. https://doi.org/10.1080/01616412.2018.1548792


Erickson, S. L., & Lewis, D. A. (2004). Cortical connections of the lateral mediodorsal thalamus in cynomolgus monkeys. Journal of Comparative Neurology, 473(1), 107-127. doi. 

Erisir, A., Levey, A. I., & Aoki, C. (2001). Muscarinic receptor M2 in cat visual cortex: Laminar distribution, relationship to γ-aminobutyric acidergic neurons, and effect of cingulate lesions. Journal of Comparative Neurology, 441(2), 168-185. doi. 

Ernst, L., Darschnik, S., Roos, J., González-Gómez, M., Beemelmans, C., Beemelmans, C., . . . Wahle, P. (2018). Fast prenatal development of the NPY neuron system in the neocortex of the European wild boar, Sus scrofa. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-018-1725-y. https://doi.org/10.1007/s00429-018-1725-y


Ertürk, A., Becker, K., Jährling, N., Mauch, C. P., Hojer, C. D., Egen, J. G., . . . Dodt, H. U. (2012). Three-dimensional imaging of solvent-cleared organs using 3DISCO. Nature Protocols, 7(11), 1983-1995. doi. 

Esclapez, M., Hirsch, J. C., Ben-Ari, Y., & Bernard, C. (1999). Newly formed excitatory pathways provide a substrate for hyperexcitability in experimental temporal lobe epilepsy. Journal of Comparative Neurology, 408(4), 449-460. doi. 

Esclapez, M., Hirsch, J. C., Khazipov, R., Ben-Ari, Y., & Bernard, C. (1997). Operative GABAergic inhibition in hippocampal CA1 pyramidal neurons in experimental epilepsy. Proceedings of the National Academy of Sciences, 94(22), 12151-12156. doi. 

Escobar, C. M., Krajewski, S. J., Sandoval-Guzman, T., Voytko, M. L., & Rance, N. E. (2004). Neuropeptide Y Gene Expression Is Increased in the Hypothalamus of Older Women. Journal of Clinical Endocrinological Metabolism, 89(5), 2338-2343. doi: 10.1210/jc.2003-031899. http://jcem.endojournals.org/cgi/content/abstract/89/5/2338 


Espallergues, J., Teegarden, S. L., Veerakumar, A., Boulden, J., Challis, C., Jochems, J., . . . Berton, O. (2012). HDAC6 Regulates Glucocorticoid Receptor Signaling in Serotonin Pathways with Critical Impact on Stress Resilience. Journal of Neuroscience, 32(13), 4400-4416. doi: 10.1523/jneurosci.5634-11.2012. http://www.jneurosci.org/content/32/13/4400.abstract


Evans, R. C., Twedell, E. L., Zhu, M., Ascencio, J., Zhang, R., & Khaliq, Z. M. (2020). Functional Dissection of Basal Ganglia Inhibitory Inputs onto Substantia Nigra Dopaminergic Neurons. Cell Reports, 32(11), 108156. doi: https://doi.org/10.1016/j.celrep.2020.108156. http://www.sciencedirect.com/science/article/pii/S2211124720311451


Evers, J. F., Schmitt, S., Sibila, M., & Duch, C. (2005). Progress in Functional Neuroanatomy: Precise Automatic Geometric Reconstruction of Neuronal Morphology From Confocal Image Stacks. Journal of Neurophysiology, 93(4), 2331-2342. doi: 10.1152/jn.00761.2004. http://jn.physiology.org/cgi/content/abstract/93/4/2331 


Evstratova, A., Chamberland, S., & Topolnik, L. (2011). Cell type-specific and activity-dependent dynamics of action potential-evoked Ca2+ signals in dendrites of hippocampal inhibitory interneurons. Journal of Physiology, 589(8), 1957-1977. doi: 10.1113/jphysiol.2010.204255. http://jp.physoc.org/content/589/8/1957.abstract


Eyo, U., & Dailey, M. (2012). Effects of oxygen-glucose deprivation on microglial mobility and viability in developing mouse hippocampal tissues. Glia, 60, 1747 - 1760. doi. 

Eyre, M. D., Antal, M., & Nusser, Z. (2008). Distinct Deep Short-Axon Cell Subtypes of the Main Olfactory Bulb Provide Novel Intrabulbar and Extrabulbar GABAergic Connections. Journal of Neuroscience, 28(33), 8217-8229. doi: 10.1523/jneurosci.2490-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/33/8217 


Eyre, M. D., Kerti, K., & Nusser, Z. (2009). Molecular diversity of deep short-axon cells of the rat main olfactory bulb. European Journal of Neuroscience, 29(7), 1397-1407. doi. 

Eyre, M. D., & Nusser, Z. (2016). Only a minority of the inhibitory inputs to cerebellar Golgi cells originates from local GABAergic cells. [10.1523/ENEURO.0055-16.2016]. eneuro. doi. http://eneuro.org/content/early/2016/05/09/ENEURO.0055-16.2016.abstract


Eyre, M. D., Renzi, M., Farrant, M., & Nusser, Z. (2012). Setting the Time Course of Inhibitory Synaptic Currents by Mixing Multiple GABAA Receptor α Subunit Isoforms. Journal of Neuroscience, 32(17), 5853-5867. doi: 10.1523/jneurosci.6495-11.2012. http://www.jneurosci.org/content/32/17/5853.abstract


Ezerman, E. B., & Forehand, C. J. (1996). Development and segmental organization of rostrocaudal dendrites of rat sympathetic preganglionic neurons. Journal of the Autonomic Nervous System, 57(1-2), 29-35. doi. 

Fabel, K., Fabel, K., Tam, B., Kaufer, D., Baiker, A., Simmons, N., . . . Palmer, T. D. (2003). VEGF is necessary for exercise-induced adult hippocampal neurogenesis. European Journal of Neuroscience, 18(10), 2803-2812. doi. http://www.blackwell-synergy.com/links/doi/10.1111/j.1460-9568.2003.0304...


Fabene, P. F., Correia, L., Carvalho, R. A., Cavalheiro, E. A., & Bentivoglio, M. (2001). The spiny rat Proechimys guyannensis as model of resistance to epilepsy: chemical characterization of hippocampal cell populations and pilocarpine-induced changes. Neuroscience, 104(4), 979-1002. doi. 

Fabris, C., Ballarin, C., Massa, R., Granato, A., Fabiani, O., Panzica, G. C., & Cozzi, B. (2009). The vasotocinergic system in the hypothalamus and limbic region of the budgerigar (Melopsittacus undulatus). European Journal of Histochemistry, 48(4), 367-372. doi. 

Faden, A. I., Fox, G. B., Di, X., Knoblach, S. M., Cernak, I., Mullins, P., . . . Kozikowski, A. P. (2003). Neuroprotective and Nootropic Actions of a Novel Cyclized Dipeptide After Controlled Cortical Impact Injury in Mice. Journal of Cerebral Blood Flow AND Metabolism, 23, 355-363. doi. 

Fagel, D. M., Ganat, Y., Cheng, E., Silbereis, J., Ohkubo, Y., Ment, L. R., & Vaccarino, F. M. (2009). Fgfr1 Is Required for Cortical Regeneration and Repair after Perinatal Hypoxia. Journal of Neuroscience, 29(4), 1202-1211. doi: 10.1523/jneurosci.4516-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/4/1202 


Faherty, C. J., Kerley, D., & Smeyne, R. J. (2003). Golgi-Cox morphological analysis of neuronal changes induced by environmental enrichment. Developmental Brain Research, 141(1-2), 55-61. doi. 

Fahimi, A., Baktir, M. A., Moghadam, S., Mojabi, F. S., Sumanth, K., McNerney, M. W., . . . Salehi, A. (2016). Physical exercise induces structural alterations in the hippocampal astrocytes: exploring the role of BDNF-TrkB signaling. [journal article]. Brain Structure and Function, 1-12. doi: 10.1007/s00429-016-1308-8. http://dx.doi.org/10.1007/s00429-016-1308-8


Fairén, A. (2007). Cajal and Lorente de Nó on cortical interneurons: Coincidences and progress. Brain Research Reviews, 55(2), 430-444. doi. 

Fakira, A. K., Gaspers, L. D., Thomas, A. P., Li, H., Jain, M. R., & Elkabes, S. (2012). Purkinje cell dysfunction and delayed death in plasma membrane calcium ATPase 2-heterozygous mice. Molecular and Cellular Neuroscience, (0). doi: 10.1016/j.mcn.2012.07.001. http://www.sciencedirect.com/science/article/pii/S1044743112001091


Falcone, C., Wolf-Ochoa, M., Amina, S., Hong, T., Vakilzadeh, G., Hopkins, W. D., . . . Martínez-Cerdeño, V. (2018). Cortical interlaminar astrocytes across the therian mammal radiation. Journal of Comparative Neurology, 0(ja). doi: doi:10.1002/cne.24605. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24605


Fan, C., Zheng, Y., Cheng, X., Qi, X., Bu, P., Luo, X., . . . Cao, Q. (2013). Transplantation of D15A-Expressing Glial-Restricted-Precursor-Derived Astrocytes Improves Anatomical and Locomotor Recovery after Spinal Cord Injury. International Journal of Biological Sciences, 9(1), 78. doi. 

Fan, X. M., Hendley, E. D., & Forehand, C. J. (1995). Enhanced vascular neuropeptide Y–immunoreactive innervation in two hypertensive rat strains. Hypertension, 26(5), 758-763. doi. 

Fan, X.-W., Chen, F., Chen, Y., Chen, G.-H., Liu, H.-H., Guan, S.-K., . . . Wu, K.-L. (2015). Electroacupuncture Prevents Cognitive Impairments by Regulating the Early Changes after Brain Irradiation in Rats. PLoS ONE, 10(4), e0122087. doi: 10.1371/journal.pone.0122087. http://dx.doi.org/10.1371%2Fjournal.pone.0122087


Fan, X.-W., Liu, H.-H., Wang, H.-B., Chen, F., Yang, Y., Chen, Y., . . . Wu, K.-L. (2017). Electroacupuncture Improves Cognitive Function and Hippocampal Neurogenesis after Brain Irradiation. Radiation Research, 0(0), null. doi: 10.1667/rr14561.1. http://www.rrjournal.org/doi/abs/10.1667/RR14561.1


Fan, Y., Zou, B., Ruan, Y., Pang, Z., & Xu, Z. C. (2005). In Vivo Demonstration of a Late Depolarizing Postsynaptic Potential in CA1 Pyramidal Neurons. Journal of Neurophysiology, 93(3), 1326-1335. doi: 10.1152/jn.00734.2004. http://jn.physiology.org/cgi/content/abstract/93/3/1326 


Fan, Z., Liang, Z., Yang, H., Pan, Y., Zheng, Y., & Wang, X. (2017). Tenuigenin protects dopaminergic neurons from inflammation via suppressing NLRP3 inflammasome activation in microglia. [journal article]. Journal of Neuroinflammation, 14(1), 256. doi: 10.1186/s12974-017-1036-x. https://doi.org/10.1186/s12974-017-1036-x


Fang, M., Lorke, D. E., Li, J., Gong, X., Yew, J. C. C., & Yew, D. T. (2005). Postnatal Changes in Functional Activities of the Pig's Brain: A Combined Functional Magnetic Resonance Imaging and Immunohistochemical Study. Neurosignals, 14(5), 222-233. doi. http://www.karger.com/DOI/10.1159/000088638 


Faralli, A., Dagna, F., Albera, A., Bekku, Y., Oohashi, T., Albera, R., . . . Carulli, D. (2015). Modifications of perineuronal nets and remodelling of excitatory and inhibitory afferents during vestibular compensation in the adult mouse. Brain Structure and Function, 1-17. doi: 10.1007/s00429-015-1095-7. http://dx.doi.org/10.1007/s00429-015-1095-7


Fares, T., & Stepanyants, A. (2009). Cooperative synapse formation in the neocortex. Proceedings of the National Academy of Sciences, 106(38), 16463-16468. doi: 10.1073/pnas.0813265106. http://www.pnas.org/content/106/38/16463.abstract 


Farfel-Becker, T., Vitner, E. B., Pressey, S. N. R., Eilam, R., Cooper, J. D., & Futerman, A. H. (2011). Spatial and temporal correlation between neuron loss and neuroinflammation in a mouse model of neuronopathic Gaucher disease. Human Molecular Genetics, 20(7), 1375-1386. doi: 10.1093/hmg/ddr019. http://hmg.oxfordjournals.org/cgi/content/abstract/20/7/1375


Fargo, K. N., & Sengelaub, D. R. (2004). Exogenous testosterone prevents motoneuron atrophy induced by contralateral motoneuron depletion. Journal of Neurobiology, 60(3), 348-359. doi. 

Fargo, K. N., & Sengelaub, D. R. (2004). Testosterone manipulation protects motoneurons from dendritic atrophy after contralateral motoneuron depletion. Journal of Comparative Neurology, 469(1), 96-106. doi. 

Fargo, K. N., & Sengelaub, D. R. (2007). Androgenic, but not estrogenic, protection of motoneurons from somal and dendritic atrophy induced by the death of neighboring motoneurons. Developmental Neurobiology, 67(8), 1094-1106. doi. 

Farrell, M. R., Holland, F. H., Shansky, R. M., & Brenhouse, H. C. (2016). Sex-specific effects of early life stress on social interaction and prefrontal cortex dendritic morphology in young rats. Behavioural Brain Research. doi: http://dx.doi.org/10.1016/j.bbr.2016.05.009. http://www.sciencedirect.com/science/article/pii/S0166432816302753


Farrow, K., Teixeira, M., Szikra, T., Viney, Tim J., Balint, K., Yonehara, K., & Roska, B. (2013). Ambient Illumination Toggles a Neuronal Circuit Switch in the Retina and Visual Perception at Cone Threshold. Neuron, (0). doi: http://dx.doi.org/10.1016/j.neuron.2013.02.014. http://www.sciencedirect.com/science/article/pii/S0896627313001724


Fasolino, M., Sabatini, P., Cuomo, T., & Liguori, G. (2004). Paraneoplastic subacute sensory neuronopathy associated with anti-ri antibodies. Journal of the Peripheral Nervous System, 9(2), 109-109. doi. 

Faulkner, J. R., Herrmann, J. E., Woo, M. J., Tansey, K. E., Doan, N. B., & Sofroniew, M. V. (2004). Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury. Journal of Neuroscience, 24(9), 2143-2155. doi. http://www.jneurosci.org/cgi/content/abstract/24/9/2143


Faunes, M., Botelho, J. F., & Wild, J. M. (2017). Innervation of the syrinx of the zebra finch (Taeniopygia guttata). Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24236. http://dx.doi.org/10.1002/cne.24236


Faunes, M., Fernández, S., Gutiérrez-Ibáñez, C., Iwaniuk, A. N., Wylie, D. R., Mpodozis, J., . . . Marín, G. (2012). Laminar segregation of GABAergic neurons in the avian nucleus isthmi pars magnocelluraris: A retrograde tracer and comparative study. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23253. http://dx.doi.org/10.1002/cne.23253


Faunes, M., & Wild, J. M. (2017). The ascending projections of the nuclei of the descending trigeminal tract (nTTD) in the zebra finch (Taeniopygia guttata). Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24247. http://dx.doi.org/10.1002/cne.24247


Faunes, M., & Wild, J. M. (2017). The sensory trigeminal complex and the organisation of its primary afferents in the zebra finch (Taeniopygia guttata). Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24249. http://dx.doi.org/10.1002/cne.24249


Favero, M., & Castro-Alamancos, M. A. (2013). Synaptic Cooperativity Regulates Persistent Network Activity in Neocortex. Journal of Neuroscience, 33(7), 3151-3163. doi: 10.1523/jneurosci.4424-12.2013. http://www.jneurosci.org/content/33/7/3151.abstract


Fawley, J. A., Pouliot, W. A., & Dudek, F. E. (2011). Pilocarpine-induced status epilepticus and subsequent spontaneous seizures: lack of effect on the number of gonadotropin-releasing hormone-positive neurons in a mouse model of temporal lobe epilepsy. Neuroscience. doi. 

Fazeli, W., Zappettini, S., Marguet, S. L., Grendel, J., Esclapez, M., Bernard, C., & Isbrandt, D. (2017). Early-life exposure to caffeine affects the construction and activity of cortical networks in mice. Experimental Neurology, 295, 88-103. doi: https://doi.org/10.1016/j.expneurol.2017.05.013. http://www.sciencedirect.com/science/article/pii/S001448861730136X


Fazio, R., Malaguti, M. C., Molinari, E., Previtali, S., Del Carro, U., Amadio, S., . . . Quattrini, A. (2004). CIDP associated with lung cancer: a paraneoplastic disease? Journal of the Peripheral Nervous System, 9(2), 108-108. doi: doi:10.1111/j.1085-9489.2004.009209m.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Fazzari, P., Paternain, A. V., Valiente, M., Pla, R., Luján, R., Lloyd, K., . . . Rico, B. (2010). Control of cortical GABA circuitry development by Nrg1 and ErbB4 signalling. Nature, 464(7293), 1376-1380. doi. 

Federer, F., Ichida, J. M., Jeffs, J., Schiessl, I., McLoughlin, N., & Angelucci, A. (2009). Four Projection Streams from Primate V1 to the Cytochrome Oxidase Stripes of V2. Journal of Neuroscience, 29(49), 15455-15471. doi: 10.1523/jneurosci.1648-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/49/15455 


Federer, F., Williams, D., Ichida, J. M., Merlin, S., & Angelucci, A. (2013). Two Projection Streams from Macaque V1 to the Pale Cytochrome Oxidase Stripes of V2. Journal of Neuroscience, 33(28), 11530-11539. doi: 10.1523/jneurosci.5053-12.2013. http://www.jneurosci.org/content/33/28/11530.abstract


Feingold, J., Desrochers, T. M., Fujii, N., Harlan, R., Tierney, P. L., Shimazu, H., . . . Graybiel, A. M. (2011). A system for recording neural activity chronically and simultaneously from multiple cortical and subcortical regions in non-human primates. Journal of Neurophysiology. doi. 

Fekete, Z., Pálfi, E., Márton, G., Handbauer, M., Bérces, Z., Ulbert, I., . . . Négyessy, L. (2016). Combined in vivo recording of neural signals and iontophoretic injection of pathway tracers using a hollow silicon microelectrode. Sensors and Actuators B: Chemical. doi: http://dx.doi.org/10.1016/j.snb.2015.12.099. http://www.sciencedirect.com/science/article/pii/S0925400515308236


Feldmann, M., Beckmann, D., Eysel, U. T., & Manahan-Vaughan, D. (2018). Early Loss of Vision Results in Extensive Reorganization of Plasticity-Related Receptors and Alterations in Hippocampal Function That Extend Through Adulthood. Cerebral Cortex, bhy297-bhy297. doi: 10.1093/cercor/bhy297. http://dx.doi.org/10.1093/cercor/bhy297


Feldmeyer, D., Brecht, M., Helmchen, F., Petersen, C. C. H., Poulet, J. F. A., Staiger, J. F., . . . Schwarz, C. (2012). Barrel cortex function. Progress in Neurobiology, (0). doi: http://dx.doi.org/10.1016/j.pneurobio.2012.11.002. http://www.sciencedirect.com/science/article/pii/S0301008212001700


Feldmeyer, D., Egger, V., Lubke, J., & Sakmann, B. (1999). Reliable synaptic connections between pairs of excitatory layer 4 neurones within a single 'barrel' of developing rat somatosensory cortex. Journal of Physiology, 521(1), 169-190. doi. http://jp.physoc.org/cgi/content/abstract/521/1/169 


Feldmeyer, D., Kask, K., Brusa, R., Kornau, H.-C., Kolhekar, R., Rozov, A., . . . Seeburg, P. H. (1999). Neurological dysfunctions in mice expressing different levels of the Q/R site-unedited AMPAR subunit GluR-B. Nature Neuroscience, 2, 54-64. doi. 

Feldmeyer, D., Lubke, J., & Sakmann, B. (2006). Efficacy and connectivity of intracolumnar pairs of layer 2/3 pyramidal cells in the barrel cortex of juvenile rats. Journal of Physiology, 575(2), 583-602. doi: 10.1113/jphysiol.2006.105106. http://jp.physoc.org/cgi/content/abstract/575/2/583 


Feldmeyer, D., Lubke, J., Silver, R. A., & Sakmann, B. (2002). Synaptic connections between layer 4 spiny neurone- layer 2/3 pyramidal cell pairs in juvenile rat barrel cortex: physiology and anatomy of interlaminar signalling within a cortical column. Journal of Physiology, 538(3), 803-822. doi: 10.1113/jphysiol.2001.012959. http://jp.physoc.org/cgi/content/abstract/538/3/803 


Feldmeyer, D., Qi, G., Emmenegger, V., & Staiger, J. F. (2017). Inhibitory interneurons and their circuit motifs in the many layers of the barrel cortex. Neuroscience. doi: https://doi.org/10.1016/j.neuroscience.2017.05.027. http://www.sciencedirect.com/science/article/pii/S0306452217303524


Feldmeyer, D., Roth, A., & Sakmann, B. (2005). Monosynaptic Connections between Pairs of Spiny Stellate Cells in Layer 4 and Pyramidal Cells in Layer 5A Indicate That Lemniscal and Paralemniscal Afferent Pathways Converge in the Infragranular Somatosensory Cortex. Journal of Neuroscience, 25(13), 3423-3431. doi. http://www.jneurosci.org/cgi/content/abstract/25/13/3423


Felleman, D. J., Xiao, Y., & McClendon, E. (1997). Modular Organization of Occipito-Temporal Pathways: Cortical Connections between Visual Area 4 and Visual Area 2 and Posterior Inferotemporal Ventral Area in Macaque Monkeys. Journal of Neuroscience, 17(9), 3185-3200. doi. http://www.jneurosci.org/cgi/content/abstract/17/9/3185


Fellous, J. M., Rudolph, M., Destexhe, A., & Sejnowski, T. J. (2003). Synaptic background noise controls the input/output characteristics of single cells in an in vitro model of in vivo activity. Neuroscience, 122(3), 811-829. doi. 

Feng, N., Ning, G., & Zheng, X. (2005). A framework for simulating axon guidance. Neurocomputing, 68, 70-84. doi. 

Fenrich, K. K., & Rose, P. K. (2009). Spinal Interneuron Axons Spontaneously Regenerate after Spinal Cord Injury in the Adult Feline. Journal of Neuroscience, 29(39), 12145-12158. doi: 10.1523/jneurosci.0897-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/39/12145 


Fenrich, K. K., & Rose, P. K. (2011). Axons with highly branched terminal regions successfully regenerate across spinal midline transections in the adult cat. Journal of Comparative Neurology, 519(16), 3240-3258. doi: 10.1002/cne.22686. http://dx.doi.org/10.1002/cne.22686


Fenrich, K. K., Skelton, N., MacDermid, V. E., Meehan, C. F., Armstrong, S., Neuber-Hess, M. S., & Rose, P. K. (2007). Axonal regeneration and development of de novo axons from distal dendrites of adult feline commissural interneurons after a proximal axotomy. Journal of Comparative Neurology, 502(6), 1079-1097. doi. 

Fenstermaker, V., Chen, Y., Ghosh, A., & Yuste, R. (2004). Regulation of dendritic length and branching by semaphorin 3A. Journal of Neurobiology, 58(3), 403-412. doi. 

Fenton, E. Y., Fournier, N. M., Lussier, A. L., Romay-Tallon, R., Caruncho, H. J., & Kalynchuk, L. E. (2015). Imipramine protects against the deleterious effects of chronic corticosterone on depression-like behavior, hippocampal reelin expression, and neuronal maturation. Progress in Neuro-Psychopharmacology and Biological Psychiatry, (0). doi: http://dx.doi.org/10.1016/j.pnpbp.2015.02.001. http://www.sciencedirect.com/science/article/pii/S0278584615000275


Ferdman, N., Murmu, R. P., Bock, J., Braun, K., & Leshem, M. (2007). Weaning age, social isolation, and gender, interact to determine adult explorative and social behavior, and dendritic and spine morphology in prefrontal cortex of rats. Behavioural Brain Research, 180(2), 174-182. doi. 

Ferger, B., Leng, A., Mura, A., Hengerer, B., & Feldon, J. (2004). Genetic ablation of tumor necrosis factor-alpha (TNF-α) and pharmacological inhibition of TNF-synthesis attenuates MPTP toxicity in mouse striatum. Journal of Neurochemistry, 89(4), 822-833. doi. 

Fernandez, D. C., Chang, Y.-T., Hattar, S., & Chen, S.-K. (2016). Architecture of retinal projections to the central circadian pacemaker. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1523629113. http://www.pnas.org/content/early/2016/05/05/1523629113.abstract


Fernández de Cossío, L., Guzmán, A., van der Veldt, S., & Luheshi, G. N. (2016). Prenatal infection leads to ASD-like behavior and altered synaptic pruning in the mouse offspring. Brain, Behavior, and Immunity. doi: http://dx.doi.org/10.1016/j.bbi.2016.09.028. http://www.sciencedirect.com/science/article/pii/S0889159116304524


Fernández, J., Fernández, L., Benavides-Piccione, R., Ballesteros-Yañez, I., DeFelipe, J., & Peña, J. M. (2010). A model for generating synthetic dendrites of cortical neurons. Trends in Applied Intelligent Systems, 129-138. doi. 

Fernandez, K. A., Jeffers, P. W., Lall, K., Liberman, M. C., & Kujawa, S. G. (2015). Aging after Noise Exposure: Acceleration of Cochlear Synaptopathy in “Recovered” Ears. The Journal of Neuroscience, 35(19), 7509-7520. doi. http://www.jneurosci.org/content/35/19/7509.short


Fernández, M., Morales, C., Durán, E., Fernandez-Colleman, S., Sentis, E., Mpodozis, J., . . . Marín, G. J. (2019). Parallel organization of the avian sensorimotor arcopallium: Tectofugal visual Pathway in the pigeon (Columba livia). Journal of Comparative Neurology, 0(ja). doi: 10.1002/cne.24775. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24775


Fernández, M. E., Croce, S., Boutin, C., Cremer, H., & Raineteau, O. (2011). Targeted electroporation of defined lateral ventricular walls: a novel and rapid method to study fate specification during postnatal forebrain neurogenesis. Neural Development, 6(1), 1-12. doi. 

Fernandez-Gonzalez, P., Benavides-Piccione, R., Leguey, I., Bielza, C., Larrañaga, P., & DeFelipe, J. (2016). Dendritic-branching angles of pyramidal neurons of the human cerebral cortex. [journal article]. Brain Structure and Function, 1-13. doi: 10.1007/s00429-016-1311-0. http://dx.doi.org/10.1007/s00429-016-1311-0


Ferrante, A., Boussadia, Z., Borreca, A., Mallozzi, C., Pedini, G., Pacini, L., . . . Martire, A. (2021). Adenosine A2A receptor inhibition reduces synaptic and cognitive hippocampal alterations in Fmr1 KO mice. Translational Psychiatry, 11(1), 112. doi: 10.1038/s41398-021-01238-5. https://doi.org/10.1038/s41398-021-01238-5


Ferrante, M., Tahvildari, B., Duque, A., Hadzipasic, M., Salkoff, D., Zagha, E. W., . . . McCormick, D. A. (2016). Distinct Functional Groups Emerge from the Intrinsic Properties of Molecularly Identified Entorhinal Interneurons and Principal Cells. Cerebral Cortex. doi: 10.1093/cercor/bhw143. http://cercor.oxfordjournals.org/content/early/2016/06/06/cercor.bhw143....


Ferrante, R. J., Andreassen, O. A., Dedeoglu, A., Ferrante, K. L., Jenkins, B. G., Hersch, S. M., & Beal, M. F. (2002). Therapeutic Effects of Coenzyme Q10 and Remacemide in Transgenic Mouse Models of Huntington's Disease. Journal of Neuroscience, 22(5), 1592-1599. doi. http://www.jneurosci.org/cgi/content/abstract/22/5/1592


Ferrante, R. J., Andreassen, O. A., Jenkins, B. G., Dedeoglu, A., Kuemmerle, S., Kubilus, J. K., . . . Beal, M. F. (2000). Neuroprotective Effects of Creatine in a Transgenic Mouse Model of Huntington's Disease. Journal of Neuroscience, 20(12), 4389-4397. doi. http://www.jneurosci.org/cgi/content/abstract/20/12/4389


Ferrante, R. J., Klein, A. M., Dedeoglu, A., & Flint Beal, M. (2001). Therapeutic efficacy of EGb761 (Gingko biloba extract) in a transgenic mouse model of amyotrophic lateral sclerosis. Journal of Molecular Neuroscience, 17(1), 89-96. doi. 

Ferrante, R. J., Kubilus, J. K., Lee, J., Ryu, H., Beesen, A., Zucker, B., . . . Hersch, S. M. (2003). Histone Deacetylase Inhibition by Sodium Butyrate Chemotherapy Ameliorates the Neurodegenerative Phenotype in Huntington's Disease Mice. Journal of Neuroscience, 23(28), 9418-9427. doi. http://www.jneurosci.org/cgi/content/abstract/23/28/9418 


Ferrante, R. J., Ryu, H., Kubilus, J. K., D'Mello, S., Sugars, K. L., Lee, J., . . . Ratan, R. R. (2004). Chemotherapy for the Brain: The Antitumor Antibiotic Mithramycin Prolongs Survival in a Mouse Model of Huntington's Disease. Journal of Neuroscience, 24(46), 10335-10342. doi. http://www.jneurosci.org/cgi/content/abstract/24/46/10335


Ferrarese, L., Jouhanneau, J.-S., Remme, M. W. H., Kremkow, J., Katona, G., Rózsa, B., . . . Poulet, J. F. A. (2018). Dendrite-Specific Amplification of Weak Synaptic Input during Network Activity In Vivo. Cell Reports, 24(13), 3455-3465.e3455. doi: https://doi.org/10.1016/j.celrep.2018.08.088. http://www.sciencedirect.com/science/article/pii/S2211124718314074


Ferrari, D. C., Mdzomba, B. J., Dehorter, N., Lopez, C., Michel, F. J., Libersat, F., & Hammond, C. (2012). Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups. [Original Research]. Frontiers in Cellular Neuroscience, 6. doi: 10.3389/fncel.2012.00007. http://www.frontiersin.org/Journal/Abstract.aspx?s=156&name=cellular_neu...


Ferrari, S., Cavallaro, T., Lanzafame, M., Malena, M., & Rizzuto, N. (2004). Painful neuropathy vasculitis in HIV infection. Journal of the Peripheral Nervous System, 9(2), 123-124. doi: doi:10.1111/j.1085-9489.2004.009209bl.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Ferreira, J. G. P., Duarte, J. C. G., Diniz, G. B., & Bittencourt, J. C. (2017). Litter size determines the number of melanin-concentrating hormone neurons in the medial preoptic area of Sprague Dawley lactating dams. Physiology and Behavior. doi: http://dx.doi.org/10.1016/j.physbeh.2017.08.028. http://www.sciencedirect.com/science/article/pii/S0031938417302664


Ferreira, T. A., Iacono, L. L., & Gross, C. T. (2010). Serotonin receptor 1A modulates actin dynamics and restricts dendritic growth in hippocampal neurons. European Journal of Neuroscience, 32(1), 18-26. doi. 

Festa, L., Gutoskey, C. J., Graziano, A., Waterhouse, B. D., & Meucci, O. (2015). Induction of Interleukin-1β by Human Immunodeficiency Virus-1 Viral Proteins Leads to Increased Levels of Neuronal Ferritin Heavy Chain, Synaptic Injury, and Deficits in Flexible Attention. The Journal of Neuroscience, 35(29), 10550-10561. doi. http://www.jneurosci.org/content/35/29/10550.short


Fetoni, A. R., De Bartolo, P., Eramo, S. L. M., Rolesi, R., Paciello, F., Bergamini, C., . . . Troiani, D. (2013). Noise-Induced Hearing Loss (NIHL) as a Target of Oxidative Stress-Mediated Damage: Cochlear and Cortical Responses after an Increase in Antioxidant Defense. Journal of Neuroscience, 33(9), 4011-4023. doi: 10.1523/jneurosci.2282-12.2013. http://www.jneurosci.org/content/33/9/4011.abstract


Fiala, J. C. (2005). Reconstruct: a free editor for serial section microscopy. Journal of Microscopy, 218(1), 52-61. doi: doi:10.1111/j.1365-2818.2005.01466.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1365-2818.2005.01466.x 


Fieblinger, T., & Cenci, M. A. (2015). Zooming in on the small: The plasticity of striatal dendritic spines in l-DOPA–Induced dyskinesia. Movement Disorders, n/a-n/a. doi: 10.1002/mds.26139. http://dx.doi.org/10.1002/mds.26139


Fieblinger, T., Graves, S. M., Sebel, L. E., Alcacer, C., Plotkin, J. L., Gertler, T. S., . . . Cenci, M. A. (2014). Cell type-specific plasticity of striatal projection neurons in parkinsonism and L-DOPA-induced dyskinesia. Nature Communications, 5. doi. http://www.nature.com/ncomms/2014/141031/ncomms6316/full/ncomms6316.html


Fiesel, F. C., Schurr, C., Weber, S. S., & Kahle, P. J. (2011). TDP-43 knockdown impairs neurite outgrowth dependent on its target histone deacetylase 6. Molecular neurodegeneration, 6(1), 1-10. doi. 

Filho, C. S., de Lima, C. M., Fôro, C. A. R., de Oliveira, M. A., Magalhães, N. G. M., Diniz, C. G., . . . Diniz, C. W. P. (2014). Visuospatial learning and memory in the Cebus apella and microglial morphology in the molecular layer of the dentate gyrus and CA1 lacunosum molecular layer. Journal of Chemical Neuroanatomy, (0). doi: http://dx.doi.org/10.1016/j.jchemneu.2014.10.001. http://www.sciencedirect.com/science/article/pii/S0891061814000908


Filiano, A. J., Martens, L. H., Young, A. H., Warmus, B. A., Zhou, P., Diaz-Ramirez, G., . . . Roberson, E. D. (2013). Dissociation of Frontotemporal Dementia–Related Deficits and Neuroinflammation in Progranulin Haploinsufficient Mice. Journal of Neuroscience, 33(12), 5352-5361. doi: 10.1523/jneurosci.6103-11.2013. http://www.jneurosci.org/content/33/12/5352.abstract


Filipchuk, A. A., & Durand, J. (2012). Postnatal dendritic development in lumbar motoneurons in mutant superoxide dismutase 1 mouse model of amyotrophic lateral sclerosis. Neuroscience. doi. 

Filipovic, R., Rakic, S., & Zecevic, N. (2002). Expression of Golli proteins in adult human brain and multiple sclerosis lesions. Journal of Neuroimmunology, 127(1), 1-12. doi. 

Fillinger, C., Yalcin, I., Barrot, M., & Veinante, P. (2016). Afferents to anterior cingulate areas 24a and 24b and midcingulate areas 24a′ and 24b′ in the mouse. [journal article]. Brain Structure and Function, 1-24. doi: 10.1007/s00429-016-1290-1. http://dx.doi.org/10.1007/s00429-016-1290-1


Fink, J. S., Kalda, A., Ryu, H., Stack, E. C., Schwarzschild, M. A., Chen, J.-F., & Ferrante, R. J. (2004). Genetic and pharmacological inactivation of the adenosine A2A receptor attenuates 3-nitropropionic acid-induced striatal damage. Journal of Neurochemistry, 88(3), 538-544. doi: doi:10.1046/j.1471-4159.2003.02145.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1471-4159.2003.02145.x 


Finkelstein, Y., Milatovic, D., Lazarovici, P., Ophir, A., Richter, E. D., Aschner, M., . . . others. (2010). Peaceful use of disastrous neurotoxicants. Neurotoxicology, 31(5), 608-620. doi. 

Finlay, B. L., Charvet, C. J., Bastille, I., Cheung, D. T., Muniz, J. A. P. C., & de Lima Silveira, L. C. (2013). Scaling the primate lateral geniculate nucleus: Niche and neurodevelopment in the regulation of magnocellular and parvocellular cell number and nucleus volume. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23505. http://dx.doi.org/10.1002/cne.23505


Fino, E., & Yuste, R. (2011). Dense inhibitory connectivity in neocortex. Neuron, 69(6), 1188-1203. doi. 

Finsterwald, C., Fiumelli, H., Cardinaux, J.-R., & Martin, J.-L. (2010). Regulation of Dendritic Development by BDNF Requires Activation of CRTC1 by Glutamate. Journal of Biological Chemistry, 285(37), 28587-28595. doi: 10.1074/jbc.M110.125740. http://www.jbc.org/content/285/37/28587.abstract


Finsterwald, C., & Martin, J.-L. (2011). Cellular mechanisms underlying the regulation of dendritic development by hepatocyte growth factor. European Journal of Neuroscience, 34(7), 1053-1061. doi: 10.1111/j.1460-9568.2011.07839.x. http://dx.doi.org/10.1111/j.1460-9568.2011.07839.x


Fiorentino, H., Kuczewski, N., Diabira, D., Ferrand, N., Pangalos, M. N., Porcher, C., & Gaiarsa, J.-L. (2009). GABAB Receptor Activation Triggers BDNF Release and Promotes the Maturation of GABAergic Synapses. Journal of Neuroscience, 29(37), 11650-11661. doi: 10.1523/jneurosci.3587-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/37/11650 


Fischer, A. K., von Rosenstiel, P., Fuchs, E., Goula, D., Almeida, O. F. X., & Czéh, B. (2002). The prototypic mineralocorticoid receptor agonist aldosterone influences neurogenesis in the dentate gyrus of the adrenalectomized rat. Brain Research, 947(2), 290-293. doi. 

Fischer, T., Faus-Kessler, T., Welzl, G., Simeone, A., Wurst, W., & Prakash, N. (2011). Fgf15-mediated control of neurogenic and proneural gene expression regulates dorsal midbrain neurogenesis. Developmental Biology, 350(2), 496-510. doi. 

Fish, K. N., Gonzales-Burgos, G., Zaitsev, A. V., & Lewis, D. A. (2012). Histological characterization of physiologically determined fast spiking interneurons in slices of the primate dorsolateral prefrontal cortex. Isolated Central Nervous System Circuits (Ed K Ballanyi), Neuromethods Series, 73, 159-181. doi. 

Fiske, B. K., & Brunjes, P. C. (2001). Cell death in the developing and sensory-deprived rat olfactory bulb. Journal of Comparative Neurology, 431(3), 311-319. doi. 

Fitting, S., Booze, R. M., & Mactutus, C. F. (2006). Neonatal hippocampal Tat injections: developmental effects on prepulse inhibition (PPI) of the auditory startle response. International Journal of Developmental Neuroscience, 24(4), 275-283. doi. 

Fitzgerald, P. J., Lane, J. W., Thakur, P. H., & Hsiao, S. S. (2004). Receptive Field Properties of the Macaque Second Somatosensory Cortex: Evidence for Multiple Functional Representations. Journal of Neuroscience, 24(49), 11193-11204. doi: 10.1523/jneurosci.3481-04.2004. http://www.jneurosci.org/cgi/content/abstract/24/49/11193 


Fitzgerald, P. J., Lane, J. W., Thakur, P. H., & Hsiao, S. S. (2006). Receptive Field (RF) Properties of the Macaque Second Somatosensory Cortex: RF Size, Shape, and Somatotopic Organization. Journal of Neuroscience, 26(24), 6485-6495. doi: 10.1523/jneurosci.5061-05.2006. http://www.jneurosci.org/cgi/content/abstract/26/24/6485 


Fitzgerald, P. J., Lane, J. W., Thakur, P. H., & Hsiao, S. S. (2006). Receptive Field Properties of the Macaque Second Somatosensory Cortex: Representation of Orientation on Different Finger Pads. Journal of Neuroscience, 26(24), 6473-6484. doi: 10.1523/jneurosci.5057-05.2006. http://www.jneurosci.org/cgi/content/abstract/26/24/6473 


FitzGibbon, T. (2006). Does the development of the perigeniculate nucleus support the notion of a hierarchical progression within the visual pathway? Neuroscience, 140(2), 529-546. doi. 

FitzGibbon, T. (2007). Do first order and higher order regions of the thalamic reticular nucleus have different developmental timetables? Experimental Neurology, 204(1), 339-354. doi. 

FitzGibbon, T. (2007). Do< i> first order</i> and< i> higher order</i> regions of the thalamic reticular nucleus have different developmental timetables? Experimental Neurology, 204(1), 339-354. doi. 

FitzGibbon, T., Eriköz, B., Grünert, U., & Martin, P. R. (2015). Analysis of the lateral geniculate nucleus in dichromatic and trichromatic marmosets. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23772. http://dx.doi.org/10.1002/cne.23772


Fitzgibbon, T., Szmajda, B. A., Martin, P. R., Adams, J. C., Ahlsen, G., Lindstrom, S., . . . Avanzini, G. (2007). First order connections of the visual sector of the thalamic reticular nucleus in marmoset monkeys (Callithrix jacchus). Visual Neuroscience, 24(6), 857-857. doi. 

Fiumelli, H., Briner, A., Puskarjov, M., Blaesse, P., Belem, B. J., Dayer, A. G., . . . Vutskits, L. (2012). An Ion Transport-Independent Role for the Cation-Chloride Cotransporter KCC2 in Dendritic Spinogenesis In Vivo. Cerebral Cortex, bhs027. doi: 10.1093/cercor/bhs027. http://cercor.oxfordjournals.org/cgi/content/abstract/bhs027v1


Flanigan, T. J., Anderson, J. E., Elayan, I., Allen, A. R., & Ferguson, S. A. (2017). Effects of Cyclophosphamide (CYP) and/or Doxorubicin (DOX) in a Murine Model of Post-Chemotherapy Cognitive Impairment. Toxicological Sciences, kfx267-kfx267. doi: 10.1093/toxsci/kfx267. http://dx.doi.org/10.1093/toxsci/kfx267


Fletcher, L. N., & Williams, S. R. (2018). Neocortical Topology Governs the Dendritic Integrative Capacity of Layer 5 Pyramidal Neurons. Neuron. doi: https://doi.org/10.1016/j.neuron.2018.10.048. http://www.sciencedirect.com/science/article/pii/S0896627318309565


Florencia, M., A., S. C., & Carol, M. (2018). Distinct timing of neurogenesis of ipsilateral and contralateral retinal ganglion cells. Journal of Comparative Neurology, 0(ja). doi: doi:10.1002/cne.24467. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24467


Flores, C., Wen, X., Labelle-Dumais, C., & Kolb, B. (2007). Chronic phencyclidine treatment increases dendritic spine density in prefrontal cortex and nucleus accumbens neurons. Synapse, 61(12), 978-984. doi. 

Flores, C. E., Nikonenko, I., Mendez, P., Fritschy, J.-M., Tyagarajan, S. K., & Muller, D. (2014). Activity-dependent inhibitory synapse remodeling through gephyrin phosphorylation. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1411170112. http://www.pnas.org/content/early/2014/12/17/1411170112.abstract


Flügel, A., Berkowicz, T., Ritter, T., Labeur, M., Jenne, D. E., Li, Z., . . . Wekerle, H. (2001). Migratory activity and functional changes of green fluorescent effector cells before and during experimental autoimmune encephalomyelitis. Immunity, 14(5), 547-560. doi. 

Foeller, E., Celikel, T., & Feldman, D. E. (2005). Inhibitory Sharpening of Receptive Fields Contributes to Whisker Map Plasticity in Rat Somatosensory Cortex. Journal of Neurophysiology, 94(6), 4387-4400. doi: 10.1152/jn.00553.2005. http://jn.physiology.org/cgi/content/abstract/94/6/4387 


Fogaça, M. V., Campos, A. C., Coelho, L. D., Duman, R. S., & Guimarães, F. S. (2018). The anxiolytic effects of cannabidiol in chronically stressed mice are mediated by the endocannabinoid system: Role of neurogenesis and dendritic remodeling. Neuropharmacology, 135, 22-33. doi: https://doi.org/10.1016/j.neuropharm.2018.03.001. https://www.sciencedirect.com/science/article/pii/S0028390818301023


Fogarty, M. J., Kanjhan, R., Bellingham, M. C., & Noakes, P. G. (2016). Glycinergic Neurotransmission: A Potent Regulator of Embryonic Motor Neuron Dendritic Morphology and Synaptic Plasticity. The Journal of Neuroscience, 36(1), 80-87. doi. http://www.jneurosci.org/content/36/1/80.short


Fogarty, M. J., Kanjhan, R., Yanagawa, Y., Noakes, P. G., & Bellingham, M. C. (2017). Alterations in hypoglossal motor neurons due to GAD67 and VGAT deficient mice. Experimental Neurology. doi: http://dx.doi.org/10.1016/j.expneurol.2016.12.004. http://www.sciencedirect.com/science/article/pii/S0014488616304046


Fogarty, M. J., Klenowski, P. M., Lee, J. D., Drieberg-Thompson, J. R., Bartlett, S. E., Ngo, S. T., . . . Noakes, P. G. (2016). Cortical synaptic and dendritic spine abnormalities in a presymptomatic TDP-43 model of amyotrophic lateral sclerosis. [Article]. Scientific Reports, 6, 37968. doi: 10.1038/srep37968. http://dx.doi.org/10.1038/srep37968


Fogarty, M. J., Mu, E. W. H., Lavidis, N. A., Noakes, P. G., & Bellingham, M. C. (2017). Motor Areas Show Altered Dendritic Structure in an Amyotrophic Lateral Sclerosis Mouse Model. [Original Research]. Frontiers in Neuroscience, 11(609). doi: 10.3389/fnins.2017.00609. https://www.frontiersin.org/article/10.3389/fnins.2017.00609


Fogarty, M. J., Mu, E. W. H., Lavidis, N. A., Noakes, P. G., & Bellingham, M. C. (2019). Size-dependent vulnerability of lumbar motor neuron dendritic degeneration in SOD1G93A mice. The anatomical record, 0(ja). doi: 10.1002/ar.24255. https://anatomypubs.onlinelibrary.wiley.com/doi/abs/10.1002/ar.24255


Fogarty, M. J., Mu, E. W. H., Noakes, P. G., Lavidis, N. A., & Bellingham, M. C. (2016). Marked changes in dendritic structure and spine density precede significant neuronal death in vulnerable cortical pyramidal neuron populations in the SOD1G93A mouse model of amyotrophic lateral sclerosis. [journal article]. Acta Neuropathologica Communications, 4(1), 1-21. doi: 10.1186/s40478-016-0347-y. http://dx.doi.org/10.1186/s40478-016-0347-y


Fogarty, M. J., Noakes, P. G., & Bellingham, M. C. (2015). Motor Cortex Layer V Pyramidal Neurons Exhibit Dendritic Regression, Spine Loss, and Increased Synaptic Excitation in the Presymptomatic hSOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis. The Journal of Neuroscience, 35(2), 643-647. doi. http://www.jneurosci.org/content/35/2/643.short


Fohlmeister, J. F., Cohen, E. D., & Newman, E. A. (2010). Mechanisms and distribution of ion channels in retinal ganglion cells: Using temperature as an independent variable. Journal of Neurophysiology, 00123.02009. doi: 10.1152/jn.00123.2009. http://jn.physiology.org/cgi/content/abstract/00123.2009v1 


Földy, C., Malenka, Robert C., & Südhof, Thomas C. (2013). Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling. Neuron, (0). doi: http://dx.doi.org/10.1016/j.neuron.2013.02.036. http://www.sciencedirect.com/science/article/pii/S0896627313002250


Fong, A. Y., & Potts, J. T. (2006). Neurokinin-1 receptor activation in Botzinger complex evokes bradypnoea. Journal of Physiology, 575(3), 869-885. doi: 10.1113/jphysiol.2006.114314. http://jp.physoc.org/cgi/content/abstract/575/3/869 


Fonken, L. K., Kitsmiller, E., Smale, L., & Nelson, R. J. (2012). Dim Nighttime Light Impairs Cognition and Provokes Depressive-Like Responses in a Diurnal Rodent. Journal of Biological Rhythms, 27(4), 319-327. doi: 10.1177/0748730412448324. http://jbr.sagepub.com/content/27/4/319.abstract


Fonken, L. K., Xu, X., Weil, Z. M., Chen, G., Sun, Q., Rajagopalan, S., & Nelson, R. J. (2011). Air pollution impairs cognition, provokes depressive-like behaviors and alters hippocampal cytokine expression and morphology. Molecular Psychiatry. doi: http://www.nature.com/mp/journal/vaop/ncurrent/suppinfo/mp201176s1.html. http://dx.doi.org/10.1038/mp.2011.76


Fontilla, M. F., & Peterson, E. H. (2000). Kinocilia heights on utricular hair cells. Hearing Research, 145(1-2), 8-16. doi. 

