Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction (Q43575854)

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scientific article published in April 2001

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English	Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction	scientific article published in April 2001

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11303694

retrieved

24 November 2017

title

Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11303694

retrieved

24 November 2017

main subject

myocardial infarction

1 reference

based on heuristic

inferred from title

author

Irem Dincer

series ordinal

7

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

author name string

S Gülec

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

O Aras

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

E Akar

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

E Tutar

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

K Omürlü

series ordinal

5

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

F Avci

series ordinal

6

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

N Akar

series ordinal

8

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

D Oral

series ordinal

9

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

publication date

1 April 2001

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11303694

retrieved

24 November 2017

published in

Clinical Cardiology

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

volume

24

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

issue

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

page(s)

281-284

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

cites work

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FCLC.4960240405

retrieved

21 January 2018

Methylene tetrahydrofolate reductase genotype and the risk and extent of coronary artery disease in a population with low plasma folate.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thermolabile methylenetetrahydrofolate reductase: an inherited risk factor for coronary artery disease.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma homocyst(e)ine levels in men with premature coronary artery disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteinemia due to folate deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and properties of methylenetetrahydrofolate reductase from pig liver.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Treatment of mild hyperhomocysteinemia in vascular disease patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relative risk of factors for coronary heart disease in population with low cholesterol levels

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteinemia: association of a metabolic disorder with vascular disease and thrombosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine and coronary atherosclerosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase mutation and coronary artery disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular variant of 5,10-methylenetetrahydrofolate reductase is a risk factor of ischemic heart disease in the Japanese population

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Mutation in the Methylenetetrahydrofolate Reductase Gene Is Not Associated With Increased Risk for Coronary Artery Disease or Myocardial Infarction

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thermolabile methylenetetrahydrofolate reductase in coronary artery disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

677-->CT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11303694

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1002/CLC.4960240405

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

PMC publication ID

6654870

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

PubMed publication ID

11303694

1 reference

stated in

Europe PubMed Central

PMC publication ID

6654870

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6654870&resulttype=core&format=json

retrieved

15 May 2020

ResearchGate publication ID

229860967

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