Selective Lengthening of the Cell Cycle in the Neurogenic Subpopulation of Neural Progenitor Cells during Mouse Brain Development

Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases

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A small step for the cell, a giant leap for mankind: a hypothesis of neocortical expansion during evolution

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Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: A major site of neurogenesis

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Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells

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Characterization of CNS Precursor Subtypes and Radial Glia

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Bromodeoxyuridine immunohistochemical determination of the lengths of the cell cycle and the DNA-synthetic phase for an anatomically defined population

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Signalling, cell cycle and pluripotency in embryonic stem cells

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The cell cycle of the pseudostratified ventricular epithelium of the embryonic murine cerebral wall

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Numbers, time and neocortical neuronogenesis: a general developmental and evolutionary model

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Constructing the cerebral cortex: Neurogenesis and fate determination

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Bre1a, a Histone H2B Ubiquitin Ligase, Regulates the Cell Cycle and Differentiation of Neural Precursor Cells

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MALS-3 regulates polarity and early neurogenesis in the developing cerebral cortex

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New Insights into Mechanisms of Stem Cell Daughter Fate Determination in Regenerative Tissues

Sada, A., & Tumbar, T. (2012) · International review of cytology · doi:10.1016/b978-0-12-405210-9.00001-1 · Cited by 24

Neurogenic decisions require a cell cycle independent function of the CDC25B phosphatase

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Regulation of size and scale in vertebrate spinal cord development

Kuzmicz‐Kowalska, K., & Kicheva, A. (2020) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.383 · Cited by 24

Cell proliferation and cell death are disturbed during prenatal and postnatal brain development after uranium exposure

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A single-cell–resolution fate map of endoderm reveals demarcation of pancreatic progenitors by cell cycle

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LRIG1-Mediated Inhibition of EGF Receptor Signaling Regulates Neural Precursor Cell Proliferation in the Neocortex

Jeong, D., Casasbuenas, D. L., Gengatharan, A., Edwards, K. M., Saghatelyan, A., Kaplan, D. R., Miller, F. D., & Yuzwa, S. A. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108257 · Cited by 23

Cyclin-Dependent Kinase-Dependent Phosphorylation of Sox2 at Serine 39 Regulates Neurogenesis

Lim, S., Bhinge, A., Alonso, S. B., Aksoy, I., Aprea, J., Cheok, C. F., Calegari, F., Stanton, L. W., & Kaldis, P. (2017) · Molecular and Cellular Biology · doi:10.1128/mcb.00201-17 · Cited by 24

Who's your daddy? Behavioral and epigenetic consequences of paternal drug exposure

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Phf21b imprints the spatiotemporal epigenetic switch essential for neural stem cell differentiationPreprint

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Lack of placental neurosteroid alters cortical development and female somatosensory function

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The disarrayed mutation results in cell cycle and neurogenesis defects during retinal development in zebrafish

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Terminal differentiation of adult hippocampal progenitor cells is a step functionally dissociable from proliferation and is controlled by Tis21, Id3 and NeuroD2

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Control of cerebral size and thickness

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miR‐30c and semaphorin 3A determine adult neurogenesis by regulating proliferation and differentiation of stem cells in the subventricular zones of mouse

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Neurogenesis of the spiral ganglion cells in the cochlea requires the transcriptional cofactor TIS21

Yamada, T., Minoda, R., Miwa, T., Ise, M., Takeda, H., & Yumoto, E. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.10.001 · Cited by 19

Formula G1: Cell cycle in the driver's seat of stem cell fate determination

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Role of FOXC1 in regulating APSCs self-renewal via STI-1/PrPC signaling

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Nonselective Sister Chromatid Segregation in Mouse Embryonic Neocortical Precursor Cells

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Bi-modal reprogramming of cell cycle by MiRNA-4673 amplifies human neurogenic capacity

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Stemming out of a new PML era?