Foo, K. S., Hellysaz, A., & Broberger, C. (2014). Expression and colocalization patterns of calbindin-D28K, calretinin and parvalbumin in the rat hypothalamic arcuate nucleus. Journal of Chemical Neuroanatomy, (0). doi: http://dx.doi.org/10.1016/j.jchemneu.2014.06.008. http://www.sciencedirect.com/science/article/pii/S0891061814000490


Forehand, C. J. (1990). Morphology of sympathetic preganglionic neurons in the neonatal rat spinal cord: An intracellular horseradish peroxidase study. Journal of Comparative Neurology, 298(3), 334-342. doi. http://dx.doi.org/10.1002/cne.902980306 


Forehand, C. J., & Konopka, L. M. (1989). Frog sympathetic ganglion cells have local axon collaterals. Journal of Comparative Neurology, 289(2), 294-303. doi. http://dx.doi.org/10.1002/cne.902890209 


Forgione, N., Karadimas, S. K., Foltz, W. D., Satkunendrarajah, K., Lip, A., & Fehlings, M. (2014). Bilateral Contusion-Compression Model of Incomplete Traumatic Cervical Spinal Cord Injury (SCI). Journal of Neurotrauma, (ja). doi. http://online.liebertpub.com/doi/abs/10.1089/neu.2014.3388


Fornai, M., Pellegrini, C., Antonioli, L., Segnani, C., Ippolito, C., Barocelli, E., . . . Colucci, R. (2015). Enteric dysfunctions in experimental Parkinson’s disease: alterations of excitatory cholinergic neurotransmission regulating colonic motility in rats. Journal of Pharmacology and Experimental Therapeutics. doi: 10.1124/jpet.115.228510. http://jpet.aspetjournals.org/content/early/2015/11/18/jpet.115.228510.a...


Forner, S., Martini, A. C., Prieto, G. A., Dang, C. T., Rodriguez-Ortiz, C. J., Reyes-Ruiz, J. M., . . . LaFerla, F. M. (2019). Intra- and extracellular β-amyloid overexpression via adeno-associated virus-mediated gene transfer impairs memory and synaptic plasticity in the hippocampus. Scientific Reports, 9(1), 15936. doi: 10.1038/s41598-019-52324-0. https://doi.org/10.1038/s41598-019-52324-0


Forny-Germano, L., e Silva, N. M. L., Batista, A. F., Brito-Moreira, J., Gralle, M., Boehnke, S. E., . . . Martinez, A. M. B. (2014). Alzheimer's Disease-Like Pathology Induced by Amyloid-β Oligomers in Nonhuman Primates. The Journal of Neuroscience, 34(41), 13629-13643. doi. http://www.jneurosci.org/content/34/41/13629.short


Forro, T., Valenti, O., Lasztoczi, B., & Klausberger, T. (2013). Temporal Organization of GABAergic Interneurons in the Intermediate CA1 Hippocampus During Network Oscillations. Cerebral Cortex. doi: 10.1093/cercor/bht316. http://cercor.oxfordjournals.org/content/early/2013/11/22/cercor.bht316....


Forsberg, K., Wuttke, A., Quadrato, G., Chumakov, P. M., Wizenmann, A., & Di Giovanni, S. (2013). The Tumor Suppressor p53 Fine-Tunes Reactive Oxygen Species Levels and Neurogenesis via PI3 Kinase Signaling. Journal of Neuroscience, 33(36), 14318-14330. doi: 10.1523/jneurosci.1056-13.2013. http://www.jneurosci.org/content/33/36/14318.abstract


Förstera, E., Bartosb, M., & Zhaoa, S. (2005). Hippocampal Slice Cultures. Hippocampus, 3, 9-9. doi. 

Fortun, J., Puzis, R., Pearse, D. D., Gage, F. H., & Bunge, M. B. (2009). Muscle injection of AAV-NT3 promotes anatomical reorganization of CST axons and improves behavioral outcome following SCI. Journal of Neurotrauma, 26(7), 941-953. doi. 

Fortuna, M. G., Kügler, S., & Hülsmann, S. (2018). Probing the function of glycinergic neurons in the mouse respiratory network using optogenetics. Respiratory physiology & neurobiology. doi: https://doi.org/10.1016/j.resp.2018.10.008. http://www.sciencedirect.com/science/article/pii/S1569904818300740


Fortuna, M. G., Stornetta, R. L., West, G. H., & Guyenet, P. G. (2009). Activation of the retrotrapezoid nucleus by posterior hypothalamic stimulation. Journal of Physiology, 587(21), 5121-5138. doi: 10.1113/jphysiol.2009.176875. http://jp.physoc.org/content/587/21/5121.abstract 


Foscarin, S., Gianola, S., Carulli, D., Fazzari, P., Mi, S., Tamagnone, L., & Rossi, F. (2009). Overexpression of GAP-43 modifies the distribution of the receptors for myelin-associated growth-inhibitory proteins in injured Purkinje axons. European Journal of Neuroscience, 30(10), 1837-1848. doi. 

Foscarin, S., Ponchione, D., Pajaj, E., Leto, K., Gawlak, M., Wilczynski, G. M., . . . Carulli, D. (2011). Experience-dependent plasticity and modulation of growth regulatory molecules at central synapses. PLoS ONE, 6(1), e16666-e16666. doi. 

Fossati, S., Candiani, S., Nödl, M.-T., Maragliano, L., Pennuto, M., Domingues, P., . . . Zullo, L. (2014). Identification and Expression of Acetylcholinesterase in Octopus vulgaris Arm Development and Regeneration: a Conserved Role for ACHE? Molecular Neurobiology, 1-12. doi: 10.1007/s12035-014-8842-2. http://dx.doi.org/10.1007/s12035-014-8842-2


Fournier, N. M., Botterill, J. J., Marks, W. N., Guskjolen, A. J., & Kalynchuk, L. E. (2012). Impaired recruitment of seizure-generated neurons into functional memory networks of the adult dentate gyrus following long-term amygdala kindling. Experimental Neurology, (0). doi: http://dx.doi.org/10.1016/j.expneurol.2012.11.031. http://www.sciencedirect.com/science/article/pii/S0014488612004487


Fowler, M. A., Sidiropoulou, K., Ozkan, E. D., Phillips, C. W., & Cooper, D. C. (2007). Corticolimbic expression of TRPC4 and TRPC5 channels in the rodent brain. PLoS ONE, 2(6), e573-e573. doi. 

Fox, C., Dingman, A., Derugin, N., Wendland, M. F., Manabat, C., Ji, S., . . . Vexler, Z. S. (2005). Minocycline confers early but transient protection in the immature brain following focal cerebral ischemia–reperfusion. Journal of Cerebral Blood Flow and Metabolism. doi. 

Foxworthy, W. A., Clemo, H. R., & Meredith, M. A. (2012). Laminar and connectional organization of a multisensory cortex. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23264. http://dx.doi.org/10.1002/cne.23264


Foxworthy, W. A., & Meredith, M. A. (2011). An examination of somatosensory area SIII in ferret cortex. Somatosensory - 38; Motor Research, 28, 1(2), 1-10. doi. 

Francis, H. W., Rivas, A., Lehar, M., & Ryugo, D. K. (2004). Two types of afferent terminals innervate cochlear inner hair cells in C57BL/6J mice. Brain Research, 1016(2), 182-194. doi. 

Francis, H. W., Rivas, A., Lehar, M., Saito, Y., Mouton, P. R., & Ryugo, D. K. (2006). Efficient quantification of afferent cochlear ultrastructure using design-based stereology. Journal of Neuroscience Methods, 150(2), 150-158. doi. 

Franco, A., Knafo, S., Banon-Rodriguez, I., Merino-Serrais, P., Fernaud-Espinosa, I., Nieto, M., . . . Anton, I. M. (2011). WIP Is a Negative Regulator of Neuronal Maturation and Synaptic Activity. Cerebral Cortex, bhr199. doi: 10.1093/cercor/bhr199. http://cercor.oxfordjournals.org/cgi/content/abstract/bhr199v1


Frandolig, J. E., Matney, C. J., Lee, K., Kim, J., Chevée, M., Kim, S.-J., . . . Brown, S. P. (2019). The Synaptic Organization of Layer 6 Circuits Reveals Inhibition as a Major Output of a Neocortical Sublamina. Cell Reports, 28(12), 3131-3143.e3135. doi: https://doi.org/10.1016/j.celrep.2019.08.048. http://www.sciencedirect.com/science/article/pii/S2211124719310964


Frank, M., Schaeren-Wiemers, N., Schneider, R., & Schwab, M. E. (1999). Developmental Expression Pattern of the Myelin ProteolipiMAL Indicates Different Functions of MAL for Immature Schwann Cells and in a Late Step of CNS Myelinogenesis. Journal of Neurochemistry, 73(2), 587-597. doi. http://www.jneurochem.org/cgi/content/abstract/73/2/587


Frank, N. Y., Schatton, T., Kim, S., Zhan, Q., Wilson, B. J., Ma, J., . . . Frank, M. H. (2011). VEGFR-1 Expressed by Malignant Melanoma-Initiating Cells Is Required for Tumor Growth. Cancer Research, 71(4), 1474-1485. doi: 10.1158/0008-5472.can-10-1660. http://cancerres.aacrjournals.org/content/71/4/1474.abstract


Frankel, S., Concannon, J., Brusky, K., Pietrowicz, E., Giorgianni, S., Thompson, W. D., & Currie, D. A. (2009). Arsenic exposure disrupts neurite growth and complexity in vitro. Neurotoxicology, 30(4), 529-537. doi. 

Frankle, W. G., Laruelle, M., & Haber, S. N. (2006). Prefrontal Cortical Projections to the Midbrain in Primates: Evidence for a Sparse Connection. Neuropsychopharmacology, 31, 1627-1636. doi. 

Franklin, S. R., Brunso-Bechtold, J. K., & Henkel, C. K. (2006). Unilateral cochlear ablation before hearing onset disrupts the maintenance of dorsal nucleus of the lateral lemniscus projection patterns in the rat inferior colliculus. Neuroscience, 143(1), 105-115. doi. 

Franklin, S. R., Brunso-Bechtold, J. K., & Henkel, C. K. (2008). Bilateral cochlear ablation in postnatal rat disrupts development of banded pattern of projections from the dorsal nucleus of the lateral lemniscus to the inferior colliculus. Neuroscience, 154(1), 346-354. doi. 

Franklin, T. C., Wohleb, E. S., Zhang, Y., Fogaça, M., Hare, B., & Duman, R. S. (2017). Persistent increase in microglial RAGE contributes to chronic stress Induced priming of depressive-like behavior. Biological Psychiatry. doi: https://doi.org/10.1016/j.biopsych.2017.06.034. http://www.sciencedirect.com/science/article/pii/S0006322317318085


Fransen, E., D'Hooge, R., Van Camp, G., Verhoye, M., Sijbers, J., Reyniers, E., . . . Koekkoek, S. K. E. (1998). L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns. Human Molecular Genetics, 7(6), 999-1009. doi. 

Franssen, C. L., Bardi, M., Shea, E. A., Hampton, J. E., Adam Franssen, R., Kinsley, C. H., & Lambert, K. G. (2011). Fatherhood Alters Behavioural and Neural Responsiveness in a Spatial Task. Journal of Neuroendocrinology, 23(11), 1177-1187. doi: 10.1111/j.1365-2826.2011.02225.x. http://dx.doi.org/10.1111/j.1365-2826.2011.02225.x


Frappe, I., Roger, M., & Gaillard, A. (1999). Transplants of fetal frontal cortex grafted into the occipital cortex of newborn rats receive a substantial thalamic input from nuclei normally projecting to the frontal cortex. Neuroscience, 89(2), 409-421. doi. 

Frauenknecht, K., Katzav, A., Weiss Lavi, R., Sabag, A., Otten, S., Chapman, J., & Sommer, C. J. (2014). Mice with experimental antiphospholipid syndrome display hippocampal dysfunction and a reduction of dendritic complexity in hippocampal CA1 neurons. Neuropathology and Applied Neurobiology, n/a-n/a. doi: 10.1111/nan.12180. http://dx.doi.org/10.1111/nan.12180


Frazer, S., Prados, J., Niquille, M., Cadilhac, C., Markopoulos, F., Gomez, L., . . . Dayer, A. (2017). Transcriptomic and anatomic parcellation of 5-HT3AR expressing cortical interneuron subtypes revealed by single-cell RNA sequencing. [Article]. Nature Communications, 8, 14219. doi: 10.1038/ncomms14219

http://www.nature.com/articles/ncomms14219#supplementary-information. http://dx.doi.org/10.1038/ncomms14219


Freedman, L. J., Insel, T. R., & Smith, Y. (2000). Subcortical projections of area 25 (subgenual cortex) of the macaque monkey. Journal of Comparative Neurology, 421(2), 172-188. doi. 

Freedman, L. J., & Maddox, M. T. (2001). A comparison of anti-bioton and biotinylated anti-avidin double-bridge and biotinylated tyramide immunohistochemical amplification. Journal of Neuroscience Methods, 112(1), 43-49. doi. 

Freedman, L. J., & Shi, C. (2001). Monoaminergic innervation of the macaque extended amygdala. Neuroscience, 104(4), 1067-1084. doi. 

Freese, J. L., & Amaral, D. G. (2005). The organization of projections from the amygdala to visual cortical areas TE and V1 in the macaque monkey. Journal of Comparative Neurology, 486(4), 295-317. doi. 

Frega, M., Linda, K., Keller, J. M., Gümüş-Akay, G., Mossink, B., van Rhijn, J.-R., . . . Nadif Kasri, N. (2019). Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signaling. Nature Communications, 10(1), 4928. doi: 10.1038/s41467-019-12947-3. https://doi.org/10.1038/s41467-019-12947-3


Fregosi, M., Contestabile, A., Hamadjida, A., & Rouiller, E. M. (2017). Corticobulbar projections from distinct motor cortical areas to the reticular formation in macaque monkeys. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.13576. http://dx.doi.org/10.1111/ejn.13576


Fregosi, M., & Rouiller, E. M. (2017). Ipsilateral corticotectal projections from the primary, premotor and supplementary motor cortical areas in adult macaque monkeys: a quantitative anterograde tracing study. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.13709. http://dx.doi.org/10.1111/ejn.13709


Freire, M. A. M., Faber, J., Picanço-Diniz, C. W., Franca, J. G., & Pereira, A. (2011). Morphometric variability of NADPH diaphorase neurons in the primary sensory areas of the rat. Neuroscience. doi. 

Freire, M. A. M., Franca, J. G., Picanco-Diniz, C. W., Pereira, A., & others. (2005). Neuropil reactivity, distribution and morphology of NADPH diaphorase type I neurons in the barrel cortex of the adult mouse. Journal of Chemical Neuroanatomy, 30(2-3), 71-81. doi. 

Freire, M. A. M., Gomes-Leal, W., Carvalho, W. A., Guimarães, J. S., Franca, J. G., Picanço-Diniz, C. W., . . . others. (2004). A morphometric study of the progressive changes on NADPH diaphorase activity in the developing rat's barrel field. Neuroscience Research, 50(1), 55-66. doi. 

Freire, M. A. M., Morya, E., Faber, J., Santos, J. R., Guimaraes, J. S., Lemos, N. A. M., . . . Nicolelis, M. A. L. (2011). Comprehensive Analysis of Tissue Preservation and Recording Quality from Chronic Multielectrode Implants. PLoS ONE, 6(11), e27554-e27554. doi. 

Freire, M. A. M., Oliveira, R. B., Picanço-Diniz, C. W., Pereira, A., & others. (2007). Differential effects of methylmercury intoxication in the rat's barrel field as evidenced by NADPH diaphorase histochemistry. Neurotoxicology, 28(1), 175-181. doi. 

Freire, M. A. M., Rocha, E. G., Oliveira, J. L. F., Guimarães, J. S., Silveira, L. C. L., Elston, G. N., . . . Picanço-Diniz, C. W. (2010). Morphological variability of NADPH diaphorase neurons across areas V1, V2, and V3 of the common agouti. Brain Research, 1318, 52-63. doi. 

Freire, M. A. M., Tourinho, S. C., Guimarães, J. S., Oliveira, J. L. F., Picanço-Diniz, C. W., Gomes-Leal, W., & Pereira, A. (2008). Frontiers: Histochemical characterization, distribution and morphometric analysis of NADPH diaphorase neurons in the spinal cord of the agouti. Frontiers in Neuroanatomy, 2. doi. 

Freire, M. A. M., Tourinho, S. C., Guimarães, J. S., Oliveira, J. L. F., Picanço-Diniz, C. W., Gomes-Leal, W., & Pereira Jr, A. (2008). Histochemical characterization, distribution and morphometric analysis of NADPH diaphorase neurons in the spinal cord of the agouti. Frontiers in Neuroanatomy, 2. doi. 

French, C. A., Vinueza Veloz, M. F., Zhou, K., Peter, S., Fisher, S. E., Costa, R. M., & De Zeeuw, C. I. (2018). Differential effects of Foxp2 disruption in distinct motor circuits. Molecular Psychiatry. doi: 10.1038/s41380-018-0199-x. https://doi.org/10.1038/s41380-018-0199-x


Freria, C. M., Hall, J. C. E., Wei, P., Guan, Z., McTigue, D. M., & Popovich, P. G. (2017). Deletion of the fractalkine receptor, CX3CR1, improves endogenous repair, axon sprouting and synaptogenesis after spinal cord injury in mice. [10.1523/JNEUROSCI.2841-16.2017]. The Journal of Neuroscience. doi. http://www.jneurosci.org/content/early/2017/03/06/JNEUROSCI.2841-16.2017...


Freund, M., Walther, T., & von Bohlen und Halbach, O. (2013). Effects of the angiotensin-(1–7) receptor Mas on cell proliferation and on the population of doublecortin positive cells within the dentate gyrus and the piriform cortex. European Neuropsychopharmacology, (0). doi: http://dx.doi.org/10.1016/j.euroneuro.2013.06.004. http://www.sciencedirect.com/science/article/pii/S0924977X1300179X


Freund, P., Wannier, T., Schmidlin, E., Bloch, J., Mir, A., Schwab, M. E., & Rouiller, E. M. (2007). Anti-Nogo-A antibody treatment enhances sprouting of corticospinal axons rostral to a unilateral cervical spinal cord lesion in adult macaque monkey. Journal of Comparative Neurology, 502(4), 644-659. doi. 

Frick, A., Feldmeyer, D., Helmstaedter, M., & Sakmann, B. (2008). Monosynaptic Connections between Pairs of L5A Pyramidal Neurons in Columns of Juvenile Rat Somatosensory Cortex. Cerebral Cortex, 18(2), 397-406. doi: 10.1093/cercor/bhm074. http://cercor.oxfordjournals.org/cgi/content/abstract/18/2/397 


Frick, A., Feldmeyer, D., & Sakmann, B. (2007). Postnatal development of synaptic transmission in local networks of L5A pyramidal neurons in rat somatosensory cortex. Journal of Physiology, 585(1), 103-116. doi: 10.1113/jphysiol.2007.141788. http://jp.physoc.org/cgi/content/abstract/585/1/103 


Friedman, L. G., Riemslagh, F. W., Sullivan, J. M., Mesias, R., Williams, F. M., Huntley, G. W., & Benson, D. L. (2014). Cadherin-8 expression, synaptic localization and molecular control of neuronal form in prefrontal cortico-striatal circuits. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23666. http://dx.doi.org/10.1002/cne.23666


Friel, K., Chakrabarty, S., Kuo, H.-C., & Martin, J. (2012). Using Motor Behavior during an Early Critical Period to Restore Skilled Limb Movement after Damage to the Corticospinal System during Development. Journal of Neuroscience, 32(27), 9265-9276. doi: 10.1523/jneurosci.1198-12.2012. http://www.jneurosci.org/content/32/27/9265.abstract


Friel, K. M., & Martin, J. H. (2007). Bilateral Activity-Dependent Interactions in the Developing Corticospinal System. Journal of Neuroscience, 27(41), 11083-11090. doi: 10.1523/jneurosci.2814-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/41/11083 


Friese, A., Kaltschmidt, J. A., Ladle, D. R., Sigrist, M., Jessell, T. M., & Arber, S. (2009). Gamma and alpha motor neurons distinguished by expression of transcription factor Err3. Proceedings of the National Academy of Sciences, -. doi: 10.1073/pnas.0906809106. http://www.pnas.org/content/early/2009/07/24/0906809106.abstract 


Fritz, R., Yilmazer-Hanke, D., Roskoden, T., Schwegler, H., & Linke, R. (2005). Separate sets of neurons of the central nucleus of the amygdala project to the substantia innominata and the caudal pontine reticular nucleus in the rat. Neuroscience Letters, 373(2), 130-133. doi. 

Fritzsche, K., Can, A., Shen, H., Tsai, C., Turner, J., Tanenbaum, H. L., . . . Roysam, B. (2003). Automated model based segmentation, tracing and analysis of retinal vasculature from digital fundus images. State-of-The-Art Angiography, Applications and Plaque Imaging Using MR, CT, Ultrasound and X-rays, 225-298. doi. 

Frohmader, K. S., Wiskerke, J., Wise, R. A., Lehman, M. N., & Coolen, L. M. (2010). Methamphetamine acts on subpopulations of neurons regulating sexual behavior in male rats. Neuroscience, 166(3), 771-784. doi. 

Fryer, J. D., Taylor, J. W., DeMattos, R. B., Bales, K. R., Paul, S. M., Parsadanian, M., & Holtzman, D. M. (2003). Apolipoprotein E Markedly Facilitates Age-Dependent Cerebral Amyloid Angiopathy and Spontaneous Hemorrhage in Amyloid Precursor Protein Transgenic Mice. Journal of Neuroscience, 23(21), 7889-7896. doi. http://www.jneurosci.org/cgi/content/abstract/23/21/7889 


Fu, M.-m., McAlear, T. S., Nguyen, H., Oses-Prieto, J. A., Valenzuela, A., Shi, R. D., . . . Barres, B. A. (2019). The Golgi Outpost Protein TPPP Nucleates Microtubules and Is Critical for Myelination. Cell, 179(1), 132-146.e114. doi: https://doi.org/10.1016/j.cell.2019.08.025. http://www.sciencedirect.com/science/article/pii/S0092867419309134


Fu, Y. H., Tvrdik, P., Makki, N., Palombi, O., Machold, R., Paxinos, G., & Watson, C. (2009). The precerebellar linear nucleus in the mouse defined by connections, immunohistochemistry, and gene expression. Brain Research, 1271, 49-59. doi. 

Fucà, E., Guglielmotto, M., Boda, E., Rossi, F., Leto, K., & Buffo, A. (2017). Preventive motor training but not progenitor grafting ameliorates cerebellar ataxia and deregulated autophagy in tambaleante mice. Neurobiology of Disease, 102, 49-59. doi: http://dx.doi.org/10.1016/j.nbd.2017.02.005. http://www.sciencedirect.com/science/article/pii/S0969996117300360


Fuchs, E., Seress, L., & others. (2005). Mossy cells and different subpopulations of pyramidal neurons are immunoreactive for cocaine-and amphetamine-regulated transcript peptide in the hippocampal formation of non-human primates and tree shrew (Tupaia belangeri). Neuroscience, 136(1), 231-240. doi. 

Fudge, J. L., deCampo, D. M., & Becoats, K. T. (2012). Revisiting the hippocampal–amygdala pathway in primates: Association with immature-appearing neurons. Neuroscience, 212(0), 104-119. doi: 10.1016/j.neuroscience.2012.03.040. http://www.sciencedirect.com/science/article/pii/S0306452212003041


Fuentealba, Luis C., Rompani, Santiago B., Parraguez, Jose I., Obernier, K., Romero, R., Cepko, Constance L., & Alvarez-Buylla, A. (2015). Embryonic Origin of Postnatal Neural Stem Cells. Cell, 161(7), 1644-1655. doi: 10.1016/j.cell.2015.05.041. http://dx.doi.org/10.1016/j.cell.2015.05.041


Fuentealba, P., Klausberger, T., Karayannis, T., Suen, W. Y., Huck, J., Tomioka, R., . . . Somogyi, P. (2010). Expression of COUP-TFII Nuclear Receptor in Restricted GABAergic Neuronal Populations in the Adult Rat Hippocampus. Journal of Neuroscience, 30(5), 1595-1609. doi: 10.1523/jneurosci.4199-09.2010. http://www.jneurosci.org/cgi/content/abstract/30/5/1595 


Fuentes-Santamaria, V., Alvarado, J. C., Brunso-Bechtold, J. K., & Henkel, C. K. (2003). Upregulation of calretinin immunostaining in the ferret inferior colliculus after cochlear ablation. Journal of Comparative Neurology, 460(4), 585-596. doi. 

Fuentes-Santamaría, V., Alvarado, J. C., Herranz, A. S., García-Atarés, N., & López, D. E. (2007). Morphologic and neurochemical alterations in the superior colliculus of the genetically epilepsy-prone hamster (GPG/Vall). Epilepsy Research, 75(2), 206-219. doi. 

Fuentes-Santamaria, V., Alvarado, J. C., Taylor, A. R., Brunso-Bechtold, J. K., & Henkel, C. K. (2005). Quantitative changes in calretinin immunostaining in the cochlear nuclei after unilateral cochlear removal in young ferrets. Journal of Comparative Neurology, 483(4), 458-475. doi. 

Fuentes-Santamaria, V., Cantos, R., Alvarado, J. C., Garcia-Atares, N., & Lopez, D. E. (2005). Morphologic and Neurochemical Abnormalities in the Auditory Brainstem of the Genetically Epilepsy-prone Hamster (GPG/Vall). Epilepsia, 46(7), 1027-1045. doi: doi:10.1111/j.1528-1167.2005.68104.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1528-1167.2005.68104.x 


Fujii, T. G., Nixima, K. i., & Okanoya, K. (2016). Application of Optical Clearing Methods on the Songbird Brain. Ornithological Science, 15(2), 163-170. doi: 10.2326/osj.15.163. http://dx.doi.org/10.2326/osj.15.163


Fujino, T., Leslie, J. H., Eavri, R., Chen, J. L., Lin, W. C., Flanders, G. H., . . . Nedivi, E. (2011). CPG15 regulates synapse stability in the developing and adult brain. Genes and Development, 25(24), 2674-2685. doi: 10.1101/gad.176172.111. http://genesdev.cshlp.org/content/25/24/2674.abstract


Fujishima, K., Horie, R., Mochizuki, A., & Kengaku, M. (2012). Principles of branch dynamics governing shape characteristics of cerebellar Purkinje cell dendrites. Development, 139(18), 3442-3455. doi: 10.1242/dev.081315. http://dev.biologists.org/content/139/18/3442.abstract


Fujita, S., Mizoguchi, N., Aoki, R., Cui, Y., Koshikawa, N., & Kobayashi, M. (2015). Cytoarchitecture-Dependent Decrease in Propagation Velocity of Cortical Spreading Depression in the Rat Insular Cortex Revealed by Optical Imaging. Cerebral Cortex. doi: 10.1093/cercor/bhu336. http://cercor.oxfordjournals.org/content/early/2015/01/15/cercor.bhu336....


Fujita, S., Mizoguchi, N., Aoki, R., Cui, Y., Koshikawa, N., & Kobayashi, M. (2015). Cytoarchitecture-Dependent Decrease in Propagation Velocity of Cortical Spreading Depression in the Rat Insular Cortex Revealed by Optical Imaging. Cerebral Cortex. doi: 10.1093/cercor/bhu336. http://cercor.oxfordjournals.org/content/early/2015/01/15/cercor.bhu336....


Fujita, Y., Masuda, K., Bando, M., Nakato, R., Katou, Y., Tanaka, T., . . . Yamashita, T. (2017). Decreased cohesin in the brain leads to defective synapse development and anxiety-related behavior. [10.1084/jem.20161517]. The Journal of experimental medicine. doi. http://jem.rupress.org/content/early/2017/04/12/jem.20161517.abstract


Fujiwara, T., Inoue, T., Maruo, T., Rikitake, Y., Ieki, N., Mandai, K., . . . Mizoguchi, A. (2015). Nectin-1 Spots Regulate the Branching of Olfactory Mitral Cell Dendrites. Molecular and Cellular Neuroscience. doi: http://dx.doi.org/10.1016/j.mcn.2015.07.003. http://www.sciencedirect.com/science/article/pii/S1044743115300038


Fukami, H., & Bradley, R. M. (2005). Biophysical and Morphological Properties of Parasympathetic Neurons Controling the Parotid and von Ebner Salivary Glands in Rats. Journal of Neurophysiology, 93(2), 678-686. doi: 10.1152/jn.00277.2004. http://jn.physiology.org/cgi/content/abstract/93/2/678 


Fukuda, S., Maeda, H., & Sakurai, M. (2020). Reevaluation of motoneuron morphology: diversity and regularity among motoneurons innervating different arm muscles along a proximal–distal axis. Scientific Reports, 10(1), 13089. doi: 10.1038/s41598-020-69662-z. https://doi.org/10.1038/s41598-020-69662-z


Fukuda, T. (2009). Network Architecture of Gap Junction-Coupled Neuronal Linkage in the Striatum. Journal of Neuroscience, 29(4), 1235-1243. doi: 10.1523/jneurosci.4418-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/4/1235 


Fukuda, T. (2016). Structural organization of the dendritic reticulum linked by gap junctions in layer 4 of the visual cortex. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2016.10.050. http://www.sciencedirect.com/science/article/pii/S0306452216305905


Fukuda, T., & Kosaka, T. (2000). Gap Junctions Linking the Dendritic Network of GABAergic Interneurons in the Hippocampus. Journal of Neuroscience, 20(4), 1519-1528. doi. http://www.jneurosci.org/cgi/content/abstract/20/4/1519


Fukuda, T., & Kosaka, T. (2003). Ultrastructural study of gap junctions between dendrites of parvalbumin-containing GABAergic neurons in various neocortical areas of the adult rat. Neuroscience, 120(1), 5-20. doi. 

Fukuda, T., Kosaka, T., Singer, W., & Galuske, R. A. W. (2006). Gap Junctions among Dendrites of Cortical GABAergic Neurons Establish a Dense and Widespread Intercolumnar Network. Journal of Neuroscience, 26(13), 3434-3443. doi: 10.1523/jneurosci.4076-05.2006. http://www.jneurosci.org/cgi/content/abstract/26/13/3434 


Fukuda, T., Morooka, K., & Miyagi, Y. (2010). A simple but accurate method for histological reconstruction of the large-sized brain tissue of the human that is applicable to construction of digitized brain database. Neuroscience Research, 67(3), 260-265. doi. 

Fukui, H., Diaz, F., Garcia, S., & Moraes, C. T. (2007). Cytochrome c oxidase deficiency in neurons decreases both oxidative stress and amyloid formation in a mouse model of Alzheimer's disease. PNAS, 104(35), 14163-14168. doi: 10.1073/pnas.0705738104. http://www.pnas.org/cgi/content/abstract/104/35/14163 


Fukumitsu, K., Fujishima, K., Yoshimura, A., Wu, Y. K., Heuser, J., & Kengaku, M. (2015). Synergistic Action of Dendritic Mitochondria and Creatine Kinase Maintains ATP Homeostasis and Actin Dynamics in Growing Neuronal Dendrites. The Journal of Neuroscience, 35(14), 5707-5723. doi: 10.1523/jneurosci.4115-14.2015. http://www.jneurosci.org/content/35/14/5707.abstract


Fukumitsu, K., Hatsukano, T., Yoshimura, A., Heuser, J., Fujishima, K., & Kengaku, M. (2015). Mitochondrial fission protein Drp1 regulates mitochondrial transport and dendritic arborization in cerebellar Purkinje cells. Molecular and Cellular Neuroscience. doi: http://dx.doi.org/10.1016/j.mcn.2015.12.006. http://www.sciencedirect.com/science/article/pii/S1044743115300464


Fukunaga, I., Berning, M., Kollo, M., Schmaltz, A., & Schaefer, Andreas T. (2012). Two Distinct Channels of Olfactory Bulb Output. Neuron, 75(2), 320-329. doi: 10.1016/j.neuron.2012.05.017. http://www.sciencedirect.com/science/article/pii/S0896627312004837


Fukunaga, I., Herb, J. T., Kollo, M., Boyden, E. S., & Schaefer, A. T. (2014). Independent control of gamma and theta activity by distinct interneuron networks in the olfactory bulb. Nature Neuroscience. doi. http://www.nature.com/neuro/journal/vaop/ncurrent/full/nn.3760.html


Fullerton, B. C., & Pandya, D. N. (2007). Architectonic analysis of the auditory-related areas of the superior temporal region in human brain. Journal of Comparative Neurology, 504(5), 470-498. doi. 

Funamizu, Y., Nishijima, H., Ueno, T., Ueno, S., Mizukami, H., Yagihashi, S., & Tomiyama, M. (2017). Morphological dendritic spine changes of medium spiny neurons in the nucleus accumbens in 6-hydroxydopamine-lesioned rats treated with levodopa. Neuroscience Research. doi: http://doi.org/10.1016/j.neures.2017.03.010. http://www.sciencedirect.com/science/article/pii/S0168010216302486


Fung, J. C. L., & Cho, E. Y. P. (2020). Methylene blue promotes survival and GAP-43 expression of retinal ganglion cells after optic nerve transection. Life Sciences, 118462. doi: https://doi.org/10.1016/j.lfs.2020.118462. http://www.sciencedirect.com/science/article/pii/S0024320520312157


Funka-Lea, G. D., & Schwaber, J. S. (1994). A digital brain atlas and its application to the visceral neuraxis. Journal of Neuroscience Methods, 54(2), 253-260. doi. 

Furman, M., & Crair, M. C. (2012). Synapse maturation is enhanced in the binocular region of the retinocollicular map prior to eye opening. Journal of Neurophysiology. doi: 10.1152/jn.00943.2011. http://jn.physiology.org/content/early/2012/03/02/jn.00943.2011.abstract


Furman, M., Xu, H.-P., & Crair, M. C. (2013). Competition driven by retinal waves promotes the morphological and functional synaptic development of neurons in the superior colliculus. Journal of Neurophysiology. doi: 10.1152/jn.01066.2012. http://jn.physiology.org/content/early/2013/06/05/jn.01066.2012.abstract


Furtak, S. C., Moyer Jr, J. R., & Brown, T. H. (2007). Morphology and ontogeny of rat perirhinal cortical neurons. Journal of Comparative Neurology, 505(5), 493-510. doi. 

Furtak, S. C., Wei, S. M., Agster, K. L., & Burwell, R. D. (2007). Functional neuroanatomy of the parahippocampal region in the rat: the perirhinal and postrhinal cortices. Hippocampus, 17(9), 709-722. doi. 

Furuta, T., Deschênes, M., & Kaneko, T. (2011). Anisotropic Distribution of Thalamocortical Boutons in Barrels. Journal of Neuroscience, 31(17), 6432-6439. doi: 10.1523/jneurosci.6154-10.2011. http://www.jneurosci.org/content/31/17/6432.abstract


Furuta, T., Kaneko, T., & Deschenes, M. (2009). Septal Neurons in Barrel Cortex Derive Their Receptive Field Input from the Lemniscal Pathway. Journal of Neuroscience, 29(13), 4089-4095. doi: 10.1523/jneurosci.5393-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/13/4089 


Furutani, R., & Kibayashi, K. (2011). Morphological Alteration and Reduction of MAP2-Immunoreactivity in Pyramidal Neurons of Cerebral Cortex in a Rat Model of Focal Cortical Compression. Journal of Neurotrauma. doi. 

Fuzik, J., Zeisel, A., Mate, Z., Calvigioni, D., Yanagawa, Y., Szabo, G., . . . Harkany, T. (2015). Integration of electrophysiological recordings with single-cell RNA-seq data identifies neuronal subtypes. [Research]. Nat Biotech, advance online publication. doi: 10.1038/nbt.3443

http://www.nature.com/nbt/journal/vaop/ncurrent/abs/nbt.3443.html#supple.... http://dx.doi.org/10.1038/nbt.3443


Gabbott, P., Warner, T. A., Brown, J., Salway, P., Gabbott, T., & Busby, S. (2012). Amygdala afferents monosynaptically innervate corticospinal neurones in rat medial prefrontal cortex (mPFC). Journal of Comparative Neurology. doi. 

Gabbott, P. L. A., Warner, T. A., Jays, P. R. L., Salway, P., & Busby, S. J. (2005). Prefrontal cortex in the rat: projections to subcortical autonomic, motor, and limbic centers. Journal of Comparative Neurology, 492(2), 145-177. doi. 

Gaborieau, E., Hurtado-Chong, A., Fernández, M., Azim, K., & Raineteau, O. (2018). A dual role for the transcription factor Sp8 in postnatal neurogenesis. Scientific Reports, 8(1), 14560. doi: 10.1038/s41598-018-32134-6. https://doi.org/10.1038/s41598-018-32134-6


Gabr, U., Won, Y. S., Boonlayangoor, S., Thompson, K., Baroody, F. M., & Naclerio, R. M. (2001). C57Bl/6 and BALB/c mice have similar neutrophil response to acute Streptococcus pneumoniae sinus infections. Archives of Otolaryngology- Head and Neck Surgery, 127(8), 985-985. doi. 

Gabriele, M. L., Brubaker, D. Q., Chamberlain, K. A., Kross, K. M., Simpson, N. S., & Kavianpour, S. M. (2011). EphA4 and ephrin-B2 expression patterns during inferior colliculus projection shaping prior to experience. Developmental Neurobiology, 71(2), 182-199. doi: 10.1002/dneu.20842. http://dx.doi.org/10.1002/dneu.20842


Gabriele, M. L., Brunso-Bechtold, J. K., & Henkel, C. K. (2000). Development of afferent patterns in the inferior colliculus of the rat: projection from the dorsal nucleus of the lateral lemniscus. Journal of Comparative Neurology, 416(3), 368-382. doi. 

Gabriele, M. L., Brunso-Bechtold, J. K., & Henkel, C. K. (2000). Plasticity in the Development of Afferent Patterns in the Inferior Colliculus of the Rat after Unilateral Cochlear Ablation. Journal of Neuroscience, 20(18), 6939-6949. doi. http://www.jneurosci.org/cgi/content/abstract/20/18/6939


Gagnon, D., & Parent, M. (2014). Distribution of VGLUT3 in Highly Collateralized Axons from the Rat Dorsal Raphe Nucleus as Revealed by Single-Neuron Reconstructions. PLoS ONE, 9(2), e87709. doi: 10.1371/journal.pone.0087709. http://dx.doi.org/10.1371%2Fjournal.pone.0087709


Gagnon, M., Inhorn, S., Hancock, J., Keller, B., Carpenter, D., Merlin, T., . . . Whalen, R. (2004). Comparison of Cytology Proficiency Testing: Glass Slides vs. Virtual Slides. Acta Cytologica, November-December, 788-794. doi. 

Gahring, L. C., Persiyanov, K., Days, E. L., & Rogers, S. W. (2005). Age-related loss of neuronal nicotinic receptor expression in the aging mouse hippocampus corresponds with cyclooxygenase-2 and PPARγ expression and is altered by long-term NS398 administration. Journal of Neurobiology, 62(4), 453-468. doi. 

Gahring, L. C., Persiyanov, K., Dunn, D., Weiss, R., Meyer, E. L., & Rogers, S. W. (2004). Mouse strain-specific nicotinic acetylcholine receptor expression by inhibitory interneurons and astrocytes in the dorsal hippocampus. Journal of Comparative Neurology, 468(3), 334-346. doi. 

Gahring, L. C., Persiyanov, K., & Rogers, S. W. (2005). Mouse strain-specific changes in nicotinic receptor expression with age. Neurobiology of Aging, 26(6), 973-980. doi. 

Gaillard, A., Nasarre, C., & Roger, M. (2003). Early (E12) cortical progenitors can change their fate upon heterotopic transplantation. European Journal of Neuroscience, 17(7), 1375-1383. doi: doi:10.1046/j.1460-9568.2003.02576.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.2003.02576.x 


Gal, R., & Libersat, F. (2006). New vistas on the initiation and maintenance of insect motor behaviors revealed by specific lesions of the head ganglia. Journal of Comparative Physiology A: Neuroethology, Sensory, Neural, and Behavioral Physiology, 192(9), 1003-1020. doi. 

Galarreta, M., Erdelyi, F., Szabo, G., & Hestrin, S. (2004). Electrical Coupling among Irregular-Spiking GABAergic Interneurons Expressing Cannabinoid Receptors. Journal of Neuroscience, 24(44), 9770-9778. doi. http://www.jneurosci.org/cgi/content/abstract/24/44/9770


Galarreta, M., & Hestrin, S. (2002). Electrical and chemical synapses among parvalbumin fast-spiking GABAergic interneurons in adult mouse neocortex. Proceedings of the National Academy of Sciences, 99(19), 12438-12443. doi: 10.1073/pnas.192159599. http://www.pnas.org/cgi/content/abstract/99/19/12438 


Galassi, G., Ruggeri, A., Leone, M., & Cappelli, G. (2004). Chronic ataxic neuropathy initially diagnosed as ataxic variant of guillain barré syndrome. Journal of the Peripheral Nervous System, 9(2), 119-119. doi. 

Galazo, M. J., Martinez-Cerdeno, V., Porrero, C., & Clasca, F. (2008). Embryonic and Postnatal Development of the Layer I-Directed ("Matrix") Thalamocortical System in the Rat. Cerebral Cortex, 18(2), 344-363. doi: 10.1093/cercor/bhm059. http://cercor.oxfordjournals.org/cgi/content/abstract/18/2/344 


Gale, S. D., & Murphy, G. J. (2014). Distinct Representation and Distribution of Visual Information by Specific Cell Types in Mouse Superficial Superior Colliculus. The Journal of Neuroscience, 34(40), 13458-13471. doi. http://www.jneurosci.org/content/34/40/13458.short


Gallay, D. S., Gallay, M. N., Jeanmonod, D., Rouiller, E. M., & Morel, A. (2012). The Insula of Reil Revisited: Multiarchitectonic Organization in Macaque Monkeys. Cerebral Cortex, 22(1), 175-190. doi. 

Galliano, E., Gao, Z., Schonewille, M., Todorov, B., Simons, E., Pop, Andreea S., . . . De Zeeuw, Chris I. (2013). Silencing the Majority of Cerebellar Granule Cells Uncovers Their Essential Role in Motor Learning and Consolidation. Cell Reports, (0). doi: http://dx.doi.org/10.1016/j.celrep.2013.03.023. http://www.sciencedirect.com/science/article/pii/S2211124713001307


Galvan, A., Charara, A., Pare, J. F., Levey, A. I., & Smith, Y. (2004). Differential subcellular and subsynaptic distribution of GABAA and GABAB receptors in the monkey subthalamic nucleus. Neuroscience, 127(3), 709-721. doi. 

Galvan, C. D., Wenzel, J. H., Dineley, K. T., Lam, T. T., Schwartzkroin, P. A., Sweatt, J. D., & Swann, J. W. (2003). Postsynaptic contributions to hippocampal network hyperexcitability induced by chronic activity blockade in vivo. European Journal of Neuroscience, 18(7), 1861-1872. doi: doi:10.1046/j.1460-9568.2003.02920.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.2003.02920.x 


Galvan, E. J., Calixto, E., & Barrionuevo, G. (2008). Bidirectional Hebbian Plasticity at Hippocampal Mossy Fiber Synapses on CA3 Interneurons. Journal of Neuroscience, 28(52), 14042-14055. doi: 10.1523/jneurosci.4848-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/52/14042 


Galván, E. J., Pérez-Rosello, T., Gómez-Lira, G., Lara, E., Gutiérrez, R., & Barrionuevo, G. (2015). Synapse-specific compartmentalization of signaling cascades for LTP induction in CA3 interneurons. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2015.01.024. http://www.sciencedirect.com/science/article/pii/S0306452215000792


Gama, C. I., Tully, S. E., Sotogaku, N., Clark, P. M., Rawat, M., Vaidehi, N., . . . Hsieh-Wilson, L. C. (2006). Sulfation patterns of glycosaminoglycans encode molecular recognition and activity. Nature of Chemical Biology. doi. 

Gambino, F., Pagès, S., Kehayas, V., Baptista, D., Tatti, R., Carleton, A., & Holtmaat, A. (2014). Sensory-evoked LTP driven by dendritic plateau potentials in vivo. Nature. doi. http://www.nature.com/nature/journal/vaop/ncurrent/full/nature13664.html


Ganat, Y. M., Silbereis, J., Cave, C., Ngu, H., Anderson, G. M., Ohkubo, Y., . . . Vaccarino, F. M. (2006). Early Postnatal Astroglial Cells Produce Multilineage Precursors and Neural Stem Cells In Vivo. Journal of Neuroscience, 26(33), 8609-8621. doi: 10.1523/jneurosci.2532-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/33/8609 


Gantelet, E., Kraftsik, R., Delaloye, S., Gourdon, G., Kuntzer, T., & Barakat-Walter, I. (2007). The expansion of 300 CTG repeats in myotonic dystrophy transgenic mice does not induce sensory or motor neuropathy. Acta Neuropathologica, 114(2), 175-185. doi. 

Gao, H., Glatzer, N. R., Williams, K. W., Derbenev, A. V., Liu, D., & Smith, B. N. (2009). Morphological and electrophysiological features of motor neurons and putative interneurons in the dorsal vagal complex of rats and mice. Brain Research, 1291, 40-52. doi. 

Gao, K., & Mason, P. (2001). Physiological and anatomic evidence for functional subclasses of serotonergic raphe magnus cells. Journal of Comparative Neurology, 439(4), 426-439. doi. 

