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Measurement of von Willebrand factor‐cleaving protease (ADAMTS‐13) activity in plasma: a multicenter comparison of different assay methods

Journal of thrombosis and haemostasis, 2003-09, Vol.1 (9), p.1882-1887

2003

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Measurement of von Willebrand factor cleaving protease (ADAMTS‐13): results of an international collaborative study involving 11 methods testing the same set of coded plasmas

Journal of thrombosis and haemostasis, 2004-09, Vol.2 (9), p.1601-1609

2004

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Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)

Journal of thrombosis and haemostasis, 2004-03, Vol.2 (3), p.424-429

2004

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Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen

Thrombosis and haemostasis, 2001-09, Vol.86 (3), p.848-854

2001

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von Willebrand factor: structure and function

Thrombosis and haemostasis, 1993, Vol.70 (1), p.99-104

1993

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The von Willebrand factor self‐association is modulated by a multiple domain interaction

Journal of thrombosis and haemostasis, 2005-03, Vol.3 (3), p.552-561

2005

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Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF

Thrombosis and haemostasis, 1999-11, Vol.82 (5), p.1382-1385

1999

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Specific von Willebrand factor–cleaving protease in thrombotic microangiopathies: a study of 111 cases

Blood, 2001-09, Vol.98 (6), p.1765-1772

2001

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Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion

Journal of thrombosis and haemostasis, 2006-01, Vol.4 (1), p.148-157

2006

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Conformational Changes in the A3 Domain of von Willebrand Factor Modulate the Interaction of the A1 Domain With Platelet Glycoprotein Ib

Blood, 1999-03, Vol.93 (6), p.1959-1968

1999

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Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS‐13

Journal of thrombosis and haemostasis, 2007-02, Vol.5 (2), p.321-328

2007

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Generation of von Willebrand factor epitope libraries expressed in E. coli

BioTechniques, 2002-02, Vol.32 (2), p.402-409

2002

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Platelet aggregation induced by a monoclonal antibody to the A1 domain of von Willebrand factor

Blood, 1998-05, Vol.91 (10), p.3792-3799

1998

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Mapping and functional studies of two alloantibodies developed in patients with type 3 von Willebrand disease

Thrombosis and haemostasis, 2000-02, Vol.83 (2), p.274-281

2000

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Characterization of bitiscetin‐2, a second form of bitiscetin from the venom of Bitis arietans : comparison of its binding site with the collagen‐binding site on the von Willebrand factor A3‐domain

Journal of thrombosis and haemostasis, 2006-07, Vol.4 (7), p.1596-1601

2006

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Structure-Function Relationship of Human Von Willebrand Factor

Blood, 1987-09, Vol.70 (3), p.605-611

1987

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Ristocetin and botrocetin involve two distinct domains of von Willebrand factor for binding to platelet membrane glycoprotein Ib

Thrombosis and haemostasis, 1990-10, Vol.64 (2), p.326

1990

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New assay for measuring binding of platelet glycoprotein IIb/IIIa to unpurified von Willebrand factor

Thrombosis and haemostasis, 1999-07, Vol.82 (1), p.134-139

1999

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Discrepancy Between IIA Phenotype and IIB Genotype in a Patient With a Variant of von Willebrand Disease

Blood, 1994-02, Vol.83 (3), p.833-841

1994

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Impaired prothrombin consumption in Bernard-Soulier syndrome is corrected in vitro by human factor VIII

Thrombosis and haemostasis, 1997-02, Vol.77 (2), p.383-386

1997

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Improvement of von Willebrand factor proteolysis after prostacyclin infusion in severe pulmonary arterial hypertension

Circulation (New York, N.Y.), 2000-11, Vol.102 (20), p.2460-2462

2000

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Influence of Mutations and Size of Multimers in Type II von Willebrand Disease Upon the Function of von Willebrand Factor

Blood, 1994-06, Vol.83 (12), p.3553-3561

1994

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The binding domain of von Willebrand factor to sulfatides is distinct from those interacting with glycoprotein Ib, heparin, and collagen and resides between amino acid residues Leu 512 and Lys 673

Blood, 1991-11, Vol.78 (9), p.2310-2317

1991

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Characterization of recombinant von Willebrand factors mutated on cysteine 509 or 695

Thrombosis and haemostasis, 1996-09, Vol.76 (3), p.453-459

1996

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Localization of a Collagen-Interactive Domain of Human von Willebrand Factor Between Amino Acid Residues Gly 911 and Glu 1,365

Blood, 1987-11, Vol.70 (5), p.1577-1583

1987

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Measurement of von Willebrand factor‐cleaving protease (ADAMTS‐13) activity in plasma: a multicenter comparison of different assay methods

Measurement of von Willebrand factor cleaving protease (ADAMTS‐13): results of an international collaborative study involving 11 methods testing the same set of coded plasmas

Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome)

Ser968Thr mutation within the A3 domain of von Willebrand factor (VWF) in two related patients leads to a defective binding of VWF to collagen

von Willebrand factor: structure and function

The von Willebrand factor self‐association is modulated by a multiple domain interaction

Estimation of the von Willebrand factor-cleaving protease in plasma using monoclonal antibodies to vWF

Specific von Willebrand factor–cleaving protease in thrombotic microangiopathies: a study of 111 cases

Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion

Conformational Changes in the A3 Domain of von Willebrand Factor Modulate the Interaction of the A1 Domain With Platelet Glycoprotein Ib

Effect of von Willebrand disease type 2B and type 2M mutations on the susceptibility of von Willebrand factor to ADAMTS‐13

Generation of von Willebrand factor epitope libraries expressed in E. coli

Platelet aggregation induced by a monoclonal antibody to the A1 domain of von Willebrand factor

Mapping and functional studies of two alloantibodies developed in patients with type 3 von Willebrand disease

Characterization of bitiscetin‐2, a second form of bitiscetin from the venom of Bitis arietans : comparison of its binding site with the collagen‐binding site on the von Willebrand factor A3‐domain

Structure-Function Relationship of Human Von Willebrand Factor

Ristocetin and botrocetin involve two distinct domains of von Willebrand factor for binding to platelet membrane glycoprotein Ib

New assay for measuring binding of platelet glycoprotein IIb/IIIa to unpurified von Willebrand factor

Discrepancy Between IIA Phenotype and IIB Genotype in a Patient With a Variant of von Willebrand Disease

Impaired prothrombin consumption in Bernard-Soulier syndrome is corrected in vitro by human factor VIII

Improvement of von Willebrand factor proteolysis after prostacyclin infusion in severe pulmonary arterial hypertension

Influence of Mutations and Size of Multimers in Type II von Willebrand Disease Upon the Function of von Willebrand Factor

The binding domain of von Willebrand factor to sulfatides is distinct from those interacting with glycoprotein Ib, heparin, and collagen and resides between amino acid residues Leu 512 and Lys 673

Characterization of recombinant von Willebrand factors mutated on cysteine 509 or 695

Localization of a Collagen-Interactive Domain of Human von Willebrand Factor Between Amino Acid Residues Gly 911 and Glu 1,365

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