[von Willebrand factor (vWF)]. 1995

Y Takahashi
Division of Neonatology, Nara Medical University.

UI MeSH Term Description Entries
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D014841 von Willebrand Factor A high-molecular-weight plasma protein, produced by endothelial cells and megakaryocytes, that is part of the factor VIII/von Willebrand factor complex. The von Willebrand factor has receptors for collagen, platelets, and ristocetin activity as well as the immunologically distinct antigenic determinants. It functions in adhesion of platelets to collagen and hemostatic plug formation. The prolonged bleeding time in VON WILLEBRAND DISEASES is due to the deficiency of this factor. Factor VIII-Related Antigen,Factor VIIIR-Ag,Factor VIIIR-RCo,Plasma Factor VIII Complex,Ristocetin Cofactor,Ristocetin-Willebrand Factor,von Willebrand Protein,Factor VIII Related Antigen,Factor VIIIR Ag,Factor VIIIR RCo,Ristocetin Willebrand Factor

Related Publications

Y Takahashi
February 1985, Rinsho byori. The Japanese journal of clinical pathology,
Y Takahashi
November 2022, Arteriosclerosis, thrombosis, and vascular biology,
Y Takahashi
January 2019, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis,
Y Takahashi
August 1990, Nucleic acids research,
Y Takahashi
November 2008, Brain and nerve = Shinkei kenkyu no shinpo,
Y Takahashi
March 2018, Haemophilia : the official journal of the World Federation of Hemophilia,
Copied contents to your clipboard!