Gao, L., Tian, M., Zhao, H.-Y., Xu, Q.-Q., Huang, Y.-M., Si, Q.-C., . . . Zeng, Y. (2015). TrkB Activation by 7, 8-Dihydroxyflavone Increases Synapse AMPA Subunits and Ameliorates Spatial Memory Deficits in a Mouse Model of Alzheimer's Disease. Journal of Neurochemistry, n/a-n/a. doi: 10.1111/jnc.13432. http://dx.doi.org/10.1111/jnc.13432


Gao, P., Postiglione, Maria P., Krieger, Teresa G., Hernandez, L., Wang, C., Han, Z., . . . Shi, S.-H. (2014). Deterministic Progenitor Behavior and Unitary Production of Neurons in the Neocortex. Cell, 159(4), 775-788. doi: http://dx.doi.org/10.1016/j.cell.2014.10.027. http://www.sciencedirect.com/science/article/pii/S0092867414013154


Gao, R., Asano, S. M., Upadhyayula, S., Pisarev, I., Milkie, D. E., Liu, T.-L., . . . Betzig, E. (2019). Cortical column and whole-brain imaging with molecular contrast and nanoscale resolution. Science, 363(6424), eaau8302. doi: 10.1126/science.aau8302. http://science.sciencemag.org/content/363/6424/eaau8302.abstract


Gao, W. J., & Pallas, S. L. (1999). Cross-Modal Reorganization of Horizontal Connectivity in Auditory Cortex without Altering Thalamocortical Projections. Journal of Neuroscience, 19(18), 7940-7950. doi. http://www.jneurosci.org/cgi/content/abstract/19/18/7940 


Gao, W. J., Wormington, A. B., Newman, D. E., & Pallas, S. L. (2000). Development of inhibitory circuitry in visual and auditory cortex of postnatal ferrets: Immunocytochemical localization of calbindin-and parvalbumin-containing neurons. Journal of Comparative Neurology, 422(1), 140-157. doi. 

Gao, W.-J., & Goldman-Rakic, P. S. (2003). Selective modulation of excitatory and inhibitory microcircuits by dopamine. Proceedings of the National Academy of Sciences, 100(5), 2836-2841. doi: 10.1073/pnas.262796399. http://www.pnas.org/cgi/content/abstract/100/5/2836 


Gao, W.-J., Krimer, L. S., & Goldman-Rakic, P. S. (2001). Presynaptic regulation of recurrent excitation by D1 receptors in prefrontal circuits. Neurobiology, 98, 295-300. doi. 

Gao, W.-J., Wang, Y., & Goldman-Rakic, P. S. (2003). Dopamine modulation of perisomatic and peridendritic inhibition in prefrontal cortex. Journal of Neuroscience, 23(5), 1622-1630. doi. 

Gao, X., & Chen, J. (2011). Mild Traumatic Brain Injury Results in Extensive Neuronal Degeneration in the Cerebral Cortex. Journal of Neuropathology and Experimental Neurology, 70(3), 183-183. doi. 

Gao, X., Deng, P., Xu, Z. C., & Chen, J. (2011). Moderate Traumatic Brain Injury Causes Acute Dendritic and Synaptic Degeneration in the Hippocampal Dentate Gyrus. PLoS ONE, 6(9), e24566-e24566. doi. 

Gao, X., Grendel, J., Muhia, M., Castro-Gomez, S., Süsens, U., Isbrandt, D., . . . Ohana, O. (2019). Disturbed prefrontal cortex activity in the absence of schizophrenia-like behavioral dysfunction in Arc/Arg3.1 deficient mice. The Journal of Neuroscience, 0623-0619. doi: 10.1523/jneurosci.0623-19.2019. http://www.jneurosci.org/content/early/2019/09/05/JNEUROSCI.0623-19.2019...


Gao, Y., Hu, S., Li, Q., Wang, M., Zhi, Z., Kuang, X., . . . Wang, Y. (2018). Neonatal inflammation induces reorganization in dendritic morphology of retinal ganglion cells but not their retinogeniculate projection in mice. Neuroscience Letters, 676, 34-40. doi: https://doi.org/10.1016/j.neulet.2018.04.012. https://www.sciencedirect.com/science/article/pii/S0304394018302672


Gao, Y., Jiang, T., Qu, C., Tao, H., Cao, H., Zhao, Y., . . . Chen, J.-G. (2013). Atlastin-1 regulates dendritic morphogenesis in mouse cerebral cortex. Neuroscience Research, (0). doi: http://dx.doi.org/10.1016/j.neures.2013.08.007. http://www.sciencedirect.com/science/article/pii/S0168010213001922


Gao, Y., Liu, L., Li, Q., & Wang, Y. (2015). Differential alterations in the morphology and electrophysiology of layer II pyramidal cells in the primary visual cortex of a mouse model prenatally exposed to LPS. Neuroscience Letters, 591(0), 138-143. doi: http://dx.doi.org/10.1016/j.neulet.2015.02.043. http://www.sciencedirect.com/science/article/pii/S0304394015001573


Gao, Y., Shen, M., Gonzalez, J. C., Dong, Q., Kannan, S., Hoang, J. T., . . . Zhao, X. (2020). RGS6 Mediates Effects of Voluntary Running on Adult Hippocampal Neurogenesis. Cell Reports, 32(5), 107997. doi: https://doi.org/10.1016/j.celrep.2020.107997. http://www.sciencedirect.com/science/article/pii/S2211124720309827


Gao, Y., Su, J., Guo, W., Polich, E. D., Magyar, D. P., Xing, Y., . . . Zhao, X. (2015). Inhibition of miR-15a promotes BDNF expression and rescues dendritic maturation deficits in MeCP2-deficient neurons. Stem Cells, n/a-n/a. doi: 10.1002/stem.1950. http://dx.doi.org/10.1002/stem.1950


Gao, Z., Proietti-Onori, M., Lin, Z., ten Brinke, Michiel M., Boele, H.-J., Potters, J.-W., . . . De Zeeuw, Chris I. (2016). Excitatory Cerebellar Nucleocortical Circuit Provides Internal Amplification during Associative Conditioning. Neuron, 89(3), 645-657. doi: http://dx.doi.org/10.1016/j.neuron.2016.01.008. http://www.sciencedirect.com/science/article/pii/S089662731600009X


Garbossa, D., Fontanella, M., Pagni, C. A., & Vercelli, A. (2001). Nitric oxide synthase and cytochrome c oxidase changes in the tumoural and peritumoural cerebral cortex. Acta Neurochirurgica, 143(9), 897-908. doi. 

Garbossa, D., Fontanella, M., Tomasi, S., Ducati, A., & Vercelli, A. (2005). Differential distribution of NADPH-diaphorase histochemistry in human cerebral cortex. Brain Research, 1034(1), 1-10. doi. 

Garbossa, D., & Vercelli, A. (2003). Experimentally-induced microencephaly: effects on cortical neurons. Brain Research Bulletin, 60(4), 329-338. doi. 

Garcia, B. G., Neely, M. D., & Deutch, A. Y. (2010). Cortical Regulation of Striatal Medium Spiny Neuron Dendritic Remodeling in Parkinsonism: Modulation of Glutamate Release Reverses Dopamine Depletion–Induced Dendritic Spine Loss. Cerebral Cortex, 20(10), 2423-2423. doi. 

Garcia, I., Quast, Kathleen B., Huang, L., Herman, Alexander M., Selever, J., Deussing, Jan M., . . . Arenkiel, Benjamin R. (2014). Local CRH Signaling Promotes Synaptogenesis and Circuit Integration of Adult-Born Neurons. Developmental cell, (0). doi: http://dx.doi.org/10.1016/j.devcel.2014.07.001. http://www.sciencedirect.com/science/article/pii/S1534580714004213


García, N. V. D. M., Karayannis, T., & Fishell, G. (2011). Neuronal activity is required for the development of specific cortical interneuron subtypes. Nature, 472(7343), 351-355. doi. 

García-Cabezas, M. Á., & Barbas, H. (2016). Anterior Cingulate Pathways May Affect Emotions Through Orbitofrontal Cortex. Cerebral Cortex. doi: 10.1093/cercor/bhw284. http://cercor.oxfordjournals.org/content/early/2016/09/20/cercor.bhw284....


Garcia-Cabezas, M. A., Martinez-Sanchez, P., Sanchez-Gonzalez, M. A., Garzon, M., & Cavada, C. (2008). Dopamine Innervation in the Thalamus: Monkey versus Rat. Cerebral Cortex, bhn093. doi: 10.1093/cercor/bhn093. http://cercor.oxfordjournals.org/cgi/content/abstract/bhn093v1 


García-Cabezas, M. Á., Rico, B., Sánchez-González, M. Á., & Cavada, C. (2007). Distribution of the dopamine innervation in the macaque and human thalamus. Neuroimage, 34(3), 965-984. doi. 

Garcia-Cairasco, N. (2009). Learning about brain physiology and complexity from the study of the epilepsies. Brazilian Journal of Medical and Biological Research, 42(1), 76-86. doi. 

Garcia-Cairasco, N. (2009). Puzzling challenges in contemporary neuroscience: insights from complexity and emergence in epileptogenic circuits. Epilepsy & Behavior, 14(1), 54-63. doi. 

Garcia-Cairasco, N., Umeoka, E. H. L., & Cortes de Oliveira, J. A. (2017). The Wistar Audiogenic Rat (WAR) strain and its contributions to epileptology and related comorbidities: History and perspectives. Epilepsy & Behavior. doi: https://doi.org/10.1016/j.yebeh.2017.04.001. http://www.sciencedirect.com/science/article/pii/S1525505017302688


García-Calero, E., Martínez-de-la-Torre, M., & Puelles, L. (2002). The avian griseum tectale: cytoarchitecture, NOS expression and neurogenesis. Brain Research Bulletin, 57(3-4), 353-357. doi. 

Garcia-Junco-Clemente, P., Chow, D. K., Tring, E., Lazaro, M. T., Trachtenberg, J. T., & Golshani, P. (2013). Overexpression of calcium-activated potassium channels underlies cortical dysfunction in a model of PTEN-associated autism. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1309207110. http://www.pnas.org/content/early/2013/10/16/1309207110.abstract


Garcia-Marin, V., Blazquez-Llorca, L., Rodriguez, J. R., Boluda, S., Muntane, G., Ferrer, I., & DeFelipe, J. (2009). Diminished perisomatic GABAergic terminals on cortical neurons adjacent to amyloid plaques. Frontiers in Neuroanatomy, 3. doi. 

Garcia-Marin, V., Sundiang, M., & Hawken, M. (2014). Reduced density of geniculocortical terminals in foveal layer 4A in the macaque primary visual cortex: relationship to S-cone density. Brain Structure and Function, 1-14. doi: 10.1007/s00429-014-0826-5. http://dx.doi.org/10.1007/s00429-014-0826-5


Garden, D. L. F., Dodson, P. D., O'Donnell, C., White, M. D., & Nolan, M. F. (2008). Tuning of synaptic integration in the medial entorhinal cortex to the organization of grid cell firing fields. Neuron, 60(5), 875-889. doi. 

Gardian, G., Browne, S. E., Choi, D.-K., Klivenyi, P., Gregorio, J., Kubilus, J. K., . . . Beal, M. F. (2005). Neuroprotective Effects of Phenylbutyrate in the N171-82Q Transgenic Mouse Model of Huntington's Disease. Journal of Biological Chemistry, 280(1), 556-563. doi: 10.1074/jbc.M410210200. http://www.jbc.org/cgi/content/abstract/280/1/556 


Gariépy, J. F., Missaghi, K., Chartré, S., Robert, M., Auclair, F., & Dubuc, R. (2011). Bilateral connectivity in the brainstem respiratory networks of lampreys. Journal of Comparative Neurology. doi. 

Gariépy, J.-F., Missaghi, K., Chevallier, S., Chartré, S., Robert, M., Auclair, F., . . . Dubuc, R. (2012). Specific neural substrate linking respiration to locomotion. Proceedings of the National Academy of Sciences, 109(2), E84–E92. doi: 10.1073/pnas.1113002109. http://www.pnas.org/content/109/2/E84.abstract


Garner, H. L., Whittington, M. A., & Henderson, Z. (2005). Induction by kainate of theta frequency rhythmic activity in the rat medial septum-diagonal band complex in vitro. Journal of Physiology, 564(1), 83-102. doi: 10.1113/jphysiol.2004.080622. http://jp.physoc.org/cgi/content/abstract/564/1/83 


Garrett, J. E., Kim, I., Wilson, R. E., & Wellman, C. L. (2006). Effect of N-methyl-d-aspartate receptor blockade on plasticity of frontal cortex after cholinergic deafferentation in rat. Neuroscience, 140(1), 57-66. doi. 

Garrett, J. E., & Wellman, C. L. (2009). Chronic stress effects on dendritic morphology in medial prefrontal cortex: sex differences and estrogen dependence. Neuroscience, 162(1), 195-207. doi. 

Garrett, L., Ung, M. C., Heermann, T., Niedermeier, K. M., & Hölter, S. (2018). Analysis of Neuropsychiatric Disease‐Related Functional Neuroanatomical Markers in Mice. Current Protocols in Mouse Biology, 8(1), 79-128. doi: doi:10.1002/cpmo.37. https://currentprotocols.onlinelibrary.wiley.com/doi/abs/10.1002/cpmo.37


Garrido-Sanabria, E. R., Perez, M. G., Banuelos, C., Reyna, T., Hernandez, S., Castaneda, M. T., & Colom, L. V. (2007). Electrophysiological and morphological heterogeneity of slow firing neurons in medial septal/diagonal band complex as revealed by cluster analysis. Neuroscience, 146(3), 931-945. doi. 

Garske, A. K., Lawyer, C. R., Peterson, B. M., & Illig, K. R. (2013). Adolescent Changes in Dopamine D1 Receptor Expression in Orbitofrontal Cortex and Piriform Cortex Accompany an Associative Learning Deficit. PLoS ONE, 8(2), e56191. doi. 

Gärtner, U., Alpár, A., Behrbohm, J., Heumann, R. H., Rolf, & Arendt, T. (2005). Enhanced Ras activity promotes spine formation in synRas mice neocortex. Neuroreport, 16(2), 149-149. doi. 

Gärtner, U., Alpár, A., Reimann, F., Seeger, G., Heumann, R., & Arendt, T. (2004). Constitutive Ras activity induces hippocampal hypertrophy and remodeling of pyramidal neurons in synRas mice. Journal of Neuroscience Research, 77(5), 630-641. doi. 

Gärtner, U., Alpár, A., Seeger, G., Heumann, R., & Arendt, T. (2004). Enhanced Ras activity in pyramidal neurons induces cellular hypertrophy and changes in afferent and intrinsic connectivity in synRas mice. International Journal of Developmental Neuroscience, 22(3), 165-173. doi. 

Garvey, L., Pavese, N., Politis, M., Ramlackhansingh, A., Brooks, D., Taylor-Robinson, S., & Winston, A. (2013). Increased microglia activation in neurologically asymptomatic HIV-infected patients receiving effective ART; an 11C-PK11195 PET study. AIDS, 28(1), 67 - 72. doi. 

Garzotto, D., Giacobini, P., Crepaldi, T., Fasolo, A., & De Marchis, S. (2008). Hepatocyte Growth Factor Regulates Migration of Olfactory Interneuron Precursors in the Rostral Migratory Stream through Met-Grb2 Coupling. Journal of Neuroscience, 28(23), 5901-5909. doi: 10.1523/jneurosci.1083-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/23/5901 


Garzotto, D., Giacobini, P., Crepaldi, T., Fasolo, A., & De Marchis, S. (2008). Hepatocyte growth factor regulates migration of olfactory interneuron precursors in the rostral migratory stream through Met–Grb2 coupling. Journal of Neuroscience, 28(23), 5901-5909. doi. 

Gashi, E., Avallone, J., Webster, T., & Friedman, L. K. (2007). Altered excitability and distribution of NMDA receptor subunit proteins in cortical layers of rat pups following multiple perinatal seizures. Brain Research, 1145, 56-65. doi. 

Gaspar, R., Soares-Cunha, C., Domingues, A. V., Coimbra, B., Baptista, F. I., Pinto, L., . . . Gomes, C. A. (2021). Resilience to stress and sex-specific remodeling of microglia and neuronal morphology in a rat model of anxiety and anhedonia. Neurobiology of Stress, 14, 100302. doi: https://doi.org/10.1016/j.ynstr.2021.100302. https://www.sciencedirect.com/science/article/pii/S2352289521000102


Gastinger, M. J., Barber, A. J., Khin, S. A., McRill, C. S., Gardner, T. W., & Marshak, D. W. (2001). Abnormal centrifugal axons in streptozotocin-diabetic rat retinas. Investigative Ophthalmology and Visual Science, 42(11), 2679-2685. doi. 

Gastinger, M. J., Bordt, A. S., Bernal, M. P., & Marshak, D. W. (2005). Serotonergic retinopetal axons in the monkey retina. Current Eye Research, 30(12), 1089-1095. doi. 

Gastinger, M. J., O'Brien, J. J., Larsen, N. B., & Marshak, D. W. (1999). Histamine immunoreactive axons in the macaque retina. Investigative Ophthalmology and Visual Science, 40(2), 487-487. doi. 

Gastinger, M. J., Tian, N., Horvath, T., & Marshak, D. W. (2006). Retinopetal axons in mammals: emphasis on histamine and serotonin. Current Eye Research, 31(7-8), 655-667. doi. 

Gáti, G., Lendvai, D., Hökfelt, T., Harkany, T., & Alpár, A. (2014). Revival of Calcium-Binding Proteins for Neuromorphology: Secretagogin Typifies Distinct Cell Populations in the Avian Brain. Brain, Behavior and Evolution, 83(2), 82-92. doi. http://www.karger.com/Article/FullText/357834


Gaub, P., Joshi, Y., Wuttke, A., Naumann, U., Schnichels, S., Heiduschka, P., & Di Giovanni, S. (2011). The histone acetyltransferase p300 promotes intrinsic axonal regeneration. Brain, 134(7), 2134-2148. doi: 10.1093/brain/awr142. http://brain.oxfordjournals.org/cgi/content/abstract/134/7/2134


Gaub, P., Tedeschi, A., Puttagunta, R., Nguyen, T., Schmandke, A., & Di Giovanni, S. (2010). HDAC inhibition promotes neuronal outgrowth and counteracts growth cone collapse through CBP/p300 and P/CAF-dependent p53 acetylation. Cell Death and Differentiation, 17(9), 1392-1408. doi. 

Gaudet, C. M. A., Lim, Y.-P., Stonestreet, B. S., & Threlkeld, S. W. (2016). Effects of Age, Experience and Inter-alpha Inhibitor Proteins on Working Memory and Neuronal Plasticity after Neonatal Hypoxia-Ischemia. Behavioural Brain Research. doi: http://dx.doi.org/10.1016/j.bbr.2016.01.016. http://www.sciencedirect.com/science/article/pii/S0166432816300134


Gaugler, M. N., Genc, O., Bobela, W., Mohanna, S., Ardah, M. T., El-Agnaf, O. M., . . . others. (2012). Nigrostriatal overabundance of α-synuclein leads to decreased vesicle density and deficits in dopamine release that correlate with reduced motor activity. Acta Neuropathologica, 1-17. doi. 

Gauron, C., Meda, F., Dupont, E., Albadri, S., Quenech’Du, N., Ipendey, E., . . . Rampon, C. (2016). Hydrogen peroxide (H 2 O 2) controls axon pathfinding during zebrafish development. Developmental Biology. doi. http://www.sciencedirect.com/science/article/pii/S0012160615303110


Gautschi, M., & Clarke, P. G. H. (2007). Neuronal death in the lateral geniculate nucleus of young ferrets following a cortical lesion: Time-course, age dependence and involvement of caspases. Brain Research, 1167, 20-30. doi. 

Gaykema, R. P., & Zaborszky, L. (1996). Direct Catecholaminergic-Cholinergic Interactions in the Basal Forebrain. II. Substantia Nigra-Ventral Tegmental Area Projections to holinergic Neurons. Journal Comparative Neurology, 374, 555-577. doi. 

Gazula, V. R., Roberts, M., Luzzio, C., Jawad, A. F., & Kalb, R. G. (2004). Effects of limb exercise after spinal cord injury on motor neuron dendrite structure. Journal of Comparative Neurology, 476(2), 130-145. doi. 

Gazzerro, E., Baldassari, S., Giacomini, C., Musante, V., Fruscione, F., La Padula, V., . . . Minetti, C. (2012). Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein. PLoS ONE, 7(3), e32180. doi: 10.1371/journal.pone.0032180. http://dx.doi.org/10.1371%2Fjournal.pone.0032180


Gazzerro, E., Baldassari, S., Giacomini, C., Musante, V., Fruscione, F., La Padula, V., . . . others. (2012). Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein. PLoS ONE, 7(3), e32180-e32180. doi. 

Ge, W.-P., Zhou, W., Luo, Q., Jan, L. Y., & Jan, Y. N. (2009). Dividing glial cells maintain differentiated properties including complex morphology and functional synapses. Proceedings of the National Academy of Sciences, 106(1), 328-333. doi: 10.1073/pnas.0811353106. http://www.pnas.org/content/106/1/328.abstract 


Geary, C. G., Wilk, V. C., Barton, K. L., Jefferson, P. O., Binder, T., Bhutani, V., . . . Bergstrom, H. C. (2021). Sex differences in gut microbiota modulation of aversive conditioning, open field activity, and basolateral amygdala dendritic spine density. [https://doi.org/10.1002/jnr.24848]. Journal of Neuroscience Research, n/a(n/a). doi: https://doi.org/10.1002/jnr.24848. https://doi.org/10.1002/jnr.24848


Gebäck, T., & Koumoutsakos, P. (2009). Edge detection in microscopy images using curvelets. BMC bioinformatics, 10(1), 75-75. doi. 

Geiger, J. R. P., Lubke, J., Roth, A., Frotscher, M., & Jonas, P. (1997). Submillisecond AMPA receptor-mediated signaling at a principal neuron-interneuron synapse. Neuron, 18(6), 1009-1023. doi. 

Geis, H. R. A. P., & Borst, J. G. G. (2012). Large GABAergic neurons form a distinct subclass within the mouse dorsal cortex of the inferior colliculus with respect to intrinsic properties, synaptic inputs, sound responses, and projections. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23170. http://dx.doi.org/10.1002/cne.23170


Geisler, S., & Zahm, D. S. (2005). Afferents of the ventral tegmental area in the rat-anatomical substratum for integrative functions. Journal of Comparative Neurology, 490(3), 270-294. doi. 

Geisler, S., & Zahm, D. S. (2006). Neurotensin afferents of the ventral tegmental area in the rat: [1] re-examination of their origins and [2] responses to acute psychostimulant and antipsychotic drug administration. European Journal of Neuroscience, 24(1), 116-134. doi: doi:10.1111/j.1460-9568.2006.04928.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2006.04928.x 


Geisler, S., & Zahm, D. S. (2006). On the retention of neurotensin in the ventral tegmental area (VTA) despite destruction of the main neurotensinergic afferents of the VTA—Implications for the organization of forebrain projections to the VTA. Brain Research, 1087(1), 87-104. doi. 

Gelfo, F., De Bartolo, P., Giovine, A., Petrosini, L., & Leggio, M. G. (2009). Layer and regional effects of environmental enrichment on the pyramidal neuron morphology of the rat. Neurobiology of Learning and Memory, 91(4), 353-365. doi. 

Gelfo, F., Petrosini, L., Graziano, A., De Bartolo, P., Burello, L., Vitale, E., . . . Mandolesi, L. (2013). Cortical Metabolic Deficits in a Rat Model of Cholinergic Basal Forebrain Degeneration. Neurochemical Research, 1-10. doi: 10.1007/s11064-013-1120-2. http://dx.doi.org/10.1007/s11064-013-1120-2


Gelman, D., Griveau, A., Dehorter, N., Teissier, A., Varela, C., Pla, R., . . . Marín, O. (2011). A Wide Diversity of Cortical GABAergic Interneurons Derives from the Embryonic Preoptic Area. Journal of Neuroscience, 31(46), 16570-16580. doi: 10.1523/jneurosci.4068-11.2011. http://www.jneurosci.org/content/31/46/16570.abstract


Gelman, D. M., Martini, F. J., Nobrega-Pereira, S., Pierani, A., Kessaris, N., & Marin, O. (2009). The Embryonic Preoptic Area Is a Novel Source of Cortical GABAergic Interneurons. Journal of Neuroscience, 29(29), 9380-9389. doi: 10.1523/jneurosci.0604-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/29/9380 


Gely-Pernot, A., Coronas, V., Harnois, T., Prestoz, L., Mandairon, N., Didier, A., . . . others. (2012). An Endogenous Vitamin K-Dependent Mechanism Regulates Cell Proliferation in the Brain Subventricular Stem Cell Niche. Stem Cells. doi. 

Gemignani, F., Brindani, F., Zinno, L., Allegri, I., Alfieri, S., & Marbini, A. (2004). Frequency of clinically diagnosed small fiber neuropathy in a neuropathy population. Journal of the Peripheral Nervous System, 9(2), 119-119. doi: doi:10.1111/j.1085-9489.2004.009209aw.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Gendron, L., Lucido, A. L., Mennicken, F., O'Donnell, D., Vincent, J.-P., Stroh, T., & Beaudet, A. (2006). Morphine and Pain-Related Stimuli Enhance Cell Surface Availability of Somatic Δ -Opioid Receptors in Rat Dorsal Root Ganglia. Journal of Neuroscience, 26, 953-962. doi. 

Gennarino, V. A., Palmer, E. E., McDonell, L. M., Wang, L., Adamski, C. J., Koire, A., . . . Zoghbi, H. Y. (2018). A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures. Cell, 172(5), 924-936.e911. doi: https://doi.org/10.1016/j.cell.2018.02.006. http://www.sciencedirect.com/science/article/pii/S0092867418301508


Genoud, C., Houades, V., Kraftsik, R., Welker, E., & Giaume, C. (2015). Proximity of excitatory synapses and astroglial gap junctions in layer IV of the mouse barrel cortex. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2015.01.051. http://www.sciencedirect.com/science/article/pii/S0306452215001086


Genoud, C., Knott, G. W., Sakata, K., Lu, B., & Welker, E. (2004). Altered Synapse Formation in the Adult Somatosensory Cortex of Brain-Derived Neurotrophic Factor Heterozygote Mice. Journal of Neuroscience, 24(10), 2394-2400. doi. http://www.jneurosci.org/cgi/content/abstract/24/10/2394


Genoud, C., Quairiaux, C., Steiner, P., Hirling, H., Welker, E., & Knott, G. W. (2006). Plasticity of astrocytic coverage and glutamate transporter expression in adult mouse cortex. PLoS Biology, 4(11), e343. doi. 

Gentet, L. J., Avermann, M., Matyas, F., Staiger, J. F., & Petersen, C. C. H. (2010). Membrane potential dynamics of GABAergic neurons in the barrel cortex of behaving mice. Neuron, 65(3), 422-435. doi. 

Gentet, L. J., Kremer, Y., Taniguchi, H., Huang, Z. J., Staiger, J. F., & Petersen, C. C. H. (2012). Unique functional properties of somatostatin-expressing GABAergic neurons in mouse barrel cortex. Nature Neuroscience. doi. 

George, I., Hara, E., & Hessler, N. A. (2006). Behavioral and neural lateralization of vision in courtship singing of the zebra finch. Journal of Neurobiology, 66(10), 1164-1173. doi. 

Georgeann S, O. B., Sandra, R., Seanna M, M., Ann M, C., Carlos, P. C., Alvaro, S., & others. (2009). Two-photon axotomy and time-lapse confocal imaging in live zebrafish embryos. Journal of Visualized Experiments, (24). doi. 

Georgiev, D., González-Burgos, G., Kikuchi, M., Minabe, Y., Lewis, D. A., & Hashimoto, T. (2012). Selective Expression of KCNS3 Potassium Channel α-Subunit in Parvalbumin-Containing GABA Neurons in the Human Prefrontal Cortex. PLoS ONE, 7(8), e43904. doi: 10.1371/journal.pone.0043904. http://dx.doi.org/10.1371%2Fjournal.pone.0043904


Gerashchenko, D., Kohls, M. D., Greco, M., Waleh, N. S., Salin-Pascual, R., Kilduff, T. S., . . . Shiromani, P. J. (2001). Hypocretin-2-Saporin Lesions of the Lateral Hypothalamus Produce Narcoleptic-Like Sleep Behavior in the Rat. Journal of Neuroscience, 21(18), 7273-7283. doi. http://www.jneurosci.org/cgi/content/abstract/21/18/7273


Gerecke, K. M., Kishore, R., Jasnow, A., Quadros-Menella, P., Parker, S., Kozub, F. J., . . . Kinsley, C. H. (2012). Alterations of sex-typical microanatomy: Prenatal stress modifies the structure of medial preoptic area neurons in rats. Developmental Psychobiology. doi. 

Gerfen, Charles R., Paletzki, R., & Heintz, N. (2013). GENSAT BAC Cre-Recombinase Driver Lines to Study the Functional Organization of Cerebral Cortical and Basal Ganglia Circuits. Neuron, 80(6), 1368-1383. doi: http://dx.doi.org/10.1016/j.neuron.2013.10.016. http://www.sciencedirect.com/science/article/pii/S0896627313009197


Gerkin, R., Tripathy, S., Crook, S., & Kotaleski, J. (2014). Databases and Data Repositories in Computational Neuroscience: Overview. In D. Jaeger & R. Jung (Eds.), Encyclopedia of Computational Neuroscience (pp. 1-4): Springer New York.

Gerlach, S., & Hersch, R. D. (2002). A real-time navigator for the visible human. IEEE Internet Computing, 5(2), 27-33. doi. http://diwww.epfl.ch/w3lsp/publications/gigaserver/artnftvh.pdf


German, D. C., Liang, C. L., Manaye, K. F., Lane, K., & Sonsalla, P. K. (2000). Pharmacological inactivation of the vesicular monoamine transporter can enhance 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine-induced neurodegeneration of midbrain dopaminergic neurons, but not locus coeruleus noradrenergic neurons. Neuroscience, 101(4), 1063-1069. doi. 

German, D. C., Manaye, K. F., Wu, D., Hersh, L. B., & Zweig, R. M. (1999). Mesopontine cholinergic and non-cholinergic neurons in schizophrenia. Journal of Neuroscience, 94(1), 33-38. doi. 

German, D. C., Quintero, E. M., Liang, C. L., Ng, B., Punia, S., Xie, C., & Dietschy, J. M. (2001). Selective neurodegeneration, without neurofibrillary tangles, in a mouse model of Niemann-Pick C disease. Journal of Comparative Neurology, 433(3), 415-425. doi. 

German, D. C., Yazdani, U., Speciale, S. G., Pasbakhsh, P., Games, D., & Liang, C. L. (2003). Cholinergic neuropathology in a mouse model of Alzheimer's disease. Journal of Comparative Neurology, 462(4), 371-381. doi. 

Germuska, M., Saha, S., Fiala, J., & Barbas, H. (2006). Synaptic distinction of laminar-specific prefrontal-temporal pathways in primates. Cerebral Cortex, 16(6), 865-875. doi. 

Gerrits, P. O., Kortekaas, R., Veening, J. G., De Weerd, H., Algra, A., Mouton, L. J., & van der Want, J. J. L. (2008). Estrous cycle-dependent neural plasticity in the caudal brainstem in the female golden hamster: ultrastructural and immunocytochemical studies of axo-dendritic relationships and dynamic remodeling. Hormones and Behavior, 54(5), 627-639. doi. 

Gerrits, P. O., Krukerink, M., & Veening, J. G. (2009). Columnar organization of estrogen receptor-α immunoreactive neurons in the periaqueductal gray projecting to the nucleus para-retroambiguus in the caudal brainstem of the female golden hamster. Neuroscience, 161(2), 459-474. doi. 

Gerrits, P. O., Veening, J. G., Blomsma, S. A., & Mouton, L. J. (2008). The nucleus para-retroambiguus: A new group of estrogen receptive cells in the caudal ventrolateral medulla of the female golden hamster. Hormones and Behavior, 53(2), 329-341. doi. 

Gertler, T. S., Chan, C. S., & Surmeier, D. J. (2008). Dichotomous Anatomical Properties of Adult Striatal Medium Spiny Neurons. Journal of Neuroscience, 28(43), 10814-10824. doi: 10.1523/jneurosci.2660-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/43/10814 


Gervais, N. J., Mumby, D. G., & Brake, W. G. (2015). Attenuation of dendritic spine density in the perirhinal cortex following 17β-estradiol replacement in the rat. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22479. http://dx.doi.org/10.1002/hipo.22479


Gharbawie, O., Stepniewska, I., & Kaas, J. (2015). The origins of thalamic inputs to grasp zones in frontal cortex of macaque monkeys. Brain Structure and Function, 1-18. doi: 10.1007/s00429-015-1091-y. http://dx.doi.org/10.1007/s00429-015-1091-y


Gharbawie, O. A., Stepniewska, I., Burish, M. J., & Kaas, J. H. (2010). Thalamocortical Connections of Functional Zones in Posterior Parietal Cortex and Frontal Cortex Motor Regions in New World Monkeys. Cerebral Cortex, bhp308. doi: 10.1093/cercor/bhp308. http://cercor.oxfordjournals.org/cgi/content/abstract/bhp308v1 


Gharbawie, O. A., Stepniewska, I., & Kaas, J. H. (2011). Cortical Connections of Functional Zones in Posterior Parietal Cortex and Frontal Cortex Motor Regions in New World Monkeys. Cerebral Cortex. doi: 10.1093/cercor/bhq260. http://cercor.oxfordjournals.org/content/early/2011/01/24/cercor.bhq260....


Gharbawie, O. A., Stepniewska, I., Qi, H., & Kaas, J. H. (2011). Multiple Parietal–Frontal Pathways Mediate Grasping in Macaque Monkeys. Journal of Neuroscience, 31(32), 11660-11677. doi: 10.1523/jneurosci.1777-11.2011. http://www.jneurosci.org/content/31/32/11660.abstract


Ghashghaei, H. T., & Barbas, H. (2001). Neural interaction between the basal forebrain and functionally distinct prefrontal cortices in the rhesus monkey. Neuroscience, 103(3), 593-614. doi. 

Ghashghaei, H. T., & Barbas, H. (2002). Pathways for emotion: interactions of prefrontal and anterior temporal pathways in the amygdala of the rhesus monkey. Neuroscience, 115(4), 1261-1279. doi. 

Ghashghaei, H. T., Hilgetag, C. C., & Barbas, H. (2007). Sequence of information processing for emotions based on the anatomic dialogue between prefrontal cortex and amygdala. Neuroimage, 34(3), 905-923. doi. 

Ghashghaei, H. T., Weber, J., Pevny, L., Schmid, R., Schwab, M. H., Lloyd, K. C. K., . . . Anton, E. S. (2006). The role of neuregulin-ErbB4 interactions on the proliferation and organization of cells in the subventricular zone. PNAS, 0510410103. doi: 10.1073/pnas.0507729103. http://www.pnas.org/cgi/content/abstract/0510410103v1 


Gheorghita, F., Kraftsik, R., Dubois, R., & Welker, E. (2006). Structural Basis for Map Formation in the Thalamocortical Pathway of the Barrelless Mouse. Journal of Neuroscience, 26(39), 10057-10067. doi: 10.1523/jneurosci.1263-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/39/10057 


Ghergherehchi, C. L., Hibbard, E. A., Mikesh, M., Bittner, G. D., & Sengelaub, D. R. (2019). Behavioral recovery and spinal motoneuron remodeling after polyethylene glycol fusion repair of singly cut and ablated sciatic nerves. PLoS ONE, 14(10), e0223443. doi: 10.1371/journal.pone.0223443. https://doi.org/10.1371/journal.pone.0223443


Ghiglione, E., Beronio, A., Reni, L., & Abruzzese, M. (2004). Leprous neuropathy: a clinical and neurophysiological study. Journal of the Peripheral Nervous System, 9(2), 120-121. doi: doi:10.1111/j.1085-9489.2004.009209bb.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Ghosh, A., Haiss, F., Sydekum, E., Schneider, R., Gullo, M., Wyss, M. T., . . . others. (2009). Rewiring of hindlimb corticospinal neurons after spinal cord injury. Nature Neuroscience, 13(1), 97-104. doi. 

Ghosh, A., Peduzzi, S., Snyder, M., Schneider, R., Starkey, M., & Schwab, M. E. (2011). Heterogeneous Spine Loss in Layer 5 Cortical Neurons after Spinal Cord Injury. Cerebral Cortex, bhr191. doi: 10.1093/cercor/bhr191. http://cercor.oxfordjournals.org/cgi/content/abstract/bhr191v1


Ghosh, A., Sydekum, E., Haiss, F., Peduzzi, S., Zorner, B., Schneider, R., . . . Schwab, M. E. (2009). Functional and Anatomical Reorganization of the Sensory-Motor Cortex after Incomplete Spinal Cord Injury in Adult Rats. Journal of Neuroscience, 29(39), 12210-12219. doi: 10.1523/jneurosci.1828-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/39/12210 


Ghosh, S., Larson, S. D., Hefzi, H., Marnoy, Z., Cutforth, T., Dokka, K., & Baldwin, K. K. (2011). Sensory maps in the olfactory cortex defined by long-range viral tracing of single neurons. Nature, 472(7342), 217-220. doi. 

Giacomini, C., La Padula, V., Schenone, A., Leandri, M., Contestabile, A., Moruzzo, D., . . . Corradi, A. (2011). Both Schwann cell and axonal defects cause motor peripheral neuropathy in Ebf2-/-mice. Neurobiology of Disease. doi. 

Giacomini, C., Mahajani, S., Ruffilli, R., Marotta, R., & Gasparini, L. (2015). Lamin B1 protein is required for dendrite development in primary mouse cortical neurons. Molecular Biology of the Cell. doi: 10.1091/mbc.E15-05-0307. http://www.molbiolcell.org/content/early/2015/10/26/mbc.E15-05-0307.abst...


Giampà, C., Laurenti, D., Anzilotti, S., Bernardi, G., Menniti, F. S., & Fusco, F. R. (2010). Inhibition of the striatal specific phosphodiesterase PDE10A ameliorates striatal and cortical pathology in R6/2 mouse model of Huntington's disease. PLoS ONE, 5(10), e13417-e13417. doi. 

Giampà, C., Montagna, E., Dato, C., Melone, M. A. B., Bernardi, G., & Fusco, F. R. (2013). Systemic Delivery of Recombinant Brain Derived Neurotrophic Factor (BDNF) in the R6/2 Mouse Model of Huntington’s Disease. PLoS ONE, 8(5), e64037. doi: 10.1371/journal.pone.0064037. http://dx.doi.org/10.1371%2Fjournal.pone.0064037


Gianaris, A., Liu, N.-K., Wang, X.-F., Oakes, E., Brenia, J., Gianaris, T., . . . Xu, X.-M. (2016). Unilateral microinjection of acrolein into thoracic spinal cord produces acute and chronic injury and functional deficits. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2016.03.054. http://www.sciencedirect.com/science/article/pii/S0306452216300410


Giannetti, S., Gaglini, P., Di Rocco, F., Di Rocco, C., & Granato, A. (2000). Organization of cortico-cortical associative projections in a rat model of microgyria. Neuroreport, 11(10), 2185-2185. doi. 

Gianola, S., De Castro, F., & Rossi, F. (2009). Anosmin-1 stimulates outgrowth and branching of developing Purkinje axons. Neuroscience, 158(2), 570-584. doi. 

Gianola, S., & Rossi, F. (2001). Evolution of the Purkinje cell response to injury and regenerative potential during postnatal development of the rat cerebellum. Journal of Comparative Neurology, 430(1), 101-117. doi. 

Gianola, S., & Rossi, F. (2004). GAP-43 overexpression in adult mouse Purkinje cells overrides myelin-derived inhibition of neurite growth. European Journal of Neuroscience, 19(4), 819-830. doi: doi:10.1111/j.0953-816X.2004.03190.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.0953-816X.2004.03190.x 


Gianola, S., Savio, T., Schwab, M. E., & Rossi, F. (2003). Cell-Autonomous Mechanisms and Myelin-Associated Factors Contribute to the Development of Purkinje Axon Intracortical Plexus in the Rat Cerebellum. Journal of Neuroscience, 23, 4613-4624. doi. 

Gibbs, S., Chattopadhyaya, B., Desgent, S., Awad, P. N., Clerk-Lamalice, O., Levesque, M., . . . others. (2011). Long-term consequences of a prolonged febrile seizure in a dual pathology model. Neurobiology of Disease. doi. 

Gibson, Daniel A., Tymanskyj, S., Yuan, Rachel C., Leung, Haiwen C., Lefebvre, Julie L., Sanes, Joshua R., . . . Ma, L. (2014). Dendrite Self-Avoidance Requires Cell-Autonomous Slit/Robo Signaling in Cerebellar Purkinje Cells. Neuron, 81(5), 1040-1056. doi: http://dx.doi.org/10.1016/j.neuron.2014.01.009. http://www.sciencedirect.com/science/article/pii/S0896627314000142


Giele, J. L. P., Nabers, A. F., Veening, J. G., van Egmond, J., & Vissers, K. C. P. (2009). The Effect of a Thoracic Spinal Block on Fos Expression in the Lumbar Spinal Cord of the Rat Induced by a Noxious Electrical Stimulus at the Hindpaw. Anesthesia and Analgesia, 109(5), 1659-1665. doi. 

Gielow, M. R., & Zaborszky, L. (2017). The Input-Output Relationship of the Cholinergic Basal Forebrain. Cell Reports, 18(7), 1817-1830. doi: http://dx.doi.org/10.1016/j.celrep.2017.01.060. http://www.sciencedirect.com/science/article/pii/S2211124717301171


Giesert, F., Glasl, L., Zimprich, A., Ernst, L., Piccoli, G., Stautner, C., . . . Wurst, W. (2017). The pathogenic LRRK2 R1441C mutation induces specific deficits modeling the prodromal phase of Parkinson's disease in the mouse. Neurobiology of Disease. doi: https://doi.org/10.1016/j.nbd.2017.05.013. http://www.sciencedirect.com/science/article/pii/S0969996117301237


Gilbert, M. T., & Soderstrom, K. (2013). Novel song-stimulated dendritic spine formation and Arc/Arg3.1 expression in zebra finch auditory telencephalon are disrupted by cannabinoid agonism. Brain Research, (0). doi: http://dx.doi.org/10.1016/j.brainres.2013.10.012. http://www.sciencedirect.com/science/article/pii/S0006899313013772


Gilchrist, L. S., Cain, D. M., Harding-Rose, C., Kov, A. N., Wendelschafer-Crabb, G., Kennedy, W. R., & Simone, D. A. (2005). Re-organization of P2X< sub> 3</sub> receptor localization on epidermal nerve fibers in a murine model of cancer pain. Brain Research, 1044(2), 197-205. doi. 

Gill, K. M., Bernstein, I. L., & Mizumori, S. J. Y. (2007). Immediate early gene activation in hippocampus and dorsal striatum: Effects of explicit place and response training. Neurobiology of Learning and Memory, 87(4), 583-596. doi. 

Gillani, R. L., Tsai, S. Y., Wallace, D. G., O'Brien, T. E., Arhebamen, E., Tole, M., . . . Kartje, G. L. (2010). Cognitive recovery in the aged rat after stroke and anti-Nogo-A immunotherapy. Behavioural Brain Research, 208(2), 415-424. doi. 

Gillette, T. A., & Ascoli, G. A. (2012). Measuring and Modeling Morphology: How Dendrites Take Shape

Computational Systems Neurobiology. In N. Le Novère (Ed.), (pp. 387-427): Springer Netherlands.

Gillette, T. A., Brown, K. M., & Ascoli, G. A. (2011). The DIADEM metric: Comparing multiple reconstructions of the same neuron. Neuroinformatics, 1-13. doi. 

Gilmore, J. H., Jarskog, L. F., Vadlamudi, S., & Lauder, J. M. (2004). Prenatal Infection and Risk for Schizophrenia: IL-1, IL-6, and TNF Inhibit Cortical Neuron Dendrite development. Neuropsychopharmacology, (29), 1221-1229. doi. 

Ginet, V., Puyal, J., Magnin, G., Clarke, P. G. H., & Truttmann, A. C. (2009). Limited role of the c-Jun N-terminal kinase pathway in a neonatal rat model of cerebral hypoxia–ischemia. Journal of Neurochemistry, 108(3), 552-562. doi. 

Giordano, G., & Costa, L. G. (2012). Morphological Assessment of Neurite Outgrowth in Hippocampal Neuron-Astrocyte Co-Cultures. Current Protocols in Toxicology, 11-16. doi. 

Giorgio, A. D., & Granato, A. (2015). Reduced density of dendritic spines in pyramidal neurons of rats exposed to alcohol during early postnatal life. International Journal of Developmental Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.ijdevneu.2015.01.005. http://www.sciencedirect.com/science/article/pii/S0736574815000076


Gisabella, B., Scammell, T., Bandaru, S. S., & Saper, C. B. (2019). Regulation of hippocampal dendritic spines following sleep deprivation. Journal of Comparative Neurology, 0(ja). doi: 10.1002/cne.24764. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24764


Gittins, R., & Harrison, P. (2004). A quantitative morphometric study of the human anterior cingulate cortex. Brain Research, 1013, 212 - 222. doi. 

Gittis, A. H., Hang, G. B., LaDow, E. S., Shoenfeld, L. R., Atallah, B. V., Finkbeiner, S., & Kreitzer, A. C. (2011). Rapid target-specific remodeling of fast-spiking inhibitory circuits after loss of dopamine. Neuron, 71(5), 858-868. doi. 

Giza, J. I., Kim, J., Meyer, H. C., Anastasia, A., Dincheva, I., Zheng, C. I., . . . Lee, F. S. (2018). The BDNF Val66Met Prodomain Disassembles Dendritic Spines Altering Fear Extinction Circuitry and Behavior. Neuron. doi: https://doi.org/10.1016/j.neuron.2018.05.024. https://www.sciencedirect.com/science/article/pii/S0896627318304227


Gladden, M. H., Maxwell, D. J., Sahal, A., & Jankowska, E. (2000). Coupling between serotoninergic and noradrenergic neurones and γ-motoneurones in the cat. Journal of Physiology, 527(2), 213-223. doi. 

Glanzer, J., Enose, Y., Wang, T., Kadiu, I., Gong, N., Rozek, W., . . . Gendelman, H. (2007). Genomic and proteomic microglial profiling: pathways for neuroprotective inflammatory responses following nerve fragment clearance and activation. Journal of Neurochemistry, 102, 627 - 645. doi. 

Glaser, E., & Loos, H. V. D. (1965). A semi-quantitative computer-microscope for the analysis of neuronal morphometry. IEEE Transactions on Bio-Medical Engineering. doi. 

Glaser, J. R., & Glaser, E. M. (1990). Neuron imaging with Neurolucida–a PC-based system for image combining microscopy. Computerized Medical Imaging and Graphics, 14(5), 307-317. doi. 

Glasgow, S. D., & Chapman, C. A. (2013). Muscarinic Depolarization of Layer II Neurons of the Parasubiculum. PLoS ONE, 8(3), e58901. doi: 10.1371/journal.pone.0058901. http://dx.doi.org/10.1371%2Fjournal.pone.0058901


Glasl, L., Kloos, K., Giesert, F., Roethig, A., Di Benedetto, B., Kühn, R., . . . others. (2012). Pink1-deficiency in mice impairs gait, olfaction and serotonergic innervation of the olfactory bulb. Experimental Neurology. doi. 

