Neurotrophic Factors and Their Potential Applications in Tissue Regeneration

Epigenetic Regulations of GABAergic Neurotransmission: Relevance for Neurological Disorders and Epigenetic Therapy

Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,949 · see citing works

Neurotrophins: Roles in Neuronal Development and Function

Huang, E. J., & Reichardt, L. F. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.677 · Cited by 4,394 · see citing works

Translational Findings on Brain-Derived Neurotrophic Factor and Anxiety: Contributions from Basic Research to Clinical Practice

da Luz, A. C. D. D. S., Dias, G. P., Bevilaqua, M. C. D. N., Cocks, G. D., Gardino, P. F., Thuret, S., & Nardi, A. E. (2013) · Neuropsychobiology · doi:10.1159/000353269 · Cited by 4,012 · see citing works

GDNF: a Glial Cell Line-Derived Neurotrophic Factor for Midbrain Dopaminergic Neurons

Lin, L.-F. H., Doherty, D. H., Lile, J. D., Bektesh, S. L., & Collins, F. (1993) · Science · doi:10.1126/science.8493557 · Cited by 3,206 · see citing works

Neurotrophin-regulated signalling pathways

Reichardt, L. F. (2006) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2006.1894 · Cited by 2,195 · see citing works

The GDNF family: Signalling, biological functions and therapeutic value

Airaksinen, M. S., & Saarma, M. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn812 · Cited by 1,832 · see citing works

Purification of a new neurotrophic factor from mammalian brain.

Barde, Y. A., Edgar, D., & Thoenen, H. (1982) · The EMBO Journal · doi:10.1002/j.1460-2075.1982.tb01207.x · Cited by 1,822 · see citing works

Adult Bone Marrow Stromal Cells Differentiate into Neural Cells in Vitro

Sanchez‐Ramos, J., Song, S., Cardozo‐Pelaez, F., Hazzi, C., Stedeford, T. J., Willing, A. E., Freeman, T. B., Saporta, S., Janssen, W. E., Patel, N. A., et al. (2000) · Experimental Neurology · doi:10.1006/exnr.2000.7389 · Cited by 1,562 · see citing works

Hippocampal long-term potentiation is impaired in mice lacking brain-derived neurotrophic factor.

Korte, M., Carroll, P., Wolf, E., Brem, G., Thoenen, H., & Bonhoeffer, T. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.19.8856 · Cited by 1,426 · see citing works

Regulation of Cell Fate Decision of Undifferentiated Spermatogonia by GDNF

Meng, X., Lindahl, M., Hyvönen, M. E., Parvinen, M., de Rooij, D. G., Hess, M. W., Raatikainen-Ahokas, A., Sainio, K., Rauvala, H., Lakso, M., et al. (2000) · Science · doi:10.1126/science.287.5457.1489 · Cited by 1,404 · see citing works

Long-Lasting Neurotrophin-Induced Enhancement of Synaptic Transmission in the Adult Hippocampus

Kang, H., & Schuman, E. M. (1995) · Science · doi:10.1126/science.7886457 · Cited by 1,354 · see citing works

Neurotrophin-3: a Neurotrophic Factor Related to NGF and BDNF

Maisonpierre, P. C., Belluscio, L., Squinto, S., Ip, N. Y., Furth, M. E., Lindsay, R. M., & Yancopoulos, G. D. (1990) · Science · doi:10.1126/science.2321006 · Cited by 1,322 · see citing works

Loss of Huntingtin-Mediated BDNF Gene Transcription in Huntington's Disease

Zuccato, C., Ciammola, A., Rigamonti, D., Leavitt, B. R., Goffredo, D., Conti, L., MacDonald, M. E., Friedlander, R. M., Silani, V., Hayden, M. R., et al. (2001) · Science · doi:10.1126/science.1059581 · Cited by 1,319 · see citing works

Direct brain infusion of glial cell line–derived neurotrophic factor in Parkinson disease

Gill, S. S., Patel, N. K., Hotton, G. R., O'Sullivan, K., McCarter, R., Bunnage, M., Brooks, D. J., Svendsen, C. N., & Heywood, P. (2003) · Nature Medicine · doi:10.1038/nm850 · Cited by 1,290 · see citing works

Nerve Growth Factor Signaling, Neuroprotection, and Neural Repair

Sofroniew, M. V., Howe, C. L., & Mobley, W. C. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1217 · Cited by 1,284 · see citing works

Recombinant BDNF Rescues Deficits in Basal Synaptic Transmission and Hippocampal LTP in BDNF Knockout Mice

Patterson, S. L., Abel, T., Deuel, T. A. S., Martin, K. C., Rose, J. C., & Kandel, E. R. (1996) · Neuron · doi:10.1016/s0896-6273(00)80140-3 · Cited by 1,233 · see citing works

Renal agenesis and the absence of enteric neurons in mice lacking GDNF

Sánchez, M. P., Silos‐Santiago, I., Frisén, J., He, B., Lira, S. A., & Barbacid, M. (1996) · Nature · doi:10.1038/382070a0 · Cited by 1,196 · see citing works

Defects in enteric innervation and kidney development in mice lacking GDNF

Pichel, J. G., Shen, L., SHENG, H. Z., Granholm, A., Drago, J., Grinberg, A., Lee, E. J., Huang, S. P., Saarma, M., Hoffer, B. J., et al. (1996) · Nature · doi:10.1038/382073a0 · Cited by 1,153 · see citing works

Identification and characterization of a novel member of the nerve growth factor/brain-derived neurotrophic factor family

Hohn, A., Leibrock, J., Bailey, K., & Barde, Y.-A. (1990) · Nature · doi:10.1038/344339a0 · Cited by 1,145 · see citing works

Mice lacking brain-derived neurotrophic factor develop with sensory deficits

Ernfors, P., Lee, K.-F., & Jaenisch, R. (1994) · Nature · doi:10.1038/368147a0 · Cited by 1,067 · see citing works

TrkB signalling pathways in LTP and learning

Minichiello, L. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2738 · Cited by 1,055 · see citing works

A phase 1 clinical trial of nerve growth factor gene therapy for Alzheimer disease

Tuszynski, M. H., Thal, L., Pay, M., Salmon, D. P., U, H. S., Bakay, R., Patel, P., Blesch, A., Vahlsing, H. L., Ho, G., et al. (2005) · Nature Medicine · doi:10.1038/nm1239 · Cited by 1,050 · see citing works

Targeted disruption of the BDNF gene perturbs brain and sensory neuron development but not motor neuron development

Jones, K. R., Fariñas, I., Backus, C., & Reichardt, L. F. (1994) · Cell · doi:10.1016/0092-8674(94)90377-8 · Cited by 1,041 · see citing works

Randomized controlled trial of intraputamenal glial cell line–derived neurotrophic factor infusion in Parkinson disease

Lang, A. E., Gill, S., Patel, N., Lozano, A., Nutt, J. G., Penn, R., Brooks, D. J., Hotton, G. R., Moro, E., Heywood, P., et al. (2006) · Annals of Neurology · doi:10.1002/ana.20737 · Cited by 987 · see citing works

Severe sensory and sympathetic neuropathies in mice carrying a disrupted Trk/NGF receptor gene

Smeyne, R. J., Klein, R., Schnapp, A., Long, L. K., Bryant, S., Lewin, A. C., Lira, S. A., & Barbacid, M. (1994) · Nature · doi:10.1038/368246a0 · Cited by 980 · see citing works

Selective growth stimulating effects of mouse sarcoma on the sensory and sympathetic nervous system of the chick embryo

Levi‐Montalcini, R., & Hamburger, V. (1951) · Journal of Experimental Zoology · doi:10.1002/jez.1401160206 · Cited by 958 · see citing works

Targeted mutation of the gene encoding the low affinity NGF receptor p75 leads to deficits in the peripheral sensory nervous system

Lee, K., Li, E., Huber, L. J., Landis, S. C., Sharpe, A. H., Chao, M. V., & Jaenisch, R. (1992) · Cell · doi:10.1016/0092-8674(92)90286-l · Cited by 946 · see citing works

BDNF mRNA is decreased in the hippocampus of individuals with Alzheimer's disease

Phillips, H. S., Hains, J. M., Armanini, M., Laramee, G. R., Johnson, S. A., & Winslow, J. W. (1991) · Neuron · doi:10.1016/0896-6273(91)90273-3 · Cited by 921 · see citing works

Brain-derived neurotrophic factor-deficient mice develop aggressiveness and hyperphagia in conjunction with brain serotonergic abnormalities

Lyons, W. E., Mamounas, L. A., Ricaurte, G. A., Coppola, V., Reid, S. W., Bora, S. H., Wihler, C., Koliatsos, V. E., & Tessarollo, L. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.26.15239 · Cited by 862 · see citing works

Neurotrophin-5: A novel neurotrophic factor that activates trk and trkB

Berkemeier, L. R., Winslow, J. W., Kaplan, D. R., Nikolics, K., Goeddel, D. V., & Rosenthal, A. (1991) · Neuron · doi:10.1016/0896-6273(91)90287-a · Cited by 836 · see citing works

Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genes

Zuccato, C., Tartari, M., Crotti, A., Goffredo, D., Valenza, M., Conti, L., Cataudella, T., Leavitt, B. R., Hayden, M. R., Timmusk, T., et al. (2003) · Nature Genetics · doi:10.1038/ng1219 · Cited by 814 · see citing works

BDNF regulates eating behavior and locomotor activity in mice

Kernie, S. G., Liebl, D. J., & Parada, L. F. (2000) · The EMBO Journal · doi:10.1093/emboj/19.6.1290 · Cited by 806 · see citing works

Lack of neurotrophin-3 leads to deficiencies in the peripheral nervous system and loss of limb proprioceptive afferents

Ernfors, P., Lee, K., Kučera, J., & Jaenisch, R. (1994) · Cell · doi:10.1016/0092-8674(94)90213-5 · Cited by 805 · see citing works

A BDNF autocrine loop in adult sensory neurons prevents cell death

Acheson, A., Conover, J. C., Fandl, J. P., DeChiara, T. M., Russell, M., Thadani, A., Squinto, S. P., Yancopoulos, G. D., & Lindsay, R. M. (1995) · Nature · doi:10.1038/374450a0 · Cited by 765 · see citing works

Rapid and selective induction of BDNF expression in the hippocampus during contextual learning

Hall, J., Thomas, K. L., & Everitt, B. (2000) · Nature Neuroscience · doi:10.1038/75698 · Cited by 669 · see citing works

Novel functions and signalling pathways for GDNF

Sariola, H. V., & Saarma, M. (2003) · Journal of Cell Science · doi:10.1242/jcs.00786 · Cited by 648 · see citing works

Mammalian neurotrophin-4: structure, chromosomal localization, tissue distribution, and receptor specificity.

Ip, N. Y., Ibáñez, C. F., Nye, S. H., McClain, J., Jones, P. F., Gies, D. R., Belluscio, L., Le Beau, M. M., Espinosa, R., & Squinto, S. P. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.7.3060 · Cited by 626 · see citing works

The Neural Cell Adhesion Molecule NCAM Is an Alternative Signaling Receptor for GDNF Family Ligands

Paratcha, G., Ledda, F., & Ibáñez, C. F. (2003) · Cell · doi:10.1016/s0092-8674(03)00435-5 · Cited by 624 · see citing works

Brain-Derived Neurotrophic Factor/TrkB Signaling in Memory Processes

Yamada, K., & Nabeshima, T. (2003) · Journal of Pharmacological Sciences · doi:10.1254/jphs.91.267 · Cited by 585 · see citing works

BDNF-induced TrkB activation down-regulates the K+–Cl− cotransporter KCC2 and impairs neuronal Cl− extrusion

Rivera, C., Li, H., Thomas-Crusells, J., Lahtinen, H., Viitanen, T., Nanobashvili, A., Kokaia, Z., Airaksinen, M. S., Voipio, J., Kaila, K., et al. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200209011 · Cited by 566 · see citing works

Studies on the expression of the beta nerve growth factor (NGF) gene in the central nervous system: level and regional distribution of NGF mRNA suggest that NGF functions as a trophic factor for several distinct populations of neurons.

