NEUROTROPHINS AND SYNAPTIC PLASTICITY

Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor.

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The Organization of Behavior; A Neuropsychological Theory.

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The Organization of Behavior: A Neuropsychological Theory

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The Nerve Growth Factor 35 Years Later

Levi‐Montalcini, R. (1987) · Science · doi:10.1126/science.3306916 · Cited by 3,109

Cell death during development of the nervous system

Oppenheim, R. W. (1991) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.14.030191.002321 · Cited by 3,084

Synaptic Activity and the Construction of Cortical Circuits

Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048

The period of susceptibility to the physiological effects of unilateral eye closure in kittens

Hubel, D. H., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009022 · Cited by 3,030

Physiology of the Neurotrophins

Lewin, G. R., & Barde, Y. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.001445 · Cited by 1,959

Neurotrophins and Neuronal Plasticity

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Trophic factors and neuronal survival

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Neuro-Immune Crosstalk in CNS Diseases

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Putative roles of soluble trophic factors in facial nerve regeneration, target reinnervation, and recovery of vibrissal whisking

Bendella, H., Rink, S., Grosheva, M., Sarıkçıoğlu, L., Gordon, T., & Angelov, D. N. (2017) · Experimental Neurology · doi:10.1016/j.expneurol.2017.10.029 · Cited by 26

Spatiotemporal Dynamics of Brain-Derived Neurotrophic Factor mRNA Induction in the Vestibulo-Olivary Network during Vestibular Compensation

Li, Y. X., Hashimoto, T., Tokuyama, W., Miyashita, Y., & Okuno, H. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02738.2001 · Cited by 26

BDNF Boosts Spike Fidelity in Chaotic Neural Oscillations

Fujisawa, S., Yamada, M. K., Nishiyama, N., Matsuki, N., & Ikegaya, Y. (2004) · Biophysical Journal · doi:10.1016/s0006-3495(04)74249-6 · Cited by 26

Soya phytoestrogens change cortical and hippocampal expression of BDNF mRNA in male rats

File, S. E., Hartley, D. E., Alom, N., & Rattray, M. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(02)01391-5 · Cited by 26

ErbB receptor signalling regulates dendrite formation in mouse cerebellar granule cells in vivo

Rieff, H. I., & Corfas, G. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04727.x · Cited by 26

Synapse disassembly: Figure 1.Preprint

Eaton, B. A., & Davis, G. W. (2003) · Genes & Development · doi:10.1101/gad.1113703 · Cited by 26

State-of-the-Art: Inflammatory and Metabolic Markers in Mood Disorders

Mucci, F., Marazziti, D., Vecchia, A. D., Baroni, S., Morana, P., Carpita, B., Mangiapane, P., Morana, F., Morana, B., & Dell’Osso, L. (2020) · Life · doi:10.3390/life10060082 · Cited by 29

Brain-derived neurotrophic factor scales presynaptic calcium transients to modulate excitatory neurotransmission

Wang, C. S., McCarthy, C. I., Guzikowski, N. J., Kavalali, E. T., & Monteggia, L. M. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2303664121 · Cited by 26

Real-Time qPCR Identifies Suitable Reference Genes for Borna Disease Virus-Infected Rat Cortical Neurons

Zhang, L., Liu, S., Zhang, L., You, H., Huang, R., Sun, L., He, P., Chen, S., Zhang, H., & Xie, P. (2014) · International Journal of Molecular Sciences · doi:10.3390/ijms151221825 · Cited by 25

Flat and tubular membrane systems for the reconstruction of hippocampal neuronal network

Morelli, S., Piscioneri, A., Salerno, S., Rende, M., Campana, C., Tasselli, F., Vito, A. D., Giusi, G., Canonaco, M., Drioli, E., et al. (2011) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.434 · Cited by 25

Interleukin-1β interferes with signal transduction induced by neurotrophin-3 in cortical neurons

Soi‐ampornkul, R., Tong, L., Thangnipon, W., Balázs, R., & Cotman, C. W. (2007) · Brain Research · doi:10.1016/j.brainres.2007.10.051 · Cited by 25

