Maternal genome-wide DNA methylation patterns and congenital heart defects. - sprookjes - yvandenbroek - TriplyDB

Maternal genome-wide DNA methylation patterns and congenital heart defects.

Maternal genome-wide DNA methylation patterns and congenital heart defects.

http://www.wikidata.org/entity/Q33812860

about

Developments in our understanding of the genetic basis of birth defects Epigenetic diet: impact on the epigenome and cancer Genetic networks governing heart development.Decoding the complex genetic causes of heart diseases using systems biology DNA hypermethylation and DNA hypomethylation is present at different loci in chronic kidney disease Hypermethylation of the enolase gene (ENO2) in autism PhenomeNET: a whole-phenome approach to disease gene discovery.LINE-1 methylation status and its association with tetralogy of fallot in infants DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samples.Differential DNA methylation in purified human blood cells: implications for cell lineage and studies on disease susceptibility Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic Networks Kidney Dysfunction in Adult Offspring Exposed In Utero to Type 1 Diabetes Is Associated with Alterations in Genome-Wide DNA Methylation Karyotypic and molecular genetic changes associated with fetal cardiovascular abnormalities: results of a retrospective 4-year ultrasonic diagnosis study Comparative DNA methylation among females with neurodevelopmental disorders and seizures identifies TAC1 as a MeCP2 target gene.Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot.CITED2 mutation and methylation in children with congenital heart disease Hypermethylation of brain natriuretic peptide gene is associated with the risk of rheumatic heart disease.Inhibition of Gata4 and Tbx5 by Nicotine-Mediated DNA Methylation in Myocardial Differentiation.Folate, homocysteine and the cardiac neural crest.Genome-wide DNA methylation analysis in alcohol dependence.Congenital heart disease: the crossroads of genetics, epigenetics and environment.Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases.Perinatal management of pregnancies with severe fetal heart defects and epigenetic aspects.Promoter methylation and expression of the VANGL2 gene in the myocardium of pediatric patients with tetralogy of fallot.Semiparametric tests for identifying differentially methylated loci with case-control designs using Illumina arrays.Steroidogenic factor-1 hypermethylation in maternal rat blood could serve as a biomarker for intrauterine growth retardation.Epigenome-wide association study for Parkinson's disease.Intrauterine growth retardation-associated syncytin b hypermethylation in maternal rat blood revealed by DNA methylation array analysis.Genome-wide analysis of DNA methylation in human amnion.

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P2860

Maternal genome-wide DNA methylation patterns and congenital heart defects.

http://www.wikidata.org/entity/Q33812860

description

2011 nî lūn-bûn

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2011 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2011 թվականի հունվարին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Maternal genome-wide DNA methylation patterns and congenital heart defects.

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Maternal genome-wide DNA methylation patterns and congenital heart defects.

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type

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Maternal genome-wide DNA methylation patterns and congenital heart defects.

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Maternal genome-wide DNA methylation patterns and congenital heart defects.

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Maternal genome-wide DNA methylation patterns and congenital heart defects.

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Maternal genome-wide DNA methylation patterns and congenital heart defects.

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Maternal genome-wide DNA methylation patterns and congenital heart defects.

@en

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Charlotte A Hobbs

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

Mario A Cleves

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Mohammad A Karim

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Ping Hu

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

Shimul Chowdhury

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

Stephen W Erickson

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

Stewart L MacLeod

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P2860

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.

DNA methylation profiling of human chromosomes 6, 20 and 22

Neural tube defects and folate: case far from closed

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

Intra-individual change over time in DNA methylation with familial clustering

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

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DNA methylation

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