Neurotrophins and neuronal differentiation in the central nervous system

McAllister, A.K.

doi:10.1007/pl00000920

Cited by 175Nerve injury and regenerationNeurogenesis and neuroplasticity mechanismsAxon Guidance and Neuronal Signaling

Neurotrophins and neuronal differentiation in the central nervous system

Open access

McAllister, A.K.·2001·Cellular and Molecular Life Sciences

DOI 10.1007/pl00000920PMC PMC11337387

Open this paper in CoChat — free account

Abstract

The central nervous system requires the proper formation of exquisitely precise circuits to function properly. These neuronal circuits are assembled during development by the formation of synaptic connections between hundreds of thousands of differentiating neurons. For these circuits to form correctly, neurons must elaborate precisely patterned axonal and dendritic arbors. Although the cellular and molecular mechanisms that guide neuronal differentiation and formation of connections remain mostly unknown, the neurotrophins have emerged recently as attractive candidates for regulating neuronal differentiation in the developing brain. The experiments reviewed here provide strong support for a bifunctional role for the neurotrophins in axonal and dendritic growth and are consistent with the exciting possibility that the neurotrophins might mediate activity-dependent synaptic plasticity.

Integrity signals

Registry

Crossref · 10.1007/pl00000920

Cites

61 of 61 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

BDNF regulates neuron survival, plasticity, and synaptic function, plays an integral role in differentiation during development, is affected by stress, and is associated with major depression and suicidal behavior.
“Brain-derived neurotrophic factor (BDNF) regulates neuron survival, plasticity, and synaptic function (169-174), plays an integral role in differentiation during development (175, 176), is affected by stress (177), and is associated with major depression and suicidal behavior (178).”
From A brain-centric model of suicidal behavior (2020) · cites this paper as [170]

