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]
Citations
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Research works printed but not linked: 2
- Polleux, F., Dehay, C. & Kennedy, H. Gradients and timing of the arrival of thalamic axons in the mouse neocortex. Soc. Neurosci. Abstr. 22, 1012 (1996).
- Kennedy, H., Douglas, R. J., Knoblauch, K. & Dehay, C. Self-organization and pattern formation in cortical networks in the primate. Novartis Found. Symp. in the press.
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“Moreover, IPCs are largely absent in the reptile cortex, which lacks the neuron-abundant upper layers (Cheung et al , 2007, 2010), whereas primates typically display an expanded SVZ that produces massive numbers of IPCs and upper layer neurons (Dehay & Kennedy, 2007; Thor, 2024).”
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“In mouse retina, the main representative p27/Kip1 is expressed throughout retinogenesis in cells that exit the cell cycle and differentiate (Dehay and Kennedy, 2007).”
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“…Figure 8 : Expression et cibles des gènes du locus INK4-Arf (d'après Sherr and Roberts, 1995) ..........................36 Figure 9 : Rôle des inhibiteurs du cycle cellulaire CIP/KIP et INK (d'après Dehay and Kennedy, 2007) ................37 Figure 10.”
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“…and notably bRG ( 14 , 20 ); lower diversity and proliferative potential of progenitors in the oSVZ ( 22 , 23 ); a bias toward neurogenic versus self-renewing divisions ( 17 , 24 ); and differences in progenitor cell-cycle dynamics, such as longer G 1 or reduced proliferative capacity ( 25 , 26 ).”
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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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