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The Glial Nature of Embryonic and Adult Neural Stem Cells
Open accessAbstract
Glial cells were long considered end products of neural differentiation, specialized supportive cells with an origin very different from that of neurons. New studies have shown that some glial cells—radial glia (RG) in development and specific subpopulations of astrocytes in adult mammals—function as primary progenitors or neural stem cells (NSCs). This is a fundamental departure from classical views separating neuronal and glial lineages early in development. Direct visualization of the behavior of NSCs and lineage-tracing studies reveal how neuronal lineages emerge. In development and in the adult brain, many neurons and glial cells are not the direct progeny of NSCs, but instead originate from transit amplifying, or intermediate, progenitor cells (IPCs). Within NSCs and IPCs, genetic programs unfold for generating the extraordinary diversity of cell types in the central nervous system. The timing in development and location of NSCs, a property tightly linked to their neuroepithelial origin, appear to be the key determinants of the types of neurons generated. Identification of NSCs and IPCs is critical to understand brain development and adult neurogenesis and to develop new strategies for brain repair.
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“GFAP is also expressed by progenitor cells15 and its expression depends on developmental stages16,17.”
From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [15]
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In the citing paper
“In particular, and by taking advantage of Btg2 and Tubb3 expression, our group has generated a combinatorial, double-reporter mouse line in which RFP and or GFP expression allowed the isolation specifically of PP, DP and N based on their endogenous fluorescence (RFP-, RFP+ and GFP+, respectively) (31).”
From MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis (2020) · cites this paper as [31]
Experimental — accuracy not yet measuredThe check wasn’t confident either way, so it gives no verdict — never disputed.
In the citing paper
“Unsurprisingly, when analyzing the expression pattern of the host genes of switch miRNAs (data retrieved from ( 31)), we found a high degree of overlap in their differential expression within different cell populations (Figure 3).”
From MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis (2020) · cites this paper as [31]
Experimental — accuracy not yet measuredIn the citing paper
“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 [108]
In the citing paper
“The predicted progenitors expressed proliferation (Mki67) and known markers (Pax6, Rspo2/3, Wnt5a/3a/1, Fabp7, clusters 7 and 8 in Figure 2A,B S2B; STAR Methods), previously reported for precursors of ependymal cells and cortical neurons (Kriegstein and Alvarez-Buylla, 2009), with Wnt1 having the most specific expression (Figure S2G).”
From A cellular and spatial map of the choroid plexus across brain ventricles and ages (2021) · cites this paper as Kriegstein and Alvarez-Buylla, 2009
In the citing paper
“In embryos, subsets of glial cells expressed markers of neural progenitor/stem-like cells (e.g. Pax6, Nes, Sox2, Rspo2/3) or of oligodendrocyte precursor cells (OPCs, e.g. Olig1, Olig2) (Kriegstein and Alvarez-Buylla, 2009) (Figure 2A, S2A,B).”
From A cellular and spatial map of the choroid plexus across brain ventricles and ages (2021) · cites this paper as Kriegstein and Alvarez-Buylla, 2009
In the citing paper
“Validation and use of this mouse line revealed to be very powerful in the identification of several new genes and biological processes regulating cortical development (31).”
From MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis (2020) · cites this paper as [31]
In the citing paper
“our group previously concluded that a transient up-or down-regulation specifically in DP compared to both their PP progenitors and N progeny (on-and off-switch transcripts, respectively) represented a hallmark of functional commitment to the neurogenic lineage (31,36).”
From MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis (2020) · cites this paper as [31]
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Citations
Cites
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
Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants
Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S., Weisstaub, N., Lee, J., Duman, R., Arancio, O., et al. (2003) · Science · doi:10.1126/science.1083328 · Cited by 4,321
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
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
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
Specification of Cerebral Cortical Areas
Rakic, P. (1988) · Science · doi:10.1126/science.3291116 · Cited by 3,127 · cited 1×
“Astrocytes may retain fundamental properties and positional information linked to the original array of RG in the developing brain (Rakic 1988).”
