(Q46166687)

English

Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects

scientific article published in January 2008

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Statements

scholarly article

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects (English)

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

6

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

author name string

Ingrid M van Beynum

1

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

Christiaan Mooij

2

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

Livia Kapusta

3

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

Sandra Heil

4

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

Martin den Heijer

5

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

publication date

1 January 2008

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

Clinical Chemistry and Laboratory Medicine

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

46

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

10

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

1369-1375

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

The incidence of congenital heart disease

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Hungarian cohort-controlled trial of periconceptional multivitamin supplementation shows a reduction in certain congenital abnormalities

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Association of the C677T methylenetetrahydrofolate reductase mutation and elevated homocysteine levels with congenital cardiac malformations

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

The L-arginine-nitric oxide pathway

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Nitric oxide as a bioregulator of apoptosis

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Genetic evidence that nitric oxide modulates homocysteine: the NOS3 894TT genotype is a risk factor for hyperhomocystenemia

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Dysfunctional endothelial nitric oxide biosynthesis in healthy smokers with impaired endothelium-dependent vasodilatation

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

The Glu298Asp polymorphism of the NOS 3 gene as a determinant of the baseline production of nitric oxide

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Genotype-dependent expression of endothelial nitric oxide synthase (eNOS) and its regulatory proteins in cultured endothelial cells

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Nitric oxide inhibits apoptosis by preventing increases in caspase-3-like activity via two distinct mechanisms

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Homocysteine induces congenital defects of the heart and neural tube: effect of folic acid

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Congenital heart defects and maternal derangement of homocysteine metabolism.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Maternal hyperhomocysteinaemia is a risk factor for congenital heart disease.

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2008.271

21 January 2018

Identifiers

10.1515/CCLM.2008.271

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/18844489

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