Environmental Enrichment Alters Neurotrophin Levels After Fetal Alcohol Exposure in Rats

Parks, E. A., McMechan, A. P., Hannigan, J. H., & Berman, R. F. (2008) · Alcoholism Clinical and Experimental Research · doi:10.1111/j.1530-0277.2008.00759.x · Cited by 25

Distinct actions of ancestral vinclozolin and juvenile stress on neural gene expression in the male rat

Gillette, R., Miller-Crews, I., Skinner, M. K., & Crews, D. P. (2015) · Frontiers in Genetics · doi:10.3389/fgene.2015.00056 · Cited by 25

Effect of Long-Term Body-Mass-Based Resistance Exercise on Cognitive Function in Elderly People

Ikudome, S., Mori, S., Unenaka, S., Kawanishi, M., Kitamura, T., & Nakamoto, H. (2016) · Journal of Applied Gerontology · doi:10.1177/0733464815625834 · Cited by 28

Programmed Cell Death and Neurotrophic Factors

Oppenheim, R. W., Milligan, C. E., & von Bartheld, C. S. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-385870-2.00018-4 · Cited by 25

The interplay of BDNF-TrkB with NMDA receptor in propofol-induced cognition dysfunction

Zhou, J., Wang, F., Zhang, J., Li, J., Ma, L., Dong, T., & Zhuang, Z. (2018) · BMC Anesthesiology · doi:10.1186/s12871-018-0491-y · Cited by 25

Effect of lurasidone vs olanzapine on neurotrophic biomarkers in unmedicated schizophrenia: A randomized controlled trial

Jena, M., Ranjan, R., Mishra, B. R., Mishra, A., Nath, S., Sahu, P., Meher, B. R., Srinivasan, A., & Maiti, R. (2019) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2019.02.007 · Cited by 25

Neurotrophin 4/5 is required for the normal development of the slow muscle fiber phenotype in the rat soleus

Carrasco, D. I., & ENGLISH, A. W. (2003) · Journal of Experimental Biology · doi:10.1242/jeb.00412 · Cited by 25

Passive avoidance training decreases synapse density in the hippocampus of the domestic chick

Nikolakopoulou, A. M., Davies, H. A., & Stewart, M. G. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04619.x · Cited by 25

Effects of Soft-diet Feeding on BDNF Expression in Hippocampus of Mice

Yamamoto, T., Hirayama, A., Hosoe, N., Furube, M., & Hirano, S. (2008) · The Bulletin of Tokyo Dental College · doi:10.2209/tdcpublication.49.185 · Cited by 25

Activity-dependent change in the protein level of brain-derived neurotrophic factor but no change in other neurotrophins in the visual cortex of young and adult ferrets

Ichisaka, S., Katoh‐Semba, R., Hata, Y., Ohshima, M., Kameyama, K., & Tsumoto, T. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00771-6 · Cited by 25

Neurotrophins and Cortical Development

McAllister, A. K. (2002) · Results and problems in cell differentiation · doi:10.1007/978-3-540-46006-0_5 · Cited by 25

Transient domoic acid excitotoxicity increases BDNF expression and activates both MEK- and PKA-dependent neurogenesis in organotypic hippocampal slices

Pérez‐Gómez, A., & Tasker, R. A. (2013) · BMC Neuroscience · doi:10.1186/1471-2202-14-72 · Cited by 24

Melatonin in Synaptic Impairments of Alzheimer’s Disease

Shi, Y., Fang, Y., Wei, Y., Jiang, Q., Zeng, P. H., Tang, N., Lu, Y., & Tian, Q. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-171178 · Cited by 24

The Genetic Association with Athlete Status, Physical Performance, and Injury Risk in Soccer

Murtagh, C. F., Hall, E. C. R., Brownlee, T. E., Drust, B., Williams, A. G., & Erskine, R. M. (2023) · International Journal of Sports Medicine · doi:10.1055/a-2103-0165 · Cited by 27

Syntaxin 8 Modulates the Post-synthetic Trafficking of the TrkA Receptor and Inflammatory Pain Transmission*

Chen, B., Zhao, L., Li, X., Ji, Y.-S., Li, N., Xu, X., & Chen, Z.-Y. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.567925 · Cited by 24

