Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice. - Wikidata - awgldk - TriplyDB

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

http://www.wikidata.org/entity/Q34121996

about

Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions Integrative annotation of variants from 1092 humans: application to cancer genomics Epigenetic regulation of the INK4b-ARF-INK4a locus: in sickness and in health Long noncoding RNA in genome regulation: prospects and mechanisms Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1 Genome-wide association study of intracranial aneurysm identifies three new risk loci Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene Genomics era and complex disorders: Implications of GWAS with special reference to coronary artery disease, type 2 diabetes mellitus, and cancers Mechanisms of long noncoding RNA function in development and disease Expanding Horizons for Abdominal Aortic Aneurysms The association of 9p21-3 locus with coronary atherosclerosis: a systematic review and meta-analysis Identifying novel biomarkers for cardiovascular disease risk prediction Human genetics of diabetic vascular complications DNA damage and repair in atherosclerosis: current insights and future perspectives Long non-coding RNAs and complex human diseases Functional anatomy of distant-acting mammalian enhancers Genome-wide association studies of late-onset cardiovascular disease The gene desert mammary carcinoma susceptibility locus Mcs1a regulates Nr2f1 modifying mammary epithelial cell differentiation and proliferation Multiple knockout mouse models reveal lincRNAs are required for life and brain development The short and long of noncoding sequences in the control of vascular cell phenotypes ANRIL: molecular mechanisms and implications in human health Common genetic variants in the 9p21 region and their associations with multiple tumours Effect of 9p21.3 coronary artery disease locus neighboring genes on atherosclerosis in mice Bone marrow p16INK4a-deficiency does not modulate obesity, glucose homeostasis or atherosclerosis development Large scale association analysis identifies three susceptibility loci for coronary artery disease Genetics and beyond--the transcriptome of human monocytes and disease susceptibility Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk.Long noncoding RNA variations in cardiometabolic diseases.Islet biology, the CDKN2A/B locus and type 2 diabetes risk.An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes.Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk.Genome-wide identification of expression quantitative trait loci (eQTLs) in human heart Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis.Towards a molecular systems model of coronary artery disease Integrated genomics of susceptibility to alkylator-induced leukemia in mice CDKN2B Methylation and Aortic Arch Calcification in Patients with Ischemic Stroke Combining genome-wide data from humans and animal models of dyslipidemia and atherosclerosis.Roles of lncRNAs in pancreatic beta cell identity and diabetes susceptibility.Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction.

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P2860

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

http://www.wikidata.org/entity/Q34121996

description

2010 nî lūn-bûn

@nan

2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի փետրվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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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

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@ast

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@en

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@nl

type

label

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@ast

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@en

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@nl

prefLabel

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@ast

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@en

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

@nl

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Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

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Dalit May

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Elaine Gong

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Jonathan C Cohen

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Len A Pennacchio

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Veena Afzal

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Yiwen Zhu

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P2860

INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis

A biomarker that identifies senescent human cells in culture and in aging skin in vivo

A common allele on chromosome 9 associated with coronary heart disease

A single-nucleotide polymorphism in the human p27kip1 gene (-838C>A) affects basal promoter activity and the risk of myocardial infarction

Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals

Heart disease and stroke statistics--2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

Severe hypercholesterolemia and atherosclerosis in apolipoprotein E-deficient mice created by homologous recombination in ES cells

The UCSC Genome Browser Database: 2008 update

A common variant on chromosome 9p21 affects the risk of myocardial infarction

Spontaneous hypercholesterolemia and arterial lesions in mice lacking apolipoprotein E

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Catia Attanasio

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