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Distribution of Brain-Derived Neurotrophic Factor (BDNF) Protein and mRNA in the Normal Adult Rat CNS: Evidence for Anterograde Axonal Transport
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A sensitive immunohistochemical technique was used, along with highly specific affinity-purified antibodies to brain-derived neurotrophic factor (BDNF), to generate a detailed mapping of BDNF immunoreactivity (BDNF-ir) throughout the adult rat CNS. A parallel analysis of sites of BDNF synthesis was performed with in situ hybridization techniques using a cRNA probe to the exon encoding mature rat BDNF protein. These combined data revealed (1) groups of cell bodies containing diffuse BDNF-ir throughout the CNS that were strongly correlated with fields of cells containing BDNF mRNA; (2) varying degrees of BDNF-ir outside of cell bodies, in what appeared to be fibers and/or terminals; and (3) many regions containing extremely heavy BDNF-immunoreactive fiber/terminal labeling that lacked BDNF mRNA (e.g., medial habenula, central nucleus of the amygdala, bed nucleus of stria terminalis, lateral septum, and spinal cord). The latter observation suggested that in these regions BDNF was derived from anterograde axonal transport by afferent systems. In the two cases in which this hypothesis was tested by the elimination of select afferents, BDNF immunostaining was completely eliminated. These data, along with the observation that BDNF-ir was rarely found within dendrites or fibers en passage, suggest that BDNF protein produced in adult CNS neurons is polarized primarily along axonal processes and is preferentially stored in terminals within the innervation target.
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“BDNF is involved in multiple levels of neuroplasticity like synaptic modulation, adult neurogenesis, and dendritic growth (29–32).”
From Psychedelics and Neuroplasticity: A Systematic Review Unraveling the Biological Underpinnings of Psychedelics. (2021) · cites this paper as [29]
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Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
AChE-stained horizontal sections of the rat brain in stereotaxic coordinates
Paxinos, G., WATSON, C. R. R., & Emson, P. C. (1980) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(80)90021-7 · Cited by 4,501
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 4,015
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
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
Maisonpierre, P. C., Belluscio, L., Friedman, B., Alderson, R. F., Wiegand, S. J., Furth, M. E., Lindsay, R. M., & Yancopoulos, G. D. (1990) · Neuron · doi:10.1016/0896-6273(90)90089-x · Cited by 1,250
Korsching, S. I., Auburger, G. W. J., Heumann, R., Scott, J., & Thoenen, H. (1985) · The EMBO Journal · doi:10.1002/j.1460-2075.1985.tb03791.x · Cited by 938
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
Ernfors, P., Wetmore, C., Olson, L., & Persson, H. (1990) · Neuron · doi:10.1016/0896-6273(90)90090-3 · Cited by 819
Potentiation of developing neuromuscular synapses by the neurotrophins NT-3 and BDNF
Lohof, A. M., Ip, N. Y., & Poo, M.-M. (1993) · Nature · doi:10.1038/363350a0 · Cited by 755
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Szapacs, M. E., Numis, A. L., & Andrews, A. M. (2004) · Neurobiology of Disease · doi:10.1016/j.nbd.2004.04.010 · Cited by 49
Silasi, G., Klahr, A. C., Hackett, M. J., Auriat, A. M., Nichol, H., & Colbourne, F. (2012) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2012.38 · Cited by 41
Li, T., Jiang, L., Zhang, X., & Chen, H. (2009) · Neuroreport · doi:10.1097/wnr.0b013e32832000c8 · Cited by 41
Haematopoietic cells produce BDNF and regulate appetite upon migration to the hypothalamus