Contribution of BDNF/TrkB signalling in the rACC to the development of pain-related aversion via activation of ERK in rats with spared nerve injury

Wang, X., Zhang, L., Zhan, Y., Li, D., Zhang, Y., Wang, G., & Zhang, M. (2017) · Brain Research · doi:10.1016/j.brainres.2017.07.010 · Cited by 24

Investigation of the mechanisms of neuroprotection mediated by Ro5-4864 in brain injury

Palzur, E., Sharon, A., Shehadeh, M., & Soustiel, J. F. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.014 · Cited by 26

A novel prophylactic effect of furosemide treatment on autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE)

Yamada, J., Zhu, G., Okada, M., Hirose, S., Yoshida, S., Shiba, Y., Migita, K., Mori, F., Sugawara, T., Chen, L., et al. (2013) · Epilepsy Research · doi:10.1016/j.eplepsyres.2013.08.018 · Cited by 23

BDNF Val66Met polymorphism and cognitive impairment in Parkinson’s disease—a meta-analysis

Yin, Y., Su, X., Pan, L., & Li, C. (2019) · Neurological Sciences · doi:10.1007/s10072-019-03907-2 · Cited by 23

SNAP-25 is abundantly expressed in enteric neuronal networks and upregulated by the neurotrophic factor GDNF

Barrenschee, M., Böttner, M., Harde, J., Lange, C., Cossais, F., Ebsen, M., Vogel, I., & Wedel, T. (2015) · Histochemistry and Cell Biology · doi:10.1007/s00418-015-1310-x · Cited by 22

Effects of unilateral and bilateral labyrinthectomy on rat postural muscle properties: the soleus

Kasri, M., Picquet, F., & Falempin, M. (2003) · Experimental Neurology · doi:10.1016/j.expneurol.2003.09.006 · Cited by 23

Adaptation of Slow Myofibers: The Effect of Sustained BDNF Treatment of Extraocular Muscles in Infant Nonhuman Primates

Willoughby, C. L., Fleuriet, J., Walton, M. M. G., Mustari, M. J., & McLoon, L. K. (2015) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.15-16852 · Cited by 23

Sensory Input–Based Adaptation and Brain Architecture

Ptito, M., & Desgent, S. (2006) · Cambridge University Press eBooks · doi:10.1017/cbo9780511499722.007 · Cited by 22

Körperliche Aktivität fördert Gehirngesundheit und -leistungsfähigkeit

Strüder, H. K., Tagarakis, C. V. M., & Hollmann, W. (2003) · Nervenheilkunde · doi:10.1055/s-0038-1626335 · Cited by 23

Comparative Analysis of Neurotrophin Receptors and Ligands in Vertebrate Neurons: Tools for Evolutionary Stability or Changes in Neural Circuits?

von Bartheld, C. S., & Fritzsch, B. (2006) · Brain Behavior and Evolution · doi:10.1159/000094085 · Cited by 23

Ultrastructural Identification of Storage Compartments and Localization of Activity-Dependent Secretion of Neurotrophin 6 in Hippocampal Neurons

Gärtner, A., Shostak, Y., Hackel, N., Ethell, I. M., & Thoenen, H. (2000) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1999.0825 · Cited by 23

Adolescent maturation of inhibitory inputs onto cingulate cortex neurons is cell-type specific and TrkB dependent

Vandenberg, A., Piekarski, D. J., Caporale, N., Munoz-Cuevas, F. J., & Wilbrecht, L. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00005 · Cited by 22

Reservoir computing using back-end-of-line SiC-based memristors

Guo, D., Kapur, O. R., Dai, P., Han, Y., Beanland, R., Jiang, L., de Groot, C. H., & Huang, R. (2023) · Materials Advances · doi:10.1039/d3ma00141e · Cited by 22

Glycoprotein M6a as a signaling transducer in neuronal lipid rafts

Ito, Y., Honda, A., & Igarashi, M. (2017) · Neuroscience Research · doi:10.1016/j.neures.2017.11.002 · Cited by 22

The Seed of Zizyphus jujuba var. spinosa Attenuates Alzheimer’s Disease-Associated Hippocampal Synaptic Deficits through BDNF/TrkB Signaling

Kwon, H., Jung, I. H., Yi, J. H., Kim, J. H., Park, J. H., Lee, S., Jung, J. W., Lee, Y. C., Ryu, J. H., & Kim, D. H. (2017) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b17-00378 · Cited by 22

Future treatment strategies for neuropathic pain.