BackgroundMechanisms and Functional Implications of Adult Neurogenesis
Zhao, C., Deng, W., & Gage, F. H. (2008) · Cell · doi:10.1016/j.cell.2008.01.033 · Cited by 3,007
Running enhances neurogenesis, learning, and long-term potentiation in mice
van Praag, H., Christie, B. R., Sejnowski, T. J., & Gage, F. H. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.23.13427 · Cited by 2,904
Inflammatory Blockade Restores Adult Hippocampal Neurogenesis
Monje, M. L., Toda, H., & Palmer, T. D. (2003) · Science · doi:10.1126/science.1088417 · Cited by 2,426
Research works printed but not linked: 7
- 10.1016/S0092-8674(00)80783-7 · DOI · Paper page
- Hajós F, 1981, Acta Morphol. Acad. Sci. Hung., 29, 361
- Magini J, 1888, Arch. Ital. Biol., 10, 384
- Miyata T, 2008, Dev. Growth Differ., 50, S105
- Retzius G, 1894, Biol. Unters., 6, 1
- Smart IH, 1973, J. Anat., 116, 67
- 10.1523/JNEUROSCI.18-20-08331.1998 · DOI
Cited by
Sorted by citations
Items 701–800 of 1,011
Calió, M. L., Mosini, A. C., Marinho, D. S., Salles, G. N., Massinhani, F. H., Ko, G. M., & Porcionatto, M. A. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105219 · Cited by 48
Lindsey, B. W., Donato, S. D., Kaslin, J., & Tropepe, V. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12729 · Cited by 46
Lifetime modulation of the pain system via neuroimmune and neuroendocrine interactions
Zouikr, I., & Karshikoff, B. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00276 · Cited by 45
From Progenitors to Progeny: Shaping Striatal Circuit Development and Function
Knowles, R., Dehorter, N., & Ellender, T. J. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0620-21.2021 · Cited by 49
Ortega, F., Costa, M. R., Simon‐Ebert, T., Schroeder, T., Götz, M., & Berninger, B. (2011) · Nature Protocols · doi:10.1038/nprot.2011.404 · Cited by 45
Genetic approaches to study glial cells in the rodent brain
Pfrieger, F. W., & Ślęzak, M. (2011) · Glia · doi:10.1002/glia.22283 · Cited by 47
DeBoer, E., Kraushar, M. L., Hart, R. P., & Rašin, M. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.05.042 · Cited by 47
Rolseth, V., Krokeide, S. Z., Kunke, D., Neurauter, C. G., Suganthan, R., Sejersted, Y., Hildrestrand, G. A., Bjørås, M., & Luna, L. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2012.12.024 · Cited by 45
Achuta, V. S., Grym, H., Putkonen, N., Louhivuori, V., Kärkkäinen, V., Koıstınaho, J., Roybon, L., & Castrén, M. L. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22419 · Cited by 46
Shu, P., Fu, H., Zhao, X., Wu, C., Ruan, X., Zeng, Y., Liu, W., Wang, M., Hou, L., Chen, P., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-08450-8 · Cited by 45
Transcriptional and Post-Transcriptional Mechanisms of the Development of Neocortical Lamination
Popovitchenko, T., & Rašin, M. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00102 · Cited by 45
Brocca, M. E., & García‐Segura, L. M. (2018) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-018-0607-4 · Cited by 45
Embryonic microglia influence developing hypothalamic glial populations
