Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease.

Samankaltaisia teoksia

• von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure.
  Tekijä: Holmberg, L, et al.
  Julkaistu: (1993)
• von Willebrand Factor Variant p.Arg924Gln Marks an Allele Associated with Reduced von Willebrand Factor and Factor VIII Levels
  Tekijä: HICKSON, N., et al.
  Julkaistu: (2010)
• Subunit composition of plasma von Willebrand factor. Cleavage is present in normal individuals, increased in IIA and IIB von Willebrand disease, but minimal in variants with aberrant structure of individual oligomers (types IIC, IID, and IIE).
  Tekijä: Zimmerman, T S, et al.
  Julkaistu: (1986)
• The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF
  Tekijä: Haberichter, Sandra L., et al.
  Julkaistu: (2010)
• D’ domain region Arg782-Cys799 of von Willebrand factor contributes to factor VIII binding
  Tekijä: Przeradzka, Małgorzata A., et al.
  Julkaistu: (2020)