Marchand, F., Jones, N. G., & McMahon, S. (2009) · Handbook of Experimental Pharmacology · doi:10.1007/978-3-540-79090-7_17 · Cited by 20

An Analysis of Synaptic Normalization in a General Class of Hebbian Models

Elliott, T. (2003) · Neural Computation · doi:10.1162/08997660360581967 · Cited by 22

Impact of High Intensity Exercise on Muscle Morphology in EAE Rats

Wens, I., Dalgas, U., Verboven, K., Kosten, L., STEVENS, A., Hens, N., & Eijnde, B. O. (2015) · Physiological Research · doi:10.33549/physiolres.932824 · Cited by 22

Molecular Mechanisms in Perirhinal Cortex Selectively Necessary for Discrimination of Overlapping Memories, but Independent of Memory Persistence

Miranda, M., Kent, B. A., Morici, J. F., Gallo, F. T., Weisstaub, N., Saksida, L. M., Bussey, T. J., & Bekinschtein, P. (2017) · eNeuro · doi:10.1523/eneuro.0293-17.2017 · Cited by 22

Increased expression of endogenous biotin, but not BDNF, in telencephalic song regions during zebra finch vocal learning

Johnson, F., Norstrom, E. M., & Soderstrom, K. (2000) · Developmental Brain Research · doi:10.1016/s0165-3806(00)00002-x · Cited by 22

Ca2+, CREB and krüppel: A novel KLF7-binding element conserved in mouse and human TRKB promoters is required for CREB-dependent transcription

Kingsbury, T. J., & Krueger, B. K. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.04.004 · Cited by 22

Presynaptic neurotrophin‐3 increases the number of tectal synapses, vesicle density, and number of docked vesicles in chick embryos

Wang, X., Butowt, R., & von Bartheld, C. S. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10558 · Cited by 22

Cellular mechanisms of the acute increase of glutamate release induced by nerve growth factor in rat cerebral cortex

Raiteri, L., Giovedı̀, S., Benfenati, F., Raiteri, M., & Bonanno, G. (2003) · Neuropharmacology · doi:10.1016/s0028-3908(02)00403-3 · Cited by 22

Book Review: Neurotrophins and Plasticity in the Visual Cortex

Caleo, M., & Maffei, L. (2002) · The Neuroscientist · doi:10.1177/107385840200800110 · Cited by 22

Long-Term Brain and Behavioral Consequences of Early-Life Iron Deficiency

Kennedy, B. C., Wallin, D. J., Tran, P. V., & Georgieff, M. (2016) · Springer eBooks · doi:10.1007/978-3-319-22023-9_15 · Cited by 19

A human systems biology approach to discover new drug targets in epilepsy

Loeb, J. A. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02635.x · Cited by 21

Susceptibility to ethanol sensitization is differentially associated with changes in pCREB, trkB and BDNF mRNA expression in the mouse brain

Nona, C. N., Guirguis, S. M. E., & Nobrega, J. N. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.12.035 · Cited by 21

Impact of sound exposure and aging on brain-derived neurotrophic factor and tyrosine kinase B receptors levels in dorsal cochlear nucleus 80 days following sound exposure

Wang, H., Brozoski, T. J., Ling, L. L., Hughes, L. F., & Caspary, D. M. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.10.056 · Cited by 22

Developmental robotics: manifesto and application

Elliott, T., & Shadbolt, N. R. (2003) · Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rsta.2003.1250 · Cited by 21

Expression of Trk receptors in otolith-related neurons in the vestibular nucleus of rats

Zhang, F. X., Lai, C. H., Tse, Y. C., Shum, D. K., & Chan, Y. (2005) · Brain Research · doi:10.1016/j.brainres.2005.09.025 · Cited by 21

