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Migration and distribution of two populations of hippocampal granule cell precursors during the perinatal and postnatal periods
Abstract
Methacrylate‐embedded sections and short‐survival thymidine radiograms of the hippocampal dentate gyrus were examined in perinatal and postnatal rats in order to trace the site of origin and migration of the precursors of granule cells and study the morphogenesis of the granular layer. The densely packed, spindle‐shaped cells of the secondary dentate matrix (a derivative of the primary dentate neuroepithelium) stream in a subpial position towards the granular layer of the internal dentate limb during the perinatal and early postnatal periods. By an accretionary process, the crest of the granular layer forms on day E21 and on the subsequent days the granular layer of the internal dentate limb expands progressively in a lateral direction. Granule cells differentiation, as judged by the transformation of polymorph, darkly staining small cells into rounder, lightly staining larger granule cells, follows the same gradient from the external dentate limb to the internal dentate limb. The secondary dentate matrix is in a process of dissolution by day P5. This matrix is the source of what will later become the outer shell of the granular layer composed of early generated granule cells. The thicker inner shell of the granular layer, formed during the infantile and juvenile periods, derives from an intrinsic, tertiary germinal matrix. On day E22, the dentate migration of the secondary dentate matrix becomes partitioned into two components: (a) the subpial component of extradentate origin, referred to in this context as the first dentate migration, and (b) the second dentate migration. The latter is distributed in the basal polymorph layer throughout the entire dentate gyrus and is henceforth recognized as the tertiary dentate matrix. The tertiary dentate matrix is prominent between days P3 and P10. It is postulated that the great increase in granule cell population during the infantile period is principally due to cells derived from this intrinsic matrix of the dentate gyrus. Between days P20 and P30 the tertiary dentate matrix disappears in the basal polymorph layer and henceforth proliferative cells become largely confined to the subgranular zone at the base of the granular layer. The subgranular zone is the source of granule cells produced during the juvenile and adult periods.
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“reduction in PTB triggered radial glial-like cells to convert into new granular neurons through what appears to be the typical developmental process by which new hippocampal neurons mature during development39 and in young adult animals40.”
From Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB (2021) · cites this paper as [39]
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Cites
Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats
Altman, J., & Das, G. D. (1965) · Journal of Comparative Neurology · doi:10.1002/cne.901240303 · Cited by 3,592
Self-citationBayer, S. A. (1980) · The Journal of Comparative Neurology · doi:10.1002/cne.901900107 · Cited by 913
Self-citationAutoradiographic 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-citationTime of neuron origin in the hippocampal region. An autoradiographic study in the mouse.
Angevine, J. B. (1965) · PubMed · Cited by 476
Evidence that granule cells generated in the dentate gyrus of adult rats extend axonal projections
Stanfield, B. B., & Trice, J. (1988) · Experimental Brain Research · doi:10.1007/bf00250261 · Cited by 431
Altman, J., & Bayer, S. A. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903010302 · Cited by 401
