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A new subtype of progenitor cell in the mouse embryonic neocortex
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A hallmark of mammalian brain evolution is cortical expansion, which reflects an increase in the number of cortical neurons established by the progenitor cell subtypes present and the number of their neurogenic divisions. Recent studies have revealed a new class of radial glia-like (oRG) progenitor cells in the human brain, which reside in the outer subventricular zone. Expansion of the subventricular zone and appearance of oRG cells may have been essential evolutionary steps leading from lissencephalic to gyrencephalic neocortex. Here we show that oRG-like progenitor cells are present in the mouse embryonic neocortex. They arise from asymmetric divisions of radial glia and undergo self-renewing asymmetric divisions to generate neurons. Moreover, mouse oRG cells undergo mitotic somal translocation whereby centrosome movement into the basal process during interphase precedes nuclear translocation. Our finding of oRG cells in the developing rodent brain fills a gap in our understanding of neocortical expansion.
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“The oRG population is largely missing in mouse brain development47, and human cellular models therefore provide a unique opportunity to study this cell population.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [47]
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Cites
Specification of Cerebral Cortical Areas
Rakic, P. (1988) · Science · doi:10.1126/science.3291116 · Cited by 3,127 · cited 1×
“Although the laminar organization of the cortex is relatively similar in all mammals, an expansion in cortical surface area underlies the transformation from smooth cortex to the highly folded primate neocortex, and the associated alteration of cortical architecture that is the substrate for the 'higher' cortical func…”
BackgroundThe Glial Nature of Embryonic and Adult Neural Stem Cells
Kriegstein, A., & Alvarez-Buylla, A. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135600 · Cited by 2,475
Self-citationNoctor, S. C., Martínez-Cerdeño, V., Ivic, L., & Kriegstein, A. R. (2004) · Nature Neuroscience · doi:10.1038/nn1172 · Cited by 2,229
Self-citationThe cell biology of neurogenesis
Götz, M., & Huttner, W. B. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1739 · Cited by 2,130
Neurons derived from radial glial cells establish radial units in neocortex
Noctor, S. C., Flint, A. C., Weissman, T. A., Dammerman, R. S., & Kriegstein, A. R. (2001) · Nature · doi:10.1038/35055553 · Cited by 2,016
Self-citationEvolution of the neocortex: a perspective from developmental biology
Rakic, P. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2719 · Cited by 1,565
Neurogenic radial glia in the outer subventricular zone of human neocortex
Hansen, D. V., Lui, J. H., Parker, P. R. L., & Kriegstein, A. R. (2010) · Nature · doi:10.1038/nature08845 · Cited by 1,388
Self-citationEnglund, C., Fink, A., Lau, C., Pham, D., Daza, R. A. M., Bulfone, A., Kowalczyk, T., & Hevner, R. F. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2899-04.2005 · Cited by 1,261
Rakic, P. (1974) · Science · doi:10.1126/science.183.4123.425 · Cited by 1,161
Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage
Malatesta, P., Hartfuss, E., & Götz, M. (2000) · Development · doi:10.1242/dev.127.24.5253 · Cited by 1,157
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Items 101–200 of 506
Metabolic Regulation of Neocortical Expansion in Development and Evolution
Namba, T., Nardelli, J., Gressèns, P., & Huttner, W. Β. (2020) · Neuron · doi:10.1016/j.neuron.2020.11.014 · Cited by 92
Shaping the brain: The emergence of cortical structure and folding