Glasper, E. R., Hyer, M. M., Katakam, J., Harper, R., Ameri, C., & Wolz, T. (2015). Fatherhood contributes to increased hippocampal spine density and anxiety regulation in California mice. Brain and Behavior, n/a-n/a. doi: 10.1002/brb3.416. http://dx.doi.org/10.1002/brb3.416


Glass, R., Synowitz, M., Kronenberg, G., Walzlein, J.-H., Markovic, D. S., Wang, L.-P., . . . Kettenmann, H. (2005). Glioblastoma-Induced Attraction of Endogenous Neural Precursor Cells Is Associated with Improved Survival. Journal of Neuroscience, 25(10), 2637-2646. doi: 10.1523/jneurosci.5118-04.2005. http://www.jneurosci.org/cgi/content/abstract/25/10/2637 


Glatzer, N. R., Hasney, C. P., Bhaskaran, M. D., & Smith, B. N. (2003). Synaptic and morphologic properties in vitro of premotor rat nucleus tractus solitarius neurons labeled transneuronally from the stomach. Journal of Comparative Neurology, 464(4), 525-539. doi. 

Glavaski-Joksimovic, A., Virag, T., Chang, Q. A., West, N. C., Mangatu, T. A., McGrogan, M. P., . . . Bohn, M. C. (2009). Reversal of dopaminergic degeneration in a parkinsonian rat following micrografting of human bone marrow-derived neural progenitors. Cell Transplantation, 18(7), 801-814. doi. 

Gleeson, P., Crook, S., Cannon, R. C., Hines, M. L., Billings, G. O., Farinella, M., . . . others. (2010). NeuroML: a language for describing data driven models of neurons and networks with a high degree of biological detail. PLoS computational biology, 6(6), e1000815-e1000815. doi. 

Gleeson, P., Steuber, V., & Silver, R. A. (2007). neuroConstruct: a tool for modeling networks of neurons in 3D space. Neuron, 54(2), 219-235. doi. 

Gleeson, P., Steuber, V., & Silver, R. A. (2008). Using neuroConstruct to develop and modify biologically detailed 3D neuronal network models in health and disease. Computational Neuroscience in Epilepsy. doi. 

Glendenning, M. L., Lovekamp-Swan, T., & Schreihofer, D. A. (2008). Protective effect of estrogen in endothelin-induced middle cerebral artery occlusion in female rats. Neuroscience Letters, 445(2), 188-192. doi. 

Glezer, I., Chernomoretz, A., David, S., Plante, M. M., & Rivest, S. (2007). Genes involved in the balance between neuronal survival and death during inflammation. PLoS ONE, 2(3), e310-e310. doi. 

Glickfeld, L. L., Atallah, B. V., & Scanziani, M. (2008). Complementary Modulation of Somatic Inhibition by Opioids and Cannabinoids. Journal of Neuroscience, 28(8), 1824-1832. doi: 10.1523/jneurosci.4700-07.2008. http://www.jneurosci.org/cgi/content/abstract/28/8/1824 


Glickfeld, L. L., & Scanziani, M. (2006). Distinct timing in the activity of cannabinoid-sensitive and cannabinoid-insensitive basket cells. Nature of Neuroscience, 9, 807-815. doi. 

Glickstein, S. B., Hof, P. R., & Schmauss, C. (2002). Mice Lacking Dopamine D2 and D3 Receptors Have Spatial Working Memory Deficits. Journal of Neuroscience, 22(13), 5619-5629. doi: 20026543. http://www.jneurosci.org/cgi/content/abstract/22/13/5619 


Gloor, C., Luft, A. R., & Hosp, J. A. (2015). Biphasic plasticity of dendritic fields in layer V motor neurons in response to motor learning. Neurobiology of Learning and Memory. doi: http://dx.doi.org/10.1016/j.nlm.2015.08.009. http://www.sciencedirect.com/science/article/pii/S1074742715001574


Gloveli, T., Booker, S. A., Kopell, N., & Dugladze, T. (2018). Cell Type-Specific Activity During Hippocampal Network Oscillations In Vitro. In V. Cutsuridis, B. P. Graham, S. Cobb & I. Vida (Eds.), Hippocampal Microcircuits: A Computational Modeler's Resource Book (pp. 327-364). Cham: Springer International Publishing.

Gloveli, T., Dugladze, T., Rotstein, H. G., Traub, R. D., Monyer, H., Heinemann, U., . . . Kopell, N. J. (2005). Orthogonal arrangement of rhythm-generating microcircuits in the hippocampus. PNAS, 102(37), 13295-13300. doi. http://www.pnas.org/cgi/content/abstract/102/37/13295


Gloveli, T., Dugladze, T., Saha, S., Monyer, H., Heinemann, U., Traub, R. D., . . . Buhl, t. l. E. H. (2005). Differential involvement of oriens/pyramidale interneurones in hippocampal network oscillations in vitro. Journal of Physiology, 562(1), 131-147. doi: 10.1113/jphysiol.2004.073007. http://jp.physoc.org/cgi/content/abstract/562/1/131 


Gloveli, T., Kopell, N., & Dugladze, T. (2010). Neuronal activity patterns during hippocampal network oscillations in vitro. Hippocampal Microcircuits, 247-276. doi. 

Godavarthi, S. K., Dey, P., Sharma, A., & Jana, N. R. (2015). Impaired adult hippocampal neurogenesis and its partial reversal by chronic treatment of fluoxetine in a mouse model of Angelman syndrome. Biochemical and Biophysical Research Communications. doi: http://dx.doi.org/10.1016/j.bbrc.2015.07.103. http://www.sciencedirect.com/science/article/pii/S0006291X15303338


Godavarthi, S. K., Sharma, A., & Jana, N. R. (2014). Reversal of reduced parvalbumin neurons in hippocampus and amygdala of Angelman syndrome model mice by chronic treatment of fluoxetine. Journal of Neurochemistry, n/a-n/a. doi: 10.1111/jnc.12726. http://dx.doi.org/10.1111/jnc.12726


Godfrey, D. A., Chen, K., Godfrey, M. A., Jin, Y. M., Robinson, K. T., & Hair, C. (2008). Effects of cochlear ablation on amino acid concentrations in the chinchilla posteroventral cochlear nucleus, as compared to rat. Neuroscience, 154(1), 304-314. doi. 

Godfrey, D. A., Chen, K., Godfrey, M. A., Lee, A. C., Crass, S. P., Shipp, D., . . . Robinson, K. T. (2015). Cochlear ablation effects on amino acid levels in the chinchilla cochlear nucleus. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2015.03.055. http://www.sciencedirect.com/science/article/pii/S0306452215003048


Godfrey, D. A., Chen, K., O'Toole, T. R., & Mustapha, A. I. A. A. (2017). Amino acid and acetylcholine chemistry in the central auditory system of young, middle-aged and old rats. Hearing Research. doi: https://doi.org/10.1016/j.heares.2017.05.002. http://www.sciencedirect.com/science/article/pii/S0378595517301181


Godfrey, D. A., Kaltenbach, J. A., Chen, K., Ilyas, O., Liu, X., Licari, F., . . . McKnight, D. (2012). Amino acid concentrations in the hamster central auditory system and long-term effects of intense tone exposure. Journal of Neuroscience Research, n/a-n/a. doi: 10.1002/jnr.23095. http://dx.doi.org/10.1002/jnr.23095


Godfrey, D. A., Lee, A. C., Hamilton, W. D., Benjamin Iii, L. C., Vishwanath, S., Simo, H., . . . Heffner, R. S. (2016). Volumes of Cochlear Nucleus Regions in Rodents. Hearing Research. doi: http://dx.doi.org/10.1016/j.heares.2016.07.003. http://www.sciencedirect.com/science/article/pii/S0378595516302660


Goeke, C. M., Hashimoto, J. G., Guizzetti, M., & Vitalone, A. (2021). Effects of ethanol-and choline-treated astrocytes on hippocampal neuron neurite outgrowth in vitro. Science Progress, 104(2), 00368504211018943. doi: 10.1177/00368504211018943. https://doi.org/10.1177/00368504211018943


Goeke, C. M., Roberts, M. L., Hashimoto, J. G., Finn, D. A., & Guizzetti, M. (2018). Neonatal Ethanol and Choline Treatments Alter the Morphology of Developing Rat Hippocampal Pyramidal Neurons in Opposite Directions. Neuroscience, 374, 13-24. doi: https://doi.org/10.1016/j.neuroscience.2018.01.031. https://www.sciencedirect.com/science/article/pii/S0306452218300472


Goings, G. E., Kozlowski, D. A., & Szele, F. G. (2006). Differential activation of microglia in neurogenic versus non-neurogenic regions of the forebrain. Glia, 54(4), 329-342. doi. 

Goings, G. E., Wibisono, B. L., & Szele, F. G. (2002). Cerebral cortex lesions decrease the number of bromodeoxyuridine-positive subventricular zone cells in mice. Neuroscience Letters, 329(2), 161-164. doi. 

Gold, C., Henze, D. A., Koch, C., & Buzsaki, G. (2006). On the Origin of the Extracellular Action Potential Waveform: A Modeling Study. Journal of Neurophysiology, 95(5), 3113-3128. doi: 10.1152/jn.00979.2005. http://jn.physiology.org/cgi/content/abstract/95/5/3113 


Goldberg, J., Hamzei-Sichani, F., MacLean, J., Tamas, G., Urban, R., & Yuste, R. (2006). From Dendrites to Networks: Optically Probing the Living Brain Slice and Using Principal Component Analysis to Characterize Neuronal Morphology. Neuroanatomical Tract-Tracing 3, 452-476. doi. 

Goldberg, J. H., Lacefield, C. O., & Yuste, R. (2004). Global dendritic calcium spikes in mouse layer 5 low threshold spiking interneurones: implications for control of pyramidal cell bursting. Journal of Physiology, 558(2), 465-478. doi: 10.1113/jphysiol.2004.064519. http://jp.physoc.org/cgi/content/abstract/558/2/465 


Goldberg, J. H., Tamas, G., Aronov, D., & Yuste, R. (2003). Calcium microdomains in aspiny dendrites. Neuron, 40(4), 807-821. doi. 

Goldberg, J. H., Tamas, G., & Yuste, R. (2003). Ca2+ imaging of mouse neocortical interneurone dendrites: Ia-type K+ channels control action potential backpropagation. Journal of Physiology, 551(1), 49-65. doi: 10.1113/jphysiol.2003.042580. http://jp.physoc.org/cgi/content/abstract/551/1/49 


Goldberg, J. H., Yuste, R., & Tamas, G. (2003). Ca2+ imaging of mouse neocortical interneurone dendrites: Contribution of Ca2+-permeable AMPA and NMDA receptors to subthreshold Ca2+dynamics. Journal of Physiology, 551(1), 67-78. doi: 10.1113/jphysiol.2003.042598. http://jp.physoc.org/cgi/content/abstract/551/1/67 


Golden, K. L., Pearse, D. D., Blits, B., Garg, M. S., Oudega, M., Wood, P. M., & Bunge, M. B. (2007). Transduced Schwann cells promote axon growth and myelination after spinal cord injury. Experimental Neurology, 207(2), 203-217. doi. 

Goldin, M., Epsztein, J., Jorquera, I., Represa, A., Ben-Ari, Y., Crepel, V., & Cossart, R. (2007). Synaptic Kainate Receptors Tune Oriens-Lacunosum Moleculare Interneurons to Operate at Theta Frequency. Journal of Neuroscience, 27(36), 9560-9572. doi: 10.1523/jneurosci.1237-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/36/9560 


Golding, N. L., Kath, W. L., & Spruston, N. (2001). Dichotomy of Action-Potential Backpropagation in CA1 Pyramidal Neuron Dendrites. Journal of Neurophysiology, 86(6), 2998-3010. doi. http://jn.physiology.org/cgi/content/abstract/86/6/2998 


Golding, N. L., Mickus, T. J., Katz, Y., Kath, W. L., & Spruston, N. (2005). Factors mediating powerful voltage attenuation along CA1 pyramidal neuron dendrites. Journal of Physiology, 568(1), 69-82. doi: 10.1113/jphysiol.2005.086793. http://jp.physoc.org/cgi/content/abstract/568/1/69 


Goldowitz, D., Cushing, R. C., Laywell, E., D'Arcangelo, G., Sheldon, M., Sweet, H. O., . . . Curran, T. (1997). Cerebellar Disorganization Characteristic of Reeler in Scrambler Mutant Mice Despite Presence of Reelin. Journal of Neuroscience, 17(22), 8767-8777. doi. http://www.jneurosci.org/cgi/content/abstract/17/22/8767


Goldowitz, D., Hamre, K. M., Przyborski, S. A., & Ackerman, S. L. (2000). Granule Cells and Cerebellar Boundaries: Analysis of Unc5h3 Mutant Chimeras. Journal of Neuroscience, 20(11), 4129-4137. doi. http://www.jneurosci.org/cgi/content/abstract/20/11/4129


Goldstein, A. Y. N., Jan, Y.-N., & Luo, L. (2005). Function and regulation of Tumbleweed (RacGAP50C) in neuroblast proliferation and neuronal morphogenesis. PNAS, 102(10), 3834-3839. doi. http://www.pnas.org/cgi/content/abstract/102/10/3834


Goldwater, D. S., Pavlides, C., Hunter, R. G., Bloss, E. B., Hof, P. R., McEwen, B. S., & Morrison, J. H. (2009). Structural and functional alterations to rat medial prefrontal cortex following chronic restraint stress and recovery. Neuroscience, 164(2), 798-808. doi. 

Gombash, S. E., Cowley, C. J., Fitzgerald, J. A., Iyer, C. C., Fried, D., McGovern, V. L., . . . Foust, K. D. (2015). SMN Deficiency Disrupts Gastrointestinal and Enteric Nervous System Function in Mice. Human Molecular Genetics. doi: 10.1093/hmg/ddv127. http://hmg.oxfordjournals.org/content/early/2015/04/09/hmg.ddv127.abstract


Gombash, S. E., Lipton, J. W., Collier, T. J., Madhavan, L., Steece-Collier, K., Cole-Strauss, A., . . . others. (2011). Striatal Pleiotrophin Overexpression Provides Functional and Morphological Neuroprotection in the 6-Hydroxydopamine Model. Molecular Therapy, 20(3), 544-554. doi. 

Gomes, G. F., Peixoto, R. D. d. F., Maciel, B. G., Santos, K. F. d., Bayma, L. R., Feitoza Neto, P. A., . . . Diniz, C. W. P. (2019). Differential Microglial Morphological Response, TNFα, and Viral Load in Sedentary-like and Active Murine Models After Systemic Non-neurotropic Dengue Virus Infection. Journal of Histochemistry and Cytochemistry, 0022155419835218. doi: 10.1369/0022155419835218. https://doi.org/10.1369/0022155419835218


Gomez, C., Brinon, J. G., Orio, L., Colado, M. I., Lawrence, A. J., Zhou, F. C., . . . Alonso, J. R. (2007). Changes in the serotonergic system in the main olfactory bulb of rats unilaterally deprived from birth to adulthood. Journal of Neurochemistry, 100(4), 924-938. doi: doi:10.1111/j.1471-4159.2006.04229.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1471-4159.2006.04229.x 


Gomez, C., Brinon, J. G., Valero, J., Recio, J. S., Murias, A. R., Curto, G. G., . . . Alonso, J. R. (2007). Sex differences in catechol contents in the olfactory bulb of control and unilaterally deprived rats. European Journal of Neuroscience, 25(5), 1517-1528. doi: doi:10.1111/j.1460-9568.2007.05407.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05407.x 


Gómez, C., Curto, G. G., Baltanás, F. C., Valero, J., O'Shea, E., Colado, M. I., . . . Alonso, J. R. (2011). Changes in the serotonergic system and in BDNF distribution in the main olfactory bulb of pcd mice before and after mitral cell loss. Neuroscience. doi. 

Gómez, C., Jimeno, D., Fernández-Medarde, A., García-Navas, R., Calzada, N., & Santos, E. (2017). Ras-GRF2 regulates nestin-positive stem cell density and onset of differentiation during adult neurogenesis in the mouse dentate gyrus. Molecular and Cellular Neuroscience. doi: https://doi.org/10.1016/j.mcn.2017.09.006. http://www.sciencedirect.com/science/article/pii/S1044743117301392


Gómez-Álvarez, M., & Saldaña, E. (2015). Different tonotopic regions of the lateral superior olive receive a similar combination of afferent inputs. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23942. http://dx.doi.org/10.1002/cne.23942


Gómez-Chacón, B., Gámiz, F., & Gallo, M. (2012). Basolateral amygdala lesions attenuate safe taste memory-related c-fos expression in the rat perirhinal cortex. Behavioural Brain Research. doi. 

Gómez-Galán, M., De Bundel, D., Van Eeckhaut, A., Smolders, I., & Lindskog, M. (2012). Dysfunctional astrocytic regulation of glutamate transmission in a rat model of depression. Molecular Psychiatry. doi. 

Gomez-Gonzalez, B., & Escobar, A. (2010). Prenatal stress alters microglial development and distribution in postnatal rat brain. Acta Neuropathol, 119, 303 - 315. doi. 

Goncalves, J. T., Bloyd, C. W., Shtrahman, M., Johnston, S. T., Schafer, S. T., Parylak, S. L., . . . Gage, F. H. (2016). In vivo imaging of dendritic pruning in dentate granule cells. [Brief Communication]. Nature Neuroscience, advance online publication. doi: 10.1038/nn.4301

http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.4301.html#suppl.... http://dx.doi.org/10.1038/nn.4301


Gonçalves, L., Silva, R., Pinto-Ribeiro, F., Pêgo, J. M., Bessa, J. M., Pertovaara, A., . . . Almeida, A. (2008). Neuropathic pain is associated with depressive behaviour and induces neuroplasticity in the amygdala of the rat. Experimental Neurology, 213(1), 48-56. doi. 

Gong, H., McGinty, D., Guzman-Marin, R., Chew, K.-T., Stewart, D., & Szymusiak, R. (2004). Activation of c-fos in GABAergic neurones in the preoptic area during sleep and in response to sleep deprivation. Journal of Physiology, 556(3), 935-946. doi: 10.1113/jphysiol.2003.056622. http://jp.physoc.org/cgi/content/abstract/556/3/935 


Gong, H., Szymusiak, R., King, J., Steininger, T., & McGinty, D. (2000). Sleep-related c-Fos protein expression in the preoptic hypothalamus: effects of ambient warming. American Journal Physiological Regulatory Integrative Comparative Physiology, 279(6), R2079-2088. doi. http://ajpregu.physiology.org/cgi/content/abstract/279/6/R2079 


Gong, H., Xu, D., Yuan, J., Li, X., Guo, C., Peng, J., . . . Luo, Q. (2016). High-throughput dual-colour precision imaging for brain-wide connectome with cytoarchitectonic landmarks at the cellular level. [Article]. Nat Commun, 7. doi: 10.1038/ncomms12142. http://dx.doi.org/10.1038/ncomms12142


Gong, S., Doughty, M., Harbaugh, C. R., Cummins, A., Hatten, M. E., Heintz, N., & Gerfen, C. R. (2007). Targeting Cre Recombinase to Specific Neuron Populations with Bacterial Artificial Chromosome Constructs

Journal of Neuroscience 27(37), 9817-9823. doi. 

Gong, S., Zhou, Q., & LeDoux, M. S. (2003). Blink-related sensorimotor anatomy in the rat. Anatomy and Embryology, 207(3), 193-208. doi. 

Gong, X., Jiang, Y., Zhang, X., An, Y., Zhang, J., Wu, Y., . . . others. (2012). High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability. PLoS ONE, 7(4), e34739-e34739. doi. 

Gong, X., Jiang, Y.-w., Zhang, X., An, Y., Zhang, J., Wu, Y., . . . Wang, H. (2012). High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability. PLoS ONE, 7(4), e34739. doi: 10.1371/journal.pone.0034739. http://dx.doi.org/10.1371%2Fjournal.pone.0034739


Gonzalez, F. F., McQuillen, P., Mu, D., Chang, Y., Wendland, M., Vexler, Z., & Ferriero, D. M. (2007). Erythropoietin Enhances Long-Term Neuroprotection and Neurogenesis in Neonatal Stroke. Developmental Neuroscience, 29(4-5), 321-330. doi. http://www.karger.com/DOI/10.1159/000105473 


González, G., Fleuret, F., & Fua, P. (2008). Automated delineation of dendritic networks in noisy image stacks. Computer Vision–ECCV 2008, 214-227. doi. 

Gonzalez, I., Arévalo-Serrano, J., Perez, J. L., Gonzalo, P., & Gonzalo-Ruiz, A. (2008). Effects of β-amyloid peptide on the density of M2 muscarinic acetylcholine receptor protein in the hippocampus of the rat: relationship with GABA-, calcium-binding protein and somatostatin-containing cells. Neuropathology and Applied Neurobiology, 34(5), 506-522. doi. 

González, I., Arévalo-Serrano, J., Sanz-Anquela, J. M., & Gonzalo-Ruiz, A. (2007). Effects of β-amyloid protein on M1 and M2 subtypes of muscarinic acetylcholine receptors in the medial septum-diagonal band complex of the rat: relationship with cholinergic, GABAergic, and calcium-binding protein perikarya. Acta Neuropathologica, 113(6), 637-651. doi. 

González, J. F. G., Mel, B. W., & Poirazi, P. (2011). Distinguishing linear vs. non-linear integration in CA1 radial oblique dendrites: it’s about time. Frontiers in computational neuroscience, 5. doi. 

González-Aparicio, R., & Moratalla, R. (2013). Oleoylethanolamide reduces L-DOPA-induced dyskinesia via TRPV1 receptor in a mouse model of Parkinson´s disease. Neurobiology of Disease, (0). doi: http://dx.doi.org/10.1016/j.nbd.2013.10.008. http://www.sciencedirect.com/science/article/pii/S0969996113002830


Gonzalez-Burgos, G., Krimer, L. S., Povysheva, N. V., Barrionuevo, G., & Lewis, D. A. (2005). Functional Properties of Fast Spiking Interneurons and Their Synaptic Connections With Pyramidal Cells in Primate Dorsolateral Prefrontal Cortex. Journal of Neurophysiology, 93(2), 942-953. doi: 10.1152/jn.00787.2004. http://jn.physiology.org/cgi/content/abstract/93/2/942 


González-Burgos, G., Krimer, L. S., Urban, N. N., Barrionuevo, G., & Lewis, D. A. (2004). Synaptic efficacy during repetitive activation of excitatory inputs in primate dorsolateral prefrontal cortex. Cerebral Cortex, 14(5), 530-542. doi. 

González-Burgos, G., Krimer, L. S., Urban, N. N., Barrionuevo, G., & Lewis, D. A. (2004). Synaptic efficacy during repetitive activation of excitatory inputs in primate dorsolateral prefrontal cortex. Cerebral Cortex, 14(5), 530-542. doi. 

Gonzalez-Burgos, G., Kroener, S., Seamans, J. K., Lewis, D. A., & Barrionuevo, G. (2005). Dopaminergic Modulation of Short-Term Synaptic Plasticity in Fast-Spiking Interneurons of Primate Dorsolateral Prefrontal Cortex. Journal of Neurophysiology, 94(6), 4168-4177. doi: 10.1152/jn.00698.2005. http://jn.physiology.org/cgi/content/abstract/94/6/4168 


Gonzalez-Burgos, G., Kroener, S., Zaitsev, A. V., Povysheva, N. V., Krimer, L. S., Barrionuevo, G., & Lewis, D. A. (2008). Functional Maturation of Excitatory Synapses in Layer 3 Pyramidal Neurons during Postnatal Development of the Primate Prefrontal Cortex. Cerebral Cortex, 18(3), 626-637. doi: 10.1093/cercor/bhm095. http://cercor.oxfordjournals.org/cgi/content/abstract/18/3/626 


Gonzalez-Burgos, G., Miyamae, T., Pafundo, D. E., Yoshino, H., Rotaru, D. C., Hoftman, G., . . . Lewis, D. A. (2014). Functional Maturation of GABA Synapses During Postnatal Development of the Monkey Dorsolateral Prefrontal Cortex. Cerebral Cortex. doi: 10.1093/cercor/bhu122. http://cercor.oxfordjournals.org/content/early/2014/06/05/cercor.bhu122....


Gonzalez-Burgos, G., Rotaru, D. C., Zaitsev, A. V., Povysheva, N. V., & Lewis, D. A. (2008). The GABA transporter GAT1 prevents spillover at proximal and distal GABA synapses onto primate prefrontal cortex neurons. Journal of Neurophysiology, 91161.92008. doi: 10.1152/jn.91161.2008. http://jn.physiology.org/cgi/content/abstract/91161.2008v1 


González-Cabrera, C., Meza, R., Ulloa, L., Merino-Sepúlveda, P., Luco, V., Sanhueza, A., . . . Henny, P. (2017). Characterization of the axon initial segment of mice substantia nigra dopaminergic neurons. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24288. http://dx.doi.org/10.1002/cne.24288


Gonzalo-Ruiz, A., & Arévalo-Serrano, J. (2012). Interaction between?-amyloid protein and the? 7 nicotinic acetylcholine receptor in cholinergic, gabaergic and calcium-binding proteins-containing neurons in the septum-diagonal band complex of the rat. European Journal of Anatomy, 10(3), 127-142. doi. 

Gonzalo-Ruiz, A., Gonzalez, I., & Sanz-Anquela, J. M. (2003). Effects of β-amyloid protein on serotoninergic, noradrenergic, and cholinergic markers in neurons of the pontomesencephalic tegmentum in the rat. Journal of Chemical Neuroanatomy, 26(3), 153-169. doi. 

Gonzalo-Ruiz, A., Perez, J. L., Sanz, J. M., Geula, C., & Arevalo, J. (2006). Effects of lipids and aging on the neurotoxicity and neuronal loss caused by intracerebral injections of the amyloid-β peptide in the rat. Experimental Neurology, 197(1), 41-55. doi. 

Goodliffe, J. W., Song, H., Rubakovic, A., Chang, W., Medalla, M., Weaver, C. M., & Luebke, J. I. (2018). Differential changes to D1 and D2 medium spiny neurons in the 12-month-old Q175+/- mouse model of Huntington’s Disease. PLoS ONE, 13(8), e0200626. doi: 10.1371/journal.pone.0200626. https://doi.org/10.1371/journal.pone.0200626


Goodman, R. L., Maltby, M. J., Millar, R. P., Hileman, S. M., Nestor, C. C., Whited, B., . . . Lehman, M. N. (2012). Evidence that Dopamine Acts via Kisspeptin to Hold GnRH Pulse Frequency in Check in Anestrous Ewes. Endocrinology. doi: 10.1210/en.2012-1611. http://endo.endojournals.org/content/early/2012/10/03/en.2012-1611.abstract


Gordon, M., Shepherd, G., Stepanyants, A., Bureau, I., Chklovskii, D., & Svoboda, K. (2005). Geometric and functional organization of cortical circuits. Nature Neuroscience, 8, 782-790. doi. 

Gordon, R. J., Tattersfield, A. S., Vazey, E. M., Kells, A. P., McGregor, A. L., Hughes, S. M., & Connor, B. (2007). Temporal profile of subventricular zone progenitor cell migration following quinolinic acid-induced striatal cell loss. Neuroscience, 146(4), 1704-1718. doi. 

Gos, T., Bock, J., Poeggel, G., & Braun, K. (2008). Stress-induced synaptic changes in the rat anterior cingulate cortex are dependent on endocrine developmental time windows. Synapse, 62(3), 229-232. doi. 

Goshen, I., Avital, A., Kreisel, T., Licht, T., Segal, M., & Yirmiya, R. (2009). Environmental Enrichment Restores Memory Functioning in Mice with Impaired IL-1 Signaling via Reinstatement of Long-Term Potentiation and Spine Size Enlargement. Journal of Neuroscience, 29(11), 3395-3403. doi: 10.1523/jneurosci.5352-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/11/3395 


Goto, J., Talos, D. M., Klein, P., Qin, W., Chekaluk, Y. I., Anderl, S., . . . Kwiatkowski, D. J. (2011). Regulable neural progenitor-specific Tsc1 loss yields giant cells with organellar dysfunction in a model of tuberous sclerosis complex. Proceedings of the National Academy of Sciences, 108(45), E1070–E1079. doi: 10.1073/pnas.1106454108. http://www.pnas.org/content/108/45/E1070.abstract


Goto, K., Kutsuna, N., Yamashita, A., Oshima, H., Suma, T., & Yoshino, A. (2018). Changes of Doublecortin-Immunoreactive Cells from the Acute Phase to Chronic Phase After Transient Global Brain Ischemia in Rat Cingulate Cortex. In O. Thews, J. C. LaManna & D. K. Harrison (Eds.), Oxygen Transport to Tissue XL (pp. 69-75). Cham: Springer International Publishing.

Gottlieb, J. P., & Keller, A. (1997). Intrinsic circuitry and physiological properties of pyramidal neurons in rat barrel cortex. Experimental Brain Research, 115, 47-60. doi. 

Gould, E., Vail, N., Wagers, M., & Gross, C. (2001). Adult-generated hippocampal and neocortical neurons in macaques have a transient existence. Proceedings of the National Academy of Sciences, 98(19), 10910-10917. doi. 

Gourley, S. L., Swanson, A. M., & Koleske, A. J. (2013). Corticosteroid-Induced Neural Remodeling Predicts Behavioral Vulnerability and Resilience. Journal of Neuroscience, 33(7), 3107-3112. doi: 10.1523/jneurosci.2138-12.2013. http://www.jneurosci.org/content/33/7/3107.abstract


Gouty-Colomer, L. A., Hosseini, B., Marcelo, I. M., Schreiber, J., Slump, D. E., Yamaguchi, S., . . . Kushner, S. A. (2015). Arc expression identifies the lateral amygdala fear memory trace. [Original Article]. Molecular Psychiatry. doi: 10.1038/mp.2015.18. http://dx.doi.org/10.1038/mp.2015.18


Grachev, P., Porter, K. L., Coolen, L. M., McCosh, R. B., Connors, J. M., Hileman, S. M., . . . Goodman, R. L. (2016). Surge-like LH secretion induced by retrochiasmatic area NK3R activation is mediated primarily by ARC kisspeptin neurones in the ewe. Journal of Neuroendocrinology, n/a-n/a. doi: 10.1111/jne.12393. http://dx.doi.org/10.1111/jne.12393


Gradari, S., Pérez-Dómper, P., Butler, R. G., Martínez-Cué, C., de Polavieja, G. G., & Trejo, J. L. (2016). The relationship between behavior acquisition and persistence abilities: Involvement of adult hippocampal neurogenesis. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22568. http://dx.doi.org/10.1002/hipo.22568


Graebenitz, S., Lesting, J., Sosulina, L., Seidenbecher, T., & Pape, H. C. (2010). Alteration of NMDA receptor–mediated synaptic interactions in the lateral amygdala associated with seizure activity in a mouse model of chronic temporal lobe epilepsy. Epilepsia, 51(9), 1754-1762. doi. 

Graeber, M., & Streit, W. (2010). Microglia: biology and pathology. Acta Neuropathol, 119, 89 - 105. doi. 

Graf, W., Gerrits, N., Yatim-Dhiba, N., & Ugolini, G. (2002). Mapping the oculomotor system: the power of transneuronal labelling with rabies virus. European Journal of Neuroscience, 15(9), 1557. doi. 

Grafe, L. A., Geng, E., Corbett, B., Urban, K., & Bhatnagar, S. (2019). Sex- and Stress-Dependent Effects on Dendritic Morphology and Spine Densities in Putative Orexin Neurons. Neuroscience. doi: https://doi.org/10.1016/j.neuroscience.2019.08.026. http://www.sciencedirect.com/science/article/pii/S0306452219305998


Grahn, P. J., Vaishya, S., Knight, A., Chen, B. K., Schmeichel, A., Currier, B., . . . Windebank, A. (2014). Implantation of cauda equina nerve roots through a biodegradable scaffold at the conus medullaris in rat. The Spine Journal, (0). doi: http://dx.doi.org/10.1016/j.spinee.2014.01.059. http://www.sciencedirect.com/science/article/pii/S1529943014001375


Granato, A. (2006). Altered organization of cortical interneurons in rats exposed to ethanol during neonatal life. Brain Research, 1069(1), 23-30. doi. 

Granato, A., Di Rocco, F., Zumbo, A., Toesca, A., & Giannetti, S. (2003). Organization of cortico-cortical associative projections in rats exposed to ethanol during early postnatal life. Brain Research Bulletin, 60(4), 339-344. doi. 

Granato, A., & Van Pelt, J. (2003). Effects of early ethanol exposure on dendrite growth of cortical pyramidal neurons: inferences from a computational model. Developmental Brain Research, 142(2), 223-227. doi. 

Grande, V., Manassero, G., & Vercelli, A. (2014). Neuroprotective and Anti-Inflammatory Roles of the Phosphatase and Tensin Homolog Deleted on Chromosome Ten (PTEN) Inhibition in a Mouse Model of Temporal Lobe Epilepsy. PLoS ONE, 9(12), e114554. doi: 10.1371/journal.pone.0114554. http://dx.doi.org/10.1371%2Fjournal.pone.0114554


Grandis, M., Jain, M., La Padula, V., Balsamo, J., Lilien, J., Kamholz, J., . . . Shy, M. E. (2004). Mutations disrupting extracellular structure of MPZ cause early onset severe forms of CMT1B. Journal of the Peripheral Nervous System, 9(2), 111-112. doi: doi:10.1111/j.1085-9489.2004.009209y.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Grant, A., Hoops, D., Labelle-Dumais, C., Prevost, M., Rajabi, H., Kolb, B., . . . Flores, C. (2007). Netrin-1 receptor-deficient mice show enhanced mesocortical dopamine transmission and blunted behavioural responses to amphetamine. European Journal of Neuroscience, 26(11), 3215-3228. doi: doi:10.1111/j.1460-9568.2007.05888.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05888.x 


Grantyn, A., Brandi, A. M., Dubayle, D., Graf, W., Ugolini, G., Hadjidimitrakis, K., & Moschovakis, A. (2002). Density gradients of trans-synaptically labeled collicular neurons after injections of rabies virus in the lateral rectus muscle of the rhesus monkey. Journal of Comparative Neurology, 451(4), 346-361. doi. 

Grantyn, A., Kuze, B., Brandi, A. M., Thomas, M. A., & Quenech'du, N. (2010). Direct projections of omnipause neurons to reticulospinal neurons: A double-labeling light microscopic study in the cat. Journal of Comparative Neurology, 518(23), 4792-4812. doi. 

Grau-Perales, A., Gómez-Chacón, B., Morillas, E., & Gallo, M. (2018). Flavor recognition memory related activity of the posterior piriform cortex in adult and aged rats. Behavioural Brain Research. doi: https://doi.org/10.1016/j.bbr.2018.12.016. http://www.sciencedirect.com/science/article/pii/S0166432818311689


Grau-Perales, A. B., Gámiz, F., & Gallo, M. (2021). Effect of hippocampal 6-OHDA lesions on the contextual modulation of taste recognition memory. Behavioural Brain Research, 409, 113320. doi: https://doi.org/10.1016/j.bbr.2021.113320. https://www.sciencedirect.com/science/article/pii/S0166432821002084


Grau-Perales, A. B., Levy, E. R. J., Fenton, A. A., & Gallo, M. (2019). Dorsal hippocampal damage disrupts the auditory context-dependent attenuation of taste neophobia in mice. Neurobiology of Learning and Memory, 157, 121-127. doi: https://doi.org/10.1016/j.nlm.2018.12.009. http://www.sciencedirect.com/science/article/pii/S1074742718302855


Graves, Austin R., Moore, Shannon J., Bloss, Erik B., Mensh, Brett D., Kath, William L., & Spruston, N. (2012). Hippocampal Pyramidal Neurons Comprise Two Distinct Cell Types that Are Countermodulated by Metabotropic Receptors. Neuron, 76(4), 776-789. doi: http://dx.doi.org/10.1016/j.neuron.2012.09.036. http://www.sciencedirect.com/science/article/pii/S0896627312008902


Graziano, A., & Jones, E. G. (2009). Early Withdrawal of Axons from Higher Centers in Response to Peripheral Somatosensory Denervation. Journal of Neuroscience, 29(12), 3738-3748. doi: 10.1523/jneurosci.5388-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/12/3738 


Greco, M. A., Magner, M., &amp, D. O., & Shiromani, P. J. (1998). Expression of cholinergic markers in the pons of Flinders rats. Molecular Brain Research, 55(2), 232-236. doi. 

Greco, M. A., & Shiromani, P. J. (2001). Hypocretin receptor protein and mRNA expression in the dorsolateral pons of rats. Molecular Brain Research, 88(1-2), 176-182. doi. 

Greminger, A. R., Lee, D. L., Shrager, P., & Mayer-Pröschel, M. (2014). Gestational Iron Deficiency Differentially Alters the Structure and Function of White and Gray Matter Brain Regions of Developing Rats. The Journal of Nutrition. doi: 10.3945/jn.113.187732. http://jn.nutrition.org/content/early/2014/04/16/jn.113.187732.abstract


Gribaudo, S., Bovetti, S., Friard, O., Denorme, M., Oboti, L., Fasolo, A., & De Marchis, S. (2012). Transitory and activity-dependent expression of Neurogranin in olfactory bulb tufted cells during mouse postnatal development. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23150. http://dx.doi.org/10.1002/cne.23150


Gribaudo, S., Bovetti, S., Garzotto, D., Fasolo, A., & De Marchis, S. (2009). Expression and localization of the calmodulin-binding protein neurogranin in the adult mouse olfactory bulb. Journal of Comparative Neurology, 517(5), 683-694. doi. 

Griffiths, B. B., Sahbaie, P., Rao, A., Arvola, O., Xu, L., Liang, D., . . . Stary, C. M. (2019). Pre-treatment with microRNA-181a Antagomir Prevents Loss of Parvalbumin Expression and Preserves Novel Object Recognition Following Mild Traumatic Brain Injury. [journal article]. Neuromolecular medicine. doi: 10.1007/s12017-019-08532-y. https://doi.org/10.1007/s12017-019-08532-y


Grill, J. D., & Riddle, D. R. (2002). Age-related and laminar-specific dendritic changes in the medial frontal cortex of the rat. Brain Research, 937(1-2), 8-21. doi. 

Grill, J. D., Sonntag, W. E., & Riddle, D. R. (2005). Dendritic stability in a model of adult-onset IGF-I deficiency. Growth Hormone and IGF Research, 15(5), 337-348. doi. 

Grillo, C. A., Risher, M., Macht, V. A., Bumgardner, A. L., Hang, A., Gabriel, C., . . . Reagan, L. P. (2014). Repeated restraint stress-induced atrophy of glutamatergic pyramidal neurons and decreases in glutamatergic efflux in the rat amygdala are prevented by the antidepressant agomelatine. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2014.09.047. http://www.sciencedirect.com/science/article/pii/S0306452214007982


Grimaldi, P., Saleem, Kadharbatcha S., & Tsao, D. (2016). Anatomical Connections of the Functionally Defined “Face Patches” in the Macaque Monkey. Neuron. doi: http://dx.doi.org/10.1016/j.neuron.2016.05.009. http://www.sciencedirect.com/science/article/pii/S0896627316301696


Grimm, J., Barnes, J., Koerber, J., Glueck, E., Ginder, D., Hyde, J., & Eaton, L. (2015). Effects of acute or chronic environmental enrichment on regional Fos protein expression following sucrose cue-reactivity testing in rats. Brain Structure and Function, 1-14. doi: 10.1007/s00429-015-1074-z. http://dx.doi.org/10.1007/s00429-015-1074-z


Grisot, G., Haber, S. N., & Yendiki, A. (2021). Diffusion MRI and anatomic tracing in the same brain reveal common failure modes of tractography. Neuroimage, 239, 118300. doi: https://doi.org/10.1016/j.neuroimage.2021.118300. https://www.sciencedirect.com/science/article/pii/S1053811921005760


Gritti, I., Henny, P., Galloni, F., Mainville, L., Mariotti, M., & Jones, B. E. (2006). Stereological estimates of the basal forebrain cell population in the rat, including neurons containing choline acetyltransferase, glutamic acid decarboxylase or phosphate-activated glutaminase and colocalizing vesicular glutamate transporters. Neuroscience, 143(4), 1051-1064. doi. 

Groc, L., Petanjek, Z., Gustafsson, B., Ben-Ari, Y., Hanse, E., & Khazipov, R. (2002). In vivo blockade of neural activity 

                    alters dendritic development of neonatal CA1 pyramidal cells. European Journal of Neuroscience, 16(10), 1931. doi. 

Groc, L., Petanjek, Z., Gustafsson, B., Ben-Ari, Y., Khazipov, R., & Hanse, E. (2003). Compensatory dendritic growth of CA1 pyramidal cells following growth impairment in the neonatal period. European Journal of Neuroscience, 18, 1332-1336. doi. 

Groen, M. R., Paulsen, O., Perez-Garci, E., Nevian, T., Wortel, J., Dekker, M. P., . . . Meredith, R. M. (2014). Development of dendritic tonic GABAergic inhibition regulates excitability and plasticity in CA1 pyramidal neurons. Journal of Neurophysiology. doi: 10.1152/jn.00066.2014. http://jn.physiology.org/content/early/2014/04/18/jn.00066.2014.abstract


Gröger, N., Mannewitz, A., Bock, J., de Schultz, T. F., Guttmann, K., Poeggel, G., & Braun, K. (2017). Infant avoidance training alters cellular activation patterns in prefronto-limbic circuits during adult avoidance learning: I. Cellular imaging of neurons expressing the synaptic plasticity early growth response protein 1 (Egr1). [journal article]. Brain Structure and Function, 1-13. doi: 10.1007/s00429-017-1423-1. http://dx.doi.org/10.1007/s00429-017-1423-1


Groh, A., Bokor, H., Mease, R. A., Plattner, V. M., Hangya, B., Stroh, A., . . . Acsády, L. (2013). Convergence of Cortical and Sensory Driver Inputs on Single Thalamocortical Cells. Cerebral Cortex. doi: 10.1093/cercor/bht173. http://cercor.oxfordjournals.org/content/early/2013/07/03/cercor.bht173....


Groh, A., de Kock, C. P. J., Wimmer, V. C., Sakmann, B., & Kuner, T. (2008). Driver or Coincidence Detector: Modal Switch of a Corticothalamic Giant Synapse Controlled by Spontaneous Activity and Short-Term Depression. Journal of Neuroscience, 28(39), 9652-9663. doi: 10.1523/jneurosci.1554-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/39/9652 


Groh, A., Meyer, H. S., Schmidt, E. F., Heintz, N., Sakmann, B., & Krieger, P. (2010). Cell-type specific properties of pyramidal neurons in neocortex underlying a layout that is modifiable depending on the cortical area. Cerebral Cortex, 20(4), 826-836. doi. 

Gröhn, O. H. J., Kettunen, M. I., Mäkelä, H. I., Penttonen, M., Pitkänen, A., Lukkarinen, J. A., & Kauppinen, R. A. (2000). Early Detection of Irreversible Cerebral Ischemia in the Rat Using Dispersion of the Magnetic Resonance Imaging Relaxation Time, T1ρ. Journal of Cerebral Blood Flow AND Metabolism, 20, 1457-1466. doi. 

Grońska-Pęski, M., Schachner, M., & Hébert, J. M. (2020). L1cam curbs the differentiation of adult-born hippocampal neurons. Stem Cell Research, 48, 101999. doi: https://doi.org/10.1016/j.scr.2020.101999. http://www.sciencedirect.com/science/article/pii/S1873506120303007


Groom, A., Potter, K., Turcot, V., Pearce, M. S., Embleton, N. D., & Relton, C. L. (2011). Postnatal Growth Is Associated with DNA Methylation and Childhood Adiposity: Using Genetic Variation to Infer the Direction of Causation. Journal of Developmental Origins of Health and Disease, 2(1), S2–S34-S32–S34. doi. 

Grosso, A., Cambiaghi, M., Milano, L., Renna, A., Sacco, T., & Sacchetti, B. (2016). Region- and Layer-Specific Activation of the Higher Order Auditory Cortex Te2 after Remote Retrieval of Fear or Appetitive Memories. Cerebral Cortex. doi: 10.1093/cercor/bhw159. http://cercor.oxfordjournals.org/content/early/2016/05/31/cercor.bhw159....


Groves, T. R., Farris, R., Anderson, J. E., Alexander, T. C., Kiffer, F., Carter, G., . . . Allen, A. R. (2017). 5-Fluorouracil chemotherapy upregulates cytokines and alters hippocampal dendritic complexity in aged mice. Behavioural Brain Research, 316, 215-224. doi: http://dx.doi.org/10.1016/j.bbr.2016.08.039. http://www.sciencedirect.com/science/article/pii/S0166432816305575


Groves, T. R., Wang, J., Boerma, M., Allen, A., & o, R. (2017). Assessment of Hippocampal Dendritic Complexity in Aged Mice Using the Golgi-Cox Method. (124), e55696. doi: doi:10.3791/55696. https://www.jove.com/video/55696


Gruene, T. M., Roberts, E., Thomas, V., Ronzio, A., & Shansky, R. M. (2014). Sex-specific neuroanatomical correlates of fear expression in prefrontal-amygdala circuits. Biological Psychiatry, (0). doi: http://dx.doi.org/10.1016/j.biopsych.2014.11.014. http://www.sciencedirect.com/science/article/pii/S0006322314008944


Grünewald, L., Becker, N., Camphausen, A., O‘Leary, A., Lesch, K.-P., Freudenberg, F., & Reif, A. (2018). Expression of the ADHD candidate gene Diras2 in the brain. [journal article]. Journal of Neural Transmission. doi: 10.1007/s00702-018-1867-3. https://doi.org/10.1007/s00702-018-1867-3


Grzanna, R., Dubin, J. R., Dent, G. W., Ji, Z., Zhang, W., Ho, S. P., & Hartig, P. R. (1998). Intrastriatal and intraventricular injections of oligodeoxynucleotides in the rat brain: tissue penetration, intracellular distribution and c-fos antisense effects. Molecular Brain Research, 63, 35-52. doi. 

Gu, F., Parada, I., Shen, F., Li, J., Bacci, A., Graber, K., . . . Prince, D. A. (2017). Structural alterations in fast-spiking GABAergic interneurons in a model of posttraumatic neocortical epileptogenesis. Neurobiology of Disease. doi: http://dx.doi.org/10.1016/j.nbd.2017.08.008. http://www.sciencedirect.com/science/article/pii/S0969996117301894


Gu, H. H., & Han, D. D. (2017). Chapter 14 - Use of Knock-In Mice to Investigate the Molecular Mechanism of Cocaine Action A2 - Preedy, Victor R The Neuroscience of Cocaine (pp. 135-142). San Diego: Academic Press.

Gu, H. Y., Chai, H., Zhang, J. Y., Yao, Z. B., Zhou, L. H., Wong, W. M., . . . Wu, W. T. (2005). Survival, regeneration and functional recovery of motoneurons after delayed reimplantation of avulsed spinal root in adult rat. Experimental Neurology, 192(1), 89-99. doi. 

Gu, H.-Y., Chai, H., Zhang, J.-Y., Yao, Z.-B., Zhou, L.-H., Wong, W.-M., . . . Wu, W.-T. (2004). Survival, regeneration and functional recovery of motoneurons in adult rats by reimplantation of ventral root following spinal root avulsion. European Journal of Neuroscience, 19(8), 2123-2131. doi. http://www.blackwell-synergy.com/links/doi/10.1111/j.0953-816X.2004.0329...


Gu, W., Fu, S., Wang, Y., Li, Y., Lu, H., Xu, X., & Lu, P. (2009). Chondroitin sulfate proteoglycans regulate the growth, differentiation and migration of multipotent neural precursor cells through the integrin signaling pathway. BMC Neuroscience, 10(1), 128. doi. http://www.biomedcentral.com/1471-2202/10/128 


Gu, W., Zhang, F., Xue, Q., Ma, Z., Lu, P., & Yu, B. (2010). Transplantation of bone marrow mesenchymal stem cells reduces lesion volume and induces axonal regrowth of injured spinal cord. Neuropathology, 30(3), 205-217. doi. 

