The DOI matches its Crossref record; 170 of the 170 references it cites were found in a registry or an index.
Cell-cycle control and cortical development
Abstract
The spatio-temporal timing of the last round of mitosis, followed by the migration of neuroblasts to the cortical plate leads to the formation of the six-layered cortex that is subdivided into functionally defined cortical areas. Whereas many of the cellular and molecular mechanisms have been established in rodents, there are a number of unique features that require further elucidation in primates. Recent findings both in rodents and in primates indicate that regulation of the cell cycle, specifically of the G1 phase has a crucial role in controlling area-specific rates of neuron production and the generation of cytoarchitectonic maps.
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“oRGs are present in large numbers in gyrencephalic primates22,23,40–44 and are considered pivotal to the evolutionary increase in human cortex size and complexity45,46.”
From The use of brain organoids to investigate neural development and disease (2017) · cites this paper as [43]
In the citing paper
“Interestingly, G1/S transition rates might be associated with these cell decisions as symmetric divisions can have shorter G1/S transition times than asymmetric divisions [93, 101].”
From The ASD Living Biology: from cell proliferation to clinical phenotype (2019) · cites this paper as [93]
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“…and time lapse imaging studies of brain slices indicated that the percentage of G1-phase AP cells increases during mammalian neuronal development (Takahashi et al. 1994, 1995; Calegari & Huttner 2003; Dehay & Kennedy 2007; Lange & Calegari 2010; Salomoni & Calegari 2010; Betizeau et al. 2013).”
BackgroundMechanisms of Cortical Differentiation
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Mcl1 regulates the terminal mitosis of neural precursor cells in the mammalian brain through p27Kip1
Hasan, S. M. M., Sheen, A. D., Power, A. M., Langevin, L. M., Xiong, J., Furlong, M., Day, K., Schuurmans, C., Opferman, J. T., & Vanderluit, J. L. (2013) · Development · doi:10.1242/dev.090910 · Cited by 29
“As a result, the location of a cell along the apical-basal axis provides information on its proliferation status (Dehay and Kennedy, 2007; Götz and Huttner, 2005; Takahashi and Liu, 2006).”
BackgroundMicroRNA-182 Regulates Neurite Outgrowth Involving the PTEN/AKT Pathway
Wang, W. M., Lü, G., Su, X. W., Lyu, H., & Poon, W. S. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00096 · Cited by 31
“Keywords: microRNA-182, axon outgrowth, dendrite, AKT, BCAT2 INTRODUCTION During brain development, neurons are generated in the ventricular zone and subventricular zone (SVZ) (Dehay and Kennedy, 2007).”
BackgroundInfluentialKim, S. N., Viswanadham, V., Doan, R. N., Dou, Y., Bizzotto, S., Khoshkhoo, S., Huang, A. Y., Yeh, R. C., Chhouk, B. H., Truong, A., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.06.565899 · Cited by 29
“…observations in non-human primates of a higher density of neurons in adult primary compared to secondary visual cortex (Collins et al., 2010; Dehay and Kennedy, 2007; Rockel et al., 1980) and constrained radial migration across the border during development (Li et al., 2012; Ohtsuki et al.,…”
A role for the serotonin 2A receptor in the expansion and functioning of human transmodal cortex
Luppi, A. I., Girn, M., Rosas, F. E., Timmermann, C., Roseman, L., Erritzøe, D., Nutt, D., Stamatakis, E. A., Spreng, R. N., Xing, L., et al. (2023) · Brain · doi:10.1093/brain/awad311 · Cited by 31
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A common mechanism for microcephaly
Wollnik, B. (2010) · Nature Genetics · doi:10.1038/ng1110-923 · Cited by 28
Jiang, S., Li, X., Jin, W., Duan, X., Bo, L., Jiang-li, W., Zhang, R., Wang, Y., Kang, R., & Huang, L. (2018) · Neuroscience Letters · doi:10.1016/j.neulet.2018.02.051 · Cited by 27
Xu, X., Chini, M., Bitzenhofer, S. H., & Hanganu‐Opatz, I. L. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2170-18.2018 · Cited by 28
“The cerebral cortex emerges as the result of complex developmental processes, such as neurogenesis, neuronal migration, and differentiation (Rakic, 1988; Dehay and Kennedy, 2007).”
