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Human endothelial cells synthesize and release ADAMTS‐13

Journal of thrombosis and haemostasis, 2006-06, Vol.4 (6), p.1396-1404

2006

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Thrombotic Thrombocytopenic Purpura Associated with Clopidogrel

The New England journal of medicine, 2000-06, Vol.342 (24), p.1773-1777

2000

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Platelets adhered to endothelial cell‐bound ultra‐large von Willebrand factor strings support leukocyte tethering and rolling under high shear stress

Journal of thrombosis and haemostasis, 2005-03, Vol.3 (3), p.562-570

2005

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Diagnostic criteria for hematopoietic stem cell transplant-associated microangiopathy: results of a consensus process by an International Working Group

Haematologica (Roma), 2007-01, Vol.92 (1), p.95-100

2007

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Disulfide bond reduction of von Willebrand factor by ADAMTS‐13

Journal of thrombosis and haemostasis, 2010-12, Vol.8 (12), p.2778-2788

2010

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Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura

Annals of internal medicine, 2000-05, Vol.132 (10), p.794

2000

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Covalent regulation of ULVWF string formation and elongation on endothelial cells under flow conditions

Journal of thrombosis and haemostasis, 2008-07, Vol.6 (7), p.1135-1143

2008

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Platelet-derived VWF-cleaving metalloprotease ADAMTS-13

Journal of thrombosis and haemostasis, 2005-11, Vol.3 (11), p.2536-2544

2005

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Platelets and shear stress

Blood, 1996-09, Vol.88 (5), p.1525-1541

1996

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Platelet‐derived VWF‐cleaving metalloprotease ADAMTS‐13

Journal of thrombosis and haemostasis, 2005-11, Vol.3 (11), p.2536-2544

2005

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Haemolytic-uraemic syndrome: basic science

The Lancet (British edition), 1994-02, Vol.343 (8894), p.393-397

Moake, J.L.

1994

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Moschcowitz, Multimers, and Metalloprotease

The New England journal of medicine, 1998-11, Vol.339 (22), p.1629-1631

Moake, Joel L

1998

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Novel ADAMTS‐13 mutations in an adult with delayed onset thrombotic thrombocytopenic purpura

Journal of thrombosis and haemostasis, 2006-09, Vol.4 (9), p.1931-1935

2006

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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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Defective processing of unusually large von Willebrand factor multimers and thrombotic thrombocytopenic purpura

Journal of thrombosis and haemostasis, 2004-09, Vol.2 (9), p.1515-1521

Moake, J. L.

2004

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ADAMTS‐13 cleaves long von Willebrand factor multimeric strings anchored to endothelial cells in the absence of flow, platelets or conformation‐altering chemicals

Journal of thrombosis and haemostasis, 2009-01, Vol.7 (1), p.229-232

2009

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Protein phosphatase 2B inhibition promotes the secretion of von Willebrand factor from endothelial cells

Journal of thrombosis and haemostasis, 2009-06, Vol.7 (6), p.1009-1018

2009

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Attack of the acronyms: TTP, VWF, ADAMTS‐13 and SELDI‐TOF‐MS

Journal of thrombosis and haemostasis, 2006-02, Vol.4 (2), p.329-332

2006

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ADAMTS‐13 activity in plasma is rapidly measured by a new ELISA method that uses recombinant VWF‐A2 domain as substrate

Journal of thrombosis and haemostasis, 2004-03, Vol.2 (3), p.485-491

2004

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Blockade of adenosine diphosphate receptors P2Y(12) and P2Y(1) is required to inhibit platelet aggregation in whole blood under flow

Blood, 2001-12, Vol.98 (12), p.3340-3345

2001

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Real-Time Analysis of Shear-Dependent Thrombus Formation and Its Blockade by Inhibitors of von Willebrand Factor Binding to Platelets

Blood, 1993-03, Vol.81 (5), p.1263-1276

1993

Volltextzugriff (PDF)

Studies on the pathophysiology of thrombotic thrombocytopenic purpura

Seminars in hematology, 1997-04, Vol.34 (2), p.83-89

Moake, J L

1997

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Thrombotic microangiopathies and the linkage between von Willebrand factor and the alternative complement pathway

Seminars in thrombosis and hemostasis, 2014-07, Vol.40 (5), p.544-550

2014

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Thrombotic thrombocytopenic purpura

Thrombosis and haemostasis, 1995, Vol.74 (1), p.240-245

Moake, J L

1995

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Thrombotic thrombocytopenic purpura: understanding a disease no longer rare

The American journal of the medical sciences, 1998-08, Vol.316 (2), p.105-119

1998

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Human endothelial cells synthesize and release ADAMTS‐13

Thrombotic Thrombocytopenic Purpura Associated with Clopidogrel

Platelets adhered to endothelial cell‐bound ultra‐large von Willebrand factor strings support leukocyte tethering and rolling under high shear stress

Diagnostic criteria for hematopoietic stem cell transplant-associated microangiopathy: results of a consensus process by an International Working Group

Disulfide bond reduction of von Willebrand factor by ADAMTS‐13

Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura

Covalent regulation of ULVWF string formation and elongation on endothelial cells under flow conditions

Platelet-derived VWF-cleaving metalloprotease ADAMTS-13

Platelets and shear stress

Platelet‐derived VWF‐cleaving metalloprotease ADAMTS‐13

Haemolytic-uraemic syndrome: basic science

Moschcowitz, Multimers, and Metalloprotease

Novel ADAMTS‐13 mutations in an adult with delayed onset thrombotic thrombocytopenic purpura

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

Defective processing of unusually large von Willebrand factor multimers and thrombotic thrombocytopenic purpura

ADAMTS‐13 cleaves long von Willebrand factor multimeric strings anchored to endothelial cells in the absence of flow, platelets or conformation‐altering chemicals

Protein phosphatase 2B inhibition promotes the secretion of von Willebrand factor from endothelial cells

Attack of the acronyms: TTP, VWF, ADAMTS‐13 and SELDI‐TOF‐MS

ADAMTS‐13 activity in plasma is rapidly measured by a new ELISA method that uses recombinant VWF‐A2 domain as substrate

Blockade of adenosine diphosphate receptors P2Y(12) and P2Y(1) is required to inhibit platelet aggregation in whole blood under flow

Real-Time Analysis of Shear-Dependent Thrombus Formation and Its Blockade by Inhibitors of von Willebrand Factor Binding to Platelets

Studies on the pathophysiology of thrombotic thrombocytopenic purpura

Thrombotic microangiopathies and the linkage between von Willebrand factor and the alternative complement pathway

Thrombotic thrombocytopenic purpura

Thrombotic thrombocytopenic purpura: understanding a disease no longer rare

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