Gu, W., Zhang, F., Xue, Q., Ma, Z., Lu, P., & Yu, B. (2012). Bone mesenchymal stromal cells stimulate neurite outgrowth of spinal neurons by secreting neurotrophic factors. Neurological Research, 34(2), 172-180. doi. 

Gu, Y. W., Su, D. S., Tian, J., & Wang, X. R. (2008). Attenuating phosphorylation of p38 MAPK in the activated microglia: a new mechanism for intrathecal lidocaine reversing tactile allodynia following chronic constriction injury in rats. Neuroscience Letters, 431(2), 129-134. doi. 

Guadagno, A., Wong, T. P., & Walker, C.-D. (2018). Morphological and functional changes in the preweaning basolateral amygdala induced by early chronic stress associate with anxiety and fear behavior in adult male, but not female rats. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 81(Supplement C), 25-37. doi: https://doi.org/10.1016/j.pnpbp.2017.09.025. http://www.sciencedirect.com/science/article/pii/S0278584617306437


Guadaño-Ferraz, A., Viñuela, A., Oeding, G., Bernal, J., & Rausell, E. (2005). RC3/neurogranin is expressed in pyramidal neurons of motor and somatosensory cortex in normal and denervated monkeys. Journal of Comparative Neurology, 493(4), 554-570. doi. 

Guagliardo, N. A., & Hill, D. L. (2007). Fungiform taste bud degeneration in C57BL/6J mice following chorda-lingual nerve transection. Journal of Comparative Neurology, 504(2), 206-216. doi. 

Guagliardo, N. A., Yao, J., Stipes, E. J., Cechova, S., Le, T. H., Bayliss, D. A., . . . Barrett, P. Q. (2018). Adrenal Tissue-Specific Deletion of TASK Channels Causes Aldosterone-Driven Angiotensin II-Independent Hypertension. Hypertension, 0(0), HYPERTENSIONAHA.118.11962. doi: doi:10.1161/HYPERTENSIONAHA.118.11962. https://www.ahajournals.org/doi/abs/10.1161/HYPERTENSIONAHA.118.11962 %X The renin-angiotensin system tightly controls aldosterone synthesis. Dysregulation is evident in hypertension (primary aldosteronism), low renin, and resistant hypertension) but also can exist in normotension. Whether chronic, mild aldosterone autonomy can elicit hypertension remains untested. Previously, we reported that global genetic deletion of 2 pore-domain TWIK-relative acid-sensitive potassium channels, TASK-1 and TASK-3, from mice produces striking aldosterone excess, low renin, and hypertension. Here, we deleted TASK-1 and TASK-3 channels selectively from zona glomerulosa cells and generated a model of mild aldosterone autonomy with attendant hypertension that is aldosterone-driven and Ang II (angiotensin II)-independent. This study shows that a zona glomerulosa–specific channel defect can produce mild autonomous hyperaldosteronism sufficient to cause chronic blood pressure elevation.

Guan, H., & Maness, P. F. (2010). Perisomatic GABAergic Innervation in Prefrontal Cortex Is Regulated by Ankyrin Interaction with the L1 Cell Adhesion Molecule. Cerebral Cortex, 20(11), 2684-2693. doi: 10.1093/cercor/bhq016. http://cercor.oxfordjournals.org/content/20/11/2684.abstract


Guerra, L., McGarry, L. M., Robles, V., Bielza, C., Larrañaga, P., & Yuste, R. (2011). Comparison between supervised and unsupervised classifications of neuronal cell types: A case study. Developmental Neurobiology, 71(1), 71-82. doi: 10.1002/dneu.20809. http://dx.doi.org/10.1002/dneu.20809


Guest, J. D., Herrera, L., Margitich, I., Oliveria, M., Marcillo, A., & Casas, C. E. (2008). Xenografts of expanded primate olfactory ensheathing glia support transient behavioral recovery that is independent of serotonergic or corticospinal axonal regeneration in nude rats following spinal cord transection. Experimental Neurology, 212(2), 261-274. doi. 

Guet-McCreight, A., Camiré, O., Topolnik, L., & Skinner, F. K. (2016). Using A Semi-Automated Strategy To Develop Multi-Compartment Models That Predict Biophysical Properties Of Interneuron Specific 3 (IS3) Cells In Hippocampus. [10.1523/ENEURO.0087-16.2016]. eneuro. doi. http://eneuro.sfn.org/content/early/2016/08/29/ENEURO.0087-16.2016.abstract


Guha, U., Gomes, W. A., Samanta, J., Gupta, M., Rice, F. L., & Kessler, J. A. (2004). Target-derived BMP signaling limits sensory neuron number and the extent of peripheral innervation in vivo. Development, 131(5), 1175-1186. doi: 10.1242/dev.01013. http://dev.biologists.org/cgi/content/abstract/131/5/1175 


Guillamon-Vivancos, T., Tyler, W. A., Medalla, M., Chang, W. W.-e., Okamoto, M., Haydar, T. F., & Luebke, J. I. (2018). Distinct Neocortical Progenitor Lineages Fine-tune Neuronal Diversity in a Layer-specific Manner. Cerebral Cortex. doi: 10.1093/cercor/bhy019. http://dx.doi.org/10.1093/cercor/bhy019


Guillery, R. W., Feig, S. L., & Van Lieshout, D. P. (2001). Connections of higher order visual relays in the thalamus: a study of corticothalamic pathways in cats. Journal of Comparative Neurology, 438(1), 66-85. doi. 

Guilloux, J.-P., David, I., Pehrson, A., Guiard, B. P., Repérant, C., Orvoën, S., . . . David, D. J. (2013). Antidepressant and anxiolytic potential of the multimodal antidepressant vortioxetine (Lu AA21004) assessed by behavioural and neurogenesis outcomes in mice. Neuropharmacology, (0). doi: http://dx.doi.org/10.1016/j.neuropharm.2013.05.014. http://www.sciencedirect.com/science/article/pii/S0028390813002244


Guilloux, J.-P., Samuels, B. A., Mendez-David, I., Hu, A., Levinstein, M., Faye, C., . . . Hen, R. (2017). S 38093, a histamine H3 antagonist/inverse agonist, promotes hippocampal neurogenesis and improves context discrimination task in aged mice. Scientific Reports, 7, 42946. doi. 

Guimaraes, B. d. P. P. F., Curado, M. R., Nogueira-Campos, A. A., Houzel, J. C., & Gattass, R. (2021). Nitrergic neurons of the forepaw representation in the rat somatosensory and motor cortices: A quantitative study. [https://doi.org/10.1002/cne.25192]. Journal of Comparative Neurology, n/a(n/a). doi: https://doi.org/10.1002/cne.25192. https://doi.org/10.1002/cne.25192


Gull, S., Ingrisch, I., Tausch, S., Witte, O. W., & Schmidt, S. (2015). Consistent and reproducible staining of glia by a modified Golgi–Cox method. Journal of Neuroscience Methods, 256, 141-150. doi: http://dx.doi.org/10.1016/j.jneumeth.2015.08.029. http://www.sciencedirect.com/science/article/pii/S0165027015003209


Gulyas, A. I., Megias, M., Emri, Z., & Freund, T. F. (1999). Total Number and Ratio of Excitatory and Inhibitory Synapses Converging onto Single Interneurons of Different Types in the CA1 Area of the Rat Hippocampus. Journal of Neuroscience, 19(22), 10082-10097. doi. http://www.jneurosci.org/cgi/content/abstract/19/22/10082


Gulyas, B., Toth, M., Schain, M., Airaksinen, A., Vas, A., Kostulas, K., . . . Halldin, C. (2012). Evolution of microglial activation in ischaemic core and peri-infarct regions after stroke: a PET study with the TSPO molecular imaging biomarker [((11))C]vinpocetine. Journal of the Neurological Sciences, 320, 110 - 117. doi. 

Gunhan, E., van der List, D., & Chalupa, L. M. (2003). Ectopic Photoreceptors and Cone Bipolar Cells in the Developing and Mature Retina. Journal of Neuroscience, 23(4), 1383-1389. doi. http://www.jneurosci.org/cgi/content/abstract/23/4/1383 


Guo, N., Garcia, M. M., & Harlan, R. E. (2008). A morphine-paired environment alters c-Fos expression in the forebrain of rats displaying conditioned place preference or aversion. Behavioral Neuroscience, 122(5), 1078-1078. doi. 

Guo, S.-L., Tan, G.-H., Li, S., Cheng, X.-W., Zhou, Y., Jia, Y.-F., . . . Xiong, Z.-Q. (2011). Serum inducible kinase is a positive regulator of cortical dendrite development and is required for BDNF-promoted dendritic arborization. Cell Research. doi: http://www.nature.com/cr/journal/vaop/ncurrent/suppinfo/cr2011100s1.html. http://dx.doi.org/10.1038/cr.2011.100


Guo, W., Murthy, A. C., Zhang, L., Johnson, E. B., Schaller, E. G., Allan, A. M., & Zhao, X. (2012). Inhibition of GSK3β improves hippocampus-dependent learning and rescues neurogenesis in a mouse model of fragile X syndrome. Human Molecular Genetics, 21(3), 681-691. doi. 

Guo, W., Polich, Eric D., Su, J., Gao, Y., Christopher, Devin M., Allan, Andrea M., . . . Zhao, X. (2015). Fragile X Proteins FMRP and FXR2P Control Synaptic GluA1 Expression and Neuronal Maturation via Distinct Mechanisms. Cell Reports, 11(10), 1651-1666. doi: http://dx.doi.org/10.1016/j.celrep.2015.05.013. http://www.sciencedirect.com/science/article/pii/S2211124715005252


Guo, Y., & Udin, S. B. (2000). The Development of Abnormal Axon Trajectories after Rotation of One Eye in Xenopus. Journal of Neuroscience, 20(11), 4189-4197. doi. http://www.jneurosci.org/cgi/content/abstract/20/11/4189


Guo, Z. V., Inagaki, H. K., Daie, K., Druckmann, S., Gerfen, C. R., & Svoboda, K. (2017). Maintenance of persistent activity in a frontal thalamocortical loop. [Article]. Nature, advance online publication. doi: 10.1038/nature22324

http://www.nature.com/nature/journal/vaop/ncurrent/abs/nature22324.html#.... http://dx.doi.org/10.1038/nature22324


Gupta, A., Elgammal, F. S., Proddutur, A., Shah, S., & Santhakumar, V. (2012). Decrease in Tonic Inhibition Contributes to Increase in Dentate Semilunar Granule Cell Excitability after Brain Injury. Journal of Neuroscience, 32(7), 2523-2537. doi: 10.1523/jneurosci.4141-11.2012. http://www.jneurosci.org/content/32/7/2523.abstract


Gupta, A., Wang, Y., & Markram, H. (2000). Organizing Principles for a Diversity of GABAergic Interneurons and Synapses in the Neocortex. Science, 287, 273-278. doi. 

Gupta, N., Greenberg, G., de Tilly, L. N., Gray, B., Polemidiotis, M., & Yucel, Y. H. (2009). Atrophy of the lateral geniculate nucleus in human glaucoma detected by magnetic resonance imaging. British Journal of Ophthalmology, 93(1), 56-60. doi: 10.1136/bjo.2008.138172. http://bjo.bmj.com/cgi/content/abstract/93/1/56 


Gupta, N., Ly, T., Zhang, Q., Kaufman, P. L., Weinreb, R. N., & Yücel, Y. H. (2007). Chronic ocular hypertension induces dendrite pathology in the lateral geniculate nucleus of the brain. Experimental Eye Research, 84(1), 176-184. doi. 

Gupta, R. C., Milatovic, S., Dettbarn, W. D., Aschner, M., & Milatovic, D. (2007). Neuronal oxidative injury and dendritic damage induced by carbofuran: protection by memantine. Toxicology and Applied Pharmacology, 219(2-3), 97-105. doi. 

Gurevicius, K., Gureviciene, I., Sivukhina, E., Irintchev, A., Schachner, M., & Tanila, H. (2007). Increased hippocampal and cortical beta oscillations in mice deficient for the HNK-1 sulfotransferase. Molecular and Cellular Neuroscience, 34(2), 189-198. doi. 

Gurevicius, K., Kuang, F., Stoenica, L., Irintchev, A., Gureviciene, I., Dityatev, A., . . . Tanila, H. (2009). Genetic ablation of tenascin-C expression leads to abnormal hippocampal CA1 structure and electrical activity in vivo. Hippocampus, 19(12), 1232-1246. doi. 

Gurung, B., & Fritzsch*, B. (2004). Time Course of Embryonic Midbrain and Thalamic Auditory Connection Development in Mice as Revealed by Carbocyanine Dye Tracing. Journal of Comparative Neurology, 479, 309-327. doi. 

Guseva, D., Angelov, D. N., Irintchev, A., & Schachner, M. (2009). Ablation of adhesion molecule L1 in mice favours Schwann cell proliferation and functional recovery after peripheral nerve injury. Brain, awp160. doi: 10.1093/brain/awp160. http://brain.oxfordjournals.org/cgi/content/abstract/awp160v1 


Guseva, D., Loers, G., & Schachner, M. (2014). Function-Triggering Antibodies to the Adhesion Molecule L1 Enhance Recovery after Injury of the Adult Mouse Femoral Nerve. PLoS ONE, 9(11), e112984. doi: 10.1371/journal.pone.0112984. http://dx.doi.org/10.1371%2Fjournal.pone.0112984


Guseva, D., Zerwas, M., Xiao, M., Jakovcevski, I., Irintchev, A., & Schachner, M. (2011). Adhesion molecule L1 overexpressed under the control of the neuronal Thy-1 promoter improves myelination after peripheral nerve injury in adult mice. Experimental Neurology. doi. 

Gutarts, R., Nusstein, J., Reader, A., & Beck, M. (2005). In vivo debridement efficacy of ultrasonic irrigation following hand-rotary instrumentation in human mandibular molars. Journal of Endodontics, 31(3), 166-170. doi. 

Gutierrez-Mecinas, M., Davis, O., Polgár, E., Shahzad, M., Navarro-Batista, K., Furuta, T., . . . Todd, A. J. (2018). Expression of Calretinin Among Different Neurochemical Classes of Interneuron in the Superficial Dorsal Horn of the Mouse Spinal Cord. Neuroscience. doi: https://doi.org/10.1016/j.neuroscience.2018.12.009. http://www.sciencedirect.com/science/article/pii/S0306452218308182


Gutierrez-Mecinas, M., Kuehn, E. D., Abraira, V. E., Polgár, E., Watanabe, M., & Todd, A. J. (2016). Immunostaining for Homer reveals the majority of excitatory synapses in laminae I–III of the mouse spinal dorsal horn. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2016.05.009. http://www.sciencedirect.com/science/article/pii/S0306452216301580


Gutierrez-Mecinas, M., Polgár, E., Bell, A. M., Herau, M., & Todd, A. J. (2018). Substance P-expressing excitatory interneurons in the mouse superficial dorsal horn provide a propriospinal input to the lateral spinal nucleus. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-018-1629-x. https://doi.org/10.1007/s00429-018-1629-x


Guy, J., Sachkova, A., Möck, M., Witte, M., Wagener, R. J., & Staiger, J. F. (2016). Intracortical Network Effects Preserve Thalamocortical Input Efficacy in a Cortex Without Layers. Cerebral Cortex. doi: 10.1093/cercor/bhw281. http://cercor.oxfordjournals.org/content/early/2016/09/12/cercor.bhw281....


Guy, J., Wagener, R. J., Möck, M., & Staiger, J. F. (2014). Persistence of Functional Sensory Maps in the Absence of Cortical Layers in the Somsatosensory Cortex of Reeler Mice. Cerebral Cortex. doi: 10.1093/cercor/bhu052. http://cercor.oxfordjournals.org/content/early/2014/04/23/cercor.bhu052....


Guyenet, P. G., Abbott, S. B. G., & Stornetta, R. L. (2012). The respiratory chemoreception conundrum: Light at the end of the tunnel? Brain Research, (0). doi: 10.1016/j.brainres.2012.10.028. http://www.sciencedirect.com/science/article/pii/S0006899312016745


Guyenet, P. G., Sevigny, C. P., Weston, M. C., & Stornetta, R. L. (2002). Neurokinin-1 Receptor-Expressing Cells of the Ventral Respiratory Group Are Functionally Heterogeneous and Predominantly Glutamatergic. Journal of Neuroscience, 22(9), 3806-3816. doi. http://www.jneurosci.org/cgi/content/abstract/22/9/3806


Guyenet, P. G., Stornetta, R. L., Riley, T., Norton, F. R., Rosin, D. L., & Lynch, K. R. (1994). Alpha< sub> 2A</sub>-adrenergic receptors are present in lower brainstem catecholaminergic and serotonergic neurons innervating spinal cord. Brain Research, 638(1), 285-294. doi. 

Guyenet, P. G., & Wang, H. (2001). Pre-Botzinger Neurons With Preinspiratory Discharges "In Vivo" Express NK1 Receptors in the Rat. Journal of Neurophysiology, 86(1), 438-446. doi. http://jn.physiology.org/cgi/content/abstract/86/1/438 


Guzik-Kornacka, A., van der Bourg, A., Vajda, F., Joly, S., Christ, F., Schwab, M., & Pernet, V. (2014). Nogo-A deletion increases the plasticity of the optokinetic response and changes retinal projection organization in the adult mouse visual system. Brain Structure and Function, 1-13. doi: 10.1007/s00429-014-0909-3. http://dx.doi.org/10.1007/s00429-014-0909-3


Gvilia, I., Angara, C., McGinty, D., & Szymusiak, R. (2005). Different neuronal populations of the rat median preoptic nucleus express c-fos during sleep and in response to hypertonic saline or angiotensin-II. Journal of Physiology, 569(2), 587-599. doi: 10.1113/jphysiol.2005.097212. http://jp.physoc.org/cgi/content/abstract/569/2/587 


Gvilia, I., Suntsova, N., Angara, B., McGinty, D., & Szymusiak, R. (2011). Maturation of sleep homeostasis in developing rats: a role for preoptic area neurons. American Journal of Physiology - Regulatory, Integrative and Comparative Physiology, 300(4), R885-R894. doi: 10.1152/ajpregu.00727.2010. http://ajpregu.physiology.org/content/300/4/R885.abstract


Gvilia, I., Turner, A., McGinty, D., & Szymusiak, R. (2006). Preoptic Area Neurons and the Homeostatic Regulation of Rapid Eye Movement Sleep. Journal of Neuroscience, 26(11), 3037-3044. doi: 10.1523/jneurosci.4827-05.2006. http://www.jneurosci.org/cgi/content/abstract/26/11/3037 


Gvilia, I., Xu, F., McGinty, D., & Szymusiak, R. (2006). Homeostatic Regulation of Sleep: A Role for Preoptic Area Neurons. Journal of Neuroscience, 26(37), 9426-9433. doi: 10.1523/jneurosci.2012-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/37/9426 


Gyengesi, E., Calabrese, E., Sherrier, M., Johnson, G. A., Paxinos, G., & Watson, C. (2013). Semi-automated 3D segmentation of major tracts in the rat brain: comparing DTI with standard histological methods. Brain Structure and Function, 1-12. doi: 10.1007/s00429-013-0516-8. http://dx.doi.org/10.1007/s00429-013-0516-8


Gyengesi, E., Mnch, G., Paxinos, G., & Zaborszky, L. (2014). Can you believe what you see: evaluation of choline acetyl transferase (ChAT) expression in the ChAT-eGFP transgenic mouse (89.1). The FASEB journal, 28(1 Supplement). doi. http://www.fasebj.org/content/28/1_Supplement/89.1.abstract


Ha, T., Swanson, D., Larouche, M., Glenn, R., Weeden, D., Zhang, P., . . . Goldowitz, D. (2014). CbGRiTS: Cerebellar gene regulation in time and space. Developmental Biology, (0). doi: http://dx.doi.org/10.1016/j.ydbio.2014.09.032. http://www.sciencedirect.com/science/article/pii/S0012160614005016


Haas, C., & Fischer, I. (2013). Human astrocytes derived from glial restricted progenitors support regeneration of the injured spinal cord. Journal of Neurotrauma, (ja). doi. 

Haas, C., Neuhuber, B., Yamagami, T., Rao, M., & Fischer, I. (2011). Phenotypic analysis of astrocytes derived from glial restricted precursors and their impact on axon regeneration. Experimental Neurology. doi. 

Haas, C. A., Dudeck, O., Kirsch, M., Huszka, C., Kann, G., Pollak, S., . . . Frotscher, M. (2002). Role for Reelin in the Development of Granule Cell Dispersion in Temporal Lobe Epilepsy. Journal of Neuroscience, 22(14), 5797-5802. doi: 20026621. http://www.jneurosci.org/cgi/content/abstract/22/14/5797 


Haas, M. A., Bell, D., Slender, A., Lana-Elola, E., Watson-Scales, S., Fisher, E. M. C., . . . Guillemot, F. (2013). Alterations to Dendritic Spine Morphology, but Not Dendrite Patterning, of Cortical Projection Neurons in Tc1 and Ts1Rhr Mouse Models of Down Syndrome. PLoS ONE, 8(10), e78561. doi: 10.1371/journal.pone.0078561. http://dx.doi.org/10.1371%2Fjournal.pone.0078561


Haber, S. N., Kim, K.-S., Mailly, P., & Calzavara, R. (2006). Reward-Related Cortical Inputs Define a Large Striatal Region in Primates That Interface with Associative Cortical Connections, Providing a Substrate for Incentive-Based Learning. Journal of Neuroscience, 26(32), 8368-8376. doi: 10.1523/jneurosci.0271-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/32/8368 


Hackett, T. A., & de la Mothe, L. A. (2009). Regional and laminar distribution of the vesicular glutamate transporter, VGluT2, in the macaque monkey auditory cortex. Journal of Chemical Neuroanatomy, 38(2), 106-116. doi. 

Hackett, T. A., De La Mothe, L. A., Ulbert, I., Karmos, G., Smiley, J., & Schroeder, C. E. (2007). Multisensory convergence in auditory cortex, II. Thalamocortical connections of the caudal superior temporal plane. Journal of Comparative Neurology, 502(6), 924-952. doi. 

Hacohen-Kleiman, G., Moaraf, S., Kapitansky, O., & Gozes, I. (2020). Sex-and Region-Dependent Expression of the Autism-Linked ADNP Correlates with Social- and Speech-Related Genes in the Canary Brain. Journal of Molecular Neuroscience. doi: 10.1007/s12031-020-01700-x. https://doi.org/10.1007/s12031-020-01700-x


Hada, Y., Yamada, Y., Imamura, K., Mataga, N., Watanabe, Y., & Yamamoto, M. (1999). Effects of monocular enucleation on parvalbumin in rat visual system during postnatal development. Investigative Ophthalmology and Visual Science, 40(11), 2535-2545. doi. 

Hadjilambreva, G., Mix, E., Rolfs, A., Muller, J., & Strauss, U. (2005). Neuromodulation by a Cytokine: Interferon-β Differentially Augments Neocortical Neuronal Activity and Excitability. Journal of Neurophysiology, 93(2), 843-852. doi: 10.1152/jn.01224.2003. http://jn.physiology.org/cgi/content/abstract/93/2/843 


Hadjimarkou, M. M., Benham, R., Schwarz, J. M., Holder, M. K., & Mong, J. A. (2008). Estradiol suppresses rapid eye movement sleep and activation of sleep-active neurons in the ventrolateral preoptic area. European Journal of Neuroscience, 27(7), 1780-1792. doi: doi:10.1111/j.1460-9568.2008.06142.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2008.06142.x 


Haeussner, E., Aschauer, B., Burton, G. J., Huppertz, B., Edler von Koch, F., Müller-Starck, J., . . . Frank, H.-G. (2015). Does 2D-Histologic identification of villous types of human placentas at birth enable sensitive and reliable interpretation of 3D structure? Placenta. doi: http://dx.doi.org/10.1016/j.placenta.2015.10.003. http://www.sciencedirect.com/science/article/pii/S0143400415300631


Haeussner, E., Schmitz, C., Frank, H.-G., & Edler von Koch, F. (2016). Novel 3D light microscopic analysis of IUGR placentas points to a morphological correlate of compensated ischemic placental disease in humans. [Article]. Scientific Reports, 6, 24004. doi: 10.1038/srep24004

http://www.nature.com/articles/srep24004#supplementary-information. http://dx.doi.org/10.1038/srep24004


Hafner, G., Guy, J., Witte, M., Truschow, P., Rüppel, A., Sirmpilatze, N., . . . Staiger, J. F. (2020). Increased Callosal Connectivity in Reeler Mice Revealed by Brain-Wide Input Mapping of VIP Neurons in Barrel Cortex. Cerebral Cortex, (bhaa280). doi: 10.1093/cercor/bhaa280. https://doi.org/10.1093/cercor/bhaa280


Hafner, G., Witte, M., Guy, J., Subhashini, N., Fenno, L. E., Ramakrishnan, C., . . . Staiger, J. F. (2019). Mapping Brain-Wide Afferent Inputs of Parvalbumin-Expressing GABAergic Neurons in Barrel Cortex Reveals Local and Long-Range Circuit Motifs. Cell Reports, 28(13), 3450-3461.e3458. doi: https://doi.org/10.1016/j.celrep.2019.08.064. http://www.sciencedirect.com/science/article/pii/S2211124719311192


Hagar, J. M., Macht, V. A., Wilson, S. P., & Fadel, J. R. (2017). Upregulation of orexin/hypocretin expression in aged rats: effects on feeding latency and neurotransmission in the insular cortex. Neuroscience. doi. http://linkinghub.elsevier.com/retrieve/pii/S0306452217301793?via=sd


Hagemann, T. L., Connor, J. X., & Messing, A. (2006). Alexander Disease-Associated Glial Fibrillary Acidic Protein Mutations in Mice Induce Rosenthal Fiber Formation and a White Matter Stress Response. Journal of Neuroscience, 26(43), 11162-11173. doi: 10.1523/jneurosci.3260-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/43/11162 


Haggerty, A. E., Al‐Ali, H., & Oudega, M. (2018). Soluble laminin polymers enhance axon growth of primary neurons in vitro. Journal of Biomedical Materials Research Part A. doi. https://onlinelibrary.wiley.com/doi/abs/10.1002/jbm.a.36429


Hahm, E., Hammond, D. L., & Proudfit, H. K. (2011). Substance P induces the reversible formation of varicosities in the dendrites of rat brainstem neurons. Brain Research, 1369, 36-45. doi. 

Hahn, K., Sirdofsky, M., Brown, A., Ebenezer, G., Hauer, P., Miller, C., & Polydefkis, M. (2006). Collateral sprouting of human epidermal nerve fibers following intracutaneous axotomy. Journal of the Peripheral Nervous System, 11(2), 142-147. doi: doi:10.1111/j.1085-9489.2006.00079.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2006.00079.x 


Hahn, T. T. G., McFarland, J. M., Berberich, S., Sakmann, B., & Mehta, M. R. (2012). Spontaneous persistent activity in entorhinal cortex modulates cortico-hippocampal interaction in vivo. Nature Neuroscience. doi. 

Hains, A. B., Vu, M. A. T., Maciejewski, P. K., van Dyck, C. H., Gottron, M., & Arnsten, A. F. T. (2009). Inhibition of protein kinase C signaling protects prefrontal cortex dendritic spines and cognition from the effects of chronic stress. Proceedings of the National Academy of Sciences, 106(42), 17957-17962. doi: 10.1073/pnas.0908563106. http://www.pnas.org/content/106/42/17957.abstract 


Hains, A. B., Yabe, Y., & Arnsten, A. F. T. (2015). Chronic Stimulation of Alpha-2A-Adrenoceptors With Guanfacine Protects Rodent Prefrontal Cortex Dendritic Spines and Cognition From the Effects of Chronic Stress. Neurobiology of Stress, (0). doi: http://dx.doi.org/10.1016/j.ynstr.2015.01.001. http://www.sciencedirect.com/science/article/pii/S2352289515000223


Hains, D. S., Sims-Lucas, S., Carpenter, A., Saha, M., Murawski, I., Kish, K., . . . Bates, C. M. (2010). High incidence of vesicoureteral reflux in mice with Fgfr2 deletion in kidney mesenchyma. Journal of Urology, 183(5), 2077-2084. doi. 

Hajszán, T., & Zaborszky, L. (2002). Direct catecholaminergic–cholinergic interactions in the basal forebrain. III. Adrenergic innervation of choline acetyltransferase-containing neurons in the rat. Journal of Comparative Neurology, 449(2), 141-157. doi. 

Hakeem, A. Y., Sherwood, C. C., Bonar, C. J., Butti, C., Hof, P. R., & Allman, J. M. (2009). Von Economo neurons in the elephant brain. The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology, 292(2), 242-248. doi. 

Hakim, J. S., Esmaeili Rad, M., Grahn, P. J., Chen, B., Knight, A. M., Schmeichel, A. M., . . . Yaszemski, M. J. (2015). Positively charged oligo[poly(ethylene glycol) fumarate] scaffold implantation results in a permissive lesion environment after spinal cord injury in rat. Tissue Engineering Part A. doi: 10.1089/ten.TEA.2015.0019. http://dx.doi.org/10.1089/ten.TEA.2015.0019


Halabisky, B., Parada, I., Buckmaster, P. S., & Prince, D. A. (2010). Excitatory Input Onto Hilar Somatostatin Interneurons Is Increased in a Chronic Model of Epilepsy. Journal of Neurophysiology, 104(4), 2214-2223. doi: 10.1152/jn.00147.2010. http://jn.physiology.org/cgi/content/abstract/104/4/2214


Halassa, Michael M., Chen, Z., Wimmer, Ralf D., Brunetti, Philip M., Zhao, S., Zikopoulos, B., . . . Wilson, Matthew A. (2014). State-Dependent Architecture of Thalamic Reticular Subnetworks. Cell, 158(4), 808-821. doi: 10.1016/j.cell.2014.06.025. http://www.cell.com/cell/abstract/S0092-8674(14)00815-0

Halavi, M., Hamilton, K. A., Parekh, R., & Ascoli, G. A. (2012). Digital reconstructions of neuronal morphology: Three decades of research trends. Frontiers in Neuroscience, 6. doi. 

Haldipur, P., Bharti, U., Alberti, C., Sarkar, C., Gulati, G., Iyengar, S., . . . Mani, S. (2011). Preterm delivery disrupts the developmental program of the cerebellum. PLoS ONE, 6(8), e23449-e23449. doi. 

Hallermann, S., de Kock, C. P. J., Stuart, G. J., & Kole, M. H. P. (2012). State and location dependence of action potential metabolic cost in cortical pyramidal neurons. [10.1038/nn.3132]. Nature Neuroscience, advance online publication. doi: http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.3132.html#suppl.... http://dx.doi.org/10.1038/nn.3132


Hallermann, S., Pawlu, C., Jonas, P., & Heckmann, M. (2003). A large pool of releasable vesicles in a cortical glutamatergic synapse. Neuroscience, 100, 8975-8980. doi. 

Halliday, G. M., Hardman, C. D., Cordato, N. J., Hely, M. A., & Morris, J. G. L. (2000). A role for the substantia nigra pars reticulata in the gaze palsy of progressive supranuclear palsy. Brain, 123(4), 724-732. doi: 10.1093/brain/123.4.724. http://brain.oxfordjournals.org/cgi/content/abstract/123/4/724 


Halliday, G. M., Macdonald, V., & Henderson, J. M. (2005). A comparison of degeneration in motor thalamus and cortex between progressive supranuclear palsy and Parkinson's disease. Brain, 128(10), 2272-2280. doi: 10.1093/brain/awh596. http://brain.oxfordjournals.org/cgi/content/abstract/128/10/2272 


Halsell, C. B., & Travers, S. P. (1997). Anterior and Posterior Oral Cavity Responsive Neurons Are Differentially Distributed Among Parabrachial Subnuclei in Rat. Journal of Neurophysiology, 78(2), 920-938. doi. http://jn.physiology.org/cgi/content/abstract/78/2/920 


Halsell, C. B., Travers, S. P., & Travers, J. B. (1996). Ascending and descending projections from the rostral nucleus of the solitary tract originate from separate neuronal populations. Neuroscience, 72(1), 185-197. doi. 

Hama, Y., Shiraki, K., Yoshida, Y., Maruyama, A., Yasuda, M., Tsuda, M., . . . others. (2010). Antibody to varicella-zoster virus immediate-early protein 62 augments allodynia in zoster via brain-derived neurotrophic factor. Journal of Virology, 84(3), 1616-1624. doi. 

Hamad, M. I. K., Ma-Högemeier, Z.-L., Riedel, C., Conrads, C., Veitinger, T., Habijan, T., . . . Wahle, P. (2011). Cell class-specific regulation of neocortical dendrite and spine growth by AMPA receptor splice and editing variants. Development, 138(19), 4301-4313. doi: 10.1242/dev.071076. http://dev.biologists.org/content/138/19/4301.abstract


Hamada, M. S., Goethals, S., de Vries, S. I., Brette, R., & Kole, M. H. P. (2016). Covariation of axon initial segment location and dendritic tree normalizes the somatic action potential. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1607548113. http://www.pnas.org/content/early/2016/11/30/1607548113.abstract


Hamada, M. S., & Kole, M. H. (2015). Myelin Loss and Axonal Ion Channel Adaptations Associated with Gray Matter Neuronal Hyperexcitability. The Journal of Neuroscience, 35(18), 7272-7286. doi. http://www.jneurosci.org/content/35/18/7272.full


Hamadjida, A., Wyss, A., Mir, A., Schwab, M., Belhaj-Saif, A., & Rouiller, E. (2012). Influence of anti-Nogo-A antibody treatment on the reorganization of callosal connectivity of the premotor cortical areas following unilateral lesion of primary motor cortex (M1) in adult macaque monkeys. Experimental Brain Research, 1-20. doi: 10.1007/s00221-012-3262-x. http://dx.doi.org/10.1007/s00221-012-3262-x


Hamaguchi, S., Hirose, T., Matsumoto, N., Akeda, Y., Irisawa, T., Seki, M., . . . Tomono, K. (2014). Neutrophil extracellular traps in bronchial aspirates: a quantitative analysis. European Respiratory Journal. doi: 10.1183/09031936.00139813. http://erj.ersjournals.com/content/early/2014/03/06/09031936.00139813.ab...


Hamam, B. N., Amaral, D. G., & Alonso, A. A. (2002). Morphological and electrophysiological characteristics of layer V neurons of the rat lateral entorhinal cortex. Journal of Comparative Neurology, 451(1), 45-61. doi. 

Hamam, B. N., Kennedy, T. E., Alonso, A., & Amaral, D. G. (2000). Morphological and electrophysiological characteristics of layer V neurons of the rat medial entorhinal cortex. Journal of Comparative Neurology, 418(4), 457-472. doi. 

Hamamoto, M., Kiyokage, E., Sohn, J., Hioki, H., Harada, T., & Toida, K. (2016). Structural Basis for Cholinergic Regulation of Neural Circuits in the Mouse Olfactory Bulb. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24088. http://dx.doi.org/10.1002/cne.24088


Hamilton, G. F., Criss, K. J., & Klintsova, A. Y. (2015). Voluntary Exercise Partially Reverses Neonatal Alcohol-Induced Deficits in mPFC Layer II/III Dendritic Morphology of Male Adolescent Rats. Synapse, n/a-n/a. doi: 10.1002/syn.21827. http://dx.doi.org/10.1002/syn.21827


Hamilton, G. F., Whitcher, L. T., & Klintsova, A. Y. (2010). Postnatal binge-like alcohol exposure decreases dendritic complexity while increasing the density of mature spines in mPFC Layer II/III pyramidal neurons. Synapse, 64(2), 127-135. doi. 

Hamilton, K. A., Parrish-Aungst, S., Margolis, F. L., Erdélyi, F., Szabó, G., & Puche, A. C. (2008). Sensory deafferentation transsynaptically alters neuronal GluR1 expression in the external plexiform layer of the adult mouse main olfactory bulb. Chemical Senses, 33(2), 201-201. doi. 

Hamity, M. V., Walder, R. Y., & Hammond, D. L. (2014). Increased Neuronal Expression of Neurokinin-1 Receptor and Stimulus-Evoked Internalization of the Receptor in the Rostral Ventromedial Medulla of the Rat after Peripheral Inflammatory Injury. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23564. http://dx.doi.org/10.1002/cne.23564


Hamlin, A. S., Buller, K. M., Day, T. A., & Osborne, P. B. (2004). Effect of naloxone-precipitated morphine withdrawal on< i> c</i>-< i> fos</i> expression in rat corticotropin-releasing hormone neurons in the paraventricular hypothalamus and extended amygdala. Neuroscience Letters, 362(1), 39-43. doi. 

Hammar, I., Bannatyne, B. A., Maxwell, D. J., Edgley, S. A., & Jankowska, E. (2004). The actions of monoamines and distribution of noradrenergic and serotoninergic contacts on different subpopulations of commissural interneurons in the cat spinal cord. European Journal of Neuroscience, 19(5), 1305-1316. doi. http://www.blackwell-synergy.com/links/doi/10.1111/j.1460-9568.2004.0323...


Hammar, I., & Maxwell, D. J. (2002). Serotoninergic and noradrenergic axons make contacts with neurons of the ventral spinocerebellar tract in the cat. Journal of Comparative Neurology, 443(3), 310-319. doi. 

Hammond, D. L., Ackerman, L., Holdsworth, R., & Elzey, B. (2004). Effects of spinal nerve ligation on immunohistochemically identified neurons in the L4 and L5 dorsal root ganglia of the rat. Journal of Comparative Neurology, 475(4), 575-589. doi. 

Hammond, V. E., Gunnersen, J. M., Goh, C.-P., Low, L.-H., Hyakumura, T., Tang, M. M., . . . Tan, S.-S. (2013). Ndfip1 Is Required for the Development of Pyramidal Neuron Dendrites and Spines in the Neocortex. Cerebral Cortex. doi: 10.1093/cercor/bht191. http://cercor.oxfordjournals.org/content/early/2013/07/26/cercor.bht191....


Hammoum, I., Benlarbi, M., Dellaa, A., Szabó, K., Dékány, B., Csaba, D., . . . Benchouacha-Chekir, R. (2017). Study of Retinal Neurodegeneration and Maculopathy in Diabetic Meriones shawi: A Particular Animal Model with Human-like Macula. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24245. http://dx.doi.org/10.1002/cne.24245


Hamodat, H., Fisk, J. D., & Darvesh, S. (2019). Cholinergic Neurons in Nucleus Subputaminalis in Primary Progressive Aphasia. Canadian Journal of Neurological Sciences, 1-10. doi. https://www.cambridge.org/core/journals/canadian-journal-of-neurological...


Han, S., Arnold, S. A., Sithu, S. D., Mahoney, E. T., Geralds, J. T., Tran, P., . . . Hagg, T. (2010). Rescuing vasculature with intravenous angiopoietin-1 and αvβ3 integrin peptide is protective after spinal cord injury. Brain, 133(4), 1026-1042. doi: 10.1093/brain/awq034. http://brain.oxfordjournals.org/cgi/content/abstract/133/4/1026 


Han, V. Z., Meek, J., Campbell, H. R., & Bell, C. C. (2006). Cell morphology and circuitry in the central lobes of the mormyrid cerebellum. Journal of Comparative Neurology, 497(3), 309-325. doi. 

Han, X., Lan, X., Li, Q., Gao, Y., Zhu, W., Cheng, T., . . . Wang, J. (2015). Inhibition of prostaglandin E2 receptor EP3 mitigates thrombin-induced brain injury. Journal of Cerebral Blood Flow and Metabolism. doi: 10.1177/0271678x15606462. http://jcb.sagepub.com/content/early/2015/09/23/0271678X15606462.abstract


Han, Y., Chang, Q. A., Virag, T., West, N. C., George, D., Castro, M. G., & Bohn, M. C. (2010). Lack of humoral immune response to the tetracycline (Tet) activator in rats injected intracranially with Tet-off rAAV vectors. Gene Therapy, 17(5), 616-625. doi. 

Handa, Y., Ozaki, N., Honda, T., Furukawa, K., Tomita, Y., Inoue, M., . . . Sugiura, Y. (2005). GD3 synthase gene knockout mice exhibit thermal hyperalgesia and mechanical allodynia but decreased response to formalin-induced prolonged noxious stimulation. Pain, 117(3), 271-279. doi. 

Hanganu, I. L., & Luhmann, H. J. (2004). Functional Nicotinic Acetylcholine Receptors on Subplate Neurons in Neonatal Rat Somatosensory Cortex. Journal of Neurophysiology, 92(1), 189-198. doi: 10.1152/jn.00010.2004. http://jn.physiology.org/cgi/content/abstract/92/1/189 


Hanganu, I. L., Staiger, J. F., Ben-Ari, Y., & Khazipov, R. (2007). Cholinergic Modulation of Spindle Bursts in the Neonatal Rat Visual Cortex In Vivo. Journal of Neuroscience, 27(21), 5694-5705. doi: 10.1523/jneurosci.5233-06.2007. http://www.jneurosci.org/cgi/content/abstract/27/21/5694 


Hanson, J. E., & Smith, Y. (1999). Group I Metabotropic Glutamate Receptors at GABAergic Synapses in Monkeys. Journal of Neuroscience, 19(15), 6488-6496. doi. http://www.jneurosci.org/cgi/content/abstract/19/15/6488


Hanson, J. E., & Smith, Y. (2002). Subcellular distribution of high-voltage-activated calcium channel subtypes in rat globus pallidus neurons. Journal of Comparative Neurology, 442(2), 89-98. doi. 

Hanson, J. E., Smith, Y., & Jaeger, D. (2004). Sodium Channels and Dendritic Spike Initiation at Excitatory Synapses in Globus Pallidus Neurons. Journal of Neuroscience, 24(2), 329-340. doi: 10.1523/jneurosci.3937-03.2004. http://www.jneurosci.org/cgi/content/abstract/24/2/329 


Hanson, J. N., Motala, M. J., Heien, M. L., Gillette, M., Sweedler, J., & Nuzzo, R. G. (2008). Textural guidance cues for controlling process outgrowth of mammalian neurons. Lab Chip, 9(1), 122-131. doi. 

Hanson, M. G., & Landmesser, L. T. (2004). Normal patterns of spontaneous activity are required for correct motor axon guidance and the expression of specific guidance molecules. Neuron, 43(5), 687-701. doi. 

Hanson, M. G., Milner, L. D., & Landmesser, L. T. (2008). Spontaneous rhythmic activity in early chick spinal cord influences distinct motor axon pathfinding decisions. Brain Research Reviews, 57(1), 77-85. doi. 

Hao, J., Rapp, P. R., Janssen, W. G. M., Lou, W., Lasley, B. L., Hof, P. R., & Morrison, J. H. (2007). Interactive effects of age and estrogen on cognition and pyramidal neurons in monkey prefrontal cortex. PNAS, 104(27), 11465-11470. doi: 10.1073/pnas.0704757104. http://www.pnas.org/cgi/content/abstract/104/27/11465 


Hao, J., Rapp, P. R., Leffler, A. E., Leffler, S. R., Janssen, W. G. M., Lou, W., . . . Morrison, J. H. (2006). Estrogen Alters Spine Number and Morphology in Prefrontal Cortex of Aged Female Rhesus Monkeys. Journal of Neuroscience, 26(9), 2571-2578. doi: 10.1523/jneurosci.3440-05.2006. http://www.jneurosci.org/cgi/content/abstract/26/9/2571 


Haque, A., Huss, D., & Dickman, J. D. (2006). Afferent Innervation Patterns of the Pigeon Horizontal Crista Ampullaris. Journal of Neurophysiology, 96(6), 3293-3304. doi: 10.1152/jn.00930.2005. http://jn.physiology.org/cgi/content/abstract/96/6/3293 


Haque, A., Zakir, M., & Dickman, J. D. (2009). Regeneration of vestibular horizontal semicircular canal afferents in pigeons. Journal of Neurophysiology, 91000.92008. doi: 10.1152/jn.91000.2008. http://jn.physiology.org/cgi/content/abstract/91000.2008v1 


Hara, E., Kubikova, L., Hessler, N. A., & Jarvis, E. D. (2007). Role of the midbrain dopaminergic system in modulation of vocal brain activation by social context. European Journal of Neuroscience, 25(11), 3406-3416. doi: doi:10.1111/j.1460-9568.2007.05600.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05600.x 


Harbom, L. J., Rudisill, T. L., Michel, N., Litwa, K. A., Beenhakker, M. P., & McConnell, M. J. (2018). The effect of rho kinase inhibition on morphological and electrophysiological maturity in iPSC-derived neurons. [journal article]. Cell and Tissue Research. doi: 10.1007/s00441-018-2942-7. https://doi.org/10.1007/s00441-018-2942-7


Harding, A. J., Stimson, E., Henderson, J. M., & Halliday, G. M. (2002). Clinical correlates of selective pathology in the amygdala of patients with Parkinson's disease. Brain, 125(11), 2431-2445. doi: 10.1093/brain/awf251. http://brain.oxfordjournals.org/cgi/content/abstract/125/11/2431 


Hardingham, N. R., Gould, T., & Fox, K. (2011). Anatomical and sensory experiential determinants of synaptic plasticity in layer 2/3 pyramidal neurons of mouse barrel cortex. Journal of Comparative Neurology, 519(11), 2090-2124. doi: 10.1002/cne.22583. http://dx.doi.org/10.1002/cne.22583


Hargus, G., Cui, Y., Schmid, J.-S., Xu, J., Glatzel, M., Schachner, M., & Bernreuther, C. (2008). Tenascin-R Promotes Neuronal Differentiation of Embryonic Stem Cells and Recruitment of Host-Derived Neural Precursor Cells After Excitotoxic Lesion of the Mouse Striatum. Stem Cells, 26(8), 1973-1984. doi: 10.1634/stemcells.2007-0929. http://stemcells.alphamedpress.org/cgi/content/abstract/26/8/1973 


Harland, B., Collings, D. A., McNaughton, N., Abraham, W. C., & Dalrymple-Alford, J. C. (2014). Anterior thalamic lesions reduce spine density in both hippocampal CA1 and retrosplenial cortex, but enrichment rescues CA1 spines only. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22309. http://dx.doi.org/10.1002/hipo.22309


Harmon, K. M., & Wellman, C. L. (2003). Differential effects of cholinergic lesions on dendritic spines in frontal cortex of young adult and aging rats. Brain Research, 992(1), 60-68. doi. 

Harrer, M. I., & Travers, S. P. (1996). Topographic organization of Fos-like immunoreactivity in the rostral nucleus of the solitary tract evoked by gustatory stimulation with sucrose and quinine. Brain Research, 711(1-2), 125-137. doi. 

Harris, C. A., Resau, J. H., Hudson, E. A., West, R. A., Moon, C., Black, A. D., & McAllister, J. P. (2011). Reduction of protein adsorption and macrophage and astrocyte adhesion on ventricular catheters by polyethylene glycol and N-acetyl-L-cysteine. Journal of Biomedical Materials Research Part A, 98A(3), 425-433. doi: 10.1002/jbm.a.33130. http://dx.doi.org/10.1002/jbm.a.33130


Harris, C. A., Resau, J. H., Hudson, E. A., West, R. A., Moon, C., & McAllister Ii, J. P. (2010). Mechanical contributions to astrocyte adhesion using a novel in vitro model of catheter obstruction. Experimental Neurology, 222(2), 204-210. doi. 

