Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor.

Lignende værker

• Deficiency of an erythrocyte membrane protein with complement regulatory activity in paroxysmal nocturnal hemoglobinuria.
  af: Pangburn, M K, et al.
  Udgivet: (1983)
• Characterization of the complement sensitivity of paroxysmal nocturnal hemoglobinuria erythrocytes.
  af: Parker, C J, et al.
  Udgivet: (1985)
• Relationship between decay accelerating factor deficiency, diminished acetylcholinesterase activity, and defective terminal complement pathway restriction in paroxysmal nocturnal hemoglobinuria erythrocytes.
  af: Medof, M E, et al.
  Udgivet: (1987)
• Enhanced complement-mediated lysis of type III paroxysmal nocturnal hemoglobinuria erythrocytes involves increased C9 binding and polymerization.
  af: Hu, V W, et al.
  Udgivet: (1985)
• Amelioration of lytic abnormalities of paroxysmal nocturnal hemoglobinuria with decay-accelerating factor.
  af: Medof, M E, et al.
  Udgivet: (1985)