Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
about
The Role of the Neurobiologist in Redefining the Diagnosis of AutismAdvances in autism genetics: on the threshold of a new neurobiologyInteraction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardationMaternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans.The CHARGE study: an epidemiologic investigation of genetic and environmental factors contributing to autismThe comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13Mecp2 organizes juvenile social behavior in a sex-specific mannerAbnormal transmethylation/transsulfuration metabolism and DNA hypomethylation among parents of children with autismIntegrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genesThe odyssey of MeCP2 and parental imprintingDLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disordersInhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndromeClinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.DNA modifications: function and applications in normal and disease StatesChannelopathy pathogenesis in autism spectrum disordersGenetic modifiers of MeCP2 function in Drosophila.Immunologic and neurodevelopmental susceptibilities of autismPsychosis and autism as diametrical disorders of the social brainTipping the balance of autism risk: potential mechanisms linking pesticides and autismMeCP2-dependent repression of an imprinted miR-184 released by depolarizationGene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndromeEpigenetics and human disease: translating basic biology into clinical applicationsPax6-dependent cortical glutamatergic neuronal differentiation regulates autism-like behavior in prenatally valproic acid-exposed rat offspringGenome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosisA model for neural development and treatment of Rett syndrome using human induced pluripotent stem cellsPeople with MECP2 mutation-positive Rett disorder who converse.GABA receptor subunit distribution and FMRP-mGluR5 signaling abnormalities in the cerebellum of subjects with schizophrenia, mood disorders, and autism.Expression of GABAA α2-, β1- and ε-receptors are altered significantly in the lateral cerebellum of subjects with schizophrenia, major depression and bipolar disorderSomatosensory and sensorimotor consequences associated with the heterozygous disruption of the autism candidate gene, Gabrb3.Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders.Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV dataLow-dose thyroxine attenuates autism-associated adverse effects of fetal alcohol in male offspring's social behavior and hippocampal gene expression.Proton magnetic resonance spectroscopy as a probe into the pathophysiology of autism spectrum disorders (ASD): a review.Detection of parent-of-origin effects for quantitative traits using general pedigree data.Functional Profiling of Human MeCP2 by Automated Data Comparison Analysis and Computerized Expression Pathway ModelingReduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylationThe changing impact of genes and environment on brain development during childhood and adolescence: initial findings from a neuroimaging study of pediatric twins.Detection of parent-of-origin effects using general pedigree data
P2860
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P2860
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
description
2004 nî lūn-bûn
@nan
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Epigenetic overlap in autism-s ...... expression of UBE3A and GABRB3
@nl
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@ast
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@en
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@en-gb
type
label
Epigenetic overlap in autism-s ...... expression of UBE3A and GABRB3
@nl
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@ast
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@en
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@en-gb
prefLabel
Epigenetic overlap in autism-s ...... expression of UBE3A and GABRB3
@nl
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@ast
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@en
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@en-gb
P2860
P921
P3181
P356
P1476
Epigenetic overlap in autism-s ...... xpression of UBE3A and GABRB3.
@en
P2093
Amber Hogart
P2860
P304
P3181
P356
10.1093/HMG/DDI045
P407
P577
2004-12-22T00:00:00Z