Detection of gp91-phox precursor protein in B-cell lines from patients with X-linked chronic granulomatous disease as an indicator for mutations impairing cytochrome b558 biosynthesis.

Podobne knjige/članki

• Mutations in the promoter region of the gene for gp91-phox in X-linked chronic granulomatous disease with decreased expression of cytochrome b558.
  od: Newburger, P E, et al.
  Izdano: (1994)
• A point mutation in gp91-phox of cytochrome b558 of the human NADPH oxidase leading to defective translocation of the cytosolic proteins p47-phox and p67-phox.
  od: Leusen, J H, et al.
  Izdano: (1994)
• Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).
  od: de Boer, M, et al.
  Izdano: (1992)
• Endothelial Function and Oxidative Stress in X-Linked, gp91(phox) Deficiency, Chronic Granulomatous Disease
  od: Higashi, Yukihito, et al.
  Izdano: (2020)
• Proton Conduction through gp91(phox)
  od: Henderson, Lydia M., et al.
  Izdano: (2002)