Harris, E., & Stewart, M. (2001). Propagation of synchronous epileptiform events from subiculum backward into area CA1 of rat brain slices. Brain Research, 895(1-2), 41-49. doi. 

Harris, E., Witter, M. P., Weinstein, G., & Stewart, M. (2001). Intrinsic connectivity of the rat subiculum: I. Dendritic morphology and patterns of axonal arborization by pyramidal neurons. Journal of Comparative Neurology, 435(4), 490-505. doi. 

Harris, N. G., Nogueira, M. S., Verley, D. R., & Sutton, R. L. (2013). Chondroitinase enhances cortical map plasticity and increases functionally active sprouting axons after brain injury. Journal of Neurotrauma, (ja). doi. 

Harsan, L.-A., Dávid, C., Reisert, M., Schnell, S., Hennig, J., von Elverfeldt, D., & Staiger, J. F. (2013). Mapping remodeling of thalamocortical projections in the living reeler mouse brain by diffusion tractography. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1218330110. http://www.pnas.org/content/early/2013/04/19/1218330110.abstract


Hart, M. G. C. v. d., Czéh, B., Biurrun, G. d., Michaelis, T., Watanabe, T., Natt, O., . . . Fuchs, E. (2002). Substance P receptor antagonist and clomipramine prevent stress-induced alterations in cerebral metabolites, cytogenesis in the dentate gyrus and hippocampal volume. Molecular Psychiatry, 7, 933-941. doi. 

Hartle, K. D., Jeffers, M. S., & Ivanco, T. L. (2010). Changes in dendritic morphology and spine density in motor cortex of the adult rat after stroke during infancy. Synapse, 64(8), 602-610. doi. 

Hartman, R. E., Laurer, H., Longhi, L., Bales, K. R., Paul, S. M., McIntosh, T. K., & Holtzman, D. M. (2002). Apolipoprotein E4 Influences Amyloid Deposition But Not Cell Loss after Traumatic Brain Injury in a Mouse Model of Alzheimer's Disease. Journal of Neuroscience, 22, 10083-10087. doi. 

Hartveit, E., Zandt, B.-J., & Veruki, M. L. (2019). Multiphoton Excitation Microscopy for the Reconstruction and Analysis of Single Neuron Morphology. In E. Hartveit (Ed.), Multiphoton Microscopy (pp. 161-194). New York, NY: Springer New York.

Hartwich, K., Pollak, T., & Klausberger, T. (2009). Distinct Firing Patterns of Identified Basket and Dendrite-Targeting Interneurons in the Prefrontal Cortex during Hippocampal Theta and Local Spindle Oscillations. Journal of Neuroscience, 29(30), 9563-9574. doi: 10.1523/jneurosci.1397-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/30/9563 


Harty, R. C., Kim, T. H., Thomas, E. A., Cardamone, L., Jones, N. C., Petrou, S., & Wimmer, V. C. (2013). Axon initial segment structural plasticity in animal models of genetic and acquired epilepsy. Epilepsy Research, (0). doi: http://dx.doi.org/10.1016/j.eplepsyres.2013.03.004. http://www.sciencedirect.com/science/article/pii/S0920121113000892


Haruta, M., & Hata, Y. (2007). Experience-driven axon retraction without binocular imbalance in developing visual cortex. Current Biology, 17(1), 37-42. doi. 

Harvey, A. R., Ehlert, E., de Wit, J., Drummond, E. S., Pollett, M. A., Ruitenberg, M., . . . Levelt, C. N. (2009). Use of GFP to analyze morphology, connectivity, and function of cells in the central nervous system. Viral Applications of Green Fluorescent Protein, 63-63. doi. 

Harvey, A. R., Hellström, M., & Rodger, J. (2009). Gene therapy and transplantation in the retinofugal pathway. Progress in Brain Research, 175, 151-161. doi. 

Harwell, Corey C., Fuentealba, Luis C., Gonzalez-Cerrillo, A., Parker, Phillip R. L., Gertz, Caitlyn C., Mazzola, E., . . . Kriegstein, A. R. (2015). Wide Dispersion and Diversity of Clonally Related Inhibitory Interneurons. Neuron. doi: http://dx.doi.org/10.1016/j.neuron.2015.07.030. http://www.sciencedirect.com/science/article/pii/S0896627315006728


Harwell, Corey C., Parker, Philip R. L., Gee, Steven M., Okada, A., McConnell, Susan K., Kreitzer, Anatol C., & Kriegstein, Arnold R. (2012). Sonic Hedgehog Expression in Corticofugal Projection Neurons Directs Cortical Microcircuit Formation. Neuron, 73(6), 1116-1126. doi: 10.1016/j.neuron.2012.02.009. http://www.sciencedirect.com/science/article/pii/S0896627312001365


Hasegawa, M., Kondo, M., Suzuki, I., Shimizu, N., Sessle, B. J., & Iwata, K. (2012). ERK is Involved in Tooth-pressure-induced Fos Expression in Vc Neurons. Journal of Dental Research. doi: 10.1177/0022034512462397. http://jdr.sagepub.com/content/early/2012/09/25/0022034512462397.abstract


Hasegawa, Y., Hojo, Y., Kojima, H., Ikeda, M., Hotta, K., Sato, R., . . . Kawato, S. (2015). Estradiol rapidly modulates synaptic plasticity of hippocampal neurons: Involvement of kinase networks. Brain Research, (0). doi: http://dx.doi.org/10.1016/j.brainres.2014.12.056. http://www.sciencedirect.com/science/article/pii/S0006899315000104


Haselmann, H., Mannara, F., Werner, C., Planagumà, J., Miguez-Cabello, F., Schmidl, L., . . . Geis, C. (2018). Human Autoantibodies against the AMPA Receptor Subunit GluA2 Induce Receptor Reorganization and Memory Dysfunction. Neuron. doi: https://doi.org/10.1016/j.neuron.2018.07.048. http://www.sciencedirect.com/science/article/pii/S0896627318306469


Hashemi-Nezhad, M., & Lyon, D. C. (2012). Orientation Tuning of the Suppressive Extraclassical Surround Depends on Intrinsic Organization of V1. Cerebral Cortex, 22(2), 308-326. doi. 

Hashimoto, K., & Spector, A. C. (2013). Extensive Lesions in the Gustatory Cortex in the Rat Do Not Disrupt the Retention of a Presurgically Conditioned Taste Aversion and Do Not Impair Unconditioned Concentration-Dependent Licking of Sucrose and Quinine. Chemical Senses. doi: 10.1093/chemse/bjt054. http://chemse.oxfordjournals.org/content/early/2013/11/12/chemse.bjt054....


Hashimoto, M., Takahara, D., Hirata, Y., Inoue, K., Miyachi, S., Nambu, A., . . . Hoshi, E. (2010). Motor and non-motor projections from the cerebellum to rostrocaudally distinct sectors of the dorsal premotor cortex in macaques. European Journal of Neuroscience, 31(8), 1402-1413. doi. 

Hashimoto-Torii, K., Torii, M., Sarkisian, M. R., Bartley, C. M., Shen, J., Radtke, F., . . . Rakic, P. (2008). Interaction between Reelin and Notch signaling regulates neuronal migration in the cerebral cortex. Neuron, 60(2), 273-284. doi. 

Hassani, O. K., Henny, P., Lee, M. G., & Jones, B. E. (2010). GABAergic neurons intermingled with orexin and MCH neurons in the lateral hypothalamus discharge maximally during sleep. European Journal of Neuroscience, 32(3), 448-457. doi. 

Hassani, O. K., Lee, M. G., Henny, P., & Jones, B. E. (2009). Discharge Profiles of Identified GABAergic in Comparison to Cholinergic and Putative Glutamatergic Basal Forebrain Neurons across the Sleep-Wake Cycle. Journal of Neuroscience, 29(38), 11828-11840. doi: 10.1523/jneurosci.1259-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/38/11828 


Hassani, O. K., Lee, M. G., & Jones, B. E. (2009). Melanin-concentrating hormone neurons discharge in a reciprocal manner to orexin neurons across the sleep–wake cycle. Proceedings of the National Academy of Sciences, 106(7), 2418-2422. doi: 10.1073/pnas.0811400106. http://www.pnas.org/content/106/7/2418.abstract 


Hastings, N. B., Seth, M. I., Tanapat, P., Rydel, T. A., & Gould, E. (2002). Granule neurons generated during development extend divergent axon collaterals to hippocampal area CA3. Journal of Comparative Neurology, 452(4), 324-333. doi. 

Hata, Y., Tsumoto, T., & Stryker, M. P. (1999). Selective pruning of more active afferents when cat visual cortex is pharmacologically inhibited. Neuron, 22(2), 375-381. doi. 

Hatanaka, Y., Hojo, Y., Mukai, H., Murakami, G., Komatsuzaki, Y., Kim, J., . . . Kawato, S. (2014). Rapid increase of spines by dihydrotestosterone and testosterone in hippocampal neurons: Dependence on synaptic androgen receptor and kinase networks. Brain Research, (0). doi: http://dx.doi.org/10.1016/j.brainres.2014.12.011. http://www.sciencedirect.com/science/article/pii/S0006899314016801


Hatanaka, Y., Mukai, H., Mitsuhashi, K., Hojo, Y., Murakami, G., Komatsuzaki, Y., . . . Kawato, S. (2009). Androgen rapidly increases dendritic thorns of CA3 neurons in male rat hippocampus. Biochemical and Biophysical Research Communications, 381(4), 728-732. doi. 

Hatanaka, Y., Wada, K., & Kabuta, T. (2016). Maternal high-fat diet leads to persistent synaptic instability in mouse offspring via oxidative stress during lactation. Neurochemistry International. doi: http://dx.doi.org/10.1016/j.neuint.2016.03.008. http://www.sciencedirect.com/science/article/pii/S0197018616300341


Hatch, R. J., Leinenga, G., & Götz, J. (2016). Scanning Ultrasound (SUS) Causes No Changes to Neuronal Excitability and Prevents Age-Related Reductions in Hippocampal CA1 Dendritic Structure in Wild-Type Mice. PLoS ONE, 11(10), e0164278. doi: 10.1371/journal.pone.0164278. http://dx.doi.org/10.1371%2Fjournal.pone.0164278


Hattiangady, B., Rao, M. S., & Shetty, A. K. (2008). Grafting of striatal precursor cells into hippocampus shortly after status epilepticus restrains chronic temporal lobe epilepsy. Experimental Neurology, 212(2), 468-481. doi. 

Hattiangady, B., Rao, M. S., Zaman, V., & Shetty, A. K. (2006). Incorporation of embryonic CA3 cell grafts into the adult hippocampus at 4-months after injury: effects of combined neurotrophic supplementation and caspase inhibition. Neuroscience, 139(4), 1369-1383. doi. 

Hattiangady, B., & Shetty, A. K. (2007). Neural Stem Cell Grafting in an Animal Model of Chronic Temporal Lobe Epilepsy Current Protocols in Stem Cell Biology: John Wiley & Sons, Inc.

Hattiangady, B., & Shetty, A. K. (2008). Aging does not alter the number or phenotype of putative stem/progenitor cells in the neurogenic region of the hippocampus. Neurobiology of Aging, 29(1), 129-147. doi. 

Haubst, N., Georges-Labouesse, E., De Arcangelis, A., Mayer, U., & Gotz, M. (2006). Basement membrane attachment is dispensable for radial glial cell fate and for proliferation, but affects positioning of neuronal subtypes. Development, 133(16), 3245-3254. doi: 10.1242/dev.02486. http://dev.biologists.org/cgi/content/abstract/133/16/3245 


Haulcomb, M. M., Mesnard, N. A., Batka, R. J., Alexander, T. D., Sanders, V. M., & Jones, K. J. (2014). Axotomy-induced target disconnection promotes an additional death mechanism involved in motoneuron degeneration in ALS transgenic mice. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23538. http://dx.doi.org/10.1002/cne.23538


Hauser, K. F., Hahn, Y. K., Adjan, V. V., Zou, S., Buch, S. K., Nath, A., . . . Knapp, P. E. (2009). HIV-1 Tat and morphine have interactive effects on oligodendrocyte survival and morphology. Glia, 57(2), 194-206. doi. 

Hausmann, O. N., Fouad, K., Wallimann, T., & Schwab, M. E. (2002). Protective effects of oral creatine supplementation on spinal cord injury in rats. Spinal Cord, 40, 449-456. doi. 

Havton, L. A., & Kellerth, J. O. (2001). Neurofilamentous hypertrophy of intramedullary axonal arbors in intact spinal motoneurons undergoing peripheral sprouting. Journal of Neurocytology, 30(11), 917-926. doi. 

Havton, L. A., & Ohara, P. T. (1994). Dendritic orientation of thalamocortical projection neurons in the ventrobasal complex of macaques. Brain Research, 638, 126-132. doi. 

Hawes, S. L., Evans, R. C., Unruh, B. A., Benkert, E. E., Gillani, F., Dumas, T. C., & Blackwell, K. T. (2015). Multimodal Plasticity in Dorsal Striatum While Learning a Lateralized Navigation Task. The Journal of Neuroscience, 35(29), 10535-10549. doi. http://www.jneurosci.org/content/35/29/10535.short


Hawley, D. F., Bardi, M., Everette, A. M., Higgins, T. J., Tu, K. M., Kinsley, C. H., & Lambert, K. G. (2009). Neurobiological constituents of active, passive, and variable coping strategies in rats: Integration of regional brain neuropeptide Y levels and cardiovascular responses. Stress: The International Journal on the Biology of Stress, 13(2), 172-183. doi. 

Haws, M. E., Jaramillo, T. C., Espinosa-Becerra, F., Widman, A., Stuber, G. D., Sparta, D. R., . . . Powell, C. M. (2013). PTEN knockdown alters dendritic spine/protrusion morphology, not density. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23488. http://dx.doi.org/10.1002/cne.23488


Hawthorne, A. L., Wylie, C. J., Landmesser, L. T., Deneris, E. S., & Silver, J. (2010). Serotonergic Neurons Migrate Radially through the Neuroepithelium by Dynamin-Mediated Somal Translocation. Journal of Neuroscience, 30(2), 420-430. doi: 10.1523/jneurosci.2333-09.2010. http://www.jneurosci.org/cgi/content/abstract/30/2/420 


Hay, E., Hill, S., Schürmann, F., Markram, H., & Segev, I. (2011). Models of neocortical layer 5b pyramidal cells capturing a wide range of dendritic and perisomatic active properties. PLoS computational biology, 7(7), e1002107-e1002107. doi. 

Hay, E., Schürmann, F., Markram, H., & Segev, I. (2013). Preserving Axo-somatic Spiking Features Despite Diverse Dendritic Morphology. Journal of Neurophysiology. doi: 10.1152/jn.00048.2013. http://jn.physiology.org/content/early/2013/03/22/jn.00048.2013.abstract


Hayano, Y., Sasaki, K., Ohmura, N., Takemoto, M., Maeda, Y., Yamashita, T., . . . Yamamoto, N. (2014). Netrin-4 regulates thalamocortical axon branching in an activity-dependent fashion. Proceedings of the National Academy of Sciences. doi: 10.1073/pnas.1402095111. http://www.pnas.org/content/early/2014/10/02/1402095111.abstract


Hayar, A., Karnup, S., Ennis, M., & Shipley, M. T. (2004). External Tufted Cells: A Major Excitatory Element That Coordinates Glomerular Activity. Journal of Neuroscience, 24(30), 6676-6685. doi. http://www.jneurosci.org/cgi/content/abstract/24/30/6676


Hayar, A., Karnup, S., Shipley, M. T., & Ennis, M. (2004). Olfactory Bulb Glomeruli: External Tufted Cells Intrinsically Burst at Theta Frequency and Are Entrained by Patterned Olfactory Input. Journal of Neuroscience, 24(5), 1190-1199. doi: 10.1523/jneurosci.4714-03.2004. http://www.jneurosci.org/cgi/content/abstract/24/5/1190 


Hayar, A., Shipley, M. T., & Ennis, M. (2005). Olfactory Bulb External Tufted Cells Are Synchronized by Multiple Intraglomerular Mechanisms. Journal of Neuroscience, 25(36), 8197-8208. doi. http://www.jneurosci.org/cgi/content/abstract/25/36/8197


Hayase, Y., Amano, S., Hashizume, K., Tominaga, T., Miyamoto, H., Kanno, Y., . . . Hoshino, M. (2020). Down syndrome cell adhesion molecule like-1 (DSCAML1) links the GABA system and seizure susceptibility. Acta Neuropathologica Communications, 8(1), 206. doi: 10.1186/s40478-020-01082-6. https://doi.org/10.1186/s40478-020-01082-6


Hayashi, K., Furuya, A., Sakamaki, Y., Akagi, T., Shinoda, Y., Sadakata, T., . . . Furuichi, T. (2017). The brain-specific RasGEF very-KIND is required for normal dendritic growth in cerebellar granule cells and proper motor coordination. PLoS ONE, 12(3), e0173175. doi: 10.1371/journal.pone.0173175. http://dx.doi.org/10.1371%2Fjournal.pone.0173175


Hayashi, M. L., Rao, B. S., Seo, J. S., Choi, H. S., Dolan, B. M., Choi, S. Y., . . . Tonegawa, S. (2007). Inhibition of p21-activated kinase rescues symptoms of fragile X syndrome in mice. Proceedings of the National Academy of Sciences, 104(27), 11489-11489. doi. 

Haynes, R. L., Billiards, S. S., Borenstein, N. S., Volpe, J. J., & Kinney, H. C. (2008). Diffuse axonal injury in periventricular leukomalacia as determined by apoptotic marker fractin. Pediatric Research, 63(6), 656-656. doi. 

Haynes, R. L., & Kinney, H. C. (2011). Central Axonal Development and Pathology in Early Life. Cytoskeleton of the Nervous System, 1-53. doi. 

Haynes, R. L., Sleeper, L. A., Volpe, J. J., & Kinney, H. C. (2013). Neuropathologic Studies of the Encephalopathy of Prematurity in the Late Preterm Infant. Clinics in Perinatology, (0). doi: http://dx.doi.org/10.1016/j.clp.2013.07.003. http://www.sciencedirect.com/science/article/pii/S0095510813000778


Haynes, R. L., Xu, G., Folkerth, R. D., Trachtenberg, F. L., Volpe, J. J., & Kinney, H. C. (2011). Potential neuronal repair in cerebral white matter injury in the human neonate. Pediatric Research, 69(1), 62-62. doi. 

Haynes, W. I. A., & Haber, S. N. (2013). The Organization of Prefrontal-Subthalamic Inputs in Primates Provides an Anatomical Substrate for Both Functional Specificity and Integration: Implications for Basal Ganglia Models and Deep Brain Stimulation. The Journal of Neuroscience, 33(11), 4804-4814. doi: 10.1523/jneurosci.4674-12.2013. http://www.jneurosci.org/content/33/11/4804.abstract


Hays, S. A., Ruiz, A., Bethea, T., Khodaparast, N., Carmel, J. B., Rennaker, R. L., II, & Kilgard, M. P. (2016). Vagus Nerve Stimulation during Rehabilitative Training Enhances Recovery of Forelimb Function after Ischemic Stroke in Aged Rats. Neurobiology of Aging. doi: 10.1016/j.neurobiolaging.2016.03.030. http://dx.doi.org/10.1016/j.neurobiolaging.2016.03.030


Hazra, A., Gu, F., Aulakh, A., Berridge, C., Eriksen, J. L., & Žiburkus, J. (2013). Inhibitory Neuron and Hippocampal Circuit Dysfunction in an Aged Mouse Model of Alzheimer's Disease. PLoS ONE, 8(5), e64318. doi: 10.1371/journal.pone.0064318. http://dx.doi.org/10.1371%2Fjournal.pone.0064318


He, H., Mahnke, A. H., Doyle, S., Fan, N., Wang, C.-C., Hall, B. J., . . . Erickson, J. D. (2012). Neurodevelopmental Role for VGLUT2 in Pyramidal Neuron Plasticity, Dendritic Refinement, and in Spatial Learning. Journal of Neuroscience, 32(45), 15886-15901. doi: 10.1523/jneurosci.4505-11.2012. http://www.jneurosci.org/content/32/45/15886.abstract


He, J., Nixon, K., Shetty, A. K., & Crews, F. T. (2005). Chronic alcohol exposure reduces hippocampal neurogenesis and dendritic growth of newborn neurons. European Journal of Neuroscience, 21(10), 2711-2720. doi: doi:10.1111/j.1460-9568.2005.04120.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2005.04120.x 


He, M., Tucciarone, J., Lee, S., Nigro, Maximiliano J., Kim, Y., Levine, Jesse M., . . . Huang, Z. J. (2016). Strategies and Tools for Combinatorial Targeting of GABAergic Neurons in Mouse Cerebral Cortex. Neuron. doi: 10.1016/j.neuron.2016.08.021. http://dx.doi.org/10.1016/j.neuron.2016.08.021


He, S., Shao, L. R., Rittase, W. B., & Bausch, S. B. (2012). Increased Kv1 Channel Expression May Contribute to Decreased sIPSC Frequency Following Chronic Inhibition of NR2B-Containing NMDAR. Neuropsychopharmacology. doi. 

He, T., Mortensen, X., Wang, P., & Tian, N. (2017). The effects of immune protein CD3ζ development and degeneration of retinal neurons after optic nerve injury. PLoS ONE, 12(4), e0175522. doi: 10.1371/journal.pone.0175522. https://doi.org/10.1371/journal.pone.0175522


He, Z., Jia, C., Feng, S., Zhou, K., Tai, Y., Bai, X., & Wang, Y. (2012). TRPC5 Channel Is the Mediator of Neurotrophin-3 in Regulating Dendritic Growth via CaMKIIα in Rat Hippocampal Neurons. Journal of Neuroscience, 32(27), 9383-9395. doi: 10.1523/jneurosci.6363-11.2012. http://www.jneurosci.org/content/32/27/9383.abstract


Head, B. P., Hu, Y., Finley, J. C., Saldana, M. D., Bonds, J. A., Miyanohara, A., . . . Patel, P. M. (2011). Neuron-targeted Caveolin-1 Protein Enhances Signaling and Promotes Arborization of Primary Neurons. Journal of Biological Chemistry, 286(38), 33310-33321. doi. 

Hebbeler, S. L., & Sengelaub, D. R. (2003). Development of a sexually dimorphic neuromuscular system in male rats after spinal transection: morphologic changes and implications for estrogen sites of action. Journal of Comparative Neurology, 467(1), 80-96. doi. 

Hebbeler, S. L., Verhovshek, T., & Sengelaub, D. R. (2001). Ovariectomy attenuates dendritic growth in hormone-sensitive spinal motoneurons. Journal of Neurobiology, 48(4), 301-314. doi. 

Hebbeler, S. L., Verhovshek, T., & Sengelaub, D. R. (2002). NMDA receptor blockade inhibits estrogenic support of dendritic growth in a sexually dimorphic rat spinal nucleus. Journal of Comparative Neurology, 142-152. doi. 

Hebbeler, S. L., Verhovshek, T., & Sengelaub, D. R. (2002). N-methyl-D-aspartate receptor blockade inhibits estrogenic support of dendritic growth in a sexually dimorphic rat spinal nucleus. Journal of Comparative Neurology, 451(2), 142-152. doi. 

Hefti, B. J., & Smith, P. H. (2000). Anatomy, Physiology, and Synaptic Responses of Rat Layer V Auditory Cortical Cells and Effects of Intracellular GABAA Blockade. Journal of Neurophysiology, 83(5), 2626-2638. doi. http://jn.physiology.org/cgi/content/abstract/83/5/2626 


Hegedus, B., Hughes, W. F., Garbow, J. R., Gianino, S., Banerjee, D., Kim, K., . . . Gutmann, D. H. (2009). Optic nerve dysfunction in a mouse model of neurofibromatosis-1 optic glioma. Journal of Neuropathology and Experimental Neurology, 68(5), 542-542. doi. 

Heidger, P. M., Dee, F., Consoer, D., Leaven, T., Duncan, J., & Kreiter, C. (2002). Integrated Approach to Teaching and Testing in Histology with Real and Virtual Imaging. The Anatomical Record, 269, 107-112. doi. 

Heilbronner, S. R., & Haber, S. N. (2014). Frontal Cortical and Subcortical Projections Provide a Basis for Segmenting the Cingulum Bundle: Implications for Neuroimaging and Psychiatric Disorders. The Journal of Neuroscience, 34(30), 10041-10054. doi. http://www.jneurosci.org/content/34/30/10041.short


Heilbronner, S. R., Meyer, M. A. A., Choi, E. Y., & Haber, S. N. (2018). How do cortico-striatal projections impact on downstream pallidal circuitry? [journal article]. Brain Structure and Function. doi: 10.1007/s00429-018-1662-9. https://doi.org/10.1007/s00429-018-1662-9


Heilbronner, S. R., Rodriguez-Romaguera, J., Quirk, G. J., Groenewegen, H. J., & Haber, S. N. (2016). Circuit Based Cortico-Striatal Homologies between Rat and Primate. Biological Psychiatry. doi: 10.1016/j.biopsych.2016.05.012. http://dx.doi.org/10.1016/j.biopsych.2016.05.012


Heine, C., Heimrich, B., Vogt, J., Wegner, A., Illes, P., & Franke, H. (2006). P2 receptor-stimulation influences axonal outgrowth in the developing hippocampus in vitro. Neuroscience, 138(1), 303-311. doi. 

Heine, C., Sygnecka, K., Scherf, N., Grohmann, M., Bräsigk, A., & Franke, H. (2015). P2Y1 receptor mediated neuronal fibre outgrowth in organotypic co-cultures. Neuropharmacology, (0). doi: http://dx.doi.org/10.1016/j.neuropharm.2015.02.001. http://www.sciencedirect.com/science/article/pii/S0028390815000477


Heinrichs, S. C., Leite-Morris, K. A., Guy, M. D., Goldberg, L. R., Young, A. J., & Kaplan, G. B. (2013). Dendritic structural plasticity in the basolateral amygdala after fear conditioning and its extinction in mice. Behavioural Brain Research, (0). doi: http://dx.doi.org/10.1016/j.bbr.2013.03.048. http://www.sciencedirect.com/science/article/pii/S0166432813001903


Heistek, T. S., Ruiperez-Alonso, M., Timmerman, A. J., Brussaard, A. B., & Mansvelder, H. D. (2012). α2-containing GABAA receptors expressed in hippocampal region CA3 control fast network oscillations. Journal of Physiology, no-no. doi: 10.1113/jphysiol.2012.243725. http://dx.doi.org/10.1113/jphysiol.2012.243725


Helmeke, C., Ovtscharoff Jr, W., Poeggel, G., & Braun, K. (2001). Juvenile emotional experience alters synaptic inputs on pyramidal neurons in the anterior cingulate cortex. Cerebral Cortex, 11(8), 717-727. doi. 

Helmeke, C., Poeggel, G., & Braun, K. (2001). Differential emotional experience induces elevated spine densities on basal dendrites of pyramidal neurons in the anterior cingulate cortex of Octodon degus. Neuroscience, 104(4), 927-931. doi. 

Helmeke, C., Seidel, K., Poeggel, G., Bredy, T. W., Abraham, A., & Braun, K. (2009). Paternal deprivation during infancy results in dendrite-and time-specific changes of dendritic development and spine formation in the orbitofrontal cortex of the biparental rodent< i> Octodon degus</i>. Neuroscience, 163(3), 790-798. doi. 

Helmstaedter, M., Sakmann, B., & Feldmeyer, D. (2009). L2/3 interneuron groups defined by multiparameter analysis of axonal projection, dendritic geometry, and electrical excitability. Cerebral Cortex, 19(4), 951-962. doi. 

Helmstaedter, M., Sakmann, B., & Feldmeyer, D. (2009). Neuronal correlates of local, lateral, and translaminar inhibition with reference to cortical columns. Cerebral Cortex, 19(4), 926-937. doi. 

Helmstaedter, M., Sakmann, B., & Feldmeyer, D. (2009). The relation between dendritic geometry, electrical excitability, and axonal projections of L2/3 interneurons in rat barrel cortex. Cerebral Cortex, 19(4), 938-950. doi. 

Helmstaedter, M., Staiger, J. F., Sakmann, B., & Feldmeyer, D. (2008). Efficient Recruitment of Layer 2/3 Interneurons by Layer 4 Input in Single Columns of Rat Somatosensory Cortex. Journal of Neuroscience, 28(33), 8273-8284. doi: 10.1523/jneurosci.5701-07.2008. http://www.jneurosci.org/cgi/content/abstract/28/33/8273 


Helton, T. D., Zhao, M., Farris, S., & Dudek, S. M. (2018). Diversity of dendritic morphology and entorhinal cortex synaptic effectiveness in mouse CA2 pyramidal neurons. Hippocampus, 0(ja). doi: doi:10.1002/hipo.23012. https://onlinelibrary.wiley.com/doi/abs/10.1002/hipo.23012


Helwig, M., Hoshino, A., Berridge, C., Lee, S.-N., Lorenzen, N., Otzen, D. E., . . . Lindberg, I. (2012). The neuroendocrine protein 7B2 suppresses the aggregation of neurodegenerative disease-related proteins. Journal of Biological Chemistry. doi: 10.1074/jbc.M112.417071. http://www.jbc.org/content/early/2012/11/21/jbc.M112.417071.abstract


Helyes, Z., Tékus, V., Szentes, N., Pohóczky, K., Botz, B., Kiss, T., . . . Goebel, A. (2019). Transfer of complex regional pain syndrome to mice via human autoantibodies is mediated by interleukin-1–induced mechanisms. Proceedings of the National Academy of Sciences, 201820168. doi: 10.1073/pnas.1820168116. http://www.pnas.org/content/early/2019/06/04/1820168116.abstract


Henckens, M. J. A. G., van der Marel, K., van der Toorn, A., Pillai, A. G., Fernández, G., Dijkhuizen, R. M., & Joëls, M. (2014). Stress-induced alterations in large-scale functional networks of the rodent brain. Neuroimage, (0). doi: http://dx.doi.org/10.1016/j.neuroimage.2014.10.037. http://www.sciencedirect.com/science/article/pii/S1053811914008635


Henderson, B. W., Greathouse, K. M., Ramdas, R., Walker, C. K., Rao, T. C., Bach, S. V., . . . Herskowitz, J. H. (2019). Pharmacologic inhibition of LIMK1 provides dendritic spine resilience against β-amyloid. Science Signaling, 12(587), eaaw9318. doi. https://stke.sciencemag.org/content/12/587/eaaw9318.abstract


Henderson, C., Wijetunge, L., Kinoshita, M. N., Shumway, M., Hammond, R. S., Postma, F. R., . . . Paylor, R. (2012). Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofen. Sci Transl Med, 4(152), 152ra128. doi. 

Henderson, J. M., Carpenter, K., Cartwright, H., & Halliday, G. M. (2000). Loss of thalamic intralaminar nuclei in progressive supranuclear palsy and Parkinson's disease: clinical and therapeutic implications. Brain, 123(7), 1410-1421. doi: 10.1093/brain/123.7.1410. http://brain.oxfordjournals.org/cgi/content/abstract/123/7/1410 


Henderson, Z., Fiddler, G., Saha, S., Boros, A., & Halasy, K. (2004). A parvalbumin-containing, axosomatic synaptic network in the rat medial septum: relevance to rhythmogenesis*. European Journal of Neuroscience, 19(10), 2753-2768. doi: doi:10.1111/j.0953-816X.2004.03399.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.0953-816X.2004.03399.x 


Hendricks, S. J., Brunjes, P. C., & Hill, D. L. (2004). Taste bud cell dynamics during normal and sodium-restricted development. Journal of Comparative Neurology, 472(2), 173-182. doi. 

Hendrickson, E. B., Edgerton, J. R., & Jaeger, D. (2011). The capabilities and limitations of conductance-based compartmental neuron models with reduced branched or unbranched morphologies and active dendrites. Journal of Computational Neuroscience, 30(2), 301-321. doi. 

Hendrickson, E. B., Edgerton, J. R., & Jaeger, D. (2011). The use of automated parameter searches to improve ion channel kinetics for neural modeling. Journal of Computational Neuroscience, 1-18. doi. 

Heng, M. Y., Tallaksen-Greene, S. J., Detloff, P. J., & Albin, R. L. (2007). Longitudinal Evaluation of the Hdh(CAG)150 Knock-In Murine Model of Huntington's Disease. Journal of Neuroscience, 27(34), 8989-8998. doi: 10.1523/jneurosci.1830-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/34/8989 


Henkel, C. K., Fuentes-Santamaria, V., Alvarado, J. C., & Brunso-Bechtold, J. K. (2003). Quantitative measurement of afferent layers in the ferret inferior colliculus: DNLL projections to sublayers. Hearing Research, 177(1-2), 32-42. doi. 

Henkel, C. K., & Gabriele, M. L. (1999). Organization of the disynaptic pathway from the anteroventral cochlear nucleus to the lateral superior olivary nucleus in the ferret. Anatomy and Embryology, 199(2), 149-160. doi. 

Hennou, S., Khalilov, I., Diabira, D., Ben-Ari, Y., & Gozlan, H. (2002). Early sequential formation of functional GABAA and glutamatergic synapses on CA1 interneurons of the rat foetal hippocampus. European Journal of Neuroscience, 16(2), 197-208. doi: doi:10.1046/j.1460-9568.2002.02073.x. http://www.blackwell-synergy.com/doi/abs/10.1046/j.1460-9568.2002.02073.x 


Henny, P., Brown, M. C., Micklem, B., Magill, P., & Bolam, J. P. (2013). Stereological and ultrastructural quantification of the afferent synaptome of individual neurons. Brain Structure and Function, 1-10. doi: 10.1007/s00429-013-0523-9. http://dx.doi.org/10.1007/s00429-013-0523-9


Henny, P., Brown, M. T. C., Northrop, A., Faunes, M., Ungless, M. A., Magill, P. J., & Bolam, J. P. (2012). Structural correlates of heterogeneous in vivo activity of midbrain dopaminergic neurons. Nature Neuroscience. doi. 

Henny, P., & Jones, B. E. (2006). Innervation of orexin/hypocretin neurons by GABAergic, glutamatergic or cholinergic basal forebrain terminals evidenced by immunostaining for presynaptic vesicular transporter and postsynaptic scaffolding proteins. Journal of Comparative Neurology, 499(4), 645-661. doi. 

Henny, P., & Jones, B. E. (2006). Vesicular glutamate (VGlut), GABA (VGAT), and acetylcholine (VACht) transporters in basal forebrain axon terminals innervating the lateral hypothalamus. Journal of Comparative Neurology, 496(4), 453-467. doi. 

Henny, P., & Jones, B. E. (2008). Projections from basal forebrain to prefrontal cortex comprise cholinergic, GABAergic and glutamatergic inputs to pyramidal cells or interneurons. European Journal of Neuroscience, 27(3), 654-670. doi: doi:10.1111/j.1460-9568.2008.06029.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2008.06029.x 


Henriksen, E. J., Colgin, L. L., Barnes, C. A., Witter, M. P., Moser, M. B., & Moser, E. I. (2010). Spatial representation along the proximodistal axis of CA1. Neuron, 68(1), 127-137. doi. 

Henriques, C. F. S., Mateus-Pinheiro, M. M. R., Gaspar, A. R. G., de Carvalho Pinheiro, H. A. R., Duarte, J. F. M., Baptista, F. I. C., . . . dos Reis Vale Gomes, C. A. (2019). Microglia cytoarchitecture in the brain of adenosine A2A receptor knockout mice: brain region and sex specificities. European Journal of Neuroscience, 0(ja). doi: 10.1111/ejn.14561. https://onlinelibrary.wiley.com/doi/abs/10.1111/ejn.14561


Henry, R. A., Hughes, S. M., & Connor, B. (2007). AAV-mediated delivery of BDNF augments neurogenesis in the normal and quinolinic acid-lesioned adult rat brain. European Journal of Neuroscience, 25(12), 3513-3525. doi: doi:10.1111/j.1460-9568.2007.05625.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05625.x 


Henry, S. M., Held, J. M., Vietje, B. P., & Wells, J. (1995). The role of somatosensory information in a constrained locomotor task. Experimental Neurology, 131(2), 251-265. doi. 

Henschke, J. U., Oelschlegel, A. M., Angenstein, F., Ohl, F. W., Goldschmidt, J., Kanold, P. O., & Budinger, E. (2017). Early sensory experience influences the development of multisensory thalamocortical and intracortical connections of primary sensory cortices. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-017-1549-1. https://doi.org/10.1007/s00429-017-1549-1


Hequembourg, S., & Liberman, M. C. (2001). Spiral ligament pathology: a major aspect of age-related cochlear degeneration in C57BL/6 mice. Jaro-Journal of the Association for Research in Otolaryngology, 2(2), 118-129. doi. 

Hercher, C., Canetti, L., Turecki, G., & Mechawar, N. (2010). Anterior cingulate pyramidal neurons display altered dendritic branching in depressed suicides. Journal of Psychiatric Research, 44(5), 286-293. doi. 

Hercher, C., Parent, M., Flores, C., Canetti, L., Turecki, G., & Mechawar, N. (2009). Alcohol dependence-related increase of glial cell density in the anterior cingulate cortex of suicide completers. Journal of Psychiatry and Neuroscience, 34, 281 - 288. doi. 

Herfst, L., Burgalossi, A., Haskic, K., Tukker, J. J., Schmidt, M., & Brecht, M. (2012). Friction-Based Stabilization of Juxtacellular Recordings in Freely-Moving Rats. Journal of Neurophysiology. doi: 10.1152/jn.00910.2011. http://jn.physiology.org/content/early/2012/04/13/jn.00910.2011.abstract


Hernandez, M. X., Jiang, S., Cole, T. A., Chu, S.-H., Fonseca, M. I., Fang, M. J., . . . Tenner, A. J. (2017). Prevention of C5aR1 signaling delays microglial inflammatory polarization, favors clearance pathways and suppresses cognitive loss. [journal article]. Molecular neurodegeneration, 12(1), 66. doi: 10.1186/s13024-017-0210-z. https://doi.org/10.1186/s13024-017-0210-z


Herring, A., Münster, Y., Metzdorf, J., Bolczek, B., Krüssel, S., Krieter, D., . . . Keyvani, K. (2016). Late running is not too late against Alzheimer's pathology. Neurobiology of Disease, 94, 44-54. doi: http://dx.doi.org/10.1016/j.nbd.2016.06.003. http://www.sciencedirect.com/science/article/pii/S096999611630136X


Herrmann, J. E., Imura, T., Song, B., Qi, J., Ao, Y., Nguyen, T. K., . . . Sofroniew, M. V. (2008). STAT3 is a Critical Regulator of Astrogliosis and Scar Formation after Spinal Cord Injury. Journal of Neuroscience, 28(28), 7231-7243. doi: 10.1523/jneurosci.1709-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/28/7231 


Hester, M. S., & Danzer, S. C. (2013). Accumulation of Abnormal Adult-Generated Hippocampal Granule Cells Predicts Seizure Frequency and Severity. Journal of Neuroscience, 33(21), 8926-8936. doi: 10.1523/jneurosci.5161-12.2013. http://www.jneurosci.org/content/33/21/8926.abstract


Hester, M. S., Hosford, B. E., Santos, V. R., Singh, S. P., Rolle, I., LaSarge, C. L., . . . Danzer, S. C. (2016). Impact of rapamycin on status epilepticus induced hippocampal pathology and weight gain. Experimental Neurology. doi: http://dx.doi.org/10.1016/j.expneurol.2016.03.015. http://www.sciencedirect.com/science/article/pii/S0014488616300589


Heukelum, S. V., Geers, F. E., Tulva, K., van Dulm, S., Beckmann, C. F., Buitelaar, J. K., . . . França, A. S. C. (2021). Structural Degradation in Midcingulate Cortex Is Associated with Pathological Aggression in Mice. Brain Sciences, 11(7). doi: 10.3390/brainsci11070868. 

Heun-Johnson, H., & Levitt, P. (2018). Differential impact of Met receptor gene interaction with early-life stress on neuronal morphology and behavior in mice. Neurobiology of Stress, 8, 10-20. doi: https://doi.org/10.1016/j.ynstr.2017.11.003. https://www.sciencedirect.com/science/article/pii/S2352289517300164


Heyden, A., Angenstein, F., Sallaz, M., Seidenbecher, C., & Montag, D. (2008). Abnormal axonal guidance and brain anatomy in mouse mutants for the cell recognition molecules close homolog of L1 and NgCAM-related cell adhesion molecule. Neuroscience, 155(1), 221-233. doi. 

Heyden, A., Ionescu, M. C. S., Romorini, S., Kracht, B., Ghiglieri, V., Calabresi, P., . . . Gundelfinger, E. D. (2011). Hippocampal enlargement in Bassoon-mutant mice is associated with enhanced neurogenesis, reduced apoptosis, and abnormal BDNF levels. Cell and Tissue Research, 1-16. doi. 

Heydendael, W., Sharma, K., Iyer, V., Luz, S., Piel, D., Beck, S., & Bhatnagar, S. (2011). Orexins/Hypocretins Act in the Posterior Paraventricular Thalamic Nucleus During Repeated Stress to Regulate Facilitation to Novel Stress. Endocrinology, 152(12), 4738-4752. doi. 

Heysieattalab, S., & Sadeghi, L. (2021). Dynamic structural neuroplasticity during and after epileptogenesis in a pilocarpine rat model of epilepsy. Acta Epileptologica, 3(1), 3. doi: 10.1186/s42494-020-00037-7. https://doi.org/10.1186/s42494-020-00037-7


Hickey, W. (1991). Migration of hematogenous cells through the blood-brain barrier and the initiation of CNS inflammation. Brain Pathology, 1, 97 - 105. doi. 

Higo, S., Hojo, Y., Ishii, H., Komatsuzaki, Y., Ooishi, Y., Murakami, G., . . . others. (2011). Endogenous synthesis of corticosteroids in the hippocampus. PLoS ONE, 6(7), e21631-e21631. doi. 

Hilal, M. L., Moreau, M. M., Racca, C., Pinheiro, V. L., Piguel, N. H., Santoni, M.-J., . . . Sans, N. (2016). Activity-Dependent Neuroplasticity Induced by an Enriched Environment Reverses Cognitive Deficits in Scribble Deficient Mouse. Cerebral Cortex. doi: 10.1093/cercor/bhw333. http://cercor.oxfordjournals.org/content/early/2016/10/26/cercor.bhw333....


Hill, A. A. V., & Cattaert, D. (2008). Recruitment in a heterogeneous population of motor neurons that innervates the depressor muscle of the crayfish walking leg muscle. Journal of Experimental Biology, 211(4), 613-629. doi: 10.1242/jeb.006270. http://jeb.biologists.org/cgi/content/abstract/211/4/613 


Hill, J. J., Kolluri, N., Hashimoto, T., Wu, Q., Sampson, A. R., Monteggia, L. M., & Lewis, D. A. (2005). Analysis of pyramidal neuron morphology in an inducible knockout of brain-derived neurotrophic factor. Biological Psychiatry, 57(8), 932-934. doi. 

Hill, J. L., Hardy, N. F., Jimenez, D. V., Maynard, K. R., Kardian, A. S., Pollock, C. J., . . . Martinowich, K. (2016). Loss of promoter IV-driven BDNF expression impacts oscillatory activity during sleep, sensory information processing and fear regulation. [Original Article]. Transl Psychiatry, 6, e873. doi: 10.1038/tp.2016.153. http://dx.doi.org/10.1038/tp.2016.153


Hill, M. N., Hillard, C. J., & McEwen, B. S. (2011). Alterations in Corticolimbic Dendritic Morphology and Emotional Behavior in Cannabinoid CB1 Receptor–Deficient Mice Parallel the Effects of Chronic Stress. Cerebral Cortex. doi: 10.1093/cercor/bhq280. http://cercor.oxfordjournals.org/content/early/2011/01/24/cercor.bhq280....


Hill, M. N., Kumar, S. A., Filipski, S. B., Iverson, M., Stuhr, K. L., Keith, J. M., . . . McEwen, B. S. (2012). Disruption of fatty acid amide hydrolase activity prevents the effects of chronic stress on anxiety and amygdalar microstructure. Molecular Psychiatry. doi: http://www.nature.com/mp/journal/vaop/ncurrent/suppinfo/mp201290s1.html. http://dx.doi.org/10.1038/mp.2012.90


Hill, R. L., Zhang, Y. P., Burke, D. A., DeVries, W. H., Zhang, Y., Magnuson, D. S. K., . . . Shields, C. B. (2009). Anatomical and functional outcomes following a precise, graded, dorsal laceration spinal cord injury in C57BL/6 mice. Journal of Neurotrauma, 26(1), 1-15. doi. 

Hillen, H., Barghorn, S., Striebinger, A., Labkovsky, B., Muller, R., Nimmrich, V., . . . Ebert, U. (2010). Generation and Therapeutic Efficacy of Highly Oligomer-Specific β-Amyloid Antibodies. Journal of Neuroscience, 30(31), 10369-10379. doi: 10.1523/jneurosci.5721-09.2010. http://www.jneurosci.org/cgi/content/abstract/30/31/10369 


Hilton, G. D., Ndubuizu, A., Nunez, J. L., & McCarthy, M. M. (2005). Simultaneous glutamate and GABAA receptor agonist administration increases calbindin levels and prevents hippocampal damage induced by either agent alone in a model of perinatal brain injury. Developmental Brain Research, 159(2), 99-111. doi. 

Hilton, G. D., Ndubuizu, A. N., & McCarthy, M. M. (2004). Neuroprotective effects of estradiol in newborn female rat hippocampus. Developmental Brain Research, 150(2), 191-198. doi. 

Hilton, G. D., Nuez, J. L., & McCarthy, M. M. (2003). Sex differences in response to kainic acid and estradiol in the hippocampus of newborn rats. Neuroscience, 116(2), 383-391. doi. 

Hilton, G. D., Nunez, J. L., Bambrick, L., Thompson, S. M., & McCarthy, M. M. (2006). Glutamate-mediated excitotoxicity in neonatal hippocampal neurons is mediated by mGluR-induced release of Ca++ from intracellular stores and is prevented by estradiol. European Journal of Neuroscience, 24(11), 3008-3016. doi: doi:10.1111/j.1460-9568.2006.05189.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2006.05189.x 


Hilz, M. J., Axelrod, F. B., Bickel, A., Stemper, B., Brys, M., Wendelschafer-Crabb, G., & Kennedy, W. R. (2004). Assessing function and pathology in familial dysautonomia: assessment of temperature perception, sweating and cutaneous innervation. Brain, 127(9), 2090-2098. doi: 10.1093/brain/awh235. http://brain.oxfordjournals.org/cgi/content/abstract/127/9/2090 


Hindman, H. B., DeMagistris, M., Callan, C., McDaniel, T., Bubel, T., & Huxlin, K. R. (2019). Impact of topical anti-fibrotics on corneal nerve regeneration in vivo. Experimental Eye Research, 181, 49-60. doi: https://doi.org/10.1016/j.exer.2019.01.017. http://www.sciencedirect.com/science/article/pii/S001448351830561X


Hines, M. L., Davison, A. P., & Muller, E. (2009). NEURON and Python. Frontiers in Neuroinformatics, 3. doi. 

