(Q28369118)

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A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9789068%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9789068%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

Pamela J Bagley

1

1 reference

Europe PubMed Central

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5 December 2019

2

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J Selhub

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Europe PubMed Central

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5 December 2019

language of work or name

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publication date

1 October 1998

1 reference

Europe PubMed Central

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5 December 2019

Proceedings of the National Academy of Sciences of the United States of America

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Europe PubMed Central

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5 December 2019

95

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5 December 2019

13217-13220

1 reference

Europe PubMed Central

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5 December 2019

22

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Europe PubMed Central

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5 December 2019

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

20 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

29 September 2017

Intermediate homocysteinemia: a thermolabile variant of methylenetetrahydrofolate reductase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

29 September 2017

The pathogenesis of homocysteinemia: interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

29 September 2017

Folate distribution in cultured human cells. Studies on 5,10-CH2-H4PteGlu reductase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

29 September 2017

The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

2 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

2 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

2 June 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

Methylenetetrahydrofolate reductase polymorphism, dietary interactions, and risk of colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=23763

27 November 2018

Studies of folate compounds in nature. Folate compounds in rat kidney and red blood cells

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

Analysis of folates using combined affinity and ion-pair chromatography

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

Spina bifida, 677T-->C mutation, and role of folate

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

Is mutated MTHFR a risk factor for neural tube defects?

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.22.13217

21 January 2018

Folate derivatives in human cells: studies on normal and 5,10-methylenetetrahydrofolate reductase-deficient fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A methylenetetrahydrofolate reductase polymorphism and the risk of colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzymatic deconjugation of erythrocyte polyglutamyl folates during preparation for folate assay: investigation with reversed-phase liquid chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9789068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.95.22.13217

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9789068%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1998PNAS...9513217B

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9789068%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9789068%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

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