von Willebrand factor (MESH entry database)
Studies of the human factor VIII/von Willebrand factor protein III Qualitative defects in von Willebrand's disease
15
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
On the miscellaneous aspects of von Willebrand factor
197
Substructure of human von Willebrand factor
11
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
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
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
Evidence that the primary binding site of von Willebrand factor that mediates platelet adhesion on subendothelium is not collagen
10
Carbohydrate of the Factor VIII/von Willebrand Factor in von Willebrand's Disease
6
Inactivation of human factor VIII by activated protein C Cofactor activity of protein S and protective effect of von Willebrand factor
9
Interaction of von Willebrand factor with human platelets in the plasma milieu
9
Human von Willebrand factor/factor VIII concentrates in the management of pediatric patients with von Willebrand disease/hemophilia A
9
Disulfide Bonds and the Quaternary Structure of Factor VIII/von Willebrand Factor
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
Intracellular trafficking of factor VIII to von Willebrand factor storage granules
13
The role of von Willebrand factor alterations in thyroid disorders
15
von Willebrand factor binds to platelets and induces aggregation in platelet type but not type IIB von Willebrand disease
12
Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease
13
The Effects of Ristocetin and von Willebrand Factor on Platelet Electrophoretic Mobility
9
Superiority of the Rapid Von Willebrand Factor (VWF) VWF:GPIbR and VWF:GPIbM Assays in Type 2A, 2B and 2M Von Willebrand Disease
12