Akula, S. K., Exposito-Alonso, D., & Walsh, C. A. (2023) · Developmental Cell · doi:10.1016/j.devcel.2023.11.004 · Cited by 104
Coevolution of radial glial cells and the cerebral cortex
Romero, C. D. J., & Borrell, V. (2015) · Glia · doi:10.1002/glia.22827 · Cited by 102
The secondary loss of gyrencephaly as an example of evolutionary phenotypical reversal
Kelava, I., Lewitus, É., & Huttner, W. Β. (2013) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00016 · Cited by 93
Miyata, T., Okamoto, M., Shinoda, T., & Kawaguchi, A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00473 · Cited by 103
Cerebral cortex assembly: generating and reprogramming projection neuron diversity
Lodato, S., Shetty, A. S., & Arlotta, P. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.11.003 · Cited by 100
Relationship Between Cortical Gyrification, White Matter Connectivity, and Autism Spectrum Disorder
Ecker, C., Andrews, D., Dell’Acqua, F., Daly, E., Murphy, C., Catani, M., de Schotten, M. T., Baron‐Cohen, S., Lai, M.-C., Lombardo, M. V., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw098 · Cited by 94
Basal Progenitor Morphology and Neocortex Evolution
Kalebic, N., & Huttner, W. Β. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.07.009 · Cited by 86
Molecular and cellular evolution of corticogenesis in amniotes
Cárdenas, A., & Borrell, V. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03315-x · Cited by 86
Li, Z., Tyler, W. A., Zeldich, E., Santpere, G., Okamoto, M., Gao, T., Li, M., Šestan, N., & Haydar, T. F. (2020) · Science Advances · doi:10.1126/sciadv.abd2068 · Cited by 78
Multimodal Single-Cell Analysis Reveals Physiological Maturation in the Developing Human Neocortex
Mayer, S., Chen, J., Velmeshev, D., Mayer, A., Eze, U. C., Bhaduri, A., da Cunha, C. E., Jung, D., Arjun, A., Li, E., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.01.027 · Cited by 82
Self-citationInterkinetic nuclear migration: beyond a hallmark of neurogenesis
Kosodo, Y. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-0952-2 · Cited by 84
Dual Effect of CTCF Loss on Neuroprogenitor Differentiation and Survival
Watson, L. A., Wang, X., Elbert, A., Kernohan, K. D., Galjart, N., & Bérubé, N. G. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3769-13.2014 · Cited by 82
Self-citationTyler, W. A., & Haydar, T. F. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.5380-12.2013 · Cited by 81
Evolution of the mammalian dentate gyrus
Hevner, R. F. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23851 · Cited by 80
Mechanisms of brain evolution: Regulation of neural progenitor cell diversity and cell cycle length
Borrell, V., & Calegari, F. (2014) · Neuroscience Research · doi:10.1016/j.neures.2014.04.004 · Cited by 82
Lineage origins of GABAergic versus glutamatergic neurons in the neocortex
Marín, Ó., & Müller, U. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.015 · Cited by 87
Cellular and Molecular Mechanisms Linking Human Cortical Development and Evolution
Libé-Philippot, B., & Vanderhaeghen, P. (2021) · Annual Review of Genetics · doi:10.1146/annurev-genet-071719-020705 · Cited by 78
Bertacchi, M., Romano, A. L., Loubat, A., Mau‐Them, F. T., Willems, M., Faivre, L. O., Kien, P. K. V., Perrin, L., Devillard, F., Sorlin, A., et al. (2020) · The EMBO Journal · doi:10.15252/embj.2019104163 · Cited by 74
Cellular and molecular properties of neural progenitors in the developing mammalian hypothalamus
Zhou, X., Zhong, S., Peng, H., Liu, J., Ding, W., Sun, L., Ma, Q., Liu, Z., Chen, R., Wu, Q., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17890-2 · Cited by 74
Self-citationLv, X., Ren, S., Zhang, X., Shen, Z., Ghosh, T., Xianyu, A., Gao, P., Li, Z., Lin, S., Yu, Y., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11854-x · Cited by 79
From sauropsids to mammals and back: New approaches to comparative cortical development