BackgroundNCAM regulates temporal specification of neural progenitor cells via profilin2 during corticogenesis
Huang, R., Yuan, D., Li, S., Liang, X.-S., Gao, Y., Lan, X., Qin, H., Ma, Y., Xu, G., Schachner, M., et al. (2019) · The Journal of Cell Biology · doi:10.1083/jcb.201902164 · Cited by 29
“83 Regulation of the cell cycle plays a crucial role in controlling temporal and spatial 84 production of neural cells (Dehay and Kennedy, 2007; Politis et al., 2008).”
BackgroundWu, X., Gu, X., Han, X., Du, A., Jiang, Y., Zhang, X., Wang, Y., Cao, G., & Zhao, C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2549-13.2014 · Cited by 27
“…AP self-renewal and the transition to BPs The progenitor cell decision to undergo self-renewal or differentiation is one of the key programs in neurogenesis (Calegari et al., 2005; Dehay and Kennedy, 2007; Fietz and Huttner, 2011), and both INM and the cell cycle are involved in this process.”
BackgroundMaternal-fetal unit interactions and eutherian neocortical development and evolution
Montiel, J. F., Kaune, H., & Maliqueo, M. A. (2013) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00022 · Cited by 27
Diffusion MR Microscopy of Cortical Development in the Mouse Embryo
Aggarwal, M., Gobius, I., Richards, L. J., & Mori, S. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu006 · Cited by 28
“Keywords: cortex, development, diffusion MRI, microimaging, mouse embryo”
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“…cell cycle exit and differentiation in the CNS; however, whether the cell cycle kinetics are the cause or consequence of neuronal progenitor fate decisions is still debated (Gotz and Huttner, 2005; Dehay and Kennedy, 2007; Wilcock et al., 2007; Lange and Calegari, 2010; Arai et al., 2011).”
BackgroundFame, R. M., Dehay, C., Kennedy, H., & Macklis, J. D. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw023 · Cited by 27
Self-citationPodmirseg, S. R., Jäkel, H., Ranches, G., Kullmann, M. K., Sohm, B., Villunger, A., Lindner, H. H., & Hengst, L. (2016) · Oncogene · doi:10.1038/onc.2015.524 · Cited by 27
“As caspases fulfil non-lethal roles in neuron cell differentiation 28, 73, 77 , processing of p27 during neuronal development could be an important regulatory mechanism to mediate a robust cell cycle exit as well as trigger cytoskeletal remodelling.”
Vancamp, P., Deprez, M.-A., Remmerie, M., & Darras, V. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1917-17.2017 · Cited by 26
“While this initially favors neuroblast production, it probably quickly exhausts the progenitor cell pool, resulting in a hypoplastic cortex (Dehay and Kennedy, 2007).”
BackgroundDifferential function of NBS1 and ATR in neurogenesis
Zhou, Z., Bruhn, C., & Wang, Z. (2011) · DNA repair · doi:10.1016/j.dnarep.2011.10.021 · Cited by 26
RhoG Promotes Neural Progenitor Cell Proliferation in Mouse Cerebral Cortex
Fujimoto, S., Negishi, M., & Katoh, H. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-03-0200 · Cited by 26
“…cortical development, the VZ is abundant in neural progenitor cells (NPCs), whose proliferative activity is spatially and temporally controlled by various molecules including cell cycle regulators, transcription factors, and extracellular factors (Götz and Huttner, 2005; Dehay and Kennedy, 2007).”
BackgroundAbdullah, A. I., Zhang, H., Nie, Y., Tang, W., & Sun, T. (2016) · Stem Cell Reports · doi:10.1016/j.stemcr.2016.06.005 · Cited by 29
“Lengthening of the NP cell cycle is thought to be one of the major factors regulating this switch (Dehay and Kennedy, 2007).”
BackgroundEnhancing our brains: Genomic mechanisms underlying cortical evolution
Mitchell, C., & Silver, D. L. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.08.045 · Cited by 28
“Moreover progenitor cell cycle is distinct amongst humans, non-human primates and rodents [5,15,23,24], and diverse across cortical areas [25].”
Saito, K., Mizuguchi, K., Hamabe‐Horiike, T., Duong, T. A. D., Shinmyo, Y., & Kawasaki, H. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy312 · Cited by 26
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Maturin is a novel protein required for differentiation during primary neurogenesis
Luna, R. I. M., Ku, R. Y., Lyou, Y., & Zuber, M. E. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.09.028 · Cited by 26
“Keywords Pak3; primary neurogenesis; neuronal differentiation; neural plate Introduction Normal neural development requires a precise balance of proliferation and differentiation (Dehay and Kennedy, 2007; Donovan and Dyer, 2005; Salomoni and Calegari, 2010).”
