Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women (Q80376584)

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scientific article published on 23 May 2007

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English	Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women	scientific article published on 23 May 2007

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scholarly article

1 reference

Europe PubMed Central

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31 December 2019

Association between decreased vitamin levels and MTHFR, MTR and MTRR gene polymorphisms as determinants for elevated total homocysteine concentrations in pregnant women (English)

1 reference

Europe PubMed Central

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31 December 2019

pregnant person

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Elvira M Guerra-Shinohara

9

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31 December 2019

author name string

Barbosa PR

1

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31 December 2019

Stabler SP

2

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31 December 2019

Machado AL

3

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31 December 2019

Braga RC

4

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31 December 2019

Hirata RD

5

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31 December 2019

Hirata MH

6

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31 December 2019

Sampaio-Neto LF

7

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31 December 2019

Allen RH

8

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31 December 2019

publication date

23 May 2007

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31 December 2019

European Journal of Clinical Nutrition

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31 December 2019

62

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31 December 2019

8

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31 December 2019

1010-1021

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31 December 2019

https://scigraph.springernature.com/pub.10.1038/sj.ejcn.1602810

0 references

Elevated midtrimester serum methylmalonic acid levels as a risk factor for neural tube defects.

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Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in Brazilian children

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Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect.

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Metabolic abnormalities in cobalamin (vitamin B12) and folate deficiency.

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Prevalence of the mutation C677 --> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil

1 reference

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Changes of some vitamin levels during and after normal pregnancy

1 reference

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

1 reference

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7 January 2021

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Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects

1 reference

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7 January 2021

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Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects

1 reference

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7 January 2021

based on heuristic

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A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJCN.1602810

7 January 2021

based on heuristic

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The MTHFR 1298A>C polymorphism and genomic DNA methylation in human lymphocytes.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

1 reference

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Elevated serum S-adenosylhomocysteine in cobalamin-deficient megaloblastic anemia

1 reference

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7 January 2021

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Low ratio of S-adenosylmethionine to S-adenosylhomocysteine is associated with vitamin deficiency in Brazilian pregnant women and newborns.

1 reference

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7 January 2021

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Relationship between total homocysteine and folate levels in pregnant women and their newborn babies according to maternal serum levels of vitamin B12.

1 reference

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7 January 2021

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Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations

1 reference

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7 January 2021

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Homocysteine is lower in the third trimester of pregnancy in women with enhanced folate status from continued folic acid supplementation.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJCN.1602810

7 January 2021

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Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study.

1 reference

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7 January 2021

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The 2756A>G variant in the gene encoding methionine synthase: its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study

1 reference

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7 January 2021

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Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

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Genetic polymorphisms predisposing to hyperhomocysteinemia in cardiac transplant patients

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7 January 2021

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Maternal and fetal plasma homocysteine concentrations at birth: the influence of folate, vitamin B12, and the 5,10-methylenetetrahydrofolate reductase 677C-->T variant.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJCN.1602810

7 January 2021

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Methylenetetrahydrofolate reductase C677T and A1298C polymorphism and changes in homocysteine concentrations in women with idiopathic recurrent pregnancy losses

1 reference

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7 January 2021

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Maternal homocysteine before conception and throughout pregnancy predicts fetal homocysteine and birth weight

1 reference

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7 January 2021

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The pregnancy-related decrease in fasting plasma homocysteine is not explained by folic acid supplementation, hemodilution, or a decrease in albumin in a longitudinal study.

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

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7 January 2021

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Methylenetetrahydrofolate reductase (MTHFR) c677t gene variant modulates the homocysteine folate correlation in a mild folate-deficient population

1 reference

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Age and Gender Affect the Relation between Methylenetetrahydrofolate Reductase C677T Genotype and Fasting Plasma Homocysteine Concentrations in the Framingham Offspring Study Cohort

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Pathogenesis of subacute combined degeneration: a result of methyl group deficiency

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The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

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Quantification of serum and urinary S-adenosylmethionine and S-adenosylhomocysteine by stable-isotope-dilution liquid chromatography-mass spectrometry

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Quantitation of total homocysteine, total cysteine, and methionine in normal serum and urine using capillary gas chromatography-mass spectrometry

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Assay of methylmalonic acid in the serum of patients with cobalamin deficiency using capillary gas chromatography-mass spectrometry

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Neural-tube defects are associated with low concentrations of cobalamin (vitamin B12) in amniotic fluid

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

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Methionine synthase reductase 66A->G polymorphism is associated with increased plasma homocysteine concentration when combined with the homozygous methylenetetrahydrofolate reductase 677C->T variant

1 reference

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Changes in homocysteine levels during normal pregnancy

1 reference

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7 January 2021

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

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Human methionine synthase reductase is a molecular chaperone for human methionine synthase

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Increased frequency of combined methylenetetrahydrofolate reductase C677T and A1298C mutated alleles in spontaneously aborted embryos

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