von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure.

Podobne zapisy

• Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease.
  od: Schneppenheim, R, i wsp.
  Wydane: (1996)
• Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC).
  od: Ruggeri, Z M, i wsp.
  Wydane: (1982)
• The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF
  od: Haberichter, Sandra L., i wsp.
  Wydane: (2010)
• 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.
  od: Ware, J, i wsp.
  Wydane: (1991)
• Variant von Willebrand's Disease: CHARACTERIZATION OF TWO SUBTYPES BY ANALYSIS OF MULTIMERIC COMPOSITION OF FACTOR VIII/VON WILLEBRAND FACTOR IN PLASMA AND PLATELETS
  od: Ruggeri, Zaverio M., i wsp.
  Wydane: (1980)