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The American Journal of Medicine, 1963
M, BLOMBACK, J E, JORPES, I M, NILSSON
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M, BLOMBACK, J E, JORPES, I M, NILSSON
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von Willebrand's factor and von Willebrand's disease.
Current opinion in hematology, 1997von Willebrand's factor is required for platelet adhesion to subendothelium, and for normal factor VIII survival in the circulation. These functions require the assembly of von Willebrand's factor into multimers that exhibit properly regulated binding to platelet glycoprotein lb. Recent studies suggest that the propeptide of von Willebrand's factor may
T, Matsushita, Z, Dong, J E, Sadler
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[Von Willebrand factor and Von Willebrand disease].
Nederlands tijdschrift voor geneeskunde, 2014Von Willebrand factor (VWF) is a multimeric adhesive protein that binds platelets to exposed subendothelium and carries factor VIII in the circulation. VWD is classified into three major subtypes, distinguished by a quantitative deficiency of VWF (type 1: partial deficiency; type 3: complete deficiency) or qualitative defects of VWF (type 2A, 2B, 2M ...
Paul W M, Verhezen +2 more
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von Willebrand factor and von Willebrand disease.
Blood, 1987Progress has occurred in the past several years in the understanding of the structure and function of von Willebrand factor (vWF). This multimeric glycoprotein exhibits a dual role, that of mediating platelet adhesion and aggregation onto thrombogenic surfaces, and that of functioning as carrier in plasma for the factor VIII procoagulant protein.
Z M, Ruggeri, T S, Zimmerman
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