Urabe, H., Kojima, H., Chan, L., Terashima, T., Ogawa, N., Katagi, M., Fujino, K., Kumagai, A., Kawai, H., Asakawa, A., et al. (2013) · Nature Communications · doi:10.1038/ncomms2536 · Cited by 41
Trigeminal Mechanisms of Nociception: Peripheral and Brainstem Organization
Bereiter, D. A., Hargreaves, K. M., & Hu, J. W. (2008) · Elsevier eBooks · doi:10.1016/b978-012370880-9.00174-2 · Cited by 42
Neurotrophins in the dentate gyrus
Binder, D. K. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63022-2 · Cited by 43
Kramer, B. M. R., Cruijsen, P. M. J. M., Ouwens, D. T. W. M., Coolen, M. W., Martens, G. J. M., Roubos, E. W., & Jenks, B. G. (2002) · Endocrinology · doi:10.1210/en.143.4.1337 · Cited by 41
Revisiting the expression of BDNF and its receptors in mammalian development
Esvald, E., Tuvikene, J., Kiir, C. S., Avarlaid, A., Tamberg, L., Sirp, A., Shubina, A., Cabrera-Cabrera, F., Pihlak, A., Koppel, I., et al. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1182499 · Cited by 43
Hatami, H., Oryan, S., Semnanian, S., Kazemi, B., Bandepour, M., & Ahmadiani, A. (2007) · Neuropeptides · doi:10.1016/j.npep.2007.04.007 · Cited by 40
Dosage Effects of BDNF Val66Met Polymorphism on Cortical Surface Area and Functional Connectivity
Wang, C., Zhang, Y., Liu, B., Long, H., Yu, C., & Jiang, T. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3501-13.2014 · Cited by 43
Daftary, S. S., Calderon, G., & Rios, M. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.025 · Cited by 43
Will, T. J., Tushev, G., Kochen, L., Nassim-Assir, B., Cajigas, I. J., Dieck, S. T., & Schuman, E. M. (2013) · Science Signaling · doi:10.1126/scisignal.2004520 · Cited by 44
Allaman, I., Papp, M., Kraftsik, R., Fiumelli, H., Magistretti, P. J., & Martin, J. (2008) · PubMed · Cited by 40
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Guillin, O., Griffon, N., Díaz, J., Foll, B. L., Bézard, E., Gross, C. E., Lammers, C., Stark, H., Carroll, P., & Schwartz, J.-C. (2004) · International review of neurobiology · doi:10.1016/s0074-7742(04)59016-5 · Cited by 42
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Weible, M. W., & Hendry, I. A. (2003) · Journal of Neurobiology · doi:10.1002/neu.10318 · Cited by 40
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Rohe, M., Hartl, D., Fjorback, A. N., Klose, J., & Willnow, T. E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072164 · Cited by 42
Ortiz, J. B., Mathewson, C. M., Hoffman, A. N., Hanavan, P. D., Terwilliger, E. F., & Conrad, C. D. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12703 · Cited by 40
Wiciński, M., Malinowski, B., Węclewicz, M. M., Grześk, E., & Grześk, G. (2017) · BioMed Research International · doi:10.1155/2017/9202954 · Cited by 40
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Miller, K. M., Patterson, J. R., Kochmanski, J. J., Kemp, C. J., Stoll, A. C., Onyekpe, C. U., Cole-Strauss, A., Steece‐Collier, K., Howe, J. W., Luk, K. C., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1952-20.2020 · Cited by 37
Tebano, M. T., Martire, A., Chiodi, V., Ferrante, A., & Popoli, P. (2010) · The Scientific World JOURNAL · doi:10.1100/tsw.2010.164 · Cited by 39
Eagleson, K. L., Fairfull, L. D., Salton, S. R., & Levitt, P. R. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-23-09315.2001 · Cited by 39
Behrendt, T., Kirschnick, F., Kröger, L., Beileke, P., Rezepin, M., Brigadski, T., Leßmann, V., & Schega, L. (2021) · BMC Neuroscience · doi:10.1186/s12868-021-00675-8 · Cited by 48
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Venney, C. J., Johansson, M. L., & Heath, D. D. (2016) · Molecular Ecology · doi:10.1111/mec.13777 · Cited by 41
Do estrogens enhance activation of brown and beiging of adipose tissues?