The Molecular Biology of Axon Guidance
Tessier‐Lavigne, M., & Goodman, C. S. (1996) · Science · doi:10.1126/science.274.5290.1123 · Cited by 3,295 · see citing works
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 · see citing works
Functions of the neurotrophins during nervous system development: What the knockouts are teaching us
Snider, W. D. (1994) · Cell · doi:10.1016/0092-8674(94)90048-5 · Cited by 1,428 · see citing works
NEUROTROPHINS AND SYNAPTIC PLASTICITY
McAllister, A. K., Katz, L. C., & Lo, D. C. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.295 · Cited by 1,337 · see citing works
Self-citation
Netrin-1 Is Required for Commissural Axon Guidance in the Developing Vertebrate Nervous System
Serafini, T. A., Colamarino, S. A., Leonardo, E. D., Wang, H., Beddington, R. S. P., Skarnes, W. C., & Tessier‐Lavigne, M. (1996) · Cell · doi:10.1016/s0092-8674(00)81795-x · Cited by 1,286 · see citing works
Neurotrophins regulate dendritic growth in developing visual cortex
McAllister, A. K., Lo, D. C., & Katz, L. C. (1995) · Neuron · doi:10.1016/0896-6273(95)90171-x · Cited by 959 · see citing works
Self-citation
The changing scene of neurotrophic factors
Thoenen, H. (1991) · Trends in Neurosciences · doi:10.1016/0166-2236(91)90097-e · Cited by 820 · see citing works
Conversion of Neuronal Growth Cone Responses from Repulsion to Attraction by Cyclic Nucleotides
Song, H., Ming, G., He, Z., Lehmann, M., McKerracher, L. J., Tessier‐Lavigne, M., & Poo, M.-M. (1998) · Science · doi:10.1126/science.281.5382.1515 · Cited by 796 · see citing works
Neurotrophic factors: from molecule to man
Lindsay, R. M., Wiegand, S. J., Altar, C. A., & DiStefano, P. S. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90099-x · Cited by 789 · see citing works
Impulse activity and the patterning of connections during cns development
Shatz, C. J. (1990) · Neuron · doi:10.1016/0896-6273(90)90333-b · Cited by 766 · see citing works
Effects of brain-derived neurotrophic factor on optic axon branching and remodelling in vivo
Cohen-Cory, S., & Fraser, S. E. (1995) · Nature · doi:10.1038/378192a0 · Cited by 580 · see citing works
Opposing Roles for Endogenous BDNF and NT-3 in Regulating Cortical Dendritic Growth
McAllister, A. K., Katz, L. C., & Lo, D. C. (1997) · Neuron · doi:10.1016/s0896-6273(00)80316-5 · Cited by 570 · see citing works
Self-citation
Neurotrophin-evoked rapid excitation through TrkB receptors
Kafitz, K. W., Rose, C. R., Thoenen, H., & Konnerth, A. (1999) · Nature · doi:10.1038/44847 · Cited by 542 · see citing works
Neuronal Chemotaxis: Chick Dorsal-Root Axons Turn Toward High Concentrations of Nerve Growth Factor
Gundersen, R. W., & Barrett, J. N. (1979) · Science · doi:10.1126/science.493992 · Cited by 523 · see citing works
Neurotrophin Binding to the p75 Receptor Modulates Rho Activity and Axonal Outgrowth
Yamashita, T., Tucker, K. L., & Barde, Y. (1999) · Neuron · doi:10.1016/s0896-6273(00)81114-9 · Cited by 521 · see citing works
Light regulates expression of brain-derived neurotrophic factor mRNA in rat visual cortex.
Castrén, E., Zafra, F., Thoenen, H., & Lindholm, D. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.20.9444 · Cited by 513 · see citing works
Neurotrophin Regulation of Cortical Dendritic Growth Requires Activity
McAllister, A. K., Katz, L. C., & Lo, D. C. (1996) · Neuron · doi:10.1016/s0896-6273(00)80239-1 · Cited by 503 · see citing works
Self-citation
Impairments in High-Frequency Transmission, Synaptic Vesicle Docking, and Synaptic Protein Distribution in the Hippocampus of BDNF Knockout Mice
Pozzo‐Miller, L. D., Gottschalk, W., Zhang, L., McDermott, K., Du, J., Gopalakrishnan, R., Oho, C., Sheng, Z., & Lu, B. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-12-04972.1999 · Cited by 471 · see citing works
In Vitro Experiments on the Effects of Mouse Sarcomas 180 and 37 on the Spinal and Sympathetic Ganglia of the Chick Embryo
Levi‐Montalcini, R., Meyer, H., & Hamburger, V. (1997) · World Scientific series in 20th century biology · doi:10.1142/9789812830319_0007 · Cited by 446 · see citing works
Abnormal Cerebellar Development and Foliation in BDNF−/− Mice Reveals a Role for Neurotrophins in CNS Patterning
Schwartz, P. M., Borghesani, P. R., Levy, R. L., Pomeroy, S. L., & Segal, R. A. (1997) · Neuron · doi:10.1016/s0896-6273(00)80938-1 · Cited by 438 · see citing works
Human trks: molecular cloning, tissue distribution, and expression of extracellular domain immunoadhesins
Shelton, D., Sutherland, J. S., Gripp, J. T., Camerato, T., Armanini, M. P., Phillips, H., Carroll, K., Spencer, S., & Levinson, A. D. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00477.1995 · Cited by 398 · see citing works
Lamina-Specific Connectivity in the Brain: Regulation by N-Cadherin, Neurotrophins, and Glycoconjugates
Akihiro, I., & Sanes, J. R. (1997) · Science · doi:10.1126/science.276.5317.1428 · Cited by 388 · see citing works
Cellular and Molecular Mechanisms of Dendrite Growth
McAllister, A. K. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.963 · Cited by 382 · see citing works
Self-citation
Brain-derived neurotrophic factor mediates the activity-dependent regulation of inhibition in neocortical cultures
Rutherford, L. C., DeWan, A., Lauer, H. M., & Turrigiano, G. G. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-12-04527.1997 · Cited by 381 · see citing works
Destabilization of Cortical Dendrites and Spines by BDNF
Horch, H. W., Krüttgen, A., Portbury, S. D., & Katz, L. C. (1999) · Neuron · doi:10.1016/s0896-6273(00)80785-0 · Cited by 345 · see citing works
Growth factor signaling: Where is the specificity?
Chao, M. V. (1992) · Cell · doi:10.1016/0092-8674(92)90068-n · Cited by 341 · see citing works
Trophic regulation of nerve cell morphology and innervation in the autonomic nervous system
Purves, D., Snider, W. D., & Voyvodic, J. T. (1988) · Nature · doi:10.1038/336123a0 · Cited by 338 · see citing works
Development of sympathetic neurons in compartmentalized cultures
Campenot, R. B. (1982) · Developmental Biology · doi:10.1016/0012-1606(82)90233-0 · Cited by 298 · see citing works
Neurotrophins and activity-dependent development of the neocortex
Bonhoeffer, T. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80017-1 · Cited by 297 · see citing works
Brain-Derived Neurotrophic Factor Enhances Long-Term Potentiation in Rat Visual Cortex
Akaneya, Y., Tsumoto, T., Kinoshita, S., & Hatanaka, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-17-06707.1997 · Cited by 284 · see citing works
Synaptic Innervation Density Is Regulated by Neuron-Derived BDNF
Causing, C. G., Gloster, A. T., Aloyz, R. S., Bamji, S. X., Chang, E., Fawcett, J., Kuchel, G. A., & Miller, F. D. (1997) · Neuron · doi:10.1016/s0896-6273(00)80266-4 · Cited by 283 · see citing works
Cortical Degeneration in the Absence of Neurotrophin Signaling
Xu, B., Zang, K., Ruff, N. L., Zhang, Y. A., McConnell, S. K., Stryker, M. P., & Reichardt, L. F. (2000) · Neuron · doi:10.1016/s0896-6273(00)81153-8 · Cited by 279 · see citing works
Truncated and full-length TrkB receptors regulate distinct modes of dendritic growth