Montiel, J. F., Vasistha, N. A., García‐Moreno, F., & Molnár, Z. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23871 · Cited by 74
Cell Division Modes and Cleavage Planes of Neural Progenitors during Mammalian Cortical DevelopmentPreprint
Matsuzaki, F., & Shitamukai, A. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a015719 · Cited by 80
Beyond Axon Guidance: Roles of Slit-Robo Signaling in Neocortical Formation
Gonda, Y., Namba, T., & Hanashima, C. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.607415 · Cited by 77
Folding brains: from development to disease modeling
Del-Valle-Anton, L., & Borrell, V. (2021) · Physiological Reviews · doi:10.1152/physrev.00016.2021 · Cited by 79
Evolution of the Chordate Telencephalon
Briscoe, S. D., & Ragsdale, C. W. (2019) · Current Biology · doi:10.1016/j.cub.2019.05.026 · Cited by 75
Untangling Cortical Complexity During Development
Mukhtar, T., & Taylor, V. (2018) · Journal of Experimental Neuroscience · doi:10.1177/1179069518759332 · Cited by 81
The regulation of cortical neurogenesis
Villalba, A., Götz, M., & Borrell, V. (2020) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2020.10.003 · Cited by 80
Cellular dynamics of neuronal migration in the hippocampus
Hayashi, K., Kubo, K., Kitazawa, A., & Nakajima, K. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00135 · Cited by 80
Betancourt, J., Katzman, S. J., & Chen, B. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23373 · Cited by 67
Distinct progenitor behavior underlying neocortical gliogenesis related to tumorigenesis
Shen, Z., Lin, Y., Yang, J., Jörg, D. J., Peng, Y., Zhang, X., Xu, Y., Hernandez, L., Ma, J., Simons, B. D., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108853 · Cited by 70
Neocortical neurogenesis and neuronal migration
Tan, X., & Shi, S. (2012) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.88 · Cited by 85
Kitazawa, A., Kubo, K., Hayashi, K., Matsunaga, Y., Ishii, K., & Nakajima, K. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2254-13.2014 · Cited by 75
LSD1 co-repressor Rcor2 orchestrates neurogenesis in the developing mouse brain
Wang, Y., Wu, Q., Yang, P., Wang, C., Liu, J., Ding, W., Liu, W., Bai, Y., Yang, Y., Wang, H., et al. (2016) · Nature Communications · doi:10.1038/ncomms10481 · Cited by 75
Self-citationLiu, W. A., Chen, S., Li, Z., Lee, C. H., Mirzaa, G., Dobyns, W. B., Ross, M. E., Zhang, J., & Shi, S. (2018) · Genes & Development · doi:10.1101/gad.313171.118 · Cited by 77
Cerrato, V., Parmigiani, E., Figueres‐Oñate, M., Betizeau, M., Aprato, J., Nanavaty, I. N., Berchialla, P., Luzzati, F., de’Sperati, C., López‐Mascaraque, L., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2005513 · Cited by 64
Garcίa, M. T., Chang, Y., Arai, Y., & Huttner, W. Β. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23801 · Cited by 77
Inside-Out Radial Migration Facilitates Lineage-Dependent Neocortical Microcircuit Assembly
He, S., Li, Z., Ge, S., Yu, Y., & Shi, S. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.002 · Cited by 74
Wang, H., Xiao, Z., Zheng, J., Wu, J., Hu, X.-L., Yang, X., & Shen, Q. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.04.081 · Cited by 73
A molecular and cellular perspective on human brain evolution and tempo
Lindhout, F. W., Krienen, F. M., Pollard, K. S., & Lancaster, M. A. (2024) · Nature · doi:10.1038/s41586-024-07521-x · Cited by 80
Kostic, M., Paridaen, J. T. M. L., Long, K. R., Kalebic, N., Langen, B., Grübling, N., Wimberger, P., Kawasaki, H., Namba, T., & Huttner, W. Β. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.091 · Cited by 67
The multifaceted roles of primary cilia in the development of the cerebral cortex
Hasenpusch-Theil, K., & Theil, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.630161 · Cited by 66
