Common DNA methylation alterations in multiple brain regions in autism. - Wikidata - wikimedia - TriplyDB

Common DNA methylation alterations in multiple brain regions in autism.

Common DNA methylation alterations in multiple brain regions in autism.

http://www.wikidata.org/entity/Q34287640

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Gene-environment interactions in human health: case studies and strategies for developing new paradigms and research methodologies An AUTS2-Polycomb complex activates gene expression in the CNS.The Interaction between the Immune System and Epigenetics in the Etiology of Autism Spectrum Disorders Epigenetic Effect of Environmental Factors on Autism Spectrum Disorders DNA methylation biomarkers: cancer and beyond Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder Placental methylome analysis from a prospective autism study Exaggerated CpH methylation in the autism-affected brain.Merging data from genetic and epigenetic approaches to better understand autistic spectrum disorder."Gap hunting" to characterize clustered probe signals in Illumina methylation array data Methylomic changes in individuals with psychosis, prenatally exposed to endocrine disrupting compounds: Lessons from diethylstilbestrol.Paternal age effects on sperm FOXK1 and KCNA7 methylation and transmission into the next generation Increasing maternal or post-weaning folic acid alters gene expression and moderately changes behavior in the offspring Bio-collections in autism research.DNA methylation analysis of the autistic brain reveals multiple dysregulated biological pathways.Implications of prenatal steroid perturbations for neurodevelopment, behavior, and autism Cerebellar oxidative DNA damage and altered DNA methylation in the BTBR T+tf/J mouse model of autism and similarities with human post mortem cerebellum.Genetic epidemiology and insights into interactive genetic and environmental effects in autism spectrum disorders The breadth and type of systemic inflammation and the risk of adverse neurological outcomes in extremely low gestation newborns.Methylomic trajectories across human fetal brain development.Epigenetic mechanisms underlying the pathogenesis of neurogenetic diseases Dissociable deficits of executive function caused by gestational adversity are linked to specific transcriptional changes in the prefrontal cortex.Differential DNA methylation profiles of coding and non-coding genes define hippocampal sclerosis in human temporal lobe epilepsy.Genomics in neurological disorders.Circuit- and Diagnosis-Specific DNA Methylation Changes at γ-Aminobutyric Acid-Related Genes in Postmortem Human Hippocampus in Schizophrenia and Bipolar Disorder Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin Modulation of the genome and epigenome of individuals susceptible to autism by environmental risk factors Concordant and discordant DNA methylation signatures of aging in human blood and brain.The Role of Epigenetic Change in Autism Spectrum Disorders.Decreased Brain Levels of Vitamin B12 in Aging, Autism and Schizophrenia.Maternal body mass index during early pregnancy, gestational weight gain, and risk of autism spectrum disorders: Results from a Swedish total population and discordant sibling study Hypomethylation of miR-142 promoter and upregulation of microRNAs that target the oxytocin receptor gene in the autism prefrontal cortex.Association of DNA methylation in the brain with age in older persons is confounded by common neuropathologies.Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23 Paternal sperm DNA methylation associated with early signs of autism risk in an autism-enriched cohort DNA extracted from saliva for methylation studies of psychiatric traits: evidence tissue specificity and relatedness to brain.Autism-Like Behavior and Epigenetic Changes Associated with Autism as Consequences of In Utero Exposure to Environmental Pollutants in a Mouse Model.Epigenetic effects of casein-derived opioid peptides in SH-SY5Y human neuroblastoma cells.Pediatric asthma and autism-genomic perspectives.Interindividual methylomic variation across blood, cortex, and cerebellum: implications for epigenetic studies of neurological and neuropsychiatric phenotypes

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Common DNA methylation alterations in multiple brain regions in autism.

http://www.wikidata.org/entity/Q34287640

description

2013 nî lūn-bûn

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2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Common DNA methylation alterations in multiple brain regions in autism.

@ast

Common DNA methylation alterations in multiple brain regions in autism.

@en

Common DNA methylation alterations in multiple brain regions in autism.

@nl

type

label

Common DNA methylation alterations in multiple brain regions in autism.

@ast

Common DNA methylation alterations in multiple brain regions in autism.

@en

Common DNA methylation alterations in multiple brain regions in autism.

@nl

prefLabel

Common DNA methylation alterations in multiple brain regions in autism.

@ast

Common DNA methylation alterations in multiple brain regions in autism.

@en

Common DNA methylation alterations in multiple brain regions in autism.

@nl

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Molecular Psychiatry

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Common DNA methylation alterations in multiple brain regions in autism

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C Ladd-Acosta

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E Briem

http://www.w3.org/2001/XMLSchema#string

M D Fallin

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W E Kaufmann

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P2860

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

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

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints

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

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

Pathogenic SYNGAP1 mutations impair cognitive development by disrupting maturation of dendritic spine synapses.

ENCODE whole-genome data in the UCSC genome browser (2011 update)

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

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10.1038/MP.2013.114

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8

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19

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Kasper D. Hansen

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2013-09-03T00:00:00Z

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23999529

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DNA methylation

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4184909

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