Self-citationBayer, S. A. (1982) · Experimental Brain Research · doi:10.1007/bf00238626 · Cited by 285
Self-citationEckenhoff, M. F., & RAKIC, P. T. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902230102 · Cited by 239
Altman, J., & Bayer, S. A. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903010303 · Cited by 198
Self-citationOn the number of neurons in the dentate gyrus of the rat
Boss, B. D., Peterson, G. M., & Cowan, W. M. (1985) · Brain Research · doi:10.1016/0006-8993(85)90257-4 · Cited by 178
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Orr, M. E., Garbarino, V. R., Salinas, A., & Buffenstein, R. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00504 · Cited by 58
Tuoc, T., Dere, E., Radyushkin, K., Pham, L., Nguyen, H., Tonchev, A. B., Sun, G., Ronnenberg, A., Shi, Y., Staiger, J. F., et al. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9948-5 · Cited by 53
Long-term effects of neonatal treatment with fluoxetine on cognitive performance in Ts65Dn mice
Stagni, F., Giacomini, A., Guidi, S., Ciani, E., Ragazzi, E., Filonzi, M., IASIO, R. D., Rimondini, R., & Bartesaghi, R. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.12.005 · Cited by 55
You, L., Yan, K., Zhou, J., Hong, Z., Bertos, N., Park, M., Wang, E., & Yang, X. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005034 · Cited by 53
Kerloch, T., Clavreul, S., Goron, A., Abrous, D. N., & Pacary, E. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy224 · Cited by 58
Pedersen, K. M., Finsen, B. R., Celis, J. E., & Jensen, N. A. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.47.31494 · Cited by 53
Early survival and delayed death of developmentally‐born dentate gyrus neurons
Cahill, S. P., Yu, R. Q., Green, D., Todorova, E., & Snyder, J. S. (2017) · Hippocampus · doi:10.1002/hipo.22760 · Cited by 53
Possible mechanisms inducing granule cell dispersion in humans with temporal lobe epilepsy
Lurton, D., Sundström, L., Brana, C., Bloch, B., & Rougier, A. (1997) · Epilepsy Research · doi:10.1016/s0920-1211(96)01002-9 · Cited by 53
Huang, S., Slomianka, L., Farmer, A. J., Kharlamova, A. V., Gulevich, R. G., Herbeck, Y. E., Trut, L. N., Wolfer, D. P., & Amrein, I. (2015) · Hippocampus · doi:10.1002/hipo.22420 · Cited by 52
A fight for survival: The challenges faced by a newborn neuron integrating in the adult hippocampus
Bergami, M., & Berninger, B. (2012) · Developmental Neurobiology · doi:10.1002/dneu.22025 · Cited by 55
Bone Morphogenic Protein Signaling Is a Major Determinant of Dentate Development
Choe, Y., Kozlova, A., Graf, D., & Pleasure, S. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.0128-13.2013 · Cited by 52
Aslan, H., Songür, A., Tunc, A. T., Özen, O. A., Baş, O., Yağmurca, M., Turgut, M., Sarsılmaz, M., & Kaplan, S. (2006) · Brain Research · doi:10.1016/j.brainres.2006.09.005 · Cited by 53
Zhao, X., Kohen, R., Parent, R., Duan, Y., Fisher, G. L., Korn, M. J., Ji, L., Wan, G., Jin, J., Püschel, A. W., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.044 · Cited by 50
Neurotrophin expression by spinal motoneurons in adult and developing rats
Buck, C. R., Seburn, K. L., & Cope, T. C. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000117)416:3 · Cited by 80
Transient increase of tenascin-C in immature hippocampus: astroglial and neuronal expression
Ferhat, L., Chevassus-au-Louis, N., Jorquera, I., Niquet, J., Khrestchatisky, M., Ben‐Ari, Y., & Represa, A. (1996) · Journal of Neurocytology · doi:10.1007/bf02284785 · Cited by 52
Zhang, J., Moats‐Staats, B. M., Ye, P., & D’Ercole, A. J. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21289 · Cited by 52
Ageing stem and progenitor cells: implications for rejuvenation of the central nervous system
