Citations for
1CYBA, CYBB
Identification of NOX2 regions for normal biosynthesis of cytochrome b558 in phagocytes highlighting essential residues for p22phox binding.
Beaumel S, Grunwald D, Fieschi F, Stasia MJ.
Biochem J 464(3):425-37. doi: 10.1042/BJ20140555. 2014
2CYBA, CYP1A1, CYP1A2
CYP1A1, CYP1A2 and CYBA gene polymorphisms associated with oxidative stress in COPD.
Vibhuti A, Arif E, Mishra A, Deepak D, Singh B, Rahman I, Mohammad G, Pasha MA.
Clin Chim Acta 411(7-8):474-80. Epub 2010 Jan 18.PMID: 20080081 2010
3CYBA, MAPK14, NOX4
Nox4 overexpression activates reactive oxygen species and p38 MAPK in human endothelial cells.
Goettsch C, Goettsch W, Muller G, Seebach J, Schnittler HJ, Morawietz H.
Biochem Biophys Res Commun iochem Biophys Res Commun. 2009 Jan 23. [Epub ahead of print] 2009
4CYBA, AKR1A1
Genetic polymorphisms in the oxidative stress pathway and susceptibility to non-Hodgkin lymphoma.
Lan Q, Zheng T, Shen M, Zhang Y, Wang SS, Zahm SH, Holford TR, Leaderer B, Boyle P, Chanock S.
Hum Genet 121(2):161-8. Epub 2006 Dec 6. 2007
5CBFA2T3, CYBA, MAP1LC3B, MVD, TSG16C, FBXO31
Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes.
Powell J, Gardner A, Bais A, Hinze S, Baker E, Whitmore S, Crawford J, Kochetkova M, Spendlove H, Doggett N, Sutherland G, Callen D, Kremmidiotis G.
Genomics 80(3):303. 2002
6CYBA, CYBB, NCF2
Assembly of the neutrophil respiratory burst oxidase: A direct interaction between p67PHOX and cytochrome b558.
Dang PM, Cross AR, Babior BM.
Proc Natl Acad Sci U S A 98(6):3001-5. 2001
7CYBA
A variant of p22(phox), involved in generation of reactive oxygen species in the vessel wall, is associated with progression of coronary atherosclerosis.
Cahilly C, Ballantyne CM, Lim DS, Gotto A, Marian AJ.
Circ Res 86(4):391-5. 2000
8CYBA
Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients.
Yamada M, Ariga T, Kawamura N, Ohtsu M, Imajoh-Ohmi S, Ohshika E, Tatsuzawa O, Kobayashi K, Sakiyama Y.
Br J Haematol 108(3):511-7. 2000
9CYBA
Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox).
Rae J, Noack D, Heyworth PG, Ellis BA, Curnutte JT, Cross AR.
Blood 96(3):1106-12. 2000
10CYBA
Identification of allele-specific p22-phox mutations in a compound heterozygous patient with chronic granulomatous disease by mismatch PCR and restriction enzyme analysis.
Hossle JP, et al.
Hum Genet 93 : 437-442. 1994
11CYBA, CYBB, NCF1
Role of Src homology 3 domains in assembly and activation of the phagocyte NADPH oxidase.
Sumimoto H, Kage Y, Nunoi H, Sasaki H, Nose T, Fukumaki Y, Ohno M, Minakami S, Takeshige K.
Proc Natl Acad Sci U S A 91(12):5345-9. 1994
12CYBA
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease : two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).
de Boer M, et al.
Am J Hum Genet 51 : 1127-1135. 1992
13CYBA
Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.
Dinauer MC, et al.
Proc Natl Acad Sci U S A 88 : 11231-11235. 1991
14CYBA
Human neutrophil cytochrome-b light chain (p22-phox): gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
Dinauer MC, et al.
J Clin Invest 86 : 1729-1737. 1990
15CYBA
The alpha subunit of cytochrome b(-245) mapped to chromosome 16.
Bu-Ghanim HN, et al.
Genomics 8 : 568-570. 1990
16CYBA, CYBB, GDCC2, NCF1, NCF2
Genetic variants of chronic granulomatous disease : prevalence of deficiencies of two cytosolic components of the NADPH oxidase system.
Clark RA, et al.
N Engl J Med 321 : 647-652. 1989