The DOI matches its Crossref record; 123 of the 123 references it cites were found in a registry or an index.
Neurotrophin signal transduction in the nervous system
Abstract
Neurotrophins use two types of receptors, the Trk tyrosine kinase receptors and the p75 neurotrophin receptor (p75NTR), to regulate the growth, development, survival and repair of the nervous system. These receptors can either collaborate with or inhibit each other's actions to mediate neurotrophin effects. The development and survival of neurons is thus based upon the functional interplay of the signals generated by Trk and p75NTR. In the past two years, the signaling pathways used by these receptors, including Akt and MAPK-induced signaling via Trk, and JNK, p53, and NF-kappaB signaling via p75NTR, have been identified. In addition, a number of novel p75NTR-interacting proteins have been identified that transmit growth, survival, and apoptotic signals.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“It regulates many different cellular processes involved in the development and maintenance of normal brain function by binding and activating the TrkB, a member of the larger family of Trk receptors.”
From Neurotrophic Factor BDNF, Physiological Functions and Therapeutic Potential in Depression, Neurodegeneration and Brain Cancer (2020) · cites this paper as [86]
In the citing paper
“BDNF signals through the tropomycin receptor kinase B (TrkB) and the low affinity p75 neurotrophin receptor (p75NTR).”
From Neurotrophic Factor BDNF, Physiological Functions and Therapeutic Potential in Depression, Neurodegeneration and Brain Cancer (2020) · cites this paper as [86]
In the citing paper
“Both proBDNF and mBDNF are active, eliciting opposing effects via the p75 neurotrophin receptor (p75NTR), a member of the tumor necrosis factor (TNF) receptor family and TrkB receptor, respectively.”
From Neurotrophic Factor BDNF, Physiological Functions and Therapeutic Potential in Depression, Neurodegeneration and Brain Cancer (2020) · cites this paper as [86]
In the citing paper
“mBDNF binds with the high-affinity TrkB receptor, the receptor dimerizes, and the intracellular tyrosine residues are autophosphorylated [86].”
From Neurotrophic Factor BDNF, Physiological Functions and Therapeutic Potential in Depression, Neurodegeneration and Brain Cancer (2020) · cites this paper as [86]
In the citing paper
“where it is implicated in plasticity mechanisms hypothesized to underlie learning6.”
From Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease (2009) · cites this paper as [6]
In the citing paper
“Deficiencies in canonical signaling through Erk–mitogen-activated protein kinase kinase, but not Akt, would be predicted in a model of cell dysfunction but not death6; our findings in aged rats are consistent with this prediction, as BDNF ameliorates age-related deficiencies in Erk without detectably perturbing Akt.”
From Neuroprotective effects of brain-derived neurotrophic factor in rodent and primate models of Alzheimer's disease (2009) · cites this paper as [6]
Citations
Cites
1 retracted
Neuronal Cell Death: Retraction
Hagg, T. (1999) · Science · doi:10.1126/science.285.5426.337h · Cited by 13
RetractedAkt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery
Datta, S. R., Dudek, H., Tao, X., Masters, S., Fu, H., Gotoh, Y., & Greenberg, M. E. (1997) · Cell · doi:10.1016/s0092-8674(00)80405-5 · Cited by 5,689
Akt Promotes Cell Survival by Phosphorylating and Inhibiting a Forkhead Transcription Factor