Badouel, C., Zander, M., Liscio, N. T., Bagherie-Lachidan, M., Sopko, R., Coyaud, É., Raught, B., Miller, F. D., & McNeill, H. (2015) · Development · doi:10.1242/dev.123539 · Cited by 64
Lineage-dependent circuit assembly in the neocortex
Gao, P., Sultan, K. T., Zhang, X., & Shi, S. (2013) · Development · doi:10.1242/dev.087668 · Cited by 68
Xie, Y., Castro-Hernández, R., Sokpor, G., Pham, L., Narayanan, R., Rosenbusch, J., Staiger, J. F., & Tuoc, T. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1595-1 · Cited by 67
The role of Extracellular Vesicles during CNS development
Sangani, N. B., Gomes, A. R., Curfs, L., & Reutelingsperger, C. P. M. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102124 · Cited by 68
Wnt/β-Catenin Signaling Regulates Sequential Fate Decisions of Murine Cortical Precursor Cells
Draganova, K., Zemke, M., Zurkirchen, L., Valenta, T., Cantù, C., Okoniewski, M. J., Schmid, M.-T., Hoffmans, R., Götz, M., Basler, K., et al. (2014) · Stem Cells · doi:10.1002/stem.1820 · Cited by 71
Fine-Tuning of Neurogenesis is Essential for the Evolutionary Expansion of the Cerebral Cortex
Poluch, S., & Juliano, S. L. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht232 · Cited by 67
Foxp1 Regulates Neural Stem Cell Self-Renewal and Bias Toward Deep Layer Cortical Fates
Pearson, C. A., Moore, D. M., Tucker, H. O., Dekker, J. D., Hu, H., Miquelajáuregui, A., & Novitch, B. G. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.034 · Cited by 65
Jiang, X., Zhang, T., Zhang, S., Kendrick, K. M., & Liu, T. (2021) · Psychoradiology · doi:10.1093/psyrad/kkab002 · Cited by 65
oRGs and mitotic somal translocation — a role in development and disease
Ostrem, B., Di Lullo, E., & Kriegstein, A. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.11.007 · Cited by 61
Self-citationNeural precursor lineages specify distinct neocortical pyramidal neuron types.
Tyler, W. A., Medalla, M., Guillamon-Vivancos, T., Luebke, J. I., & Haydar, T. F. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.0335-15.2015 · Cited by 60
The Ferret as a Model System for Neocortex Development and Evolution
Gilardi, C., & Kalebic, N. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.661759 · Cited by 58
LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules
Reiner, O. (2013) · Scientifica · doi:10.1155/2013/393975 · Cited by 63
Neocortical arealization: Evolution, mechanisms, and open questions
Alfano, C., & Studer, M. (2012) · Developmental Neurobiology · doi:10.1002/dneu.22067 · Cited by 57
The (Not Necessarily) Convoluted Role of Basal Radial Glia in Cortical Neurogenesis
Hevner, R. F., & Haydar, T. F. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr336 · Cited by 56
Venkataraman, L., Fair, S. R., McElroy, C. A., Hester, M. E., & Fu, H. (2020) · Stem Cell Reviews and Reports · doi:10.1007/s12015-020-10068-9 · Cited by 55
Xing, L., Kubik‐Zahorodna, A., Namba, T., Pinson, A., Florio, M., Procházka, J., Sarov, M., Sedláček, R., & Huttner, W. Β. (2021) · The EMBO Journal · doi:10.15252/embj.2020107093 · Cited by 56
Tox: a multifunctional transcription factor and novel regulator of mammalian corticogenesis
Artegiani, B., Domingues, A. M. D. J., Alonso, S. B., Brandl, E., Massalini, S., Dahl, A., & Calegari, F. (2014) · The EMBO Journal · doi:10.15252/embj.201490061 · Cited by 53
Herr, K. J., Herr, D. R., Lee, C., Noguchi, K., & Chun, J. J. M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1106129108 · Cited by 53
Zhu, S., Wildonger, J., Barshow, S., Younger, S. H., Huang, Y., & Lee, T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046724 · Cited by 51
Morphological and functional aspects of progenitors perturbed in cortical malformations
Bizzotto, S., & Francis, F. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00030 · Cited by 62
The evolution of basal progenitors in the developing non-mammalian brain
