(Q39022051)

English

Homocysteine and methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Tunisian patients with severe coronary artery disease

scientific article published on 19 January 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Homocysteine and methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Tunisian patients with severe coronary artery disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

author name string

Lakhdar Ghazouani

1

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Nesrine Abboud

2

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Nabil Mtiraoui

3

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Walid Zammiti

4

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Faouzi Addad

5

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Haitham Amin

6

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Wassim Y Almawi

7

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Touhami Mahjoub

8

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

publication date

19 January 2008

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

Journal of Thrombosis and Thrombolysis

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

27

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

191-197

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

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

1 reference

https://api.crossref.org/works/10.1007%2FS11239-008-0194-1

21 January 2018

Urinary excretion of homocysteine-thiolactone in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene--nutrition interactions in coronary artery disease: correlation between the MTHFR C677T polymorphism and folate and homocysteine status in a Korean population

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of 677 C-->T polymorphism of methylenetetrahydrofolate reductase on medium-term prognosis after acute coronary syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The management of hypertension in ischaemic heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation A1298C of methylenetetrahydrofolate reductase: risk for early coronary disease not associated with hyperhomocysteinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effect of 677C-->T and 1298A-->C mutations on plasma homocysteine and 5,10-methylenetetrahydrofolate reductase activity in healthy subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene-gene and gene-environment interactions in mild hyperhomocysteinemia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C677T mutation of methylenetetrahydrofolate reductase gene and serum homocysteine levels in Turkish patients with coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of 5,10-methylenetetrahydrofolate reductase (C667T) polymorphism and its association with red blood cell 5-methyltetrahydrofolate in the healthy Iranians

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation of the C677T MTHFR genotype with homocysteine levels in children with sickle cell disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase gene polymorphism and its association with coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

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

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine and venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase (MTHFR) 677C>T and methionine synthase reductase (MTRR) 66A>G polymorphisms: association with serum homocysteine and angiographic coronary artery disease in the era of flour products fortified with folic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk factors for coronary artery disease in patients with elevated high-density lipoprotein cholesterol

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocyst(e)inemia and hemostatic factors: the atherosclerosis risk in communities study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms, plasma homocysteine, folate, and vitamin B12 levels and the extent of coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of MTRRA66G polymorphism (but not of MTHFR C677T and A1298C, MTRA2756G, TCN C776G) with homocysteine and coronary artery disease in the French population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine Status and Polymorphisms of Methylenetetrahydrofolate Reductase Are Not Associated With Restenosis After Stenting in Coronary Arteries

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinaemia, methylenetetrahydrofolate reductase polymorphism and risk of coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertension--a treatable component of the cardiometabolic syndrome: challenges for the primary care physician

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mild hyperhomocysteinemia in adult patients with sickle cell disease: a common finding unrelated to folate and cobalamin status

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms of homocysteine-induced atherothrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thermolabile methylenetetrahydrofolate reductase C677T polymorphism and homocysteine are risk factors for coronary artery disease in Moroccan population

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine and atherothrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine and methionine metabolism in renal failure

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relation between plasma homocysteine, gene polymorphisms of homocysteine metabolism-related enzymes, and angiographically proven coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18204887

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11239-008-0194-1

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 September 2017

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