Changes in NGF/c-Fos double staining in the structures of the limbic system in juvenile and aged rats exposed to forced swim test

Badowska‐Szalewska, E., Klejbor, I., Cecot, T., Spodnik, J. H., & Moryś, J. (2009) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2009-1756 · Cited by 21

The outgrowth response of the axons of developing and regenerating rat retinal ganglion cells in vitro to neurotrophin treatment

Avwenagha, O., Campbell, G., & Bird, M. M. (2003) · Journal of Neurocytology · doi:10.1023/b:neur.0000021902.65233.8d · Cited by 21

Effects of a 14-day period of hindpaw sensory restriction on mRNA and protein levels of NGF and BDNF in the hindpaw primary somatosensory cortex

Dupont, E., Canu, M., Stevens, L., & Falempin, M. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.09.019 · Cited by 20

BDNF enhances dendritic Ca2+ signals evoked by coincident EPSPs and back-propagating action potentials in CA1 pyramidal neurons

Pozzo‐Miller, L. D. (2006) · Brain Research · doi:10.1016/j.brainres.2006.05.067 · Cited by 20

PI-3 Kinase and IP3: Partners in NT3-Induced Synaptic Transmission

Kaplan, D. R., & Cooper, E. (2001) · Nature Neuroscience · doi:10.1038/82897 · Cited by 20

Ca2+-evoked synaptic transmission and neurotransmitter receptor levels are impaired in the forebrain of trkb (−/−) mice

Carmona, M. A., Martı́nez, A., Soler-Jover, A., Blasi, J., Soriano, E., & Aguado, F. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00038-1 · Cited by 20

Actions of brain‐derived neurotrophic factor on evoked and spontaneous EPSCs dissociate with maturation of neurones cultured from rat visual cortex

Taniguchi, N., Takada, N., Kimura, F., & Tsumoto, T. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-1-00579.x · Cited by 19

Support of trigeminal sensory neurons by nonneuronal p75 neurotrophin receptors

Fan, L., Girnius, S. K., & Oakley, B. (2004) · Developmental Brain Research · doi:10.1016/j.devbrainres.2004.02.008 · Cited by 20

Involvement of hippocampal extracellular signal-regulated kinase 1/2 in spatial working memory in rats

Nagai, T., Kamei, H., Dohniwa, M., Takayanagi, M., Suzuki, M., Matsuya, T., Nabeshima, T., Takuma, K., & Yamada, K. (2006) · Neuroreport · doi:10.1097/01.wnr.0000233095.74913.88 · Cited by 21

Label-free detection of neuron–drug interactions using acoustic and Kelvin vibrational fields

Cheran, L., Cheung, S., Chawaf, A. A., Ellis, J. S., Belsham, D. D., MacKay, W. A., Lovejoy, D. A., & Thompson, M. E. (2007) · The Analyst · doi:10.1039/b615476j · Cited by 20

Afferent–target interactions during olivocerebellar development: transcommissural reinnervation indicates interdependence of Purkinje cell maturation and climbing fibre synapse elimination

Lohof, A. M., Mariani, J., & Sherrard, R. M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04493.x · Cited by 19

Hexahydrocurcumin Attenuates Neuronal Injury and Modulates Synaptic Plasticity in Chronic Cerebral Hypoperfusion in Rats

Jearjaroen, P., Thangwong, P., Tocharus, C., Lungkaphin, A., Chaichompoo, W., Srijun, J., Suksamrarn, A., & Tocharus, J. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03821-x · Cited by 19

The control of [125I]BDNF release from striatal rat brain slices

Goggi, J., Pullar, I. A., Carney, S. L., & Bradford, H. F. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02225-x · Cited by 19

Aberrant Behavioral and Neurobiologic Profiles in Rodents Exposed to Ethanol or Red Wine Early in Development

Nicolò, S. D., Carito, V., Fiore, M., & Giovanni Laviola, A. (2014) · Current Developmental Disorders Reports · doi:10.1007/s40474-014-0023-5 · Cited by 19

Maternal trans fat intake during pregnancy or lactation impairs memory and alters BDNF and TrkB levels in the hippocampus of adult offspring exposed to chronic mild stress

