(Q51565928)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9870206%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

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

1 reference

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7 December 2019

3

1 reference

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7 December 2019

7

G Montalescot

1 reference

7 December 2019

L Thuillier

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9870206%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

B Chadefaux-Vekemans

2

1 reference

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7 December 2019

A Kara

4

1 reference

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7 December 2019

J Aupetit

5

1 reference

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7 December 2019

C Rochette

6

1 reference

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7 December 2019

M C Couty

8

1 reference

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7 December 2019

P Kamoun

9

1 reference

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7 December 2019

A Ankri

10

1 reference

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7 December 2019

publication date

1 December 1998

1 reference

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Journal of Inherited Metabolic Disease

7 December 2019

published in

1 reference

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7 December 2019

volume

21

1 reference

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7 December 2019

issue

8

1 reference

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7 December 2019

page(s)

812-822

1 reference

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https://scigraph.springernature.com/pub.10.1023/a:1005414617390

7 December 2019

exact match

0 references

cites work

Radioenzymic determination of homocysteine in plasma and urine

1 reference

12 December 2020

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

1 reference

12 December 2020

Defects in human methionine synthase in cblG patients

1 reference

12 December 2020

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

1 reference

12 December 2020

Methylenetetrahydrofolate reductase gene and coronary artery disease

1 reference

12 December 2020

The mutation Ala677-->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Rapid determination of total homocysteine in plasma

1 reference

12 December 2020

Treatment of mild hyperhomocysteinemia in vascular disease patients

1 reference

12 December 2020

Factor V Leiden and thermolabile methylenetetrahydrofolate reductase in extreme old age

1 reference

12 December 2020

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

1 reference

12 December 2020

Can lowering homocysteine levels reduce cardiovascular risk?

1 reference

12 December 2020

Methylenetetrahydrofolate reductase deficiency: Prenatal diagnosis and family studies

1 reference

12 December 2020

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

1 reference

12 December 2020

Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid

1 reference

12 December 2020

Elevated total plasma homocysteine and 677C-->T mutation of the 5,10-methylenetetrahydrofolate reductase gene in thrombotic vascular disease

1 reference

12 December 2020

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

1 reference

12 December 2020

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects

1 reference

12 December 2020

Association between Plasma Homocysteine Concentrations and Extracranial Carotid-Artery Stenosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hyperhomocysteinemia: an independent risk factor for vascular disease

1 reference

12 December 2020

Homocystinuria due to 5,10-methylenetetra-hydrofolate reductase deficiency revealed by stroke in adult siblings

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Heterozygosity for Homocystinuria in Premature Peripheral and Cerebral Occlusive Arterial Disease

1 reference

Crossref

https://api.crossref.org/works/10.1023%2FA%3A1005414617390

7 January 2021