Brunet, A., Bonni, A., Zigmond, M. J., Lin, M. Z., Juo, P., Hu, L. S., Anderson, M. J., Arden, K. C., Blenis, J., & Greenberg, M. E. (1999) · Cell · doi:10.1016/s0092-8674(00)80595-4 · Cited by 5,594
Opposing Effects of ERK and JNK-p38 MAP Kinases on Apoptosis
Xia, Z., Dickens, M., Raingeaud, J., Davis, R. J., & Greenberg, M. E. (1995) · Science · doi:10.1126/science.270.5240.1326 · Cited by 5,273
Cellular survival: a play in three Akts
Datta, S. R., Brunet, A., & Greenberg, M. E. (1999) · Genes & Development · doi:10.1101/gad.13.22.2905 · Cited by 4,216
Regulation of neuronal survival by the serine-threonine protein kinase Akt
Dudek, H., Datta, S. R., Franke, T. F., Birnbaum, M. J., Yao, R., Cooper, G. M., Segal, R. A., Kaplan, D. R., & Greenberg, M. E. (1997) · Science · doi:10.1126/science.275.5300.661 · Cited by 2,436
Self-citationPhosphatidylinositol-3-OH kinase direct target of Ras
Rodriguez-Viciana, P., Warne, P. H., Dhand, R., Vanhaesebroeck, B., Gout, I., Fry, M. J., Waterfield, M. D., & Downward, J. (1994) · Nature · doi:10.1038/370527a0 · Cited by 1,954
Bonni, A., Brunet, A., West, A. E., Datta, S. R., Takasu, M. A., & Greenberg, M. E. (1999) · Science · doi:10.1126/science.286.5443.1358 · Cited by 1,908
Interleukin-3-Induced Phosphorylation of BAD Through the Protein Kinase Akt
Peso, L. D., González-Garcı́a, M., Page, C., Herrera, R., & Nuñez, G. (1997) · Science · doi:10.1126/science.278.5338.687 · Cited by 1,797
The PI3K‒PDK1 connection: more than just a road to PKB
Vanhaesebroeck, B., & Alessi, D. R. (2000) · Biochemical Journal · doi:10.1042/bj3460561 · Cited by 1,649
Cited by
Sorted by citations
Items 601–700 of 1,001
Shieh, P., Jan, C., & Liang, W.-Z. (2019) · Toxicology · doi:10.1016/j.tox.2019.02.004 · Cited by 61
Shi, G., Han, J., & Andres, D. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507364200 · Cited by 61
The Role of the p75 Neurotrophin Receptor in Cholinergic Dysfunction in Alzheimer's Disease
Coulson, E. J., May, L. M., Sykes, A. M., & Hamlin, A. S. (2009) · The Neuroscientist · doi:10.1177/1073858408331376 · Cited by 61
Kendall, S. E., Goldhawk, D. E., Kubu, C. J., Barker, P. A., & Verdi, J. M. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(02)00204-6 · Cited by 61
Guo, D.-J., Li, F., Yu, P. H., & Chan, S. (2012) · Pharmaceutical Biology · doi:10.3109/13880209.2012.716852 · Cited by 60
Transcriptome profiling in neurodegenerative disease
Courtney, E., Kornfeld, S., Janitz, K., & Janitz, M. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.08.018 · Cited by 64
Huang, Y. Y., Yasuda, H., Sarihi, A., & Tsumoto, T. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0899-08.2008 · Cited by 62
Hesperidin pretreatment protects hypoxia–ischemic brain injury in neonatal rat
Rong, Z., Pan, R., Xu, Y., Zhang, C., Cao, Y., & Liu, D. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.09.030 · Cited by 60
Patani, N., Jiang, W. G., & Mokbel, K. (2011) · Cancer Cell International · doi:10.1186/1475-2867-11-23 · Cited by 60
APPLs: More than just adiponectin receptor binding proteins
Liu, Z., Xiao, T., Peng, X., Li, G., & Hu, F. (2017) · Cellular Signalling · doi:10.1016/j.cellsig.2017.01.018 · Cited by 58
Jullien, J., Guili, V., Derrington, E. A., Darlix, J., Reichardt, L. F., & Rudkin, B. B. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m202401200 · Cited by 60
Presynaptic membrane receptors in acetylcholine release modulation in the neuromuscular synapse
Tomàs, J. M., Santafé, M. M., García, N., Lanuza, M. A., Tomàs, M., Besalduch, N., Obis, T., Priego, M., & Hurtado, E. (2014) · Journal of Neuroscience Research · doi:10.1002/jnr.23346 · Cited by 59