BackgroundKomada, M., Iguchi, T., Takeda, T., Ishibashi, M., & Sato, M. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.05.006 · Cited by 27
“More recently, the regulation of the development of the intermediate progenitor cells (IPCs) of the cortex via Shh activity has attracted attention because IPCs are important for brain evolution: IPCs give birth to the majority of layer II/III neurons, and the number of layer II/III neurons increases as the brain evol…”
BackgroundCoordination of proliferation and neuronal differentiation by the retinoblastoma protein family
Ajioka, I. (2014) · Development Growth & Differentiation · doi:10.1111/dgd.12127 · Cited by 28
“For example, the Cip/Kip family of cyclin dependent kinase (Cdk) inhibitors was shown to regulate the timing of neuronal progenitor cell cycle exit, thereby contributing to the generation of different neuronal subtypes in the correct ratios (Dehay & Kennedy 2007).”
BackgroundZander, M. A., Burns, S. E., Yang, G., Kaplan, D. R., & Miller, F. D. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0370-14.2014 · Cited by 26
“Radial precursor nuclei move between the VZ and SVZ as they proliferate, and they undergo G2 and mitosis when they are most proximal to the apical VZ (Dehay and Kennedy, 2007; Salomoni and Calegari, 2010).”
BackgroundPicco, N., García‐Moreno, F., Maini, P. K., Woolley, T. E., & Molnár, Z. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy068 · Cited by 28
“Among the many factors determining the development of a normal cortex in mammalian species are: the size of the founder population present at the beginning of cortical neurogenesis, the length of neurogenesis, the dynamics of cell cycle length, the proportion of different cortical progenitor types, and the fine-tuned…”
BackgroundMethodInfluentialA distinct response to endogenous DNA damage in the development of Nbs1-deficient cortical neurons
Li, R., Yang, Y., Gao, Y., Wang, Z., & Tong, W. (2012) · Cell Research · doi:10.1038/cr.2012.3 · Cited by 26
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“Cerebral cortical excitatory neurons are generated from apical progenitors (radial glia cells), basal progenitors (intermediate progenitor cells), and outer radial glialike progenitors, with coupling to the cell cycle exit of these progenitors (Dehay and Kennedy, 2007; Guillemot et al., 2006; Kriegstein and Alvarez-Bu…”
BackgroundMinamide, R., Fujiwara, K., Hasegawa, K., & Yoshikawa, K. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084460 · Cited by 24
“Cell cycle regulators are expressed in the neocortex at early stages of mammalian development [2,3].”
BackgroundOkazawa, H. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.06.005 · Cited by 26
“The result was in reverse consistent with the concept that abnormal M phase affects asymmetrical cell division, increases neurogenesis from NSCs, and changes of thickness ratio among multiple cortical layers (Caviness et al., 2003; Cox et al., 2006; Dehay and Kennedy, 2007; Fietz and Huttner, 2011; Gotz and Huttner, 2…”
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How to keep proliferative neural stem/progenitor cells
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Genetic architecture of human brain evolution
Fair, T., & Pollen, A. A. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102710 · Cited by 24
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BackgroundSecondary loss of miR-3607 reduced cortical progenitor amplification during rodent evolution
Chinnappa, K., Cárdenas, A., Prieto‐Colomina, A., Villalba, A., Márquez-Galera, Á., Soler, R., Nomura, Y., Llorens, E., Tomasello, U., López‐Atalaya, J. P., et al. (2022) · Science Advances · doi:10.1126/sciadv.abj4010 · Cited by 22
“…progenitor cells increases massively during development, particularly bRGCs, and the SVZ becomes subdivided into inner SVZ (ISVZ) and outer SVZ (OSVZ) ( 3 , 12 – 16 ). bRGCs contribute critically to increase neurogenesis and to promote cerebral cortex growth and folding in these species ( 17 ).”
Niggl, E., Bouman, A., Briere, L. C., Hoogenboezem, R. M., Wallaard, I., Park, J., Admard, J., Wilke, M., Harris-Mostert, E. D. R. O., Elgersma, M., et al. (2023) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2023.07.005 · Cited by 24
Homman‐Ludiye, J. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00079 · Cited by 24
“(Smart et al., 2002; Lukaszewicz et al., 2005; Zecevic et al., 2005; Dehay and Kennedy, 2007; Bayatti et al., 2008; Martínez-Cerdeño et al., 2012).”
