(Q43951023)

28 November 2017

title

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

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28 November 2017

1

Henrik Zetterberg

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28 November 2017

9

Kaj Blennow

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28 November 2017

8

Demetrios A Spandidos

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28 November 2017

Björn Regland

2

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28 November 2017

Mona Palmér

3

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28 November 2017

Anne Ricksten

4

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28 November 2017

Lars Palmqvist

5

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28 November 2017

Lars Rymo

6

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28 November 2017

Demetrios A Arvanitis

7

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28 November 2017

publication date

1 February 2002

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European Journal of Human Genetics

28 November 2017

published in

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28 November 2017

volume

10

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28 November 2017

issue

2

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28 November 2017

page(s)

113-118

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200767

28 November 2017

exact match

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cites work

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

1 reference

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

21 January 2018

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Neural-tube defects and derangement of homocysteine metabolism

21 January 2018

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Homocysteine metabolism in pregnancies complicated by neural-tube defects.

21 January 2018

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Hyperhomocysteinaemia and recurrent spontaneous abortion or abruptio placentae

21 January 2018

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Hyperhomocysteinemia and recurrent early pregnancy loss: a meta-analysis.

21 January 2018

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Homocysteine induces congenital defects of the heart and neural tube: effect of folic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

The effects of folic acid supplementation on plasma total homocysteine are modulated by multivitamin use and methylenetetrahydrofolate reductase genotypes.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

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

21 January 2018

1 reference

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The validation of short tandem repeat (STR) loci for use in forensic casework

21 January 2018

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Microsatellite instability in squamous cell carcinoma of the head and neck.

21 January 2018

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Molecular genetics of methylenetetrahydrofolate reductase deficiency

21 January 2018

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Neural tube defects in relation to use of folic acid antagonists during pregnancy

21 January 2018

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Folic acid antagonists during pregnancy and the risk of birth defects.

21 January 2018

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Mutations in coagulation factors in women with unexplained late fetal loss.

21 January 2018

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Hyperhomocysteinemia: a risk factor in women with unexplained recurrent early pregnancy loss

21 January 2018

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7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

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7 January 2021

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

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

Genetic risk factor for unexplained recurrent early pregnancy loss

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

Polymorphism for mutation of cytosine to thymine at location 677 in the methylenetetrahydrofolate reductase gene is associated with recurrent early fetal loss

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

Microsatellite mutations in spontaneously aborted embryos

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

Accelerated folate breakdown in pregnancy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

The relationship between increased folate catabolism and the increased requirement for folate in pregnancy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200767

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200767

1 reference

Dimensions Publication ID

28 November 2017

1013039268

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1 reference