Frank, A. P., Palmer, B. F., & Clegg, D. J. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.09.026 · Cited by 37
Primary Afferent-Derived BDNF Contributes Minimally to the Processing of Pain and Itch
Dembo, T., Braz, J. M., Hamel, K. A., Kuhn, J., & Basbaum, A. I. (2018) · eNeuro · doi:10.1523/eneuro.0402-18.2018 · Cited by 38
Hu, Y., Liu, P., Guo, D., Rahman, K., Wang, D., & Xie, T. (2010) · Pharmaceutical Biology · doi:10.3109/13880200903280034 · Cited by 38
Glutamatergic axon-derived BDNF controls GABAergic synaptic differentiation in the cerebellum
Chen, A. I., Zang, K., Masliah, E., & Reichardt, L. F. (2016) · Scientific Reports · doi:10.1038/srep20201 · Cited by 37
Hughes, P. E., Young, D., Preston, K. M., Yan, Q., & Dragunow, M. (1998) · Molecular Brain Research · doi:10.1016/s0169-328x(97)00288-x · Cited by 38
Self-citationPoulsen, F. R., Jahnsen, H., Blaabjerg, M., & Zimmer, J. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03009-3 · Cited by 38
Zaman, V., & Shetty, A. K. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00478-x · Cited by 38
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Song, M.-S., Learman, C. R., Ahn, K.-C., Baker, G. B., Kippe, J., Field, E. M., & Dunbar, G. L. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.08.011 · Cited by 33
Serra, M. P., Poddighe, L., Boi, M., Sanna, F., Piludu, M. A., Sanna, F., Corda, M. G., Giorgi, O., & Quartu, M. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19123745 · Cited by 40
Li, Y., Yu, H., Chen, C., Li, S., Zhang, Z., Xu, H., Zhu, F., Liu, J., Spencer, P. S., Dai, Z., et al. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/5408452 · Cited by 37
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Campbell, T. S., Donoghue, K. M., Ghosh, U., Nelson, C. M., & Roth, T. L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911729 · Cited by 39
Rearrangement of Retinogeniculate Projection Patterns after Eye-Specific Segregation in Mice
Hayakawa, I., & Kawasaki, H. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011001 · Cited by 37
Chigr, F., Rachidi, F., Segura, S., Mahaut, S., Tardivel, C., Jean, A., Najimi, M., & Moyse, E. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.10.040 · Cited by 37
Suzuki, R., Lumeng, L., McBride, W. J., Li, T., & Hwang, B. H. (2004) · Brain Research · doi:10.1016/j.brainres.2004.04.037 · Cited by 36
Gatt, J. M., Clark, C. R., Kemp, A. H., Liddell, B. J., Dobson‐Stone, C., Kuan, S. A., Schofield, P. R., & Williams, L. M. (2007) · Journal of Integrative Neuroscience · doi:10.1142/s0219635207001398 · Cited by 37
Pal, A., Severin, F. F., Höpfner, S., & Zerial, M. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(07)38017-8 · Cited by 37
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Tao, W., Chen, Q., Zhou, W., Wang, Y., Wang, L., & Zhang, Z. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.580381 · Cited by 37
Yin, J.-B., Wu, H., Dong, Y., Zhang, T., Wang, J., Zhang, Y., Wei, Y., Lu, Y.-C., Wu, S., Wang, W., et al. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00137 · Cited by 38
Quinn, C. R., Dobson‐Stone, C., Outhred, T., Harris, A. W. F., & Kemp, A. H. (2012) · Australian & New Zealand Journal of Psychiatry · doi:10.1177/0004867411430878 · Cited by 36
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Ehlers, M. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130081 · Cited by 37
Avwenagha, O., Bird, M. M., Lieberman, A. R., Yan, Q., & Campbell, G. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.02.056 · Cited by 35
Self-citationCardiorespiratory Fitness Is Associated with Better Executive Function in Young Women
Scott, S., Souza, M. J. D., Koehler, K., Petkus, D. L., & Murray‐Kolb, L. E. (2016) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000974 · Cited by 36
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Zhou, J., Cao, X., Mar, A. C., Ding, Y.-Q., Wang, X., Li, Q., & Li, L. (2014) · Psychopharmacology · doi:10.1007/s00213-013-3350-z · Cited by 36
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Wang, Y., Diao, Z., Li, J., Ren, B., Zhu, D., Liu, Q., Liu, Z., & Liu, X. (2017) · RSC Advances · doi:10.1039/c7ra06325c · Cited by 35