BackgroundGarcía-García, E., Pino-Barrio, M. J., López-Medina, L., & Martı́nez-Serrano, A. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-06-0524 · Cited by 22
“One is the rate of progression through the cell cycle (Dehay and Kennedy, 2007; Doe, 2008).”
BackgroundSelf-organization and interareal networks in the primate cortex
Kennedy, H., & Dehay, C. (2012) · Progress in brain research · doi:10.1016/b978-0-444-53860-4.00016-7 · Cited by 22
“As discussed above modulation of mode of division of cortical precursors has been implicated in determining cytoarchitecture via specifying the laminar thickness and hence arealisation (Dehay and Kennedy, 2007).”
InfluentialSelf-citationFBXL5 Inactivation in Mouse Brain Induces Aberrant Proliferation of Neural Stem Progenitor Cells
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MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis
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Phf21b imprints the spatiotemporal epigenetic switch essential for neural stem cell differentiationPreprint
Basu, A., Mestres, I., Sahu, S. K., Tiwari, N., Khongwir, B., Baumgart, J., Singh, A. P., Calegari, F., & Tiwari, V. K. (2020) · Genes & Development · doi:10.1101/gad.333906.119 · Cited by 24
“2A) very well fitted with the concept that a shorter G1 promotes the expansion of neural progenitors at the expense of neurogenic divisions (Dehay and Kennedy 2007; Lange and Calegari 2010; Salomoni and Calegari 2010).”
InfluentialChao, M., Chen, C., Yang, Y.-H., Chuang, Y.-C., Chu, T.-Y., & Tseng, C. (2016) · Scientific Reports · doi:10.1038/srep32373 · Cited by 22
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BackgroundMolecular investigations of the brain of higher mammals using gyrencephalic carnivore ferrets
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“…to uncover 4 the mechanisms regulating the differentiation and proliferation of neural progenitors in the cerebral cortex during development (Borrell and Reillo, 2012; Dehay and Kennedy, 2007; Fietz and Huttner, 2011; Hevner and Haydar, 2012; Lui et al., 2011; Molnar and Clowry, 2012; Rakic, 2009).”
BackgroundTheoretical Models of Neural Development
Goodhill, G. J. (2018) · iScience · doi:10.1016/j.isci.2018.09.017 · Cited by 19
“…of learning rules based on spike-timing-dependent plasticity (STDP; Dan and Poo (2006) and Markram et al. (2012)) have been extensively investigated (Morrison et al., 2008), including their potential role in visual map development (Song and Abbott, 2001; Wenisch et al., 2005) (Figures 5E and 5F).”
BackgroundCiliary resorption modulates G1length and cell cycle progression
Sung, C.-H., & Li, A. (2011) · Cell Cycle · doi:10.4161/cc.10.17.16943 · Cited by 21
Hanging by the tail: progenitor populations proliferate
Molnár, Z., Vasistha, N. A., & García‐Moreno, F. (2011) · Nature Neuroscience · doi:10.1038/nn.2817 · Cited by 23
Lombino, F. L., Muhia, M., Lopez‐Rojas, J., Brill, M. S., Thies, E., Ruschkies, L., Lutz, D., Richter, M., Hausrat, T. J., Lopes, A. T., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-52367-3 · Cited by 20
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“Interestingly, local regulation of cell cycle kinetics has been previously linked to the genesis of region-specific cortical cytoarchitectures [65].”
BackgroundControl of cerebral size and thickness
Tuoc, T., Pavlakis, E., Tylkowski, M. A., & Stoykova, A. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1590-7 · Cited by 25
“The delayed initiation of the asymmetric mode of Ne/RGCs division results in amplification of the progenitor pool [44].”
BackgroundDevelopment and evolution of cortical fields
Arai, Y., & Pierani, A. (2014) · Neuroscience Research · doi:10.1016/j.neures.2014.06.005 · Cited by 24
Zhang, H., Zhang, L., & Sun, T. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00044 · Cited by 21
“…precisely regulated proliferation, survival and differentiation of neural stem cells (NSCs) and neural progenitors (NPs) determine normal development of themammalian cerebral cortex (Dehay and Kennedy, 2007; Rakic, 2007, 2009; Aguirre et al., 2010; Delaunay et al., 2017; Subramanian et al., 2017).”
