Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms: impact on plasma homocysteine levels and development of coronary artery disease. (Q43546767)

From Wikidata

Jump to navigation Jump to search

scientific article published in February 2001

Language	Label	Description	Also known as
English	Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms: impact on plasma homocysteine levels and development of coronary artery disease.	scientific article published in February 2001

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms: impact on plasma homocysteine levels and development of coronary artery disease (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Ingolf Cascorbi

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

author name string

C Meisel

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

T Gerloff

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

V Stangl

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

M Laule

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

J M Müller

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

K D Wernecke

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

G Baumann

8

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

I Roots

9

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

K Stangl

10

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 February 2001

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Atherosclerosis

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

154

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

651-658

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Recent data are not in conflict with homocysteine as a cardiovascular risk factor

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Homocysteine and atherothrombosis

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Plasma homocysteine levels and mortality in patients with coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A prospective study of plasma homocyst(e)ine and risk of myocardial infarction in US physicians

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Serum homocysteine and risk of coronary heart disease and cerebrovascular disease in elderly men: a 10-year follow-up

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Methylenetetrahydrofolate reductase and apolipoprotein E polymorphisms are independent risk factors for coronary heart disease in Japanese: a case-control study

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: the Atherosclerosis Risk in Communities (ARIC) study.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A mutation in the methylenetetrahydrofolate reductase gene is not associated with increased risk for coronary artery disease or myocardial infarction.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Relation of a common mutation in methylenetetrahydrofolate reductase to plasma homocysteine and early onset coronary artery disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine metabolism and late-onset vascular disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A common mutation in the methylenetetrahydrofolate reductase gene and risk of coronary heart disease: results among U.S. men.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Methylenetetrahydrofolate reductase gene and coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

The TT genotype of the methylenetetrahydrofolate reductase C677T gene polymorphism is associated with the extent of coronary atherosclerosis in patients at high risk for coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Genetic analysis of thermolabile methylenetetrahydrofolate reductase as a risk factor for myocardial infarction.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Genetic polymorphism of methylenetetrahydrofolate reductase and myocardial infarction. A case-control study

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Nomenclature and criteria for diagnosis of ischemic heart disease. Report of the Joint International Society and Federation of Cardiology/World Health Organization task force on standardization of clinical nomenclature

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

A1/A2 polymorphism of glycoprotein IIIa and association with excess procedural risk for coronary catheter interventions: a case-controlled study.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Nomenclature for human CYP2D6 alleles.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Nomenclature for N-acetyltransferases

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2800%2900679-1

7 January 2021

Identifiers

10.1016/S0021-9150(00)00679-1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11257266%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

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=Q43546767&oldid=2098230689"