Production of oxygen radicals by fibroblasts and neutrophils from a patient with x‐linked chronic granulomatous disease
暂无分享,去创建一个
[1] A. Jesaitis,et al. The cytochrome b-558 molecules involved in the fibroblast and polymorphonuclear leucocyte superoxide-generating NADPH oxidase systems are structurally and genetically distinct. , 1993, Biochemical Journal.
[2] J. Hancock,et al. Functional expression of NADPH oxidase components (alpha- and beta-subunits of cytochrome b558 and 45-kDa flavoprotein) by intrinsic human glomerular mesangial cells. , 1991, The Journal of biological chemistry.
[3] P. Baeuerle,et al. A role for oxygen radicals as second messengers. , 1991, Trends in cell biology.
[4] G. Rothe,et al. Flow cytometric measurement of the respiratory burst activity of phagocytes using dihydrorhodamine 123. , 1991, Journal of immunological methods.
[5] A R Cross,et al. Identification of a superoxide-generating NADPH oxidase system in human fibroblasts. , 1991, The Biochemical journal.
[6] J. Curnutte,et al. Molecular basis of chronic granulomatous disease [see comments] , 1991 .
[7] R. M. Smith,et al. Molecular basis of chronic granulomatous disease. , 1991, Blood.
[8] G. Habermehl,et al. Human fibroblasts release low amounts of reactive oxygen species in response to the potent phagocyte stimulants, serum-treated zymosan, N-formyl-methionyl-leucyl-phenylalanine, leukotriene B4 or 12-O-tetradecanoylphorbol 13-acetate. , 1990, Biological chemistry Hoppe-Seyler.
[9] M. Lohmann‐Matthes,et al. A fast and easy method to determine the production of reactive oxygen intermediates by human and murine phagocytes using dihydrorhodamine 123. , 1990, Journal of immunological methods.
[10] G. Habermehl,et al. Human fibroblasts release reactive oxygen species in response to interleukin-1 or tumour necrosis factor-alpha. , 1989, The Biochemical journal.
[11] D. Roos,et al. Immunocytochemical discovery of the 22- to 23-Kd subunit of cytochrome b558 at the surface of human peripheral phagocytes. , 1988, Blood.
[12] A. Segal. Absence of both cytochrome b−245 subunits from neutrophils in X-linked chronic granulomatous disease , 1987, Nature.
[13] D. Wara,et al. Prenatal diagnosis of chronic granulomatous disease. , 1984, American journal of medical genetics.
[14] R. Seger,et al. PRENATAL DIAGNOSIS OF CHRONIC GRANULOMATOUS DISEASE: UNRELIABILITY OF FIBROBLAST NITROBLUE TETRAZOLIUM TEST , 1981, The Lancet.
[15] R. Good,et al. FIBROBLAST NITROBLUE TETRAZOLIUM TEST AND THE IN-UTERO DIAGNOSIS OF CHRONIC GRANULOMATOUS DISEASE , 1980, The Lancet.
[16] B. Babior,et al. Defective superoxide production by granulocytes from patients with chronic granulomatous disease. , 1974, The New England journal of medicine.
[17] L. Flohé,et al. Respiratory chain linked H2O2 production in pigeon heart mitochondria , 1971, FEBS letters.
[18] I. Fridovich,et al. Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). , 1969, The Journal of biological chemistry.
[19] R. B. Sandin,et al. Synthesis of Some Cyclic Iodonium Salts , 1956 .
[20] Tyler K. Nygaard,et al. Phagocytes , 1891, The Indian medical gazette.