BackgroundNew Aspects of Axonal Structure and Function
Feldmeyer, D., & Lübke, J. H. R. (2010) · Springer eBooks · doi:10.1007/978-1-4419-1676-1 · Cited by 21
Abramowicz, I., Carpenter, G., Alfieri, M., Colnaghi, R., Outwin, E. A., Parent, P., Thauvin‐Robinet, C., Iaconis, D., Franco, B., & O’Driscoll, M. (2016) · Human Molecular Genetics · doi:10.1093/hmg/ddw364 · Cited by 19
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Cortical Organoids to Model Microcephaly
Farcy, S., Albert, A., Gressèns, P., Baffet, A. D., & Ghouzzi, V. E. (2022) · Cells · doi:10.3390/cells11142135 · Cited by 20
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
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“Indeed, starting at E11 in mice and E12 in rats, neuronal progenitors from the ventricular zone migrate towards the apical surface of the developing cortex (Dehay and Kennedy, 2007).”
BackgroundEvolutionary development of neural systems in vertebrates and beyond
O’Connell, L. A. (2013) · Journal of Neurogenetics · doi:10.3109/01677063.2013.789511 · Cited by 17
“Context-appropriate behavioral decisions are critical for an individual ’ s fi tness and are carried out by evaluating the salience of external stimuli and integrating this information with internal physiological cues.”
BackgroundThe Principle of Cortical Development and Evolution
Yang, Z. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01259-2 · Cited by 19
“In contrast to mice, non-human primate and human cortical RG cell cycles can be up to 44-63 hours, and the lengthening of cortical RG cell cycles is a well-documented feature of primates with larger brains [66, 120, 125–127].”
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
Requirement of Mouse BCCIP for Neural Development and Progenitor Proliferation
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“It derives from a germinal layer of the dorsal telencephalon at E11 and begins to form during mouse midembryogenesis [21,22].”
BackgroundGrison, A., Gaiser, C., Bieder, A., Baranek, C., & Atanasoski, S. (2018) · Developmental Neurobiology · doi:10.1002/dneu.22588 · Cited by 16
“The transitions through the mitotic phases are controlled by cyclincdk complexes, and the cell cycle dynamics are determined by the balance of positive (cyclins) and negative (cdk inhibitors) regulators (Dehay and Kennedy, 2007).”
BackgroundCortay, V., Delaunay, D., Patti, D., Gautier, E., Doerflinger, N., Giroud, P., Knoblauch, K., Huissoud, C., Kennedy, H., & Dehay, C. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.588814 · Cited by 17
“, 1995a,b), primate cortical neuron production is characterized by a late upsurge of proliferation of the outer subventricular zone (OSVZ) progenitors generating the SG layers (Lukaszewicz et al., 2005; Dehay and Kennedy, 2007; Hansen et al., 2010; Betizeau et al., 2013).”
BackgroundSelf-citationRole of NDE1 in the Development and Evolution of the Gyrified Cortex
Soto‐Perez, J., Baumgartner, M., & Kanadia, R. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.617513 · Cited by 17
“In gyrencephalic species, the oRGC pool is large enough to represent a distinct cellular layer of the developing cortex, known as the outer subventricular zone (OSVZ), which has been correlated with cortical complexity and folding (Dehay and Kennedy, 2007; Reillo et al., 2010; Borrell and Götz, 2014; Llinares-Benadero…”
BackgroundPrimate-specific RFPL1 gene controls cell-cycle progression through cyclin B1/Cdc2 degradation
Bonnefont, J., Laforge, T., Plastre, O., Beck, B., Sorce, S., Dehay, C., & Krause, K.-H. (2010) · Cell Death and Differentiation · doi:10.1038/cdd.2010.102 · Cited by 18
Self-citationChen, Y., Bian, S., Zhang, J., Zhang, H., Tang, B., & Sun, T. (2014) · Frontiers in Neurology · doi:10.3389/fneur.2014.00132 · Cited by 17
“The rate and timing of NP proliferation and differentiation are tightly regulated by various cell cycle regulators (11, 12).”