Yacoubian, T. A., & Lo, D. C. (2000) · Nature Neuroscience · doi:10.1038/73911 · Cited by 278 · see citing works
TrkB and TrkC Signaling Are Required for Maturation and Synaptogenesis of Hippocampal Connections
Martı́nez, A., Alcántara, S., Borrell, V., del Rı́o, J. A., Blasi, J., Otal, R., Campos, N., Boronat, A., Barbacid, M., Silos‐Santiago, I., et al. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-18-07336.1998 · Cited by 262 · see citing works
Neurotrophins promote maturation of developing neuromuscular synapses
Wang, T., Xie, K., & Lu, B. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-04796.1995 · Cited by 249 · see citing works
Brain-Derived Neurotrophic Factor Differentially Regulates Retinal Ganglion Cell Dendritic and Axonal ArborizationIn Vivo
Lom, B., & Cohen‐Cory, S. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-22-09928.1999 · Cited by 247 · see citing works
Nerve growth factor regulates sympathetic ganglion cell morphology and survival in the adult mouse
Ruit, K. G., Osborne, P., Schmidt, R., Johnson, E., & Snider, W. D. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-07-02412.1990 · Cited by 229 · see citing works
Axonal growth and fasciculation linked to differential expression of BDNF and NT3 receptors in developing cerebellar granule cells
Segal, R. A., Pomeroy, S. L., & Stiles, C. D. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-04970.1995 · Cited by 212 · see citing works
NT-4-mediated rescue of lateral geniculate neurons from effects of monocular deprivation
Riddle, D. R., Lo, D. C., & Katz, L. C. (1995) · Nature · doi:10.1038/378189a0 · Cited by 200 · see citing works
Granule Neuron Regulation of Purkinje Cell Development: Striking a Balance Between Neurotrophin and Glutamate Signaling
Morrison, M. E., & Mason, C. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03563.1998 · Cited by 172 · see citing works
Nerve growth factor enhances dendritic arborization of sympathetic ganglion cells in developing mammals
Snider, W. D. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-07-02628.1988 · Cited by 168 · see citing works
The effects of nerve growth factor and its antiserum on synapses in the superior cervical ganglion of the guinea‐pig.
Njå, A., & Purves, D. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012260 · Cited by 168 · see citing works
TrkB Signaling Modulates Spine Density and Morphology Independent of Dendrite Structure in Cultured Neonatal Purkinje Cells
Shimada, A., Mason, C. A., & Morrison, M. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08559.1998 · Cited by 164 · see citing works
Neurotrophin 3 potentiates neuronal activity and inhibits gamma-aminobutyratergic synaptic transmission in cortical neurons.
Kim, H. G., Wang, T., Olafsson, P., & Lu, B. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.25.12341 · Cited by 161 · see citing works
Brain‐Derived Neurotrophic Factor Increases the Stimulation‐Evoked Release of Glutamate and the Levels of Exocytosis‐Associated Proteins in Cultured Cortical Neurons from Embryonic Rats
Takei, N., Sasaoka, K., Inoue, K., Takahashi, M., Endo, Y., & Hatanaka, H. (1997) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1997.68010370.x · Cited by 148 · see citing works
NGF and BDNF are differentially modulated by visual experience in the developing geniculocortical pathway
Schoups, A. A., Elliott, R. C., Friedman, W., & Black, I. B. (1995) · Developmental Brain Research · doi:10.1016/0165-3806(95)00043-d · Cited by 145 · see citing works
Rapid dendritic movements during synapse formation and rearrangement
Wong, W. T., & Wong, R. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)00059-8 · Cited by 121 · see citing works
Nerve growth factor and brain-derived neurotrophic factor increase neurotransmitter release in the rat visual cortex
Sala, R., Viegi, A., Rossi, F., Pizzorusso, T., Bonanno, G., Raiteri, M., & Maffei, L. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00227.x · Cited by 120 · see citing works
Nerve growth factor prevents the amblyopic effects of monocular deprivation.
Domenici, L., Berardi, N., Carmignoto, G., Vantini, G., & Maffei, L. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.19.8811 · Cited by 115 · see citing works
Brain-derived neurotrophic factor alters the synaptic modification threshold in visual cortex
Huber, K. M., Sawtell, N. B., & Bear, M. F. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00050-1 · Cited by 107 · see citing works
Neurotrophins as in vitro growth cone guidance molecules for embryonic sensory neurons
Paves, H., & Saarma, M. (1997) · Cell and Tissue Research · doi:10.1007/s004410050933 · Cited by 105 · see citing works
Changing Patterns of Expression and Subcellular Localization of TrkB in the Developing Visual System
Cabelli, R. J., Allendoerfer, K. L., Radeke, M. J., Welcher, A. A., Feinstein, S. C., & Shatz, C. J. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-24-07965.1996 · Cited by 102 · see citing works
Brain-derived neurotrophic factor blocks long-term depression in rat visual cortex
Akaneya, Y., Tsumoto, T., & Hatanaka, H. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.6.4198 · Cited by 98 · see citing works
Neurotrophic Factors Increase Neuregulin Expression in Embryonic Ventral Spinal Cord Neurons
Loeb, J. A., & Fischbach, G. D. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-04-01416.1997 · Cited by 94 · see citing works
Monoclonal antibodies to nerve growth factor affect the postnatal development of the visual system.
Berardi, N., Cellerino, A., Domenici, L., Fagiolini, M., Pizzorusso, T., Cattaneo, A., & Maffei, L. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.2.684 · Cited by 88 · see citing works
Rapid Regulation of Brain-Derived Neurotrophic Factor mRNA within Eye-Specific Circuits during Ocular Dominance Column Formation
Lein, E. S., & Shatz, C. J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-04-01470.2000 · Cited by 86 · see citing works
cAMP-Mediated Regulation of Neurotrophin-Induced Collapse of Nerve Growth Cones
Wang, Q., & Zheng, J. Q. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-13-04973.1998 · Cited by 77 · see citing works
Acute Morphogenic and Chemotropic Effects of Neurotrophins on Cultured EmbryonicXenopusSpinal Neurons
Ming, G., Lohof, A. M., & Zheng, J. Q. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-20-07860.1997 · Cited by 75 · see citing works
Dynamic regulation of BDNF and NT-3 expression during visual system development
Lein, E. S., Hohn, A., & Shatz, C. J. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000424)420:1 · Cited by 73 · see citing works
Administration or deprivation of nerve growth factor during development permanently alters neuronal geometry
Ruit, K. G., & Snider, W. D. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903140110 · Cited by 64 · see citing works
Opposing roles for neurotrophin-3 in targeting and collateral formation of distinct sets of developing cortical neurons
Castellani, V., & Bolz, J. (1999) · Development · doi:10.1242/dev.126.15.3335 · Cited by 46 · see citing works

