Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences.

Samankaltaisia teoksia

• von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib.
  Tekijä: Rabinowitz, I, et al.
  Julkaistu: (1992)
• Structural basis of von Willebrand factor binding to platelet glycoprotein Ib and collagen. Effects of disulfide reduction and limited proteolysis of polymeric von Willebrand factor.
  Tekijä: Bockenstedt, P, et al.
  Julkaistu: (1986)
• Structural Basis of Regulation of von Willebrand Factor Binding to Glycoprotein Ib
  Tekijä: Blenner, Mark A., et al.
  Julkaistu: (2014)
• Asialo von Willebrand factor interactions with platelets. Interdependence of glycoproteins Ib and IIb/IIIa for binding and aggregation.
  Tekijä: Grainick, H R, et al.
  Julkaistu: (1985)
• The membrane-proximal intermolecular disulfide bonds in glycoprotein Ib influence the receptor binding to von Willebrand factor
  Tekijä: Mo, Xi, et al.
  Julkaistu: (2008)