Explaining inter-individual variability in phenotype: is epigenetics up to the challenge? - Wikidata - awgldk - TriplyDB

Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

http://www.wikidata.org/entity/Q33691436

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Epigenetic Alterations in Alzheimer's Disease DNA methylation differences at growth related genes correlate with birth weight: a molecular signature linked to developmental origins of adult disease?Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences.Involvement of promoter methylation in the regulation of Pregnane X receptor in colon cancer cells.Validation of methylation biomarkers that distinguish normal colon mucosa of cancer patients from normal colon mucosa of patients without cancer.Epigenome mapping in normal and disease States.A remarkable age-related increase in SIRT1 protein expression against oxidative stress in elderly: SIRT1 gene variants and longevity in human Epigenetics and cardiovascular disease.MicroRNA expression profile in human macrophages in response to Leishmania major infection Deep bisulfite sequencing of aberrantly methylated loci in a patient with multiple methylation defects SIRT1 gene polymorphisms affect the protein expression in cardiovascular diseases.Life or death? A physiogenomic approach to understand individual variation in responses to hemorrhagic shock.Epigenetic differences in normal colon mucosa of cancer patients suggest altered dietary metabolic pathways.Global LINE-1 DNA methylation is associated with blood glycaemic and lipid profiles Postnatal development- and age-related changes in DNA-methylation patterns in the human genome.Type 2 diabetes mellitus in relation to global LINE-1 DNA methylation in peripheral blood: a cohort study.Homeobox gene expression profile indicates HOXA5 as a candidate prognostic marker in oral squamous cell carcinoma.A Conceptual Model of Psychoneurological Symptom Cluster Variation in Women with Breast Cancer: Bringing Nursing Research to Personalized Medicine Pharmacoepigenetics in heart failure.Epigenetics and chromatin remodeling in adult cardiomyopathy.Genetic and epigenetic associations to obesity-related appetite phenotypes among African-American children.Efficacy of statins on sirtuin 1 and endothelial nitric oxide synthase expression: the role of sirtuin 1 gene variants in human coronary atherosclerosis.Epidemiology, epigenetics and the 'Gloomy Prospect': embracing randomness in population health research and practice.

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Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

http://www.wikidata.org/entity/Q33691436

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

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Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

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type

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Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

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Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

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Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

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Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

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Explaining inter-individual variability in phenotype: is epigenetics up to the challenge?

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Carmen Sapienza

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Christos Coutifaris

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Nahid Turan

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Sunita Katari

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P2860

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Revealing the architecture of gene regulation: the promise of eQTL studies

A genome-wide association study identifies novel risk loci for type 2 diabetes

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

A genome-wide association study of global gene expression

A HapMap harvest of insights into the genetics of common disease

Population genomics of human gene expression

Genetic analysis of genome-wide variation in human gene expression

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16-19

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scholarly article

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10.4161/EPI.5.1.10557

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1

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5

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2010-01-06T00:00:00Z

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41056509

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20083905

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