Regulation of neuronal survival by the extracellular signal-regulated protein kinase 5
Finegan, K. G., Wang, X., Lee, E.-J., Robinson, A., & Tournier, C. (2009) · Cell Death and Differentiation · doi:10.1038/cdd.2008.193 · Cited by 59
Yang, S., Tang, W., He, Y., Wen, L., Sun, B., & Li, S. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0155-8 · Cited by 58
Halvorsen, E. M., Dennis, J., Keeney, P. M., Sturgill, T. W., Tuttle, J. B., & Bennett, J. P. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03216-x · Cited by 59
Kosacka, J., Figiel, M., Engele, J., Hilbig, H., Majewski, M. K., & Spanel‐Borowski, K. (2005) · Cell and Tissue Research · doi:10.1007/s00441-004-1068-2 · Cited by 60
Neurotoxic mechanisms of DNA damage: focus on transcriptional inhibition
Hetman, M., Vashishta, A., & Rempała, G. A. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06859.x · Cited by 58
Sodero, A. O., Trovò, L., Iannilli, F., Veldhoven, P. P. V., Dotti, C. G., & Martín, M. G. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.07079.x · Cited by 62
Neurotrophin-3-induced PI-3 kinase/Akt signaling rescues cortical neurons from apoptosis
Liot, G., Gabriel, C., Cacquevel, M., Ali, C., MacKenzie, E. T., Buisson, A., & Vivien, D. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.01.002 · Cited by 58
Brain-Derived Neurotrophic Factor in TNF-α Modulation of Ca2+ in Human Airway Smooth Muscle
Prakash, Y. S., Thompson, M. A., & Pabelick, C. M. (2009) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2008-0151oc · Cited by 59
Ligand-independent signaling by disulfide-crosslinked dimers of the p75 neurotrophin receptor
Vilar, M., Charalampopoulos, I., Kenchappa, R. S., Reversi, A., Klos, J. M., Karaca, E., Simi, A., Spuch, C., Choi, S., Friedman, W., et al. (2009) · Journal of Cell Science · doi:10.1242/jcs.055061 · Cited by 58
Effect of general anesthetics on the developing brain
Reddy, S. (2012) · Journal of Anaesthesiology Clinical Pharmacology · doi:10.4103/0970-9185.92426 · Cited by 58
Stahl, K., Mylonakou, M. N., Skare, Ø., Amiry-Moghaddam, M. R., & Torp, R. (2011) · Brain Research · doi:10.1016/j.brainres.2010.12.090 · Cited by 63
Lee, S. J., Li, G. G., Kim, S. T., Hong, M. E., Jang, J., Yoon, N., Ahn, S. M., Murphy, D., Christiansen, J., Wei, G., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.5494 · Cited by 60
Role of BDNF/TrkB pathway in the visual system: therapeutic implications for glaucoma
Mysona, B. A., Zhao, J., & Bollinger, K. E. (2016) · Expert Review of Ophthalmology · doi:10.1080/17469899.2017.1259566 · Cited by 57
Sharma, M., Dierkes, T., & Sajikumar, S. (2017) · Aging Cell · doi:10.1111/acel.12634 · Cited by 57
Redox Signaling Mechanisms in Nervous System Development
Olguín‐Albuerne, M., & Morán, J. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7284 · Cited by 59
Presgraves, S. P., Borwege, S., Millan, M. J., & Joyce, J. N. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.06.021 · Cited by 58
Akt-dependent Expression of NAIP-1 Protects Neurons against Amyloid-β Toxicity
Lesné, S., Gabriel, C., Nelson, D. A., White, E., MacKenzie, E. T., Vivien, D., & Buisson, A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413495200 · Cited by 58
Moore, D. B., Madorsky, I., Paiva, M., & Heaton, M. B. (2004) · Journal of Neurobiology · doi:10.1002/neu.20010 · Cited by 59
Sympathetic neurons synthesize and secrete pro‐nerve growth factor protein
