Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation - Wikidata - awgldk - TriplyDB

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation

http://www.wikidata.org/entity/Q33283941

about

Biomarkers in autism Genomic and epigenetic evidence for oxytocin receptor deficiency in autism Diet and the epigenetic (re)programming of phenotypic differences in behavior The epigenetics of sex differences in the brain Mecp2 organizes juvenile social behavior in a sex-specific manner Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders Modifiers and Readers of DNA Modifications and Their Impact on Genome Structure, Expression, and Stability in Disease DNA modifications: function and applications in normal and disease States Inhibition-Based Biomarkers for Autism Spectrum Disorder.Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes Influence of developmental lead exposure on expression of DNA methyltransferases and methyl cytosine-binding proteins in hippocampus A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome Placental methylome analysis from a prospective autism study Mechanisms of Functional Hypoconnectivity in the Medial Prefrontal Cortex of Mecp2 Null Mice.Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.Genetic mapping of social interaction behavior in B6/MSM consomic mouse strains.Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation.Gadd45b is an epigenetic regulator of juvenile social behavior and alters local pro-inflammatory cytokine production in the rodent amygdala Exaggerated CpH methylation in the autism-affected brain.A study of the influence of sex on genome wide methylation.Merging data from genetic and epigenetic approaches to better understand autistic spectrum disorder.DNA methylation in the human cerebral cortex is dynamically regulated throughout the life span and involves differentiated neurons.Chromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains.The role of MeCP2 in brain development and neurodevelopmental disorders Sex hormones in autism: androgens and estrogens differentially and reciprocally regulate RORA, a novel candidate gene for autism.Bio-collections in autism research.Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain.Hypermethylation of the enolase gene (ENO2) in autism A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism Cerebral folate receptor autoantibodies in autism spectrum disorder.Rett syndrome and the impact of MeCP2 associated transcriptional mechanisms on neurotransmission Epigenetic organization of brain sex differences and juvenile social play behavior.Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis.Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autism Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models.Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model.Genomic imprinting in the development and evolution of psychotic spectrum conditions.Neuronal nucleus and cytoplasm volume deficit in children with autism and volume increase in adolescents and adults.

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P2860

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation

http://www.wikidata.org/entity/Q33283941

description

2006 nî lūn-bûn

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2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

Reduced MeCP2 expression is fr ...... ant MECP2 promoter methylation

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Reduced MeCP2 expression is fr ...... ant MECP2 promoter methylation

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Reduced MeCP2 expression is fr ...... nt MECP2 promoter methylation.

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type

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Reduced MeCP2 expression is fr ...... ant MECP2 promoter methylation

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Reduced MeCP2 expression is fr ...... ant MECP2 promoter methylation

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Reduced MeCP2 expression is fr ...... nt MECP2 promoter methylation.

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prefLabel

Reduced MeCP2 expression is fr ...... ant MECP2 promoter methylation

@ast

Reduced MeCP2 expression is fr ...... ant MECP2 promoter methylation

@en

Reduced MeCP2 expression is fr ...... nt MECP2 promoter methylation.

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@en

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Amber R Hogart

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Michelle R Martin

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Raman P Nagarajan

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Ynnez Gwye

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P2860

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

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

Epigenetic differences arise during the lifetime of monozygotic twins

Reelin promoter hypermethylation in schizophrenia

Transposable elements: targets for early nutritional effects on epigenetic gene regulation

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions

A decade of molecular studies of fragile X syndrome

Identification of MeCP2 mutations in a series of females with autistic disorder

Mutation analysis of the coding sequence of the MECP2 gene in infantile autism

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

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e1-11

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scholarly article

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10.4161/EPI.1.4.3514

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4

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1

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Janine M. LaSalle

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2006-10-01T00:00:00Z

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5879747

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1866172

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