Salomoni, P. (2009) · Cell Death and Differentiation · doi:10.1038/cdd.2009.63 · Cited by 19

Growth rate controls the sensitivity of gene regulatory circuits

Julou, T., Gervais, T., de Groot, D. H., & van Nimwegen, E. (2025) · Science Advances · doi:10.1126/sciadv.adu9279 · Cited by 16

Cyclin D1 acts as a barrier to pluripotent reprogramming by promoting neural progenitor fate commitment

Chen, C.-L., Wang, L.-J., Yan, Y., Hsu, H.-W., Su, H., Chang, F., Hsieh, P. C. H., Hwang, S., & Shen, C. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.08.039 · Cited by 18

A Branching Process to Characterize the Dynamics of Stem Cell Differentiation

Míguez, D. G. (2015) · Scientific Reports · doi:10.1038/srep13265 · Cited by 18

Enhanced Abventricular Proliferation Compensates Cell Death in the Embryonic Cerebral Cortex

Freret-Hodara, B., Cui, Y., Griveau, A., Vigier, L., Arai, Y., Touboul, J., & Pierani, A. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw264 · Cited by 20

An epigenetic circuit controls neurogenic programs during neocortex development

Wang, A., Wang, J., Tian, K., Huo, D., Ye, H., Li, S., Zhao, C. N., Zhang, B., Zheng, Y., Xu, L., et al. (2021) · Development · doi:10.1242/dev.199772 · Cited by 18

Choosing Cell Fate Through a Dynamic Cell Cycle

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Ablation of cdk4 and cdk6 affects proliferation of basal progenitor cells in the developing dorsal and ventral forebrain

Grison, A., Gaiser, C., Bieder, A., Baranek, C., & Atanasoski, S. (2018) · Developmental Neurobiology · doi:10.1002/dneu.22588 · Cited by 16

Histone Deacetylase Inhibition Mediates Urocortin‐Induced Antiproliferation and Neuronal Differentiation in Neural Stem Cells

Huang, H., Liu, D. D., Chang, H., Chen, W.-F., Hsu, H., Kuo, J., & Wang, M.-J. (2012) · Stem Cells · doi:10.1002/stem.1226 · Cited by 17

Self‐Organization and Pattern Formation in Primate Cortical Networks

Kennedy, H., Douglas, R. J., Kenneth Knoblauch, B., & Dehay, C. (2008) · Novartis Foundation symposium · doi:10.1002/9780470994030.ch13 · Cited by 17

Cytokinetics of adult rat SVZ after EAE

Sajad, M., Chawla, R., Zargan, J., Umar, S., Sadaqat, M., & Khan, H. A. (2010) · Brain Research · doi:10.1016/j.brainres.2010.11.050 · Cited by 16

Induction of Excess Centrosomes in Neural Progenitor Cells during the Development of Radiation-Induced Microcephaly

Shimada, M., Matsuzaki, F., Kato, A., Kobayashi, J., Matsumoto, T., & Komatsu, K. (2016) · PLoS ONE · doi:10.1371/journal.pone.0158236 · Cited by 16

Genetic Influences on the Amount of Cell Death in the Neural Tube of BXD Mice Exposed to Acute Ethanol at Midgestation

Théberge, E. T., Baker, J. A., Dubose, C., Boyle, J. K., Balce, K., Goldowitz, D., & Hamre, K. M. (2018) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13947 · Cited by 15

Modeling glioma intratumoral heterogeneity with primary human neural stem and progenitor cells

Liu, D. D., Liu, D. D., Eastman, A. E., Womack, N. L., Ohene-Gambill, B. F., Baez, M., & Weissman, I. L. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102597 · Cited by 14

Population Dynamics and Neuronal Polyploidy in the Developing Neocortex

Jungas, T., Joseph, M., Fawal, M.-A., & Davy, A. (2020) · Cerebral Cortex Communications · doi:10.1093/texcom/tgaa063 · Cited by 15

Autism-associated CHD8 keeps proliferation of human neural progenitors in check by lengthening the G1 phase of the cell cycle

Coakley-Youngs, E., Shorter, S. A., Ranatunga, M., Richardson, S., Getti, G., & Fivaz, M. L. (2022) · Biology Open · doi:10.1242/bio.058941 · Cited by 15

In vitrolocalization of human neural stem cell neurogenesis by engineered FGF-2 gradients

