Relationship between decay accelerating factor deficiency, diminished acetylcholinesterase activity, and defective terminal complement pathway restriction in paroxysmal nocturnal hemoglobinuria erythrocytes.

Lignende værker

• Amelioration of lytic abnormalities of paroxysmal nocturnal hemoglobinuria with decay-accelerating factor.
  af: Medof, M E, et al.
  Udgivet: (1985)
• Characterization of the complement sensitivity of paroxysmal nocturnal hemoglobinuria erythrocytes.
  af: Parker, C J, et al.
  Udgivet: (1985)
• Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor.
  af: Nicholson-Weller, A, et al.
  Udgivet: (1983)
• Normal polymorphic variations and transcription of the decay accelerating factor gene in paroxysmal nocturnal hemoglobinuria cells.
  af: Stafford, H A, et al.
  Udgivet: (1988)
• Synthesis of aberrant decay-accelerating factor proteins by affected paroxysmal nocturnal hemoglobinuria leukocytes.
  af: Carothers, D J, et al.
  Udgivet: (1990)