Shelton, D. L., & Reichardt, L. F. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.8.2714 · Cited by 532 · see citing works

Reduced BDNF mRNA Expression in the Parkinson's Disease Substantia Nigra

Howells, D. W., Porritt, M. J., Wong, J. Y. F., Batchelor, P. E., Kalnins, R., Hughes, A. J., & Donnan, G. A. (2000) · Experimental Neurology · doi:10.1006/exnr.2000.7483 · Cited by 513 · see citing works

Persephin, a Novel Neurotrophic Factor Related to GDNF and Neurturin

Milbrandt, J., de Sauvage, F. J., Fahrner, T. J., Baloh, R. H., Leitner, M. L., Tansey, M. G., Lampe, P. A., Heuckeroth, R. O., Kotzbauer, P. T., Simburger, K. S., et al. (1998) · Neuron · doi:10.1016/s0896-6273(00)80453-5 · Cited by 494 · see citing works

Neurotrophins and Time: Different Roles for TrkB Signaling in Hippocampal Long-Term Potentiation

Kang, H., Welcher, A. A., Shelton, D., & Schuman, E. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)80378-5 · Cited by 481 · see citing works

Improvement of bilateral motor functions in patients with Parkinson disease through the unilateral intraputaminal infusion of glial cell line—derived neurotrophic factor

Slevin, J. T., Gerhardt, G. A., Smith, C. D., Gash, D. M., Kryscio, R. J., & Young, B. A. (2005) · Journal of neurosurgery · doi:10.3171/jns.2005.102.2.0216 · Cited by 474 · see citing works

Learning deficit in BDNF mutant mice.

Linnarsson, S., Björklund, A., & Ernfors, P. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01687.x · Cited by 471 · 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

Neuronal deficits, not involving motor neurons, in mice lacking BDNF and/or NT4

Conover, J., Erickson, J., Katz, D. M., Bianchi, L., Poueymirou, W., Mcclain, J., Pan, L., Helgren, M. E., Ip, N. Y., Boland, P., et al. (1995) · Nature · doi:10.1038/375235a0 · Cited by 428 · see citing works

BDNF and Full-length and Truncated TrkB Expression in Alzheimer Disease. Implications in Therapeutic Strategies

Ferrer, I., Marı́n, C., Rey, M. J., Ribalta, T., Goutan, E., Blanco, R., Tolosa, E. S., & Martı́, E. (1999) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-199907000-00007 · Cited by 407 · see citing works

The effect of systemically administered recombinant human nerve growth factor in healthy human subjects

Petty, B. G., Cornblath, D. R., Adornato, B. T., Chaudhry, V., Flexner, C. W., Wachsman, M., Sinicropi, D. V., Burton, L. E., & Peroutka, S. J. (1994) · Annals of Neurology · doi:10.1002/ana.410360221 · Cited by 402 · see citing works

Mesenchymal stem cells that produce neurotrophic factors reduce ischemic damage in the rat middle cerebral artery occlusion model

Kurozumi, K., Nakamura, K., Tamiya, T., Kawano, Y., Ishii, K., Kobune, M., Hirai, S., Uchida, H., Sasaki, K., Ito, Y., et al. (2004) · Molecular Therapy · doi:10.1016/j.ymthe.2004.09.020 · Cited by 398 · see citing works

Arrest of Motor Neuron Disease in wobbler Mice Cotreated with CNTF and BDNF

Mitsumoto, H., Ikeda, K., Klinkosz, B., Cedarbaum, J. M., Wong, V., & Lindsay, R. M. (1994) · Science · doi:10.1126/science.8066451 · Cited by 386 · see citing works

Sensory but not motor neuron deficits in mice lacking NT4 and BDNF

Liu, X., Ernfors, P., Wu, H.-L., & Jaenisch, R. (1995) · Nature · doi:10.1038/375238a0 · Cited by 379 · see citing works

The Neurotrophin Family of Neurotrophic Factors: An Overview

Skaper, S. D. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-536-7_1 · Cited by 379 · see citing works

Virus-mediated gene transfer into hippocampal CA1 region restores long-term potentiation in brain-derived neurotrophic factor mutant mice.

Korte, M., Griesbeck, O., Gravel, C., Carroll, P., Staiger, V, Thoenen, H., & Bonhoeffer, T. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.22.12547 · Cited by 351 · cited 2× · see citing works

The trk B tyrosine protein kinase is a receptor for neurotrophin-4

Klein, R., Lamballe, F., Bryant, S., & Barbacid, M. (1992) · Neuron · doi:10.1016/0896-6273(92)90209-v · Cited by 325 · see citing works

Glial Cell Line-derived Neurotrophic Factor Regulation of Genes Essential for Self-renewal of Mouse Spermatogonial Stem Cells Is Dependent on Src Family Kinase Signaling

Oatley, J. M., Avarbock, M. R., & Brinster, R. L. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m703474200 · Cited by 324 · see citing works

ERM is required for transcriptional control of the spermatogonial stem cell niche

Chen, C., Ouyang, W., Grigura, V., Zhou, Q., Carnes, K. I., Lim, H. J., Zhao, G.-Q., Arber, S., Kurpios, N. A., Murphy, T. L., et al. (2005) · Nature · doi:10.1038/nature03894 · Cited by 320 · see citing works

Mice Lacking Brain-Derived Neurotrophic Factor Exhibit Visceral Sensory Neuron Losses Distinct from Mice Lacking NT4 and Display a Severe Developmental Deficit in Control of Breathing

Erickson, J., Conover, J., Borday, V., Champagnat, J., Barbacid, M., Yancopouloš, G., & Katz, D. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05361.1996 · Cited by 310 · see citing works

Glial cell line–derived neurotrophic factor induces neuronal sprouting in human brain

Love, S., Plaha, P., Patel, N. K., Hotton, G. R., Brooks, D. J., & Gill, S. S. (2005) · Nature Medicine · doi:10.1038/nm0705-703 · Cited by 285 · see citing works

Brain-Derived Neurotrophic Factor Modulates Fast Synaptic Inhibition by Regulating GABA_AReceptor 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

Neurotrophic cross‐talk between the nervous and immune systems: Implications for neurological diseases

Kerschensteiner, M., Stadelmann, C., Dechant, G., Wekerle, H., & Hohlfeld, R. (2003) · Annals of Neurology · doi:10.1002/ana.10446 · Cited by 273 · see citing works

Nerves Regulate Cardiomyocyte Proliferation and Heart Regeneration

Mahmoud, A. I., O'Meara, C. C., Gemberling, M. P., Zhao, L., Bryant, D. M., Zheng, R., Gannon, J., Cai, L., Choi, W.-Y., Egnaczyk, G. F., et al. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.06.017 · Cited by 267 · see citing works

Neurotrophin-3 regulates ribbon synapse density in the cochlea and induces synapse regeneration after acoustic trauma

Wan, G., Gómez‐Casati, M. E., Gigliello, A. R., Liberman, M. C., & Corfas, G. (2014) · eLife · doi:10.7554/elife.03564 · Cited by 267 · see citing works

GABAergic Stimulation Regulates the Phenotype of Hippocampal Interneurons through the Regulation of Brain-Derived Neurotrophic Factor

Marty, S., Berninger, B., Carroll, P., & Thoenen, H. (1996) · Neuron · doi:10.1016/s0896-6273(00)80075-6 · Cited by 263 · see citing works

Etv4 and Etv5 are required downstream of GDNF and Ret for kidney branching morphogenesis

Lu, B. C., Cebrián, C., Chi, X., Kuure, S., Kuo, R., Bates, C. M., Arber, S., Hassell, J. A., MacNeil, L. T., Hoshi, M., et al. (2009) · Nature Genetics · doi:10.1038/ng.476 · Cited by 238 · see citing works

Cystamine and cysteamine increase brain levels of BDNF in Huntington disease via HSJ1b and transglutaminase

Borrell-Pagés, M. (2006) · Journal of Clinical Investigation · doi:10.1172/jci27607 · Cited by 236 · see citing works

Neurturin and GDNF Promote Proliferation and Survival of Enteric Neuron and Glial Progenitorsin Vitro

Heuckeroth, R. O., Lampe, P. A., Johnson, E. M., & Milbrandt, J. (1998) · Developmental Biology · doi:10.1006/dbio.1998.8955 · Cited by 233 · see citing works

RESEARCH ARTICLE: Systematic Assessment of BDNF and Its Receptor Levels in Human Cortices Affected by Huntington's Disease

Zuccato, C., Marullo, M., Conforti, P., MacDonald, M. E., Tartari, M., & Cattaneo, E. (2008) · Brain Pathology · doi:10.1111/j.1750-3639.2007.00111.x · Cited by 231 · see citing works

Nerve growth factor promotes human hemopoietic colony growth and differentiation.

Matsuda, H., Coughlin, M. D., Bienenstock, J., & Denburg, J. A. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.17.6508 · Cited by 228 · see citing works

Targeted mutation in the neurotrophin-3 gene results in loss of muscle sensory neurons.

Tessarollo, L., Vogel, K. S., Palko, M. E., Reid, S. W., & Parada, L. F. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.25.11844 · Cited by 224 · see citing works

Ultrastructural Localization of Full-Length trkB Immunoreactivity in Rat Hippocampus Suggests Multiple Roles in Modulating Activity-Dependent Synaptic Plasticity

Drake, C. T., Milner, T. A., & Patterson, S. L. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-18-08009.1999 · Cited by 221 · see citing works

Intraputaminal Infusion of Nerve Growth Factor to Support Adrenal Medullary Autografts in Parkinson's Disease

Olson, L. (1991) · Archives of Neurology · doi:10.1001/archneur.1991.00530160037011 · Cited by 216 · see citing works

Phenotypic Knockout of Nerve Growth Factor in Adult Transgenic Mice Reveals Severe Deficits in Basal Forebrain Cholinergic Neurons, Cell Death in the Spleen, and Skeletal Muscle Dystrophy

Ruberti, F., Capsoni, S., Comparini, A., Daniel, E. D., Franzot, J., Gonfloni, S., Rossi, G., Berardi, N., & Cattaneo, A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02589.2000 · Cited by 212 · see citing works

Brain-Derived Neurotrophic Factor Modulation of GABAergic Synapses by Postsynaptic Regulation of Chloride Transport

Wardle, R. A., & Poo, M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-25-08722.2003 · Cited by 201 · see citing works

Brain-Derived Neurotrophic Factor (BDNF) Modulates Inhibitory, But Not Excitatory, Transmission in the CA1 Region of the Hippocampus

Frerking, M. E., Malenka, R. C., & Nicoll, R. A. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.6.3383 · Cited by 201 · see citing works

Nerve Growth Factor Promotes Cardiac Repair following Myocardial Infarction

Meloni, M., Caporali, A., Graiani, G., Lagrasta, C. A. M., Katare, R., Linthout, S. V., Spillmann, F., Campesi, I., Madeddu, P. R., Quaini, F., et al. (2010) · Circulation Research · doi:10.1161/circresaha.109.210088 · Cited by 193 · see citing works