Nomura, T., Ohtaka‐Maruyama, C., Yamashita, W., Wakamatsu, Y., Murakami, Y., Calegari, F., Suzuki, K., Gotoh, H., & Ono, K. (2016) · Development · doi:10.1242/dev.127100 · Cited by 52
An oblique view on the role of spindle orientation in vertebrate neurogenesis
Peyre, E., & Morin, X. (2012) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2012.01350.x · Cited by 61
Stepien, B. K., Vaid, S., & Huttner, W. Β. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.676911 · Cited by 59
Tocco, C., Bertacchi, M., & Studer, M. (2021) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.767965 · Cited by 53
Regulation of cerebral cortex development by Rho GTPases: insights from in vivo studies
Azzarelli, R., Kerloch, T., & Pacary, E. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00445 · Cited by 51
Kawaue, T., Shitamukai, A., Nagasaka, A., Tsunekawa, Y., Shinoda, T., Saito, K., Terada, R., Bilgic, M., Miyata, T., Matsuzaki, F., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10730-y · Cited by 50
Roles of chromatin remodeling BAF complex in neural differentiation and reprogramming
Narayanan, R., & Tuoc, T. (2014) · Cell and Tissue Research · doi:10.1007/s00441-013-1791-7 · Cited by 49
Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex
Bendriem, R. M., Singh, S., Aleem, A. K. A., Antonetti, D. A., & Ross, M. E. (2019) · eLife · doi:10.7554/elife.49376 · Cited by 49
Proneural Genes Define Ground State Rules to Regulate Neurogenic Patterning and Cortical Folding
Han, S., Okawa, S., Wilkinson, G., Ghazale, H., Adnani, L., Dixit, R., Tavares, L., Faisal, I., Brooks, M. J., Cortay, V., et al. (2020) · Neuron · doi:10.1016/j.neuron.2021.07.007 · Cited by 50
Coquand, L., Avalos, C. B., Macé, A., Farcy, S., Di-Cicco, A., Lampič, M., Wimmer, R., Bessières, B., Attié‐Bitach, T., Fraisier, V., et al. (2024) · Nature Cell Biology · doi:10.1038/s41556-024-01393-z · Cited by 60
Reprogramming patient-derived cells to study the epilepsies
Parent, J. M., & Anderson, S. A. (2015) · Nature Neuroscience · doi:10.1038/nn.3944 · Cited by 53
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
Kawauchi, T., Shikanai, M., & Kosodo, Y. (2013) · Genes to Cells · doi:10.1111/gtc.12029 · Cited by 46
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
The Molecular Pathway Regulating Bergmann Glia and Folia Generation in the Cerebellum
Leung, A. W., & Li, J. Y. H. (2017) · The Cerebellum · doi:10.1007/s12311-017-0904-3 · Cited by 52
The Symmetry of Neural Stem Cell and Progenitor Divisions in the Vertebrate Brain
Gimeno, G. C., & Paridaen, J. T. M. L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.885269 · Cited by 48
Cytoarchitecture of mouse and human subventricular zone in developing cerebral neocortex
Tabata, H., Yoshinaga, S., & Nakajima, K. (2011) · Experimental Brain Research · doi:10.1007/s00221-011-2933-3 · Cited by 48
DeBoer, E., Kraushar, M. L., Hart, R. P., & Rašin, M. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.05.042 · Cited by 47
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
A Complex Code of Extrinsic Influences on Cortical Progenitor Cells of Higher Mammals
Reillo, I., Romero, C. D. J., Cárdenas, A., Clascá, F., Martínez‐Martínez, M. Á., & Borrell, V. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx171 · Cited by 44
Chromatin Remodeling BAF155 Subunit Regulates the Genesis of Basal Progenitors in Developing Cortex
Narayanan, R., Pham, L., Kerimoglu, C., Watanabe, T., Castro-Hernández, R., Sokpor, G., Ulmke, P. A., Kiszka, K. A., Tonchev, A. B., Rosenbusch, J., et al. (2018) · iScience · doi:10.1016/j.isci.2018.05.014 · Cited by 44
Ferretti, P. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07833.x · Cited by 45
Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
Bizzotto, S., Uzquiano, A., Dingli, F., Ershov, D., Houllier, A., Arras, G., Richards, M. W., Loew, D., Minc, N., Croquelois, A., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-15253-4 · Cited by 48
