B. Luken

发表

Activated protein C cofactor function of protein S: a critical role for Asp95 in the EGF1-like domain.

B. Dahlbäck, S. Rezende, D. Lane, 2010, Blood.

Extracellular histones, cell-free DNA, or nucleosomes: differences in immunostimulation

S. Zeerleder, B. M. Luken, G. Marsman, 2016, Cell Death & Disease.

Unraveling the scissile bond: how ADAMTS13 recognizes and cleaves von Willebrand factor.

D. Lane, J. Crawley, B. M. Luken, 2011, Blood.

Coagulation factor XI improves host defence during murine pneumonia-derived sepsis independent of factor XII activation

T. van der Poll, F. Castellino, C. van ′t Veer, 2017, Thrombosis and Haemostasis.

Humoral immune response to ADAMTS13 in acquired thrombotic thrombocytopenic purpura

J. Voorberg, J. K. Kremer Hovinga, Wouter Pos, 2011, Journal of thrombosis and haemostasis : JTH.

DNA and factor VII-activating protease protect against the cytotoxicity of histones.

J. Hazelzet, F. Lupu, S. Zeerleder, 2017, Blood advances.

FSAP‐mediated nucleosome release from late apoptotic cells is inhibited by autoantibodies present in SLE

C. Kallenberg, J. Westra, L. Aarden, 2016, European journal of immunology.

Control of VWF A2 domain stability and ADAMTS13 access to the scissile bond of full-length VWF.

C. Lynch, D. Lane, B. Luken, 2014, Blood.

The importance of vicinal cysteines, C1669 and C1670, for von Willebrand factor A2 domain function.

J. Emsley, D. Lane, J. Crawley, 2010, Blood.

The damage-associated molecular pattern HMGB1 is released early after clinical hepatic ischemia/reperfusion.

M. Murphy, T. V. van Gulik, G. Farrell, 2019, Biochimica et biophysica acta. Molecular basis of disease.

Dynamics of von Willebrand factor reactivity in sickle cell disease during vaso‐occlusive crisis and steady state

B. Biemond, K. Fijnvandraat, R. Urbanus, 2017, Journal of thrombosis and haemostasis : JTH.

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

J. Voorberg, R. Bertina, J. Eikenboom, 2006, Thrombosis and Haemostasis.

Amino acid regions 572–579 and 657–666 of the spacer domain of ADAMTS13 provide a common antigenic core required for binding of antibodies in patients with acquired TTP

J. V. van Mourik, J. Voorberg, Wouter Pos, 2005, Thrombosis and Haemostasis.

High VWF, low ADAMTS13, and oral contraceptives increase the risk of ischemic stroke and myocardial infarction in young women.

A. Algra, F. Rosendaal, B. Siegerink, 2012, Blood.

Searching for a Common Thrombo-Inflammatory Basis in Patients With Deep Vein Thrombosis or Peripheral Artery Disease

R. van Oerle, H. ten Cate, A. T. ten Cate‐Hoek, 2019, Front. Cardiovasc. Med..

Mouse venous thrombosis upon silencing of anticoagulants depends on tissue factor and platelets, not FXII or neutrophils.

T. Renné, P. Reitsma, D. Kirchhofer, 2019, Blood.

Inflammatory and endothelial markers during vaso‐occlusive crisis and acute chest syndrome in sickle cell disease

B. Biemond, S. Zeerleder, C. V. van Tuijn, 2017, American journal of hematology.

Conformational activation of ADAMTS13

D. Lane, K. Vanhoorelbeke, J. Crawley, 2014, Proceedings of the National Academy of Sciences.

Activated protein C cofactor function of protein S : a critical role for Asp 95 in the EGF 1-like domain

B. Dahlbäck, S. Rezende, D. Lane, 2010 .

Autoregulation of von Willebrand factor function by a disulfide bond switch

Kristina M. Cook, F. Gräter, C. Baldauf, 2018, Science Advances.

The spacer domain of ADAMTS13 contains a major binding site for antibodies in patients with thrombotic thrombocytopenic purpura

J. V. van Mourik, J. Voorberg, R. Fijnheer, 2005, Thrombosis and Haemostasis.

Circulating ADAMTS‐13–von Willebrand factor complexes: an enzyme on demand

R. de Groot, J. Crawley, B. Luken, 2009, Journal of thrombosis and haemostasis : JTH.

Role of platelets, neutrophils, and factor XII in spontaneous venous thrombosis in mice.

P. Reitsma, E. Laghmani, G. Wagenaar, 2016, Blood.

An autoantibody epitope comprising residues R660, Y661, and Y665 in the ADAMTS13 spacer domain identifies a binding site for the A2 domain of VWF.

J. Voorberg, D. Lane, R. Fijnheer, 2010, Blood.

VH1‐69 germline encoded antibodies directed towards ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura

J. Voorberg, J. K. Kremer Hovinga, Wouter Pos, 2009, Journal of thrombosis and haemostasis : JTH.

Evidence for a role of anti-ADAMTS13 autoantibodies despite normal ADAMTS13 activity in recurrent thrombotic thrombocytopenic purpura

S. Vesely, J. George, B. Lämmle, 2012, Haematologica.

Multiple B‐cell clones producing antibodies directed to the spacer and disintegrin/thrombospondin type‐1 repeat 1 (TSP1) of ADAMTS13 in a patient with acquired thrombotic thrombocytopenic purpura

J. V. van Mourik, J. Voorberg, J. K. Kremer Hovinga, 2006, Journal of thrombosis and haemostasis : JTH.

Antibodies against the CUB1-2 domains of ADAMTS13 in a patient with benign monoclonal gammopathy: no causal relationship.

J. Voorberg, M. van Deuren, I. Klasen, 2007, Haematologica.

THROMBOSIS AND HEMOSTASIS Control of VWF A 2 domain stability and ADAMTS 13 access to the scissile bond of full-length VWF

C. Lynch, D. Lane, B. Luken, 2014 .

Circulating Iron in Patients with Sickle Cell Disease Mediates the Release of Neutrophil Extracellular Traps

B. Biemond, R. van Bruggen, S. Zeerleder, 2023, Transfusion Medicine and Hemotherapy.

Complexes of factor VII-activating protease with plasminogen activator inhibitor-1 in human sepsis

J. Hazelzet, S. Zeerleder, W. Wuillemin, 2014, Thrombosis and Haemostasis.

Role of platelets, neutrophils, and factor XII in spontaneous venous thrombosis in mice.

P. Reitsma, E. Laghmani, G. Wagenaar, 2016, Blood.

Activated protein C cofactor function of protein S: a critical role for Asp95 in the EGF1-like domain

B. Dahlbäck, S. Rezende, D. Lane, 2010, Blood.

VH1‐69 germline encoded antibodies directed towards ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura

J. Voorberg, J. K. Kremer Hovinga, Wouter Pos, 2009, Journal of thrombosis and haemostasis : JTH.

Extracellular control of VWF multimer size and thiol‐disulfide exchange

B. Luken, 2008, Journal of thrombosis and haemostasis : JTH.