Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. - Wikidata - wikimedia - TriplyDB

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

http://www.wikidata.org/entity/Q34719900

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Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression The genetic signatures of noncoding RNAs Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study Chromosome 9p21 variant predicts mortality after coronary artery bypass graft surgery Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a Expression of p16(INK4a) in peripheral blood T-cells is a biomarker of human aging Mechanisms of long noncoding RNA function in development and disease Genetic epidemiology of coronary artery disease: an Asian Indian perspective Long Non-Coding RNAs as Master Regulators in Cardiovascular Diseases Non-Coding RNAs Including miRNAs and lncRNAs in Cardiovascular Biology and Disease Human genetics of diabetic vascular complications Long non-coding RNAs and complex human diseases Using epigenetic mechanisms to understand the impact of common disease causing alleles Non-coding RNAs: the "dark matter" of cardiovascular pathophysiology.Genetics of the acute coronary syndrome Noncoding RNA in age-related cardiovascular diseases The Eukaryotic Genome as an RNA Machine ANRIL: molecular mechanisms and implications in human health Ocular expression and distribution of products of the POAG-associated chromosome 9p21 gene region A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.Genotype imputation Genetic and familial predisposition to rotator cuff disease: a systematic review.Long noncoding RNA variations in cardiometabolic diseases.Islet biology, the CDKN2A/B locus and type 2 diabetes risk.Genome-wide association study of subclinical interstitial lung disease in MESA.The genetic architecture of lipoprotein subclasses in Gullah-speaking African American families enriched for type 2 diabetes: the Sea Islands Genetic African American Registry (Project SuGAR).Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk.Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.Genetic and functional association of FAM5C with myocardial infarction Analyses and comparison of accuracy of different genotype imputation methods Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population.Genetic analysis of six SNPs in candidate genes associated with high cross-race risk of development of thoracic aortic aneurysms and dissections in Chinese Han population Long non-coding RNAs as novel biomarkers and therapeutic targets in head and neck cancers.Single nucleotide polymorphisms associated with abnormal coronary microvascular function.Common genetic variants on chromosome 9p21 predict perioperative myocardial injury after coronary artery bypass graft surgery.

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P2860

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

http://www.wikidata.org/entity/Q34719900

description

2007 nî lūn-bûn

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2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2007 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2007年の論文

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Human Molecular Genetics

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Susceptibility to coronary art ...... ANRIL locus on chromosome 9p.

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Fiona Green

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Gianni Tognoni

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Helen M Broadbent

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John F Peden

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Maria Grazia Franzosi

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PROCARDIS consortium

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10.1093/HMG/DDM352

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6

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17

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Stefan Lorkowski

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