The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats
Abstract
In the autoradiograms of young rats injected with thymidine‐H 3 many of the granule cells of the dentate gyrus were found labeled. The number of labeled cells declined rapidly with increased age at the time of injection. Histological studies showed the presence in young rats of a large germinal matrix of mitotic cells in the ependymal and subependymal layers of the third and lateral ventricles. The areal extent and cell population of this germinal pool declined rapidly from birth on, with a transient rise with a peak at about 15 days. During this latter period the number of “undifferentiated” cells near the granular layer of the dentate gyrus showed a rapid rise with a subsequent decline. The decline in the number of “undifferentiated” cells was accompanied by a rise in the number of differentiated granule cells. Cell counts in homologous parts of the dentate gyrus indicated a six‐fold increase in the number of differentiated granule cells from birth to three months. We postulated that undifferentiated cells migrate postnatally from the forebrain ventricles to the hippocampus where they become differentiated. The possible functional significance of delayed hippocampal neurogenesis is discussed with reference to our finding of incorporation of testosterone‐H 3 by cells of the hippocampus, implicating that they may function as receptors of gonadal hormones.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The dentate gyrus of the hippocampus is the brain region where the most active neurogenesis has been documented to take place23–25.”
From Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB (2021) · cites this paper as [23]
In the citing paper
“since adult neurogenesis within the DG is well-established in rodents (Altman & Das 1965).”
From Perineuronal net deglycosylation associates with tauopathy‐induced gliosis and neurodegeneration (2024) · cites this paper as Altman & Das 1965
Citations
Cites
Are New Neurons Formed in the Brains of Adult Mammals?
Altman, J. (1962) · Science · doi:10.1126/science.135.3509.1127 · Cited by 975
Self-citationThe Kinetics of Cellular Proliferation
(1960) · The Medical Journal of Australia · doi:10.5694/j.1326-5377.1960.tb68825.x · Cited by 938
IMPROVEMENTS IN THE COATING TECHNIQUE OF RADIOAUTOGRAPHY
Kopriwa, B. M., & Leblond, C. P. (1962) · Journal of Histochemistry & Cytochemistry · doi:10.1177/10.3.269 · Cited by 934
Taylor, J. H., Woods, P. S., & Hughes, W. L. (1957) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.43.1.122 · Cited by 832
Autoradiographic investigation of cell proliferation in the brains of rats and cats
Altman, J. (1963) · The Anatomical Record · doi:10.1002/ar.1091450409 · Cited by 623
Self-citationSmart, I. H. M. (1961) · The Journal of Comparative Neurology · doi:10.1002/cne.901160306 · Cited by 449
Bailey, P. (1925) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1925.02200140055002 · Cited by 399
CELLULAR PROLIFERATION IN THE MOUSE AS REVEALED BY AUTORADIOGRAPHY WITH TRITIATED THYMIDINE
Hughes, W. L., Bond, V. P., Brecher, G., Cronkite, E. P., Painter, R. B., Quastler, H., & Sherman, F. G. (1958) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.44.5.476 · Cited by 357
CEREBRAL REPRESENTATION OF PENILE ERECTION
MacLean, P. D., & Ploog, D. W. (1962) · Journal of Neurophysiology · doi:10.1152/jn.1962.25.1.29 · Cited by 258
Thymidine-H3 as a tool for the investigation of the renewal of cell populations.
