| 1 |
25690668 | von Willebrand factor arginine 1205 substitution results in accelerated macrophage-dependent clearance in vivo. | 2015 May |
1 |
| 2 |
22490677 | Sequence and structure relationships within von Willebrand factor. | 2012 Jul 12 |
1 |
| 3 |
20075158 | Amino acid residues Arg(659), Arg(660), and Tyr(661) in the spacer domain of ADAMTS13 are critical for cleavage of von Willebrand factor. | 2010 Mar 18 |
5 |
| 4 |
18492952 | Extensive contacts between ADAMTS13 exosites and von Willebrand factor domain A2 contribute to substrate specificity. | 2008 Sep 1 |
1 |
| 5 |
18502798 | Mechanistic studies on ADAMTS13 catalysis. | 2008 Sep |
2 |
| 6 |
17146059 | Exosite interactions contribute to tension-induced cleavage of von Willebrand factor by the antithrombotic ADAMTS13 metalloprotease. | 2006 Dec 12 |
1 |
| 7 |
15975930 | The proximal carboxyl-terminal domains of ADAMTS13 determine substrate specificity and are all required for cleavage of von Willebrand factor. | 2005 Aug 19 |
1 |
| 8 |
15571600 | Gastrointestinal angiodysplasia in a patient with type 2 von Willebrand's disease and analysis of exon 28 of the von Willebrand factor gene. | 2004 Dec |
1 |
| 9 |
12855711 | A consensus tetrapeptide selected by phage display adopts the conformation of a dominant discontinuous epitope of a monoclonal anti-VWF antibody that inhibits the von Willebrand factor-collagen interaction. | 2003 Sep 26 |
1 |
| 10 |
11150026 | Type 2M von Willebrand disease variant characterized by abnormal von willebrand factor multimerization. | 2001 Jan |
2 |
| 11 |
11159522 | The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A-like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factor. | 2001 Feb 15 |
2 |
| 12 |
11920243 | Selective inactivation of Von Willebrand factor binding to glycoprotein IIb/IIIa and to inhibitor monoclonal antibody 9 by site-directed mutagenesis. | 2001 |
1 |
| 13 |
10739395 | Protamine sulphate inhibits platelet membrane glycoprotein Ib-von Willebrand factor activity. | 2000 Feb |
1 |
| 14 |
10845886 | Platelet thrombus formation on collagen at high shear rates is mediated by von Willebrand factor-glycoprotein Ib interaction and inhibited by von Willebrand factor-glycoprotein IIb/IIIa interaction. | 2000 Jun |
1 |
| 15 |
9792286 | Type 2N von Willebrand disease due to Arg91Gln substitution and a cytosine deletion in exon 18 of the von Willebrand factor gene. | 1998 Oct |
2 |
| 16 |
9808586 | Interaction of sickle erythrocytes with endothelial cells in the presence of endothelial cell conditioned medium induces oxidant stress leading to transendothelial migration of monocytes. | 1998 Nov 15 |
1 |
| 17 |
9845532 | A novel mutation in the D3 domain of von Willebrand factor markedly decreases its ability to bind factor VIII and affects its multimerization. | 1998 Dec 15 |
1 |
| 18 |
9858249 | Identification of new type 2B von Willebrand disease mutations: Arg543Gln, Arg545Pro and Arg578Leu. | 1998 Dec |
2 |
| 19 |
8622978 | Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease. | 1996 Apr 16 |
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| 20 |
8839833 | Dominant type 1 von Willebrand disease caused by mutated cysteine residues in the D3 domain of von Willebrand factor. | 1996 Oct 1 |
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| 21 |
7620154 | Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF. | 1995 Aug 1 |
1 |
| 22 |
7974349 | Epitope mapping of inhibitory monoclonal antibodies to human von Willebrand factor by using recombinant cDNA libraries. | 1994 Jun |
2 |
| 23 |
8483792 | Synthetic peptides inhibit the interaction of von Willebrand factor-platelet membrane glycoproteins. | 1993 Mar-Apr |
3 |
| 24 |
