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 (Q28202213)

From Wikidata

Jump to navigation Jump to search

scientific article (publication date: September 2003)

Language	Label	Description	Also known as
English	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	scientific article (publication date: September 2003)

Statements

scholarly article

0 references

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 (English)

0 references

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Paolo Bosco

1

0 references

Rosa-Maria Guéant-Rodriguez

2

0 references

Guido Anello

3

0 references

Concetta Barone

4

0 references

Farès Namour

5

0 references

Filippo Caraci

6

0 references

Antonino Romano

7

0 references

Corrado Romano

8

0 references

Jean-Louis Guéant

9

0 references

language of work or name

0 references

publication date

1 September 2003

0 references

American Journal of Medical Genetics Part A

1 reference

121A

0 references

219-24

0 references

3

0 references

Hyperhomocysteinemia is related to residual glomerular filtration and folate, but not to methylenetetrahydrofolate-reductase and methionine synthase polymorphisms, in supplemented end-stage renal disease patients undergoing hemodialysis

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

Methylenetetrahydrofolate reductase polymorphism in the etiology of Down syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

Human methionine synthase. cDNA cloning, gene localization, and expression

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

Maternal folate polymorphisms and the etiology of human nondisjunction

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

Identification of six methylenetetrahydrofolate reductase (MTHFR) genotypes resulting from common polymorphisms: impact on plasma homocysteine levels and development of coronary artery disease.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

MTRR and MTHFR polymorphism: link to Down syndrome?

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

Homocysteine metabolism in children with Down syndrome: in vitro modulation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

Biological and clinical implications of the MTHFR C677T polymorphism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

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/10.1002%2FAJMG.A.20234

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

'Spontaneous' genetic damage in man: evaluation of interindividual variability, relationship among markers of damage, and influence of nutritional status

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.20234

21 January 2018

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/10.1002%2FAJMG.A.20234

21 January 2018

Identifiers

10.1002/AJMG.A.20234

0 references

release_ufo7gyn4ivc2lizmoi6pxd7nqa

1 reference

https://api.fatcat.wiki/v0/release/ufo7gyn4ivc2lizmoi6pxd7nqa

24 November 2022

based on heuristic

mapped directly with Wikidata item

0 references

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=Q28202213&oldid=2042671403"