van Wijngaarden, P., & Franklin, R. J. M. (2013) · Development · doi:10.1242/dev.092262 · Cited by 53
Postnatal and Adult Neurogenesis in the Development of Human Disease
Danzer, S. C. (2007) · The Neuroscientist · doi:10.1177/1073858408317008 · Cited by 52
Principles Governing DNA Methylation during Neuronal Lineage and Subtype Specification
Sharma, A., Klein, S. L., Barboza, L., Lodhi, N., & Tóth, M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4037-15.2016 · Cited by 48
Suchecki, D. (2018) · Journal of Neuroendocrinology · doi:10.1111/jne.12610 · Cited by 50
Developmental patterns of torsinA and torsinB expression
Vasudevan, A., Breakefield, X. O., & Bhide, P. G. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.087 · Cited by 51
Kosten, T. A., Karanian, D. A., Yeh, J., Haile, C. N., Kim, J. J., Kehoe, P., & Bahr, B. A. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.03.011 · Cited by 51
p73 and Reelin in Cajal-Retzius Cells of the Developing Human Hippocampal Formation
Ábrahám, H. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh010 · Cited by 51
Diversity of Neural Precursors in the Adult Mammalian BrainPreprint
Bonaguidi, M. A., Stadel, R. P., Berg, D. A., Sun, J., Ming, G., & Song, H. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a018838 · Cited by 51
Sugiyama, T., Osumi, N., & Katsuyama, Y. (2013) · Developmental Dynamics · doi:10.1002/dvdy.24035 · Cited by 56
Endogenous Proliferation after Spinal Cord Injury in Animal Models
McDonough, A., & Martínez‐Cerdeño, V. (2012) · Stem Cells International · doi:10.1155/2012/387513 · Cited by 51
Hippocampal malformation associated with sudden death in early childhood: a neuropathologic study
Hefti, M. M., Cryan, J. B., Haas, E. A., Chadwick, A. E., Crandall, L. A., Trachtenberg, F. L., Armstrong, D. D., Grafe, M. R., Krous, H. F., & Kinney, H. C. (2016) · Forensic Science Medicine and Pathology · doi:10.1007/s12024-015-9731-3 · Cited by 50
Andrade, J. P., Madeira, M. D., & Paula-Barbosa, M. M. (1995) · Europe PMC (PubMed Central) · Cited by 50
Cell Therapy for Multiple Sclerosis
Ben‐Hur, T. (2011) · Neurotherapeutics · doi:10.1007/s13311-011-0073-x · Cited by 50
López‐Meraz, M. L., Wasterlain, C. G., Rocha, L. L., Allen, S., & Niquet, J. (2009) · Neurobiology of Disease · doi:10.1016/j.nbd.2009.10.019 · Cited by 49
Nuclear deterrents: Intrinsic regulators of IL-1β-induced effects on hippocampal neurogenesis
Ó’Léime, C. S., Cryan, J. F., & Nolan, Y. M. (2017) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2017.07.153 · Cited by 53
Temporal Embryonic Origin Critically Determines Cellular Physiology in the Dentate Gyrus
Save, L., Baude, A., & Cossart, R. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy132 · Cited by 49
Nakayama, A., Yoshida, M., Kagawa, N., & Nagao, T. (2019) · Journal of Applied Toxicology · doi:10.1002/jat.3776 · Cited by 49
Expression of cell cycle‐related proteins in developing and adult mouse hippocampus
Schmetsdorf, S., Gärtner, U., & Arendt, T. (2004) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2004.07.019 · Cited by 48
The mas proto-oncogene is developmentally regulated in the rat central nervous system
Martin, K. A., Grant, S. G. N., & Hockfield, S. J. (1992) · Developmental Brain Research · doi:10.1016/0165-3806(92)90249-v · Cited by 49
Coras, R., & Blümcke, I. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.08.003 · Cited by 48
Schaeffer, E. L., Novaes, B. A., Aquino, E. R. D. S., Skaf, H. D., & Mendes-Neto, Á. G. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.06.024 · Cited by 52
Fung, C. M., Ke, X., Brown, A. S., Yu, X., McKnight, R. A., & Lane, R. H. (2012) · Pediatric Research · doi:10.1038/pr.2012.32 · Cited by 48