Parasympathetic stimulation improves epithelial organ regeneration

Knox, S. M., Lombaert, I. M. A., Haddox, C. L., Abrams, S. R., Cotrim, A. P., Wilson, A. J., & Hoffman, M. P. (2013) · Nature Communications · doi:10.1038/ncomms2493 · Cited by 192 · see citing works

Cholinergic denervation of the rat hippocampus by fimbrial transection leads to a transient accumulation of nerve growth factor (NGF) without change in mRNANGF content

Korsching, S. I., Heumann, R., Thoenen, H., & Hefti, F. F. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90186-2 · Cited by 189 · see citing works

Endothelial NT-3 Delivered by Vasculature and CSF Promotes Quiescence of Subependymal Neural Stem Cells through Nitric Oxide Induction

Delgado, A. C., Ferrón, S. R., Vicente, D., Porlan, E., Pérez‐Villalba, A., Trujillo, C. M., D’Ocón, P., & Fariñas, I. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.015 · Cited by 183 · see citing works

AAV-Mediated gene delivery of BDNF or GDNF is neuroprotective in a model of huntington disease

Kells, A. P., Fong, D. M., Dragunow, M., During, M. J., Young, D., & Connor, B. J. (2004) · Molecular Therapy · doi:10.1016/j.ymthe.2004.02.016 · Cited by 179 · see citing works

Targeting the RET Pathway in Thyroid Cancer

Wells, S. A., & Santoro, M. M. (2009) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-08-2742 · Cited by 168 · see citing works

Critical and distinct roles for key RET tyrosine docking sites in renal developmentPreprint

Jain, S. R., Encinas, M., Johnson, E. M., & Milbrandt, J. (2006) · Genes & Development · doi:10.1101/gad.1387206 · Cited by 165 · see citing works

Glial Cell Line-Derived Neurotrophic Factor Is Essential for Postnatal Survival of Midbrain Dopamine Neurons

Granholm, A., Reyland, M. E., Albeck, D. S., Sanders, L., Gerhardt, G. A., Hoernig, G. R., Shen, L., Westphal, H., & Hoffer, B. J. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03182.2000 · Cited by 160 · see citing works

Encapsulated Cell Biodelivery of Nerve Growth Factor to the Basal Forebrain in Patients with Alzheimer’s Disease

Eriksdotter, M., Linderoth, B., Lind, G., Aladellie, L., Almkvist, O., Andreasen, N., Blennow, K., Bogdanović, N., Jelić, V., Kadir, A., et al. (2012) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000336051 · Cited by 158 · see citing works

Neural Cell Differentiation In Vitro from Adult Human Bone Marrow Mesenchymal Stem Cells

Long, X., Olszewski, M., Huang, W., & Kletzel, M. (2005) · Stem Cells and Development · doi:10.1089/scd.2005.14.65 · Cited by 155 · see citing works

Striatal Delivery of Neurturin by CERE-120, an AAV2 Vector for the Treatment of Dopaminergic Neuron Degeneration in Parkinson's Disease

Gasmi, M., Herzog, C. D., Brandon, E. P., Cunningham, J. J., Ramirez, G. A., Ketchum, E. T., & Bartus, R. T. (2006) · Molecular Therapy · doi:10.1038/sj.mt.6300010 · Cited by 153 · see citing works

Ureteric Bud Outgrowth in Response to RET Activation Is Mediated by Phosphatidylinositol 3-Kinase

Tang, M., Cai, Y., Tsai, S.-J., Wang, Y.-K., & Dressler, G. R. (2002) · Developmental Biology · doi:10.1006/dbio.2001.0557 · Cited by 149 · see citing works

Embryonic stromal clones reveal developmental regulators of definitive hematopoietic stem cells

Durand, C., Robin, C., Bollérot, K., Baron, M. H., Ottersbach, K., & Dzierzak, E. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706923105 · Cited by 146 · see citing works

Interventional MRI-guided Putaminal Delivery of AAV2-GDNF for a Planned Clinical Trial in Parkinson's Disease

Richardson, R. M., Kells, A. P., Rosenbluth, K. H., Salegio, E. A., Fiandaca, M. S., Larson, P., Starr, P. A., Martin, A. J., Lonser, R. R., Federoff, H. J., et al. (2011) · Molecular Therapy · doi:10.1038/mt.2011.11 · Cited by 145 · see citing works

GDNF – a stranger in the TGF‐β superfamily?

Saarma, M. (2000) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2000.01826.x · Cited by 144 · see citing works

Neurotrophin Signaling via TrkB and TrkC Receptors Promotes the Growth of Brain Tumor-initiating Cells

Lawn, S. O., Krishna, N., Pisklakova, A., Qu, X., Fenstermacher, D. A., Fournier, M., Vrionis, F. D., Tran, N., Chan, J. A.-W., Kenchappa, R. S., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.599373 · Cited by 141 · see citing works

GFRα1 released by nerves enhances cancer cell perineural invasion through GDNF-RET signaling

He, S., Chen, C., Chernichenko, N., He, S., Bakst, R. L., Barajas, F., Deborde, S., Allen, P. J., Vakiani, E., Yu, Z., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402944111 · Cited by 138 · see citing works

Neuroprotection by NGF and BDNF Against Neurotoxin-Exerted Apoptotic Death in Neural Stem Cells Are Mediated Through Trk Receptors, Activating PI3-Kinase and MAPK Pathways

Nguyen, N., Lee, S. B., Lee, Y. S., Lee, K.-H., & Ahn, J.-Y. (2008) · Neurochemical Research · doi:10.1007/s11064-008-9848-9 · Cited by 131 · see citing works

Synergistic Effects of GDNF and VEGF on Lifespan and Disease Progression in a Familial ALS Rat Model

Krakora, D., Mulcrone, P. L., Meyer, M., Lewis, C. M., Bernau, K., Gowing, G., Zimprich, C., Aebischer, P., Svendsen, C. N., & Suzuki, M. (2013) · Molecular Therapy · doi:10.1038/mt.2013.108 · Cited by 130 · see citing works

Four Cation-Selective Transporters Contribute to Apical Uptake and Accumulation of Metformin in Caco-2 Cell Monolayers

Han, T. K., Proctor, W. R., Costales, C., Cai, H., Everett, R., & Thakker, D. R. (2015) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.114.220350 · Cited by 123 · see citing works

CERE-110, an adeno-associated virus-based gene delivery vector expressing human nerve growth factor for the treatment of Alzheimer's disease.

Mandel, R. J. (2010) · PubMed · Cited by 123 · see citing works

GDNF/Ret signaling and renal branching morphogenesis

Costantini, F. D. (2010) · Organogenesis · doi:10.4161/org.6.4.12680 · Cited by 119 · see citing works

Long-term functional recovery from age-induced spatial memory impairments by nerve growth factor gene transfer to the rat basal forebrain.

Martı́nez-Serrano, A., Fischer, W., Söderström, S., Ebendal, T., & Björklund, A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6355 · Cited by 116 · see citing works

GDNF–RET Signaling in ER-Positive Breast Cancers Is a Key Determinant of Response and Resistance to Aromatase Inhibitors

Morandi, A., Martin, L., Gao, Q., Pancholi, S., Mackay, A. G., Robertson, D. M., Zvelebil, M., Dowsett, M., Plaza-Menacho, I., & Isacke, C. M. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-4265 · Cited by 116 · see citing works

Perineural growth in head and neck squamous cell carcinoma: A review

Roh, J., Muelleman, T. J., Tawfik, O. W., & Thomas, S. M. (2014) · Oral Oncology · doi:10.1016/j.oraloncology.2014.10.004 · Cited by 115 · see citing works

Neurotrophic factor GDNF promotes survival of salivary stem cells

Xiao, N., Lin, Y., Cao, H., Sirjani, D. B., Giaccia, A. J., Koong, A. C., Kong, C. S., Diehn, M., & Le, Q. (2014) · Journal of Clinical Investigation · doi:10.1172/jci74096 · Cited by 112 · see citing works

Glial-derived neurotrophic factor (GDNF) prevents ethanol-induced apoptosis and JUN kinase phosphorylation

McAlhany, R. E., West, J. R., & Miranda, R. C. (2000) · Developmental Brain Research · doi:10.1016/s0165-3806(99)00171-6 · Cited by 112 · see citing works

Identification of the prosurvival activity of nerve growth factor on cardiac myocytes

Caporali, A., Sala-Newby, G., Meloni, M., Graiani, G., Pani, E., Cristofaro, B., Newby, A., Madeddu, P., & Emanueli, C. (2007) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402263 · Cited by 105 · see citing works

Isolation, Tissue Localization, and Cellular Characterization of Progenitors Derived from Adult Human Salivary Glands

Sato, A., Okumura, K., Matsumoto, S., Hattori, K., Hattori, S., Shinohara, M., & Endo, F. (2007) · Cloning and Stem Cells · doi:10.1089/clo.2006.0054 · Cited by 102 · see citing works

gdnf Activates Midline Repulsion by Semaphorin3B via NCAM during Commissural Axon Guidance

Charoy, C., Nawabi, H., Reynaud, F., Derrington, E. A., Bozon, M., Wright, K. M., Falk, J., Helmbacher, F., Kindbeiter, K., & Castellani, V. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.021 · Cited by 98 · see citing works

Proliferation, Differentiation, and Survival of Rat Sensory Neuron Precursors in Vitro Require Specific Trophic Factors

Memberg, S. P., & Hall, A. K. (1995) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1995.1025 · Cited by 97 · see citing works

Nerve Growth Factor, Neural Stem Cells and Alzheimer’s Disease

Heese, K., Low, J. W., & Inoue, N. (2006) · Neurosignals · doi:10.1159/000094383 · Cited by 96 · see citing works

GDNF‐mediated signaling via RET tyrosine 1062 is essential for maintenance of spermatogonial stem cells

Jijiwa, M., Kawai, K., Fukihara, J., Nakamura, A., Hasegawa, M., Suzuki, C., Sato, T., Enomoto, A., Asai, N., Murakumo, Y., et al. (2008) · Genes to Cells · doi:10.1111/j.1365-2443.2008.01171.x · Cited by 91 · see citing works

Histone deacetylase inhibitors are neuroprotective and preserve NGF-mediated cell survival following traumatic brain injury

Lu, J., Frerich, J. M., Turtzo, L. C., Li, S., Chiang, J. Y., Yang, C., Wang, X., Zhang, C., Wu, C., Sun, Z., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308950110 · Cited by 89 · see citing works

Brain Changes in Alzheimer's Disease Patients with Implanted Encapsulated Cells Releasing Nerve Growth Factor

Ferreira, D., Initiative, A. D. N., Westman, E., Eyjolfsdottir, H., Almqvist, P. M., Lind, G., Linderoth, B., Seiger, Å., Blennow, K., Karami, A., et al. (2014) · Journal of Alzheimer s Disease · doi:10.3233/jad-141068 · Cited by 88 · see citing works

The neurotrophic factor neurturin contributes toward an aggressive cancer cell phenotype, neuropathic pain and neuronal plasticity in pancreatic cancer

Wang, K., Demir, İ. E., D’Haese, J. G., Tieftrunk, E., Kujundzic, K., Schorn, S., Xing, B., Kehl, T., Frieß, H., & Ceyhan, G. O. (2013) · Carcinogenesis · doi:10.1093/carcin/bgt312 · Cited by 88 · see citing works