Keenan, T. M., Grinager, J. R., Procak, A. A., & Svendsen, C. N. (2012) · Integrative Biology · doi:10.1039/c2ib20074k · Cited by 14

Pax6 Lengthens G1 Phase and Decreases Oscillating Cdk6 Levels in Murine Embryonic Cortical Progenitors

Mi, D., Manuel, M. N., Huang, Y.-T., Mason, J. O., & Price, D. J. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00419 · Cited by 13

Cortical Development and Brain Malformations: Insights From the Differential Regulation of Early Events of DNA Replication

Kalogeropoulou, A., Lygerou, Z., & Taraviras, S. L. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00029 · Cited by 14

Different neural crest populations exhibit diverse proliferative behaviors

Gonsalvez, D. G., Li‐Yuen‐Fong, M., Cane, K. N., Stamp, L. A., Young, H. M., & Anderson, C. R. (2014) · Developmental Neurobiology · doi:10.1002/dneu.22229 · Cited by 13

Non-uniform temporal scaling of developmental processes in the mammalian cortex

Paolino, A., Haines, E., Bailey, E., Black, D. A., Moey, C., García‐Moreno, F., Richards, L. J., Suárez, R., & Fenlon, L. R. (2023) · Nature Communications · doi:10.1038/s41467-023-41652-5 · Cited by 13

Replication Protein A Links Cell Cycle Progression and the Onset of Neurogenesis inDrosophilaOptic Lobe Development

Zhou, L., & Luo, H. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3357-12.2013 · Cited by 13

The art of lineage tracing: From worm to human

García‐Marqués, J., Espinosa-Medina, I., & Lee, T. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101966 · Cited by 13

Cell cycle regulation and interneuron production

Ross, M. E. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20823 · Cited by 13

Specification of Cortical Projection Neurons

MacDonald, J. L., Fame, R. M., Azim, E., Shnider, S. J., Molyneaux, B. J., Arlotta, P., & Macklis, J. D. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00098-8 · Cited by 14

The impact of TP53 activation and apoptosis in primary hereditary microcephaly

Iegiani, G., Ferraro, A., Pallavicini, G., & Cunto, F. D. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1220010 · Cited by 12

Toward a better understanding of how a gyrified brain develops

Barresi, M., Hickmott, R. A., Bosakhar, A., Quezada, S., Quigley, A. F., Kawasaki, H., Walker, D. W., & Tolcos, M. (2024) · Cerebral Cortex · doi:10.1093/cercor/bhae055 · Cited by 12

MiR-92b-3p inhibits proliferation and migration of C2C12 cells

Ye, Z., Shi, J. Y., Ning, Z., Hou, L., Hu, C. Y., & Wang, C. (2020) · Cell Cycle · doi:10.1080/15384101.2020.1827511 · Cited by 12

A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture

Romero, D. M., Zaidi, D., Cifuentes-Díaz, C., Maillard, C., Grannec, G., Selloum, M., Birling, M., Bahi‐Buisson, N., & Francis, F. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106085 · Cited by 12

Cell cycle activity of neural precursors in the diseased mammalian brain

Alonso, S. B., Schulze-Steikow, M., & Calegari, F. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00039 · Cited by 11

Notch Activation by Shootin1 Opposing Activities on 2 Ubiquitin Ligases

Sapir, T., Levy, T., Kozer, N., Shin, I., Zamor, V., Haffner‐Krausz, R., McGlade, J. C., & Reiner, O. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx180 · Cited by 13

Control of tissue development and cell diversity by cell cycle-dependent transcriptional filtering

Chakra, M. A., Isserlin, R., Tran, T. N., & Bader, G. D. (2021) · eLife · doi:10.7554/elife.64951 · Cited by 11

Modelling cell turnover in a complex tissue during development

Lefevre, J., Marshall, D. J., Combes, A. N., Ju, A. L., Little, M. H., & Hamilton, N. (2013) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2013.08.033 · Cited by 11

The influence of immunosuppressive drugs on neural stem/progenitor cell fate in vitro