Flagged first, then by citations

Sorted by citations

The neurobiology of autism
Pardo, C. A., & Eberhart, C. G. (2007) · Brain Pathology · doi:10.1111/j.1750-3639.2007.00102.x · Cited by 514 · see citing works
Nerve growth factor: from the early discoveries to the potential clinical use
Aloe, L., Rocco, M. L., Bianchi, P., & Manni, L. (2012) · Journal of Translational Medicine · doi:10.1186/1479-5876-10-239 · Cited by 460 · see citing works
A human peripheral blood monocyte-derived subset acts as pluripotent stem cells
Zhao, Y. L., Glesne, D. A., & Huberman, E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0536882100 · Cited by 458 · see citing works
Brain-derived neurotrophic factor: role in depression and suicide
Dwivedi, Y. (2009) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s5700 · Cited by 355 · see citing works
Apoptotic mechanisms and the synaptic pathology of schizophrenia
Glantz, L. A., Gilmore, J. H., Lieberman, J. A., & Jarskog, L. F. (2005) · Schizophrenia Research · doi:10.1016/j.schres.2005.08.014 · Cited by 289 · see citing works
Brain-Derived Neurotrophic Factor Modulates Fast Synaptic Inhibition by Regulating GABA<sub>A</sub>Receptor Phosphorylation, Activity, and Cell-Surface Stability
Jovanovic, J. N., Thomas, P., Kittler, J. T., Smart, T. G., & Moss, S. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3606-03.2004 · Cited by 273 · see citing works
Nerve Growth Factor: A Focus on Neuroscience and Therapy
Aloe, L., Rocco, M., Balzamino, B. O., & Micera, A. (2015) · Current Neuropharmacology · doi:10.2174/1570159x13666150403231920 · Cited by 240 · see citing works
Brain-derived neurotrophic factor (BDNF) and food intake regulation: A minireview
Lebrun, B., Bariohay, B., Moyse, E., & Jean, A. (2006) · Autonomic Neuroscience · doi:10.1016/j.autneu.2006.02.027 · Cited by 219 · see citing works
A brain-centric model of suicidal behavior
Mann, J. J., & Rizk, M. M. (2020) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2020.20081224 · Cited by 214 · see citing works
Apoptotic mechanisms in the pathophysiology of schizophrenia
Jarskog, L. F., Glantz, L. A., Gilmore, J. H., & Lieberman, J. A. (2005) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2005.03.010 · Cited by 214 · see citing works
Postsynaptic TrkC and Presynaptic PTPσ Function as a Bidirectional Excitatory Synaptic Organizing Complex
Takahashi, H., Arstikaitis, P., Prasad, T., Bartlett, T. E., Wang, Y. T., Murphy, T. H., & Craig, A. M. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.024 · Cited by 193 · see citing works
Association of BDNF Val66Met Polymorphism and Brain BDNF Levels with Major Depression and Suicide
Youssef, M. M., Underwood, M. D., Huang, Y.-Y., Hsiung, S.-C., Liu, Y., Simpson, N. R., Bakalian, M. J., Rosoklija, G. B., Dwork, A. J., Arango, V., et al. (2018) · International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyy008 · Cited by 183 · see citing works
Rasagiline: A novel anti-Parkinsonian monoamine oxidase-B inhibitor with neuroprotective activity
Weinreb, O., Amit, T., Bar‐Am, O., & Youdim, M. B. H. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.06.008 · Cited by 170 · see citing works
Brain-Derived Neurotrophic Factor, Food Intake Regulation, and Obesity
Rosas‐Vargas, H., Martínez‐Ezquerro, J. D., & Bienvenu, T. (2011) · Archives of Medical Research · doi:10.1016/j.arcmed.2011.09.005 · Cited by 160 · see citing works
Mood Stabilizers Target Cellular Plasticity and Resilience Cascades: Implications for the Development of Novel Therapeutics
Bachmann, R. F., Schloesser, R. J., Gould, T. D., & Manji, H. K. (2005) · Molecular Neurobiology · doi:10.1385/mn:32:2:173 · Cited by 149 · see citing works
Through the looking glass: Examining neuroanatomical evidence for cellular alterations in major depression
Hercher, C., Turecki, G., & Mechawar, N. (2009) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2009.01.006 · Cited by 142 · see citing works
Control of adult neurogenesis by programmed cell death in the mammalian brain
Ryu, J. R., Hong, C. J., Kim, J. Y., Kim, E. K., Sun, W., & Yu, S.-W. (2016) · Molecular Brain · doi:10.1186/s13041-016-0224-4 · Cited by 141 · see citing works
Decreased mRNA and Protein Expression of BDNF, NGF, and their Receptors in the Hippocampus from Suicide: An Analysis in Human Postmortem Brain
Banerjee, R., Ghosh, A. K., Ghosh, B., Bhattacharyya, S., & Mondal, A. C. (2013) · Clinical Medicine Insights: Pathology · doi:10.4137/cpath.s12530 · Cited by 135 · see citing works
Automated Sholl analysis of digitized neuronal morphology at multiple scales: Whole cell Sholl analysis versus Sholl analysis of arbor subregions
Langhammer, C. G., Previtera, M. L., Sweet, E. S., Sran, S. S., Chen, M., & Firestein, B. L. (2010) · Cytometry Part A · doi:10.1002/cyto.a.20954 · Cited by 135 · see citing works
An Overview of Brain-Derived Neurotrophic Factor and Implications for Excitotoxic Vulnerability in the Hippocampus
Murray, P. S., & Holmes, P. V. (2011) · International Journal of Peptides · doi:10.1155/2011/654085 · Cited by 132 · see citing works
Antidiabetic Effect of Brain-Derived Neurotrophic Factor and Its Association with Inflammation in Type 2 Diabetes Mellitus
Eyileten, C., Kapłon‐Cieślicka, A., Mirowska-Guzel, D. M., Małek, Ł. A., & Postula, M. A. (2017) · Journal of Diabetes Research · doi:10.1155/2017/2823671 · Cited by 123 · see citing works
Nature versus nurture revisited: an old idea with a new twist
Krubitzer, L. A., & Kahn, D. M. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(03)00088-1 · Cited by 123 · see citing works
Suicide Brain Is Associated with Decreased Expression of Neurotrophins
Dwivedi, Y., Mondal, A. C., Rizavi, H. S., & Conley, R. R. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.04.014 · Cited by 120 · see citing works
Curcuminoids Promote Neurite Outgrowth in PC12 Cells through MAPK/ERK- and PKC-Dependent Pathways
Liao, K.-K., Wu, M., Chen, P., Huang, S., Chiu, S.-J., Ho, C., & Yen, J.-H. (2011) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf203290r · Cited by 119 · see citing works
Methylation of BDNF in women with bulimic eating syndromes: associations with childhood abuse and borderline personality disorder
Thaler, L., Gauvin, L., Joober, R., Groleau, P., de Guzman, R., Ambalavanan, A., Israel, M., Wilson, S., & Steiger, H. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.04.010 · Cited by 117 · see citing works
Running from Stress: Neurobiological Mechanisms of Exercise-Induced Stress Resilience
Nowacka-Chmielewska, M. M., Grabowska, K., Grabowski, M., Meybohm, P., Burek, M., & Małecki, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113348 · Cited by 117 · see citing works
