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Items: 1 to 20 of 84

1.

Solution structure of human von Willebrand factor studied using small angle neutron scattering.

Singh I, Shankaran H, Beauharnois ME, Xiao Z, Alexandridis P, Neelamegham S.

J Biol Chem. 2006 Dec 15;281(50):38266-75.

2.

Substructure of human von Willebrand factor.

Fowler WE, Fretto LJ, Hamilton KK, Erickson HP, McKee PA.

J Clin Invest. 1985 Oct;76(4):1491-500.

3.

Disulfide bond reduction of von Willebrand factor by ADAMTS-13.

Yeh HC, Zhou Z, Choi H, Tekeoglu S, May W 3rd, Wang C, Turner N, Scheiflinger F, Moake JL, Dong JF.

J Thromb Haemost. 2010 Dec;8(12):2778-88. doi: 10.1111/j.1538-7836.2010.04094.x.

4.

Fluid shear induces conformation change in human blood protein von Willebrand factor in solution.

Singh I, Themistou E, Porcar L, Neelamegham S.

Biophys J. 2009 Mar 18;96(6):2313-20. doi: 10.1016/j.bpj.2008.12.3900.

5.

Structural analysis of recombinant von Willebrand factor produced at industrial scale fermentation of transformed CHO cells co-expressing recombinant furin.

Fischer BE, Schlokat U, Mitterer A, Reiter M, Mundt W, Turecek PL, Schwarz HP, Dorner F.

FEBS Lett. 1995 Nov 20;375(3):259-62.

7.

Substructure of human von Willebrand factor. Proteolysis by V8 and characterization of two functional domains.

Fretto LJ, Fowler WE, McCaslin DR, Erickson HP, McKee PA.

J Biol Chem. 1986 Nov 25;261(33):15679-89.

8.

Disulfide bonds required to assemble functional von Willebrand factor multimers.

Dong Z, Thoma RS, Crimmins DL, McCourt DW, Tuley EA, Sadler JE.

J Biol Chem. 1994 Mar 4;269(9):6753-8.

10.

A new variant of von Willebrand's disease (type I Padua): doublet-organized plasma von Willebrand factor oligomers in the presence of all size multimers.

Casonato A, Pontara E, Dannhäuser D, Bertomoro A, Sartori MT, Girolami A.

Haematologia (Budap). 1994;26(2):97-109.

PMID:
7890268
11.

Role of thrombospondin-1 in control of von Willebrand factor multimer size in mice.

Pimanda JE, Ganderton T, Maekawa A, Yap CL, Lawler J, Kershaw G, Chesterman CN, Hogg PJ.

J Biol Chem. 2004 May 14;279(20):21439-48.

12.

Clearance of normal and type 2A von Willebrand factor in the rat.

Stoddart JH Jr, Andersen J, Lynch DC.

Blood. 1996 Sep 1;88(5):1692-9.

13.

Lack of multimer organization of von Willebrand factor in an acquired von Willebrand syndrome.

Casonato A, Pontara E, Doria A, Bertomoro A, Cattini MG, Gambari PF, Girolami A.

Br J Haematol. 2002 Mar;116(4):899-904.

PMID:
11886398
14.

Conformational stability and domain unfolding of the Von Willebrand factor A domains.

Auton M, Cruz MA, Moake J.

J Mol Biol. 2007 Feb 23;366(3):986-1000.

PMID:
17187823
15.

Control of von Willebrand factor multimer size by thrombospondin-1.

Xie L, Chesterman CN, Hogg PJ.

J Exp Med. 2001 Jun 18;193(12):1341-9.

16.

Different organization of von Willebrand factor oligomers in type-2A and -2B von Willebrand disease variants: effects of DDAVP infusion and protease inhibitors.

Casonato A, Pontara E, Bertomoro A, Dannhauser D, Secchiero S, Zaninotto M, Girolami A.

Ann Hematol. 1995 Oct;71(4):189-94.

PMID:
7578526
17.

Force sensing by the vascular protein von Willebrand factor is tuned by a strong intermonomer interaction.

Müller JP, Mielke S, Löf A, Obser T, Beer C, Bruetzel LK, Pippig DA, Vanderlinden W, Lipfert J, Schneppenheim R, Benoit M.

Proc Natl Acad Sci U S A. 2016 Feb 2;113(5):1208-13. doi: 10.1073/pnas.1516214113.

18.

Shear-induced disulfide bond formation regulates adhesion activity of von Willebrand factor.

Choi H, Aboulfatova K, Pownall HJ, Cook R, Dong JF.

J Biol Chem. 2007 Dec 7;282(49):35604-11.

19.

Response of von Willebrand factor parameters to desmopressin in patients with type 1 and type 2 congenital von Willebrand disease: diagnostic and therapeutic implications.

Michiels JJ, van de Velde A, van Vliet HH, van der Planken M, Schroyens W, Berneman Z.

Semin Thromb Hemost. 2002 Apr;28(2):111-32.

PMID:
11992235
20.

Reduction of von Willebrand factor by endothelial cells.

Xie L, Chesterman CN, Hogg PJ.

Thromb Haemost. 2000 Sep;84(3):506-13.

PMID:
11019979

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