Marsters, C. M., Nesan, D., Far, R., Klenin, N., Pittman, Q. J., & Kurrasch, D. M. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01811-7 · Cited by 46
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
ATF4-induced warburg metabolism drives over-proliferation in Drosophila
Sorge, S., Theelke, J., Yildirim, K., Hertenstein, H., McMullen, E., Müller, S., Altbürger, C., Schirmeier, S., & Lohmann, I. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107659 · Cited by 44
Girard, F., Eichenberger, S., & Celio, M. R. (2014) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2014.06.010 · Cited by 46
Marichal, N., García, G., Radmilovich, M., Trujillo-Cenóz, O., & Russo, R. E. (2012) · Stem Cells · doi:10.1002/stem.1175 · Cited by 45
Matrix regulators in neural stem cell functions
Wade, A., McKinney, A., & Phillips, J. J. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.01.017 · Cited by 46
Neural stem cell heterogeneity through time and space in the ventricular-subventricular zone
Rushing, G. V., & Ihrie, R. A. (2016) · Frontiers in Biology · doi:10.1007/s11515-016-1407-1 · Cited by 50
Gangliosides in Nerve Cell Specification
Itokazu, Y., Wang, J., & Yu, R. K. (2018) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.12.008 · Cited by 44
Güven, A., Kalebic, N., Long, K. R., Florio, M., Vaid, S., Brandl, H., Stenzel, D., & Huttner, W. Β. (2020) · eLife · doi:10.7554/elife.49808 · Cited by 44
Neural stem cells in the adult human brain.
González-Pérez, Ó. (2012) · PubMed · Cited by 44
Park, S. E., Lee, J., Chang, E. H., Kim, J. H., Sung, J., Na, D. L., & Chang, J. W. (2016) · Archives of Pharmacal Research · doi:10.1007/s12272-016-0799-4 · Cited by 44
Tracking single-cell evolution using clock-like chromatin accessibility loci
Xiao, Y., Jin, W., Ju, L., Fu, J., Wang, G., Yu, M., Chen, F., Qian, K., Wang, X., & Zhang, Y. (2024) · Nature Biotechnology · doi:10.1038/s41587-024-02241-z · Cited by 46
Embryonic cerebrospinal fluid in brain development: neural progenitor control
Gato, A., Alonso, M. I., Martín, C., Carnicero, E., Moro, J. A., la Mano, A. D., Fernández, J. M. F., Lamus, F., & Desmond, M. E. (2014) · Croatian Medical Journal · doi:10.3325/cmj.2014.55.299 · Cited by 43
Redox-regulated fate of neural stem progenitor cells
Prozorovski, T., Schneider, R., Berndt, C., Hartung, H., & Aktaş, O. (2015) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2015.01.022 · Cited by 45
Epigenetic regulation of neural stem cell property from embryo to adult
Murao, N., Noguchi, H., & Nakashima, K. (2016) · Neuroepigenetics · doi:10.1016/j.nepig.2016.01.001 · Cited by 47
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
Lamin B1 levels modulate differentiation into neurons during embryonic corticogenesis
Mahajani, S. U., Giacomini, C., Marinaro, F., Tonelli, D. D. P., Contestabile, A., & Gasparini, L. (2017) · Scientific Reports · doi:10.1038/s41598-017-05078-6 · Cited by 43
T cells in the post-ischemic brain: Troopers or paramedics?
