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Immunodeficiency Reviews|January 1, 1988
Molecular genetics of chronic granulomatous diseaseM C Dinauer, S H OrkinHematology/Oncology Clinics of North America|June 1, 1988
Chronic granulomatous disease. Molecular geneticsM C Dinauer, S H OrkinThe Journal of Clinical Investigation|December 1, 1989
A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous diseaseM C Dinauer, J T Curnutte, H Rosen, et al.Nature|June 1, 1987
The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complexM C Dinauer, S H Orkin, R Brown, et al.The Journal of Clinical Investigation|November 1, 1990
Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous diseaseM C Dinauer, E A Pierce, G A Bruns, et al.Blood|May 1, 1989
Absence of both the 91kD and 22kD subunits of human neutrophil cytochrome b in two genetic forms of chronic granulomatous diseaseC A Parkos, M C Dinauer, A J Jesaitis, et al.The New England Journal of Medicine|July 21, 1988
Partial correction of the phagocyte defect in patients with X-linked chronic granulomatous disease by subcutaneous interferon gammaR A Ezekowitz, M C Dinauer, H S Jaffe, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1993
Gene targeting of X chromosome-linked chronic granulomatous disease locus in a human myeloid leukemia cell line and rescue by expression of recombinant gp91phoxL Zhen, A A King, Y Xiao, et al.Nature|November 9, 1989
Association of a Ras-related protein with cytochrome b of human neutrophilsM T Quinn, C A Parkos, L Walker, et al.Pageof 31