(Q44216053)

English

Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico

scientific article published in November 2002

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

30 November 2017

Frequency of the thermolabile variant C677T in the MTHFR gene and lack of association with neural tube defects in the State of Yucatan, Mexico (English)

1 reference

Europe PubMed Central

30 November 2017

0 references

author name string

González-Herrera L

1

1 reference

Europe PubMed Central

30 November 2017

García-Escalante G

2

1 reference

Europe PubMed Central

30 November 2017

Castillo-Zapata I

3

1 reference

Europe PubMed Central

30 November 2017

Canto-Herrera J

4

1 reference

Europe PubMed Central

30 November 2017

Ceballos-Quintal J

5

1 reference

Europe PubMed Central

30 November 2017

Pinto-Escalante D

6

1 reference

Europe PubMed Central

30 November 2017

Díaz-Rubio F

7

1 reference

Europe PubMed Central

30 November 2017

Del Angel RM

8

1 reference

Europe PubMed Central

30 November 2017

Orozco-Orozco L

9

1 reference

Europe PubMed Central

30 November 2017

publication date

1 November 2002

1 reference

Europe PubMed Central

30 November 2017

Clinical Genetics

1 reference

Europe PubMed Central

30 November 2017

62

1 reference

Europe PubMed Central

30 November 2017

5

1 reference

Europe PubMed Central

30 November 2017

394-398

1 reference

Europe PubMed Central

30 November 2017

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

High prevalence of the thermolabile methylenetetrahydrofolate reductase variant in Mexico: a country with a very high prevalence of neural tube defects

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic risk factor for unexplained recurrent early pregnancy loss

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Neural-tube defects

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Methylenetetrahydrofolate reductase and neural tube defects

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Exploring gene-gene interactions in the etiology of neural tube defects.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic admixture in three Mexican Mestizo populations based on D1S80 and HLA-DQA1 loci

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.620507.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1034/J.1399-0004.2002.620507.X

1 reference

Europe PubMed Central

30 November 2017

1 reference

Europe PubMed Central

30 November 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q44216053&oldid=2108625212"