Functional analysis of a type IIB von Willebrand disease missense mutation: increased binding of large von Willebrand factor multimers to platelets.

مواد مشابهة

• von Willebrand factor binds to platelets and induces aggregation in platelet-type but not type IIB von Willebrand disease.
  بواسطة: Miller, J L, وآخرون
  منشور في: (1983)
• The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.
  بواسطة: Cooney, K A, وآخرون
  منشور في: (1991)
• von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib.
  بواسطة: Rabinowitz, I, وآخرون
  منشور في: (1992)
• von Willebrand factor synthesized by endothelial cells from a patient with type IIB von Willebrand disease supports platelet adhesion normally but has an increased affinity for platelets.
  بواسطة: de Groot, P G, وآخرون
  منشور في: (1989)
• Low shear stress can initiate von Willebrand factor-dependent platelet aggregation in patients with type IIB and platelet-type von Willebrand disease.
  بواسطة: Murata, M, وآخرون
  منشور في: (1993)