Lagali, P. S., Corcoran, C., & Picketts, D. J. (2010) · Clinical Genetics · doi:10.1111/j.1399-0004.2010.01503.x · Cited by 49
Genetic regulation of dentate gyrus morphogenesis
Li, G., & Pleasure, S. J. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63008-8 · Cited by 48
Navarro-Quiroga, I., Hernandez-Valdes, M., Lin, S. L., & Naegele, J. R. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21037 · Cited by 48
Prospects of Cell Therapy for Disorders of Myelin
Ben‐Hur, T., & Goldman, S. A. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1444.014 · Cited by 47
Gupta, S. K., Maurya, R., Saxena, M., & Sen, J. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.03.027 · Cited by 47
Nelson, B. R., Hodge, R., Daza, R., Tripathi, P. P., Arnold, S., Millen, K., & Hevner, R. (2020) · eLife · doi:10.7554/elife.53777 · Cited by 41
Gökçımen, A., Rağbetli̇, M. Ç., Baş, O., Tunc, A. T., Aslan, H., Yazıcı, A. C., & Kaplan, S. (2006) · Brain Research · doi:10.1016/j.brainres.2006.10.026 · Cited by 47
Miki, T., Harris, S. J., Wilce, P. A., Takeuchi, Y., & Bedi, K. S. (2003) · Hippocampus · doi:10.1002/hipo.10072 · Cited by 47
Chemokine receptors in the brain: A developing story
Tran, P. B., & Miller, R. J. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10546 · Cited by 47
Ohsawa, F., Widmer, H. R., Knüsel, B., Denton, T. L., & Hefti, F. F. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90112-s · Cited by 47
Clarke, L., & van der Kooy, D. (2011) · Stem Cells · doi:10.1002/stem.692 · Cited by 46
Mixed neurotransmission in the hippocampal mossy fibers
Münster‐Wandowski, A., Gómez‐Lira, G., & Gutiérrez, R. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00210 · Cited by 47
Ketamine Affects the Neurogenesis of the Hippocampal Dentate Gyrus in 7-Day-Old Rats
Huang, H., Liu, C., Sun, J., Hao, T., Xu, C., Wang, D., & Wu, Y. (2016) · Neurotoxicity Research · doi:10.1007/s12640-016-9615-7 · Cited by 46
Development of the Telencephalon: Neural Stem Cells, Neurogenesis, and Neuronal Migration
Bayer, S. A., & Altman, J. (2004) · Elsevier eBooks · doi:10.1016/b978-012547638-6/50003-1 · Cited by 46
Self-citationSousa, N., Madeira, M. D., & Paula-Barbosa, M. M. (1997) · Journal of Neurocytology · doi:10.1023/a:1018573105987 · Cited by 46
Amrein, I., & Slomianka, L. (2010) · Brain Research · doi:10.1016/j.brainres.2010.02.075 · Cited by 45
Maintaining appearances—The role of p53 in adult neurogenesis
Medrano, S., & Scrable, H. J. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.03.194 · Cited by 45
Sharma, A. K., Valadi, N. M., Miller, A. H., & Pearce, B. D. (2002) · Neurobiology of Disease · doi:10.1006/nbdi.2002.0531 · Cited by 44
Sakurai‐Yamashita, Y., Sassone‐Corsi, P., & Gombos, G. (1991) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1991.tb01672.x · Cited by 45
Zhao, S., Zhou, Y., Gross, J., Miao, P., Qiu, L., Wang, D., Chen, Q., & Feng, G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012506 · Cited by 44
Andrade, J. P., Castanheira-Vale, A. J., Paz-Dias, P. G., Madeira, M. D., & Paula-Barbosa, M. M. (1996) · Experimental Brain Research · doi:10.1007/bf00229626 · Cited by 44
Attardo, A., Fabel, K., Krebs, J., Haubensak, W. E., Huttner, W. Β., & Kempermann, G. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp100 · Cited by 42
Pearce, B., Steffensen, S., Paoletti, A., Henriksen, S. J., & Buchmeier, M. J. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-01-00220.1996 · Cited by 43
The Doublecortin and Doublecortin-Like Kinase 1 Genes Cooperate in Murine Hippocampal Development
Tanaka, T., Koizumi, H., & Gleeson, J. G. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhk005 · Cited by 43
van Hooijdonk, L. W. A., Ichwan, M., Dijkmans, T. F., Schouten, T. G., de Backer, M. W. A., Adan, R. A. H., Verbeek, F. J., Vreugdenhil, E., & Fitzsimons, C. P. (2009) · BMC Neuroscience · doi:10.1186/1471-2202-10-2 · Cited by 43
