(Q36467477)

14 August 2017

1 reference

title

Genetic variation in genes of folate metabolism and neural-tube defect risk (English)

1 reference

14 August 2017

1 reference

1 reference

2

Lydia A Afman

1 reference

14 August 2017

Ivon J M van der Linden

series ordinal

1

1 reference

PubMed ID

16672082

14 August 2017

Sandra G Heil

series ordinal

3

1 reference

PubMed ID

16672082

14 August 2017

Henk J Blom

series ordinal

4

1 reference

14 August 2017

1 May 2006

1 reference

Proceedings of the Nutrition Society

14 August 2017

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14 August 2017

65

1 reference

14 August 2017

2

1 reference

14 August 2017

204-215

1 reference

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

14 August 2017

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

A 31 bp VNTR in the cystathionine beta-synthase (CBS) gene is associated with reduced CBS activity and elevated post-load homocysteine levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Polymorphism of human transcobalamin II: substitution of proline and/or glutamine residues by arginine

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Teratogen update: valproic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

The human cystathionine beta-synthase (CBS) gene: complete sequence, alternative splicing, and polymorphisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

A common insertion/deletion polymorphism of the thymidylate synthase (TYMS) gene is a determinant of red blood cell folate and homocysteine concentrations

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Role in translation of a triple tandemly repeated sequence in the 5'-untranslated region of human thymidylate synthase mRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

A review of folate receptor alpha cycling and 5-methyltetrahydrofolate accumulation with an emphasis on cell models in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

The role of genetic factors in the development of hyperhomocysteinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Thymidylate synthase: a novel genetic determinant of plasma homocysteine and folate levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Methionine synthase reductase MTRR 66A > G has no effect on total homocysteine, folate, and Vitamin B12 concentrations in renal transplant patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Hyperthermia and birth defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Molecular cloning, characterization, and regulation of the human mitochondrial serine hydroxymethyltransferase gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Reduced folate carrier polymorphism (80A-->G) and neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Autoantibodies against folate receptors in women with a pregnancy complicated by a neural-tube defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Prevalence of neural tube defects in Cape Town, South Africa

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

The thymidylate synthase tandem repeat polymorphism is not associated with homocysteine concentrations in healthy young subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Spatial and temporal expression of the cystathionine beta-synthase gene during early human development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Reduced folate carrier gene is a risk factor for neural tube defects in a Chinese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Effects of TCN2 776C>G on vitamin B, folate, and total homocysteine levels in kidney transplant patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Investigations of a common genetic variant in betaine-homocysteine methyltransferase (BHMT) in coronary artery disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Is maternal obesity a risk factor for anencephaly and spina bifida?

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Spina bifida and parental occupation

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Reduced vitamin B12 binding by transcobalamin II increases the risk of neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Interaction between dietary methionine and methyl donor intake on rat liver betaine-homocysteine methyltransferase gene expression and organization of the human gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Kinetic and thermodynamic characterization of the common polymorphic variants of human methionine synthase reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Gene-gene interaction between the cystathionine beta-synthase 31 base pair variable number of tandem repeats and the methylenetetrahydrofolate reductase 677C > T polymorphism on homocysteine levels and risk for neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association.

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Analysis of the human folate receptor beta gene for an association with neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Novel insertion and deletion mutations in the 5'-UTR of the folate receptor-alpha gene: an additional contributor to hyperhomocysteinemia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Susceptibility to spina bifida; an association study of five candidate genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Thymidylate synthase repeat polymorphisms and risk of neural tube defects in a population from the northern United Kingdom

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

Common variant in betaine-homocysteine methyltransferase (BHMT) and risk for spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1079%2FPNS2006495

21 January 2018

Identifiers

DOI

10.1079/PNS2006495

1 reference

14 August 2017

1 reference

PubMed ID

16672082