von Willebrand factor
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
8
Superiority of the Rapid Von Willebrand Factor (VWF) VWF:GPIbR and VWF:GPIbM Assays in Type 2A, 2B and 2M Von Willebrand Disease
12
The Effects of Ristocetin and von Willebrand Factor on Platelet Electrophoretic Mobility
9
Genetic linkage of two intragenic restriction fragment length polymorphisms with von Willebrand's disease type IIA Evidence for a defect in the von Willebrand factor gene
7
On the miscellaneous aspects of von Willebrand factor
197
Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease
13
Studies of the human factor VIII/von Willebrand factor protein III Qualitative defects in von Willebrand's disease
15
Substructure of human von Willebrand factor
11
Carbohydrate of the Factor VIII/von Willebrand Factor in von Willebrand's Disease
6
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)
6
von Willebrand factor binds to platelets and induces aggregation in platelet type but not type IIB von Willebrand disease
12
Human von Willebrand factor/factor VIII concentrates in the management of pediatric patients with von Willebrand disease/hemophilia A
9
Type IIB von Willebrand factor with normal sialic acid content induces platelet aggregation in the absence of ristocetin Role of platelet activation, fibrinogen, and two distinct membrane receptors
9
Interaction of von Willebrand factor with human platelets in the plasma milieu
9
Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC)
5
Disulfide Bonds and the Quaternary Structure of Factor VIII/von Willebrand Factor
9
Evidence that the primary binding site of von Willebrand factor that mediates platelet adhesion on subendothelium is not collagen
10
Inactivation of human factor VIII by activated protein C Cofactor activity of protein S and protective effect of von Willebrand factor
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Binding of Staphylococcus aureus Protein A to von Willebrand Factor Is Regulated by Mechanical Force
13
Functional domains on von Willebrand factor Recognition of discrete tryptic fragments by monoclonal antibodies that inhibit interaction of von Willebrand factor with platelets and with collagen
10