Neurotrophin receptor TrkB promotes lung adenocarcinoma metastasis

Sinkevicius, K. W., Kriegel, C., Bellaria, K. J., Lee, J. J., Lau, A. N., Leeman, K. T., Zhou, P., Beede, A. M., Brainson, C. F., Caswell, D. R., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1404399111 · Cited by 87 · see citing works

Human umbilical cord blood cells express neurotrophic factors

Fan, C., Zhang, Q.-J., Tang, F., Han, Z., Wang, G.-S., & Han, Z. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.01.070 · Cited by 86 · see citing works

Neurotrophin-3 in the development of the enteric nervous system

Chalazonitis, A. (2004) · Progress in brain research · doi:10.1016/s0079-6123(03)46016-0 · Cited by 85 · see citing works

Neuroprotection by GDNF-secreting stem cells in a Huntington's disease model: optical neuroimage tracking of brain-grafted cells

Pineda, J. R., Rubio, N., Åkerud, P., Urbán, N., Badimón, L., Arenas, E., Alberch, J., Blanco, J., & Canals, J. M. (2006) · Gene Therapy · doi:10.1038/sj.gt.3302847 · Cited by 84 · see citing works

RET proto-oncogene point mutations in sporadic neuroendocrine tumors

Komminoth, P., Roth, J., Muletta-Feurer, S., Saremaslani, P., Seelentag, W. K. F., & Heitz, P. U. (1996) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.81.6.2041 · Cited by 83 · see citing works

Persephin-Overexpressing Neural Stem Cells Regulate the Function of Nigral Dopaminergic Neurons and Prevent Their Degeneration in a Model of Parkinson's Disease

PKERUD, P., Holm, P. C., Castelo‐Branco, G., Sousa, K. M., Rodríguez, F. J., & Arenas, E. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1171 · Cited by 75 · see citing works

Localized Delivery of Brain-Derived Neurotrophic Factor-Expressing Mesenchymal Stem Cells Enhances Functional Recovery following Cervical Spinal Cord Injury

Gransee, H. M., Zhan, W., Sieck, G. C., & Mantilla, C. B. (2014) · Journal of Neurotrauma · doi:10.1089/neu.2014.3464 · Cited by 75 · see citing works

Sustained delivery of bioactive neurotrophin-3 to the injured spinal cord

Donaghue, I. E., Tator, C. H., & Shoichet, M. S. (2014) · Biomaterials Science · doi:10.1039/c4bm00311j · Cited by 74 · see citing works

Sonic hedgehog and neurotrophin-3 increase oligodendrocyte numbers and myelination after spinal cord injury

Thomas, A. M., Seidlits, S. K., Goodman, A. G., Kukushliev, T. V., Hassani, D. M., Cummings, B. J., Anderson, A. J., & Shea, L. D. (2014) · Integrative Biology · doi:10.1039/c4ib00009a · Cited by 71 · see citing works

Nerve Growth Factor Improves the Muscle Regeneration Capacity of Muscle Stem Cells in Dystrophic Muscle

Lavasani, M., Lu, A., Peng, H., Cummins, J., & Huard, J. (2006) · Human Gene Therapy · doi:10.1089/hum.2006.17.180 · Cited by 71 · see citing works

Neuropoietic cytokines in normal brain development and neurodevelopmental disorders

Stolp, H. B. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2012.08.009 · Cited by 70 · see citing works

Ampakines cause sustained increases in brain-derived neurotrophic factor signaling at excitatory synapses without changes in AMPA receptor subunit expression

Lauterborn, J. C., Pineda, E., Chen, L. Y., Ramirez, E. A., LYNCH, G. S., & Gall, C. M. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.12.018 · Cited by 70 · see citing works

Additional ECT increases BDNF-levels in patients suffering from major depressive disorders compared to patients treated with citalopram only

Haghighi, M., Salehi, I., Erfani, P., Jahangard, L., Bajoghli, H., Holsboer‐Trachsler, E., & Brand, S. (2013) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2013.03.006 · Cited by 70 · see citing works

Non-chromaffin tissue plus nerve growth factor reduces experimental parkinsonism in aged rats

Pezzoli, G., Fahn, S., Dwork, A. J., Truong, D. D., de Yébenes, J. G., Jackson-Lewis, V. R., Herbert, J., & Cadet, J. L. (1988) · Brain Research · doi:10.1016/0006-8993(88)90659-2 · Cited by 68 · see citing works

Deficient long-term memory and long-lasting long-term potentiation in mice with a targeted deletion of neurotrophin-4 gene

Xie, C.-W., Sayah, D. M., Chen, Q.-S., Wei, W., Smith, D., & Liu, X. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.140204597 · Cited by 68 · see citing works

BDNF prevents amyloid-dependent impairment of LTP in the entorhinal cortex by attenuating p38 MAPK phosphorylation

Criscuolo, C., Fabiani, C., Bonadonna, C., Origlia, N., & Domenici, L. (2014) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2014.11.016 · Cited by 67 · see citing works

Nerve Growth Factor Increases Insulin Secretion and Barium Current in Pancreatic β-Cells

Rosenbaum, T., Sánchez-Soto, M. C., & Hiriart, M. (2001) · Diabetes · doi:10.2337/diabetes.50.8.1755 · Cited by 67 · see citing works

Human adipose-Derived Mesenchymal Stem Cells Improve Motor Functions and are Neuroprotective in the 6-Hydroxydopamine-Rat Model for Parkinson’s Disease when Cultured in Monolayer Cultures but Suppress Hippocampal Neurogenesis and Hippocampal Memory Function when Cultured in Spheroids

Berg, J., Roch, M., Altschüler, J., Winter, C., Schwerk, A. M. K., Kurtz, A., & Steiner, B. (2014) · Stem Cell Reviews and Reports · doi:10.1007/s12015-014-9551-y · Cited by 66 · see citing works

Transplantation of neurotrophin-3-expressing bone mesenchymal stem cells improves recovery in a rat model of spinal cord injury

Wang, L., Zhang, R., & Li, J. (2014) · Acta Neurochirurgica · doi:10.1007/s00701-014-2089-6 · Cited by 65 · see citing works

TAM Receptors Support Neural Stem Cell Survival, Proliferation and Neuronal Differentiation

Ji, R., Meng, L., Jiang, X. M., Naresh Kumar, C. V. M., Ding, J., Li, Q., & Lu, Q. (2014) · PLoS ONE · doi:10.1371/journal.pone.0115140 · Cited by 63 · see citing works

Properly scaled and targeted AAV2-NRTN (neurturin) to the substantia nigra is safe, effective and causes no weight loss: Support for nigral targeting in Parkinson's disease

Bartus, R. T., Brown, L., Wilson, A., Kruegel, B. R., Siffert, J. O., Johnson, E. M., Kordower, J. H., & Herzog, C. D. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.05.026 · Cited by 63 · see citing works

Development of Survival Responsiveness to Brain-Derived Neurotrophic Factor, Neurotrophin 3 and Neurotrophin 4/5, But Not to Nerve Growth Factor, in Cultured Motoneurons from Chick Embryo Spinal Cord

Becker, E., Soler, R. M., Yuste, V. J., Giné, E., Sanz-Rodrı́guez, C., Egea, J., Martı́n-Zanca, D., & Comella, J. X. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-19-07903.1998 · Cited by 61 · see citing works

Exploratory investigation of eight circulating plasma markers in brain tumor patients

Ilhan‐Mutlu, A., Wagner, L., Widhalm, G., Wöehrer, A., Bartsch, S., Czech, T., Heinzl, H., Leutmezer, F., Prayer, D., Marosi, C., et al. (2012) · Neurosurgical Review · doi:10.1007/s10143-012-0401-6 · Cited by 61 · see citing works

Paracrine regulation of glioma cells invasion by astrocytes is mediated by glial‐derived neurotrophic factor

Shabtay‐Orbach, A., Amit, M., Binenbaum, Y., Na’ara, S., & Gil, Z. (2014) · International Journal of Cancer · doi:10.1002/ijc.29380 · Cited by 61 · see citing works

Modification of the brain-derived neurotrophic factor gene: a portal to transform mesenchymal stem cells into advantageous engineering cells for neuroregeneration and neuroprotection

Zhao, L.-X., Zhang, J., Cao, F., Meng, L., Wang, D., Li, Y., Nan, X., Jiao, W.-C., Zheng, M., Xu, X.-H., et al. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.06.025 · Cited by 61 · see citing works

Citalopram enhances neurovascular regeneration and sensorimotor functional recovery after ischemic stroke in mice

Espinera, A. R., Ogle, M. E., Gu, X., & Li, W. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.04.011 · Cited by 60 · see citing works

BDNF protects retinal neurons from hyperglycemia through the TrkB/ERK/MAPK pathway

Liu, Y., Tao, L., Xiao, F., Zhao, Y., & Xu, X. (2013) · Molecular Medicine Reports · doi:10.3892/mmr.2013.1433 · Cited by 60 · see citing works

Islet injury induces neurotrophin expression in pancreatic cells and reactive gliosis of peri-islet Schwann cells

Teitelman, G., Guz, Y., Ivković, S., & Ehrlich, M. E. (1998) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199803)34:4 · Cited by 60 · see citing works

Intraventricular nerve growth factor infusion improves cerebral blood flow and stimulates doublecortin expression in two infants with hypoxic–ischemic brain injury

Chiaretti, A., Antonelli, A., Genovese, O., Fernández, E., Giuda, D. D., Mariotti, P., & Riccardi, R. (2008) · Neurological Research · doi:10.1179/016164107x247948 · Cited by 58 · see citing works

DNA damage induces GDNF secretion in the tumor microenvironment with paracrine effects promoting prostate cancer treatment resistance

Huber, R. M., Lucas, J. M., Gomez-Sarosi, L., Coleman, I. M., Zhao, S. Q., COLEMAN, R. T., & Nelson, P. S. (2014) · Oncotarget · doi:10.18632/oncotarget.3040 · Cited by 55 · see citing works

The TrkB+ cancer stem cells contribute to post-chemotherapy recurrence of triple-negative breast cancers in an orthotopic mouse model

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 · see citing works

Neuroprotective Effects of Oligodendrocyte Progenitor Cell Transplantation in Premature Rat Brain following Hypoxic-Ischemic Injury

Chen, L.-X., Ma, S., Zhang, P., Fan, Z.-C., Xiong, M., Cheng, G., Yang, Y., Qiu, Z., Zhou, W., & Li, J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0115997 · Cited by 55 · see citing works

Cytokine Preconditioning Promotes Codifferentiation of Human Fetal Liver CD133 + Stem Cells Into Angiomyogenic Tissue

Shmelkov, S. V., Meeus, S., Moss, N. S., Kermani, P., Rashbaum, W. K., Rabbany, S. Y., Hanson, M. A., Lane, W. J., Clair, R. S., Walsh, K. A., et al. (2005) · Circulation · doi:10.1161/01.cir.0000157155.44008.0f · Cited by 55 · see citing works

Human adipose-derived mesenchymal stromal cells increase endogenous neurogenesis in the rat subventricular zone acutely after 6-hydroxydopamine lesioning

Schwerk, A. M. K., Altschüler, J., Roch, M., Gossen, M., Winter, C., Berg, J., Kurtz, A., & Steiner, B. (2014) · Cytotherapy · doi:10.1016/j.jcyt.2014.09.005 · Cited by 53 · see citing works

Influence of citalopram and environmental temperature on exercise-induced changes in BDNF

Goekint, M., Roelands, B., Heyman, E., Njemini, R., & MEEUSEN, R. R. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.03.001 · Cited by 53 · see citing works

Medullary thyroid cancer: targeting the RET kinase pathway with sorafenib/tipifarnib