Cramer, J. V., Benakis, C., & Liesz, A. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.11.006 · Cited by 44
Guo, T., Liu, G., Du, H., Wen, Y. F., Wei, S., Li, Z., Tao, G., Shang, Z., Song, X., Zhang, Z., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz018 · Cited by 45
Romero-Morales, A. I., O’Grady, B. J., Balotin, K. M., Bellan, L. M., Lippmann, E. S., & Gama, V. (2019) · HardwareX · doi:10.1016/j.ohx.2019.e00084 · Cited by 45
de Jong, C. G. H. M., Gabius, H., & Baron, W. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03327-7 · Cited by 44
YAP1/TAZ drives ependymoma-like tumour formation in mice
Eder, N., Roncaroli, F., Domart, M., Horswell, S. D., Andreiuolo, F. D. M., Flynn, H. R., Lopes, A. T., Claxton, S., Kilday, J., Collinson, L., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16167-y · Cited by 43
Adult-Born Neurons in the Olfactory Bulb: Integration and Functional Consequences
Gheusi, G., Lepousez, G., & Lledo, P. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2012_228 · Cited by 43
Stem cell therapy for central nerve system injuries: glial cells hold the key
Xiao, L., Saiki, C., & Ide, R. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.137570 · Cited by 44
Bossuyt, J., Herrewegen, Y. V. D., Nestor, L., Buckinx, A., Bundel, D. D., & Smolders, I. J. (2023) · Glia · doi:10.1002/glia.24390 · Cited by 44
Fate specification in the adult brain – lessons for eliciting neurogenesis from glial cells
Ninkovic, J., & Götz, M. (2013) · BioEssays · doi:10.1002/bies.201200108 · Cited by 44
Notch Receptor Expression in Neurogenic Regions of the Adult Zebrafish Brain
Carlos, V., Ganz, J., Hans, S., Kaslin, J., & Brand, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073384 · Cited by 42
Fei, J., Haffner, C., & Huttner, W. Β. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.03.033 · Cited by 44
Boyan, G., & Williams, L. (2011) · Arthropod Structure & Development · doi:10.1016/j.asd.2011.02.005 · 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
Ferretti, P. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07833.x · Cited by 45
Adult Astrogenesis and the Etiology of Cortical Neurodegeneration
Mohn, T. C., & Koob, A. O. (2015) · Journal of Experimental Neuroscience · doi:10.4137/jen.s25520 · Cited by 44
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
Nkx2.1 regulates the generation of telencephalic astrocytes during embryonic development
Minocha, S., Valloton, D., Arsenijévic, Y., Cardinaux, J., Guidi, R., Hornung, J., & Lebrand, C. (2017) · Scientific Reports · doi:10.1038/srep43093 · Cited by 46
Braccioli, L., Vervoort, S. J., Puma, G., Nijboer, C. H. A., & Coffer, P. J. (2018) · Stem Cell Research · doi:10.1016/j.scr.2018.10.005 · Cited by 42
Cabello-Rivera, D., Sarmiento‐Soto, H., López‐Barneo, J., & Muñoz-Cabello, A. M. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00664 · Cited by 42
Luzuriaga, J., Pineda, J. R., Irastorza, I., Uribe‐Etxebarria, V., García-Gallastegui, P., Encinas, J. M., Chamero, P., Unda, F. J., & Ibarretxe, G. (2019) · Cellular Physiology and Biochemistry · doi:10.33594/000000096 · Cited by 42
Casingal, C. R., Descant, K. D., & Anton, E. S. (2022) · Neuron · doi:10.1016/j.neuron.2022.01.034 · Cited by 46
Differentiating human stem cells into neurons and glial cells for neural repair
Selvaraj, V. (2011) · Frontiers in bioscience · doi:10.2741/3916 · Cited by 42
Wagenführ, L., Meyer, A. K., Braunschweig, L., Marrone, L., & Storch, A. (2015) · Development · doi:10.1242/dev.121939 · Cited by 46
Lattke, M., & Guillemot, F. (2022) · WIREs Mechanisms of Disease · doi:10.1002/wsbm.1557 · Cited by 45
Neural stem cell-derived extracellular vesicles: The light of central nervous system diseases
Li, Y., & Fang, B. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115092 · Cited by 43