Hinova-Palova, D., Kotov, G., Landzhov, B., Edelstein, L., Iliev, A., Stanchev, S., . . . Paloff, A. (2019). Cytoarchitecture of the dorsal claustrum of the cat: a quantitative Golgi study. [journal article]. Journal of Molecular Histology. doi: 10.1007/s10735-019-09839-7. https://doi.org/10.1007/s10735-019-09839-7


Hinwood, M., Tynan, R. J., Charnley, J. L., Beynon, S. B., Day, T. A., & Walker, F. R. (2012). Chronic Stress Induced Remodeling of the Prefrontal Cortex: Structural Re-Organization of Microglia and the Inhibitory Effect of Minocycline. Cerebral Cortex. doi: 10.1093/cercor/bhs151. http://cercor.oxfordjournals.org/content/early/2012/06/16/cercor.bhs151....


Hioki, H. (2014). Compartmental organization of synaptic inputs to parvalbumin-expressing GABAergic neurons in mouse primary somatosensory cortex. Anatomical Science International, 1-15. doi: 10.1007/s12565-014-0264-8. http://dx.doi.org/10.1007/s12565-014-0264-8


Hirai, Y., Morishima, M., Karube, F., & Kawaguchi, Y. (2012). Specialized Cortical Subnetworks Differentially Connect Frontal Cortex to Parahippocampal Areas. Journal of Neuroscience, 32(5), 1898-1913. doi: 10.1523/jneurosci.2810-11.2012. http://www.jneurosci.org/content/32/5/1898.abstract


Hirayama, T., Tarusawa, E., Yoshimura, Y., Galjart, N., & Yagi, T. (2012). CTCF Is Required for Neural Development and Stochastic Expression of Clustered Pcdh Genes in Neurons. Cell Reports, (0). doi: 10.1016/j.celrep.2012.06.014. http://www.sciencedirect.com/science/article/pii/S221112471200174X


Hirose, K., Discolo, C. M., Keasler, J. R., & Ransohoff, R. (2005). Mononuclear phagocytes migrate into the murine cochlea after acoustic trauma. Journal of Comparative Neurology, 489(2), 180-194. doi. 

Hirose, K., Li, S.-Z., Ohlemiller, K., & Ransohoff, R. (2014). Systemic Lipopolysaccharide Induces Cochlear Inflammation and Exacerbates the Synergistic Ototoxicity of Kanamycin and Furosemide. Journal of the Association for Research in Otolaryngology, 1-16. doi: 10.1007/s10162-014-0458-8. http://dx.doi.org/10.1007/s10162-014-0458-8


Hirose, K., & Liberman, M. C. (2003). Lateral wall histopathology and endocochlear potential in the noise-damaged mouse cochlea. Jaro-Journal of the Association for Research in Otolaryngology, 4(3), 339-352. doi. 

Hirose, K., & Sato, E. (2011). Comparative analysis of combination kanamycin-furosemide versus kanamycin alone in the mouse cochlea. Hearing Research, 272(1), 108-116. doi. 

Hirota, Y., Sawada, M., Kida, Y. S., Huang, S., Yamada, O., Sakaguchi, M., . . . Sawamoto, K. (2012). Roles of Planar Cell Polarity Signaling in Maturation of Neuronal Precursor Cells in the Postnatal Mouse Olfactory Bulb. Stem Cells. doi. 

Hirsch, E., Pozzato, M., Vercelli, A., Barberis, L., Azzolino, O., Russo, C., . . . Altruda, F. (2002). Defective Dendrite Elongation but Normal Fertility in Mice Lacking the Rho-Like GTPase Activator Dbl. Molecular Cell Biology, 22(9), 3140-3148. doi. 

Hirsch, J. A., Alonso, J. M., Reid, R. C., & Martinez, L. M. (1998). Synaptic Integration in Striate Cortical Simple Cells. Journal of Neuroscience, 18, 9517-9528. doi. 

Hirsch, J. A., Gallagher, C. A., Alonso, J. M., & Martinez, L. M. (1998). Ascending Projections of Simple and Complex Cells in Layer 6 of the Cat Striate Cortex. Journal of Neuroscience, 18(19), 8086-8094. doi. 

Hirsch, M., Knight, J., Tobita, M., Soltys, J., Panitch, H., & Mao-Draayer, Y. (2009). The effect of interferon-β on mouse neural progenitor cell survival and differentiation. Biochemical and Biophysical Research Communications, 388(2), 181-186. doi. 

Ho, S. Y., Chao, C. Y., Huang, H. L., Chiu, T. W., Charoenkwan, P., & Hwang, E. (2011). NeurphologyJ: An automatic neuronal morphology quantification method and its application in pharmacological discovery. BMC bioinformatics, 12(1), 230-230. doi. 

Hoard, J. L., Hoover, D. B., & Wondergem, R. (2007). Phenotypic properties of adult mouse intrinsic cardiac neurons maintained in culture. American Journal of Physiology - Cell Physiology, 293(6), C1875-1883. doi: 10.1152/ajpcell.00113.2007. http://ajpcell.physiology.org/cgi/content/abstract/293/6/C1875 


Hockly, E., Cordery, P. M., Woodman, B., Mahal, A., Van Dellen, A., Blakemore, C., . . . Bates, G. P. (2002). Environmental enrichment slows disease progression in R6/2 Huntington's disease mice. Annals of Neurology, 51(2), 235-242. doi. 

Hodde, D., Gerardo-Nava, J., Wöhlk, V., Weinandy, S., Jockenhövel, S., Kriebel, A., . . . Brook, G. A. (2015). Characterisation of cell-substrate interactions between Schwann cells and three-dimensional fibrin hydrogels containing orientated nanofibre topographical cues. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.13026. http://dx.doi.org/10.1111/ejn.13026


Hodges, T. E., Louth, E. L., Bailey, C. D. C., & McCormick, C. M. (2018). Adolescent social instability stress alters markers of synaptic plasticity and dendritic structure in the medial amygdala and lateral septum in male rats. [journal article]. Brain Structure and Function. doi: 10.1007/s00429-018-1789-8. https://doi.org/10.1007/s00429-018-1789-8


Hodgson, J. A., Finni, T., Lai, A. M., Edgerton, V. R., & Sinha, S. (2006). Influence of structure on the tissue dynamics of the human soleus muscle observed in MRI studies during isometric contractions. Journal of Morphology, 267(5), 584-601. doi. 

Hoe, H.-S., Lee, K. J., Carney, R. S. E., Lee, J., Markova, A., Lee, J.-Y., . . . Rebeck, G. W. (2009). Interaction of Reelin with Amyloid Precursor Protein Promotes Neurite Outgrowth. Journal of Neuroscience, 29(23), 7459-7473. doi: 10.1523/jneurosci.4872-08.2009. http://www.jneurosci.org/cgi/content/abstract/29/23/7459 


Hoebeek, F. E., Khosrovani, S., Witter, L., & De Zeeuw, C. I. (2008). Purkinje cell input to cerebellar nuclei in tottering: ultrastructure and physiology. The Cerebellum, 7(4), 547-558. doi. 

Hoekstra, J. G., Cook, T. J., Stewart, T., Mattison, H., Dreisbach, M. T., Hoffer, Z. S., & Zhang, J. (2014). Astrocytic Dynamin-Like Protein 1 Regulates Neuronal Protection against Excitotoxicity in Parkinson Disease. The American journal of pathology, (0). doi: http://dx.doi.org/10.1016/j.ajpath.2014.10.022. http://www.sciencedirect.com/science/article/pii/S0002944014006555


Hoeltje, M., Djalali, S., Hofmann, F., Muenster-Wandowski, A., Hendrix, S., Boato, F., . . . others. (2009). A 29-amino acid fragment of Clostridium botulinum C3 protein enhances neuronal outgrowth, connectivity, and reinnervation. FASEB Journal, 23(4), 1115-1126. doi. 

Hoffman, E. J., Mintz, C. D., Wang, S., McNickle, D. G., Salton, S. R. J., & Benson, D. L. (2008). Effects of ethanol on axon outgrowth and branching in developing rat cortical neurons. Neuroscience, 157(3), 556-565. doi. 

Hoffman, J. F., Wright, C. L., & McCarthy, M. M. (2016). A Critical Period in Purkinje Cell Development Is Mediated by Local Estradiol Synthesis, Disrupted by Inflammation, and Has Enduring Consequences Only for Males. The Journal of Neuroscience, 36(39), 10039-10049. doi. http://www.jneurosci.org/content/36/39/10039.short


Hoffman, L. F., Choy, K. R., Sultemeier, D. R., & Simmons, D. D. (2018). Oncomodulin Expression Reveals New Insights into the Cellular Organization of the Murine Utricle Striola. [journal article]. Journal of the Association for Research in Otolaryngology. doi: 10.1007/s10162-017-0652-6. https://doi.org/10.1007/s10162-017-0652-6


Hoffmann, C. J., Hohberg, M., Chlench, S., Maroski, J., Drab, M., Siegel, G., . . . Zakrzewicz, A. (2011). Suppression of zinc finger protein 580 by high oxLDL/LDL-ratios is followed by enhanced expression of endothelial IL-8. Atherosclerosis. doi. 

Hoffmann, J. H. O., Meyer, H. S., Schmitt, A. C., Straehle, J., Weitbrecht, T., Sakmann, B., & Helmstaedter, M. (2015). Synaptic Conductance Estimates of the Connection Between Local Inhibitor Interneurons and Pyramidal Neurons in Layer 2/3 of a Cortical Column. Cerebral Cortex. doi: 10.1093/cercor/bhv039. http://cercor.oxfordjournals.org/content/early/2015/03/10/cercor.bhv039....


Hoffmann, K., Sivukhina, E., Potschka, H., Schachner, M., Löscher, W., & Dityatev, A. (2009). Retarded kindling progression in mice deficient in the extracellular matrix glycoprotein tenascin-R. Epilepsia, 50(4), 859-869. doi. 

Höfling, C., Indrischek, H., Höpcke, T., Waniek, A., Cynis, H., Koch, B., . . . Hartlage-Rübsamen, M. (2014). Mouse strain and brain region-specific expression of the glutaminyl cyclases QC and isoQC. International Journal of Developmental Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.ijdevneu.2014.05.008. http://www.sciencedirect.com/science/article/pii/S0736574814000781


Hofmann, G. C., Hasser, E. M., & Kline, D. D. (2021). Unilateral vagotomy alters astrocyte and microglial morphology in the nucleus tractus solitarii of the rat. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. doi: 10.1152/ajpregu.00019.2021. https://doi.org/10.1152/ajpregu.00019.2021


Hogan, M. K., Kovalycsik, T., Sun, Q., Rajagopalan, S., & Nelson, R. J. (2015). Combined Effects of Exposure to Dim Light at Night and Fine Particulate Matter on C3H/HeNHsd Mice. Behavioural Brain Research. doi: http://dx.doi.org/10.1016/j.bbr.2015.07.033. http://www.sciencedirect.com/science/article/pii/S0166432815301042


Hohberg, M., Knöchel, J., Hoffmann, C. J., Chlench, S., Wunderlich, W., Alter, A., . . . Zakrzewicz, A. (2011). Expression of ADAMTS1 in endothelial cells is induced by shear stress and suppressed in sprouting capillaries. Journal of Cellular Physiology, 226(2), 350-361. doi: 10.1002/jcp.22340. http://dx.doi.org/10.1002/jcp.22340


Höistad, M., & Barbas, H. (2008). Sequence of information processing for emotions through pathways linking temporal and insular cortices with the amygdala. Neuroimage, 40(3), 1016-1033. doi. 

Hojo, Y., Higo, S., Kawato, S., Hatanaka, Y., Ooishi, Y., Murakami, G., . . . others. (2011). Frontiers: Hippocampal Synthesis of Sex Steroids and Corticosteroids: Essential for Modulation of Synaptic Plasticity. Frontiers in Neuroendocrine Science, 2. doi. 

Hojo, Y., Munetomo, A., Mukai, H., Ikeda, M., Sato, R., Hatanaka, Y., . . . Kawato, S. (2015). Estradiol rapidly modulates spinogenesis in hippocampal dentate gyrus: Involvement of kinase networks. Hormones and Behavior, (0). doi: http://dx.doi.org/10.1016/j.yhbeh.2015.06.008. http://www.sciencedirect.com/science/article/pii/S0018506X15001178


Holden, J. E., Farah, E. N., & Jeong, Y. (2005). Stimulation of the lateral hypothalamus produces antinociception mediated by 5-HT1A, 5-HT1B and 5-HT3 receptors in the rat spinal cord dorsal horn. Neuroscience, 135(4), 1255-1268. doi. 

Holden, J. E., & Naleway, E. (2001). Microinjection of carbachol in the lateral hypothalamus produces opposing actions on nociception mediated by α 1-and α 2-adrenoceptors. Brain Research, 911(1), 27-36. doi. 

Holden, J. E., & Pizzi, J. A. (2008). Lateral hypothalamic-induced antinociception may be mediated by a substance P connection with the rostral ventromedial medulla. Brain Research, 1214, 40-49. doi. 

Holden, J. E., Pizzi, J. A., & Jeong, Y. (2009). An NK1 receptor antagonist microinjected into the periaqueductal gray blocks lateral hypothalamic-induced antinociception in rats. Neuroscience Letters, 453(2), 115-119. doi. 

Holden, J. E., Van Poppel, A. Y., & Thomas, S. (2002). Antinociception from lateral hypothalamic stimulation may be mediated by NK1 receptors in the A7 catecholamine cell group in rat. Brain Research, 953(1-2), 195-204. doi. 

Holden, J. E., Wang, E., Moes, J. R., Wagner, M., Maduko, A., & Jeong, Y. (2014). Differences in carbachol dose, pain condition, and sex following lateral hypothalamic stimulation. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2014.04.020. http://www.sciencedirect.com/science/article/pii/S0306452214003157


Holder, M. K., Hadjimarkou, M. M., Zup, S. L., Blutstein, T., Benham, R. S., McCarthy, M. M., & Mong, J. A. (2010). Methamphetamine facilitates female sexual behavior and enhances neuronal activation in the medial amygdala and ventromedial nucleus of the hypothalamus. Psychoneuroendocrinology, 35(2), 197-208. doi. 

Holder, M. K., Veichweg, S. S., & Mong, J. A. (2014). Methamphetamine-Enhanced Female Sexual Motivation is Dependent on Dopamine and Progesterone Signaling in the Medial Amygdala. Hormones and Behavior, (0). doi: http://dx.doi.org/10.1016/j.yhbeh.2014.10.004. http://www.sciencedirect.com/science/article/pii/S0018506X14002165


Holderith, N., Lorincz, A., Katona, G., Rozsa, B., Kulik, A., Watanabe, M., & Nusser, Z. (2012). Release probability of hippocampal glutamatergic terminals scales with the size of the active zone. [10.1038/nn.3137]. Nature Neuroscience, advance online publication. doi: http://www.nature.com/neuro/journal/vaop/ncurrent/abs/nn.3137.html#suppl.... http://dx.doi.org/10.1038/nn.3137


Holland, T. L., & Soderstrom, K. (2017). Chronic CB1 cannabinoid receptor antagonism persistently increases dendritic spine densities in brain regions important to zebra finch vocal learning and production in an antidepressant-sensitive manner. Brain Research, 1672, 1-9. doi: https://doi.org/10.1016/j.brainres.2017.07.015. http://www.sciencedirect.com/science/article/pii/S0006899317303141


Holler, S., Köstinger, G., Martin, K. A. C., Schuhknecht, G. F. P., & Stratford, K. J. (2021). Structure and function of a neocortical synapse. Nature. doi: 10.1038/s41586-020-03134-2. https://doi.org/10.1038/s41586-020-03134-2


Holliday, E. D., Nucero, P., Kutlu, M. G., Oliver, C., Connelly, K. L., Gould, T. J., & Unterwald, E. M. (2016). Long-term effects of chronic nicotine on emotional and cognitive behaviors and hippocampus cell morphology in mice: comparisons of adult and adolescent nicotine exposure. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.13398. http://dx.doi.org/10.1111/ejn.13398


Hollis, E. R., Jamshidi, P., Löw, K., Blesch, A., & Tuszynski, M. H. (2009). Induction of corticospinal regeneration by lentiviral trkB-induced Erk activation. Proceedings of the National Academy of Sciences, 106(17), 7215-7215. doi. 

Holloway, B. B., Viar, K. E., Stornetta, R. L., & Guyenet, P. G. (2015). The retrotrapezoid nucleus stimulates breathing by releasing glutamate in adult conscious mice. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.12996. http://dx.doi.org/10.1111/ejn.12996


Holmes, G. M., Browning, K. N., Babic, T., Fortna, S. R., Coleman, F. H., & Travagli, R. A. (2013). Vagal afferent fibres determine the oxytocin-induced modulation of gastric tone. The Journal of Physiology, 591(12), 3081-3100. doi: doi:10.1113/jphysiol.2013.253732. https://physoc.onlinelibrary.wiley.com/doi/abs/10.1113/jphysiol.2013.253732


Holmes, T. J., & O'connor, N. J. (2000). Blind deconvolution of 3D transmitted light brightfield micrographs. Journal of Microscopy, 200(2), 114. doi. 

Holmes, W. R., Huwe, J. A., Williams, B., Rowe, M. H., & Peterson, E. H. (2017). Models of utricular bouton afferents: Role of afferent-hair cell connectivity in determining spike train regularity. [10.1152/jn.00895.2016]. Journal of Neurophysiology. doi. http://jn.physiology.org/content/early/2017/02/10/jn.00895.2016.abstract


Höltje, M., Djalali, S., Hofmann, F., Münster-Wandowski, A., Hendrix, S., Boato, F., . . . Ahnert-Hilger, G. (2009). A 29-amino acid fragment of Clostridium botulinum C3 protein enhances neuronal outgrowth, connectivity, and reinnervation. The FASEB journal, 23(4), 1115-1126. doi: 10.1096/fj.08-116855. http://www.fasebj.org/content/23/4/1115.abstract


Holtje, M., Hoffmann, A., Hofmann, F., Mucke, C., Grosse, G., Van Rooijen, N., . . . Ahnert-Hilger, G. (2005). Role of Rho GTPase in astrocyte morphology and migratory response during in vitro wound healing. Journal of Neurochemistry, 95(5), 1237-1248. doi: doi:10.1111/j.1471-4159.2005.03443.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1471-4159.2005.03443.x 


Holtmaat, A., Wilbrecht, L., Knott, G. W., Welker, E., & Svoboda, K. (2006). Experience-dependent and cell-type-specific spine growth in the neocortex. Nature, 441, 979-983. doi. 

Homberg, J. R., Olivier, J. D. A., Blom, T., Arentsen, T., van Brunschot, C., Schipper, P., . . . Reneman, L. (2011). Fluoxetine exerts age-dependent effects on behavior and amygdala neuroplasticity in the rat. PLoS ONE, 6(1), e16646-e16646. doi. 

Honda, C. N. (1995). Differential distribution of calbindin-D28k and parvalbumin in somatic and visceral sensory neurons. Neuroscience, 68(3), 883-892. doi. 

Honda, Y., & Ishizuka, N. (2004). Organization of Connectivity of the Rat Presubiculum: I. Efferent Projections to the Medial Entorhinal Cortex. Journal of Comparative Neurology, 473, 463-484. doi. 

Honda, Y., & Ishizuka, N. (2014). Topographic distribution of cortical projection cells in the rat subiculum. Neuroscience Research, (0). doi: http://dx.doi.org/10.1016/j.neures.2014.11.011. http://www.sciencedirect.com/science/article/pii/S0168010214003204


Honda, Y., Sasaki, H., Umitsu, Y., & Ishizuka, N. (2012). Zonal distribution of perforant path cells in layer III of the entorhinal area projecting to CA1 and subiculum in the rat. Neuroscience Research, (0). doi: 10.1016/j.neures.2012.10.005. http://www.sciencedirect.com/science/article/pii/S016801021200199X


Honda, Y., & Shibata, H. (2017). Organizational connectivity among the CA1, subiculum, presubiculum, and entorhinal cortex in the rabbit. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24297. http://dx.doi.org/10.1002/cne.24297


Honda, Y., Umitsu, Y., & Ishizuka, N. (2008). Organization of connectivity of the rat presubiculum: II. Associational and commissural connections. Journal of Comparative Neurology, 506(4), 640-658. doi. 

Hönigsperger, C., Marosi, M., Murphy, R., & Storm, J. F. (2014). Dorso-ventral differences in Kv7/M-current and its impact on resonance, temporal summation, and excitability in rat hippocampal pyramidal cells. The Journal of Physiology, n/a-n/a. doi: 10.1113/jphysiol.2014.280826. http://dx.doi.org/10.1113/jphysiol.2014.280826


Hood, J. E., Jenkins, J. W., Milatovic, D., Rongzhu, L., & Aschner, M. (2010). Mefloquine induces oxidative stress and neurodegeneration in primary rat cortical neurons. Neurotoxicology, 31(5), 518-523. doi. 

Hook, M., Woller, S., Bancroft, E., Aceves, M., Funk, M. K., Hartman, J., & Garraway, S. M. (2016). Neurobiological effects of Morphine following Spinal Cord Injury. Journal of Neurotrauma. doi: 10.1089/neu.2016.4507. http://dx.doi.org/10.1089/neu.2016.4507


Hooks, B. M., Hires, S. A., Zhang, Y. X., Huber, D., Petreanu, L., Svoboda, K., & Shepherd, G. M. G. (2011). Laminar analysis of excitatory local circuits in vibrissal motor and sensory cortical areas. PLoS Biology, 9(1), e1000572-e1000572. doi. 

Hooks, B. M., Papale, A. E., Paletzki, R. F., Feroze, M. W., Eastwood, B. S., Couey, J. J., . . . Gerfen, C. R. (2018). Topographic precision in sensory and motor corticostriatal projections varies across cell type and cortical area. Nature Communications, 9(1), 3549. doi: 10.1038/s41467-018-05780-7. https://doi.org/10.1038/s41467-018-05780-7


Horie, S., Kiyokage, E., Hayashi, S., Inoue, K., Sohn, J., Hioki, H., . . . Toida, K. (2020). Structural basis for noradrenergic regulation of neural circuits in the mouse olfactory bulb. [https://doi.org/10.1002/cne.25085]. Journal of Comparative Neurology, n/a(n/a). doi: https://doi.org/10.1002/cne.25085. https://doi.org/10.1002/cne.25085


Horjales-Araujo, E., Hellysaz, A., & Broberger, C. (2014). Lateral hypothalamic thyrotropin-releasing hormone neurons: Distribution and relationship to histochemically defined cell populations in the rat. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2014.06.043. http://www.sciencedirect.com/science/article/pii/S0306452214005284


Hormigo, S., Gómez-Nieto, R., Castellano, O., Herrero-Turrión, M. J., López, D., & Anchieta de Castro e Horta-Júnior, J. (2014). The noradrenergic projection from the locus coeruleus to the cochlear root neurons in rats. Brain Structure and Function, 1-20. doi: 10.1007/s00429-014-0739-3. http://dx.doi.org/10.1007/s00429-014-0739-3


Hormigo, S., Vega-Flores, G., & Castro-Alamancos, M. A. (2016). Basal Ganglia Output Controls Active Avoidance Behavior. The Journal of Neuroscience, 36(40), 10274-10284. doi. http://www.jneurosci.org/content/36/40/10274.short


Hormigo, S., Vega-Flores, G., Rovira, V., & Castro-Alamancos, M. A. (2019). Circuits that mediate expression of signaled active avoidance converge in the pedunculopontine tegmentum. The Journal of Neuroscience, 0049-0019. doi: 10.1523/jneurosci.0049-19.2019. http://www.jneurosci.org/content/early/2019/03/29/JNEUROSCI.0049-19.2019...


Horn, Katherine E., Glasgow, Stephen D., Gobert, D., Bull, S.-J., Luk, T., Girgis, J., . . . Kennedy, Timothy E. (2013). DCC Expression by Neurons Regulates Synaptic Plasticity in the Adult Brain. Cell Reports, (0). doi: http://dx.doi.org/10.1016/j.celrep.2012.12.005. http://www.sciencedirect.com/science/article/pii/S2211124712004299


Horn, K. E., Xu, B., Gobert, D., Hamam, B. N., Thompson, K. M., Wu, C.-L., . . . Kennedy, T. E. (2012). Receptor protein tyrosine phosphatase sigma regulates synapse structure, function and plasticity. Journal of Neurochemistry. doi: 10.1111/j.1471-4159.2012.07762.x. http://dx.doi.org/10.1111/j.1471-4159.2012.07762.x


Hornfeld, S. H., Terkel, J., & Barnea, A. (2010). Neurons recruited in the nidopallium caudale, following changes in social environment, derive from the same original population. Behavioural Brain Research, 208(2), 643-645. doi. 

Hornung, J. P. (2003). The human raphe nuclei and the serotonergic system. Journal of Chemical Neuroanatomy, 26(4), 331-343. doi. 

Horowitz, J., Nagai, M., Desai, T., Pytte, C. L., & Harding, C. (2015). Exposure to the mold Stachybotrys alters microglial morphology differentially in CA1 and CA2-3 of the dorsomedial hippocampus. Brain, Behavior, and Immunity, 49, Supplement, e32. doi: http://dx.doi.org/10.1016/j.bbi.2015.06.127. http://www.sciencedirect.com/science/article/pii/S088915911500344X


Horowitz, P. M., Patterson, K. R., Guillozet-Bongaarts, A. L., Reynolds, M. R., Carroll, C. A., Weintraub, S. T., . . . Binder, L. I. (2004). Early N-Terminal Changes and Caspase-6 Cleavage of Tau in Alzheimer's Disease. Journal of Neuroscience, 24(36), 7895-7902. doi: 10.1523/jneurosci.1988-04.2004. http://www.jneurosci.org/cgi/content/abstract/24/36/7895 


Horváth, Á., Tékus, V., Bencze, N., Szentes, N., Scheich, B., Bölcskei, K., . . . Helyes, Z. (2018). Analgesic effects of the novel semicarbazide-sensitive amine oxidase inhibitor SZV 1287 in mouse pain models with neuropathic mechanisms: involvement of transient receptor potential vanilloid 1 and ankyrin 1 receptors. Pharmacological Research. doi: https://doi.org/10.1016/j.phrs.2018.02.006. https://www.sciencedirect.com/science/article/pii/S1043661817309313


Hosford, B. E., Rowley, S., Liska, J. P., & Danzer, S. C. (2017). Ablation of peri-insult generated granule cells after epilepsy onset halts disease progression. Scientific Reports, 7(1), 18015. doi: 10.1038/s41598-017-18237-6. https://doi.org/10.1038/s41598-017-18237-6


Hoshino, A., Helwig, M., Rezaei, S., Berridge, C., Eriksen, J. L., & Lindberg, I. (2013). A novel function for proSAAS as an amyloid anti-aggregant in Alzheimer's disease. Journal of Neurochemistry, n/a-n/a. doi: 10.1111/jnc.12454. http://dx.doi.org/10.1111/jnc.12454


Hosp, J., Nolan, H., & Luft, A. (2015). Topography and collateralization of dopaminergic projections to primary motor cortex in rats. Experimental Brain Research, 1-11. doi: 10.1007/s00221-015-4211-2. http://dx.doi.org/10.1007/s00221-015-4211-2


Hosp, J. A., Strüber, M., Yanagawa, Y., Obata, K., Vida, I., Jonas, P., & Bartos, M. (2013). Morpho-physiological criteria divide dentate gyrus interneurons into classes. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22214. http://dx.doi.org/10.1002/hipo.22214


Hossain, W. A., Antic, S. D., Yang, Y., Rasband, M. N., & Morest, D. K. (2005). Where Is the Spike Generator of the Cochlear Nerve? Voltage-Gated Sodium Channels in the Mouse Cochlea. Journal of Neuroscience, 25(29), 6857-6868. doi. http://www.jneurosci.org/cgi/content/abstract/25/29/6857


Hossaini, M., French, P. J., & Holstege, J. C. (2007). Distribution of glycinergic neuronal somata in the rat spinal cord. Brain Research, 1142, 61-69. doi. 

Hossaini, M., Jongen, J., Biesheuvel, K., Kuhl, D., & Holstege, J. (2010). Nociceptive stimulation induces expression of Arc/Arg3.1 in the spinal cord with a preference for neurons containing enkephalin. Molecular Pain, 6(1), 43. doi. http://www.molecularpain.com/content/6/1/43 


Hota, S. K., Barhwal, K., Baitharu, I., Prasad, D., Singh, S. B., & Ilavazhagan, G. (2009). < i> Bacopa monniera</i> leaf extract ameliorates hypobaric hypoxia induced spatial memory impairment. Neurobiology of Disease, 34(1), 23-39. doi. 

Hou, G., & Zhang, Z.-W. (2017). NMDA Receptors Regulate the Development of Neuronal Intrinsic Excitability through Cell-Autonomous Mechanisms. [Original Research]. Frontiers in cellular neuroscience, 11(353). doi: 10.3389/fncel.2017.00353. https://www.frontiersin.org/article/10.3389/fncel.2017.00353


Hou, P.-S., Miyoshi, G., & Hanashima, C. (2019). Sensory cortex wiring requires preselection of short- and long-range projection neurons through an Egr-Foxg1-COUP-TFI network. Nature Communications, 10(1), 3581. doi: 10.1038/s41467-019-11043-w. https://doi.org/10.1038/s41467-019-11043-w


Hou, W.-H., Kuo, N., Fang, G.-W., Huang, H.-S., Wu, K.-P., Zimmer, A., . . . Lien, C.-C. (2016). Wiring Specificity and Synaptic Diversity in the Mouse Lateral Central Amygdala. The Journal of Neuroscience, 36(16), 4549-4563. doi. http://www.jneurosci.org/content/36/16/4549.short


Hou, Y., Zhang, Q., Liu, H., Wu, J., Shi, Y., Qi, Y., . . . He, M. (2021). Topographical organization of mammillary neurogenesis and efferent projections in the mouse brain. Cell Reports, 34(6), 108712. doi: https://doi.org/10.1016/j.celrep.2021.108712. https://www.sciencedirect.com/science/article/pii/S2211124721000255


Hough, L. H., & Brownl, M. E. (2017). Labeling of Neuronal Morphology using Custom Diolistic Techniques. Journal of Neuroscience Methods. doi: http://dx.doi.org/10.1016/j.jneumeth.2017.03.004. http://www.sciencedirect.com/science/article/pii/S0165027017300614


Hough, L. H., Hill, K., Staudt, L., Grubb, C., & Green, A. (2019). Stereological Investigation of the Rat Ventral Thalamic Nuclei Following Developmental Hyperserotonemia. Neuroscience, 411, 202-210. doi: https://doi.org/10.1016/j.neuroscience.2019.05.054. http://www.sciencedirect.com/science/article/pii/S0306452219303847


Hough, L. H., & Segal, S. (2016). Effects of Developmental Hyperserotonemia on the Morphology of Rat Dentate Nuclear Neurons. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2016.02.021. http://www.sciencedirect.com/science/article/pii/S0306452216001445


House, D. R. C., Elstrott, J., Koh, E., Chung, J., & Feldman, D. E. (2011). Parallel Regulation of Feedforward Inhibition and Excitation during Whisker Map Plasticity. Neuron, 72(5), 819-831. doi. 

Houzel, J. C., Carvalho, M. L., & Lent, R. (2002). Interhemispheric connections between primary visual areas: beyond the midline rule. Brazilian Journal of Medical and Biological Research, 35(12), 1441-1453. doi. 

Houzel, J. C., & Milleret, C. (1999). Visual inter-hemispheric processing: constraints and potentialities set by axonal morphology. Journal of Physiology-Paris, 93(4), 271-284. doi. 

Houzel, J.-C., Milleret, C., & Innocenti, G. (1994). Morphology of Callosal Axons Interconnecting Areas 17 and 18 of the Cat. European Journal of Neuroscience, 6(6), 898-917. doi: doi:10.1111/j.1460-9568.1994.tb00585.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.1994.tb0058...


Hovis, K. R., Ramnath, R., Dahlen, J. E., Romanova, A. L., LaRocca, G., Bier, M. E., & Urban, N. N. (2012). Activity Regulates Functional Connectivity from the Vomeronasal Organ to the Accessory Olfactory Bulb. Journal of Neuroscience, 32(23), 7907-7916. doi: 10.1523/jneurosci.2399-11.2012. http://www.jneurosci.org/content/32/23/7907.abstract


Howard, B., Chen, Y., & Zecevic, N. (2006). Cortical progenitor cells in the developing human telencephalon. Glia, 53(1), 57-66. doi. 

Hoxha, E., Gabriele, R. M. C., Balbo, I., Ravera, F., Masante, L., Zambelli, V., . . . Tempia, F. (2017). Motor Deficits and Cerebellar Atrophy in Elovl5 Knock Out Mice. [Original Research]. Frontiers in cellular neuroscience, 11(343). doi: 10.3389/fncel.2017.00343. https://www.frontiersin.org/article/10.3389/fncel.2017.00343


Hoy Jr, K. C., & Alilain, W. J. (2015). Acute theophylline exposure modulates breathing activity through a cervical contusion. Experimental Neurology, 271(0), 72-76. doi: http://dx.doi.org/10.1016/j.expneurol.2015.04.024. http://www.sciencedirect.com/science/article/pii/S0014488615001508


Hozumi, Y., Kakefuda, K., Yamasaki, M., Watanabe, M., Hara, H., & Goto, K. (2014). Involvement of diacylglycerol kinase β in the spine formation at distal dendrites of striatal medium spiny neurons. Brain Research, (0). doi: http://dx.doi.org/10.1016/j.brainres.2014.11.012. http://www.sciencedirect.com/science/article/pii/S0006899314015595


Hsieh, J. T., Lei, B., Sheng, H., Venkatraman, T., Lascola, C. D., Warner, D. S., & James, M. L. (2015). Sex-Specific Effects of Progesterone on Early Outcome of Intracerebral Hemorrhage. Neuroendocrinology. doi. http://www.karger.com/Article/Abstract/440883


Hsieh, K. C., Gvilia, I., Kumar, S., Uschakov, A., McGinty, D., Alam, M. N., & Szymusiak, R. (2011). c-Fos expression in neurons projecting from the preoptic and lateral hypothalamic areas to the ventrolateral periaqueductal gray in relation to sleep states. Neuroscience. doi. 

Hsu, J. E., & Jones, T. A. (2005). Time-sensitive enhancement of motor learning with the less-affected forelimb after unilateral sensorimotor cortex lesions in rats. European Journal of Neuroscience, 22(8), 2069-2080. doi: doi:10.1111/j.1460-9568.2005.04370.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2005.04370.x 


Hsu, J. E., & Jones, T. A. (2006). Contralesional neural plasticity and functional changes in the less-affected forelimb after large and small cortical infarcts in rats. Experimental Neurology, 201(2), 479-494. doi. 

Hsu, J. Y. C., Stein, S. A., & Xu, X. M. (2006). Development of the corticospinal tract in the mouse spinal cord: a quantitative ultrastructural analysis. Brain Research, 1084(1), 16-27. doi. 

Hsu, J. Y. C., Stein, S. A., & Xu, X. M. (2008). Abnormal growth of the corticospinal axons into the lumbar spinal cord of the hyt/hyt mouse with congenital hypothyroidism. Journal of Neuroscience Research, 86(14), 3126-3139. doi. 

Hsu, J. Y. C., & Xu, X. M. (2005). Early profiles of axonal growth and astroglial response after spinal cord hemisection and implantation of Schwann cell-seeded guidance channels in adult rats. Journal of Neuroscience Research, 82(4), 472-483. doi. 

Hsu, J.-Y. C., McKeon, R., Goussev, S., Werb, Z., Lee, J.-U., Trivedi, A., & Noble-Haeusslein, L. J. (2006). Matrix Metalloproteinase-2 Facilitates Wound Healing Events That Promote Functional Recovery after Spinal Cord Injury. Journal of Neuroscience, 26(39), 9841-9850. doi: 10.1523/jneurosci.1993-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/39/9841 


Hu, H., & Agmon, A. (2016). Differential Excitation of Distally versus Proximally Targeting Cortical Interneurons by Unitary Thalamocortical Bursts. The Journal of Neuroscience, 36(26), 6906-6916. doi. http://www.jneurosci.org/content/36/26/6906.short


Hu, H., & Jonas, P. (2014). A supercritical density of Na+ channels ensures fast signaling in GABAergic interneuron axons. Nature Neuroscience. doi. 

Hu, H., Liu, Y., Bampoe, K., He, Y., & Yu, M. (2016). Postnatal Gene Therapy Improves Spatial Learning Despite the Presence of Neuronal Ectopia in a Model of Neuronal Migration Disorder. Genes, 7(12), 105. doi. http://www.mdpi.com/2073-4425/7/12/105


Hu, H., Roth, F. C., Vandael, D., & Jonas, P. (2018). Complementary Tuning of Na+ and K+ Channel Gating Underlies Fast and Energy-Efficient Action Potentials in GABAergic Interneuron Axons. Neuron, 98(1), 156-165.e156. doi: https://doi.org/10.1016/j.neuron.2018.02.024. https://www.sciencedirect.com/science/article/pii/S0896627318301454


Hu, J., Deng, L., Wang, X., & Xu, X. M. (2009). Effects of extracellular matrix molecules on the growth properties of oligodendrocyte progenitor cells in vitro. Journal of Neuroscience Research, 87(13), 2854-2862. doi. 

Hu, J.-G., Shi, L.-L., Chen, Y.-J., Xie, X.-M., Zhang, N., Zhu, A.-Y., . . . Lü, H.-Z. (2016). Differential effects of myelin basic protein-activated Th1 and Th2 cells on the local immune microenvironment of injured spinal cord. Experimental Neurology, 277, 190-201. doi: http://dx.doi.org/10.1016/j.expneurol.2016.01.002. http://www.sciencedirect.com/science/article/pii/S0014488616300012


Hu, X.-L., Cheng, X., Cai, L., Tan, G.-H., Xu, L., Feng, X.-Y., . . . Xiong, Z.-Q. (2011). Conditional Deletion of NRSF in Forebrain Neurons Accelerates Epileptogenesis in the Kindling Model. Cerebral Cortex. doi: 10.1093/cercor/bhq284. http://cercor.oxfordjournals.org/content/early/2011/02/21/cercor.bhq284....


Hua, K., Forbes, M. E., Lichtenwalner, R. J., Sonntag, W. E., & Riddle, D. R. (2009). Adult-onset deficiency in growth hormone and insulin-like growth factor-I alters oligodendrocyte turnover in the corpus callosum. Glia, 57(10), 1062-1071. doi. 

Hua, K., Schindler, M. K., McQuail, J. A., Forbes, M. E., & Riddle, D. R. (2012). Regionally Distinct Responses of Microglia and Glial Progenitor Cells to Whole Brain Irradiation in Adult and Aging Rats. PLoS ONE, 7(12), e52728. doi: 10.1371/journal.pone.0052728. http://dx.doi.org/10.1371%2Fjournal.pone.0052728


Huang, A., Noga, B. R., Carr, P. A., Fedirchuk, B., & Jordan, L. M. (2000). Spinal Cholinergic Neurons Activated During Locomotion: Localization and Electrophysiological Characterization. Journal of Neurophysiology, 83(6), 3537-3547. doi. http://jn.physiology.org/cgi/content/abstract/83/6/3537 


Huang, C. C. Y., Muszynski, K. J., Bolshakov, V. Y., & Balu, D. T. (2019). Deletion of Dtnbp1 in mice impairs threat memory consolidation and is associated with enhanced inhibitory drive in the amygdala. Translational Psychiatry, 9(1), 132. doi: 10.1038/s41398-019-0465-y. https://doi.org/10.1038/s41398-019-0465-y


Huang, C. L., & Winer, J. A. (2000). Auditory thalamocortical projections in the cat: laminar and areal patterns of input. Journal of Comparative Neurology, 427(2), 302-331. doi. 

Huang, C.-W., Chen, Y.-W., Lin, Y.-R., Chen, P.-H., Chou, M.-H., Lee, L.-J., . . . Chen, S.-L. (2016). Conditional Knockout of Breast Carcinoma Amplified Sequence 2 (BCAS2) in Mouse Forebrain Causes Dendritic Malformation via β-catenin. [Article]. Scientific Reports, 6, 34927. doi: 10.1038/srep34927

http://www.nature.com/articles/srep34927#supplementary-information. http://dx.doi.org/10.1038/srep34927


Huang, J., Furuya, A., Hayashi, K., & Furuichi, T. (2011). Interaction between very-KIND Ras guanine exchange factor and microtubule-associated protein 2, and its role in dendrite growth – structure and function of the second kinase noncatalytic C-lobe domain. FEBS Journal, no-no. doi: 10.1111/j.1742-4658.2011.08085.x. http://dx.doi.org/10.1111/j.1742-4658.2011.08085.x


Huang, J., Polgár, E., Solinski, H. J., Mishra, S. K., Tseng, P.-Y., Iwagaki, N., . . . Hoon, M. A. (2018). Circuit dissection of the role of somatostatin in itch and pain. Nature Neuroscience. doi: 10.1038/s41593-018-0119-z. https://doi.org/10.1038/s41593-018-0119-z


Huang, L., & Pallas, S. L. (2001). NMDA Antagonists in the Superior Colliculus Prevent Developmental Plasticity But Not Visual Transmission or Map Compression. Journal of Neurophysiology, 86(3), 1179-1194. doi. http://jn.physiology.org/cgi/content/abstract/86/3/1179 


Huang, L.-W., Simonnet, J., Nassar, M., Richevaux, L., Lofredi, R., & Fricker, D. (2017). Laminar Localization and Projection-Specific Properties of Presubicular Neurons Targeting the Lateral Mammillary Nucleus, Thalamus or Medial Entorhinal Cortex. [10.1523/ENEURO.0370-16.2017]. eneuro. doi. http://eneuro.org/content/early/2017/04/28/ENEURO.0370-16.2017.abstract


Huang, T., & Krimm, R. F. (2013). BDNF and NT4 play interchangeable roles in gustatory development. Developmental Biology, (0). doi: http://dx.doi.org/10.1016/j.ydbio.2013.12.031. http://www.sciencedirect.com/science/article/pii/S0012160613006933


Huang, T., Ma, L., & Krimm, R. F. (2015). Postnatal reduction of BDNF regulates the developmental remodeling of taste bud innervation. Developmental Biology. doi: http://dx.doi.org/10.1016/j.ydbio.2015.07.006. http://www.sciencedirect.com/science/article/pii/S0012160615300403


Huang, W.-C., Chen, Y., & Page, D. T. (2016). Hyperconnectivity of prefrontal cortex to amygdala projections in a mouse model of macrocephaly/autism syndrome. [Article]. Nature Communications, 7, 13421. doi: 10.1038/ncomms13421

http://www.nature.com/articles/ncomms13421#supplementary-information. http://dx.doi.org/10.1038/ncomms13421


Huang, Z., Yu, Y., Shimoda, Y., Watanabe, K., & Liu, Y. (2012). Loss of neural recognition molecule NB-3 delays the normal projection and terminal branching of developing corticospinal tract axons in the mouse. Journal of Comparative Neurology, 520(6), 1227-1245. doi: 10.1002/cne.22772. http://dx.doi.org/10.1002/cne.22772


Huangfu, D., & Guyenet, P. G. (1997). Autoactivity of A5 neurons: role of subthreshold oscillations and persistent Na+ current. American Journal of Physiology - Heart and Circulatory Physiology

273(5), H2280-2289. doi. http://ajpheart.physiology.org/cgi/content/abstract/273/5/H2280 


Huangfu, D., Schreihofer, M., & Guyenet, P. G. (1997). Effect of cholinergic agonists on bulbospinal C1 neurons in rats. Journal of Physiology - Regulatory, Integrative and Comparative Physiology, 272(1), R249-258. doi. http://ajpregu.physiology.org/cgi/content/abstract/272/1/R249 


Huber, D., Petreanu, L., Ghitani, N., Ranade, S., Hromádka, T., Mainen, Z., & Svoboda, K. (2007). Sparse optical microstimulation in barrel cortex drives learned behaviour in freely moving mice. Nature, 451(7174), 61-64. doi. 

Hubert, G. W., Paquet, M., & Smith, Y. (2001). Differential Subcellular Localization of mGluR1a and mGluR5 in the Rat and Monkey Substantia Nigra. Journal of Neuroscience, 21(6), 1838-1847. doi. http://www.jneurosci.org/cgi/content/abstract/21/6/1838


Huerta-Ocampo, I., Mena-Segovia, J., & Bolam, J. P. (2013). Convergence of cortical and thalamic input to direct and indirect pathway medium spiny neurons in the striatum. Brain Structure and Function, 1-14. doi: 10.1007/s00429-013-0601-z. http://dx.doi.org/10.1007/s00429-013-0601-z


Hüfner, K., Horn, A., Derfuss, T., Glon, C., Sinicina, I., Arbusow, V., . . . Theil, D. (2009). Fewer latent herpes simplex virus type 1 and cytotoxic T cells occur in the ophthalmic division than in the maxillary and mandibular divisions of the human trigeminal ganglion and nerve. Journal of Virology, 83(8), 3696-3703. doi. 

Hughes, D. I., Boyle, K. A., Kinnon, C. M., Bilsland, C., Quayle, J. A., Callister, R. J., & Graham, B. A. (2013). HCN4 subunit expression in fast-spiking interneurons of the rat spinal cord and hippocampus. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2013.01.028. http://www.sciencedirect.com/science/article/pii/S0306452213000651


Hughes, D. I., Polgár, E., Shehab, S. A. S., & Todd, A. J. (2004). Peripheral axotomy induces depletion of the vesicular glutamate transporter VGLUT1 in central terminals of myelinated afferent fibres in the rat spinal cord. Brain Research, 1017(1), 69-76. doi. 

Hughes, D. I., Scott, D. T., Riddell, J. S., & Todd, A. J. (2007). Upregulation of Substance P in Low-Threshold Myelinated Afferents Is Not Required for Tactile Allodynia in the Chronic Constriction Injury and Spinal Nerve Ligation Models. Journal of Neuroscience, 27(8), 2035-2044. doi: 10.1523/jneurosci.5401-06.2007. http://www.jneurosci.org/cgi/content/abstract/27/8/2035 


Hughes, D. I., Scott, D. T., Todd, A. J., & Riddell, J. S. (2003). Lack of Evidence for Sprouting of Aβ Afferents into the Superficial Laminas of the Spinal Cord Dorsal Horn after Nerve Section. Journal of Neuroscience, 23(29), 9491-9499. doi. http://www.jneurosci.org/cgi/content/abstract/23/29/9491 


Hughes, D. I., Sikander, S., Kinnon, C. M., Boyle, K. A., Watanabe, M., Callister, R. J., & Graham, B. (2012). Morphological, neurochemical and electrophysiological features of parvalbumin-expressing cells: a likely source of axo-axonic inputs in the mouse spinal dorsal horn. Journal of Physiology. doi: 10.1113/jphysiol.2012.235655. http://jp.physoc.org/content/early/2012/06/06/jphysiol.2012.235655.abstract


Huguenard, A. L., Fernando, S. M., Monks, D. A., & Sengelaub, D. R. (2011). Overexpression of androgen receptors in target musculature confers androgen sensitivity to motoneuron dendrites. Endocrinology, 152(2), 639-650. doi. 

