Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans (Q44482015)

3 December 2017

title

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

1 reference

3 December 2017

Guéant-Rodriguez RM

1

1 reference

3 December 2017

Rendeli C

2

1 reference

3 December 2017

Namour B

3

1 reference

3 December 2017

Venuti L

4

1 reference

3 December 2017

Romano A

5

1 reference

3 December 2017

Anello G

6

1 reference

3 December 2017

Bosco P

7

1 reference

3 December 2017

Debard R

8

1 reference

3 December 2017

Gérard P

9

1 reference

3 December 2017

Viola M

10

1 reference

3 December 2017

Salvaggio E

11

1 reference

3 December 2017

Guéant JL

12

1 reference

3 December 2017

language of work or name

English

0 references

publication date

1 July 2003

1 reference

3 December 2017

1 reference

3 December 2017

volume

344

1 reference

3 December 2017

issue

3

1 reference

3 December 2017

page(s)

189-192

1 reference

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

3 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Spina bifida, 677T-->C mutation, and role of folate

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Maternal folate status and risk of neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Genetic selection and folate intake during pregnancy

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Isoelectrofocusing phenotype and relative concentration of transcobalamin II isoproteins related to the codon 259 Arg/Pro polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Inborn errors of metabolism: a cause of abnormal brain development

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Methylenetetrahydrofolate reductase and neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

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/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-3940%2803%2900468-3

7 January 2021

10.1016/S0304-3940(03)00468-3

Identifiers

DOI

1 reference

3 December 2017

1 reference