Simon, R., Baumann, L., Fischer, J., Seigfried, F. A., Bruyckere, E. D., Liu, P., Jenkins, N. A., Copeland, N. G., Schwegler, H., & Britsch, S. (2016) · Genes Brain & Behavior · doi:10.1111/gbb.12287 · Cited by 45
Patterns of cell death in the perinatal mouse forebrain
Mosley, M., Shah, C. R., Morse, K. A., Miloro, S. A., Holmes, M. M., Ahern, T. H., & Forger, N. G. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24041 · Cited by 44
Gilbert, M. E., Goodman, J. H., Gomez, J., Johnstone, A. F. M., & Ramos, R. L. (2017) · NeuroToxicology · doi:10.1016/j.neuro.2016.12.009 · Cited by 44
Protocols for Studying Adult Neurogenesis: Insights and Recent Developments
Taupin, P. (2006) · Regenerative Medicine · doi:10.2217/17460751.2.1.51 · Cited by 42
Solberg, N. T., Machoň, O., & Krauss, S. J. K. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21586 · Cited by 43
Sarsılmaz, M., Kaplan, S., Songür, A., Çolakoğlu, S., Aslan, H., Tunc, A. T., Özen, O. A., Turgut, M., & Baş, O. (2007) · Brain Research · doi:10.1016/j.brainres.2007.01.139 · Cited by 44
Wang, X., Zhang, D., & Lu, X. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.75 · Cited by 42
Bustamante, C., Bilbao, P., Contreras, W., Martínez, M., Mendoza, A., Reyes, A. P., & Pascual, R. (2010) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2010.07.229 · Cited by 42
Siegel, J. A., Craytor, M. J., & Raber, J. (2010) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e32833e7e44 · Cited by 43
Distribution of p120 catenin during rat brain development:
Chauvet, N., Prieto, M., Fabre, C., Hooten, N. N., & Privat, A. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00030-7 · Cited by 42
Age-dependent kinetics of dentate gyrus neurogenesis in the absence of cyclin D2
Ansorg, A., Witte, O. W., & Urbach, A. (2012) · BMC Neuroscience · doi:10.1186/1471-2202-13-46 · Cited by 41
Ribeiro-Carvalho, A., Lima, C. S., Medeiros, A. H., Siqueira, N. R., Filgueiras, C. C., Manhães, A. C., & Abreu-Villaça, Y. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.05.032 · Cited by 40
Dorsal Dentate Gyrus, a Key Regulator for Mood and Psychiatric Disorders
Sun, D., Mei, L., & Xiong, W. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.01.005 · Cited by 47
Hou, J., Xue, J., Lee, M.-R., Sun, M., Zhao, X., Zheng, Y., & Sung, C. K. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.05.087 · Cited by 40
Radic, T., Frieß, L., Vijikumar, A., Jungenitz, T., Deller, T., & Schwarzacher, S. W. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00104 · Cited by 41
Behavioral and cognitive changes after early postnatal lesions of the rat mediodorsal thalamus
Ouhaz, Z., Ba-M’hamed, S., Mitchell, A. S., Idrissi, A. E., & Bennis, M. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.06.017 · Cited by 39
Simonati, A., Tosati, C., Rosso, T., Piazzola, E., & Rizzuto, N. (1999) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19990615)45:6 · Cited by 34
Differential properties of dentate gyrus and CA1 neural precursors
Becq, H., Jorquera, I., Ben‐Ari, Y., Weiss, S., & Represa, A. (2004) · Journal of Neurobiology · doi:10.1002/neu.20089 · Cited by 40
Neuronal functions of FOXO/DAF-16
Kim, S. Y., & Webb, A. E. (2016) · Nutrition and Healthy Aging · doi:10.3233/nha-160009 · Cited by 41
Danzer, S. C. (2017) · Brain Plasticity · doi:10.3233/bpl-170056 · Cited by 38
Nicotine and ethanol interact during adolescence: Effects on the central cholinergic systems
Ribeiro‐Carvalho, A., Lima, C. S., Filgueiras, C. C., Manhães, A. C., & Abreu‐Villaça, Y. (2008) · Brain Research · doi:10.1016/j.brainres.2008.07.062 · Cited by 41
Effects of neonatal corticosterone treatment on maze performance and HPA axis in juvenile rats
