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MECP2 promoter methylation and X chromosome inactivation in autism

MECP2 promoter methylation and X chromosome inactivation in autism

http://www.wikidata.org/entity/Q37039904

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The role of immune dysfunction in the pathophysiology of autism Developmental Dynamics of Rett Syndrome From genes to environment: using integrative genomics to build a "systems-level" understanding of autism spectrum disorders DNA modifications: function and applications in normal and disease States Daily rhythmic behaviors and thermoregulatory patterns are disrupted in adult female MeCP2-deficient mice Involvement of MeCP2 in Regulation of Myelin-Related Gene Expression in Cultured Rat Oligodendrocytes Placental methylome analysis from a prospective autism study New perspectives on rodent models of advanced paternal age: relevance to autism.Merging data from genetic and epigenetic approaches to better understand autistic spectrum disorder.Hypermethylation of the enolase gene (ENO2) in autism Impact of induced pluripotent stem cells on the study of central nervous system disease Behavioral epigenetics Common DNA methylation alterations in multiple brain regions in autism.A review of the role of female gender in autism spectrum disorders.Prenatal maternal immune activation causes epigenetic differences in adolescent mouse brain.Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues Brain transcriptional and epigenetic associations with autism.Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis.Brain region-specific expression of MeCP2 isoforms correlates with DNA methylation within Mecp2 regulatory elements.A genomic point-of-view on environmental factors influencing the human brain methylome Environmental risk factors for autism.Epigenetic approaches to psychiatric disorders.Large-scale methylation domains mark a functional subset of neuronally expressed genes.The Role of Epigenetic Change in Autism Spectrum Disorders.Metabolic imbalance associated with methylation dysregulation and oxidative damage in children with autism.Sex differences in DNA methylation may contribute to risk of PTSD and depression: a review of existing evidence Levels of select PCB and PBDE congeners in human postmortem brain reveal possible environmental involvement in 15q11-q13 duplication autism spectrum disorder Epigenetics, autism spectrum, and neurodevelopmental disorders.Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition Decitabine alters the expression of Mecp2 isoforms via dynamic DNA methylation at the Mecp2 regulatory elements in neural stem cells.Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure.Sensitive periods in epigenetics: bringing us closer to complex behavioral phenotypes.Dynamic Akt/mTOR Signaling in Children with Autism Spectrum Disorder Synaptic plasticity and signaling in Rett syndrome.The contribution of epigenetics to understanding genetic factors in autism.Rett syndrome and MeCP2.Genetic architecture, epigenetic influence and environment exposure in the pathogenesis of Autism.Breathing abnormalities in animal models of Rett syndrome a female neurogenetic disorder.Epigenetic Regulation of Infant Neurobehavioral Outcomes.Genetic and epigenetic methylation defects and implication of the ERMN gene in autism spectrum disorders.

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MECP2 promoter methylation and X chromosome inactivation in autism

http://www.wikidata.org/entity/Q37039904

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on June 2008

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

MECP2 promoter methylation and X chromosome inactivation in autism

@en

MECP2 promoter methylation and X chromosome inactivation in autism.

@nl

type

label

MECP2 promoter methylation and X chromosome inactivation in autism

@en

MECP2 promoter methylation and X chromosome inactivation in autism.

@nl

prefLabel

MECP2 promoter methylation and X chromosome inactivation in autism

@en

MECP2 promoter methylation and X chromosome inactivation in autism.

@nl

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Autism Research

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MECP2 promoter methylation and X chromosome inactivation in autism

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Dag H Yasui

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Isaac N Pessah

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Judy Van de Water

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Katherine A Patzel

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Michelle Martin

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Raman P Nagarajan

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Robin L Hansen

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Ruby Jiang

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Wendy P Robinson

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

An exceptionally conserved transcriptional repressor, CTCF, employs different combinations of zinc fingers to bind diverged promoter sequences of avian and mammalian c-myc oncogenes

The CHARGE study: an epidemiologic investigation of genetic and environmental factors contributing to autism

Strong association of de novo copy number mutations with autism

Absence of methylation of a CpG-rich region at the 5' end of the MIC2 gene on the active X, the inactive X, and the Y chromosome

Structural variation of chromosomes in autism spectrum disorder

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

Boundaries between chromosomal domains of X inactivation and escape bind CTCF and lack CpG methylation during early development

Gene action in the X-chromosome of the mouse (Mus musculus L.)

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169-178

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scholarly article

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10.1002/AUR.24

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3

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1

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Susan E Swanberg

Janine M. LaSalle

Irva Hertz-Picciotto

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2008-06-01T00:00:00Z

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23766919

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19132145

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