Hasan, W., Pedchenko, T. V., Krizsan‐Agbas, D., Baum, L. L., & Smith, P. G. (2003) · Journal of Neurobiology · doi:10.1002/neu.10250 · Cited by 64
In vivo insular cortex LTP induced by brain-derived neurotrophic factor
Escobar, M. L., Figueroa-Guzmán, Y., & Gómez-Palacio-Schjetnan, A. (2003) · Brain Research · doi:10.1016/j.brainres.2003.08.015 · Cited by 58
Tongiorgi, E., Domenici, L., & Simonato, M. (2005) · Molecular Neurobiology · doi:10.1385/mn:33:1:017 · Cited by 58
Driving effect of BDNF in the spinal dorsal horn on neuropathic pain
Zhou, W., Xie, Z., Li, C., Xing, Z., Xie, S., Li, M., & Yao, J. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135965 · Cited by 59
Sigma-1 Receptor Enhances Neurite Elongation of Cerebellar Granule Neurons via TrkB Signaling
Kimura, Y., Fujita, Y., Shibata, K., Mori, M., & Yamashita, T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075760 · Cited by 58
The role of neurotrophins in bipolar disorder
Scola, G., & Andreazza, A. C. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.08.013 · Cited by 62
Fields, J. A., Dumaop, W., Langford, D., Rockenstein, E. M., & Masliah, E. (2014) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-013-9520-2 · Cited by 57
Yin, B., Y, Z., Zhou, Z., Gao, W., Du, Z., Zhao, Z., & Li, Q.-Q. (2014) · Oncogene · doi:10.1038/onc.2014.8 · Cited by 55
Inhibitors of neuronal regeneration: mediators and signaling mechanisms
Tang, B. L. (2002) · Neurochemistry International · doi:10.1016/s0197-0186(02)00094-3 · Cited by 57
Theoretical aspects of autism: biomarkers—a review
Ratajczak, H. V. (2011) · Journal of Immunotoxicology · doi:10.3109/1547691x.2010.538749 · Cited by 61
Neurotrophins modulate monocyte chemotaxis without affecting macrophage function
Samah, B., Porcheray, F., & Gras, G. S. (2008) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2007.03578.x · Cited by 57
Гудашева, Т. А., Povarnina, P. Y., Антипова, Т. А., Firsova, Y. N., Konstantinopolsky, M. A., & Середенин, С. Б. (2015) · Journal of Biomedical Science · doi:10.1186/s12929-015-0198-z · Cited by 57
Neuronal Survival and p73/p63/p53: A Family Affair
Jacobs, W. B., Walsh, G. S., & Miller, F. D. (2004) · The Neuroscientist · doi:10.1177/1073858404263456 · Cited by 57
Self-citationChen, D., Brahimi, F., Angell, Y., Li, Y.-C., Moscowicz, J., Saragovi, H. U., & Burgess, K. (2009) · ACS Chemical Biology · doi:10.1021/cb9001415 · Cited by 56
Onyango, I. G., Bennett, J. P., & Tuttle, J. B. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2005.01.026 · Cited by 56
Molecular and Cell‐Based Approaches for Neuroprotection in Glaucoma
Lebrun-Julien, F., & Polo, A. D. (2008) · Optometry and Vision Science · doi:10.1097/opx.0b013e31817841f7 · Cited by 56
ETV6–NTRK3 as a therapeutic target of small molecule inhibitor PKC412
Thanh, H., Lý, B. T. K., Kano, Y., Tojo, A., Watanabe, T., & Sato, Y. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.10.087 · Cited by 56
Nerve growth factor activates aorta endothelial cells causing PI3K/Akt- and ERK-dependent migration
Rahbek, U. L., Dissing, S., Thomassen, C., Hansen, A. J., & Tritsaris, K. (2005) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-005-1436-0 · Cited by 58
Neuritogenic effect of standardized extract of Centella asiatica ECa233 on human neuroblastoma cells
Wanakhachornkrai, O., Pongrakhananon, V., Chunhacha, P., Wanasuntronwong, A., Vattanajun, A., Tantisira, B., Pithi Chanvorachote, B., & Tantisira, M. H. (2013) · BMC Complementary and Alternative Medicine · doi:10.1186/1472-6882-13-204 · Cited by 56
