(Q43678276)

English

Mutations in the genes regulating methylene tetrahydrofolate reductase (MTHFR C-->T677) and cystathione beta-synthase (CBS G-->A919, CBS T-->c833) are not associated with myocardial infarction in African Americans

scientific article published in July 2001

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scholarly article

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Europe PubMed Central

PubMed publication ID

25 November 2017

Mutations in the genes regulating methylene tetrahydrofolate reductase (MTHFR C-->T677) and cystathione beta-synthase (CBS G-->A919, CBS T-->c833) are not associated with myocardial infarction in African Americans (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

myocardial infarction

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based on heuristic

inferred from title

6

object named as

Evatt BL

1 reference

Europe PubMed Central

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25 November 2017

W. Craig Hooper

2

object named as

Hooper WC

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Europe PubMed Central

PubMed publication ID

25 November 2017

author name string

Dilley A

1

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Europe PubMed Central

PubMed publication ID

25 November 2017

El-Jamil M

3

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Renshaw M

4

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Wenger NK

5

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

publication date

1 July 2001

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

Thrombosis Research

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Europe PubMed Central

PubMed publication ID

25 November 2017

103

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Europe PubMed Central

PubMed publication ID

25 November 2017

2

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25 November 2017

109-115

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Europe PubMed Central

PubMed publication ID

25 November 2017

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

1 reference

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Molecular basis of phenotype expression in homocystinuria

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Prevalence of moderate hyperhomocysteinemia in patients with early-onset venous and arterial occlusive disease.

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

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7 January 2021

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Distribution in healthy and coronary populations of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation

1 reference

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7 January 2021

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The prevalence of two genetic traits related to venous thrombosis in whites and African-Americans

1 reference

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The incidence of the gene for thermolabile methylene tetrahydrofolate reductase in African Americans

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Screening for mutations by expressing patient cDNA segments in E. coli: homocystinuria due to cystathionine beta-synthase deficiency

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Familial thrombophilia associated with homozygosity for the cystathionine beta-synthase 833T-->C mutation

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Microheterogeneity in the Distribution of the 844ins68 in the Cystathionine β-Synthase Gene in Italy

1 reference

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A common 844INS68 insertion variant in the cystathionine beta-synthase gene

1 reference

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Relation between plasma homocysteine concentration, the 844ins68 variant of the cystathionine beta-synthase gene, and pyridoxal-5'-phosphate concentration.

1 reference

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Polygenic influence on plasma homocysteine: association of two prevalent mutations, the 844ins68 of cystathionine beta-synthase and A(2756)G of methionine synthase, with lowered plasma homocysteine levels.

1 reference

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Is the common 844ins68 polymorphism in the cystathionine beta-synthase gene associated with atherosclerosis?

1 reference

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Molecular basis of cystathionine beta-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuria

1 reference

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High frequency (71%) of cystathionine β-synthase mutation G307S in Irish homocystinuria patients

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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Methylenetetrahydrofolate reductase gene and coronary artery disease

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Exploring gene-gene interactions in the etiology of neural tube defects.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Heterogeneous ethnic distribution of the 844ins68 in the cystathionine beta-synthase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900278-X

7 January 2021

based on heuristic

inferred from DOI database lookup

World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological marker

1 reference

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7 January 2021

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inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(01)00278-X

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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