Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome? (Q35600454)

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21 December 2019

review article

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title

Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome? (English)

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21 December 2019

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21 December 2019

Raffaele Ferri

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21 December 2019

author name string

Jean-Louis Guéant

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21 December 2019

Rosa-Maria Guéant-Rodriguez

2

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21 December 2019

Paolo Bosco

4

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21 December 2019

Laurent Brunaud

5

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21 December 2019

Corrado Romano

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21 December 2019

Antonino Romano

8

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21 December 2019

Mirande Candito

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21 December 2019

Bernard Namour

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21 December 2019

publication date

1 November 2003

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Clinical Chemistry and Laboratory Medicine

21 December 2019

published in

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21 December 2019

volume

41

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21 December 2019

issue

11

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21 December 2019

page(s)

1473-1477

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Biological and clinical implications of the MTHFR C677T polymorphism

21 December 2019

cites work

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

21 January 2018

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

21 January 2018

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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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A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status.

21 January 2018

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

21 January 2018

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Transcobalamin polymorphism and homocysteine

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females

21 January 2018

1 reference

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Homocysteine metabolism in children with Down syndrome: in vitro modulation

21 January 2018

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Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome

21 January 2018

1 reference

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MTRR and MTHFR polymorphism: link to Down syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.226

Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.226

Maternal folate polymorphisms and the etiology of human nondisjunction

21 January 2018

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Frequency of Down's syndrome and neural-tube defects in the same family

21 January 2018

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https://api.crossref.org/works/10.1515%2FCCLM.2003.226

Methylenetetrahydrofolate reductase and neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.226

21 January 2018

Identifiers

DOI

10.1515/CCLM.2003.226

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14656028%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

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