Proliferation and apoptosis in the developing human neocortex
Chan, W. Y., Lorke, D. E., Tiu, S. C., & Yew, D. T. W. (2002) · The Anatomical Record · doi:10.1002/ar.10100 · Cited by 111 · see citing works
Evidence demonstrating role of microRNAs in the etiopathology of major depression
Dwivedi, Y. (2011) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2011.04.002 · Cited by 107 · see citing works
Neurotrophins and acupuncture
Manni, L., Albanesi, M., Guaragna, M., Paparo, S. B., & Aloe, L. (2010) · Autonomic Neuroscience · doi:10.1016/j.autneu.2010.03.020 · Cited by 103 · see citing works
Does PGC1α/FNDC5/BDNF Elicit the Beneficial Effects of Exercise on Neurodegenerative Disorders?
Jodeiri Farshbaf, M., Ghaedi, K., Megraw, T. L., Curtiss, J., Shirani Faradonbeh, M., Vaziri, P., & Nasr-Esfahani, M. H. (2016) · NeuroMolecular Medicine · doi:10.1007/s12017-015-8370-x · Cited by 101 · see citing works
The Effect of sequential bilateral low‐frequency rTMS over dorsolateral prefrontal cortex on serum level of BDNF and GABA in patients with primary insomnia
Feng, J., Zhang, Q., Zhang, C., Wen, Z., & Zhou, X. (2019) · Brain and Behavior · doi:10.1002/brb3.1206 · Cited by 94 · see citing works
Induction of Neurotrophic Factors GDNF and BDNF Associated with the Mechanism of Neurorescue Action of Rasagiline and Ladostigil
Weinreb, O., Amit, T., Bar‐Am, O., & Youdim, M. B. H. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1403.011 · Cited by 93 · see citing works
Hippocampal dysfunctions caused by cranial irradiation: A review of the experimental evidence
Son, Y., Yang, M., Wang, H., & Moon, C. (2015) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2015.01.007 · Cited by 84 · see citing works
BDNF and VEGF in the pathogenesis of stress-induced affective diseases: An insight from experimental studies
Nowacka-Chmielewska, M. M., & Obuchowicz, E. (2013) · Pharmacological Reports · doi:10.1016/s1734-1140(13)71031-4 · Cited by 82 · see citing works
Serum BDNF Levels in Suicide Attempters Related to Psychosocial Stressors: A Comparative Study with Depression
Deveci, A., Aydemir, O., Taşkin, O., Taneli, F., & Esen-Danacı, A. (2007) · Neuropsychobiology · doi:10.1159/000111539 · Cited by 80 · see citing works
MicroRNA-107 inhibits tumor growth and metastasis by targeting the BDNF-mediated PI3K/AKT pathway in human non-small lung cancer
Xia, H., Yang, L., & Lv, X. (2016) · International Journal of Oncology · doi:10.3892/ijo.2016.3628 · Cited by 81 · see citing works
Retracted
The role of microRNAs in synaptic plasticity, major affective disorders and suicidal behavior
Serafini, G., Pompili, M., Innamorati, M., Giordano, G., Montebovi, F., Sher, L., Dwivedi, Y., & Girardi, P. (2012) · Neuroscience Research · doi:10.1016/j.neures.2012.04.001 · Cited by 80 · see citing works
A Review of Brain-derived Neurotrophic Factor as a Candidate Biomarker in Schizophrenia
Nurjono, M., Lee, J., & Chong, S. A. (2012) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2012.10.2.61 · Cited by 75 · see citing works
Requirement of TrkB for synapse elimination in developing cerebellar Purkinje cells
Bosman, L. W. J., Hartmann, J., Barski, J. J., Lepier, A., Noll‐Hussong, M., Reichardt, L. F., & Konnerth, A. (2007) · Journal of Neurocytology · doi:10.1007/s11068-006-9002-z · Cited by 72 · see citing works
Age-dependent Spontaneous Hyperexcitability and Impairment of GABAergic Function in the Hippocampus of Mice Lacking trkB
Carmona, M. A., Pozas, E., Martı́nez, A., Espinosa‐Parrilla, J. F., Soriano, E., & Aguado, F. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi083 · Cited by 69 · see citing works
Reduced brain‐derived neurotrophic factor is associated with a loss of serotonergic innervation in the hippocampus of aging mice
Luellen, B. A., Bianco, L. E., Schneider, L., & Andrews, A. M. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00279.x · Cited by 68 · see citing works
MicroRNA-15a-5p suppresses cancer proliferation and division in human hepatocellular carcinoma by targeting BDNF
Long, J., Jiang, C., Liu, B., Shi, F., & Kuang, M. (2015) · Tumor Biology · doi:10.1007/s13277-015-4427-6 · Cited by 62 · see citing works
Corticotropin‐releasing factor and urocortin differentially modulate rat Purkinje cell dendritic outgrowth and differentiation in vitro
Swinny, J. D., Metzger, F., Ijkema‐Paassen, J., Gounko, N. V., Gramsbergen, A., & van der Want, J. J. L. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03279.x · Cited by 59 · see citing works
Hippocampal dysfunction during the chronic phase following a single exposure to cranial irradiation
Son, Y., Yang, M., Kim, J., Kim, J., Kim, S., Kim, J.-C., Shin, T., Wang, H., Jo, S., Jung, U., et al. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.01.018 · Cited by 57 · see citing works
Social isolation mediated anxiety like behavior is associated with enhanced expression and regulation of BDNF in the female mouse brain
Kumari, A., Singh, P., Baghel, M. S., & Thakur, M. K. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.02.032 · Cited by 57 · see citing works
Calcitonin gene-related peptide pre-administration acts as a novel antidepressant in stressed mice
Hashikawa‐Hobara, N., Ogawa, T., Sakamoto, Y., Matsuo, Y., Ogawa, M., Zamami, Y., & Hashikawa, N. (2015) · Scientific Reports · doi:10.1038/srep12559 · Cited by 56 · see citing works
Lichen-derived compounds show potential for central nervous system therapeutics
Reddy, R. G., Veeraval, L., Maitra, S., Chollet‐Krugler, M., Tomasi, S., Dévéhat, F. L., Boustié, J., & Chakravarty, S. (2016) · Phytomedicine · doi:10.1016/j.phymed.2016.08.010 · Cited by 55 · see citing works
Clinical, molecular genetics and therapeutic aspects of syndromic obesity
Geets, E., Meuwissen, M. E. C., & Hul, W. V. (2018) · Clinical Genetics · doi:10.1111/cge.13367 · Cited by 55 · see citing works
Brain-Derived Neurotrophic Factor in Infants <32 Weeks Gestational Age: Correlation With Antenatal Factors and Postnatal Outcomes
Rao, R., Mashburn, C. B., Mao, J., Wadhwa, N., Smith, G. M., & Desai, N. S. (2009) · Pediatric Research · doi:10.1203/pdr.0b013e31819d9ea5 · Cited by 53 · see citing works
Low-Intensity Pulsed Ultrasound Enhances Nerve Growth Factor-Induced Neurite Outgrowth through Mechanotransduction-Mediated ERK1/2–CREB–Trx-1 Signaling
Zhao, L., Feng, Y., Hu, H., Shi, A., Zhang, L., & Wan, M. (2016) · Ultrasound in Medicine & Biology · doi:10.1016/j.ultrasmedbio.2016.07.017 · Cited by 52 · see citing works
Expression patterns and different subcellular localization of the growth factors HDGF (hepatoma-derived growth factor) and HRP-3 (HDGF-related protein-3) suggest functions in addition to their mitogenic activity
