Varaico: Literature-Extracted Genetic Variants

Gene:CYBB
Variant:p.I214V
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CYBB

NM_000397.4:p.I214V

Associated Papers

The -930A>G polymorphism of the CYBA gene is associated with premature coronary artery disease. A case-control study and gene-risk factors interactions.

Niemiec P et al.

Molecular Biology Reports, 2014

Polymorphisms of C242T and A640G in CYBA gene and the risk of coronary artery disease: a meta-analysis.

Xu Q et al.

Plos One, 2014

Association of NADPH oxidase p22phox gene C242T, A640G and -930A/G polymorphisms with primary knee osteoarthritis in the Greek population.

Lepetsos P et al.

Molecular Biology Reports, 2013

The CYBA gene A640G polymorphism influences predispositions to coronary artery disease through interactions with cigarette smoking and hypercholesterolemia.

Niemiec P et al.

Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals, 2011

A polymorphism of NADPH oxidase p22 phox is associated with reduced susceptibility to acute rejection in renal allograft recipients.

Bhandary UV et al.

Transplant Immunology, 2011

The A640G CYBA polymorphism associates with subclinical atherosclerosis in diabetes.

Moreno MU et al.

Frontiers in Bioscience (elite Edition), 2011

Haplotype analysis of the NADPH oxidase p22 phox gene in patients with bronchial asthma.

Izakovicova Holla L et al.

International Archives of Allergy and Immunology, 2009

NADPH oxidase polymorphisms in cerebral small vessel disease.

Khan U et al.

Cerebrovascular Diseases (basel, Switzerland), 2007

Haplotype analysis of NAD(P)H oxidase p22 phox polymorphisms in end-stage renal disease.

Doi K et al.

Journal of Human Genetics, 2005

C242T CYBA polymorphism of the NADPH oxidase is associated with reduced respiratory burst in human neutrophils.

Wyche KE et al.

Hypertension (dallas, Tex. : 1979), 2004

The A640G and C242T p22(phox) polymorphisms in patients with coronary artery disease.

Zafari AM et al.

Antioxidants & Redox Signaling, 2002

Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox).

Rae J et al.

Blood, 2000

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

Inoue N et al.

Circulation, 1998

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."