(Q43228764)

English

Endothelial nitric oxide synthase and nicotinamide adenosine dinucleotide phosphate oxidase p22phox gene (C242T) polymorphisms and systemic lupus erythematosus in a Chinese Population

scientific article published on 4 December 2009

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Europe PubMed Central

PubMed publication ID

16 November 2017

Endothelial nitric oxide synthase and nicotinamide adenosine dinucleotide phosphate oxidase p22phox gene (C242T) polymorphisms and systemic lupus erythematosus in a Chinese Population (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

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author name string

F-Y Tang

1

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

X-W Xie

2

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

G-H Ling

3

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

F-Y Liu

4

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

publication date

4 December 2009

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Europe PubMed Central

PubMed publication ID

16 November 2017

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Europe PubMed Central

PubMed publication ID

16 November 2017

19

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Europe PubMed Central

PubMed publication ID

16 November 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

192-196

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

T-786-->C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene is associated with coronary spasm

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Endothelial function and carotid intima-media thickness in young healthy subjects among endothelial nitric oxide synthase Glu298-->Asp and T-786-->C polymorphisms

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Endothelial nitric oxide synthase genotype and ischemic heart disease: meta-analysis of 26 studies involving 23028 subjects

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Association of ecNOS gene polymorphisms with end stage renal diseases.

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Normal endothelial cell function

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

p22phox is a critical component of the superoxide-generating NADH/NADPH oxidase system and regulates angiotensin II-induced hypertrophy in vascular smooth muscle cells

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Association of angiotensin-converting enzyme and endothelial Nitric Oxide synthase gene polymorphisms with vascular disease in ESRD patients in a Chinese population

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Lack of association of eNOS (G894T) and p22phox NADPH oxidase subunit (C242T) polymorphisms with systemic sclerosis in a cohort of French Caucasian patients

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Intracellular processing of endothelial nitric oxide synthase isoforms associated with differences in severity of cardiopulmonary diseases: cleavage of proteins with aspartate vs. glutamate at position 298.

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

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/10.1177%2F0961203309348980

21 January 2018

Endothelial nitric oxide synthase gene polymorphisms in Behcet's disease and rheumatic diseases with vasculitis

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Polymorphism of the NADH/NADPH oxidase p22 phox gene in patients with coronary artery disease

1 reference

https://api.crossref.org/works/10.1177%2F0961203309348980

21 January 2018

Identifiers

10.1177/0961203309348980

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 November 2017

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