Huh, C. Y., Amilhon, B., Ferguson, K. A., Manseau, F., Torres-Platas, S. G., Peach, J. P., . . . Williams, S. (2016). Excitatory Inputs Determine Phase-Locking Strength and Spike-Timing of CA1 Stratum Oriens/Alveus Parvalbumin and Somatostatin Interneurons during Intrinsically Generated Hippocampal Theta Rhythm. The Journal of Neuroscience, 36(25), 6605-6622. doi. http://www.jneurosci.org/content/36/25/6605.short


Huma, Z., Ireland, K., & Maxwell, D. J. (2015). The spino–bulbar–cerebellar pathway: Activation of neurons projecting to the lateral reticular nucleus in the rat in response to noxious mechanical stimuli. Neuroscience Letters, 591(0), 197-201. doi: http://dx.doi.org/10.1016/j.neulet.2015.02.047. http://www.sciencedirect.com/science/article/pii/S0304394015001615


Hung, J., Chansard, M., Ousman, S., Nguyen, M., & Colicos, M. (2010). Activation of microglia by neuronal activity: results from a new in vitro paradigm based on neuronal-silicon interfacing technology. Brain, Behavior, and Immunity, 24, 31 - 40. doi. 

Hung, V. K. L., Yeung, P. K. K., Lai, A. K. W., Ho, M. C. Y., Lo, A. C. Y., Chan, K. C., . . . Chung, S. K. (2015). Selective astrocytic endothelin-1 overexpression contributes to dementia associated with ischemic stroke by exaggerating astrocyte-derived amyloid secretion. [Original Article]. Journal of Cerebral Blood Flow and Metabolism. doi: 10.1038/jcbfm.2015.109. http://dx.doi.org/10.1038/jcbfm.2015.109


Huppenbauer, C. B., Tanzer, L., DonCarlos, L. L., & Jones, K. J. (2005). Gonadal Steroid Attenuation of Developing Hamster Facial Motoneuron Loss by Axotomy: Equal Efficacy of Testosterone, Dihydrotestosterone, and 17-β Estradiol. Journal of Neuroscience, 25(16), 4004-4013. doi. http://www.jneurosci.org/cgi/content/abstract/25/16/4004


Hur, E. E., & Zaborszky, L. (2005). Vglut2 afferents to the medial prefrontal and primary somatosensory cortices: a combined retrograde tracing in situ hybridization. Journal of Comparative Neurology, 483(3), 351-373. doi. 

Hurley, P., Pytte, C., & Kirn, J. R. (2008). Nest of origin predicts adult neuron addition rates in the vocal control system of the zebra finch. Brain, Behavior and Evolution, 71(4), 263-270. doi. 

Hurliman, E., Groth, D., Wendelschafer-Crabb, G., Kennedy, W., Kavand, S., Ericson, M., & Hordinsky, M. (2016). Small fiber neuropathy in a patient with dermatomyositis and severe scalp pruritus. British Journal of Dermatology, n/a-n/a. doi: 10.1111/bjd.14678. http://dx.doi.org/10.1111/bjd.14678


Hurtado, A., Marcillo, A., Frydel, B., Bunge, M. B., Bramlett, H. M., & Dietrich, W. D. (2010). Anti-CD11d monoclonal antibody treatment for rat spinal cord compression injury. Experimental Neurology. doi. 

Hurtado, A., Podinin, H., Oudega, M., & Grimpe, B. (2008). Deoxyribozyme-mediated knockdown of xylosyltransferase-1 mRNA promotes axon growth in the adult rat spinal cord. Brain. doi: 10.1093/brain/awn206. http://brain.oxfordjournals.org/cgi/content/abstract/awn206v1 


Hurtado, O., Cárdenas, A., Pradillo, J. M., Morales, J. R., Ortego, F., Sobrino, T., . . . Lizasoain, I. (2007). A chronic treatment with CDP-choline improves functional recovery and increases neuronal plasticity after experimental stroke. Neurobiology of Disease, 26(1), 105-111. doi. 

Huss, D., Navaluri, R., Faulkner, K. F., & David Dickman, J. (2010). Development of otolith receptors in Japanese quail. Developmental Neurobiology, 70(6), 436-455. doi. 

Huxlin, K. R., Williams, J. M., & Price, T. (2008). A neurochemical signature of visual recovery after extrastriate cortical damage in the adult cat. Journal of Comparative Neurology, 508(1), 45-61. doi. 

Hwang, D. H., Shin, H. Y., Kwon, M. J., Choi, J. Y., Ryu, B.-Y., & Kim, B. G. (2014). Survival of Neural Stem Cell Grafts in the Lesioned Spinal Cord Is Enhanced by a Combination of Treadmill Locomotor Training via Insulin-Like Growth Factor-1 Signaling. The Journal of Neuroscience, 34(38), 12788-12800. doi. http://www.jneurosci.org/content/34/38/12788.short


Hwang, E., Willis, B. S., & Burwell, R. D. (2017). Prefrontal connections of the perirhinal and postrhinal cortices in the rat. Behavioural Brain Research. doi: http://dx.doi.org/10.1016/j.bbr.2017.07.032. http://www.sciencedirect.com/science/article/pii/S0166432816313316


Hwang, I. K., Kim, I. Y., Joo, E. J., Shin, J. H., Choi, J. W., Won, M. H., . . . Seong, J. K. (2010). Metformin normalizes type 2 diabetes-induced decrease in cell proliferation and neuroblast differentiation in the rat dentate gyrus. Neurochemical Research, 35(4), 645-650. doi. 

Hwang, I. K., Yi, S. S., Song, W., Won, M. H., Yoon, Y. S., & Seong, J. K. (2010). Effects of age and treadmill exercise in chronic diabetic stages on neuroblast differentiation in a rat model of type 2 diabetes. Brain Research, 1341, 63-71. doi. 

Hwang, I. K., Yi, S. S., Yoo, K. Y., Park, O. K., Yan, B., Kim, I. Y., . . . others. (2010). Effects of treadmill exercise on cyclooxygenase-2 in the hippocampus in type 2 diabetic rats: Correlation with the neuroblasts. Brain Research, 1341, 84-92. doi. 

Hyer, M. M., Hunter, T. J., Katakam, J., Wolz, T., & Glasper, E. R. (2016). Neurogenesis and anxiety-like behavior in male California mice during the mate's postpartum period. European Journal of Neuroscience, n/a-n/a. doi: 10.1111/ejn.13168. http://dx.doi.org/10.1111/ejn.13168


Iannotti, C., Li, H., Stemmler, M., Perman, W. H., & Xu, X. M. (2002). Identification of regenerative tissue cables using in vivo MRI after spinal cord hemisection and schwann cell bridging transplantation. Journal of Neurotrauma, 19(12), 1543-1554. doi. 

Iannotti, C., Li, H., Yan, P., Lu, X., Wirthlin, L., & Xu, X. M. (2003). Glial cell line-derived neurotrophic factor-enriched bridging transplants promote propriospinal axonal regeneration and enhance myelination after spinal cord injury. Experimental Neurology, 183(2), 379-393. doi. 

Iannotti, C., Ping Zhang, Y., Shields, C. B., Han, Y., Burke, D. A., & Xu, X. M. (2004). A neuroprotective role of glial cell line-derived neurotrophic factor following moderate spinal cord contusion injury. Experimental Neurology, 189(2), 317-332. doi. 

Iannotti, C., Zhang, Y. P., Shields, L. B. E., Han, Y., Burke, D. A., Xu, X. M., & Shields, C. B. (2006). Dural repair reduces connective tissue scar invasion and cystic cavity formation after acute spinal cord laceration injury in adult rats. Journal of Neurotrauma, 23(6), 853-865. doi. 

Ibi, D., Nagai, T., Nakajima, A., Mizoguchi, H., Kawase, T., Tsuboi, D., . . . Yamada, K. (2013). Astroglial IFITM3 mediates neuronal impairments following neonatal immune challenge in mice. Glia, n/a-n/a. doi: 10.1002/glia.22461. http://dx.doi.org/10.1002/glia.22461


Íbias, J., Soria-Molinillo, E., Kastanauskaite, A., Orgaz, C., DeFelipe, J., Pellón, R., & Miguéns, M. (2015). Schedule-induced polydipsia is associated with increased spine density in dorsolateral striatum neurons. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2015.05.026. http://www.sciencedirect.com/science/article/pii/S0306452215004583


Ibrahim, S., Hu, W., Wang, X., Gao, X., He, C., & Chen, J. (2016). Traumatic Brain Injury Causes Aberrant Migration of Adult-Born Neurons in the Hippocampus. [Article]. Scientific Reports, 6, 21793. doi: 10.1038/srep21793

http://www.nature.com/articles/srep21793#supplementary-information. http://dx.doi.org/10.1038/srep21793


Ichinohe, N. (2014). On-going elucidation of mechanisms of primate specific synaptic spine development using the common marmoset (Callithrix jacchus). Neuroscience Research, (0). doi: http://dx.doi.org/10.1016/j.neures.2014.10.019. http://www.sciencedirect.com/science/article/pii/S0168010214002429


Ichinohe, N., Borra, E., & Rockland, K. (2012). Distinct Feedforward and Intrinsic Neurons in Posterior Inferotemporal Cortex Revealed by in Vivo Connection Imaging. Scientific Reports, 2. doi. 

Ichinohe, N., Fujiyama, F., Kaneko, T., & Rockland, K. S. (2003). Honeycomb-Like Mosaic at the Border of Layers 1 and 2 in the Cerebral Cortex. Journal of Neuroscience, 23, 1372-1382. doi. 

Ichinohe, N., Hayashi, M., Wakabayashi, K., & Rockland, K. S. (2009). Distribution and progression of amyloid-[beta] deposits in the amygdala of the aged macaque monkey, and parallels with zinc distribution. Neuroscience, 159(4), 1374-1383. doi. 

Ichinohe, N., Knight, A., Ogawa, M., Ohshima, T., Mikoshiba, K., Yoshihara, Y., . . . Rockland, K. S. (2008). Unusual Patch-Matrix Organization in the Retrosplenial Cortex of the reeler Mouse and Shaking Rat Kawasaki. Cerebral Cortex, 18(5), 1125-1138. doi: 10.1093/cercor/bhm148. http://cercor.oxfordjournals.org/cgi/content/abstract/18/5/1125 


Ichinohe, N., Matsushita, A., Ohta, K., & Rockland, K. S. (2010). Pathway-Specific Utilization of Synaptic Zinc in the Macaque Ventral Visual Cortical Areas. Cerebral Cortex, bhq028. doi: 10.1093/cercor/bhq028. http://cercor.oxfordjournals.org/cgi/content/abstract/bhq028v1 


Ichinohe, N., & Rockland, K. S. (2002). Parvalbumin positive dendrites co-localize with apical dendritic bundles in rat retrosplenial cortex. Neuroreport, 13(6), 757-757. doi. 

Ichinohe, N., & Rockland, K. S. (2004). Region specific micromodularity in the uppermost layers in primate cerebral cortex. Cerebral Cortex, 14(11), 1173-1184. doi. 

Ichinohe, N., & Rockland, K. S. (2005). Zinc-enriched amygdalo-and hippocampo-cortical connections to the inferotemporal cortices in macaque monkey. Neuroscience Research, 53(1), 57-68. doi. 

Ichinohe, N., Teng, B., & Kitai, S. T. (2000). Morphological study of the tegmental pedunculopontine nucleus, substantia nigra and subthalamic nucleus, and their interconnections in rat organotypic culture. Anatomy and Embryology, 201(6), 435-453. doi. 

Igarashi, K. M., Ieki, N., An, M., Yamaguchi, Y., Nagayama, S., Kobayakawa, K., . . . Mori, K. (2012). Parallel Mitral and Tufted Cell Pathways Route Distinct Odor Information to Different Targets in the Olfactory Cortex. Journal of Neuroscience, 32(23), 7970-7985. doi: 10.1523/jneurosci.0154-12.2012. http://www.jneurosci.org/content/32/23/7970.abstract


Igarashi, K. M., Lu, L., Colgin, L. L., Moser, M.-B., & Moser, E. I. (2014). Coordination of entorhinal-hippocampal ensemble activity during associative learning. Nature. doi. http://www.nature.com/nature/journal/vaop/ncurrent/full/nature13162.html


Ikebuchi, M., Nanbu, S., Okanoya, K., Suzuki, R., & Bischof, H. J. (2012). Very Early Development of Nucleus Taeniae of the Amygdala. Brain, Behavior and Evolution. doi. 

Ikeda, M., Hojo, Y., Komatsuzaki, Y., Okamoto, M., Kato, A., Takeda, T., & Kawato, S. (2015). Hippocampal spine changes across the sleep-wake cycle: corticosterone and kinases. Journal of Endocrinology. doi: 10.1530/joe-15-0078. http://joe.endocrinology-journals.org/content/early/2015/06/01/JOE-15-00...


Ikeda, Y., Zabbarova, I., Schaefer, C. M., Bushnell, D. S., de Groat, W. C., Kanai, A. J., & Bates, C. M. (2017). Fgfr2 is integral for bladder mesenchyme patterning and function. [10.1152/ajprenal.00463.2016]. American Journal of Physiology - Renal Physiology. doi. http://ajprenal.physiology.org/content/early/2017/01/03/ajprenal.00463.2...


Ikeno, T., & Nelson, R. J. (2014). Acute Melatonin Treatment Alters Dendritic Morphology and Circadian Clock Gene Expression in the Hippocampus of Siberian Hamsters. Hippocampus, n/a-n/a. doi: 10.1002/hipo.22358. http://dx.doi.org/10.1002/hipo.22358


Ikeno, T., Weil, Z. M., & Nelson, R. J. (2013). Photoperiod affects the diurnal rhythm of hippocampal neuronal morphology of siberian hamsters. Chronobiology International, 0(0), 1-12. doi: doi:10.3109/07420528.2013.800090. http://informahealthcare.com/doi/abs/10.3109/07420528.2013.800090


Ikeno, T., Weil, Z. M., & Nelson, R. J. (2014). Timing of light pulses and photoperiod on the diurnal rhythm of hippocampal neuronal morphology of Siberian hamsters. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2014.04.002. http://www.sciencedirect.com/science/article/pii/S0306452214002905


Ikin, A. F., Sabo, S. L., Lanier, L. M., & Buxbaum, J. D. (2007). A macromolecular complex involving the amyloid precursor protein (APP) and the cytosolic adapter FE65 is a negative regulator of axon branching. Molecular and Cellular Neuroscience, 35(1), 57-63. doi. 

Ilango, A., Kesner, A. J., Keller, K. L., Stuber, G. D., Bonci, A., & Ikemoto, S. (2014). Similar Roles of Substantia Nigra and Ventral Tegmental Dopamine Neurons in Reward and Aversion. Journal of Neuroscience, 34(3), 817-822. doi. http://www.jneurosci.org/content/34/3/817.short


Illig, K. R. (2005). Projections from orbitofrontal cortex to anterior piriform cortex in the rat suggest a role in olfactory information processing. Journal of Comparative Neurology, 488(2), 224-231. doi. 

Illig, K. R., & Eudy, J. D. (2009). Contralateral projections of the rat anterior olfactory nucleus. Journal of Comparative Neurology, 512(1), 115-123. doi. 

Illig, K. R., King, V. R., & Spear, P. D. (1998). Monocular enucleation prevents retinal ganglion-cell loss following neonatal visual cortex damage in cats. Visual Neuroscience, 15(6), 1097-1105. doi. 

Imamura, F., & Greer, C. A. (2009). Dendritic branching of olfactory bulb mitral and tufted cells: regulation by TrkB. PLoS ONE, 4(8), e6729-e6729. doi. 

Inan, M., Blázquez-Llorca, L., Merchán-Pérez, A., Anderson, S. A., DeFelipe, J., & Yuste, R. (2013). Dense and Overlapping Innervation of Pyramidal Neurons by Chandelier Cells. Journal of Neuroscience, 33(5), 1907-1914. doi: 10.1523/jneurosci.4049-12.2013. http://www.jneurosci.org/content/33/5/1907.abstract


Inan, M., Lu, H.-C., Albright, M. J., She, W.-C., & Crair, M. C. (2006). Barrel Map Development Relies on Protein Kinase A Regulatory Subunit IIbeta-Mediated cAMP Signaling. Journal of Neuroscience, 26(16), 4338-4349. doi: 10.1523/jneurosci.3745-05.2006. http://www.jneurosci.org/cgi/content/abstract/26/16/4338 


Inda, M. C., DeFelipe, J., & Munoz, A. (2007). The Distribution of Chandelier Cell Axon Terminals that Express the GABA Plasma Membrane Transporter GAT-1 in the Human Neocortex. Cerebral Cortex, 17(9), 2060-2071. doi: 10.1093/cercor/bhl114. http://cercor.oxfordjournals.org/cgi/content/abstract/17/9/2060 


Inda, M. C., DeFelipe, J., & Munoz, A. (2009). Morphology and Distribution of Chandelier Cell Axon Terminals in the Mouse Cerebral Cortex and Claustroamygdaloid Complex. Cerebral Cortex, 19, 41-54. doi: 10.1093/cercor/bhn057. http://cercor.oxfordjournals.org/cgi/content/abstract/bhn057v1 


Inglis, F., Lee, K., Chiu, K., Purcell, O., Didier, P., Russell-Lodrigue, K., . . . MacLean, A. (2015). Neuropathogenesis of Chikungunya infection: astrogliosis and innate immune activation. Journal of Neurovirology, 1-9. doi: 10.1007/s13365-015-0378-3. http://dx.doi.org/10.1007/s13365-015-0378-3


Inglis, F. M., Crockett, R., Korada, S., Abraham, W. C., Hollmann, M., & Kalb, R. G. (2002). The AMPA Receptor Subunit GluR1 Regulates Dendritic Architecture of Motor Neurons. Journal of Neuroscience, 22(18), 8042-8051. doi. http://www.jneurosci.org/cgi/content/abstract/22/18/8042 

Inglis, F. M., Furia, F., Zuckerman, K. E., Strittmatter, S. M., & Kalb, R. G. (1998). The Role of Nitric Oxide and NMDA Receptors in the Development of Motor Neuron Dendrites. Journal of Neuroscience, 18(24), 10493-10501. doi. http://www.jneurosci.org/cgi/content/abstract/18/24/10493


Inglis, F. M., Zuckerman, K. E., & Kalb, R. G. (2000). Experience-dependent development of spinal motor neurons. Neuron, 26(2), 299-305. doi. 

Ingraham, J. P., Forbes, M. E., Riddle, D. R., & Sonntag, W. E. (2008). Aging reduces hypoxia-induced microvascular growth in the rodent hippocampus. Journals of Gerontology Series A: Biological Sciences and Medical Sciences, 63(1), 12-12. doi. 

Ingraham, S. E., Saha, M., Carpenter, A. R., Robinson, M., Ismail, I., Singh, S., . . . others. (2010). Pathogenesis of renal injury in the megabladder mouse: A genetic model of congenital obstructive nephropathy. Pediatric Research, 68(6), 500-507. doi. 

Ingram, E. A., Toyoda, I., Wen, X., & Buckmaster, P. S. (2009). Prolonged infusion of inhibitors of calcineurin or L-type calcium channels does not block mossy fiber sprouting in a model of temporal lobe epilepsy. Epilepsia, 50(1), 56-64. doi. 

Ingram, N. T., Khankan, R. R., & Phelps, P. E. (2016). Olfactory Ensheathing Cells Express ?7 Integrin to Mediate Their Migration on Laminin. PLoS ONE, 11(4), e0153394. doi: 10.1371/journal.pone.0153394. http://dx.doi.org/10.1371%2Fjournal.pone.0153394


Innocenti, G. M. (2013). A Dynamic Approach To Brain Connectivity. [Abstract]. Frontiers in Neuroinformatics. doi: 10.3389/conf.fninf.2013.09.00059. http://www.frontiersin.org/Journal/Abstract.aspx?s=752&name=neuroinforma...


Innocenti, G. M., & Caminiti, R. (2016). Axon diameter relates to synaptic bouton size: structural properties define computationally different types of cortical connections in primates. [journal article]. Brain Structure and Function, 1-9. doi: 10.1007/s00429-016-1266-1. http://dx.doi.org/10.1007/s00429-016-1266-1


Innocenti, G. M., Caminiti, R., & Hof, P. R. (2010). Fiber composition in the planum temporale sector of the corpus callosum in chimpanzee and human. Brain Structure and Function, 215(2), 123-128. doi. 

Innocenti, G. M., Caminiti, R., Rouiller, E. M., Knott, G., Dyrby, T. B., Descoteaux, M., & Thiran, J.-P. (2018). Diversity of Cortico-descending Projections: Histological and Diffusion MRI Characterization in the Monkey. Cerebral Cortex. doi: 10.1093/cercor/bhx363. http://dx.doi.org/10.1093/cercor/bhx363


Innocenti, G. M., Dyrby, T. B., Andersen, K. W., Rouiller, E. M., & Caminiti, R. (2016). The Crossed Projection to the Striatum in Two Species of Monkey and in Humans: Behavioral and Evolutionary Significance. Cerebral Cortex. doi: 10.1093/cercor/bhw161. http://cercor.oxfordjournals.org/content/early/2016/06/09/cercor.bhw161....


Innocenti, G. M., Lehmann, P., & Houzel, J.-C. (1994). Computational Structure of Visual Callosal Axons. European Journal of Neuroscience, 6(6), 918-935. doi: doi:10.1111/j.1460-9568.1994.tb00586.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.1994.tb0058...


Innocenti, G. M., Manger, P. R., Masiello, I., Colin, I., & Tettoni, L. (2002). Architecture and callosal connections of visual areas 17, 18, 19 and 21 in the ferret (Mustela putorius). Cerebral Cortex, 12(4), 411-411. doi. 

Innocenti, G. M., & Vercelli, A. (2010). Dendritic bundles, minicolumns, columns, and cortical output units. Frontiers in Neuroanatomy, 4. doi. 

Innocenti, G. M., Vercelli, A., & Caminiti, R. (2013). The Diameter of Cortical Axons Depends Both on the Area of Origin and Target. Cerebral Cortex. doi: 10.1093/cercor/bht070. http://cercor.oxfordjournals.org/content/early/2013/03/23/cercor.bht070....


Inoue, K.-i., Miyachi, S., Nishi, K., Okado, H., Nagai, Y., Minamimoto, T., . . . Takada, M. (2018). Recruitment of calbindin into nigral dopamine neurons protects against MPTP-Induced parkinsonism. Movement Disorders, 0(0). doi: doi:10.1002/mds.107. https://onlinelibrary.wiley.com/doi/abs/10.1002/mds.107


Iorgulescu, J. B., Patel, S. P., Louro, J., Andrade, C. M., Sanchez, A. R., & Pearse, D. D. (2015). Acute Putrescine Supplementation with Schwann Cell Implantation Improves Sensory and Serotonergic Axon Growth and Functional Recovery in Spinal Cord Injured Rats. Neural Plasticity. doi. http://www.hindawi.com/journals/np/aa/186385/cta/


Ip, E. Y. Y., Giza, C. C., Griesbach, G. S., & Hovda, D. A. (2002). Effects of enriched environment and fluid percussion injury on dendritic arborization within the cerebral cortex of the developing rat. Journal of Neurotrauma, 19(5), 573-585. doi. 

Irie, T., Matsuzaki, Y., Sekino, Y., & Hirai, H. (2013). Kv3.3 channels harboring a mutation of spinocerebellar ataxia type 13 alter excitability and induce cell death in cultured cerebellar Purkinje cells. The Journal of Physiology. doi: 10.1113/jphysiol.2013.264309. http://jp.physoc.org/content/early/2013/11/11/jphysiol.2013.264309.abstract


Irintchev, A., Rollenhagen, A., Troncoso, E., Kiss, J. Z., & Schachner, M. (2005). Structural and Functional Aberrations in the Cerebral Cortex of Tenascin-C Deficient Mice. Cerebral Cortex, 15(7), 950-962. doi: 10.1093/cercor/bhh195. http://cercor.oxfordjournals.org/cgi/content/abstract/15/7/950 


Irvine, A. D., Sun, P., Kos, L., Wang, X. Q., & Paller, A. S. (2002). A colorimetric bead-binding assay for detection of intermolecular interactions. Experimental Dermatology, 11(5), 462-467. doi: doi:10.1034/j.1600-0625.2002.110510.x. http://www.blackwell-synergy.com/doi/abs/10.1034/j.1600-0625.2002.110510...


Isayama, T., Berson, D. M., & Pu, M. (2000). Theta ganglion cell type of cat retina. Journal of Comparative Neurology, 417(1), 32-48. doi. 

Isayama, T., O'Brien, B. J., Ugalde, I., Muller, J. F., Frenz, A., Aurora, V., . . . Berson, D. M. (2009). Morphology of retinal ganglion cells in the ferret (Mustela putorius furo). Journal of Comparative Neurology, 517(4), 459-480. doi. 

Ishihara, Y., & Fukuda, T. (2016). Immunohistochemical investigation of the internal structure of the mouse subiculum. Neuroscience. doi: http://dx.doi.org/10.1016/j.neuroscience.2016.09.027. http://www.sciencedirect.com/science/article/pii/S0306452216304651


Ishihara, Y., Fukuda, T., & Sato, F. (2019). Internal structure of the rat subiculum characterized by diverse immunoreactivities and septotemporal differences. Neuroscience Research. doi: https://doi.org/10.1016/j.neures.2019.02.001. http://www.sciencedirect.com/science/article/pii/S0168010218305388


Ishikawa, H., Honda, T., Toriyama, K., Torii, S., & Sugiura, Y. (2003). Origin and course of nerves immunoreactive for calcitonin gene-related peptide surrounding the femoral artery in rat. Anatomy and Embryology, 207(4), 299-305. doi. 

Isoardo, G., Rota, E., Ciaramitaro, P., Tavella, A., Poglio, F., Prolasso, I., & Cocito, D. (2004). Predictive value of clinical, electrophysiological and immunological features for response to IVIg in patients with CIDP. Journal of the Peripheral Nervous System, 9(2), 107-107. doi: doi:10.1111/j.1085-9489.2004.009209l.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1085-9489.2004.009209...


Isomura, Y., Sirota, A., Özen, S., Montgomery, S., Mizuseki, K., Henze, D. A., & Buzsáki, G. (2006). Integration and segregation of activity in entorhinal-hippocampal subregions by neocortical slow oscillations. Neuron, 52(5), 871-882. doi. 

Ito, D., Imai, Y., Ohsawa, K., Nakajima, K., Fukuuchi, Y., & Kohsaka, S. (1998). Microglia-specific localisation of a novel calcium binding protein, Iba1. Brain Research. Molecular Brain Research, 57, 1 - 9. doi. 

Ito, T., & Atoji, Y. (2016). Tectothalamic inhibitory projection neurons in the avian torus semicircularis. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23979. http://dx.doi.org/10.1002/cne.23979


Ito, T., Bishop, D. C., & Oliver, D. L. (2009). Two Classes of GABAergic Neurons in the Inferior Colliculus. Journal of Neuroscience, 29(44), 13860-13869. doi: 10.1523/jneurosci.3454-09.2009. http://www.jneurosci.org/cgi/content/abstract/29/44/13860 


Ito, T., Furuyama, T., Hase, K., Kobayasi, K. I., Hiryu, S., & Riquimaroux, H. (2018). Organization of subcortical auditory nuclei of Japanese house bat (Pipistrellus abramus) identified with cytoarchitecture and molecular expression. Journal of Comparative Neurology, 0(ja). doi: doi:10.1002/cne.24529. https://onlinelibrary.wiley.com/doi/abs/10.1002/cne.24529


Ito, T., Hioki, H., Sohn, J., Okamoto, S., Kaneko, T., Iino, S., & Oliver, D. L. (2015). Convergence of lemniscal and local excitatory inputs on large gabaergic tectothalamic neurons. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23789. http://dx.doi.org/10.1002/cne.23789


Ito, T., & Oliver, D. L. (2010). Origins of glutamatergic terminals in the inferior colliculus identified by retrograde transport and expression of VGLUT1 and VGLUT2 genes. Frontiers in Neuroanatomy, 4. doi. 

Ito, T., & Oliver, D. L. (2014). Local and Commissural IC Neurons Make Axosomatic Inputs on Large GABAergic Tectothalamic Neurons. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23623. http://dx.doi.org/10.1002/cne.23623


Ivakhnitskaia, E., Chin, M. R., Siegel, D., & Guaiquil, V. H. (2021). Vinaxanthone inhibits Semaphorin3A induced axonal growth cone collapse in embryonic neurons but fails to block its growth promoting effects on adult neurons. Scientific Reports, 11(1), 13019. doi: 10.1038/s41598-021-92375-w. https://doi.org/10.1038/s41598-021-92375-w


Ivankovic, D., Drew, J., Lesept, F., White, I. J., López Doménech, G., Tooze, S. A., & Kittler, J. T. (2019). Axonal autophagosome maturation defect through failure of ATG9A sorting underpins pathology in AP-4 deficiency syndrome. Autophagy, 1-17. doi: 10.1080/15548627.2019.1615302. https://doi.org/10.1080/15548627.2019.1615302


Ivanov, A., Esclapez, M., Pellegrino, C., Shirao, T., & Ferhat, L. (2009). Drebrin A regulates dendritic spine plasticity and synaptic function in mature cultured hippocampal neurons. Journal of Cell Science, jcs.033464. doi: 10.1242/jcs.033464. http://jcs.biologists.org/cgi/content/abstract/jcs.033464v1 


Iwai, L., Ramos, A., Schaler, A., Weinreb, S., Blazeski, R., & Mason, C. (2016). Retinal pigment epithelial integrity is compromised in the developing albino mouse retina. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24025. http://dx.doi.org/10.1002/cne.24025


Iwasa, M., Kawabe, K., & Sapru, H. N. (2013). Activation of melanocortin receptors in the intermediololateral cell column of the upper thoracic cord elicits tachycardia in the rat. American Journal of Physiology - Heart and Circulatory Physiology. doi: 10.1152/ajpheart.00443.2013. http://ajpheart.physiology.org/content/early/2013/07/03/ajpheart.00443.2...


Iwasato, T., Inan, M., Kanki, H., Erzurumlu, R. S., Itohara, S., & Crair, M. C. (2008). Cortical Adenylyl Cyclase 1 Is Required for Thalamocortical Synapse Maturation and Aspects of Layer IV Barrel Development. Journal of Neuroscience, 28(23), 5931-5943. doi: 10.1523/jneurosci.0815-08.2008. http://www.jneurosci.org/cgi/content/abstract/28/23/5931 


Iwata, K., Miyachi, S., Imanishi, M., Tsuboi, Y., Kitagawa, J., Teramoto, K., . . . Takada, M. (2011). Ascending multisynaptic pathways from the trigeminal ganglion to the anterior cingulate cortex. Experimental Neurology, 227(1), 69-78. doi. 

Iwata, Y., Ozaki, N., Hirata, H., Sugiura, Y., Horii, E., Nakao, E., . . . others. (2006). Fibroblast growth factor-2 enhances functional recovery of reinnervated muscle. Muscle and Nerve, 34(5), 623-630. doi. 

Iyengar, S., Qi, H. X., Jain, N., & Kaas, J. H. (2007). Cortical and thalamic connections of the representations of the teeth and tongue in somatosensory cortex of new world monkeys. Journal of Comparative Neurology, 501(1), 95-120. doi. 

Izquierdo, A., Wellman, C. L., & Holmes, A. (2006). Brief Uncontrollable Stress Causes Dendritic Retraction in Infralimbic Cortex and Resistance to Fear Extinction in Mice. Journal of Neuroscience, 26(21), 5733-5738. doi: 10.1523/jneurosci.0474-06.2006. http://www.jneurosci.org/cgi/content/abstract/26/21/5733 


Jaarsma, D., Ruigrok, T. J. H., Caffé, R., Cozzari, C., Levey, A. I., Mugnaini, E., & Voogd, J. (1997). Cholinergic innervation and receptors in the cerebellum. Progress in Brain Research, 114, 67-96. doi. 

Jaarsma, D., van der Pluijm, I., de Waard, M. C., Haasdijk, E. D., Brandt, R., Vermeij, M., . . . others. (2011). Age-Related Neuronal Degeneration: Complementary Roles of Nucleotide Excision Repair and Transcription-Coupled Repair in Preventing Neuropathology. PLoS genetics, 7(12), e1002405-e1002405. doi. 

Jacinto, L. R., Mata, R., Novais, A., Marques, F., & Sousa, N. (2016). The habenula as a critical node in chronic stress-related anxiety. Experimental Neurology. doi: http://dx.doi.org/10.1016/j.expneurol.2016.12.003. http://www.sciencedirect.com/science/article/pii/S0014488616304034


Jack, A., Hamad, M. I. K., Gonda, S., Gralla, S., Pahl, S., Hollmann, M., & Wahle, P. (2018). Development of Cortical Pyramidal Cell and Interneuronal Dendrites: a Role for Kainate Receptor Subunits and NETO1. [journal article]. Molecular Neurobiology. doi: 10.1007/s12035-018-1414-0. https://doi.org/10.1007/s12035-018-1414-0


Jackson, M. E., & Cauller, L. J. (1997). Evaluation of simplified compartmental models of reconstructed neocortical neurons for use in large-scale simulations of biological neural networks. Brain Research Bulletin, 44(1), 7-17. doi. 

Jacob, A. G., O'Brien, D., Singh, R. K., Comiskey Jr, D. F., Littleton, R. M., Mohammad, F., . . . Bolinger, C. (2013). Stress-Induced Isoforms of MDM2 and MDM4 Correlate with High-Grade Disease and an Altered Splicing Network in Pediatric Rhabdomyosarcoma. Neoplasia (New York, NY), 15(9), 1049. doi. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3769884/


Jacob, J., Kent, M., Benson-Amram, S., Herculano-Houzel, S., Raghanti, M. A., Ploppert, E., . . . Lambert, K. (2021). Cytoarchitectural characteristics associated with cognitive flexibility in raccoons. [https://doi.org/10.1002/cne.25197]. Journal of Comparative Neurology, n/a(n/a). doi: https://doi.org/10.1002/cne.25197. https://doi.org/10.1002/cne.25197


Jacob, V., Petreanu, L., Wright, N., Svoboda, K., & Fox, K. (2012). Regular Spiking and Intrinsic Bursting Pyramidal Cells Show Orthogonal Forms of Experience-Dependent Plasticity in Layer V of Barrel Cortex. Neuron, 73(2), 391-404. doi. 

Jacobs, B., Creswell, J., J.P., B., Ford, K. L., J.E., B., & Zaidel, E. (2003). Quantitative analysis of cortical pyramidal neurons following corpus callosotomy. Annals of Neurology, 54, 126-130. doi. 

Jacobs, B., Driscol, L., & Schall, M. (1997). Life Span Dendritic and Spine Changes in Areas 10 and 18 of Human Cortex: A Quantitative Golgi Study. Journal of Comparative Neurology, 386(4), 661-680. doi. 

Jacobs, B., Garcia, M. E., Shea-Shumsky, N. B., Tennison, M. E., Schall, M., Saviano, M. S., . . . Manger, P. R. (2017). Comparative Morphology of Gigantopyramidal Neurons in Primary Motor Cortex Across Mammals. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.24349. http://dx.doi.org/10.1002/cne.24349


Jacobs, B., Harland, T., Kennedy, D., Schall, M., Wicinski, B., Butti, C., . . . Manger, P. (2014). The neocortex of cetartiodactyls. II. Neuronal morphology of the visual and motor cortices in the giraffe (Giraffa camelopardalis). Brain Structure and Function, 1-22. doi: 10.1007/s00429-014-0830-9. http://dx.doi.org/10.1007/s00429-014-0830-9


Jacobs, B., Lee, L., Schall, M., Raghanti, M. A., Lewandowski, A. H., Kottwitz, J. J., . . . Sherwood, C. C. (2015). Neocortical neuronal morphology in the newborn giraffe (Giraffa camelopardalis tippelskirchi) and African elephant (Loxodonta africana). Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23841. http://dx.doi.org/10.1002/cne.23841


Jacobs, B., Lubs, J., Hannan, M., Anderson, K., Butti, C., Sherwood, C. C., . . . Manger, P. R. (2010). Neuronal morphology in the African elephant (Loxodonta africana) neocortex. Brain Structure and Function. doi. 

Jacobs, B., Schall, M., Prather, M., Kapler, E., Driscoll, L., Baca, S., . . . Treml, M. (2001). Regional dendritic and spine variation in human cerebral cortex: a quantitative Golgi study. Cerebral Cortex, 11(6), 558-558. doi. 

Jacobs, G. A., & Pittendrigh, C. S. (2002). Predicting emergent properties of neuronal ensembles using a database of individual neurons. Computational Neuroanatomy: Principles and Methods, 151-170. doi. 

Jacobson, L. (2019). Glucocorticoid receptor deletion from locus coeruleus norepinephrine neurons promotes depression-like social withdrawal in female but not male mice. Brain Research, 1710, 82-91. doi: https://doi.org/10.1016/j.brainres.2018.12.026. http://www.sciencedirect.com/science/article/pii/S0006899318306449


Jacoby, R. A., & Marshak, D. W. (2000). Synaptic connections of DB3 diffuse bipolar cell axons in macaque retina. Journal of Comparative Neurology, 416(1), 19-29. doi. 

Jacques, A., Chaaya, N., Hettiarachchi, C., Carmody, M.-L., Beecher, K., Belmer, A., . . . Johnson, L. R. (2019). Microtopography of fear memory consolidation and extinction retrieval within prefrontal cortex and amygdala. [journal article]. Psychopharmacology. doi: 10.1007/s00213-018-5068-4. https://doi.org/10.1007/s00213-018-5068-4


Jaeger, D. (2005). Realistic single cell modeling–from experiment to simulation. Special Issue on Realistic Neural Modeling WAM-BAMM. doi. 

Jaeger, D., & Kita, H. (2011). Functional connectivity and integrative properties of globus pallidus neurons. Neuroscience. doi. 

Jáidar, O., Carrillo-Reid, L., Nakano, Y., Lopez-Huerta, V. G., Hernandez-Cruz, A., Bargas, J., . . . Arbuthnott, G. W. (2019). Synchronized activation of striatal direct and indirect pathways underlies the behavior in unilateral dopamine-depleted mice. European Journal of Neuroscience, 0(ja). doi: doi:10.1111/ejn.14344. https://onlinelibrary.wiley.com/doi/abs/10.1111/ejn.14344


Jain, A., McKeon, R. J., Brady-Kalnay, S. M., & Bellamkonda, R. V. (2011). Sustained delivery of activated Rho GTPases and BDNF promotes axon growth in CSPG-rich regions following spinal cord injury. PLoS ONE, 6(1), e16135-e16135. doi. 

Jain, M., Budinger, G. R. S., Lo, A., Urich, D., Rivera, S. E., Ghosh, A. K., . . . others. (2011). Leptin Promotes Fibroproliferative Acute Respiratory Distress Syndrome by Inhibiting Peroxisome Proliferator–activated Receptor-γ. American Journal of Respiratory and Critical Care Medicine, 183(11), 1490-1498. doi. 

Jakobs, T. (2014). Analysis of Morphology and Structural Remodeling of Astrocytes. In L. Bakota & R. Brandt (Eds.), Laser Scanning Microscopy and Quantitative Image Analysis of Neuronal Tissue (Vol. 87, pp. 129-143): Springer New York.

Jakobs, T. C., Ben, Y., & Masland, R. H. (2003). CD15 immunoreactive amacrine cells in the mouse retina. Journal of Comparative Neurology, 465(3), 361-371. doi. 

Jakobs, T. C., Ben, Y., & Masland, R. H. (2007). Expression of mRNA for glutamate receptor subunits distinguishes the major classes of retinal neurons, but is less specific for individual cell types. Molecular Vision, 13, 933-933. doi. 

Jakobs, T. C., Koizumi, A., & Masland, R. H. (2008). The spatial distribution of glutamatergic inputs to dendrites of retinal ganglion cells. Journal of Comparative Neurology, 510(2), 221-236. doi. 

Jakovcevski, I., Djogo, N., Hölters, L. S., Szpotowicz, E., & Schachner, M. (2013). Transgenic overexpression of the cell adhesion molecule L1 in neurons facilitates recovery after mouse spinal cord injury. Neuroscience, (0). doi: http://dx.doi.org/10.1016/j.neuroscience.2013.07.067. http://www.sciencedirect.com/science/article/pii/S0306452213006684


Jakovcevski, I., Mayer, N., & Zecevic, N. (2011). Multiple origins of human neocortical interneurons are supported by distinct expression of transcription factors. Cerebral Cortex, 21(8), 1771-1782. doi. 

Jakovcevski, I., Siering, J., Hargus, G., Karl, N., Hoelters, L., Djogo, N., . . . Irintchev, A. (2009). Close homologue of adhesion molecule L1 promotes survival of Purkinje and granule cells and granule cell migration during murine cerebellar development. Journal of Comparative Neurology, 513(5), 496-510. doi. 

Jakovcevski, I., Wu, J., Karl, N., Leshchyns'ka, I., Sytnyk, V., Chen, J., . . . Schachner, M. (2007). Glial Scar Expression of CHL1, the Close Homolog of the Adhesion Molecule L1, Limits Recovery after Spinal Cord Injury. Journal of Neuroscience, 27(27), 7222-7233. doi: 10.1523/jneurosci.0739-07.2007. http://www.jneurosci.org/cgi/content/abstract/27/27/7222 


Jakubowska-Dogru, E., Elibol, B., Dursun, I., & Yürüker, S. (2017). Effects of prenatal binge-like ethanol exposure and maternal stress on postnatal morphological development of hippocampal neurons in rats. International Journal of Developmental Neuroscience, 61, 40-50. doi: https://doi.org/10.1016/j.ijdevneu.2017.06.002. http://www.sciencedirect.com/science/article/pii/S0736574817300953


Jalilian, E., Putra, I., Katz, E., Yazdanpanah, G., Guaiquil, V. H., Shen, X., . . . Djalilian, A. R. (2021). Interactions between mesenchymal stem cells (MSCs) and trigeminal ganglion (TGs) improve neurite growth and elongation. Investigative Ophthalmology and Visual Science, 62(8), 892-892. doi. 

Jamieson, J., Boyd, H. D., & McLachlan, E. M. (2003). Simulations to Derive Membrane Resistivity in Three Phenotypes of Guinea Pig Sympathetic Postganglionic Neuron. Journal of Neurophysiology, 89(5), 2430-2440. doi: 10.1152/jn.01000.2002. http://jn.physiology.org/cgi/content/abstract/89/5/2430 


Jang, H., Boltz, D., McClaren, J., Pani, A. K., Smeyne, M., Korff, A., . . . Smeyne, R. J. (2012). Inflammatory Effects of Highly Pathogenic H5N1 Influenza Virus Infection in the CNS of Mice. Journal of Neuroscience, 32(5), 1545-1559. doi: 10.1523/jneurosci.5123-11.2012. http://www.jneurosci.org/content/32/5/1545.abstract


Jang, H.-J., Kim, J. Y., Kim, S. Y., & Cho, K.-O. (2018). Persistent Lin28 Expression Impairs Neurite Outgrowth and Cognitive Function in the Developing Mouse Neocortex. [journal article]. Molecular Neurobiology. doi: 10.1007/s12035-018-1297-0. https://doi.org/10.1007/s12035-018-1297-0


Jankowsky, J. L., Melnikova, T., Fadale, D. J., Xu, G. M., Slunt, H. H., Gonzales, V., . . . Savonenko, A. V. (2005). Environmental Enrichment Mitigates Cognitive Deficits in a Mouse Model of Alzheimer's Disease. Journal of Neuroscience, 25(21), 5217-5224. doi: 10.1523/jneurosci.5080-04.2005. http://www.jneurosci.org/cgi/content/abstract/25/21/5217 


Jann, S., Beretta, S., & Bramerio, M. (2004). Idiopathic CIDP (I-CIDP) and CIDP associated with diabetes mellitus or monoclonal gammopathy of undetermined significance have different clinical course and response to treatment. Journal of the Peripheral Nervous System, 9(2), 118-118. doi. 

Janoos, F., Mosaliganti, K., Xu, X., Machiraju, R., Huang, K., & Wong, S. T. C. (2009). Robust 3D reconstruction and identification of dendritic spines from optical microscopy imaging. Medical Image Analysis, 13(1), 167-179. doi. 

Janova, H., Arinrad, S., Balmuth, E., Mitjans, M., Hertel, J., Habes, M., . . . Nave, K.-A. (2017). Microglia ablation alleviates myelin-associated catatonic signs in mice. The Journal of clinical investigation, 128(2). doi: 10.1172/jci97032. https://doi.org/10.1172/JCI97032


Jarosik, J., Legutko, B., Werner, S., Unsicker, K., & von Bohlen und Halbach, O. (2011). Roles of exogenous and endogenous FGF-2 in animal models of depression. Restorative Neurology and Neuroscience, 29(3), 153-165. doi. 

Jarsky, T., Mady, R., Kennedy, B., & Spruston, N. (2008). Distribution of bursting neurons in the CA1 region and the subiculum of the rat hippocampus. Journal of Comparative Neurology, 506(4), 535-547. doi. 

Jasmin, L., Janni, G., Moallem, T. M., Lappi, D. A., & Ohara, P. T. (2000). Schwann Cells Are Removed from the Spinal Cord after Effecting Recovery from Paraplegia. Journal of Neuroscience, 20(24), 9215-9223. doi. http://www.jneurosci.org/cgi/content/abstract/20/24/9215 


Jasnow, A. M., Ressler, K. J., Hammack, S. E., Chhatwal, J. p., & Rainnie, D. G. (2009). Distinct Subtypes of Cholecystokinin-containing Interneurons of the Basolateral Amygdala Identified using a CCK Promoter-Specific Lentivirus. Journal of Neurophysiology, 91149.92008. doi: 10.1152/jn.91149.2008. http://jn.physiology.org/cgi/content/abstract/91149.2008v1 


Javdani, F., Holló, K., Hegedűs, K., Kis, G., Hegyi, Z., Dócs, K., . . . Antal, M. (2015). Differential expression patterns of K+/Cl- co-transporter 2 in neurons within the superficial spinal dorsal horn of rats. Journal of Comparative Neurology, n/a-n/a. doi: 10.1002/cne.23774. http://dx.doi.org/10.1002/cne.23774


Jawerka, M., Colak, D., Dimou, L., Spiller, C., Lagger, S., Montgomery, R. L., . . . Götz, M. (2010). The specific role of histone deacetylase 2 in adult neurogenesis. Neuron Glia Biology, 6(02), 93-107. doi. 

Jedynak, J. P., Uslaner, J. M., Esteban, J. A., & Robinson, T. E. (2007). Methamphetamine-induced structural plasticity in the dorsal striatum. European Journal of Neuroscience, 25(3), 847-853. doi: doi:10.1111/j.1460-9568.2007.05316.x. http://www.blackwell-synergy.com/doi/abs/10.1111/j.1460-9568.2007.05316.x 


Jeerage, K. M., Oreskovic, T. L., Curtin, A. E., Sanders, A. W., Schwindt, R. K., & Chiaramonti, A. N. (2014). Citrate-stabilized gold nanoparticles as negative controls for measurements of neurite outgrowth. Toxicology in Vitro, (0). doi: http://dx.doi.org/10.1016/j.tiv.2014.10.007. http://www.sciencedirect.com/science/article/pii/S0887233314001970


Jeerage, K. M., Oreskovic, T. L., & Hume, S. L. (2012). Neurite outgrowth and differentiation of rat cortex progenitor cells are sensitive to lithium chloride at non-cytotoxic exposures. Neurotoxicology, (0). doi: 10.1016/j.neuro.2012.06.010. http://www.sciencedirect.com/science/article/pii/S0161813X12001428


Jeffs, J., Federer, F., Ichida, J. M., & Angelucci, A. (2012). High-Resolution