Cp, L., Messier, B., & Kopriwa, B. M. (1959) · PubMed · Cited by 213
Research works printed but not linked: 2
- Allen E., 1912, The cessation of mitosis in the central nervous system of the albino rat, J. Comp. Neur., 22, 547
- Kjellgren K., 1944, Studien über die Entwicklung der Neuronen nach der Geburt, ihre Regeneration und die Asymmetrien ihrer Verteilung beim Menschen, Acta Psychiat. Neurol. Scand., Suppl., 29, 1
Cited by
Sorted by citations
Items 501–600 of 1,014
Kaneko, N., Kudo, K., Mabuchi, T., Takemoto, K., Fujimaki, K., Wati, H., Iguchi, H., Tezuka, H., & Kanba, S. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301137 · Cited by 152
Proneural gene-linked neurogenesis in zebrafish cerebellum
Kani, S., Bae, Y., Shimizu, T., Tanabe, K., Satou, C., Parsons, M. J., Scott, E. K., Higashijima, S., & Hibi, M. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.03.024 · Cited by 151
Adult stem cell therapy in stroke
Haas, S., Weidner, N., & Winkler, J. (2005) · Current Opinion in Neurology · doi:10.1097/00019052-200502000-00012 · Cited by 153
Nerve growth factor promotes survival of new neurons in the adult hippocampus
Frielingsdorf, H., Simpson, D. R., Thal, L. J., & Pizzo, D. P. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2006.11.015 · Cited by 151
BDNF control of adult SVZ neurogenesis
Bath, K. G., Akins, M. R., & Lee, F. S. (2012) · Developmental Psychobiology · doi:10.1002/dev.20546 · Cited by 146
Human Wild-Type α-Synuclein Impairs Neurogenesis
Winner, B., Lie, D. C., Rockenstein, E. M., Aigner, R., Aigner, L., Masliah, E., Kuhn, H. G., & Winkler, J. (2004) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/63.11.1155 · Cited by 156
Kralic, J. E., Ledergerber, D., & Fritschy, J. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04386.x · Cited by 157
Yamaguchi, Y. (2001) · Seminars in Cell and Developmental Biology · doi:10.1006/scdb.2000.0238 · Cited by 151
DNA Metabolism and Cell Proliferation
Altman, J. (1969) · Springer eBooks · doi:10.1007/978-1-4899-7321-4_8 · Cited by 151
Self-citationRunning rewires the neuronal network of adult-born dentate granule cells
Vivar, C., Peterson, B. D., & van Praag, H. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.031 · Cited by 143
Functional circuits of new neurons in the dentate gyrus
Vivar, C., & van Praag, H. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00015 · Cited by 153
Functions of adult-born neurons in hippocampal memory interference and indexing
Miller, S. M., & Sahay, A. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0484-2 · Cited by 153
Neurotrophins Role in Depression Neurobiology: A Review of Basic and Clinical Evidence
Neto, F. L. M., Borges, G., Torres-Sánchez, S., Micó, J. A., & Berrocoso, E. (2011) · Current Neuropharmacology · doi:10.2174/157015911798376262 · Cited by 155
Behavioural trait of reactivity to novelty is related to hippocampal neurogenesis
Lemaire, V., Aurousseau, C., Moal, M. L., & Abrous, D. N. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00833.x · Cited by 150
Sallaz, M., Schachner, M., & Montag, D. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.22.7967-7981.2002 · Cited by 152
Thymidine analogues for tracking DNA synthesis.
Cavanagh, B. L., Walker, T., Norazit, A., & Meedeniya, A. C. B. (2011) · Molecules · doi:10.3390/molecules16097980 · Cited by 143
Ferulic acid induces neural progenitor cell proliferation in vitro and in vivo
Yabe, T., Hirahara, H., Harada, N., Ito, N., Nagai, T., Sanagi, T., & Yamada, H. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.10.023 · Cited by 148
Born this way: Hippocampal neurogenesis across the lifespan
Kozareva, D. A., Cryan, J. F., & Nolan, Y. M. (2019) · Aging Cell · doi:10.1111/acel.13007 · Cited by 155
Challenges for Brain Repair: Insights from Adult Neurogenesis in Birds and Mammals
Doetsch, F. K., & Scharff, C. (2001) · Brain Behavior and Evolution · doi:10.1159/000057572 · Cited by 147
Adult brain neurogenesis and depression
Jacobs, B. L. (2002) · Brain, Behavior, and Immunity · doi:10.1016/s0889-1591(02)00015-6 · Cited by 147
Dawirs, R. R., Hildebrandt, K., & Teuchert, G. (1998) · Journal of Neural Transmission · doi:10.1007/s007020050061 · Cited by 148
Christie, K. J., & Turnley, A. M. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00070 · Cited by 152
Genetic Approaches to Neurotrauma Research: Opportunities and Potential Pitfalls of Murine Models
Steward, O., Schauwecker, P. E., Guth, L., Zhang, Z., Fujiki, M., Inman, D. M., Wrathall, J. R., Kempermann, G., Gage, F. H., Saatman, K. E., et al. (1999) · Experimental Neurology · doi:10.1006/exnr.1999.7040 · Cited by 149
Involvement of Sphingosine-1-Phosphate in Glutamate Secretion in Hippocampal Neurons
Kajimoto, T., Okada, T., Yu, H., Goparaju, S. K., Jahangeer, S. M., & Nakamura, S. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01465-06 · Cited by 148
Kumar, D., Koyanagi, I., Carrier‐Ruiz, A., Vergara, P., Srinivasan, S., Sugaya, Y., Kasuya, M., Yu, T., Vogt, K. E., Muratani, M., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.05.008 · Cited by 151
Learning and adult neurogenesis: Survival with or without proliferation?