Yang, T., Massa, S. M., & Longo, F. M. (2006) · Journal of Neurobiology · doi:10.1002/neu.20291 · Cited by 56
Montalban, E., Mattugini, N., Ciarapica, R., Provenzano, C., Savino, M., Scagnoli, F., Prosperini, G., Carissimi, C., Fulci, V., Matrone, C., et al. (2014) · NeuroMolecular Medicine · doi:10.1007/s12017-014-8292-z · Cited by 56
Brain-metastatic melanoma: a neurotrophic perspective
Marchetti, D., Denkins, Y. M., Reiland, J., Greiter‐Wilke, A., Galjour, J., Murry, B. P., Blust, J., & Roy, M. (2003) · Pathology & Oncology Research · doi:10.1007/bf03033729 · Cited by 56
Colle, R., Deflesselle, É., Martin, S., David, D. J. P., Hardy, P., ŢĂRANU, A. M., Falissard, B., Verstuyft, C., & Corruble, E. (2015) · Pharmacogenomics · doi:10.2217/pgs.15.56 · Cited by 60
Alvarado‐Velez, M., Enam, S. F., Mehta, N., Lyon, J. G., LaPlaca, M. C., & Bellamkonda, R. V. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120419 · Cited by 56
Interaction of SH2-Bβ with RET is involved in signaling of GDNF-induced neurite outgrowth
Zhang, Y., Zhu, W., Wang, Y.-G., Liu, X.-J., Li, J., Liu, X., Zhang, Z., Lu, C., & He, C. (2006) · Journal of Cell Science · doi:10.1242/jcs.02845 · Cited by 56
Cyclic phosphatidic acid elicits neurotrophin‐like actions in embryonic hippocampal neurons
Fujiwara, Y., Sebök, Á., Meakin, S. O., Kobayashi, T., Murakami‐Murofushi, K., & Tigyi, G. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.02106.x · Cited by 56
Nuclear/cytoplasmic shuttling of the transcription factor FoxO1 is regulated by neurotrophic factors
Gan, L., Zheng, W., Chabot, J., Unterman, T. G., & Quirion, R. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03108.x · Cited by 56
The p75 receptor mediates axon growth inhibition through an association with PIR-B
Fujita, Y., Takashima, R., Endo, S., Takai, T., & Yamashita, T. (2011) · Cell Death and Disease · doi:10.1038/cddis.2011.85 · Cited by 55
Chlamydia inhibit host cell apoptosis by inducing Bag-1 via the MAPK/ERK survival pathway
Kun, D., Cheng, X., Ming, Z., & Li, Q. (2013) · APOPTOSIS · doi:10.1007/s10495-013-0865-z · Cited by 55
Şişman, A. R., Kıray, M., Çamsarı, U. M., Evren, M., Ateş, M., Baykara, B., Aksu, İ., Güvendi, G., & Uysal, N. (2014) · Disease Markers · doi:10.1155/2014/108106 · Cited by 55
Liu, M., Wang, S. R., Yao, W., Zhang, Z. J., Zhong, X., Sha, L., He, M., ZHENG, Z., & Wei, M. J. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.05.011 · Cited by 55
Raap, U., Fokkens, W. J., Bruder, M., Hoogsteden, H. C., Kapp, A., & Braunstahl, G. (2008) · Allergy · doi:10.1111/j.1398-9995.2008.01626.x · Cited by 55
García, N., Tomàs, M., Santafé, M. M., Lanuza, M. A., Besalduch, N., & Tomàs, J. M. (2010) · Journal of the Peripheral Nervous System · doi:10.1111/j.1529-8027.2010.00250.x · Cited by 55
Johnson, A. K., Zhang, Z., Clayton, S., Beltz, T. G., Hurley, S. W., Thunhorst, R. L., & Xue, B. (2015) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00037.2015 · Cited by 55
Гудашева, Т. А., Povarnina, P. Y., Logvinov, I. O., Антипова, Т. А., & Середенин, С. Б. (2016) · Drug Design Development and Therapy · doi:10.2147/dddt.s118768 · Cited by 55
Huang, S.-H., Zhao, L., Sun, Z.-P., Li, X.-Z., Geng, Z., Zhang, K.-D., Chao, M. V., & Chen, Z.-Y. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m809763200 · Cited by 54
Ito, S., Nitta, Y., Fukumitsu, H., Soumiya, H., Ikeno, K., Nakamura, T., & Furukawa, S. (2011) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2012/139140 · Cited by 55
Regulation of neurogenesis by neurotrophins in developing spinal sensory ganglia.
