HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology. - Wikidata - awgldk - TriplyDB

HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology.

HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology.

http://www.wikidata.org/entity/Q38630971

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HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology.

http://www.wikidata.org/entity/Q38630971

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology.

@en

type

label

HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology.

@en

prefLabel

HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology.

@en

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NRCARDIO.2017.115

P1433

Nature Reviews Cardiology

P1476

HDL and atherosclerotic cardiovascular disease: genetic insights into complex biology.

@en

P2093

Daniel Gaudet

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

Daniel Seung Kim

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

Eric Niesor

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

Frank M Sacks

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

H Bryan Brewer

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

Jean-Claude Tardif

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

Johan L M Björkegren

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

Kerry-Anne Rye

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

M John Chapman

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

Philip J Barter

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

P2860

'Mendelian randomization': can genetic epidemiology contribute to understanding environmental determinants of disease?

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins

Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met)

Common variants at 30 loci contribute to polygenic dyslipidemia

Variations in DNA elucidate molecular networks that cause disease

Biological, clinical and population relevance of 95 loci for blood lipids

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

Homozygous lecithin:cholesterol acyltransferase (LCAT) deficiency due to a new loss of function mutation and review of the literature

Regulation of high-density lipoprotein metabolism

P31

scholarly article

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10.1038/NRCARDIO.2017.115

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Daniel Seung Kim

Robert A. Hegele

P577

2017-08-10T00:00:00Z

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

P698

28795686

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

P921

atherosclerosis