(Q37244752)

19 August 2017

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title

Effect of ABCA1 mutations on risk for myocardial infarction (English)

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19 August 2017

main subject

myocardial infarction

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3

Isabelle Ruel

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19 August 2017

5

Jacques Genest

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19 August 2017

Iulia Iatan

1

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19 August 2017

Khalid Alrasadi

series ordinal

2

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19 August 2017

Khalid Alwaili

series ordinal

4

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19 August 2017

language of work or name

English

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publication date

1 October 2008

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Current Atherosclerosis Reports

19 August 2017

published in

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19 August 2017

volume

10

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19 August 2017

issue

5

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19 August 2017

page(s)

413-426

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https://scigraph.springernature.com/pub.10.1007/s11883-008-0064-5

19 August 2017

exact match

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cites work

Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-008-0064-5

Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-008-0064-5

Targeted inactivation of hepatic Abca1 causes profound hypoalphalipoproteinemia and kidney hypercatabolism of apoA-I

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-008-0064-5

ABCA1 polymorphisms and prognosis after myocardial infarction in young patients

21 January 2018

1 reference

12 December 2020

In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarction.

1 reference

12 December 2020

Associations between two common polymorphisms in the ABCA1 gene and subclinical atherosclerosis: Multi-Ethnic Study of Atherosclerosis (MESA)

1 reference

12 December 2020

Cardioprotective effects of high-density lipoproteins: the evidence strengthens

1 reference

12 December 2020

Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia

1 reference

12 December 2020

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

1 reference

12 December 2020

Genetic determinants of low high-density lipoprotein cholesterol

1 reference

12 December 2020

Targeted inactivation of hepatic Abca1 causes profound hypoalphalipoproteinemia and kidney hypercatabolism of apoA-I

1 reference

12 December 2020

Mutation in ABCA1 predicted risk of ischemic heart disease in the Copenhagen City Heart Study Population

1 reference

12 December 2020

Common genetic variation in the ATP-binding cassette transporter A1, plasma lipids, and risk of coronary heart disease

1 reference

12 December 2020

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

1 reference

12 December 2020

Novel polymorphisms in promoter region of atp binding cassette transporter gene and plasma lipids, severity, progression, and regression of coronary atherosclerosis and response to therapy

1 reference

12 December 2020

Decreased Frequencies of ABCA1 Polymorphisms R219K and V771M in Hungarian Patients with Cerebrovascular and Cardiovascular Diseases

1 reference

12 December 2020

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

1 reference

12 December 2020

Genotypic Effect of the −565C>T Polymorphism in the ABCA1 Gene Promoter on ABCA1 Expression and Severity of Atherosclerosis

1 reference

12 December 2020

Atheroprotective effects of high-density lipoproteins

1 reference

12 December 2020

The association of the R219K polymorphism in the ATP-binding cassette transporter 1 (ABCA1) gene with coronary heart disease and hyperlipidaemia

1 reference

12 December 2020

Variations on a gene: rare and common variants in ABCA1 and their impact on HDL cholesterol levels and atherosclerosis

1 reference

12 December 2020

Common coding polymorphisms in the ABCA1 gene and risk of early-onset coronary heart disease in northern Germany

1 reference

12 December 2020

HDL-cholesterol as a marker of coronary heart disease risk: the Québec cardiovascular study.

1 reference

12 December 2020

Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study

1 reference

12 December 2020

Common variants in the gene encoding ATP-binding cassette transporter 1 in men with low HDL cholesterol levels and coronary heart disease

1 reference

12 December 2020

Global burden of cardiovascular diseases: part I: general considerations, the epidemiologic transition, risk factors, and impact of urbanization

1 reference

12 December 2020

ABCA1 gene polymorphisms and their associations with coronary artery disease and plasma lipids in males from three ethnic populations in Singapore.

1 reference

12 December 2020

Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.

1 reference

12 December 2020

ATP-binding cassette transporter A1 gene I823M polymorphism affects plasma high-density lipoprotein cholesterol level and modifies the effect of low high-density lipoprotein cholesterol on the risk of coronary artery disease

1 reference

12 December 2020

Efflux and atherosclerosis: the clinical and biochemical impact of variations in the ABCA1 gene

1 reference

12 December 2020

Genetic variation in ABCA1 predicts ischemic heart disease in the general population

1 reference

12 December 2020

Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study

1 reference

12 December 2020

A promoter variant of the ATP-binding cassette transporter A1 gene alters the HDL cholesterol level in the general Japanese population

1 reference

12 December 2020

ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels.

1 reference

12 December 2020

Biogenesis and speciation of nascent apoA-I-containing particles in various cell lines

1 reference

12 December 2020

Lipoprotein cholesterol, apolipoprotein A-I and B and lipoprotein (a) abnormalities in men with premature coronary artery disease.

1 reference

12 December 2020

The effect of ABCA1 gene polymorphisms on ischaemic stroke risk and relationship with lipid profile.

1 reference

12 December 2020

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

12 December 2020

Functional mutations of the ABCA1 gene in subjects of French-Canadian descent with HDL deficiency

1 reference

12 December 2020

A common Ile 823 Met variant of ATP-binding cassette transporter A1 gene (ABCA1) alters high density lipoprotein cholesterol level in Japanese population

1 reference

12 December 2020

Characterization of oligomeric human ATP binding cassette transporter A1. Potential implications for determining the structure of nascent high density lipoprotein particles

1 reference

12 December 2020

Macrophage ATP-binding cassette transporter A1 overexpression inhibits atherosclerotic lesion progression in low-density lipoprotein receptor knockout mice

1 reference

12 December 2020

Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

1 reference

12 December 2020

A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia

1 reference

12 December 2020

A case-control study of lipoprotein particles in two populations at contrasting risk for coronary heart disease. The ECTIM Study.

1 reference

12 December 2020

Polymorphisms associated with cholesterol and risk of cardiovascular events

1 reference

12 December 2020

Intestinal ABCA1 directly contributes to HDL biogenesis in vivo

1 reference

12 December 2020

Quantitative analysis of ABCA1-dependent compartmentalization and trafficking of apolipoprotein A-I: implications for determining cellular kinetics of nascent high density lipoprotein biogenesis

1 reference

12 December 2020

10.1007/S11883-008-0064-5

Identifiers

DOI

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19 August 2017

1 reference