HOPX Defines Heterogeneity of Postnatal Subventricular Zone Neural Stem Cells
Zweifel, S., Marcy, G., Giudice, Q. L., Li, D., Heinrich, C., Azim, K., & Raineteau, O. (2018) · Stem Cell Reports · doi:10.1016/j.stemcr.2018.08.006 · Cited by 43
Wang, L., Bluske, K. K., Dickel, L. K., & Nakagawa, Y. (2011) · Neural Development · doi:10.1186/1749-8104-6-35 · 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
Wagenführ, L., Meyer, A. K., Braunschweig, L., Marrone, L., & Storch, A. (2015) · Development · doi:10.1242/dev.121939 · Cited by 46
Using brain organoids to study human neurodevelopment, evolution and disease
Kyrousi, C., & Cappello, S. (2019) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.347 · Cited by 41
Recent advances in understanding neocortical development
Borrell, V. (2019) · F1000Research · doi:10.12688/f1000research.20332.1 · Cited by 44
Xing, L., Kalebic, N., Namba, T., Vaid, S., Wimberger, P., & Huttner, W. Β. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.034 · Cited by 45
Hurley, S., Mohan, C., Suetterlin, P., Ellingford, R. A., Riegman, K. L. H., Ellegood, J., Caruso, A., Michetti, C., Brock, O., Evans, R., et al. (2021) · Molecular Autism · doi:10.1186/s13229-020-00409-3 · Cited by 42
Single-cell epigenomics and spatiotemporal transcriptomics reveal human cerebellar development
Zhong, S., Wang, M., Huang, L., Chen, Y., Ge, Y., Zhang, J., Shi, Y., Dong, H., Zhou, X., Wang, B., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43568-6 · Cited by 40
Self-citationSilver, D. L. (2015) · BioEssays · doi:10.1002/bies.201500108 · Cited by 41
Pinson, A., Namba, T., & Huttner, W. Β. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00305 · Cited by 41
Krubitzer, L. A., & Dooley, J. C. (2013) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2013.00620 · Cited by 41
Neurogenesis in primates versus rodents and the value of non-human primate models
Zhang, R., Quan, H., Wang, Y., & Luo, F. (2023) · National Science Review · doi:10.1093/nsr/nwad248 · Cited by 47
Division modes and physical asymmetry in cerebral cortex progenitors
Delaunay, D., Kawaguchi, A., Dehay, C., & Matsuzaki, F. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.11.009 · Cited by 39
Heng, X., Guo, Q., Leung, A. W., & Li, J. Y. H. (2017) · eLife · doi:10.7554/elife.23253 · Cited by 40
Metadata
- Authors
- Wang, X., Tsai, J.-W., LaMonica, B., & Kriegstein, A. R.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Wang, Xiaoqun
- Kriegstein, Arnold R
- Venue
- Nature Neuroscience
- Published
- 2011-04-10
- Volume
- 14
- Issue
- 5
- Pages
- 555-561
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC3083489
- OpenAlex
- W2072710787
- Cited by
- 507
- References
- 37
- Citations by year
- 2026: 13 · 2025: 24 · 2024: 26 · 2023: 36 · 2022: 29 · 2021: 39 · 2020: 45 · 2019: 42 · 2018: 27 · 2017: 34 · 2016: 19 · 2015: 34 · 2014: 43 · 2013: 50 · 2012: 26
- FWCI
- 14.56
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Bernard Osher Foundation
- National Institute of General Medical Sciences (T32GM007618)
- National Institute of Neurological Disorders and Stroke (R01NS072630, R01NS035710, 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
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Keywords
- outer radial glia, embryonic neocortex, asymmetric cell division, cortical expansion, neurogenesis, mouse brain development
- MeSH terms
- Age Factors, Animals, Cell Differentiation, Cell Division, Cell Movement, Embryo, Mammalian, Luminescent Proteins, Mice, Transgenic, Nerve Tissue Proteins, Neuroglia, Neurons, Organ Culture Techniques, Stem Cells, Time Factors, Centrosome, Gene Expression Regulation, Developmental, Microscopy, Confocal, Neocortex, Green Fluorescent Proteins, Mice
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