Abouzied, M. M., Baader, S. L., Dietz, F., Kappler, J., Gieselmann, V., & Franken, S. (2004) · Biochemical Journal · doi:10.1042/bj20030916 · Cited by 52 · see citing works
Role of sensory‐motor cortex activity in postnatal development of corticospinal axon terminals in the cat
Friel, K. M., & Martin, J. H. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20483 · Cited by 51 · see citing works
Cranial irradiation regulates CREB-BDNF signaling and variant BDNF transcript levels in the mouse hippocampus
Son, Y., Yang, M., Kang, S., Lee, S., Kim, J., Kim, J., Park, S., Kim, J., Jo, S., Jung, U., et al. (2015) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2015.03.002 · Cited by 48 · see citing works
Role of the Central Cholinergic System in the Therapeutics of Schizophrenia
Terry, A. V. (2008) · Current Neuropharmacology · doi:10.2174/157015908785777247 · Cited by 48 · see citing works
MicroRNA-497 inhibits thyroid cancer tumor growth and invasion by suppressing BDNF
Wang, P., Meng, X., Huang, Y., Lv, Z., Liu, J., Wang, G., Meng, W., Xue, S., Zhang, Q., Zhang, P., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.13747 · Cited by 47 · see citing works
Retracted
Before the loss: neuronal dysfunction in Niemann–Pick Type C disease
Paul, C. A., Boegle, A. K., & Maue, R. A. (2004) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2004.08.012 · Cited by 47 · see citing works
Neuroprotective profile of the multitarget drug rasagiline in Parkinson's disease
Weinreb, O., Amit, T., Riederer, P. F., Youdim, M. B. H., & Mandel, S. A. (2011) · International review of neurobiology · doi:10.1016/b978-0-12-386467-3.00007-8 · Cited by 45 · see citing works
Intrauterine growth restriction and development of the hippocampus: implications for learning and memory in children and adolescents
Gilchrist, C. P., Cumberland, A. L., Walker, D. W., & Tolcos, M. (2018) · The Lancet Child & Adolescent Health · doi:10.1016/s2352-4642(18)30245-1 · Cited by 45 · see citing works
BDNF and TrkB protein expression is altered in the fetal hippocampus but not cerebellum after chronic prenatal compromise
Dieni, S., & Rees, S. M. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.06.003 · Cited by 44 · see citing works
Functional Characterization of Human ProNGF and NGF Mutants: Identification of NGF P61SR100E as a “Painless” Lead Investigational Candidate for Therapeutic Applications
Malerba, F., Paoletti, F., Ercole, B. B., Materazzi, S., Nassini, R., Coppi, E., Patacchini, R., Capsoni, S., Lamba, D., & Cattaneo, A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136425 · Cited by 44 · see citing works
MicroRNA‑10a‑5p suppresses cancer proliferation and division in human cervical cancer by targeting BDNF
Zhai, L., Li, Y., Lan, X., & Ai, L. (2017) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2017.5312 · Cited by 44 · see citing works
Correlations between cognitive impairment and brain-derived neurotrophic factor expression in the hippocampus of post-stroke depression rats
Zhang, Z., Wu, L., Song, J., & Li, W. (2012) · Molecular Medicine Reports · doi:10.3892/mmr.2012.1009 · Cited by 39 · see citing works
Neuroprotective Effect of Natural Products on Peripheral Nerve Degeneration: A Systematic Review
Araújo-Filho, H. G., Quintans‐Júnior, L. J., Barreto, A. S., Almeida, J. R. G. D. S., Barreto, R. D. S. S., & Quintans, J. D. S. S. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1771-2 · Cited by 39 · see citing works
MicroRNA-16 targets mRNA involved in neurite extension and branching in hippocampal neurons during presymptomatic prion disease
Burak, K., Lamoureux, L., Boese, A. S., Majer, A., Saba, R., Niu, Y., Frost, K. L., & Booth, S. A. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.12.011 · Cited by 35 · see citing works
Neurotrophic Action of 5-Hydroxylated Polymethoxyflavones: 5-Demethylnobiletin and Gardenin A Stimulate Neuritogenesis in PC12 Cells
Chiu, S.-P., Wu, M., Chen, P., Ho, Y.-R., Tai, M., Ho, C., & Yen, J.-H. (2013) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf4024678 · Cited by 35 · see citing works
Acupuncture and Neurotrophin Modulation
Soligo, M., Nori, S. L., Protto, V., Florenzano, F., & Manni, L. (2013) · International review of neurobiology · doi:10.1016/b978-0-12-411545-3.00005-5 · Cited by 35 · see citing works
A Tale of Two Maladies? Pathogenesis of Depression with and without the Huntington’s Disease Gene Mutation
Du, X., Pang, T. Y., & Hannan, A. J. (2013) · Frontiers in Neurology · doi:10.3389/fneur.2013.00081 · Cited by 33 · see citing works
A role for the tyrosine kinase ACK1 in neurotrophin signaling and neuronal extension and branching
Torre, A. L., Masdeu, M., Cotrufo, T., Moubarak, R. S., del Rı́o, J. A., Comella, J. X., Soriano, E., & Ureña, J. M. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.99 · Cited by 31 · see citing works
Phenotype of cerebellar glutamatergic neurons is altered in stargazer mutant mice lacking brain‐derived neurotrophic factor mRNA expression
Richardson, C. A., & Leitch, B. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20386 · Cited by 31 · see citing works
Regulation of Neurogenesis and Neuronal Differentiation by Natural Compounds
Chen, B., Yang, H., An, J., Tian, D., Guo, Y., & Yan, Y. (2021) · Current Stem Cell Research & Therapy · doi:10.2174/1574888x16666210907141447 · Cited by 30 · see citing works
Multifaceted Roles of Nerve Growth Factor: A Comprehensive Review with a Special Insight into Pediatric Perspectives
Capossela, L., Gatto, A., Ferretti, S., Sarno, L. D., Graglia, B., Massese, M., Soligo, M., & Chiaretti, A. (2024) · Biology · doi:10.3390/biology13070546 · Cited by 29 · see citing works
Insight into potential mechanisms of hypobaric hypoxia–induced learning and memory deficit – Lessons from rat studies
Qaid, E. Y. A., Zakaria, R., Sulaiman, S. F., Yusof, N. A. M., Shafin, N., Othman, Z., Ahmad, A. H., & Aziz, C. A. (2017) · Human & Experimental Toxicology · doi:10.1177/0960327116689714 · Cited by 29 · see citing works
Neudesin is involved in anxiety behavior: structural and neurochemical correlates
Novais, A., Ferreira, A. C., Marques, F., Pêgo, J. M., Cerqueira, J., David-Pereira, A., Campos, F. L., Dalla, C., Kokras, N., Sousa, N., et al. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00119 · Cited by 29 · see citing works
Long non-coding RNA XIST promotes retinoblastoma cell proliferation, migration, and invasion by modulating microRNA-191-5p/brain derived neurotrophic factor
Xu, Y., Fu, Z., Gao, X., Wang, R., & Li, Q. (2021) · Bioengineered · doi:10.1080/21655979.2021.1918991 · Cited by 28 · see citing works
Effect of Purified Murine NGF on Isolated Photoreceptors of a Rodent Developing Retinitis Pigmentosa