Hong, D. S., Ye, L., Gagel, R. F., Chintala, L., El‐Naggar, A. K., Wright, J., & Kurzrock, R. (2008) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-07-2422 · Cited by 52 · see citing works

p75 neurotrophin receptor is involved in proliferation of undifferentiated mouse embryonic stem cells

Moscatelli, I., Pierantozzi, E., Camaioni, A., Siracusa, G., & Campagnolo, L. (2009) · Experimental Cell Research · doi:10.1016/j.yexcr.2009.08.014 · Cited by 49 · see citing works

Artemin Stimulates Radio- and Chemo-resistance by Promoting TWIST1-BCL-2-dependent Cancer Stem Cell-like Behavior in Mammary Carcinoma Cells

Banerjee, A., Qian, P., Wu, Z., Ren, X., Steiner, M., Bougen-Zhukov, N. M., Liu, S., Liu, D., Zhu, T., & Lobie, P. E. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.365163 · Cited by 48 · see citing works

Glial cell line-derived neurotrophic factor (GDNF) induces neuritogenesis in the cochlear spiral ganglion via neural cell adhesion molecule (NCAM)

Euteneuer, S., Yang, K. H., Chávez, E., Leichtle, A., Loers, G., Olshansky, A., Pak, K. K., Schachner, M., & Ryan, A. F. (2012) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2012.12.004 · Cited by 47 · see citing works

Neurotrophin NT3 promotes ovarian primordial to primary follicle transition

Nilsson, E. E., Dole, G., & Skinner, M. K. (2009) · Reproduction · doi:10.1530/rep-09-0179 · Cited by 46 · see citing works

Expression of nerve growth factor and its high-affinity receptor Trk-A in the rat pancreas during embryonic and fetal life

Miralles, F., Philippe‐Chomette, P., Czernichow, P., & Scharfmann, R. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1560431 · Cited by 46 · see citing works

Nerve Growth Factor Increases in Pancreatic β Cells After Streptozotocin-Induced Damage in Rats

Larrieta, M. E., Vital, P., Mendoza-Rodríguez, C. A., Cerbón, M. A., & Hiriart, M. (2006) · Experimental Biology and Medicine · doi:10.1177/153537020623100405 · Cited by 46 · see citing works

Transient Activation of Hedgehog Pathway Rescued Irradiation-Induced Hyposalivation by Preserving Salivary Stem/Progenitor Cells and Parasympathetic Innervation

Hai, B., Qin, L., Yang, Z., Zhao, Q., Shangguan, L., Ti, X., Zhao, Y., Kim, S., Rangaraj, D., & Liu, F. (2013) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-13-1434 · Cited by 46 · see citing works

GDNF increases cell motility in human colon cancer through VEGF–VEGFR1 interaction

Huang, S.-M., Chen, T.-S., Chiu, C.-M., Chang, L.-K., Liao, K., Tan, H.-M., Yeh, W., Chang, G. R., Wang, M.-Y., & Lu, D. (2013) · Endocrine Related Cancer · doi:10.1530/erc-13-0351 · Cited by 46 · see citing works

Glial-derived neurotrophic factor (GDNF) prevents ethanol (EtOH) induced B92 glial cell death by both PI3K/AKT and MEK/ERK signaling pathways

Villegas, S. N., Njaine, B., Linden, R., & Carri, N. G. (2006) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.08.014 · Cited by 44 · see citing works

In vitro and in vivo improvement of islet survival following treatment with nerve growth factor

Miao, G., Mace, J., Kirby, M., Hopper, A., Peverini, R., Chinnock, R., Shapiro, J., & Hathout, E. (2006) · Transplantation · doi:10.1097/01.tp.0000200320.16723.b3 · Cited by 44 · see citing works

The Effects of Controlled Release of Neurotrophin-3 from PCLA Scaffolds on the Survival and Neuronal Differentiation of Transplanted Neural Stem Cells in a Rat Spinal Cord Injury Model

Tang, S., Liao, X., Shi, B., Qu, Y., Huang, Z., Lin, Q., Guo, X., & Pei, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107517 · Cited by 43 · see citing works

Chronic Neurotrophin-3 Strengthens Synaptic Connections to Motoneurons in the Neonatal Rat

Arvanian, V. L., Horner, P. J., Gage, F. H., & Mendell, L. M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-25-08706.2003 · Cited by 42 · see citing works

Effects of Certain Growth Factors on In Vitro Maturation of Rat Fetal Islet-like Structures

Öberg-Welsh, C., & Welsh, M. (1996) · Pancreas · doi:10.1097/00006676-199605000-00002 · Cited by 40 · see citing works

Additive effect of glial cell line-derived neurotrophic factor and neurotrophin-4/5 on rat fetal nigral explant cultures

Meyer, M., Matarredona, E. R., Seiler, R., Zimmer, J., & Widmer, H. R. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00418-3 · Cited by 39 · see citing works

Human adipose-derived mesenchymal stem cells: a better cell source for nervous system regeneration

Han, C., Zhang, L., Song, L., Liu, Y., Zou, W., Piao, H. Z., & Liu, J. (2014) · Chinese Medical Journal · doi:10.3760/cma.j.issn.0366-6999.20120064 · Cited by 39 · see citing works

Role of motoneuron-derived neurotrophin 3 in survival and axonal projection of sensory neurons during neural circuit formation

Usui, N., Watanabe, K., Ono, K., Tomita, K., Tamamaki, N., Ikenaka, K., & Takebayashi, H. (2012) · Development · doi:10.1242/dev.069997 · Cited by 36 · see citing works

Nerve growth factor is a neurotrophic factor for forebrain cholinergic neurons; implications for Alzheimer's disease.

Hefti, F. F., & Will, B. E. (1987) · PubMed · Cited by 35 · see citing works

Neurotrophin-4 (Ntf4) Mediates Neurogenesis in Mouse Embryonic Neural Stem Cells Through the Inhibition of the Signal Transducer and Activator of Transcription-3 (Stat3) and the Modulation of the Activity of Protein Kinase B

Shen, Y., Inoue, N., & Heese, K. (2010) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-010-9520-1 · Cited by 34 · see citing works

In Vivo AAV1 Transduction With hRheb(S16H) Protects Hippocampal Neurons by BDNF Production

Jeon, M., Nam, J. H., Shin, W.-H., Leem, E., Jeong, K. H., Jung, U. J., Bae, Y., Jin, Y., Kholodilov, N. G., Burke, R. E., et al. (2014) · Molecular Therapy · doi:10.1038/mt.2014.241 · Cited by 34 · see citing works

Neurotrophin-3 gene transduction of mouse neural stem cells promotes proliferation and neuronal differentiation in organotypic hippocampal slice cultures

Lü, H., Hao, Z., Jiao, Q., Xie, W.-L., Zhang, J., Lu, Y.-F., Cai, M., Parker, T. L., & Liu, Y. (2011) · Medical Science Monitor · doi:10.12659/msm.882039 · Cited by 34 · see citing works

Transforming Growth Factor β Cooperates with Persephin for Dopaminergic Phenotype Induction

Roussa, E., Oehlke, O., Rahhal, B., Heermann, S., Heidrich, S., Wiehle, M., & KRIEGLSTEIN, K. G. (2008) · Stem Cells · doi:10.1634/stemcells.2007-0805 · Cited by 33 · see citing works

Neurotrophin-3 Gene-Modified Schwann Cells Promote TrkC Gene-Modified Mesenchymal Stem Cells to Differentiate into Neuron-Like Cells in Poly(Lactic-Acid-Co-Glycolic Acid) Multiple-Channel Conduit

Zhang, Y., He, L., Xing, B., Zeng, X., Zeng, C., Zhang, W., Quan, D., & Zeng, Y. (2011) · Cells Tissues Organs · doi:10.1159/000327724 · Cited by 33 · see citing works

Artemin, a Member of the Glial Cell Line-derived Neurotrophic Factor Family of Ligands, Is HER2-regulated and Mediates Acquired Trastuzumab Resistance by Promoting Cancer Stem Cell-like Behavior in Mammary Carcinoma Cells

Ding, K., Banerjee, A., Tan, S. H., Zhao, J., Qian, Z., Li, R. Q., Qian, P., Liu, S., Wu, Z., Lobie, P. E., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.529552 · Cited by 32 · see citing works

Overexpression of β-NGF promotes differentiation of bone marrow mesenchymal stem cells into neurons through regulation of AKT and MAPK pathway

Yuan, J. J., Huang, G., Xiao, Z., Lin, L., & Han, T.-W. (2013) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-013-1768-6 · Cited by 31 · see citing works

Survival, Differentiation, and Neuroprotective Mechanisms of Human Stem Cells Complexed With Neurotrophin-3-Releasing Pharmacologically Active Microcarriers in an Ex Vivo Model of Parkinson's Disease

Daviaud, N., Garbayo, E., Sindji, L., Martı́nez-Serrano, A., Schiller, P. C., & Montero‐Menei, C. N. (2015) · Stem Cells Translational Medicine · doi:10.5966/sctm.2014-0139 · Cited by 28 · see citing works

Brain derived neurotrophic factor (BDNF) levels in depressed women treated with open-label escitalopram.

Ladea, M., & Bran, M. (2013) · PubMed · Cited by 26 · see citing works

Neurotrophin‐3 null mutant mice display a postnatal motor neuropathy

Woolley, A. G., Sheard, P. W., & Duxson, M. J. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04052.x · Cited by 26 · see citing works

Neurotrophin-4 is required for tolerance to morphine in the mouse

Smith, D., Leil, T. A., & Liu, X. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00084-3 · Cited by 26 · see citing works

BDNF expression in olfactory bulb and epithelium during regeneration of olfactory epithelium

Uranagase, A., Katsunuma, S., Doi, K., & Nibu, K. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.03.051 · Cited by 25 · see citing works

Synergistic Effect of Mesenchymal Stem Cells Infected with Recombinant Adenovirus Expressing Human BDNF on Erectile Function in a Rat Model of Cavernous Nerve Injury

Kim, S. J., Choi, S. W., Hur, K. J., Park, S. H., Sung, Y. C., Ha, Y.-S., Cho, H. J., Hong, S., Lee, J. Y., Hwang, T.-K., et al. (2012) · Korean journal of urology · doi:10.4111/kju.2012.53.10.726 · Cited by 24 · see citing works

Stem cells for cell replacement therapy: A therapeutic strategy for HD?

