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CYBB wt Allele

Known as: GP91-1, CGD, NOX2 
Human CYBB wild-type allele is located in the vicinity of Xp21.1 and is approximately 33 kb in length. This allele, which encodes cytochrome B-245… 
National Institutes of Health

Papers overview

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Review
2014
Review
2014
Summary There is a growing body of evidence to suggest that reactive oxidant species (ROS) including O2 −, OH− or H2O2 act as… 
2012
2012
Absence of phagocyte NADPH oxidase (NOX2) activity causes chronic granulomatous disease (CGD), a primary immunodeficiency… 
Highly Cited
2009
Highly Cited
2009
Chronic cocaine exposure is associated with severe cardiac complications, but the mechanisms of cocaine cardiotoxicity remain… 
Highly Cited
2008
Highly Cited
2008
The vascular adventitia is emerging as an important modulator of vessel remodeling. Adventitial myofibroblasts migrate to the… 
Highly Cited
2008
Highly Cited
2008
c-Src has been shown to activate NF-kappaB (nuclear factor kappaB) following H/R (hypoxia/reoxygenation) by acting as a redox… 
Highly Cited
2007
Highly Cited
2007
Human immunodeficiency virus, type 1 Tat is known to exert pleiotropic effects on the vascular endothelium through mitogen… 
Highly Cited
1998
Highly Cited
1998
Chronic granulomatous disease (CGD) is a disorder of the lymphohematopoietic system, whereby phagocytes of affected patients are… 
Highly Cited
1995
Highly Cited
1995
The human neutrophil NADPH oxidase-associated H channel acts as a charge compensator for the electrogenic generation of… 
1993
1993
Chronic granulomatous disease (CGD) is an inherited immunodeficiency resulting from the inability of an individual's phagocytes…