C677T and A1298C MTHFR polymorphisms in the etiology of neural tube defects in Spanish population (Q44399592)

2 December 2017

title

C677T and A1298C MTHFR polymorphisms in the etiology of neural tube defects in Spanish population (English)

1 reference

reason for deprecated rank

2 December 2017

Implicación de los polimorfismos C677T y A1298C del gen MTHFR en el desarrollo de los defectos del tubo neural en la población española (Spanish)

marking inconsistent with the registered/official identifier/name

1 reference

https://api.crossref.org/works/10.1016/S0025-7753(03)73734-8

23 December 2023

author name string

José Ignacio Gutiérrez Revilla

1

1 reference

2 December 2017

Flora Pérez Hernández

2

1 reference

2 December 2017

Manuel Tamparillas Salvador

4

1 reference

2 December 2017

Jesús Gracia Romero

5

1 reference

2 December 2017

M. Teresa Calvo Martín

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12689549

23 December 2023

language of work or name

Spanish

0 references

publication date

1 April 2003

1 reference

2 December 2017

5 April 2003

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12689549

full work available at URL

23 December 2023

https://api.elsevier.com/content/article/PII:S0025775303737348?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0025-7753(03)73734-8

https://api.elsevier.com/content/article/PII:S0025775303737348?httpAccept=text/plain

23 December 2023

1 reference

https://api.crossref.org/works/10.1016/S0025-7753(03)73734-8

23 December 2023

1 reference

2 December 2017

volume

120

1 reference

2 December 2017

issue

12

1 reference

2 December 2017

page(s)

441-445

1 reference

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

2 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Methylenetetrahydrofolate reductase and neural tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Methylenetetrahydrofolate reductase mutation and neural tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: implications for folate intake recommendations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Homocysteine metabolism in pregnancies complicated by neural-tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

[Lowering high levels of fasting total homocysteine with folic acid and vitamins B in patients with venous thromboembolism: relationship between response and the C677T methylenetetrahydrofolate reductase (MTHRF) genotype]

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Genetic selection and folate intake during pregnancy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Polymorphisms in the methylenetetrahydrofolate reductase gene were associated with both the efficacy and the toxicity of methotrexate used for the treatment of rheumatoid arthritis, as evidenced by single locus and haplotype analyses

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

Folic acid supplementation in the prevention of neural tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

677-->CT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0025-7753%2803%2973734-8

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects

7 January 2021

4

1 reference

https://api.crossref.org/works/10.1016/S0025-7753(03)73734-8

Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia

23 December 2023

9

1 reference

https://api.crossref.org/works/10.1016/S0025-7753(03)73734-8

Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects

23 December 2023

13

1 reference

https://api.crossref.org/works/10.1016/S0025-7753(03)73734-8

A methylenetetrahydrofolate reductase polymorphism and the risk of colorectal cancer

23 December 2023

18

1 reference

https://api.crossref.org/works/10.1016/S0025-7753(03)73734-8

23 December 2023

Identifiers

1 reference

2 December 2017

1 reference