Rosser, A., & Svendsen, C. N. (2014) · Movement Disorders · doi:10.1002/mds.26026 · Cited by 24 · see citing works

Electroacupuncture Promotes the Differentiation of Transplanted Bone Marrow Mesenchymal Stem Cells Preinduced with Neurotrophin-3 and Retinoic Acid into Oligodendrocyte-Like Cells in Demyelinated Spinal Cord of Rats

Liu, Z., He, B., Zhang, R.-Y., Zhang, K. K., Ding, Y., Ruan, J., Ling, E., Wu, J., & Zeng, Y. (2014) · Cell Transplantation · doi:10.3727/096368914x682099 · Cited by 24 · see citing works

Stem cell grafting in parkinsonism – Why, how and when

de Munter, J., Melamed, E., & Wolters, E. C. (2013) · Parkinsonism & Related Disorders · doi:10.1016/s1353-8020(13)70036-1 · Cited by 23 · see citing works

The Effect of Lentivirus-Mediated PSPN Genetic Engineering Bone Marrow Mesenchymal Stem Cells on Parkinson’s Disease Rat Model

Yin, X., Xu, H., Jiang, Y., Deng, W., Wu, Z., Xiang, H., Sun, P., & Xie, J. (2014) · PLoS ONE · doi:10.1371/journal.pone.0105118 · Cited by 23 · see citing works

CXCR2 and RET Single Nucleotide Polymorphisms in Pancreatic Cancer

Donahue, T. R., & Hines, O. J. (2008) · World Journal of Surgery · doi:10.1007/s00268-008-9826-z · Cited by 23 · see citing works

Extracellular Crosstalk

Zhou, F., Zhong, J., & Snider, W. D. (2003) · Cell · doi:10.1016/s0092-8674(03)00467-7 · Cited by 23 · see citing works

NGF and TERT Co-Transfected BMSCs Improve the Restoration of Cognitive Impairment in Vascular Dementia Rats

Wang, F., Chang, G., & Geng, X. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098774 · Cited by 22 · see citing works

Human umbilical cord blood stem cells and brain-derived neurotrophic factor for optic nerve injury: a biomechanical evaluation

Zhang, Z., Li, Y., Liu, X., Huang, F.-X., Liu, T., Jiang, D., Lv, X., & Luo, M. (2015) · Neural Regeneration Research · doi:10.4103/1673-5374.160110 · Cited by 22 · see citing works

Brain-derived neurotrophic factor (BDNF) expression in normal and regenerating olfactory epithelium of Xenopus laevis

Frontera, J. L., Cervino, A. S., Jungblut, L. D., & Paz, D. A. (2014) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2014.10.010 · Cited by 21 · see citing works

Nerve Growth Factor Improves Survival and Function of Transplanted Islets Via TrkA-mediated β Cell Proliferation and Revascularization

Hata, T., Sakata, N., Yoshimatsu, G., Tsuchiya, H., Fukase, M., Ishida, M., Aoki, T., Katayose, Y., Egawa, S., & Unno, M. (2015) · Transplantation · doi:10.1097/tp.0000000000000655 · Cited by 21 · see citing works

Neurotrophin 3, Not Brain‐Derived Neurotrophic Factor or Neurotrophin 4, Knockout Mice Have Delay in Vestibular Compensation After Unilateral Labyrinthectomy

Gacek, R. R., & Khetarpal, U. (1998) · The Laryngoscope · doi:10.1097/00005537-199805000-00009 · Cited by 20 · see citing works

Pancreatic Islet Transplantation Using Vascularised Chambers Containing Nerve Growth Factor Ameliorates Hyperglycaemia in Diabetic Mice

Hussey, A. J., Winardi, M., Wilson, J., Forster, N. A., Morrison, W. A., Penington, A., Knight, K. R., & Feeney, S. J. (2010) · Cells Tissues Organs · doi:10.1159/000276595 · Cited by 19 · see citing works

GDNF‐induced seminomatous tumours in mouse – an experimental model for human seminomas?

Sariola, H. V., & Meng, X. (2003) · Apmis · doi:10.1034/j.1600-0463.2003.11101231.x · Cited by 19 · see citing works

Neurotrophin-4/5 promotes proliferation of oligodendrocyte-type-2 astrocytes (O-2A)

Scarisbrick, I. A., Asakura, K., & Rodriguez, M. (2000) · Developmental Brain Research · doi:10.1016/s0165-3806(00)00077-8 · Cited by 18 · see citing works

Intrathecal injection of lentivirus‐mediated glial cell line‐derived neurotrophic factor RNA interference relieves bone cancer‐induced pain in rats

Meng, F., Xu, Y. X. Z., Dan, Q., Wei, L., Deng, Y., Liu, J., He, M., Liu, W., Xia, Q., Zhou, F. H., et al. (2015) · Cancer Science · doi:10.1111/cas.12609 · Cited by 16 · see citing works

RET Mutations in Neuroendocrine Tumors: Including Small-Cell Lung Cancer

Rudin, C. M., Drilon, A. E. D. C., & Poirier, J. T. (2014) · Journal of Thoracic Oncology · doi:10.1097/jto.0000000000000301 · Cited by 16 · see citing works

Therapeutic Effect of Myogenic Cells Modified to Express Neurotrophic Factors in a Rat Model of Sciatic Nerve Injury

(2012) · Journal of Stem Cells and Regenerative Medicine · doi:10.46582/jsrm.0801004 · Cited by 16 · see citing works

BDNF and NT4 play interchangeable roles in gustatory development

Huang, T., & Krimm, R. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.12.031 · Cited by 15 · see citing works

Effects of neurotrophin-3 on the differentiation of neural stem cells into neurons and oligodendrocytes.

Guowei, Z., Sun, C., & Liu, W. (2012) · Europe PMC (PubMed Central) · doi:10.3969/j.issn.1673-5374.2012.19.006 · Cited by 14 · see citing works

Autophagy: A Key Regulator of Homeostasis and Disease: An Overview of Molecular Mechanisms and Modulators

Gómez-Virgilio, L., Silva-Lucero, M.-D.-C., Flores-Morelos, D.-S., Gallardo-Nieto, J., Lopez-Toledo, G., Abarca-Fernandez, A.-M., Zacapala-Gómez, A.-E., Luna-Muñoz, J., Montiel-Sosa, F., Soto-Rojas, L. O., et al. (2022) · Cells · doi:10.3390/cells11152262 · Cited by 431 · see citing works

Heparin-Poloxamer Thermosensitive Hydrogel Loaded with bFGF and NGF Enhances Peripheral Nerve Regeneration in Diabetic Rats

Li, R., Li, Y., Wu, Y., Zhao, Y., Chen, H. A., Yuan, Y., Xu, K., Zhang, H., Lu, Y., Wang, J., et al. (2018) · Biomaterials · doi:10.1016/j.biomaterials.2018.03.044 · Cited by 233 · see citing works

Recent advances on the molecular mechanisms of exercise-induced improvements of cognitive dysfunction

Lü, Y., Bu, F., Wang, F., Liu, L., Zhang, S., Wang, G., & Hu, X. (2023) · Translational Neurodegeneration · doi:10.1186/s40035-023-00341-5 · Cited by 117 · see citing works

Micro- and nanotechnology approaches to improve Parkinson's disease therapy

Torres-Ortega, P. V., Saludas, L., Hanafy, A. S., Garbayo, E., & Blanco‐Prieto, M. J. (2018) · Journal of Controlled Release · doi:10.1016/j.jconrel.2018.12.036 · Cited by 83 · see citing works

Engineering Silk Fibroin‐Based Nerve Conduit with Neurotrophic Factors for Proximal Protection after Peripheral Nerve Injury

Carvalho, C. R., Chang, W., Silva‐Correia, J., Reis, R. L., Oliveira, J. M., & Kohn, J. (2020) · Advanced Healthcare Materials · doi:10.1002/adhm.202000753 · Cited by 70 · see citing works

Hepatic Autonomic Nervous System and Neurotrophic Factors Regulate the Pathogenesis and Progression of Non-alcoholic Fatty Liver Disease

Amir, M., Yu, M. A., He, P., & Srinivasan, S. (2020) · Frontiers in Medicine · doi:10.3389/fmed.2020.00062 · Cited by 69 · see citing works

Advances in treatment of neurodegenerative diseases: Perspectives for combination of stem cells with neurotrophic factors

Wang, J., Hu, W., Jiang, Z., & Feng, M. (2020) · World Journal of Stem Cells · doi:10.4252/wjsc.v12.i5.323 · Cited by 53 · see citing works

Role of Astrocytes in Parkinson’s Disease Associated with Genetic Mutations and Neurotoxicants

Kim, S., Pajarillo, E. A. B., Nyarko‐Danquah, I., Aschner, M., & Lee, E.-S. (2023) · Cells · doi:10.3390/cells12040622 · Cited by 50 · see citing works

Safety and Efficacy of Intraventricular Delivery of Bone Marrow-Derived Mesenchymal Stem Cells in Hemorrhagic Stroke Model

Huang, P., Freeman, W. D., Edenfield, B. H., Brott, T. G., Meschia, J. F., & Zubair, A. C. (2019) · Scientific Reports · doi:10.1038/s41598-019-42182-1 · Cited by 47 · see citing works

Dental pulp-derived stem cell conditioned medium to regenerate peripheral nerves in a novel animal model of dysphagia

Tsuruta, T., Sakai, K., Watanabe, J., Katagiri, W., & Hibi, H. (2018) · PLoS ONE · doi:10.1371/journal.pone.0208938 · Cited by 45 · see citing works

Epithelial Cell Lineage and Signaling in Murine Salivary Glands

Aure, M. H., Symonds, J. M., Mays, J. W., & Hoffman, M. P. (2019) · Journal of Dental Research · doi:10.1177/0022034519864592 · Cited by 45 · see citing works

Modulation of neurotrophic factors in the treatment of dementia, stroke and TBI: Effects of Cerebrolysin

Rejdak, K., Sienkiewicz‐Jarosz, H., Bieńkowski, P., & Álvarez, A. (2023) · Medicinal Research Reviews · doi:10.1002/med.21960 · Cited by 43 · see citing works

The Epigenetics of Anxiety Pathophysiology: A DNA Methylation and Histone Modification Focused Review

Persaud, N. S., & Cates, H. M. (2023) · eneuro · doi:10.1523/eneuro.0109-21.2021 · Cited by 41 · see citing works

Effects of transcranial magnetic stimulation on neurobiological changes in Alzheimer's disease (Review)

Bashir, S., Uzair, M., Abualait, T., Arshad, M. M. U. D., Khallaf, R. A., Niaz, A., Thani, Z., Yoo, W., Túnez, I., Demirtaş-Tatlıdede, A., et al. (2022) · Molecular Medicine Reports · doi:10.3892/mmr.2022.12625 · Cited by 39 · see citing works

Current druggable targets for therapeutic control of Alzheimer's disease

Gupta, G. L., & Samant, N. P. (2021) · Contemporary Clinical Trials · doi:10.1016/j.cct.2021.106549 · Cited by 38 · see citing works

Role of Region-Specific Brain Decellularized Extracellular Matrix on In Vitro Neuronal Maturation

Reginensi, D., Ortiz, D. A., Pravia, A., Burillo, A., Morales, F. L., Morgan, C., Jimenez, L., Dave, K. R., Pérez‐Pinzón, M. A., & Gittens, R. A. (2020) · Tissue Engineering Part A · doi:10.1089/ten.tea.2019.0277 · Cited by 34 · see citing works

Overview of retinal differentiation potential of mesenchymal stem cells: A promising approach for retinal cell therapy

Salehi, H., Amirpour, N., Razavi, S., Esfandiari, E., & Zavar, R. (2016) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2016.11.010 · Cited by 34 · see citing works

Investigation of glycosaminoglycan mimetic scaffolds for neurite growth

Menezes, R., Hashemi, S., Vincent, R., Collins, G. L., Meyer, J., Foston, M. B., & Arinzeh, T. L. (2019) · Acta Biomaterialia · doi:10.1016/j.actbio.2019.03.024 · Cited by 33 · see citing works

3D-printed hyaluronic acid hydrogel scaffolds impregnated with neurotrophic factors (BDNF, GDNF) for post-traumatic brain tissue reconstruction

Mishchenko, T. A., Klimenko, M. O., Kuznetsova, A. I., Yarkov, R. S., Savelyev, A. G., Sochilina, A. V., Mariyanats, A. O., Popov, V. K., Khaydukov, E. V., Zvyagin, A. V., et al. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.895406 · Cited by 32 · see citing works

The potential neuroprotective effects of stingless bee honey

Zulkifli, N. A., Hassan, Z., Mustafa, M. Z., Azman, W. N. W., Hadie, S. N. H., Ghani, N., & Zin, A. A. M. (2023) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1048028 · Cited by 33 · see citing works

Neuroprotection and Non-Invasive Brain Stimulation: Facts or Fiction?

