The expression of 22-kD subunit of cytochrome b558 in patients with X-linked chronic granulomatous disease
- 1 January 1991
- journal article
- Published by Wiley in European Journal of Haematology
- Vol. 46 (1) , 52-54
- https://doi.org/10.1111/j.1600-0609.1991.tb00516.x
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease.Journal of Clinical Investigation, 1989
- Classification of chronic granulomatous disease on the basis of monoclonal antibody-defined surface cytochrome b deficiencyThe Journal of Pediatrics, 1988
- Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000.Journal of Clinical Investigation, 1987
- The X-linked chronic granulomatous disease gene codes for the β-chain of cytochrome b−245Nature, 1987
- The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complexNature, 1987
- Absence of both cytochrome b−245 subunits from neutrophils in X-linked chronic granulomatous diseaseNature, 1987
- Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal locationNature, 1986
- A variant form of X‐linked chronic granulomatous disease with normal nitroblue tetrazolium slide test and cytochrome bEuropean Journal of Clinical Investigation, 1983
- Antigens of the Kell blood group system on neutrophils and monocytes: Their relation to chronic granulomatous diseaseThe Journal of Pediatrics, 1975
- KELL PHENOTYPES IN CHRONIC GRANULOMATOUS DISEASE: A POTENTIAL TRANSFUSION HAZARDThe Lancet, 1971