208 related articles for article (PubMed ID: 1431553)
1. Chronic granulomatous disease with partial deficiency of cytochrome b558 and incomplete respiratory burst: variants of the X-linked, cytochrome b558-negative form of the disease.
Roos D; de Boer M; Borregard N; Bjerrum OW; Valerius NH; Seger RA; Mühlebach T; Belohradsky BH; Weening RS
J Leukoc Biol; 1992 Feb; 51(2):164-71. PubMed ID: 1431553
[TBL] [Abstract][Full Text] [Related]
2. A new X-linked variant of chronic granulomatous disease characterized by the existence of a normal clone of respiratory burst-competent phagocytic cells.
Woodman RC; Newburger PE; Anklesaria P; Erickson RW; Rae J; Cohen MS; Curnutte JT
Blood; 1995 Jan; 85(1):231-41. PubMed ID: 7803797
[TBL] [Abstract][Full Text] [Related]
3. [Molecular aspects of chronic granulomatous disease. "the NADPH oxidase complex"].
Morel F
Bull Acad Natl Med; 2007 Feb; 191(2):377-90; discussion 390-2. PubMed ID: 17969555
[TBL] [Abstract][Full Text] [Related]
4. Chronic granulomatous disease and glutathione peroxidase deficiency, revisited.
Newburger PE; Malawista SE; Dinauer MC; Gelbart T; Woodman RC; Chada S; Shen Q; van Blaricom G; Quie PG; Curnutte JT
Blood; 1994 Dec; 84(11):3861-9. PubMed ID: 7949143
[TBL] [Abstract][Full Text] [Related]
5. Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease.
Bolscher BG; de Boer M; de Klein A; Weening RS; Roos D
Blood; 1991 Jun; 77(11):2482-7. PubMed ID: 1710153
[TBL] [Abstract][Full Text] [Related]
6. 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; de Klein A; Hossle JP; Seger R; Corbeel L; Weening RS; Roos D
Am J Hum Genet; 1992 Nov; 51(5):1127-35. PubMed ID: 1415254
[TBL] [Abstract][Full Text] [Related]
7. Absence of both the 91kD and 22kD subunits of human neutrophil cytochrome b in two genetic forms of chronic granulomatous disease.
Parkos CA; Dinauer MC; Jesaitis AJ; Orkin SH; Curnutte JT
Blood; 1989 May; 73(6):1416-20. PubMed ID: 2713485
[TBL] [Abstract][Full Text] [Related]
8. Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous disease.
Roesler J; Heyden S; Burdelski M; Schäfer H; Kreth HW; Lehmann R; Paul D; Marzahn J; Gahr M; Rösen-Wolff A
Exp Hematol; 1999 Mar; 27(3):505-11. PubMed ID: 10089913
[TBL] [Abstract][Full Text] [Related]
9. NADPH-binding component of the respiratory burst oxidase system: studies using neutrophil membranes from patients with chronic granulomatous disease lacking the beta-subunit of cytochrome b558.
Tsunawaki S; Mizunari H; Namiki H; Kuratsuji T
J Exp Med; 1994 Jan; 179(1):291-7. PubMed ID: 8270871
[TBL] [Abstract][Full Text] [Related]
10. Hypoxic induction of gene expression in chronic granulomatous disease-derived B-cell lines: oxygen sensing is independent of the cytochrome b558-containing nicotinamide adenine dinucleotide phosphate oxidase.
Wenger RH; Marti HH; Schuerer-Maly CC; Kvietikova I; Bauer C; Gassmann M; Maly FE
Blood; 1996 Jan; 87(2):756-61. PubMed ID: 8555500
[TBL] [Abstract][Full Text] [Related]
11. Restitution of superoxide generation in autosomal cytochrome-negative chronic granulomatous disease (A22(0) CGD)-derived B lymphocyte cell lines by transfection with p22phax cDNA.
Maly FE; Schuerer-Maly CC; Quilliam L; Cochrane CG; Newburger PE; Curnutte JT; Gifford M; Dinauer MC
J Exp Med; 1993 Dec; 178(6):2047-53. PubMed ID: 8245781
[TBL] [Abstract][Full Text] [Related]
12. Cloning of murine gp91phox cDNA and functional expression in a human X-linked chronic granulomatous disease cell line.
Björgvinsdóttir H; Zhen L; Dinauer MC
Blood; 1996 Mar; 87(5):2005-10. PubMed ID: 8634451
[TBL] [Abstract][Full Text] [Related]
13. A novel mutation at a probable heme-binding ligand in neutrophil cytochrome b558 in atypical X-linked chronic granulomatous disease.
Tsuda M; Kaneda M; Sakiyama T; Inana I; Owada M; Kiryu C; Shiraishi T; Kakinuma K
Hum Genet; 1998 Oct; 103(4):377-81. PubMed ID: 9856476
[TBL] [Abstract][Full Text] [Related]
14. CD34+ peripheral blood progenitors as a target for genetic correction of the two flavocytochrome b558 defective forms of chronic granulomatous disease.
Li F; Linton GF; Sekhsaria S; Whiting-Theobald N; Katkin JP; Gallin JI; Malech HL
Blood; 1994 Jul; 84(1):53-8. PubMed ID: 7517218
[TBL] [Abstract][Full Text] [Related]
15. Prolonged recombinant interferon-gamma therapy in chronic granulomatous disease: evidence against enhanced neutrophil oxidase activity.
Woodman RC; Erickson RW; Rae J; Jaffe HS; Curnutte JT
Blood; 1992 Mar; 79(6):1558-62. PubMed ID: 1312372
[TBL] [Abstract][Full Text] [Related]
16. Genetic variants of chronic granulomatous disease: prevalence of deficiencies of two cytosolic components of the NADPH oxidase system.
Clark RA; Malech HL; Gallin JI; Nunoi H; Volpp BD; Pearson DW; Nauseef WM; Curnutte JT
N Engl J Med; 1989 Sep; 321(10):647-52. PubMed ID: 2770793
[TBL] [Abstract][Full Text] [Related]
17. Absence of both subunits of cytochrome b558 in the UM384 cell line relative to the inability to generate superoxide anions.
Champelovier P; Laporte F; Verhoeven AJ; Hilarius P; de Klein A; Revol C; Seigneurin D; Kolodie L
Exp Hematol; 1993 Jul; 21(7):885-92. PubMed ID: 8391470
[TBL] [Abstract][Full Text] [Related]
18. Identification of a thermolabile component of the human neutrophil NADPH oxidase. A model for chronic granulomatous disease caused by deficiency of the p67-phox cytosolic component.
Erickson RW; Malawista SE; Garrett MC; Van Blaricom G; Leto TL; Curnutte JT
J Clin Invest; 1992 May; 89(5):1587-95. PubMed ID: 1314852
[TBL] [Abstract][Full Text] [Related]
19. Characterization of two monoclonal antibodies against cytochrome b558 of human neutrophils.
Verhoeven AJ; Bolscher BG; Meerhof LJ; van Zwieten R; Keijer J; Weening RS; Roos D
Blood; 1989 May; 73(6):1686-94. PubMed ID: 2469497
[TBL] [Abstract][Full Text] [Related]
20. Chronic granulomatous disease. Molecular genetics.
Dinauer MC; Orkin SH
Hematol Oncol Clin North Am; 1988 Jun; 2(2):225-40. PubMed ID: 3292508
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