Rocco, M. L., Balzamino, B. O., Passeri, P. P., Micera, A., & Aloe, L. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124810 · Cited by 28 · see citing works
Prenatal and Early Postnatal Exposure to Cigarette Smoke Decreases BDNF/TrkB Signaling and Increases Abnormal Behaviors Later in Life
Xiao, L., Kish, V. L., Benders, K. M., & Wu, Z.-X. (2015) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyv117 · Cited by 28 · see citing works
Far-infrared ray radiation promotes neurite outgrowth of neuron-like PC12 cells through AKT1 signaling
Wang, J., Lin, Y., Young, T., & Chen, M. (2018) · Journal of the Formosan Medical Association · doi:10.1016/j.jfma.2018.08.015 · Cited by 28 · see citing works
Pituitary Adenylate Cyclase-Activating Polypeptide and Vasoactive Intestinal Peptide Inhibit Dendritic Growth in Cultured Sympathetic Neurons
Drahushuk, K. M., Connell, J. W., & Higgins, D. M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-15-06560.2002 · Cited by 28 · see citing works
Role of non-coding RNAs and exosomal non-coding RNAs in retinoblastoma progression
Davoodi, N. A., Najafi, S., Ghale-Noie, Z. N., Piranviseh, A., Mollazadeh, S., Asouri, S. A., Asemi, Z., Morshedi, M., Zadeh, S. S. T., Hamblin, M. R., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1065837 · Cited by 27 · see citing works
Conserved Cues for Axon and Dendrite Growth in the Developing Cortex
McAllister, A. K. (2002) · Neuron · doi:10.1016/s0896-6273(01)00577-3 · Cited by 27 · see citing works
Self-citation
Role of Vitamin D in Parkinson’s Disease
Lương, K. V. Q., & Nguyễn, L. (2012) · ISRN Neurology · doi:10.5402/2012/134289 · Cited by 25 · see citing works
MicroRNA-382 inhibits cell proliferation and invasion of retinoblastoma by targeting BDNF-mediated PI3K/AKT signalling pathway
Song, D., Diao, J., Yang, Y., & Chen, Y. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7396 · Cited by 25 · see citing works
Long-Term Non-Invasive Treatment via Intranasal Administration of Nerve Growth Factor Protects the Human Brain in Frontotemporal Dementia associated with Corticobasal Syndrome: A Pilot Study
de Bellis, A., de Bellis, M., & Aloe, L. (2018) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-180055 · Cited by 25 · see citing works
A comparative analysis of the structural, functional and biological differences between Mouse and Human Nerve Growth Factor
Paoletti, F., Malerba, F., Ercole, B. B., Lamba, D., & Cattaneo, A. (2014) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2014.12.005 · Cited by 25 · see citing works
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 · see citing works
Self-citation
Exploring the Effect of Acute and Regular Physical Exercise on Circulating Brain-Derived Neurotrophic Factor Levels in Individuals with Obesity: A Comprehensive Systematic Review and Meta-Analysis
Ceylan, H. İ., Silva, A. F., Ramírez‐Campillo, R., & Murawska‐Ciałowicz, E. (2024) · Biology · doi:10.3390/biology13050323 · Cited by 23 · see citing works
Developmental changes of neurotrophin mRNA expression in the layers of rat visual cortex
Patz, S., & Wahle, P. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05126.x · Cited by 22 · see citing works
Increased serum levels of apoptosis in deficit syndrome schizophrenia patients: a preliminary study
Albayrak, Y., Beyazyüz, M., Küfeciler, T., Bulut, L., Ünsal, C., Baykal, S., Akyol, E., Kuloğlu, M., & Hashimoto, K. (2016) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s106993 · Cited by 22 · see citing works
MicroRNA‑147 targets BDNF to inhibit cell proliferation, migration and invasion in non‑small cell lung cancer
Li, F., Wang, X., & Yang, L. (2020) · Oncology Letters · doi:10.3892/ol.2020.11715 · Cited by 21 · see citing works
Genetic dissection of trophic interactions in the larval optic neuropil of Drosophila melanogaster
Moncalvo, V. G. R., & Campos, A. R. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.08.030 · Cited by 21 · see citing works
Molecular mechanisms of activity-dependent changes in dendritic morphology: role of RGK proteins
Ghiretti, A. E., & Paradis, S. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.05.003 · Cited by 20 · see citing works
Brain-Derived Neurotrophic Factor in Sera of Breastfed Epileptic Infants and in Breastmilk of Their Mothers
Ismail, A. M., Babers, G. M., & Rehany, M. A. E. (2015) · Breastfeeding Medicine · doi:10.1089/bfm.2015.0008 · Cited by 20 · see citing works
Enriched environment modulates behavior, myelination and augments molecules governing the plasticity in the forebrain region of rats exposed to chronic immobilization stress
Thamizhoviya, G., & Vanisree, A. J. (2019) · Metabolic Brain Disease · doi:10.1007/s11011-018-0370-8 · Cited by 20 · see citing works
Neurological Regulation of the Bone Marrow Niche
Aerts‐Kaya, F., Ulum, B., Mammadova, A., Köse, S., Aydın, G., Korkusuz, P., & Uçkan, D. (2019) · Advances in experimental medicine and biology · doi:10.1007/5584_2019_398 · Cited by 19 · see citing works
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 · see citing works
Evaluation of the Effect of NT-3 and Biodegradable Poly-l-lactic Acid Nanofiber Scaffolds on Differentiation of Rat Hair Follicle Stem Cells into Neural Cells In Vitro
Ghoroghi, F. M., Hejazian, L. B., Esmaeilzade, B., Dodel, M., Roudbari, M., & Nobakht, M. (2013) · Journal of Molecular Neuroscience · doi:10.1007/s12031-013-0073-x · Cited by 19 · see citing works
The antibiotic doxycycline mimics the NGF signaling in PC12 cells: A relevant mechanism for neuroprotection
Amaral, L. D., Santos, N. A. G. D., Sisti, F. M., Del Bel, E., & Santos, A. C. D. (2021) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2021.109454 · Cited by 18 · see citing works
Antineurodegenerative Labdane Diterpenoid Glycosides from the Twigs of Pinus koraiensis
Park, K.-J., Khan, Z., Subedi, L., Kim, S. Y., & Lee, K. R. (2020) · Journal of Natural Products · doi:10.1021/acs.jnatprod.9b01158 · Cited by 18 · see citing works
SH2B1β Interacts with STAT3 and Enhances Fibroblast Growth Factor 1-Induced Gene Expression during Neuronal Differentiation
Chang, Y.-J., Chen, K.-W., Chen, C.-J., Lin, M.-H., Sun, Y.-J., Lee, J.-L., Chiu, I.-M., & Chen, L.-Y. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00940-13 · Cited by 20 · see citing works
Targeting the Cation-Chloride Co-Transporter NKCC1 to Re-Establish GABAergic Inhibition and an Appropriate Excitatory/Inhibitory Balance in Selective Neuronal Circuits: A Novel Approach for the Treatment of Alzheimer’s Disease
Capsoni, S., Arisi, I., Malerba, F., D’Onofrio, M., Cattaneo, A., & Cherubini, E. (2022) · Brain Sciences · doi:10.3390/brainsci12060783 · Cited by 17 · see citing works

