85 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 35491445 | VWF-Gly2752Ser, a novel non-cysteine substitution variant in the CK domain, exhibits severe secretory impairment by hampering C-terminal dimer formation. | 2022 May 1 | 1 |
2 | 33588457 | Functional Roles of the von Willebrand Factor Propeptide. | 2021 Feb | 1 |
3 | 34838051 | The disulfide bond Cys2724-Cys2774 in the C-terminal cystine knot domain of von Willebrand factor is critical for its dimerization and secretion. | 2021 Nov 27 | 2 |
4 | 31479573 | Glycosylation sterically inhibits platelet adhesion to von Willebrand factor without altering intrinsic conformational dynamics. | 2020 Jan | 1 |
5 | 30642920 | The von Willebrand factor D'D3 assembly and structural principles for factor VIII binding and concatemer biogenesis. | 2019 Apr 4 | 3 |
6 | 30936056 | von Willebrand factor self-association is regulated by the shear-dependent unfolding of the A2 domain. | 2019 Apr 9 | 1 |
7 | 29507883 | Autoregulation of von Willebrand factor function by a disulfide bond switch. | 2018 Feb | 4 |
8 | 30351116 | Correlating Conformational Dynamics with the Von Willebrand Factor Reductase Activity of Factor H Using Single Molecule Force Measurements. | 2018 Nov 29 | 2 |
9 | 31080944 | Complement Component C3 Binds to the A3 Domain of von Willebrand Factor. | 2018 | 1 |
10 | 28139814 | Von Willebrand factor processing. | 2017 Jan 31 | 1 |
11 | 28533135 | Enhanced Local Disorder in a Clinically Elusive von Willebrand Factor Provokes High-Affinity Platelet Clumping. | 2017 Jul 7 | 3 |
12 | 29059501 | Head-to-Tail Cyclic Peptide Inhibitors of the Interaction between Human von Willebrand Factor and Collagen. | 2017 Dec 7 | 1 |
13 | 26581637 | Free thiol groups in von Willebrand factor (VWF) are required for its full function under physiological flow conditions. | 2016 Jan | 1 |
14 | 26670633 | von Willebrand factor is dimerized by protein disulfide isomerase. | 2016 Mar 3 | 3 |
15 | 26099845 | Industrial production of clotting factors: Challenges of expression, and choice of host cells. | 2015 Jul | 1 |
16 | 24283831 | The von Willebrand factor predicted unpaired cysteines are essential for secretion. | 2014 Feb | 1 |
17 | 22207689 | Biogenesis of Weibel-Palade bodies in von Willebrand's disease variants with impaired von Willebrand factor intrachain or interchain disulfide bond formation. | 2012 Jun | 1 |
18 | 22490677 | Sequence and structure relationships within von Willebrand factor. | 2012 Jul 12 | 1 |
19 | 23067373 | The unfolded von Willebrand factor response in bloodstream: the self-association perspective. | 2012 Oct 15 | 2 |
20 | 21266777 | N-acetylcysteine reduces the size and activity of von Willebrand factor in human plasma and mice. | 2011 Feb | 2 |
21 | 21507943 | Platelet glycoprotein Ib beta/IX mediates glycoprotein Ib alpha localization to membrane lipid domain critical for von Willebrand factor interaction at high shear. | 2011 Jun 17 | 1 |
22 | 21911836 | Lateral self-association of VWF involves the Cys2431-Cys2453 disulfide/dithiol in the C2 domain. | 2011 Nov 10 | 7 |
23 | 20354169 | The importance of vicinal cysteines, C1669 and C1670, for von Willebrand factor A2 domain function. | 2010 Jun 10 | 2 |
24 | 20705333 | Thrombospondin-1 and ADAMTS13 competitively bind to VWF A2 and A3 domains in vitro. | 2010 Oct | 4 |
25 | 20946172 | Disulfide bond reduction of von Willebrand factor by ADAMTS-13. | 2010 Dec | 10 |
26 | 20979592 | Redox control of β2-glycoprotein I-von Willebrand factor interaction by thioredoxin-1. | 2010 Aug | 1 |
27 | 19630761 | von Willebrand factor assembly and secretion. | 2009 Jul | 2 |
28 | 19817991 | Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysis. | 2009 Dec | 2 |
29 | 18182488 | Assembly of Weibel-Palade body-like tubules from N-terminal domains of von Willebrand factor. | 2008 Jan 15 | 1 |
30 | 17895385 | Two Cys residues essential for von Willebrand factor multimer assembly in the Golgi. | 2007 Oct 2 | 5 |
31 | 17925407 | Shear-induced disulfide bond formation regulates adhesion activity of von Willebrand factor. | 2007 Dec 7 | 4 |
32 | 16409464 | Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion. | 2006 Jan | 2 |
33 | 16706977 | Intrinsic stability and functional properties of disulfide bond-stabilized coagulation factor VIIIa variants. | 2006 Jun | 3 |
34 | 17139364 | Differential effects of the loss of intrachain- versus interchain-disulfide bonds in the cystine-knot domain of von Willebrand factor on the clinical phenotype of von Willebrand disease. | 2006 Dec | 9 |
35 | 16102036 | von Willebrand factor: two sides of a coin. | 2005 Aug | 1 |
36 | 14755371 | C1272S: a new candidate mutation in type 2A von Willebrand disease that disrupts the disulfide loop responsible for the interaction of VWF with platelet GP Ib-IX. | 2004 Feb | 2 |
37 | 15507277 | Platelet physiology and thrombosis. | 2004 | 1 |
38 | 11943773 | Identification of the regulatory elements of the human von Willebrand factor for binding to platelet GPIb. Importance of structural integrity of the regions flanked by the CYS1272-CYS1458 disulfide bond. | 2002 Jun 14 | 1 |
39 | 12351392 | The von Willebrand factor-reducing activity of thrombospondin-1 is located in the calcium-binding/C-terminal sequence and requires a free thiol at position 974. | 2002 Oct 15 | 2 |
40 | 11264172 | Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand disease. | 2001 Apr 1 | 2 |
41 | 11816713 | A novel monoclonal antibody against the extracellular domain of GPIbbeta modulates vWF mediated platelet adhesion. | 2001 Nov | 2 |
42 | 10831592 | Localization of disulfide bonds in the cystine knot domain of human von Willebrand factor. | 2000 Aug 18 | 1 |
43 | 11019979 | Reduction of von Willebrand factor by endothelial cells. | 2000 Sep | 2 |
44 | 9473222 | Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to platelets. | 1998 Mar 1 | 1 |
45 | 9603957 | Porcine submaxillary mucin forms disulfide-linked multimers through its amino-terminal D-domains. | 1998 Jun 5 | 1 |
46 | 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 | 4 |
47 | 9759493 | Biochemistry and genetics of von Willebrand factor. | 1998 | 1 |
48 | 9129011 | Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. | 1997 May 1 | 2 |
49 | 8622978 | Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease. | 1996 Apr 16 | 3 |
50 | 8639781 | Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. | 1996 May 15 | 1 |