1323869 | [The glycoprotein IIb/IIIa complex of the platelets. An activation-dependent integrin]. | 1992 Feb |
2 |
| 25 |
1370885 | Comparison of the primary structure of the functional domains of human and porcine von Willebrand factor that mediate platelet adhesion. | 1992 Jan 31 |
1 |
| 26 |
1419804 | Defects in type IIA von Willebrand disease: a cysteine 509 to arginine substitution in the mature von Willebrand factor disrupts a disulphide loop involved in the interaction with platelet glycoprotein Ib-IX. | 1992 Sep |
3 |
| 27 |
1569181 | Factor VIII-East Hartford (arginine 1689 to cysteine) has procoagulant activity when separated from von Willebrand factor. | 1992 May |
1 |
| 28 |
1571548 | Preferred sequence requirements for cleavage of pro-von Willebrand factor by propeptide-processing enzymes. | 1992 May 1 |
1 |
| 29 |
1732004 | The mutation Arg (53)----Trp causes von Willebrand disease Normandy by abolishing binding to factor VIII. Studies with recombinant von Willebrand factor. | 1992 Feb 1 |
2 |
| 30 |
1737795 | Selective inactivation of the Arg-Gly-Asp-Ser (RGDS) binding site in von Willebrand factor by site-directed mutagenesis. | 1992 Feb 15 |
1 |
| 31 |
1720019 | A modified Arg-Asp-Val (RDV) peptide derived during the synthesis of Arg-Glu-Asp-Val (REDV), a tetrapeptide derived from an alternatively spliced site in fibronectin, inhibits the binding of fibrinogen, fibronectin, von Willebrand factor and vitronectin to activated platelets. | 1991 Oct 31 |
2 |
| 32 |
1871720 | Platelets adhere to sulfatides by von Willebrand factor dependent and independent mechanisms. | 1991 May 6 |
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| 33 |
1715119 | Multiple epitope specificity of monoclonal antibodies to a single synthetic peptide: use in the characterization of the GP IIb-IIIa binding domain of von Willebrand factor. | 1990 |
3 |
| 34 |
2545728 | Von Willebrand factor promotes endothelial cell adhesion via an Arg-Gly-Asp-dependent mechanism. | 1989 Jul |
4 |
| 35 |
2688759 | Molecular cloning, expression and assembly of multimeric von Willebrand factor. | 1989 Oct |
1 |
| 36 |
2453507 | Generation and characterization of peptide-specific antibodies that inhibit von Willebrand factor binding to glycoprotein IIb-IIIa without interacting with other adhesive molecules. Selectivity is conferred by Pro1743 and other amino acid residues adjacent to the sequence Arg1744-Gly1745-Asp1746. | 1988 Jun 5 |
3 |
| 37 |
3131331 | Proteolytic cleavage of the precursor of von Willebrand factor is not essential for multimer formation. | 1988 Jun 15 |
1 |
| 38 |
2447074 | Biosynthetic and functional properties of an Arg-Gly-Asp-directed receptor involved in human melanoma cell attachment to vitronectin, fibrinogen, and von Willebrand factor. | 1987 Dec 25 |
1 |
| 39 |
3037722 | Inhibition of von Willebrand factor binding to platelets by two recognition site peptides: the pentadecapeptide of the carboxy terminus of the fibrinogen gamma chain and the tetrapeptide arg-gly-asp-ser. | 1987 May 1 |
1 |
| 40 |
3500868 | The dualistic mechanisms of platelet adhesion to von Willebrand factor substrates. | 1987 Dec |
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| 41 |
2944746 | Identification of two distinct regions within the binding sites for fibrinogen and fibronectin on the IIb-IIIa human platelet membrane glycoprotein complex by monoclonal antibodies P2 and P4. | 1986 Sep 15 |
3 |
| 42 |
3019665 | Full-length von Willebrand factor (vWF) cDNA encodes a highly repetitive protein considerably larger than the mature vWF subunit. | 1986 Aug |
1 |
| 43 |
2864688 | Cloning and characterization of two cDNAs coding for human von Willebrand factor. | 1985 Oct |
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