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