Guidetti, M., Bertini, A., Pirone, F., Sala, G., Signorelli, P., Ferrarese, C., Priori, A., & Bocci, T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232213775 · Cited by 26 · see citing works

Transplantation of human dental pulp stem cells compensates for striatal atrophy and modulates neuro-inflammation in 3-nitropropionic acid rat model of Huntington’s disease

Eskandari, N., Boroujeni, M. E., Abdollahifar, M., Piryaei, A., Khodagholi, F., Mirbehbahani, S. H., Shokoofeh, S., Moghaddam, M. H., Aliaghaei, A., & Sadeghi, Y. (2020) · Neuroscience Research · doi:10.1016/j.neures.2020.12.002 · Cited by 27 · see citing works

Molecular Components of Store-Operated Calcium Channels in the Regulation of Neural Stem Cell Physiology, Neurogenesis, and the Pathology of Huntington’s Disease

Latoszek, E., & Czeredys, M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.657337 · Cited by 21 · see citing works

Botulinum Toxin and Neuronal Regeneration after Traumatic Injury of Central and Peripheral Nervous System

Luvisetto, S. (2020) · Toxins · doi:10.3390/toxins12070434 · Cited by 23 · see citing works

Neurogenic and cognitive enhancing effects of human dental pulp stem cells and its secretome in animal model of hippocampal neurodegeneration

Venugopal, C., Shobha, K., Rai, K. S., & Dhanushkodi, A. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.12.012 · Cited by 21 · see citing works

Peripheral Blood Circular RNAs as a Biomarker for Major Depressive Disorder and Prediction of Possible Pathways

Zhang, D., Ji, Y., Chen, X., Chen, R., Wei, Y., Peng, Q., Lin, J., Yin, J., He-zhan, L., Cui, L., et al. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.844422 · Cited by 22 · see citing works

Remodeling microglia to a protective phenotype in Parkinson’s disease?

Awogbindin, I. O., Ishola, I. O., St‐Pierre, M., Carrier, M., Savage, J. C., Paolo, T. D., & Tremblay, M. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.135164 · Cited by 21 · see citing works

A Review of Basic Fibroblast Growth Factor Delivery Strategies and Applications in Regenerative Medicine

Tu, Y., Li, Y., Qu, G.-E., Ning, Y., Li, B., Li, G., Wu, M., Li, S., & Huang, Y. (2024) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.37834 · Cited by 21 · see citing works

Boosting Neurogenesis in the Adult Hippocampus Using Antidepressants and Mesenchymal Stem Cells

Kot, M., Neglur, P. K., Pietraszewska, A., & Bużańska, L. (2022) · Cells · doi:10.3390/cells11203234 · Cited by 20 · see citing works

Optic nerve regeneration: Potential treatment approaches

Lee, J., Nguyen, S., & Bhattacharya, S. K. (2024) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2023.102428 · Cited by 19 · see citing works

Understanding the mechanisms of disease modifying effects of aerobic exercise in people with Alzheimer’s disease

Abdullahi, A., Wong, T. W. L., & Ng, S. S. M. (2024) · Ageing Research Reviews · doi:10.1016/j.arr.2024.102202 · Cited by 20 · see citing works

Pumping the Brakes: Neurotrophic Factors for the Prevention of Cognitive Impairment and Dementia after Traumatic Brain Injury

Corrigan, F., Arulsamy, A., Teng, J., & Collins‐Praino, L. E. (2016) · Journal of Neurotrauma · doi:10.1089/neu.2016.4589 · Cited by 20 · see citing works

Corneal Cells: Fine-tuning Nerve Regeneration

Kowtharapu, B. S., & Stachs, O. (2019) · Current Eye Research · doi:10.1080/02713683.2019.1675175 · Cited by 18 · see citing works

Promoting motor functions in a spinal cord injury model of rats using transplantation of differentiated human olfactory stem cells: A step towards future therapy

Hamidabadi, H. G., Simorgh, S., Kamrava, S. K., Namjoo, Z., Bagher, Z., Bojnordi, M. N., Niapour, A., Mojaverrostami, S., Saeb, M. R., Zarrintaj, P., et al. (2021) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113205 · Cited by 18 · see citing works

Biomaterial-Based bFGF Delivery for Nerve Repair

Huang, Q., Liu, B., & Wu, W.-C. (2023) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2023/8003821 · Cited by 19 · see citing works

Role of vascular endothelial growth factor as a critical neurotrophic factor for the survival and physiology of motoneurons

Calvo, P. M., Hernández, R. G., de la Cruz, R. R., & Pastor, Á. M. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.363194 · Cited by 16 · see citing works

Nerve growth factor protects salivary glands from irradiation-induced damage

Li, S.-S., Wu, C., Zhang, B., Qiu, L., Chen, W., Yuan, Y., Liu, X.-C., Li, C., & Li, L. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118748 · Cited by 16 · see citing works

Diversity of Microglia-Derived Molecules with Neurotrophic Properties That Support Neurons in the Central Nervous System and Other Tissues

Wiens, K. R., Wasti, N., Ulloa, O., & Klegeris, A. (2024) · Molecules · doi:10.3390/molecules29235525 · Cited by 13 · see citing works

Shaping the Microglia in Retinal Degenerative Diseases Using Stem Cell Therapy: Practice and Prospects

Jin, N., Sha, W., & Gao, L. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.741368 · Cited by 14 · see citing works

The effect of lithium chloride onBDNF, NT3, and their receptor mRNA levels in the spinal contusion rat models

Abdanipour, A., Moradi, F., Fakheri, F., Ghorbanlou, M., & Nejatbakhsh, R. (2019) · Neurological Research · doi:10.1080/01616412.2019.1588507 · Cited by 14 · see citing works

Harnessing nerve–muscle cell interactions for biomaterials‐based skeletal muscle regeneration

Narayanan, N., Lengemann, P., Kim, K. H., Kuang, L., Sobreira, T. J. P., Hedrick, V., Aryal, U. K., Kuang, S., & Deng, M. (2020) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.37022 · Cited by 13 · see citing works

Aging-Related Protein Alterations in the Brain

Syed, R. A., Hayat, M., Qaiser, H., Uzair, M., Al-Regaiey, K., Khallaf, R. A., Kaleem, I., & Bashir, S. (2024) · Journal of Alzheimer s Disease · doi:10.3233/jad-230801 · Cited by 10 · see citing works

Altered serum levels of glial cell line‐derived neurotrophic factor in male chronic schizophrenia patients with tardive dyskinesia

Ye, F., Zhan, Q., Xiao, W., Sha, W., & Zhang, X. (2018) · International Journal of Methods in Psychiatric Research · doi:10.1002/mpr.1727 · Cited by 10 · see citing works

Navigating Neurodegenerative Disorders: A Comprehensive Review of Current and Emerging Therapies for Neurodegenerative Disorders

Kharat, S., Mali, S., Korade, G. S., & Rakhi, G. (2024) · Journal of Neuroscience and Neurological Disorders · doi:10.29328/journal.jnnd.1001095 · Cited by 8 · see citing works

Decoding of the Role of TREM2 in Neuropathic Pain: Molecular Pathway and Neuroinflammatory Mechanism

Vijayan, N., Veeraveedu, P. T., & Patel, S. (2025) · Drug Development Research · doi:10.1002/ddr.70111 · Cited by 8 · see citing works

Molecular mechanisms of esophageal epithelial regeneration following repair of surgical defects with acellular silk fibroin grafts

Gündoğdu, G., Tosun, M., Morhardt, D. R., Gheinani, A. H., Algarrahi, K., Yang, X., Costa, K., Alegria, C. G., Adam, R. M., Yang, W., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-86511-9 · Cited by 7 · see citing works

Towards innervation of bioengineered muscle constructs: Development of a sustained neurotrophic factor delivery and release system

Poerio, A., Mashanov, V. S., Lai, D., Kim, M. W. S., Ju, Y. M., Kim, J. H., Lee, S. J., Cleymand, F., Mano, J. F., Atala, A., et al. (2022) · Bioprinting · doi:10.1016/j.bprint.2022.e00220 · Cited by 7 · see citing works

Targeting Amyotrophic Lateral Sclerosis with Gene Therapy: From Silencing Genes to Enhancing Neuroprotection

Verdés, S., Navarro, X., & Bosch, A. (2025) · Human Gene Therapy · doi:10.1177/10430342251372898 · Cited by 7 · see citing works

Lovastatin alters neurotrophin expression in rat hippocampus-derived neural stem cells in vitro

Fakheri, F., Abdanipour, A., Parivar, K., Anarkooli, I. J., & Rastegar, H. (2020) · Acta Neurobiologiae Experimentalis · doi:10.21307/ane-2019-038 · Cited by 6 · see citing works

Neuronal survival of DRG neurons after neurite transection in vitro promotes by nerve growth factor and brain derived neurotrophic factor

Oğuz, E. K. (2018) · Cellular and Molecular Biology · doi:10.14715/cmb/2017.64.15.7 · Cited by 6 · see citing works

Relationship Between Serum Brain-Derived Neurotrophic Factor and Neurotrophin-3 Levels and Hearing Thresholds in Patients With Age-Related Hearing Loss

Altay, D. U., Korkmaz, H., Korkmaz, M., & Noyan, T. (2024) · Journal of Speech Language and Hearing Research · doi:10.1044/2024_jslhr-23-00440 · Cited by 5 · see citing works

Neurodevelopmental origins of neurodegeneration: a lifespan perspective on brain vulnerability

Kopalli, S. R., Vadia, N., Varma, P., Mishra, S., Joshi, N., Bansal, P., Al-Hasnaawei, S., Chauhan, A. S., Jain, H., Nathiya, D., et al. (2025) · Brain Research · doi:10.1016/j.brainres.2025.150134 · Cited by 6 · see citing works

Delivery of Neuroregenerative Proteins to the Brain for Treatments of Neurodegenerative Brain Diseases

Ebert, E. T., Schwinghamer, K., & Siahaan, T. J. (2024) · Life · doi:10.3390/life14111456 · Cited by 5 · see citing works

Dietary Restriction against Parkinson’s Disease: What We Know So Far

Wang, Z., Cui, Y., Wen, L., Yu, H., Feng, J., Yuan, W., & He, X. (2022) · Nutrients · doi:10.3390/nu14194108 · Cited by 5 · see citing works

CDNF overexpression prevents motor-cognitive dysfunction by intrastriatal CPP-based delivery system in a Parkinson's disease animal model.

