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Morphological and functional aspects of progenitors perturbed in cortical malformations.

Morphological and functional aspects of progenitors perturbed in cortical malformations.

http://www.wikidata.org/entity/Q35077279

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Cerebral cortex expansion and folding: what have we learned?Recessive Mutations in POLR3B Encoding RNA Polymerase III Subunit Causing Diffuse Hypomyelination in Patients with 4H Leukodystrophy with Polymicrogyria and Cataracts.Alix is required during development for normal growth of the mouse brain.Regulation of cytokinesis during corticogenesis: focus on the midbody.Cellular Phenotypes in Human iPSC-Derived Neurons from a Genetic Model of Autism Spectrum Disorder.Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex.The splicing co-factor Barricade/Tat-SF1 is required for cell cycle and lineage progression in Drosophila neural stem cells.Neural Progenitor Cells Undergoing Yap/Tead-Mediated Enhanced Self-Renewal Form Heterotopias More Easily in the Diencephalon than in the Telencephalon.Tubulin diversity and neuronal migration.

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P2860

Morphological and functional aspects of progenitors perturbed in cortical malformations.

http://www.wikidata.org/entity/Q35077279

description

2015 nî lūn-bûn

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2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Morphological and functional aspects of progenitors perturbed in cortical malformations.

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Morphological and functional aspects of progenitors perturbed in cortical malformations.

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type

label

Morphological and functional aspects of progenitors perturbed in cortical malformations.

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Morphological and functional aspects of progenitors perturbed in cortical malformations.

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prefLabel

Morphological and functional aspects of progenitors perturbed in cortical malformations.

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Morphological and functional aspects of progenitors perturbed in cortical malformations.

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Frontiers in Cellular Neuroscience

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Morphological and functional aspects of progenitors perturbed in cortical malformations.

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Sara Bizzotto

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P2860

Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome

Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome

A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function

LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human

CDK5RAP2 is a pericentriolar protein that functions in centrosomal attachment of the gamma-tubulin ring complex

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis

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30

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