Skardelly, M., Glien, A., Groba, C., Schlichting, N. S., Kamprad, M., Meixensberger, J., & Milošević, J. (2013) · Experimental Cell Research · doi:10.1016/j.yexcr.2013.08.025 · Cited by 11

Developmental changes in interkinetic nuclear migration dynamics with respect to cell‐cycle progression in the mouse cerebral cortex ventricular zone

Fousse, J., Gautier, E., Patti, D., & Dehay, C. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24641 · Cited by 10

Dlx5 and Dlx6 can antagonize cell division at the G1/S checkpoint

MacKenzie, R. K., Sankar, P. R., & Bendall, A. J. (2019) · BMC Molecular and Cell Biology · doi:10.1186/s12860-019-0191-6 · Cited by 10

Glyphosate‐based herbicide induces long‐lasting impairment in neuronal and glial differentiation

Reis, L. T. C., Raciti, M., Rodriguez, P. G., Joseph, B., Rayyes, I. A., Uhlén, P., Falk, A., Lima, S. T. D. C., & Ceccatelli, S. (2022) · Environmental Toxicology · doi:10.1002/tox.23549 · Cited by 9

Seeing beyond the average cell: branching process models of cell proliferation, differentiation, and death during mouse brain development

MacMillan, H. R., & McConnell, M. J. (2010) · Theory in Biosciences · doi:10.1007/s12064-010-0107-7 · Cited by 9

An anxiogenic drug, FG 7142, induced an increase in mRNA of Btg2 and Adamts1 in the hippocampus of adult mice

Kurumaji, A., & Nishikawa, T. (2012) · Behavioral and Brain Functions · doi:10.1186/1744-9081-8-43 · Cited by 10

A Bromodeoxyuridine (BrdU) Based Protocol for Characterizing Proliferating Progenitors in Xenopus Embryos

Auger, H., Thuret, R., Yakoubi, W. E., & Papalopulu, N. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-992-1_26 · Cited by 10

Piriform cortex alterations in the Ts65Dn model for down syndrome

Carbonell, J., Blasco‐Ibáñez, J. M., Crespo, C., Nácher, J., & Varea, E. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147031 · Cited by 9

PDK1 regulates the lengthening of G1 phase to balance RGC proliferation and differentiation during cortical neurogenesis

Han, X., Wei, Y., Ba, R., Sun, L., & Zhao, C. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab428 · Cited by 8

Specification of cortical projection neurons

Özkan, A., MacDonald, J. L., Fame, R. M., Itoh, Y., Peter, M., Durak, O., & Macklis, J. D. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00019-9 · Cited by 9

Catecholaminergic Innervation of Periventricular Neurogenic Regions of the Developing Mouse Brain

Fauser, M., Weselek, G., Hauptmann, C., Markert, F., Gerlach, M., Hermann, A., & Storch, A. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.558435 · Cited by 10

RB: An essential player in adult neurogenesis

Fong, B. C., & Slack, R. S. (2017) · Neurogenesis · doi:10.1080/23262133.2016.1270382 · Cited by 8

Orchestrating human neocortex development across the scales; from micro to macro

Massimo, M., & Long, K. R. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.09.007 · Cited by 6

Intrinsic neural stem cell properties define brain hypersensitivity to genotoxic stress

Kalogeropoulou, A., Mougkogianni, M., Iliadou, M., Nikolopoulou, E., Flordelis, S., Κανέλλου, Α., Arbi, M., Nikou, S., Nieminuszczy, J., Niedźwiedź, W., et al. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2022.04.018 · Cited by 7

SP8 Transcriptional Regulation of Cyclin D1 During Mouse Early Corticogenesis

Borello, U., Berarducci, B., Delahaye, E., Price, D. J., & Dehay, C. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00119 · Cited by 6

In Vivo Assessment of Neural Precursor Cell Cycle Kinetics in the Amphibian RetinaPreprint

Locker, M., & Perron, M. (2019) · Cold Spring Harbor Protocols · doi:10.1101/pdb.prot105536 · Cited by 7

Defective Neural Stem and Progenitor Cell Proliferation in Neurodevelopmental Disorders