Villa-Cedillo, S. A., Matta-Yee-Chig, D., Soto-Domínguez, A., Rodríguez-Rocha, H., García-García, A., Montes-de-Oca-Saucedo, C., Loera-Arias, M. D. J., Valdés, J., & Saucedo-Cárdenas, O. (2023) · Neuropeptides · doi:10.1016/j.npep.2023.102385 · Cited by 4 · see citing works

Neuropathic pain development following nerve injury is mediated by SOX11-ARID1A-SOCS3 transcriptional regulation in the spinal cord

Le, D., Zhang, C., Liu, L., Zhao, M., Liang, Y., Liao, P., & Yang, F. (2024) · Molecular Biology Reports · doi:10.1007/s11033-023-09183-w · Cited by 5 · see citing works

The Role of Neuromodulation and Potential Mechanism in Regulating Heterotopic Ossification

Li, D., Liu, C., Wang, H., Li, Y., Wang, Y., An, S., & Sun, S. (2024) · Neurochemical Research · doi:10.1007/s11064-024-04118-8 · Cited by 5 · see citing works

In Silico Analysis to Link Insulin Resistance, Obesity and Ageing with Alzheimer’s Disease

Sarkar, P. A., Jayaraj, P., Patwardhan, K., Yeole, S., Das, S., Somaiya, Y., Desikan, R., & Thirumurugan, K. (2021) · Journal of Molecular Neuroscience · doi:10.1007/s12031-021-01875-x · Cited by 5 · see citing works

The neurotrophic potential of human platelet lysate substitution for fetal bovine serum in glial induction culture medium

Ravenkamp, M., Tchoukalova, Y. D., Myers, C. E., Madsen, C. S., Shah, M. K., Zhang, N., Lal, D., & Lott, D. G. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.135025 · Cited by 5 · see citing works

Rat adipose-derived mesenchymal stem cell-derived exosomes loaded with miR-375 promote neurite outgrowth and peripheral nerve regeneration via activation of Akt by targeting EPHA4

Liu, Z., Han, Y., & Song, C. (2025) · Regenerative Therapy · doi:10.1016/j.reth.2025.06.010 · Cited by 5 · see citing works

Application of Neurotrophic Factors as a Therapeutic Approach for Neurodegenerative Diseases

Kim, S., Lee, S. Y., Jung, U. J., & Kim, S. R. (2025) · Experimental Neurobiology · doi:10.5607/en25023 · Cited by 5 · see citing works

Traumatic brain injury as risk factor of Alzheimer’s disease and possibilities of pathogenetic therapy

Litvinenko, I., Naumov, K. M., Lobzin, V. Y., Emelin, А. Y., Dynin, P. S., Kolmakova, K. A., & Nikishin, V. O. (2024) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro202412401145 · Cited by 4 · see citing works

The therapeutic use of clonal neural stem cells in experimental Parkinson´s disease

Nelke, A., García‐López, S., Caso, J. R., & Pereira, M. P. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-03965-0 · Cited by 4 · see citing works

Neurodegenerative Diseases and Cell Reprogramming

Sallam, A., & Mousa, S. A. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-02039-5 · Cited by 4 · see citing works

Striatal dopaminergic neurons as a potential target for GDNF based ischemic stroke therapy

Beker, M. Ç., Beker, M., Çağlayan, A. B., Bolat, B., Kılıç, Ü., Köse, G. T., & Kılıç, E. (2021) · TURKISH JOURNAL OF MEDICAL SCIENCES · doi:10.3906/sag-2108-268 · Cited by 4 · see citing works

BDNF increases associated with constant troponin T levels and may protect against poor cognitive interference control: The SABPA prospective study

van Vuren, E. J., Malan, L., von Känel, R., Magnusson, M., Lammertyn, L., & Malan, N. T. (2019) · European Journal of Clinical Investigation · doi:10.1111/eci.13116 · Cited by 4 · see citing works

Etiopathogenesis of depression and experimental depression models used in preclinical studies

Kandemir, Ü. (2023) · European Journal of Life Sciences · doi:10.55971/ejls.1327521 · Cited by 2 · see citing works

Application of transcutaneous electrical nerve stimulation (TENS) for restoring sexual function after gender-affirming genital reconstruction: a hypothesis

Tahmasbi, F. (2025) · Therapeutic Advances in Urology · doi:10.1177/17562872251358125 · Cited by 2 · see citing works

Multiple Cellular Therapies Along with Neurorehabilitation in Spastic Diplegic Cerebral Palsy: A Case Report.

Sharma, A., Gokulchandran, N., Kulkarni, P., Mullangi, S. K., Bhagawanani, K., Ganar, V., Sane, H. M., & Badhe, P. B. (2020) · PubMed Central · Cited by 2 · see citing works

Neurotropic activity and safety of methylene-cycloalkylacetate (MCA) derivative 3-(3-allyl-2-methylenecyclohexyl) propanoic acid

Lahiani, A., Haham, D., Lankri, D., Cornell-Kennon, S., Schaefer, E., Tsvelikhovsky, D., & Lazarovici, P. (2020) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.0c00255 · Cited by 2 · see citing works

Linking rotigotine, Parkinson's disease, and brain-derived neurotrophic factor

Sohya, K., O'Hashi, K., & Kunugi, H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815950-7.00014-x · Cited by 2 · see citing works

Scaffolds for brain tissue reconstruction

Adewole, D. O., Das, S., Petrov, D., & Cullen, D. K. (2019) · Elsevier eBooks · doi:10.1016/b978-0-08-102561-1.00001-4 · Cited by 2 · see citing works

Neuroprotective Immunity for Neurodegenerative and Neuroinfectious Diseases

Olson, K. E., Mosley, R. L., & Gendelman, H. E. (2020) · Springer eBooks · doi:10.1007/978-3-030-33946-3_8 · Cited by 2 · see citing works

Neurotrophins and their receptors in the peripheral nervous system and non-nervous tissue of fish

Carrillo-Muñoz, A. I., Rodríguez-Jaimes, S. Y., Hernández-Hernández, G. C., & Castelán, F. (2025) · Fish Physiology and Biochemistry · doi:10.1007/s10695-025-01453-7 · Cited by 1 · see citing works

Implikacje pedagogiczne badań nad BDNF (czynnik neurotroficzny pochodzenia mózgowego). Cz. 1: BDNF a rozwój człowieka

Stopikowska, M. (2025) · Problemy Opiekuńczo-Wychowawcze · doi:10.71358/pow.2364 · Cited by 1 · see citing works

Implikacje pedagogiczne badań nad BDNF (czynnik neurotroficzny pochodzenia mózgowego). Cz. 2: BDNF a prozdrowotny styl życia

Stopikowska, M. (2025) · Problemy Opiekuńczo-Wychowawcze · doi:10.71358/pow.2692 · Cited by 1 · see citing works

Significance of the composition of conduit internal environment for the activation of axon growth in patients with extended peripheral nerve defects

Pyatin, V. F., & Tuturov, A. O. (2019) · S S Korsakov Journal of Neurology and Psychiatry · doi:10.17116/jnevro2019119041100 · Cited by 1 · see citing works

Role of Astrocyte Dysfunction in Parkinson’s Disease Pathogenesis

Datta, I., Raj, A., & Kaushal, A. (2022) · Springer eBooks · doi:10.1007/978-981-16-8313-8_10 · Cited by 2 · see citing works

Decreased body temperature during anoxia affects the endogenous BDNF level in tertiary phase of injury

Kletkiewicz, H., & Rogalska, J. (2019) · Neuroscience Letters · doi:10.1016/j.neulet.2019.134413 · Cited by 1 · see citing works

Transposon‐mediated glial cell line‐derived neurotrophic factor overexpression in human adipose tissue‐derived mesenchymal stromal cells: A potential approach for neuroregenerative medicine?

Rasińska, J., Klein, C., Stahn, L., Maidhof, F., Pfeffer, A., Schreyer, S., Gossen, M., Kurtz, A., Steiner, B., & Hemmati‐Sadeghi, S. (2022) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.3296 · Cited by 1 · see citing works

Spinal Cord Injury and Its Future Therapy - A Perspective

Maiti, S. K. (2019) · Biomedical Journal of Scientific & Technical Research · doi:10.26717/bjstr.2019.22.003762

Acetylsalicylic Acid Enhanced Neurotrophic Profile of Epidermal Neural Crest Stem Cells: A Possible Approach for the Combination Therapy

Zafarmand, S. S., Salehi, M. S., Mokhtari, M. J., Safari, A., Pandamooz, S., Dianatpour, M., & Borhani‐Haghighi, A. (2021) · Physiology and Pharmacology · doi:10.52547/phypha.26.2.1

Ophthalmological Metabolic Diseases and Stem Cells

Zúñiga-Gazcón, H., Delgado, M. A. F., Mayorga, D. E. S., Calderón, L. A. V., & Ramírez, M. H. G. (2022) · International Journal of Medical Science and Clinical Research Studies · doi:10.47191/ijmscrs/v2-i7-15

The effect of lovastatin on cell proliferation and neurotrophic factor expression of bone marrow mesenchymal stem cells in vitro

bageri, A., Ghorbanian, M., & Kosha, A. (2022) · Cell & Tissue Journal · doi:10.52547/jct.13.2.107

Traumatic Brain Injury as a Risk Factor for Alzheimer’s Disease and Potential for Pathogenetic Therapy

Litvinenko, I., Naumov, K. M., Lobzin, V. Y., Emelin, А. Y., Dynin, P. S., Kolmakova, K. A., & Nikishin, V. O. (2024) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-024-01632-8

Research Advances in the Mechanism of Action of Repetitive Transcranial Magnetic Stimulation in Treating Cognitive Impairment in Patients with Alzheimer’s Disease

史, 瑞. (2025) · Advances in Clinical Medicine · doi:10.12677/acm.2025.1541237

Dexamethasone-induced insulin resistance impaired artemin levels in the hippocampus and altered behavioural patterns

Çalışkan, H. (2025) · Scripta Medica · doi:10.5937/scriptamed56-60383

Thermo-responsive single-chain cyclized/knotted polymers for cell encapsulation

Dou, Z., He, L., Zhao, W., Wang, X., Wang, H., Lu, J., Wang, C., & Yang, L. (2026) · Materials Advances · doi:10.1039/d5ma00621j

Modélisation in vitro des effets de toxiques environnementaux responsables de sécheresse oculaire, sur des cellules épithéliales et des neurones sensoriels trigéminés

Vitoux, M.-A. (2020) · doi:10.70675/cb6ca03bzf094z42b9za1fcz272ae99aa20b

Leveraging engineered small EVs to mitigate cancer pain: a new paradigm

Sarkar, S., Roy, S., & Choudhury, L. (2026) · Journal of Microencapsulation · doi:10.1080/02652048.2026.2677813

Exploring shared genetic pathways and gene interplay in major neurodegenerative diseases: a comprehensive review

Pattnaik, P. P., Prusty, S. K., Pati, S., Jew, K. A., Bora, A. K., Sahoo, J., & Sahu, P. K. (2026) · Gene · doi:10.1016/j.gene.2026.150318

Zebrafish as a translational model for peptide-mediated synaptic dysfunction related to obesity

Rodrigues, A. C., Lacerda, A. P., Mukoyama, L. T. H., de Carvalho, G. B., da Mata, J. A. L., Buccini, D. F., Franco, O. L., & Migliolo, L. (2026) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2026.1845252

Association of Cholinergic Stimulation with Improved Functional Performance and Neurotrophic Markers in Mild Cognitive Impairment

Qaisar, R., Iqbal, M. S., Ahmad, F., & Karim, A. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-06302-z

Neurotrophic factors: promising candidates in tissue regeneration

Xiao, N. (2016) · Neural Regeneration Research · doi:10.4103/1673-5374.182696 · Cited by 13 · see citing works

Therapeutic Potential of Neurotrophic Factors

McMahon, S. B., & Murinson, B. B. (2005) · Elsevier eBooks · doi:10.1016/b978-012738903-5/50026-6 · Cited by 2 · see citing works

Roles of Neurotrophic Factors in Neuronal Survival and Nerve Regeneration

김윤희, Kim, M., Cheon, K.-A. A., Jin, S., & Kwon, Y. H. K. (1997)

Neurotrophic Factor in the Nerve Tissue Repair of the Applied Research

Meng, T. (2008) · Jilin Normal University Journal

Neurotrophic Factors

(2008) · Springer eBooks · doi:10.1007/978-3-540-29678-2_3959