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

By T. Miyata, A. Kawaguchi, Kanako Saito, Masako Kawano, T. Muto, M. Ogawa. Development, 2004

793 citations recorded by the source corpus.

Subfields: Cell Biology, Developmental Neuroscience, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/cc148767879122f5128934ee3f844466c7d86cbb

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Citations in the corpus

The cell biology of neurogenesis: toward an understanding of the development and evolution of the neocortex. (2014, background): “…progenitors, and the related transit amplifying progenitors (Betizeau et al. 2013, Fietz et al. 2010, Hansen et al. 2010, Haubensak et al. 2004, Miyata et al. 2004, Noctor et al. 2004, Reillo et al. 2011, Reillo & Borrell 2012, Shitamukai et al. 2011, Wang et al. 2011); (c) for SAPs, bipolar…”
Essential Roles of Notch Signaling in Maintenance of Neural Stem Cells in Developing and Adult Brains (2010, background): “In the embryonic brain, radial glial cells sequentially give rise to distinct types of neurons or basal progenitors (Rakic, 1995; Haubensak et al., 2004; Miyata et al., 2004; Noctor et al., 2004), and finally differentiate into astrocytes.”
Pax6, Tbr2, and Tbr1 Are Expressed Sequentially by Radial Glia, Intermediate Progenitor Cells, and Postmitotic Neurons in Developing Neocortex (2005, background): “The only discrepancy was that, in contrast to IPCs (Miyata et al., 2004; Noctor et al., 2004), most Tbr2 cells did not appear to express nestin (Fig.”
Tumorigenesis in the brain: location, location, location. (2007, background): “In this regard, studies in which the fate of specific RG populations are traced genetically in vivo (11), ex vivo studies of RG differentiation (12), and live time-lapse video microscopy studies (13) collectively suggest that dorsal and ventral telencephalic RG Requests for reprints: David H.”
Development and Evolution of the Human Neocortex (2011, positive): “Directly after RG cell division, both daughter cells startwith the sameground state ofNotchactivity and still possess neuroepithelial cell-cell interactions,having short apical fibers that contact the ventricle (Miyata et al., 2004).”
The Glial Nature of Embryonic and Adult Neural Stem Cells (2009, background): “…RG cells, which predominantly divide asymmetrically during the period of peak neurogenesis, nIPCs undergo symmetrical divisions to produce two neurons or may divide symmetrically to produce two additional IPCs (Haubensak et al. 2004; Miyata et al. 2004; Noctor et al. 2004, 2007; Wu et al. 2005).”
Visualizing spatiotemporal dynamics of multicellular cell-cycle progression. (2008, background): “In addition, exposure of slices to 40% oxygen, instead of the usual 20%, has significantly improved cell proliferation, differentiation, and migration during imaging experiments (Miyata et al., 2002, 2004).”
Neuronal subtype specification in the cerebral cortex (2007, background): “More recently, elegant studies in slice culture have shown that radial glia frequently undergo an asymmetric division to generate an intermediate progenitor, which then migrates into the SVZ before pausing and undergoing a symmetric round of cell division to produce two neuron”
Neural progenitors, neurogenesis and the evolution of the neocortex (2014, background): “4), the prevailing outputs of aRG differentiative divisions are neurogenic IPs (aIPs, neurogenic bIPs), which divide symmetrically yielding two neurons, i.e. the most frequent lineage path is aRG→neurogenic IP→neuron (Haubensak et al., 2004;Miyata et al., 2004;Noctoret al., 2004;Konno et al., 2008; ”