Mutation in the gene encoding the alpha chain of platelet glycoprotein Ib in platelet-type von Willebrand disease.

Ítems similars

• Visualizing the von Willebrand factor/glycoprotein Ib-IX axis with a platelet-type von Willebrand disease mutation
  per: Guerrero, Jose A., et al.
  Publicat: (2009)
• Expression of the phenotypic abnormality of platelet-type von Willebrand disease in a recombinant glycoprotein Ib alpha fragment.
  per: Murata, M, et al.
  Publicat: (1993)
• Identification of a point mutation in type IIB von Willebrand disease illustrating the regulation of von Willebrand factor affinity for the platelet membrane glycoprotein Ib-IX receptor.
  per: Ware, J, et al.
  Publicat: (1991)
• von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib.
  per: Rabinowitz, I, et al.
  Publicat: (1992)
• Promotion of binding of von Willebrand factor to platelet glycoprotein Ib by dimers of ristocetin.
  per: Hoylaerts, M F, et al.
  Publicat: (1995)