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Voss, A. J., Lanjewar, S. N., Sampson, M. M., King, A. T., Hill, E. J., Sing, A., Sojka, C., Bhatia, T. N., Spangle, J. M., & Sloan, S. A. (2022) · Nature Neuroscience · doi:10.1038/s41593-023-01375-8 · Cited by 41
Effects of small molecules on neurogenesis: Neuronal proliferation and differentiation
Jastrzębski, M. K., Wójcik, P., Stępnicki, P., & Kaczor, A. (2023) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2023.10.007 · Cited by 40
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
Spatial joint profiling of DNA methylome and transcriptome in tissues
Lee, C. N., Fu, H., Cardilla, A., Zhou, W., & Deng, Y. (2025) · Nature · doi:10.1038/s41586-025-09478-x · Cited by 42
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
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
Bestman, J. E., Lee‐Osbourne, J., & Cline, H. T. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22795 · Cited by 42
Role of microglia in embryonic neurogenesis
Tong, C. K., & Vidyadaran, S. (2016) · Experimental Biology and Medicine · doi:10.1177/1535370216664430 · Cited by 41
Unique Organization of the Nuclear Envelope in the Post-natal Quiescent Neural Stem Cells
Cebrián‐Silla, A., Alfaro‐Cervelló, C., Herranz‐Pérez, V., Kaneko, N., Park, D. H., Sawamoto, K., Álvarez-Buylla, A., Lim, D. A., & García‐Verdugo, J. M. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.05.024 · Cited by 41
Neuronal Activity-Dependent Control of Postnatal Neurogenesis and Gliogenesis
Káradóttir, R. T., & Kuo, C. T. (2018) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-072116-031054 · Cited by 42
Shiota, Y., Nagai, A., Sheikh, A. M., Mitaki, S., Mishima, S., Yano, S., Haque, M. A., Kobayashi, S., & Yamaguchi, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-33030-9 · Cited by 41
Halley, A. C., & Krubitzer, L. A. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.12.003 · Cited by 43
Su, Y., Zhang, W., Patro, C. P. K., Zhao, J., Mu, T., Ma, Z., Xu, J., Ban, K. H.-K., Yi, C., & Zhou, Y. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00362 · Cited by 41
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
Essential genes for astroglial development and axon pathfinding during zebrafish embryogenesis
Barresi, M. J. F., Burton, S., DiPietrantonio, K., Amsterdam, A., Hopkins, N. H., & Karlstrom, R. O. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22393 · Cited by 43
Huang, X., Kong, H., Tang, M., Lu, M., Ding, J., & Hu, G. (2012) · CNS Neuroscience & Therapeutics · doi:10.1111/j.1755-5949.2011.00276.x · Cited by 41
Cortical neurogenesis from pluripotent stem cells: complexity emerging from simplicity
Anderson, S., & Vanderhaeghen, P. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.03.012 · Cited by 40
Delgado, R. N., & Lim, D. A. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.09.008 · Cited by 40
Luzzati, F., Marchis, S. D., Parlato, R., Gribaudo, S., Schütz, G., Fasolo, A., & Peretto, P. M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025088 · Cited by 41
Proliferation, migration and differentiation in juvenile and adult Xenopus laevis brains
d'Amico, L.-A., Boujard, D., & Coumailleau, P. (2011) · Brain Research · doi:10.1016/j.brainres.2011.06.032 · Cited by 40
Barber, B. A., Liyanage, V. R. B., Zachariah, R. M., Olson, C. O., Bailey, M. A. G., & Rastegar, M. (2013) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2013.04.005 · Cited by 40
Regulation of Myelination in the Central Nervous System by Nuclear Lamin B1 and Non-coding RNAs
Lin, S.-T., Heng, M. Y., Ptáček, L. J., & Fu, Y.-H. (2014) · Translational Neurodegeneration · doi:10.1186/2047-9158-3-4 · Cited by 40
Adult neurogenesis in the decapod crustacean brain: a hematopoietic connection?