Prickaerts, J. (2003) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2003.09.001 · Cited by 149
Multipotential stem cells and progenitors in the vertebrate retina
Reh, T. A., & Levine, E. M. (1998) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199808)36:2 · Cited by 231
Scobie, K. N., Hall, B. J., Wilke, S. A., Klemenhagen, K. C., Fujii‐Kuriyama, Y., Ghosh, A., Hen, R., & Sahay, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2260-09.2009 · Cited by 151
Elliott, R. C., Miles, M. F., & Lowenstein, D. H. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-06-02218.2003 · Cited by 143
Tsai, H. M., Garber, B. B., & Larramendi, L. M. H. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901980207 · Cited by 148
The role of seizure-induced neurogenesis in epileptogenesis and brain repair
Parent, J. M. (2002) · Epilepsy Research · doi:10.1016/s0920-1211(02)00078-5 · Cited by 142
Bartlett, W. P., Li, X.-S., Williams, M., & Benkovic, S. J. (1991) · Developmental Biology · doi:10.1016/s0012-1606(05)80021-1 · Cited by 143
Nakamura, E., Kadomatsu, K., Yuasa, S., Muramatsu, H., Mamiya, T., NABESHIMA, T., Fan, Q., Ishiguro, K., Igakura, T., Matsubara, S., et al. (1998) · Genes to Cells · doi:10.1046/j.1365-2443.1998.00231.x · Cited by 144
Gritti, A., Cova, L., Parati, E. A., Galli, R., & Vescovi, A. L. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)11247-t · Cited by 140
Hippocampal neurogenesis is reduced by sleep fragmentation in the adult rat
Guzmán-Marı́n, R., Bashir, T., Suntsova, N., Szymusiak, R. S., & McGinty, D. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.05.030 · Cited by 142
Control of adult neurogenesis by programmed cell death in the mammalian brain
Ryu, J. R., Hong, C. J., Kim, J. Y., Kim, E. K., Sun, W., & Yu, S.-W. (2016) · Molecular Brain · doi:10.1186/s13041-016-0224-4 · Cited by 148
Thyroid Hormones Affect Neurogenesis in the Dentate Gyrus of Adult Rat
Ambrogini, P., Cuppini, R., Ferri, P., Mancini, C., Ciaroni, S., Voci, A., Gerdoni, E., & Gallo, G. (2005) · Neuroendocrinology · doi:10.1159/000087648 · Cited by 143
Adult hippocampal neurogenesis and aging
Klempin, F., & Kempermann, G. (2007) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-007-0731-5 · Cited by 152
Barnea, A., & Nottebohm, F. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.2.714 · Cited by 141
Store-Operated CRAC Channels Regulate Gene Expression and Proliferation in Neural Progenitor Cells
Somasundaram, A., Shum, A. K., McBride, H. J., Kessler, J. A., Feske, S., Miller, R. J., & Prakriya, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0263-14.2014 · Cited by 143
Heterogeneity and Fgf dependence of adult neural progenitors in the zebrafish telencephalon
Ganz, J., Kaslin, J., Hochmann, S., Freudenreich, D., & Brand, M. (2010) · Glia · doi:10.1002/glia.21012 · Cited by 137
Morales-Garcia, J. A., Calleja-Conde, J., Lopez-Moreno, J. A., Alonso-Gil, S., Sanz-SanCristobal, M., Riba, J., & Perez-Castillo, A. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-01011-0 · Cited by 138
Neurogenesis, cell death and regeneration in the adult gymnotiform brain
Zupanc, G. K. H. (1999) · Journal of Experimental Biology · doi:10.1242/jeb.202.10.1435 · Cited by 138
Nadler, J. V., Cotman, C. W., & LYNCH, G. S. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901710409 · Cited by 138
Estrogen Enhances Neurogenesis and Behavioral Recovery after Stroke
Li, J., Siegel, M., Yuan, M., Zeng, Z., Finnucan, L., Persky, R., Hurn, P. D., & McCullough, L. D. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.181 · Cited by 138