BackgroundHuang, 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
Zhang, J., Li, A., Sun, H., Xiong, X., Qin, S., Wang, P., Dai, L., Zhang, Z., Li, X., & Liu, Z. (2020) · Oncology Letters · doi:10.3892/ol.2020.12031 · Cited by 16
Temporal differences of neurodevelopment processes between species
Iwata, R. (2021) · Neuroscience Research · doi:10.1016/j.neures.2021.08.004 · Cited by 14
Drug Design of Cyclin-Dependent Kinase 2 Inhibitor for Melanoma from Traditional Chinese Medicine
Tang, H., & Chen, C. Y. (2014) · BioMed Research International · doi:10.1155/2014/798742 · Cited by 15
“Cyclin E-CDK2 complex guides the process from G1 to S phase, while cyclin A-CDK2 complex is required to pass through the S phase [6, 7].”
BackgroundA multiscale mathematical model of cell dynamics during neurogenesis in the mouse cerebral cortex
Postel, M., Karam, A., Pézeron, G., Schneider‐Maunoury, S., & Clément, F. (2019) · BMC Bioinformatics · doi:10.1186/s12859-019-3018-8 · Cited by 17
Expression pattern of Nav2 in the murine CNS with development
Pook, C., Ahrens, J. M., & Clagett‐Dame, M. (2020) · Gene Expression Patterns · doi:10.1016/j.gep.2020.119099 · Cited by 17
Martins, M., Galfrè, S. G., Terrigno, M., Pandolfini, L., Appolloni, I., Dunville, K., Marranci, A., Rizzo, M., Mercatanti, A., Poliseno, L., et al. (2021) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.04.020 · Cited by 16
“The evolution of the mammalian cortex is characterized by the progressive thickening of the supra-granular cell layer(s) (Dehay et al., 2015; Dehay and Kennedy, 2007).”
BackgroundThe Ups and Downs of Neural Progenitors: Cep120 and TACCs Control Interkinetic Nuclear Migration
Guerrier, S., & Polleux, F. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.019 · Cited by 16
“The SVZ first appears around E13, and increases progressively during mouse cortical neurogenesis relative to the ventricular zone (VZ) (reviewed by Dehay and Kennedy, 2007).”
BackgroundWong, C., Griffin, R. J., Hardcastle, I. R., Northen, J. S., Wang, L.-Z., & Golding, B. T. (2010) · Organic & Biomolecular Chemistry · doi:10.1039/b922717b · Cited by 16
Zhang, J., Ooi, J., Utami, K. H., Langley, S. R., Aning, O. A., Park, D. S., Renner, M., Ma, S., Cheok, C. F., Knoblich, J. A., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/850586 · Cited by 15
“The importance of cell cycle regulation in neural development is well established [41,42].”
Cephalopod retinal development shows vertebrate-like mechanisms of neurogenesis
Napoli, F. R., Daly, C. M. S., Neal, S., McCulloch, K. J., Zaloga, A. R., Liu, A., & Koenig, K. M. (2022) · Current Biology · doi:10.1016/j.cub.2022.10.027 · Cited by 16
Shukla, M., & Vincent, B. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230314142505 · Cited by 17
Differential changes in the cellular composition of the developing marsupial brain
Seelke, A. M. H., Dooley, J. C., & Krubitzer, L. A. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23301 · Cited by 15
“2616 The Journal of Comparative Neurology |Research in Systems Neuroscience been reported that the vast majority of cortical and subcortical neurons are generated in mice and rats (Dehay and Kennedy, 2007; Robinson and Dreher, 1990).”
BackgroundIdentification of MMP-2 as a novel enhancer of cerebellar granule cell proliferation
Verslegers, M., Hove, I. V., Buyens, T., Dekeyster, E., Knevels, E., & Moons, L. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.10.001 · Cited by 15
One progenitor to generate them all: new evidence for multi-fated neural progenitors
Ortiz-Álvarez, G., & Spassky, N. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.10.013 · Cited by 14
Ding, W.-H., Tian, H.-L., Yuan, F., Wang, R., Yang, D., Liu, Y., Ding, J., & Guo, Y. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.314316 · Cited by 15
“…correlated with cell cycle exit, as well as the neuronal differentiation of progenitor cells (Lukaszewicz et al., 2002); CEND1 is known to lengthen the G1/S transition of NSCs by downregulating cyclin D1 levels, thereby leading to enhanced neuronal differentiation (Dehay and Kennedy, 2007).”