Fariñas, I., Cano-Jaimez, M., Bellmunt, E., & Soriano, M. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00767-5 · Cited by 56
Liu, A., Prenger, M. S., Norton, D. D., Mei, L., Kusiak, J. W., & Bai, G. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105399200 · Cited by 55
Regulation of PC12 cell survival and differentiation by the new P2Y-like receptor GPR17
Daniele, S., Lecca, D., Trincavelli, M. L., Ciampi, O., Abbracchio, M. P., & Martini, C. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2009.12.006 · Cited by 54
Peripheral Sensory Axon Growth: From Receptor Binding to Cellular Signaling
Tucker, B. A., & Mearow, K. M. (2008) · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · doi:10.1017/s0317167100009331 · Cited by 54
Dependence of neurotrophic factor activation of Trk tyrosine kinase receptors on cellular sialidase
Woronowicz, A., Amith, S. R., Vusser, K. D., Laroy, W., Contreras, R., Basta, S., & Szewczuk, M. R. (2006) · Glycobiology · doi:10.1093/glycob/cwl049 · Cited by 54
Norman, B. H., & McDermott, J. S. (2016) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b00964 · Cited by 52
Glycogen synthase kinase 3β and the regulation of axon growth
Goold, R., & Gordon‐Weeks, P. R. (2004) · Biochemical Society Transactions · doi:10.1042/bst0320809 · Cited by 54
A novel mutation within the extracellular domain of TrkA causes constitutive receptor activation
Arévalo, J. C., Conde, B., Hempstead, B. L., Chao, M. V., Martı́n-Zanca, D., & Pérez, P. (2001) · Oncogene · doi:10.1038/sj.onc.1204215 · Cited by 55
Ip, F. C. F., Cheung, J., & Ip, N. Y. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)01603-2 · Cited by 54
Taylor, J. M., Ali, U., Iannello, R. C., Hertzog, P. J., & Crack, P. J. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02863.x · Cited by 54
Karim, F., Hu, H., Adwanikar, H., Kaplan, D. R., & Robert, W.-S. (2006) · Molecular Pain · doi:10.1186/1744-8069-2-2 · Cited by 54
Self-citationChae, K. S., Martin‐Caraballo, M., Anderson, M., & Dryer, S. E. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00796.2004 · Cited by 54
BDNF-TrkB Signaling in Mitochondria: Implications for Neurodegenerative Diseases
Soman, S. K., Swain, M., & Dagda, R. K. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04357-4 · Cited by 57
Phytochemicals Targeting BDNF Signaling for Treating Neurological Disorders
Singh, A. A., Katiyar, S., & Song, M. (2025) · Brain Sciences · doi:10.3390/brainsci15030252 · Cited by 61
Neurogenin 1 Mediates Erythropoietin Enhanced Differentiation of Adult Neural Progenitor Cells
Wang, L., Zhang, Z. G., Zhang, R. L., Jiao, Z. X., Wang, Y., D, S. P.-N., LeTourneau, Y., Gregg, S. R., & Chopp, M. (2005) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/sj.jcbfm.9600215 · Cited by 53
Tetanus Toxin C-Fragment: The Courier and the Cure?
