Benzer Materyaller

• Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease.
  Yazar:: Dinauer, M C, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)
• A missense mutation in the neutrophil cytochrome b heavy chain in cytochrome-positive X-linked chronic granulomatous disease.
  Yazar:: Dinauer, M C, ve diğerleri
  Baskı/Yayın Bilgisi: (1989)
• Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000.
  Yazar:: Parkos, C A, ve diğerleri
  Baskı/Yayın Bilgisi: (1987)
• Point mutation in the cytoplasmic domain of the neutrophil p22-phox cytochrome b subunit is associated with a nonfunctional NADPH oxidase and chronic granulomatous disease.
  Yazar:: Dinauer, M C, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)
• Ultrastructural localization of cytochrome b in the membranes of resting and phagocytosing human granulocytes.
  Yazar:: Jesaitis, A J, ve diğerleri
  Baskı/Yayın Bilgisi: (1990)