Reduced folate carrier polymorphism (80A--&gt;G) and neural tube defects (Q44389085)

2 December 2017

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

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2 December 2017

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Patrizia De Marco

1

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2 December 2017

Maria Grazia Calevo

2

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2 December 2017

Anna Moroni

3

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2 December 2017

Elisa Merello

4

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2 December 2017

Alessandro Raso

5

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2 December 2017

Richard H Finnell

6

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2 December 2017

Huiping Zhu

7

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2 December 2017

Luciano Andreussi

8

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2 December 2017

Armando Cama

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2 December 2017

Valeria Capra

10

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2 December 2017

1 March 2003

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European Journal of Human Genetics

2 December 2017

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2 December 2017

11

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2 December 2017

3

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2 December 2017

245-252

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200946

2 December 2017

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Folate coenzyme and antifolate transport proteins in normal and neoplastic cells

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7 January 2021

Characterization of the multiple transport routes for methotrexate in L1210 cells using phthalate as a model anion substrate

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7 January 2021

Structural organization of the reduced folate carrier gene in Chinese hamster ovary cells

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7 January 2021

Rescue of embryonic lethality in reduced folate carrier-deficient mice by maternal folic acid supplementation reveals early neonatal failure of hematopoietic organs

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Homocysteine metabolism in pregnancies complicated by neural-tube defects.

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7 January 2021

Mutated 5,10-methylenetetrahydrofolate reductase and moderate hyperhomocysteinaemia

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7 January 2021

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

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7 January 2021

Methylenetetrahydrofolate reductase and neural tube defects

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7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

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7 January 2021

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

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7 January 2021

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

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7 January 2021

A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations

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7 January 2021

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

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7 January 2021

Folate pathway gene alterations in patients with neural tube defects

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7 January 2021

The role of folate transport and metabolism in neural tube defect risk

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7 January 2021

A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia

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7 January 2021

Polymorphisms in genes involved in folate metabolism as risk factors for NTDs

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations

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7 January 2021

Probing the Role of Positive Residues in the ADP/ATP Carrier from Yeast. The Effect of Six Arginine Mutations on Transport and the Four ATP versus ADP Exchange Modes†

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7 January 2021

Effect of site-directed mutagenesis of the arginine residues 509 and 748 on mouse band 3 protein-mediated anion transport.

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200946

7 January 2021

The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200946

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200946

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200946

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200946

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Dimensions Publication ID

2 December 2017

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