The Potential of Stem Cells in Treatment of Traumatic Brain Injury
Weston, N. M., & Sun, D. (2018) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-018-0812-z · Cited by 139
Sorrells, S. F., Paredes, M. F., Zhang, Z., Kang, G., Pastor-Alonso, O., Biagiotti, S. W., Page, C. E., Sandoval, K., Knox, A., Connolly, A. J., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0676-20.2020 · Cited by 140
Saha, B., Péron, S., Murray, K., Jaber, M., & Gaillard, A. (2013) · Stem Cell Research · doi:10.1016/j.scr.2013.06.006 · Cited by 136
Neuronal progenitors as tools for cell replacement in the nervous system
Brüstle, O., & McKay, R. D. G. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80104-8 · Cited by 134
α-Aminoadipate Induces Progenitor Cell Properties of Müller Glia in Adult Mice
Takeda, M., Takamiya, A., Jiao, J., Cho, K., Trevino, S. G., Matsuda, T., & Chen, D. F. (2008) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.07-0434 · Cited by 139
The Wnt /β-catenin signaling pathway in the adult neurogenesis
Zhang, L., Yang, X., Yang, S., & Zhang, J. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.7483.x · Cited by 138
Barnea, A., & Витальевич, П. В. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07851.x · Cited by 137
Sun, D., Colello, R. J., Daugherty, W. P., Kwon, T. H., McGinn, M. J., Harvey, H. B., & Bullock, M. R. (2005) · Journal of Neurotrauma · doi:10.1089/neu.2005.22.95 · Cited by 137
Kitamura, T., Mishina, M., & Sugiyama, H. (2003) · Neuroscience Research · doi:10.1016/s0168-0102(03)00171-8 · Cited by 137
Strategies utilized by migrating neurons of the postnatal vertebrate forebrain
Goldman, S. A., & Luskin, M. B. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01191-0 · Cited by 134
A Role for Calcineurin in Alzheimers Disease
Reese, L. C., & Taglialatela, G. (2011) · Current Neuropharmacology · doi:10.2174/157015911798376316 · Cited by 132
Heterogeneity of Radial Glia-Like Cells in the Adult Hippocampus
Gebara, E., Bonaguidi, M. A., Beckervordersandforth, R., Sultan, S., Udry, F., Gijs, P.-J., Lie, D. C., Ming, G., Song, H., & Toni, N. (2016) · Stem Cells · doi:10.1002/stem.2266 · Cited by 139
Dendritic growth and regression in rat dentate granule cells during late postnatal development
Rihn, L. L., & Claiborne, B. J. (1990) · Developmental Brain Research · doi:10.1016/0165-3806(90)90071-6 · Cited by 133
The development of the mesencephalic nucleus of the trigeminal nerve in the chick
Rogers, L. A., & Cowan, W. M. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901470302 · Cited by 133
Pan, Y.-W., Chan, G. C. ‐., Kuo, C. T., Storm, D. R., & Xia, Z. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6076-11.2012 · Cited by 139
Blockade of Gap Junctions In Vivo Provides Neuroprotection After Perinatal Global Ischemia
Pina-Benabou, M. H. D., Szostak, V., Kyrozis, A., Rempe, D. A., Uziel, D., Urban-Maldonado, M. M., Benabou, S., Spray, D. C., Federoff, H. J., Stanton, P. K., et al. (2005) · Stroke · doi:10.1161/01.str.0000182239.75969.d8 · Cited by 132
Chapter 26 Role of Akt and Erk Signaling in the Neurogenesis Following Brain Ischemia
Shioda, N., Han, F., & Fukunaga, K. (2009) · International review of neurobiology · doi:10.1016/s0074-7742(09)85026-5 · Cited by 132
Developmental changes in expression of the three ryanodine receptor mRNAs in the mouse brain
Mori, F., Fukaya, M., Abe, H., Wakabayashi, K., & Watanabe, M. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01046-6 · Cited by 132
Stress and Traumatic Brain Injury: A Behavioral, Proteomics, and Histological Study