Authors: McAllister, A. K.
Affiliations: University of California, Davis (US)
Corresponding author: McAllister, A.K.
ORCID: McAllister, A.K.
Venue: Cellular and Molecular Life Sciences
Publisher: Springer Science and Business Media LLC
Published: 2001-07
Volume: 58
Issue: 8
Pages: 1054-1060
ISSN: 1420-682X (ISSN-L)
DOI: 10.1007/pl00000920
PMC: PMC11337387
OpenAlex: W2143920419
Cited by: 175
References: 61
Citations by year: 2026: 2 · 2025: 2 · 2024: 3 · 2023: 4 · 2022: 10 · 2021: 8 · 2020: 6 · 2019: 6 · 2018: 9 · 2017: 10 · 2016: 8 · 2015: 13 · 2014: 12 · 2013: 10 · 2012: 9
FWCI: 2.21
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: www.springer.com/tdm (tdm)
Locations: Cellular and Molecular Life Sciences (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
Keywords: neurotrophins, neuronal differentiation, central nervous system development, axon growth, dendritic growth, synaptic connectivity, activity-dependent synaptic plasticity, neural circuit formation
MeSH terms: Animals, Axons, Cell Differentiation, Central Nervous System, Dendrites, Humans, Nerve Growth Factors, Neuronal Plasticity, Neurons, Synapses

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Neurotrophins and neuronal differentiation in the central nervous system

Abstract

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks