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Adult Neurogenesis in the Mammalian Brain: Significant Answers and Significant Questions
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Adult neurogenesis, a process of generating functional neurons from adult neural precursors, occurs throughout life in restricted brain regions in mammals. The past decade has witnessed tremendous progress in addressing questions related to almost every aspect of adult neurogenesis in the mammalian brain. Here we review major advances in our understanding of adult mammalian neurogenesis in the dentate gyrus of the hippocampus and from the subventricular zone of the lateral ventricle, the rostral migratory stream to the olfactory bulb. We highlight emerging principles that have significant implications for stem cell biology, developmental neurobiology, neural plasticity, and disease mechanisms. We also discuss remaining questions related to adult neural stem cells and their niches, underlying regulatory mechanisms, and potential functions of newborn neurons in the adult brain. Building upon the recent progress and aided by new technologies, the adult neurogenesis field is poised to leap forward in the next decade.
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“The process by which newly generated neurons in normal development are incorporated into the granular cell layer is well established and involves expression of specific markers and development of defined neuronal morphology24,26,34,35.”
From Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB (2021) · cites this paper as [24]
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“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 [24]
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“There is evidence of neurogenesis from adult neural stem cells deriving from the subventricular zone (SVZ) and the subgranular zone (SGZ) of the hippocampal dentate gyrus, that can give rise to neurons, oligodendrocytes and astrocytes [107,108].”
From Ageing, Cellular Senescence and Neurodegenerative Disease (2018) · cites this paper as [107]
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Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,951
Neurogenesis in the adult human hippocampus
Eriksson, P. S., Perfilieva, E., Björk-Eriksson, T., Alborn, A.-M., Nordborg, C., Peterson, D. A., & Gage, F. H. (1998) · Nature Medicine · doi:10.1038/3305 · Cited by 6,369
Gage, F. H. (2000) · Science · doi:10.1126/science.287.5457.1433 · Cited by 4,786
Reynolds, B. A., & Weiss, S. (1992) · Science · doi:10.1126/science.1553558 · Cited by 4,482
Subventricular zone astrocytes are neural stem cells in the adult mammalian brain
Doetsch, F., Caillé, I., Lim, D. A., García-Verdugo, J. M., & Alvarez-Buylla, A. (1999) · Cell · doi:10.1016/s0092-8674(00)80783-7 · Cited by 3,898
Running increases cell proliferation and neurogenesis in the adult mouse dentate gyrus
van Praag, H., Kempermann, G., & Gage, F. H. (1999) · Nature Neuroscience · doi:10.1038/6368 · Cited by 3,880
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
The Neuroendocrinology of Stress: A Never Ending Story
Lightman, S. L. (2008) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2008.01711.x · Cited by 3,588
More hippocampal neurons in adult mice living in an enriched environment
Kempermann, G., Kuhn, H. G., & Gage, F. H. (1997) · Nature · doi:10.1038/386493a0 · Cited by 3,586
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Items 701–800 of 1,010
Rozmer, K., Gao, P., Araújo, M. G. L., Khan, M. T., Liu, J., Rong, W., Tang, Y., Franke, H., Krügel, U., Fernandes, M. J. D. S., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw178 · Cited by 45
Targeting Adult Neurogenesis to Optimize Hippocampal Circuits in Aging
McAvoy, K. M., & Sahay, A. (2017) · Neurotherapeutics · doi:10.1007/s13311-017-0539-6 · Cited by 45
Apostolopoulou, M., Kiehl, T. R., Winter, M., Cardenas De La Hoz, E., Boles, N. C., Bjornsson, C. S., Zuloaga, K. L., Goderie, S. K., Wang, Y., Cohen, A. R., et al. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.10.005 · Cited by 46
Controlling the Outgrowth and Functions of Neural Stem Cells: The Effect of Surface Topography
Simitzi, C., Karali, K., Ranella, A., & Stratakis, E. I. (2018) · ChemPhysChem · doi:10.1002/cphc.201701175 · Cited by 45
Brain Disorders and Chemical Pollutants: A Gap Junction Link?
Mesnil, M., Defamie, N., Naus, C. C. G., & Sarrouilhe, D. (2020) · Biomolecules · doi:10.3390/biom11010051 · Cited by 45
Cellular targets for neuropeptide Y-mediated control of adult neurogenesis
Geloso, M. C., Corvino, V., Maria, V. D., Marchese, E., & Michetti, F. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00085 · Cited by 45
Kim, H. J., Denli, A. M., Wright, R., Baul, T. D., Clemenson, G. D., Morcos, A. S., Zhao, C., Schafer, S. T., Gage, F. H., & Kagalwala, M. N. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.4286-14.2015 · Cited by 45
Neural plasticity and network remodeling: From concepts to pathology
Cohen, E. J., Quarta, E., Bravi, R., Granato, A., & Minciacchi, D. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2016.12.048 · Cited by 45
Qiu, L.-L., Tan, X.-X., Yang, J., Ji, M., Zhang, H., Zhao, C., Xia, J., & Sun, J. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03413-9 · Cited by 44
Prodromidou, K., Papastefanaki, F., Sklaviadis, T., & Matsas, R. (2014) · Stem Cells · doi:10.1002/stem.1663 · Cited by 44
Childhood Markers of Health Behavior Relate to Hippocampal Health, Memory, and Academic Performance
Hassevoort, K. M., Khan, N. A., Hillman, C. H., & Cohen, N. J. (2016) · Mind Brain and Education · doi:10.1111/mbe.12108 · Cited by 44
Emergence of multimodal action representations from neural network self-organization
Parisi, G. I., Tani, J., Weber, C., & Wermter, S. (2016) · Cognitive Systems Research · doi:10.1016/j.cogsys.2016.08.002 · Cited by 44
Adult NSC diversity and plasticity: the role of the niche
Llorens-Bobadilla, E., & Martín-Villalba, A. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.11.008 · Cited by 45
Nematullah, M., Hoda, M. N., & Khan, F. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0444-3 · Cited by 44
Soares, R., Ribeiro, F. F., Xapelli, S., Genebra, T., Ribeiro, M. F., Sebastião, A. M., Rodrigues, C. M. P., & Solá, S. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0592-5 · Cited by 44
Becker, K., Cana, A., Baumgärtner, W., & Spitzbarth, I. (2018) · Veterinary Pathology · doi:10.1177/0300985818781930 · Cited by 44
Li, Q., Wang, P., Huang, C., Chen, B., Liu, J., Zhao, M., & Zhao, J. (2019) · Journal of Molecular Neuroscience · doi:10.1007/s12031-019-01263-6 · Cited by 44
Aranarochana, A., Chaisawang, P., Sirichoat, A., Pannangrong, W., Wigmore, P. M., & Welbat, J. U. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.02.022 · Cited by 44
Mao, Z., Ouyang, S., Zhang, Q., Wu, Y., Wang, G., Tu, L., Luo, Z., Li, W., Kurihara, H., Li, Y., et al. (2020) · The FASEB Journal · doi:10.1096/fj.202000146rr · Cited by 44
The epitranscriptome in stem cell biology and neural development
Vissers, C. B., Sinha, A., Ming, G., & Song, H. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105139 · Cited by 44
Self-citationSantos, S. S., Moreira, J. B., Costa, M., Rodrigues, R. S., Sebastião, A. M., Xapelli, S., & Solá, S. (2021) · Cells · doi:10.3390/cells11010090 · Cited by 44
Mechanistic insight into the role of metformin in Alzheimer's disease
Sanati, M., Aminyavari, S., Afshari, A. R., & Sahebkar, A. (2022) · Life Sciences · doi:10.1016/j.lfs.2021.120299 · Cited by 44
Epigenetic Factors in Intellectual Disability
López‐Atalaya, J. P., Valor, L. M., & Barco, Á. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-800977-2.00006-1 · Cited by 44
Neural stem and progenitor cells in health and disease
Ladran, I., Tran, N., Topol, A., & Brennand, K. (2013) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1239 · Cited by 44
The multifaceted role of WNT signaling in Alzheimer’s disease onset and age-related progression.
Kostes, W. W., & Brafman, D. A. (2023) · Cells · doi:10.3390/cells12081204 · Cited by 43
Adult myelination: wrapping up neuronal plasticity
Young, K. M., O′Rourke, M., & Gasperini, R. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.137571 · Cited by 43
Prss56, a novel marker of adult neurogenesis in the mouse brain
Jourdon, A., Gresset, A., Spassky, N., Charnay, P., Topilko, P., & Santos, R. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1171-z · Cited by 43
The role of neurogenesis during development and in the adult brain
Jin, X. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13251 · Cited by 43
Transgenic mouse models for studying adult neurogenesis
Semerci, F., & Maletić‐Savatić, M. (2016) · Frontiers in Biology · doi:10.1007/s11515-016-1405-3 · Cited by 43
Morales-Garcia, J. A., Echeverry‐Alzate, V., Alonso‐Gil, S., Sanz-SanCristóbal, M., López‐Moreno, J. A., Gil, C., Martı́nez, A., Santos, Á., & Pérez‐Castillo, A. (2016) · Stem Cells · doi:10.1002/stem.2480 · Cited by 43
Modulation of Adult Hippocampal Neurogenesis by Sleep: Impact on Mental Health
Navarro-Sanchis, C., Brock, O., Winsky‐Sommerer, R., & Thuret, S. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00074 · Cited by 43
Neurogenesis during Abstinence Is Necessary for Context-Driven Methamphetamine-Related Memory
Galinato, M. H., Takashima, Y., Fannon, M. J., Quach, L. W., Silva, R. J. M., Mysore, K. K., Terranova, M. J., Dutta, R. R., Ostrom, R. W., Somkuwar, S. S., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2011-17.2018 · Cited by 43
Chen, S., Lin, M., Tsai, J.-S., He, P., Luo, W.-T., Chiu, I.-M., Herschman, H. R., & Li, H. (2020) · Stem Cells Translational Medicine · doi:10.1002/sctm.19-0174 · Cited by 43
Gordon, K. L., Zussman, J. W., Li, X., Miller, C., & Sherwood, D. R. (2020) · eLife · doi:10.7554/elife.56383 · Cited by 43
Heavy metals and adult neurogenesis
Wang, H., & Matsushita, M. T. (2021) · Current Opinion in Toxicology · doi:10.1016/j.cotox.2021.03.006 · Cited by 43
Cruz-Martinez, P., González-Granero, S., Molina‐Navarro, M. M., Pacheco‐Torres, J., García‐Verdugo, J. M., Geijo‐Barrientos, E., Jones, J., & Martı́nez, S. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.130 · Cited by 43
Hippocampal TERT Regulates Spatial Memory Formation through Modulation of Neural Development
Zhou, Q.-G., Liu, M., Lee, H., Ishikawa, F., Devkota, S., Shen, X.-R., Jin, X., Wu, H.-Y., Liu, Z., Liu, X., et al. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.06.014 · Cited by 43
Welbat, J. U., Chaisawang, P., Pannangrong, W., & Wigmore, P. (2018) · Nutrients · doi:10.3390/nu10081053 · Cited by 42
Syal, C., Kosaraju, J., Hamilton, L., Aumont, A., Chu, A., Sarma, S. N., Thomas, J., Seegobin, M., Dilworth, F. J., He, L., et al. (2020) · Theranostics · doi:10.7150/thno.44962 · Cited by 42
Ishimoto, T., Masuo, Y., Kato, Y., & Nakamichi, N. (2018) · Cellular Signalling · doi:10.1016/j.cellsig.2018.10.012 · Cited by 42
Latent tri-lineage potential of adult hippocampal neural stem cells revealed by Nf1 inactivation
Sun, G. J., Zhou, Y. F., Ito, S., Bonaguidi, M. A., Stein-O’Brien, G., Kawasaki, N. K., Modak, N., Zhu, Y., Ming, G., & Song, H. (2015) · Nature Neuroscience · doi:10.1038/nn.4159 · Cited by 42
Self-citationEndogenous neurogenesis following ischaemic brain injury: Insights for therapeutic strategies
Merson, T. D., & Bourne, J. A. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.08.003 · Cited by 42
Kühn, S., Charlet, K., Schubert, F., Kiefer, F., Zimmermann, P., Heinz, A., & Gallinat, J. (2014) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2014.352 · Cited by 42
Extended Effect of Chronic Social Defeat Stress in Childhood on Behaviors in Adulthood
Kovalenko, I. L., Galyamina, A. G., Смагин, Д. А., Michurina, T. V., Kudryavtseva, N. N., & Enikolopov, G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091762 · Cited by 42
Watanabe, Y., Khodosevich, K., & Monyer, H. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.03.022 · Cited by 42
Potential of Neural Stem Cell-Based Therapy for Parkinson’s Disease
Chou, C.-H., Fan, H., & Hueng, D. (2015) · Parkinson s Disease · doi:10.1155/2015/571475 · Cited by 42
Stem Cells in the Nervous System
Maldonado‐Soto, A. R., Oakley, D. H., Wichterle, H., Stein, J. M., Doetsch, F. K., & Henderson, C. E. (2014) · American Journal of Physical Medicine & Rehabilitation · doi:10.1097/phm.0000000000000111 · Cited by 42
Jiao, Q., Li, X., An, J., Zhang, Z., Chen, X., Tan, J., Zhang, P., Lü, H., & Liu, Y. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00200 · Cited by 42
Hill, J. D., Zuluaga‐Ramirez, V., Gajghate, S., Winfield, M., & Persidsky, Y. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14387 · Cited by 42
Leeson, H. C., Kasherman, M. A., Chan‐Ling, T., Lovelace, M. D., Brownlie, J. C., Toppinen, K. M., Gu, B. J., & Weible, M. W. (2018) · Stem Cells · doi:10.1002/stem.2894 · Cited by 42
AMPK Signaling Regulates the Age-Related Decline of Hippocampal Neurogenesis
Wang, B. Z., Yang, J. J., Zhang, H., Smith, C., & Jin, K. (2019) · Aging and Disease · doi:10.14336/ad.2019.0102 · Cited by 42
NOX4 regulates TGFβ‐induced proliferation and self‐renewal in glioblastoma stem cells
García‐Gómez, P., Golán, I., Dadras, M. S., Mezheyeuski, A., Bellomo, C., Tzavlaki, K., Morén, A., Puigvert, J. C., & Caja, L. (2022) · Molecular Oncology · doi:10.1002/1878-0261.13200 · Cited by 42
Lithopoulos, M. A., Strueby, L., O’Reilly, M., Zhong, S., Möbius, M. A., Eaton, F., Fung, M., Hurskainen, M., Cyr-Depauw, C., Suen, C., et al. (2022) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202012-4520oc · Cited by 42
Lithopoulos, M. A., Toussay, X., Zhong, S., Xu, L., Mustafa, S. B., Ouellette, J., Andrade, M. F., Comin, C. H., Bassam, H. A., Baker, A. N., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci146095 · Cited by 42
DISC1-related signaling pathways in adult neurogenesis of the hippocampus
Wu, Q., Li, Y., & Xiao, B. (2013) · Gene · doi:10.1016/j.gene.2013.01.015 · Cited by 42
The Nuclear Receptor TLX Is Required for Gliomagenesis within the Adult Neurogenic Niche
Zou, Y., Niu, W., Qin, S., Downes, M., Burns, D. K., & Zhang, C. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.01122-12 · Cited by 42
Unified theory of Alzheimer’s disease (UTAD): implications for prevention and curative therapy
Nehls, M. (2016) · Journal of Molecular Psychiatry · doi:10.1186/s40303-016-0018-8 · Cited by 41
Emerging strategies for nerve repair and regeneration in ischemic stroke: neural stem cell therapy
Wang, S., He, Q., Qu, Y., Yin, W., Zhao, R., Wang, X., Yang, Y., & Guo, Z. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.391313 · Cited by 41
Chen, C., Huang, C., & Hsu, K. (2015) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyv097 · Cited by 41
Radial glial cell: Critical functions and new perspective as a steroid synthetic cell
Xing, L., Goswami, M., & Trudeau, V. L. (2014) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2014.03.010 · Cited by 41
Garcia, I., Bhullar, P. K., Tepe, B., Ortiz‐Guzman, J., Huang, L., Herman, A. M., Chaboub, L. S., Deneen, B., Justice, N. J., & Arenkiel, B. R. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0888-4 · Cited by 41
Todkar, K. J., Scotti, A. L., & Schwaller, B. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00056 · Cited by 41
Adult Bone Marrow: Which Stem Cells for Cellular Therapy Protocols in Neurodegenerative Disorders?
Wislet‐Gendebien, S., Laudet, E., Neirinckx, V., & Rogister, B. (2012) · BioMed Research International · doi:10.1155/2012/601560 · Cited by 41
Skalecka, A., Liszewska, E., Bilinski, R., Gkogkas, C. G., Khoutorsky, A., Malik, A. R., Sonenberg, N., & Jaworski, J. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22392 · Cited by 41
miRNA-Mediated Regulation of Adult Hippocampal Neurogenesis; Implications for Epilepsy
Bielefeld, P., Mooney, C., Henshall, D. C., & Fitzsimons, C. P. (2016) · Brain Plasticity · doi:10.3233/bpl-160036 · Cited by 41
Liu, W., & Crews, F. T. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00151 · Cited by 41
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
Dlk1 dosage regulates hippocampal neurogenesis and cognition
Montalbán-Loro, R., Lassi, G., Lozano-Ureña, A., Pérez‐Villalba, A., Jiménez-Villalba, E., Charalambous, M., Vallortígara, G., Horner, A. E., Saksida, L. M., Bussey, T. J., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2015505118 · Cited by 41
Neurogenesis after Spinal Cord Injury: State of the Art
Rodríguez‐Barrera, R., Rivas-González, M., García-Sánchez, J., Mojica-Torres, D., & Ibarra, A. (2021) · Cells · doi:10.3390/cells10061499 · Cited by 41
Kako, E., Kaneko, N., Aoyama, M., Hida, H., Takebayashi, H., Ikenaka, K., Asai, K., Togari, H., Sobue, K., & Sawamoto, K. (2012) · Stem Cells · doi:10.1002/stem.1202 · Cited by 41
Progenitor Outgrowth from the Niche in Drosophila Trachea Is Guided by FGF from Decaying Branches
Chen, F., & Krasnow, M. A. (2014) · Science · doi:10.1126/science.1241442 · Cited by 41
Age-related decline in BubR1 impairs adult hippocampal neurogenesis
Yang, Z., Jun, H., Choi, C.-I., Yoo, K. H., Cho, C. H., Hussaini, S. M. Q., Simmons, A. J., Kim, S., van Deursen, J. M., Baker, D. J., et al. (2017) · Aging Cell · doi:10.1111/acel.12594 · Cited by 40
Li, L. R., Sethi, G., Zhang, X., Liu, C. L., Yan, H., Liu, Q., Ren, B. X., & Tang, F. R. (2022) · Aging · doi:10.18632/aging.203893 · Cited by 41
Zhang, Z., Lin, W., Li, Y., Yuan, X., He, X., Zhao, H., Mo, J., Lin, J., Yang, L., Liang, B., et al. (2023) · Aquaculture · doi:10.1016/j.aquaculture.2023.739651 · Cited by 40
Restoration of neuronal progenitors by partial reprogramming in the aged neurogenic niche
Xu, L., Ramirez-Matias, J., Hauptschein, M., Sun, E., Lunger, J. C., Buckley, M. T., & Brunet, A. (2024) · Nature Aging · doi:10.1038/s43587-024-00594-3 · Cited by 41
Batailler, M., Derouet, L., Butruille, L., & Migaud, M. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1101-0 · Cited by 40
Adult neurogenesis in the dentate gyrus
Benarroch, E. E. (2013) · Neurology · doi:10.1212/wnl.0b013e3182a9a156 · Cited by 40
Giacomo, E. D., Benedetti, E., Cristiano, L., Antonosante, A., d’Angelo, M., Fidoamore, A., Barone, D., Moreno, S., Ippoliti, R., Cerù, M. P., et al. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1252881 · Cited by 40
Singh, S., Mishra, A., Srivastava, N., & Shukla, S. (2016) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.6b00354 · Cited by 40