Kwon, S.-K. C., Kövesdi, E., Gyorgy, A. B., Wingo, D., Kamnaksh, A., Walker, J., Long, J. B., & Agoston, D. V. (2011) · Frontiers in Neurology · doi:10.3389/fneur.2011.00012 · Cited by 134
Neylan, T. C., Mueller, S. G., Wang, Z., Metzler, T. J., Lenoci, M., Truran, D., Marmar, C. R., Weiner, M. W., & Schuff, N. W. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.04.035 · Cited by 131
Gold, P. W., Licinio, J., & Pavlatou, M. G. (2012) · Molecular Psychiatry · doi:10.1038/mp.2012.167 · Cited by 132
Seri, B., Herrera, D. G., Gritti, A., Ferrón, S. R., Collado, L., Vescovi, A. L., García‐Verdugo, J. M., & Álvarez-Buylla, A. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhk027 · Cited by 133
Defining the NG2-expressing cell of the adult CNS
Horner, P. J., Thallmair, M., & Gage, F. H. (2002) · Journal of Neurocytology · doi:10.1023/a:1025739630398 · Cited by 133
Connection matrix of the hippocampal formation: I. The dentate gyrus
Patton, P. E., & McNaughton, B. L. (1995) · Hippocampus · doi:10.1002/hipo.450050402 · Cited by 130
Glutamate as a Modulator of Embryonic and Adult Neurogenesis
Schlett, K. (2006) · Current Topics in Medicinal Chemistry · doi:10.2174/156802606777323665 · Cited by 131
Delayed postnatal neurogenesis in the cerebral cortex of lizards
López‐García, C., Molowny, A., García‐Verdugo, J. M., & Ferrer, I. (1988) · Developmental Brain Research · doi:10.1016/0165-3806(88)90096-x · Cited by 131
Adrenalectomy increases neurogenesis but not PSA‐NCAM expression in aged dentate gyrus
Montaron, M., Petry, K. G., Rodriguez, J. J., Marinelli, M., Aurousseau, C., Rougon, G., Moal, M. L., & Abrous, D. N. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00579.x · Cited by 131
The role of cannabinoids in adult neurogenesis
Prenderville, J. A., Kelly, A. M., & Downer, E. J. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13186 · Cited by 136
Hinsch, K., & Zupanc, G. K. H. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.01.071 · Cited by 130
PSA‐NCAM: an important regulator of hippocampal plasticity
Cremer, H., Chazal, G., Lledo, P., Rougon, G., Montaron, M., Mayo, W., Moal, M. L., & Abrous, D. N. (2000) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(99)00090-8 · Cited by 131
Redefining neuroendocrinology: Epigenetics of brain-body communication over the life course
McEwen, B. S. (2018) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2017.11.001 · Cited by 129
Neural stem cell therapy—Brief review
Grochowski, C., Radzikowska, E., & Maciejewski, R. (2018) · Clinical Neurology and Neurosurgery · doi:10.1016/j.clineuro.2018.07.013 · Cited by 134
Adrenal steroid receptor immunoreactivity in cells born in the adult rat dentate gyrus
Cameron, H. A., Woolley, C. S., & Gould, E. (1993) · Brain Research · doi:10.1016/0006-8993(93)90524-q · Cited by 129
Abolition of aberrant neurogenesis ameliorates cognitive impairment after stroke in mice
Cuartero, M. I., de la Parra, J., Pérez-Ruiz, A., Bravo-Ferrer, I., Durán-Laforet, V., García-Culebras, A., García-Segura, J. M., Dhaliwal, J., Frankland, P. W., Lizasoain, I., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci120412 · Cited by 128
Saaltink, D.-J., & Vreugdenhil, E. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1568-5 · Cited by 127
Naylor, A. S., Persson, A. I., Eriksson, P. S., Jonsdottir, I. H., & Thorlin, T. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01085.2004 · Cited by 127
Jabès, A., Lavenex, P. B., Amaral, D. G., & Lavenex, P. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07061.x · Cited by 127
Adult Stem Cells for Regenerative Therapy
