| 1 |
31675465 | Unique surface-exposed hydrophobic residues in the C1 domain of factor VIII contribute to cofactor function and von Willebrand factor binding. | 2020 Feb |
2 |
| 2 |
24283831 | The von Willebrand factor predicted unpaired cysteines are essential for secretion. | 2014 Feb |
1 |
| 3 |
22754302 | Role of 14-3-3ζ in platelet glycoprotein Ibα-von Willebrand factor interaction-induced signaling. | 2012 |
1 |
| 4 |
18923835 | Impact of 789Ala/Ala genotype on quantitative type of von Willebrand disease. | 2009 May |
3 |
| 5 |
19875727 | Identification of a novel 14-3-3zeta binding site within the cytoplasmic domain of platelet glycoprotein Ibalpha that plays a key role in regulating the von Willebrand factor binding function of glycoprotein Ib-IX. | 2009 Dec 4 |
2 |
| 6 |
18369690 | Identification of amino acid residues responsible for von Willebrand factor binding to sulfatide by charged-to-alanine-scanning mutagenesis. | 2008 May |
1 |
| 7 |
15606553 | Impact of O-linked glycosylation of the VWF-A1-domain flanking regions on platelet interaction. | 2005 Jan |
1 |
| 8 |
12969981 | Deletion of alanine 2201 in the FVIII C2 domain results in mild hemophilia A by impairing FVIII binding to VWF and phospholipids and destroys a major FVIII antigenic determinant involved in inhibitor development. | 2004 Jan 1 |
1 |
| 9 |
14757772 | Identification of the amino acid residues of the platelet glycoprotein Ib (GPIb) essential for the von Willebrand factor binding by clustered charged-to-alanine scanning mutagenesis. | 2004 Apr 16 |
1 |
| 10 |
12069583 | Binding site on human von Willebrand factor of bitiscetin, a snake venom-derived platelet aggregation inducer. | 2002 Jun 25 |
1 |
| 11 |
10648402 | Requirement of leucine-rich repeats of glycoprotein (GP) Ibalpha for shear-dependent and static binding of von Willebrand factor to the platelet membrane GP Ib-IX-V complex. | 2000 Feb 1 |
1 |
| 12 |
11876992 | [Construction and transient expression of an Ala 737-->Glu mutant of vWF]. | 2000 May |
1 |
| 13 |
9657753 | Binding of factor VIII to von willebrand factor is enabled by cleavage of the von Willebrand factor propeptide and enhanced by formation of disulfide-linked multimers. | 1998 Jul 15 |
1 |
| 14 |
9865467 | Ser752 mutation to Pro or Ala in the beta3 integrin subunit differentially affects the kinetics of cell spreading to von Willebrand factor and fibrinogen. | 1998 |
1 |
| 15 |
7539426 | Identification of amino acid residues essential for von Willebrand factor binding to platelet glycoprotein Ib. Charged-to-alanine scanning mutagenesis of the A1 domain of human von Willebrand factor. | 1995 Jun 2 |
3 |
| 16 |
8120035 | Disulfide bonds required to assemble functional von Willebrand factor multimers. | 1994 Mar 4 |
1 |
| 17 |
1737795 | Selective inactivation of the Arg-Gly-Asp-Ser (RGDS) binding site in von Willebrand factor by site-directed mutagenesis. | 1992 Feb 15 |
1 |