Thyroid Hormone Regulation of Adult Neurogenesis
Fanibunda, S. E., Desouza, L. A., Kapoor, R., Vaidya, R. A., & Vaidya, V. A. (2017) · Vitamins and hormones · doi:10.1016/bs.vh.2017.04.006 · Cited by 40
Neural plasticity in developing and adult olfactory pathways – focus on the human olfactory bulb
Huart, C., Rombaux, P., & Hummel, T. R. (2019) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-018-9780-x · Cited by 40
Cadmium Exposure Impairs Adult Hippocampal Neurogenesis
Wang, H., Abel, G. M., Storm, D. R., & Xia, Z. (2019) · Toxicological Sciences · doi:10.1093/toxsci/kfz152 · Cited by 40
The dentate gyrus in depression
Umschweif, G., Greengard, P., & Sagi, Y. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14640 · Cited by 40
Shan, X., Chen, J., Dai, S., Wang, J., Huang, Z., Lv, Z., Wang, Q., & Wu, Q. (2020) · Phytomedicine · doi:10.1016/j.phymed.2020.153269 · Cited by 40
PINK1 deficiency impairs adult neurogenesis of dopaminergic neurons
Brown, S. J., Boussaad, I., Jarazo, J., Fitzgerald, J. C., Antony, P. M. A., Keatinge, M., Blechman, J., Schwamborn, J. C., Krüger, R., Placzek, M., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-84278-7 · Cited by 40
Adult Neurogenesis under Control of the Circadian System
Ali, A. A. H., & von Gall, C. (2022) · Cells · doi:10.3390/cells11050764 · Cited by 40
Berlet, R., Cabantan, D. A. G., Gonzales-Portillo, D., & Borlongan, C. V. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.798826 · Cited by 40
Impaired Autophagy in Hilar Mossy Cells of the Dentate Gyrus and Its Implication in Schizophrenia
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Metadata
- Authors
- Ming, G.-L., & Song, H.
- Affiliations
- Johns Hopkins University (US)
- Corresponding author
- Ming, Guo-li
- Song, Hongjun
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2011-05
- Volume
- 70
- Issue
- 4
- Pages
- 687-702
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC3106107
- OpenAlex
- W2135046848
- Cited by
- 2,651
- References
- 198
- Citations by year
- 2026: 87 · 2025: 135 · 2024: 140 · 2023: 149 · 2022: 168 · 2021: 189 · 2020: 164 · 2019: 204 · 2018: 205 · 2017: 209 · 2016: 225 · 2015: 177 · 2014: 219 · 2013: 188 · 2012: 160
- FWCI
- 16.60
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute on Aging (AG24984, R01AG024984)
- National Institute of Mental Health (R21MH087874, R33MH087874, MH087874)
- National Institute of Neurological Disorders and Stroke (NS 048271, R01NS047344, NS 047344, R01NS048271, R37NS047344, R56NS047344)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01HD069184, HD069184)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- adult neurogenesis, neural stem cells, dentate gyrus, hippocampus, subventricular zone, rostral migratory stream, olfactory bulb, neural stem cell niche, neuroplasticity, developmental neuroscience, disease mechanisms
- MeSH terms
- Age Factors, Animals, Brain, Humans, Nervous System Diseases, Neuronal Plasticity, Neurogenesis, Neural Stem Cells
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