Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations.
about
Cerebral cortex expansion and folding: what have we learned?Genes and brain malformations associated with abnormal neuron positioningVariants in CUL4B are associated with cerebral malformationsKatanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamicsMicrocephaly models in the developing zebrafish retinal neuroepithelium point to an underlying defect in metaphase progression.Malformations of cortical development: genetic mechanisms and diagnostic approachMutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephalyPolymicrogyria: pathology, fetal origins and mechanisms.OSVZ progenitors in the human cortex: an updated perspective on neurodevelopmental disease.Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutationPrimary microcephaly gene MCPH1 shows signatures of tumor suppressors and is regulated by miR-27a in oral squamous cell carcinoma.A novel single base pair duplication in WDR62 causes primary microcephaly.Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly.Refining the phenotype associated with CASC5 mutation.Identification and analysis of a novel dimerization domain shared by various members of c-Jun N-terminal kinase (JNK) scaffold proteins.The Role of WD40-Repeat Protein 62 (MCPH2) in Brain Growth: Diverse Molecular and Cellular Mechanisms Required for Cortical Development.A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family.A novel WDR62 mutation causes primary microcephaly in a Pakistani family.Genetic heterogeneity in Pakistani microcephaly families.Severe presentation of WDR62 mutation: is there a role for modifying genetic factors?
P2860
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P2860
Mutations in WDR62, encoding a centrosomal and nuclear protein, in Indian primary microcephaly families with cortical malformations.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
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
Mutations in WDR62, encoding a ...... s with cortical malformations.
@ast
Mutations in WDR62, encoding a ...... s with cortical malformations.
@en
Mutations in WDR62, encoding a ...... s with cortical malformations.
@nl
type
label
Mutations in WDR62, encoding a ...... s with cortical malformations.
@ast
Mutations in WDR62, encoding a ...... s with cortical malformations.
@en
Mutations in WDR62, encoding a ...... s with cortical malformations.
@nl
prefLabel
Mutations in WDR62, encoding a ...... s with cortical malformations.
@ast
Mutations in WDR62, encoding a ...... s with cortical malformations.
@en
Mutations in WDR62, encoding a ...... s with cortical malformations.
@nl
P2093
P2860
P1433
P1476
Mutations in WDR62, encoding a ...... s with cortical malformations.
@en
P2093
H R Arvinda
M R Duvvari
P Singhmar
S C Girimaji
P2860
P304
P356
10.1111/J.1399-0004.2011.01686.X
P577
2011-05-16T00:00:00Z