Gurusamy, N., Alsayari, A., Rajasingh, S., & Rajasingh, J. (2018) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2018.07.009 · Cited by 133
Unfolding the Role of BDNF as a Biomarker for Treatment of Depression
Rana, T., Behl, T., Sehgal, A., Srivastava, P., & BUNGAU, S. G. (2020) · Journal of Molecular Neuroscience · doi:10.1007/s12031-020-01754-x · Cited by 136
The Role of Astrocytes in the Neurorepair Process
Chiareli, R. A., Carvalho, G. A., Marques, B. L., Mota, L. S., Oliveira‐Lima, O. C., Gomes, R. M., Birbrair, A., Gomez, R. S., Simão, F., Klempin, F., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.665795 · Cited by 130
Steiner, B., Winter, C., Hosman, K., Siebert, E., Kempermann, G., Petrus, D. S., & Kupsch, A. R. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2005.11.004 · Cited by 127
Molecular Endocrinology and Physiology of the Aging Central Nervous System
Smith, R. G., Betancourt, L., & Sun, Y. (2005) · Endocrine Reviews · doi:10.1210/er.2002-0017 · Cited by 129
Diamond, A. D. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb48904.x · Cited by 131
Zheng, L., Kaneko, N., & Sawamoto, K. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00005 · Cited by 127
Zhao, C., Avilés, C., Abel, R., Almli, C. R., McQuillen, P. S., & Pleasure, S. J. (2005) · Development · doi:10.1242/dev.01871 · Cited by 126
Shen, L., Nam, H.-S., Song, P., Moore, H. M., & Anderson, S. A. (2006) · Hippocampus · doi:10.1002/hipo.20218 · Cited by 125
Spontaneous alternation behavior in animals: A review
Richman, C. L., Dember, W. N., & Kim, P. (1986) · Current Psychology · doi:10.1007/bf02686603 · Cited by 129
Development of microglia in the postnatal rat hippocampus
Dalmau, I., Finsen, B. R., Zimmer, J., Gonz�lez, B., & Castellano, B. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1998)8:5 · Cited by 130
Remodeling of neuronal networks by stress
Fuchs, E. (2006) · Frontiers in bioscience · doi:10.2741/2004 · Cited by 128
Clark, R. G., & Milhorat, T. H. (1970) · Journal of neurosurgery · doi:10.3171/jns.1970.32.4.0400 · Cited by 126
CHEN, Y., AI, Y., SLEVIN, J., MALEY, B., & GASH, D. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.07.010 · Cited by 126
Phillips, W., Morton, A. J., & Barker, R. A. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3796-05.2005 · Cited by 129
Bédard, A., Lévesque, M., Bernier, P. J., & Parent, A. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02263.x · Cited by 127
Neuroprotective effects of theanine and its preventive effects on cognitive dysfunction
Kakuda, T. (2011) · Pharmacological Research · doi:10.1016/j.phrs.2011.03.010 · Cited by 124
Furtado, M. D. A., Rossetti, F., Chanda, S., & Yourick, D. L. (2012) · NeuroToxicology · doi:10.1016/j.neuro.2012.09.001 · Cited by 125
Metadata
- Authors
- Altman, J., & Das, G. D.
- Affiliations
- Massachusetts Institute of Technology (US)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1965-06
- Volume
- 124
- Issue
- 3
- Pages
- 319-335
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W1980499453
- Cited by
- 3,592
- References
- 18
- Citations by year
- 2026: 55 · 2025: 79 · 2024: 66 · 2023: 92 · 2022: 112 · 2021: 131 · 2020: 130 · 2019: 136 · 2018: 116 · 2017: 128 · 2016: 132 · 2015: 143 · 2014: 142 · 2013: 145 · 2012: 160
- FWCI
- 6.21
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- dentate gyrus granule cells, germinal matrix, ependymal layer, undifferentiated cells, cell migration, rat brain development
- MeSH terms
- Animals, Animals, Newborn, Autoradiography, Cell Differentiation, Hippocampus, Testosterone, Thymidine, Tritium, Rats, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review