Chronic granulomatous disease.

Gelijkaardige items

• Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
  door: Dinauer, M C, et al.
  Gepubliceerd in: (1990)
• Gp91(phox) is the heme binding subunit of the superoxide-generating NADPH oxidase
  door: Yu, Lixin, et al.
  Gepubliceerd in: (1998)
• A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease.
  door: Dinauer, M C, et al.
  Gepubliceerd in: (1989)
• O(2) sensing is preserved in mice lacking the gp91 phox subunit of NADPH oxidase
  door: Archer, Stephen L., et al.
  Gepubliceerd in: (1999)
• 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.
  door: Erickson, R W, et al.
  Gepubliceerd in: (1992)