McCormick, C. M., Rioux, T., Fisher, R., Lang, K., MacLaury, K., & Teillon, S. (2001) · Physiology & Behavior · doi:10.1016/s0031-9384(01)00574-1 · Cited by 39
Acidic Calponin Cloned from Neural Cells is Differentially Expressed During Rat Brain Development
Ferhat, L., Charton, G., Represa, A., Ben‐Ari, Y., der Terrossian, E., & Khrestchatisky, M. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01612.x · Cited by 39
DNA Methyltransferase 1 Is Indispensable for Development of the Hippocampal Dentate Gyrus
Noguchi, H., Murao, N., Kimura, A., Matsuda, T., Namihira, M., & Nakashima, K. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0512-16.2016 · Cited by 38
Ciric, T., Cahill, S. P., & Snyder, J. S. (2019) · Brain and Behavior · doi:10.1002/brb3.1435 · Cited by 37
Probing Pedomorphy and Prolonged Lifespan in Naked Mole-Rats and Dwarf Mice
Buffenstein, R., Lewis, K. N., Gibney, P. A., Narayan, V., Grimes, K. M., Smith, M., Lin, T., & Brown‐Borg, H. M. (2020) · Physiology · doi:10.1152/physiol.00032.2019 · Cited by 39
Dupuy, S. T., & Houser, C. R. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19971222)389:3 · Cited by 38
D-serine: a new word in the glutamatergic neuro-glial language
Scolari, M., & Acosta, G. B. (2007) · Amino Acids · doi:10.1007/s00726-006-0481-0 · Cited by 36
Chitosan Nanoparticles Cause Pre- and Postimplantation Embryo Complications in Mice1
Park, M., Gurunathan, S., Choi, Y., Kwon, D., Han, J.-W., Cho, S., Park, C., Seo, H. G., & Kim, J. (2013) · Biology of Reproduction · doi:10.1095/biolreprod.112.107532 · Cited by 38
Morozov, Y. M., Ayoub, A. E., & RAKIC, P. T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0272-06.2006 · Cited by 37
Clayton, G. H., Perez, G. M., Smith, R. L., & Owens, G. C. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00074-1 · Cited by 38
Chang, G., Karatayev, O., & LEIBOWITZ, S. F. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.09.020 · Cited by 39
Todkar, K. J., Scotti, A. L., & Schwaller, B. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00056 · Cited by 41
Schaeffer, E. L., Aquino, E. R. D. S., Novaes, B. D. A., Skaf, H. D., & Gattaz, W. F. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.08.019 · Cited by 38
Reshetnikov, V. V., Kovner, A. V., Lepeshko, A. A., Pavlov, K. S., Grinkevich, L. N., & Bondar, N. P. (2018) · Genes Brain & Behavior · doi:10.1111/gbb.12541 · Cited by 37
Stagni, F., & Bartesaghi, R. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.903729 · Cited by 33
Hisaoka, T., Morikawa, Y., Kitamura, T., & Senba, E. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(03)00101-9 · Cited by 37
Metadata
- Authors
- Altman, J., & Bayer, S. A.
- Affiliations
- Purdue University West Lafayette (US)
- Indiana University – Purdue University Indianapolis (US)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1990-11-15
- Volume
- 301
- Issue
- 3
- Pages
- 365-381
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2006624547
- Cited by
- 819
- References
- 12
- Citations by year
- 2026: 8 · 2025: 11 · 2024: 9 · 2023: 9 · 2022: 18 · 2021: 17 · 2020: 24 · 2019: 29 · 2018: 28 · 2017: 37 · 2016: 33 · 2015: 35 · 2014: 31 · 2013: 35 · 2012: 39
- FWCI
- 3.40
- 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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- hippocampal granule cells, granule cell precursors, dentate gyrus, subgranular zone, perinatal development, postnatal development, cell migration, granule cell differentiation
- MeSH terms
- Aging, Animals, Autoradiography, Cell Differentiation, Cell Division, Cell Movement, Gestational Age, Hippocampus, Morphogenesis, Rats, Inbred Strains, Thymidine, Tritium, Rats
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