(Q44407272)

English

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

scientific article published on March 26, 2003

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

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

1 reference

10.1007/S00109-003-0426-Y

https://api.crossref.org/works/10.1007/S00109-003-0426-Y

25 December 2023

1 reference

based on heuristic

inferred from title

coronary artery disease

1 reference

based on heuristic

inferred from title

genetic polymorphism

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12700893

25 December 2023

molecular medicine

1 reference

10.1007/S00109-003-0426-Y

https://api.crossref.org/works/10.1007/S00109-003-0426-Y

25 December 2023

1

object named as

David Evans

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12700893

25 December 2023

author name string

F. Ulrich Beil

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12700893

25 December 2023

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12700893

25 December 2023

publication date

26 March 2003

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

full work available at URL

http://link.springer.com/content/pdf/10.1007/s00109-003-0426-y.pdf

Portable Document Format

1 reference

10.1007/S00109-003-0426-Y

https://api.crossref.org/works/10.1007/S00109-003-0426-Y

25 December 2023

http://link.springer.com/article/10.1007/s00109-003-0426-y/fulltext.html

1 reference

10.1007/S00109-003-0426-Y

https://api.crossref.org/works/10.1007/S00109-003-0426-Y

25 December 2023

http://link.springer.com/content/pdf/10.1007/s00109-003-0426-y

1 reference

10.1007/S00109-003-0426-Y

https://api.crossref.org/works/10.1007/S00109-003-0426-Y

25 December 2023

Journal of Molecular Medicine

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

81

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

264-270

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

ABC transporters in cellular lipid trafficking

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

ATP-binding cassette transporter A1 and cholesterol trafficking

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

Analysis of hABC1 gene 5' end: additional peptide sequence, promoter region, and four polymorphisms.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

A common variant in the gene for lipoprotein lipase (Asp9-->Asn). Functional implications and prevalence in normal and hyperlipidemic subjects.

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

Lipoprotein(a) and coronary heart disease. Meta-analysis of prospective studies

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

Genetic determinants of plasma triglycerides: impact of rare and common mutations

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00109-003-0426-Y

21 January 2018

Plasma triglyceride level is a risk factor for cardiovascular disease independent of high-density lipoprotein cholesterol level: a meta-analysis of population-based prospective studies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12700893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ABCA1. The gatekeeper for eliminating excess tissue cholesterol.

1 reference

https://pubmed.ncbi.nlm.nih.gov/12700893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI

1 reference

https://pubmed.ncbi.nlm.nih.gov/12700893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/12700893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cellular cholesterol efflux in heterozygotes for tangier disease is markedly reduced and correlates with high density lipoprotein cholesterol concentration and particle size

1 reference

https://pubmed.ncbi.nlm.nih.gov/12700893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patients With ApoE3 Deficiency (E2/2, E3/2, and E4/2) Who Manifest With Hyperlipidemia Have Increased Frequency of an Asn 291→Ser Mutation in the Human LPL Gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/12700893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common and rare ABCA1 variants affecting plasma HDL cholesterol

1 reference

https://pubmed.ncbi.nlm.nih.gov/12700893

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00109-003-0426-Y

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

release_7i4fsb5mvfcgtfngxkfoxtp3fq

1 reference

https://api.fatcat.wiki/v0/release/7i4fsb5mvfcgtfngxkfoxtp3fq

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q44407272&oldid=2206626512"