Ghent University Academic Bibliography

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Your filters: cql: keyword exact "factor-cleaving protease" cql: author exact 802002606306 or (type exact bookEditor and editor exact 802002606306)

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Immunogenic hotspots in the spacer domain of ADAMTS13 in immune‐mediated thrombotic thrombocytopenic purpura

Leydi Carolina Velásquez Pereira, Elien Roose, Nuno A. G. Graça, György Sinkovits, Kadri Kangro, Bérangère S. Joly, Edwige Tellier, Gilles Kaplanski, Tanja Falter, Charis Von Auer, et al.

(2021) JOURNAL OF THROMBOSIS AND HAEMOSTASIS. 19(2). p.478-488
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Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura

Elien Roose, An-Sofie Tellier, Edwige Tellier, György Sinkovits, Bérangère S Joly, Charlotte Dekimpe, Gilles Kaplanski, Maelle Le Besnerais, Ilaria Mancini, Dr. Tanja Falter, et al.

(2020) BLOOD. 136(3). p.353-361
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- Journal Article
- A1
- open access
Major changes of von Willebrand factor multimer distribution in cirrhotic patients with stable disease or acute decompensation

Eszter Palyu, Jolan Harsfalvi, Tamas Tornai, Maria Papp, Miklos Udvardy, Katalin Szekeres-Csiki, Lajos Pataki, Karen Vanhoorelbeke, Hendrik Feys (UGent) , Hans Deckmyn, et al.

(2018) THROMBOSIS AND HAEMOSTASIS. 118(8). p.1397-1408
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- Journal Article
- A1
Allosteric activation of ADAMTS13 by von Willebrand factor

Joshua Muia, Jian Zhu, Garima Gupta, Sandra L Haberichter, Kenneth D Friedman, Hendrik Feys (UGent) , Louis Deforche, Karen Vanhoorelbeke, Lisa A Westfield, Robyn Roth, et al.

(2014) PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 111(52). p.18584-18589
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- Journal Article
- A1
Inactivation of ADAMTS13 by plasmin as a potential cause of thrombotic thrombocytopenic purpura

Hendrik Feys (UGent) , N Vandeputte, R Palla, F Peyvandi, K Peerlinck, H Deckmyn, HR Lijnen and K Vanhoorelbeke

(2010) JOURNAL OF THROMBOSIS AND HAEMOSTASIS. 8(9). p.2053-2062
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- Journal Article
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The distal carboxyterminal domains of murine ADAMTS13 influence proteolysis of platelet-decorated VWF strings in vivo

B De Maeyer, SF De Meyer, Hendrik Feys (UGent) , I Pareyn, N Vandeputte, H Deckmyn and K Vanhoorelbeke

(2010) JOURNAL OF THROMBOSIS AND HAEMOSTASIS. 8(10). p.2305-2312
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- Journal Article
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Thrombotic thrombocytopenic purpura directly linked with ADAMTS13 inhibition in the baboon (Papio ursinus)

Hendrik Feys (UGent) , Jan Roodt, Nele Vandeputte, Inge Pareyn, Seb Lamprecht, Walter J Van Rensburg, Patricia J Anderson, Ulrich Budde, Vernon J Louw, Philip N Badenhorst, et al.

(2010) BLOOD. 116(12). p.2005-2010
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ADAMTS13 in health and disease

Hendrik Feys (UGent) , Hans Deckmyn and Karen Vanhoorelbeke

(2009) ACTA HAEMATOLOGICA. 121(2-3). p.183-185
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- Journal Article
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Multi-step binding of ADAMTS-13 to von Willebrand factor

Hendrik Feys (UGent) , PJ Anderson, K Vanhoorelbeke, EM Majerus and JE Sadler

(2009) JOURNAL OF THROMBOSIS AND HAEMOSTASIS. 7(12). p.2088-2095
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- Journal Article
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Mutation of the H-bond acceptor S119 in the ADAMTS13 metalloprotease domain reduces secretion and substrate turnover in a patient with congenital thrombotic thrombocytopenic purpura

Hendrik Feys (UGent) , Inge Pareyn, Renée Vancraenenbroeck, Marc De Maeyer, Hans Deckmyn, Chris Van Geet and Karen Vanhoorelbeke

(2009) BLOOD. 114(21). p.4749-4752

Academic Bibliography

Immunogenic hotspots in the spacer domain of ADAMTS13 in immune‐mediated thrombotic thrombocytopenic purpura

Open ADAMTS13, induced by antibodies, is a biomarker for subclinical immune-mediated thrombotic thrombocytopenic purpura

Major changes of von Willebrand factor multimer distribution in cirrhotic patients with stable disease or acute decompensation

Allosteric activation of ADAMTS13 by von Willebrand factor

Inactivation of ADAMTS13 by plasmin as a potential cause of thrombotic thrombocytopenic purpura

The distal carboxyterminal domains of murine ADAMTS13 influence proteolysis of platelet-decorated VWF strings in vivo

Thrombotic thrombocytopenic purpura directly linked with ADAMTS13 inhibition in the baboon (Papio ursinus)

ADAMTS13 in health and disease

Multi-step binding of ADAMTS-13 to von Willebrand factor

Mutation of the H-bond acceptor S119 in the ADAMTS13 metalloprotease domain reduces secretion and substrate turnover in a patient with congenital thrombotic thrombocytopenic purpura

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