Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects
about
Conserved roles for cytoskeletal components in determining laterality.p600 regulates spindle orientation in apical neural progenitors and contributes to neurogenesis in the developing neocortex.A point mutation in translation initiation factor eIF2B leads to function--and time-specific changes in brain gene expression.Kinesin-12 influences axonal growth during zebrafish neural developmentTranscriptomic changes in brain development.Cytoskeleton in action: lissencephaly, a neuronal migration disorderLIS1 deficiency promotes dysfunctional synaptic integration of granule cells generated in the developing and adult dentate gyrus.Integrative mechanisms of oriented neuronal migration in the developing brain.LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules.p600/UBR4 in the central nervous system.Regulation of neuronal migration, an emerging topic in autism spectrum disorders.Targeting protein for xenopus kinesin-like protein 2 (TPX2) regulates γ-histone 2AX (γ-H2AX) levels upon ionizing radiation.Identification of novel radiation-induced p53-dependent transcripts extensively regulated during mouse brain development.fosB-null mice display impaired adult hippocampal neurogenesis and spontaneous epilepsy with depressive behavior.Cell cycle networks link gene expression dysregulation, mutation, and brain maldevelopment in autistic toddlers.14-3-3 Proteins in Brain Development: Neurogenesis, Neuronal Migration and NeuromorphogenesisTranscriptome analysis reveals rod/cone photoreceptor specific signatures across mammalian retinas.Genetic associations with reflexive visual attention in infancy and childhood.Early born neurons are abnormally positioned in the doublecortin knockout hippocampus.Developmental dynamics of PAFAH1B subunits during mouse brain development.Tau's role in the developing brain: implications for intellectual disability.Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3.Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl.
P2860
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P2860
Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
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2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Global developmental gene expr ...... man neuronal migration defects
@ast
Global developmental gene expr ...... man neuronal migration defects
@en
type
label
Global developmental gene expr ...... man neuronal migration defects
@ast
Global developmental gene expr ...... man neuronal migration defects
@en
prefLabel
Global developmental gene expr ...... man neuronal migration defects
@ast
Global developmental gene expr ...... man neuronal migration defects
@en
P2093
P2860
P1433
P1476
Global developmental gene expr ...... man neuronal migration defects
@en
P2093
Anthony Wynshaw-Boris
Nicholas J Schork
Ondrej Libiger
Shinji Hirotsune
Sonia Jain
Tiziano Pramparo
Yong Ha Youn
P2860
P304
P356
10.1371/JOURNAL.PGEN.1001331
P577
2011-03-10T00:00:00Z