(Q41188766)

28 September 2017

1 reference

title

Molecular genetics of methylenetetrahydrofolate reductase deficiency (English)

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methylenetetrahydrofolate reductase deficiency

28 September 2017

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author name string

R Rozen

series ordinal

1

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28 September 2017

1 January 1996

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Journal of Inherited Metabolic Disease

28 September 2017

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28 September 2017

19

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28 September 2017

5

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28 September 2017

589-594

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https://scigraph.springernature.com/pub.10.1007/bf01799831

28 September 2017

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cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01799831

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

21 January 2018

1 reference

12 December 2020

A Quantitative Assessment of Plasma Homocysteine as a Risk Factor for Vascular Disease

1 reference

12 December 2020

Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.

1 reference

12 December 2020

Homocysteine metabolism in pregnancies complicated by neural-tube defects.

1 reference

12 December 2020

Homocyst(e)ine and arterial occlusive diseases

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

Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency

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

Vascular pathology of homocysteinemia: implications for the pathogenesis of arteriosclerosis.

1 reference

12 December 2020

Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?

1 reference

12 December 2020

Methylenetetrahydrofolate reductase. Evidence for spatially distinct subunit domains obtained by scanning transmission electron microscopy and limited proteolysis.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Folate status is the major determinant of fasting total plasma homocysteine levels in maintenance dialysis patients.

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

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01799831

1 reference

PubMed ID

8892013

Dimensions Publication ID

28 September 2017

0 references

1 reference

PubMed ID

8892013