(Q46060410)

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Methionine synthase reductase (MTRR) A66G polymorphism is not related to plasma homocysteine concentration and the risk for vascular disease

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Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

Methionine synthase reductase (MTRR) A66G polymorphism is not related to plasma homocysteine concentration and the risk for vascular disease (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

author name string

Scazzone C

1

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

Acuto S

2

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

Guglielmini E

3

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

Campisi G

4

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

Bono A

5

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

publication date

1 April 2009

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

Experimental and Molecular Pathology

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

86

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

2

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

131-133

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Methylenetetrahydrofolate reductase (MTHFR) 677C>T and methionine synthase reductase (MTRR) 66A>G polymorphisms: association with serum homocysteine and angiographic coronary artery disease in the era of flour products fortified with folic acid

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Hyperhomocysteinemia as a risk factor for deep-vein thrombosis.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Methylenetetrahydrofolate reductase polymorphism (C677T), hyperhomocysteinemia, and risk of ischemic cardiovascular disease and venous thromboembolism: prospective and case-control studies from the Copenhagen City Heart Study

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Influence of methionine synthase (A2756G) and methionine synthase reductase (A66G) polymorphisms on plasma homocysteine levels and relation to risk of coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Homocysteinemia: association of a metabolic disorder with vascular disease and thrombosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Homocysteine and cardiovascular disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

No association between MTHFR A1298C and MTRR A66G polymorphisms, and MS in an Australian cohort.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

Hyperhomocysteinaemia and vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

7 January 2021

The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXMP.2009.01.014

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%2FJ.YEXMP.2009.01.014

7 January 2021

Identifiers

10.1016/J.YEXMP.2009.01.014

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19348062

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