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6. Deficient flavoprotein component of the NADPH-dependent O2-.-generating oxidase in the neutrophils from three male patients with chronic granulomatous disease. Gabig TG; Lefker BA J Clin Invest; 1984 Mar; 73(3):701-5. PubMed ID: 6707199 [TBL] [Abstract][Full Text] [Related]
7. Comparison of NADH and NADPH oxidase activities in granules isolated from human polymorphonuclear leukocytes with a fluorometric assay. Iverson D; DeChatelet LR; Spitznagel JK; Wang P J Clin Invest; 1977 Feb; 59(2):282-90. PubMed ID: 833275 [TBL] [Abstract][Full Text] [Related]
8. Chronic granulomatous disease. Schmalzer EA; Miller DR Prog Med Genet; 1976; 1():145-84. PubMed ID: 935507 [No Abstract] [Full Text] [Related]
9. Increased phagocytic activity of polymorphonuclear leukocytes of chronic granulomatous disease as determined with flow cytometric assay. Hasui M; Hirabayashi Y; Hattori K; Kobayashi Y J Lab Clin Med; 1991 Apr; 117(4):291-8. PubMed ID: 1849170 [TBL] [Abstract][Full Text] [Related]
11. A phosphoprotein of Mr 47,000, defective in autosomal chronic granulomatous disease, copurifies with one of two soluble components required for NADPH:O2 oxidoreductase activity in human neutrophils. Bolscher BG; van Zwieten R; Kramer IM; Weening RS; Verhoeven AJ; Roos D J Clin Invest; 1989 Mar; 83(3):757-63. PubMed ID: 2537848 [TBL] [Abstract][Full Text] [Related]
13. A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox. Leusen JH; de Boer M; Bolscher BG; Hilarius PM; Weening RS; Ochs HD; Roos D; Verhoeven AJ J Clin Invest; 1994 May; 93(5):2120-6. PubMed ID: 8182143 [TBL] [Abstract][Full Text] [Related]
14. Skewing of X-chromosome inactivation in three generations of carriers with X-linked chronic granulomatous disease within one family. Köker MY; Sanal O; de Boer M; Tezcan I; Metin A; Tan C; Ersoy F; Roos D Eur J Clin Invest; 2006 Apr; 36(4):257-64. PubMed ID: 16620288 [TBL] [Abstract][Full Text] [Related]
15. [Biological and clinical aspects of chronic granulomatous disease]. Robak T; Robak E Przegl Lek; 1992; 49(5):168-71. PubMed ID: 1438921 [No Abstract] [Full Text] [Related]
16. [Chronic septic granulomatous disease in two brothers (author's transl)]. Rister M; Fröhlich G; Seiferth J Dtsch Med Wochenschr; 1974 Oct; 99(43):2172-5. PubMed ID: 4154190 [No Abstract] [Full Text] [Related]
17. Analytical subcellular fractionation of neutrophils from patients with chronic granulomatous disease. Demonstration of the enzyme defect in four cases. Segal AW; Peters TJ Q J Med; 1978 Apr; 47(186):213-20. PubMed ID: 684156 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Phagocytic NADPH oxidase and its role in chronic granulomatous disease. Pallister CJ; Hancock JT Br J Biomed Sci; 1995 Jun; 52(2):149-56. PubMed ID: 8520251 [TBL] [Abstract][Full Text] [Related]
20. Characterisation of the enzyme defect in chronic granulomatous disease. Segal AW; Peters TJ Lancet; 1976 Jun; 1(7974):1363-5. PubMed ID: 59010 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]