Beltz, B. S., Zhang, Y., Benton, J. L., & Sandeman, D. C. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07802.x · Cited by 40
Wang, W., Jossin, Y., Chai, G., Lien, W., Tissir, F., & Goffinet, A. M. (2016) · Nature Communications · doi:10.1038/ncomms10936 · Cited by 42
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Zhang, S., Burda, J. E., Anderson, M. A., Zhao, Z., Ao, Y., Cheng, Y., Sun, Y. E., Deming, T. J., & Sofroniew, M. V. (2015) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.5b00153 · Cited by 40
Arranz, J., Balducci, E., Arató, K., Sánchez‐Elexpuru, G., Najas, S., Parras, A., Rebollo, E., Pijuan, I., Erb, I., Verde, G., et al. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.02.022 · Cited by 43
Li, M., Sun, S., Priest, J., Bi, X., & Fan, Y. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1862-0 · Cited by 43
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Zhang, X., Alnafisah, R. S., Hamoud, A.-R. A., Shukla, R., Wen, Z., McCullumsmith, R. E., & O'Donovan, S. M. (2021) · Neurochemical Research · doi:10.1007/s11064-020-03212-x · Cited by 43
Decoding neuronal composition and ontogeny of individual hypothalamic nuclei
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Wu, X., Shen, Q., Zhang, Z., Zhang, D., Gu, Y., & Xing, D. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02399-2 · 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
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Schuster, A. M., Klotz, M., Schwab, T., Liddo, R. D., Bertalot, T., Schrenk, S., Martin, M., Nguyen, T. D., Nguyen, T. N. Q., Gries, M., et al. (2014) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12292 · Cited by 41
Zhou, X., Liu, F., Tian, M., Xu, Z., Liang, Q., Wang, C., Li, J., Liu, Z., Tang, K., He, M., et al. (2015) · Development · doi:10.1242/dev.115279 · Cited by 41
Ma, X., Han, Y., Song, X., Do, T., Yang, Z., Ni, J., & Xie, T. (2016) · Development · doi:10.1242/dev.141069 · Cited by 39
Falk, S., Bugeon, S., Ninkovic, J., Pilz, G.-A., Postiglione, M. P., Cremer, H., Knoblich, J. A., & Götz, M. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.009 · Cited by 39
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Gulaia, V. S., Kumeiko, V. V., Shved, N. A., Cicinskas, E., Александрович, Р. С., Ruzov, A. S., & Kagansky, A. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00388 · Cited by 39
Sirko, S., Akita, K., von Holst, A., & Faissner, A. (2010) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(10)79003-0 · Cited by 40
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Guzmán, A., Ramos-Balderas, J. L., Carrillo-Rosas, S., & Maldonado, E. (2013) · Biology Open · doi:10.1242/bio.20136023 · Cited by 39
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Kanaumi, T., Milenkovic, I., Adle-Biassette, H., Aronica, E., & Kovács, G. G. (2013) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2013.09.011 · Cited by 36
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Metadata
- Authors
- Kriegstein, A., & Alvarez-Buylla, A.
- Affiliations
- University of California, San Francisco (US)
- The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Departments of Neurology, Neurological Surgery, and School of Medicine, University of California, San Francisco, California 94143-0525;,
- ORCID
- Kriegstein, Arnold
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 2009-06-01
- Volume
- 32
- Issue
- 1
- Pages
- 149-184
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- PMC
- PMC3086722
- OpenAlex
- W2172266256
- Cited by
- 2,475
- References
- 263
- Citations by year
- 2026: 87 · 2025: 141 · 2024: 138 · 2023: 131 · 2022: 133 · 2021: 168 · 2020: 162 · 2019: 147 · 2018: 166 · 2017: 155 · 2016: 162 · 2015: 129 · 2014: 167 · 2013: 172 · 2012: 155
- FWCI
- 12.34
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS035710, R01NS028478, R01NS021223)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- neural stem cells, radial glia, astrocytes, intermediate progenitor cells, transit amplifying cells, neuronal lineage, neuroepithelium, adult neurogenesis, brain development, lineage tracing, brain repair
- MeSH terms
- Animals, Cell Differentiation, Central Nervous System, Humans, Neuroglia, Neurons, Stem Cells, Gene Expression Regulation, Developmental, Cell Lineage, Adult Stem Cells, Neurogenesis
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