Apical Polarization of SVCT2 in Apical Radial Glial Cells and Progenitors During Brain Development
Silva-Álvarez, C., Salazar, K., Cisternas, P., Martínez, F., Liour, S. S., Jara, N., Bertinat, R., & Nualart, F. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-0081-2 · Cited by 15
Chen, C., Wang, H.-W., You, L., Shang, R., & Liu, F.-C. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22293 · Cited by 15
“5 onward, the cortical projection neurons arising from the progenitors in the proliferative zones, namely the VZ and the subventricular zone (SVZ), migrate radially in an inside-out manner (for reviews, see Marin and Rubenstein, 2003; Dehay and Kennedy, 2007; Molyneaux et al., 2007).”
BackgroundArea Patterning of the Mammalian Cortex
O'Leary, D. D. M., Stocker, A. M., & Zembrzycki, A. (2013) · Patterning and Cell Type Specification in the Developing CNS and PNS · doi:10.1016/b978-0-12-397265-1.00021-6 · Cited by 14
Manansala, M., Min, S., & Cleary, M. D. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.01.025 · Cited by 14
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
“E cyclins are turned on in late G1 and together with their cognate cyclin-dependent kinase cdk2 regulate G1/S checkpoint transition in ESCs (Neganova et al., 2009, 2011) and cortical progenitors (Delalle et al., 1999; Lukaszewicz et al., 2005; Watanabe et al., 2015).”
BackgroundEmbryonic stem cells in non-human primates: An overview of neural differentiation potential
Wianny, F., Bourillot, P.-Y., & Dehay, C. (2011) · Differentiation · doi:10.1016/j.diff.2011.01.008 · Cited by 14
“Indeed, monkey brain development show features that are very specific to primates (Dehay and Kennedy, 2007), and cannot be studied in the mouse.”
BackgroundSelf-citationSculpting Cerebral Cortex with Serotonin in Rodent and Primate
Vitalis, T., & Verney, C. (2017) · InTech eBooks · doi:10.5772/intechopen.69000 · Cited by 14
“A, is adapted from [20] and B is adapted from [13, 14, 79].”
MethodChen, X., Chanda, A., Ikeuchi, Y., Zhang, X., Goodman, J. V., Reddy, N. C., Majidi, S. P., Wu, D. Y., Smith, S. E., Godec, A., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0688-18.2018 · Cited by 14
“Control of neuronal precursor cell proliferation is essential for normal brain development, and abnormalities of this process cause neurological diseases (Dehay and Kennedy, 2007).”
BackgroundMora‐Bermúdez, F., Taverna, E., & Huttner, W. Β. (2021) · FEBS Journal · doi:10.1111/febs.15793 · Cited by 14
“This shorter cell cycle is primarily due to a shorter G1 [38,39].”
The Role of Human-Specific Gene Duplications During Brain Development and Evolution
Sassa, T. (2013) · Journal of Neurogenetics · doi:10.3109/01677063.2013.789512 · Cited by 15
“In the human brain, the postmitotic neurons have to travel a longer distance before reaching the fi nal destination, as the neocortex is substantially thicker than in nonhuman primates or rodents (Dehay & Kennedy, 2007; Rakic, 2009; Sidman & Rakic, 1973).”
Background
Metadata
- Authors
- Dehay, C., & Kennedy, H.
- Affiliations
- Lyon 1 Université (FR)
- Corresponding author
- Dehay, Colette
- Venue
- Nature Reviews Neuroscience
- Published
- 2007-06
- Volume
- 8
- Issue
- 6
- Pages
- 438-450
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2010852678
- Cited by
- 655
- References
- 170
- Citations by year
- 2026: 9 · 2025: 15 · 2024: 17 · 2023: 28 · 2022: 18 · 2021: 30 · 2020: 39 · 2019: 30 · 2018: 47 · 2017: 36 · 2016: 39 · 2015: 34 · 2014: 61 · 2013: 52 · 2012: 47
- FWCI
- 3.18
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- 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 › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- cortical development, cell cycle regulation, G1 phase, neuronal proliferation, neuronal differentiation, neuroblast migration, cortical plate, cortical lamination, cortical regions, cytoarchitecture, primate cortex, rodent cortex
- MeSH terms
- Animals, Cell Communication, Cell Cycle, Cell Differentiation, Cerebral Cortex, Humans, Neurons, Stem Cells, Signal Transduction, G1 Phase, Cell Cycle Proteins, Cell Proliferation
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