Shigenaka, A., Nitta, E., Nakagawa, T., Nakagawa, M., & Hosoi, T. (2025) · Journal of Developmental Biology · doi:10.3390/jdb13040040 · Cited by 8

The Phylotypic Brain of Vertebrates, from Neural Tube Closure to Brain Diversification

Senovilla-Ganzo, R., & García‐Moreno, F. (2024) · Brain Behavior and Evolution · doi:10.1159/000537748 · Cited by 6

Learning about cell lineage, cellular diversity and evolution of the human brain through stem cell models

Bail, R. L., Bonafina, A., Espuny-Camacho, I., & Nguyen, L. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.10.018 · Cited by 6

Bacterial TLR2/6 Ligands Block Ciliogenesis, Derepress Hedgehog Signaling, and Expand the Neocortex

Mann, B., Crawford, J. C., Reddy, K., Lott, J., Youn, Y. H., Gao, G., Guy, C. S., Chou, C., Darnell, D., Trivedi, S., et al. (2023) · mBio · doi:10.1128/mbio.00510-23 · Cited by 6

Mapping neurogenesis onset in the optic tectum of Xenopus laevis

Herrgen, L., & Akerman, C. J. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22393 · Cited by 6

Plasticity in oligodendrocyte lineage progression: An OPC puzzle on our nerves

Craig, G. A., Yoo, S., D'Araujo, T. Y., & Xiao, J. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14845 · Cited by 6

Isolation, culture optimization and functional characterization of stem cell neurospheres from mouse neonatal olfactory bulb and epithelium

Minovi, A., Aguado, A., Brunert, D., Kurtenbach, S., Dazert, S., Hatt, H. H., & Conrad, H. (2017) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/s00405-017-4590-z · Cited by 6

FGF2 modulates simultaneously the mode, the rate of division and the growth fraction in cultures of radial glia

Ledesma-Terrón, M., Peralta-Cañadas, N., & Míguez, D. G. (2020) · Development · doi:10.1242/dev.189712 · Cited by 6

Cell types and clonal relations in the mouse brain revealed by single-cell and spatial transcriptomicsPreprint

Ratz, M., von Berlin, L., Larsson, L., Martin, M., Westholm, J. O., Manno, G. L., Lundeberg, J., & Frisén, J. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.31.458418 · Cited by 6

Spatiotemporal transcriptome at single-cell resolution reveals key radial glial cell population in axolotl telencephalon development and regenerationPreprint

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The microcephaly-associated transcriptional regulator AUTS2 cooperates with Polycomb complex PRC2 to produce upper-layer neurons in mice

Shimaoka, K., Hori, K., Miyashita, S., Inoue, Y., Tabe, N. K. N., Sakamoto, A., Hasegawa, I., Nishitani, K., Yamashiro, K., Egusa, S. F., et al. (2025) · The EMBO Journal · doi:10.1038/s44318-024-00343-7 · Cited by 5

Monitoring Neurogenesis in the Cerebral Cortex: an Update

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PAR3 restricts the expansion of neural precursor cells by regulating hedgehog signaling

Hirose, T., Sugitani, Y., Kurihara, H., Kazama, H., Kusaka, C., Noda, T., Takahashi, H., & Ohno, S. (2022) · Development · doi:10.1242/dev.199931 · Cited by 4

Multipotent neurogenic fate of mesenchymal stem cell is determined by Cdk4-mediated hypophosphorylation of Smad-STAT3

Kim, D. Y., Lee, J., Kang, D., Lee, D., Kim, Y.-J., Hwang, S., Kim, D.-I., Lee, C., & Lee, K.-H. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1188230 · Cited by 5

Expression of the neural specific protein, GAP‐43, dramatically lengthens the cell cycle in fibroblasts

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Revealing the Impact of Mitochondrial Fitness During Early Neural Development Using Human Brain Organoids

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SETD1A regulates psychiatric gene networks involved in genomic stability and synaptic function in rare and sporadic schizophrenia

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Region-specific mechanisms of brain growth during mouse development

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Reduction of the Cell Cycle Length by Decreasing G1 Phase and Cell Cycle Reentry Expand Neuronal Progenitor Cells in the Subventricular Zone of Adult Rat after Stroke

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