|
1
|
Expression of terminal alpha2-6-linked sialic acid on von Willebrand factor specifically enhances proteolysis by ADAMTS13.
|
Blood
|
2009
|
1.81
|
|
2
|
A novel binding site for ADAMTS13 constitutively exposed on the surface of globular VWF.
|
Blood
|
2009
|
1.51
|
|
3
|
Endothelial von Willebrand factor regulates angiogenesis.
|
Blood
|
2010
|
1.47
|
|
4
|
Bombay phenotype is associated with reduced plasma-VWF levels and an increased susceptibility to ADAMTS13 proteolysis.
|
Blood
|
2005
|
1.30
|
|
5
|
Cellular and molecular basis of von Willebrand disease: studies on blood outgrowth endothelial cells.
|
Blood
|
2013
|
1.22
|
|
6
|
Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factor.
|
Blood
|
2009
|
1.18
|
|
7
|
Mapping the N-glycome of human von Willebrand factor.
|
Biochem J
|
2012
|
0.90
|
|
8
|
O-linked glycosylation of von Willebrand factor modulates the interaction with platelet receptor glycoprotein Ib under static and shear stress conditions.
|
Blood
|
2012
|
0.87
|
|
9
|
Identification of functionally important residues in TFPI Kunitz domain 3 required for the enhancement of its activity by protein S.
|
Blood
|
2012
|
0.85
|