Interaction between common folate polymorphisms and B-vitamin nutritional status modulates homocysteine and risk for a thrombotic event (Q44509445)

3 December 2017

title

Interaction between common folate polymorphisms and B-vitamin nutritional status modulates homocysteine and risk for a thrombotic event (English)

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3 December 2017

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Zoe Yates

1

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3 December 2017

Mark Lucock

series ordinal

2

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3 December 2017

publication date

1 July 2003

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Molecular Genetics and Metabolism

3 December 2017

published in

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3 December 2017

volume

79

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3 December 2017

issue

3

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3 December 2017

page(s)

201-213

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Folic acid: nutritional biochemistry, molecular biology, and role in disease processes

3 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Cobalamin-dependent methyltransferases

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Human methionine synthase reductase, a soluble P-450 reductase-like dual flavoprotein, is sufficient for NADPH-dependent methionine synthase activation

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

The 1298A-->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Underlying disorders associated with severe early-onset preeclampsia

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Elevated homocyst(e)ine levels with preeclampsia

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Clotting and hemorrhage in the placenta--a delicate balance

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Local hypomethylation in atherosclerosis found in rabbit ec-sod gene

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Methylation of the estrogen receptor-alpha gene promoter is selectively increased in proliferating human aortic smooth muscle cells.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Polymorphisms of methylenetetrahydrofolate reductase and other enzymes: metabolic significance, risks and impact on folate requirement

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Determination of plasma total homocysteine and cysteine using HPLC with fluorescence detection and an ammonium 7-fluoro-2, 1, 3-benzoxadiazole-4-sulphonate (SBD-F) derivatization protocol optimized for antioxidant concentration, derivatization reage

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

An examination of polymorphic genes and folate metabolism in mothers affected by a spina bifida pregnancy

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

The quantitatively important relationship between homocysteine metabolism and glutathione synthesis by the transsulfuration pathway and its regulation by redox changes

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Glutathionylcobalamin as an intermediate in the formation of cobalamin coenzymes

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Betaine-homocysteine methyltransferase (BHMT): genomic sequencing and relevance to hyperhomocysteinemia and vascular disease in humans

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Influence of a glutamate carboxypeptidase II (GCPII) polymorphism (1561C-->T) on plasma homocysteine, folate and vitamin B(12) levels and its relationship to cardiovascular disease risk

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

Polymorphisms in the thymidylate synthase and serine hydroxymethyltransferase genes and risk of adult acute lymphocytic leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900093-3

7 January 2021

10.1016/S1096-7192(03)00093-3

Identifiers

DOI

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3 December 2017

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