The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
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Daily rhythmic behaviors and thermoregulatory patterns are disrupted in adult female MeCP2-deficient miceA review of Rett syndrome (RTT) with induced pluripotent stem cellsA model for neural development and treatment of Rett syndrome using human induced pluripotent stem cellsReduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylationThe role of MeCP2 in brain development and neurodevelopmental disordersMutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndromeRegulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.Molecular and comparative genetics of mental retardation.Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model.Neuroimaging endophenotypes in animal models of autism spectrum disorders: lost or found in translation?Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain.Applying the ethoexperimental approach to neurodevelopmental syndrome research reveals exaggerated defensive behavior in Mecp2 mutant mice.Evolving role of MeCP2 in Rett syndrome and autism.MeCP2: structure and function.Epigenetic factors and autism spectrum disorders.MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling.MicroRNA-432 contributes to dopamine cocktail and retinoic acid induced differentiation of human neuroblastoma cells by targeting NESTIN and RCOR1 genes.Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation.Trisomy 21 and Rett syndrome: a double burden.Review article: Breaking new ground with Rett syndrome
P2860
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P2860
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@ast
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@en
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@nl
type
label
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@ast
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@en
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@nl
prefLabel
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@ast
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@en
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@nl
P2093
P2860
P356
P1476
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
@en
P2093
Carolyn Schanen
Naghmeh Dorrani
Sara Hammer
Shinichi Kudo
P2860
P356
10.1002/MRDD.10023
P577
2002-01-01T00:00:00Z