Novel variants identified in methyl-CpG-binding domain genes in autistic individuals. - Wikidata - wikimedia - TriplyDB

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

http://www.wikidata.org/entity/Q34136181

about

Epigenetics of early child development Emerging Molecular and Biological Functions of MBD2, a Reader of DNA Methylation Transcriptional co-repressors and memory storage MBD3 expression and DNA binding patterns are altered in a rat model of temporal lobe epilepsy An epigenetic feedback regulatory loop involving microRNA-195 and MBD1 governs neural stem cell differentiation Microarray analysis reveals higher gestational folic Acid alters expression of genes in the cerebellum of mice offspring-a pilot study.Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons.Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders.The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1.Tagging methyl-CpG-binding domain proteins reveals different spatiotemporal expression and supports distinct functions.The landscape of DNA methylation amid a perfect storm of autism aetiologies.Epigenetics, autism spectrum, and neurodevelopmental disorders.Common variation contributes to the genetic architecture of social communication traits.Autism genes keep turning up chromatin Methyl-CpG-Binding Protein MBD1 Regulates Neuronal Lineage Commitment through Maintaining Adult Neural Stem Cell Identity MicroRNA regulation of neural stem cells and neurogenesis.Genetic variation in the epigenetic machinery and mental health.Crosstalk among Epigenetic Pathways Regulates Neurogenesis Structure and function insights into the NuRD chromatin remodeling complex.Methyl-CpG-binding domain proteins: readers of the epigenome.Methyl-CpG-Binding Protein (MBD) Family: Epigenomic Read-Outs Functions and Roles in Tumorigenesis and Psychiatric Diseases.Genetics and Epigenetics in Adult Neurogenesis.Prediction of autism susceptibility genes based on association rules.DNA Methylation and Adult Neurogenesis.

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P2860

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

http://www.wikidata.org/entity/Q34136181

description

2009 nî lūn-bûn

@nan

2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

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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

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@ast

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@en

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@nl

type

label

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@ast

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@en

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@nl

prefLabel

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@ast

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@en

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

@nl

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Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

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Eden R Martin

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Harry H Wright

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Ioanna Konidari

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John R Gilbert

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Mary L Baltos

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Melissa Y Rayner-Evans

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Michael L Cuccaro

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Ruth K Abramson

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P2860

Comparative study of methyl-CpG-binding domain proteins

Identification and Evaluation of Children With Autism Spectrum Disorders

Regression in Autistic Spectrum Disorders

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

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

Regulation of MBD1-mediated transcriptional repression by SUMO and PIAS proteins

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

Excess of twins among affected sibling pairs with autism: implications for the etiology of autism.

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

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