Toivonen, J. M., Oliván, S., & Osta, R. (2010) · Toxins · doi:10.3390/toxins2112622 · Cited by 54
Association of BDNF Gene Polymorphism with Bipolar Disorders in Han Chinese Population
Wang, Z., Li, Z., Chen, J., Huang, J., Yuan, C., Hong, W., Yu, S., & Fang, Y. (2012) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2012.00797.x · Cited by 53
Bella, A. J., Lin, G., Tantiwongse, K., Garcia, M. M., Lin, C.-S., Brant, W. O., & Lue, T. F. (2006) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2006.00291.x · Cited by 53
Mundy, W. R., & Freudenrich, T. M. (2005) · NeuroToxicology · doi:10.1016/j.neuro.2005.07.007 · Cited by 53
NGF Enhances Sensory Axon Growth Induced by Laminin but Not by the L1 Cell Adhesion Molecule
Liu, R.-Y., Schmid, R. S., Snider, W. D., & Maness, P. F. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1107 · Cited by 53
Pathophysiological Mechanisms for Actions of the Neurotrophins
Twiss, J. L., Chang, J., & Schanen, N. C. (2006) · Brain Pathology · doi:10.1111/j.1750-3639.2006.00039.x · Cited by 54
Purves-Tyson, T. D., & Keast, J. R. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.08.019 · Cited by 53
Groth, R. D., Coicou, L. G., Mermelstein, P. G., & Seybold, V. S. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04632.x · Cited by 52
Caleo, M., Medini, P., von Bartheld, C. S., & Maffei, L. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00287.2003 · Cited by 52
Higuchi, M., Onishi, K., Masuyama, N., & Gotoh, Y. (2003) · Genes to Cells · doi:10.1046/j.1365-2443.2003.00663.x · Cited by 52
Neuronal survival induced by neurotrophins requires calmodulin
Egea, J., Espinet, C., Soler, R. M., Dolcet, X., Yuste, V. J., Encinas, M., Iglesias, M., Rocamora, N., & Comella, J. X. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200101023 · Cited by 52
Suzuki, T., Sekido, H., Kato, N., Nakayama, Y., & Yabe‐Nishimura, C. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02824.x · Cited by 51
N -acetyl serotonin derivatives as potent neuroprotectants for retinas
Shen, J., Ghai, K., Sompol, P. M., Liu, X., Cao, X., Iuvone, P. M., & Ye, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119201109 · Cited by 51
Abcejo, A. J., Sathish, V., Smelter, D. F., Aravamudan, B., Thompson, M. A., Hartman, W. R., Pabelick, C. M., & Prakash, Y. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044343 · Cited by 51
TRPC3 regulates release of brain-derived neurotrophic factor from human airway smooth muscle
Vohra, P. K., Thompson, M. A., Sathish, V., Kiel, A. M., Jerde, C. R., Pabelick, C. M., Singh, B. B., & Prakash, Y. S. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.07.019 · Cited by 51
Unsain, N., Nuñez, N., Anastasía, A., & Mascó, D. H. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.038 · Cited by 53
de Almeida, A. A., da Silva, S. G., Lopim, G. M., Campos, D. V., Fernandes, J., Cabral, F. R., & Arida, R. M. (2017) · Neurochemical Research · doi:10.1007/s11064-016-2165-9 · Cited by 55
Madziar, B., G.‐Coviella, I. L., Zemelko, V. I., & Berse, B. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02908.x · Cited by 52
Metadata
- Authors
- Kaplan, D. R., & Miller, F. D.
- Affiliations
- Montreal Neurological Institute and Hospital (CA)
- Corresponding author
- Kaplan, David R
- Miller, Freda D
- Venue
- Current Opinion in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2000-06
- Volume
- 10
- Issue
- 3
- Pages
- 381-391
- ISSN
- 0959-4388 (ISSN-L)
- OpenAlex
- W2128960139
- Cited by
- 1,944
- References
- 122
- Citations by year
- 2026: 18 · 2025: 35 · 2024: 41 · 2023: 44 · 2022: 44 · 2021: 38 · 2020: 51 · 2019: 45 · 2018: 49 · 2017: 53 · 2016: 66 · 2015: 53 · 2014: 91 · 2013: 79 · 2012: 68
- FWCI
- 11.45
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Opinion in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- neurotrophins, signal transduction, Trk receptors, p75 neurotrophin receptor, neurotrophin receptor signaling, Akt signaling, MAPK signaling, JNK signaling, p53 pathway, NF-κB signaling, neuronal survival, neuronal development, apoptosis
- MeSH terms
- Animals, Nerve Growth Factors, Nervous System Physiological Phenomena, Neurons, Signal Transduction
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