Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
about
Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndromeSeptins promote stress fiber-mediated maturation of focal adhesions and renal epithelial motility.Septin-driven coordination of actin and microtubule remodeling regulates the collateral branching of axons.Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex.The step-wise pathway of septin hetero-octamer assembly in budding yeast.During tangential migration, SDF1 lends the cytoskeleton a guiding hand.The emerging functions of septins in metazoansTranscriptome analysis of amoeboid and ramified microglia isolated from the corpus callosum of rat brain.Spatial guidance of cell asymmetry: septin GTPases show the way.Septin functions in organ system physiology and pathology.Partial Functional Diversification of Drosophila melanogaster Septin Genes Sep2 and Sep5.Proteome rearrangements after auditory learning: high-resolution profiling of synapse-enriched protein fractions from mouse brain.SIL1, a causative cochaperone gene of Marinesco-Söjgren syndrome, plays an essential role in establishing the architecture of the developing cerebral cortexRole of a circadian-relevant gene NR1D1 in brain development: possible involvement in the pathophysiology of autism spectrum disorders.Septin roles in tumorigenesis.Application of in utero electroporation and live imaging in the analyses of neuronal migration during mouse brain development.Comparative expression analysis of Septin 14 in testes of infertile men with normal spermatogenesis and spermatogenic failure.SEPT4 is regulated by the Notch signaling pathway.SEPT9 occupies the terminal positions in septin octamers and mediates polymerization-dependent functions in abscissionDe novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic featuresMUNC18-1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development.Septin C-terminal domain interactions: implications for filament stability and assembly.Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability.Role of an adaptor protein Lin-7B in brain development: possible involvement in autism spectrum disorders.SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.Characterization of presynaptic septin complexes in mammalian hippocampal neurons.[Functional Characterization of Septin Complexes].
P2860
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P2860
Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
@ast
Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
@en
type
label
Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
@ast
Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
@en
prefLabel
Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
@ast
Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
@en
P2093
P2860
P356
P1476
Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.
@en
P2093
Hidenori Ito
Ikuko Iwamoto
Kaori Sudo
Koh-ichi Nagata
Rika Morishita
Tomoyasu Shinoda
P2860
P304
P356
10.1091/MBC.E09-10-0869
P577
2010-02-24T00:00:00Z