Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome.
about
Modifiers and Readers of DNA Modifications and Their Impact on Genome Structure, Expression, and Stability in DiseaseMECP2 disorders: from the clinic to mice and backSynaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia.Cytosine modifications in neurodevelopment and diseasesThe impact of MeCP2 loss- or gain-of-function on synaptic plasticityUnlocking epigenetic codes in neurogenesisRole of mecp2 in experience-dependent epigenetic programmingDisease mutations in disordered regions--exception to the rule?Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndromeA model for neural development and treatment of Rett syndrome using human induced pluripotent stem cellsRole of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy.Induced gamma oscillations differentiate familiar and novel voices in children with MECP2 duplication and Rett syndromes.Mild expression differences of MECP2 influencing aggressive social behavior.Binding of MBD proteins to DNA blocks Tet1 function thereby modulating transcriptional noise.Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disorders.The role of MeCP2 in brain development and neurodevelopmental disordersGABAA receptor antagonism ameliorates behavioral and synaptic impairments associated with MeCP2 overexpressionMethyl-CpG binding domain proteins inhibit interspecies courtship and promote aggression in Drosophila.A mouse model for MeCP2 duplication syndrome: MeCP2 overexpression impairs learning and memory and synaptic transmissionA review of the role of female gender in autism spectrum disorders.Genetic insights into the functional elements of language.A partial MECP2 duplication in a mildly affected adult male: a putative role for the 3' untranslated region in the MECP2 duplication phenotype.A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections.Astrocyte-specific regulation of hMeCP2 expression in Drosophila.Abnormalities in the zinc-metalloprotease-BDNF axis may contribute to megalencephaly and cortical hyperconnectivity in young autism spectrum disorder patients.Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autismDrosophila modeling of heritable neurodevelopmental disordersAbsence of preference for social novelty and increased grooming in integrin β3 knockout mice: initial studies and future directions.Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation.Genomic copy number variation in disorders of cognitive development.A genomic point-of-view on environmental factors influencing the human brain methylomeProtein interactome reveals converging molecular pathways among autism disorders.CAGE-defined promoter regions of the genes implicated in Rett Syndrome.Epigenetic mechanisms may underlie the aetiology of sex differences in mental health risk and resilience.Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome.MECP2, a gene associated with Rett syndrome in humans, shows conserved coding regions, independent Alu insertions, and a novel transcript across primate evolutionNeurodevelopmental and neurobehavioral characteristics in males and females with CDKL5 duplications.
P2860
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P2860
Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome.
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@ast
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@en
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@nl
type
label
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@ast
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@en
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@nl
prefLabel
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@ast
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@en
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@nl
P2093
P2860
P356
P1433
P1476
Autism and other neuropsychiat ...... th MeCP2 duplication syndrome.
@en
P2093
Christian P Schaaf
Claudia M B Carvalho
Daniel G Glaze
James R Lupski
Melissa B Ramocki
Ronald Richman
Sarika U Peters
Y Jane Tavyev
P2860
P304
P356
10.1002/ANA.21715
P577
2009-12-01T00:00:00Z