Pase, C. S., Roversi, K., Roversi, K., Vey, L. T., Dias, V. T., Veit, J. C., Maurer, L. H., Duarte, T., Emanuelli, T., Duarte, M. M. M. F., et al. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.11.009 · Cited by 20

Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D Gene

Aguirre, G. K., Butt, O. H., Datta, R., Román, A. J., Sumaroka, A., Schwartz, S., Cideciyan, A. V., & Jacobson, S. G. (2017) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.16-20413 · Cited by 20

Blockade of TrkB receptors in the nucleus accumbens prior to heterotypic stress alters corticotropin-releasing hormone (CRH), vesicular glutamate transporter 2 (vGluT2) and glucocorticoid receptor (GR) within the mesolimbic pathway

Azogu, I., & Plamondon, H. (2017) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.02.012 · Cited by 20

Disruption of brain-derived neurotrophic factor production from individual promoters generates distinct body composition phenotypes in mice

McAllan, L., Maynard, K. R., Kardian, A., Stayton, A., Fox, S. L., Stephenson, E. J., Kinney, C. E., Alshibli, N. K., Gomes, C., Pierre, J. F., et al. (2018) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00205.2018 · Cited by 18

Multisensory Perception, Verbal, Visuo-spatial and Motor Working Memory Modulation After a Single Open- or Closed-Skill Exercise Session in Children

O’Brien, J., Ottoboni, G., Tessari, A., & Setti, A. (2020) · Journal of Cognitive Enhancement · doi:10.1007/s41465-020-00189-x · Cited by 22

Identification of the isoforms of Ca2+/calmodulin‐dependent protein kinase II and expression of brain‐derived neurotrophic factor mRNAs in the substantia nigra

Kamata, A., Takeuchi, Y., & Fukunaga, K. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03531.x · Cited by 19

Forensic evaluation of trauma syndromes in children

Lubit, R., Hartwell, N., van Gor, W. G., & Eth, S. (2002) · Child and Adolescent Psychiatric Clinics of North America · doi:10.1016/s1056-4993(02)00026-3 · Cited by 19

Sorting Protein-related Receptor SorLA Controls Regulated Secretion of Glial Cell Line-derived Neurotrophic Factor

Geng, Z., Xu, F.-Y., Huang, S., & Chen, Z.-Y. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.246413 · Cited by 19

GDNF isoform affects intracellular trafficking and secretion of GDNF in neuronal cells

Wang, Y., Geng, Z., Zhao, L., Huang, S., Sheng, A.-L., & Chen, Z.-Y. (2008) · Brain Research · doi:10.1016/j.brainres.2008.05.087 · Cited by 18

Induction of rapid eye movement sleep by neurotrophin-3 and its co-localization with choline acetyltransferase in mesopontine neurons

Yamuy, J., Rojas, M. J., Torterolo, P., Sampogna, S. L., & Chase, M. H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00396-2 · Cited by 19

Brain-derived neurotrophic factor induces rapid morphological changes in dendritic spines of olfactory bulb granule cells in cultured slices through the modulation of glutamatergic signaling

Matsutani, S., & Yamamoto, N. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.10.030 · Cited by 19

Neural strategies for learning during sensitive periods of development

Bottjer, S. W. (2002) · Journal of Comparative Physiology A · doi:10.1007/s00359-002-0356-0 · Cited by 18

Captured in the Net of Space and Time: Understanding Cortical Field Evolution

Krubitzer, L. A., & Hunt, D. L. (2007) · Evolution of Nervous Systems · doi:10.1016/b0-12-370878-8/00058-6 · Cited by 19

Bone morphogenetic proteins regulate ionotropic glutamate receptors in human retina

Shen, W., Finnegan, S., Lein, P. J., Sullivan, S., Slaughter, M. M., & Higgins, D. M. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03681.x · Cited by 19

Antagonistic effects of TrkB and p75NTR on NMDA receptor currents in post‐synaptic densities transplanted into Xenopus oocytes

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Morphology of local axon collaterals of electrophysiologically characterised neurons in the rat medial septal/ diagonal band complex

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