Cardillo, G. D. M., de Paula, V. D. J. R., Ikenaga, E. H., Costa, L. R., Catanozi, S., Schaeffer, E. L., Gattaz, W. F., Kerr, D. S., & Forlenza, O. V. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-170838 · Cited by 35
Neurotrophin signalling in amygdala-dependent cued fear learning
Meis, S., Endres, T., & Leßmann, V. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03260-3 · Cited by 40
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Distinct types of nitric oxide–producing neurons in the developing and adult mouse claustrum
Guirado, S., Real, M. A., Olmos, J. L., & Dávila, J. C. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10835 · Cited by 35
Biogenic amine changes in brain regions and attenuating action of Ocimum sanctumin noise exposure
Jamesdaniel, S., Devi, R. S., Ravindran, R., & Senthilvelan, M. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2005.12.008 · Cited by 35
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Potenza, R. L., Tebano, M. T., Martire, A., Domenici, M. R., Pepponi, R., Armida, M., Pèzzola, A., Minghetti, L., & Popoli, P. (2007) · Purinergic Signalling · doi:10.1007/s11302-007-9066-y · Cited by 34
Epileptogenesis in the Parahippocampal Region: Parallels with the Dentate Gyrus
Scharfman, H. E. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06734.x · Cited by 35
Danzer, S. C., Pan, E., Nef, S., Parada, L. F., & McNamara, J. O. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.03.025 · Cited by 35
Reelin mRNA expression during embryonic brain development in the turtleEmys orbicularis
Bernier, B., Bar, I., Pieau, C., de Rouvroit, C. L., & Goffinet, A. M. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991025)413:3 · Cited by 62
von Bartheld, C. S., & Johnson, J. E. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1159 · Cited by 35
Mousa, H. H., Sharawy, M. H., & Nader, M. A. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.121258 · Cited by 35
Shein, N. A., Grigoriadis, N., Horowitz, M., Umschwief, G., Alexandrovich, A. G., Simeonidou, C., Grigoriadis, S., Touloumi, O., & Shohami, E. (2008) · Brain Research · doi:10.1016/j.brainres.2008.09.032 · Cited by 34
Adachi, N., Numakawa, T., Kumamaru, E., Itami, C., Chiba, S., Iijima, Y., Richards, M., Katoh‐Semba, R., & Kunugi, H. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs074 · Cited by 34
Differences in the Biological Functions of BDNF and proBDNF in the Central Nervous System
Borodinova, A. A., & Salozhin, S. V. (2017) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-017-0391-5 · Cited by 37
Factors that regulate KiSS1 gene expression in the hippocampus
Arai, A., & Orwig, N. (2008) · Brain Research · doi:10.1016/j.brainres.2008.09.031 · Cited by 35
Sushil Kumar, K., Parkash, J., Kataria, H., & Kaur, G. (2009) · Neuroscience Research · doi:10.1016/j.neures.2009.08.015 · Cited by 34
Remote limb ischemic conditioning enhances motor learning in healthy humans
Cherry‐Allen, K. M., Gidday, J. M., Lee, J., Hershey, T. G., & Lang, C. E. (2015) · Journal of Neurophysiology · doi:10.1152/jn.01028.2014 · Cited by 34
Chapter 3 BDNF/trkB signaling in the developmental sculpting of visual connections
Frost, D. O. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)34004-9 · Cited by 34
Walker, S. M., Mitchell, V. A., White, D. M., Rush, R. A., & Duggan, A. W. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02259-4 · Cited by 34
Dieni, S., & Rees, S. M. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10422 · Cited by 34
Expression of Trk receptors in the oculomotor system of the adult cat
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Karchewski, L. A., Kim, F. A., Johnston, J. M., McKnight, R. M., & Verge, V. M. K. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991018)413:2 · Cited by 81
Hemmerle, A. M., Ahlbrand, R., Bronson, S. L., Lundgren, K. H., Richtand, N. M., & Seroogy, K. B. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.07.006 · Cited by 33
Lmx1a enhances the effect of iNSCs in a PD model
Wu, J., Sheng, C., Liu, Z., Jia, W., Wang, B., Li, M., Fu, L., Ren, Z., An, J., Sang, L., et al. (2014) · Stem Cell Research · doi:10.1016/j.scr.2014.10.004 · Cited by 33
Berghauzen-Maciejewska, K., Wardas, J., Kosmowska, B., Głowacka, U., Kuter, K. Z., & Ossowska, K. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117698 · Cited by 34
Lee, I., Wang, J., Fu, C., Lin, S., & Sheu, W. H. (2016) · Medicine · doi:10.1097/md.0000000000005260 · Cited by 33
Ferrini, F., Salio, C., Boggio, E. M., & Merighi, A. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666201116143422 · Cited by 34
Candidate genes for panic disorder: insight from human and mouse genetic studies
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Torres-Reverón, A., Khalid, S., Williams, T. J., Waters, E. M., Drake, C. T., McEwen, B. S., & Milner, T. A. (2008) · Brain Research · doi:10.1016/j.brainres.2008.07.058 · Cited by 33
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Bariohay, B., Tardivel, C., Pio, J., Jean, A., & Félix, B. (2008) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.90407.2008 · Cited by 33
Piermartiri, T., Pan, H., Figueiredo, T. H., & Marini, A. M. (2015) · Molecules · doi:10.3390/molecules201119698 · Cited by 33
Obstructive sleep apnea and its controversial effects on cognition
Devita, M., Montemurro, S., Ramponi, S., Marvisi, M., Villani, D., Raimondi, M. C., Rusconi, M. L., & Mondini, S. (2016) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803395.2016.1253668 · Cited by 33
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Frost, D. O., Ma, Y., Hsieh, T., Forbes, M. E., & Johnson, J. E. (2001) · Journal of Neurobiology · doi:10.1002/neu.1073 · Cited by 33
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Kondziolka, D. S., Wechsler, L. R., & Achim, C. L. (2002) · Journal of Clinical Neuroscience · doi:10.1054/jocn.2001.1043 · Cited by 33
Serra, M. P., Poddighe, L., Boi, M., Sanna, F., Piludu, M. A., Corda, M. G., Giorgi, O., & Quartu, M. (2017) · Brain and Behavior · doi:10.1002/brb3.861 · Cited by 32
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Gangarossa, G., Siaume‐Perez, S., Dembitskaya, Y., Prokin, I., Berry, H., & Venance, L. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz081 · Cited by 33
Hormonal Regulation of Mammalian Adult Neurogenesis: A Multifaceted Mechanism
Jorgensen, C., & Wang, Z. (2020) · Biomolecules · doi:10.3390/biom10081151 · Cited by 36
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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 38
Sugiyama, N., Kanba, S., & Arita, J. (2003) · Molecular Brain Research · doi:10.1016/s0169-328x(03)00184-0 · Cited by 32
Peiris, T. S., Machaalani, R., & Waters, K. A. (2004) · Brain Research · doi:10.1016/j.brainres.2004.09.024 · Cited by 32
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Metadata
- Authors
- Conner, J. M., Lauterborn, J. C., Yan, Q., Gall, C. M., & Varon, S.
- Affiliations
- University of California San Diego (US)
- University of California, Irvine (US)
- Amgen (United States) (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1997-04-01
- Volume
- 17
- Issue
- 7
- Pages
- 2295-2313
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6573520
- OpenAlex
- W2117830068
- Cited by
- 1,097
- References
- 57
- Citations by year
- 2026: 10 · 2025: 12 · 2024: 25 · 2023: 23 · 2022: 41 · 2021: 38 · 2020: 32 · 2019: 39 · 2018: 40 · 2017: 42 · 2016: 49 · 2015: 58 · 2014: 44 · 2013: 52 · 2012: 48
- FWCI
- 13.92
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01ns016349-16, 5k02mh000974-03, 5r01ns026748-10)
- National Institute of Mental Health (MH00974)
- National Institute of Neurological Disorders and Stroke (NS-26748, NS 16349)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- brain-derived neurotrophic factor, anterograde axonal transport, BDNF mRNA, central nervous system, afferent systems, medial habenula, central amygdala, bed nucleus of the stria terminalis, lateral septum, spinal cord
- MeSH terms
- Animals, Axonal Transport, Brain, Female, Immunohistochemistry, Male, Nerve Fibers, Neurons, Organ Specificity, Reference Values, RNA, Messenger, Spinal Cord, Rats, Sprague-Dawley, In Situ Hybridization, DNA, Complementary, Brain-Derived Neurotrophic Factor, Rats
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