Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Ida Hilden"'
Publikováno v:
Blood Advances, Vol 1, Iss 27, Pp 2692-2702 (2017)
Abstract: Tissue factor pathway inhibitor α (TFPIα) inhibits prothrombinase, the thrombin-generating complex of factor Xa (FXa) and factor Va (FVa), during the initiation of coagulation. This inhibition requires binding of a conserved basic region
Externí odkaz:
https://doaj.org/article/b80cab3955024d39919b18c5139417a1
Publikováno v:
Journal of Thrombosis and Haemostasis
Background The anti‐tissue factor plasma inhibitor monoclonal antibody concizumab is under clinical investigation for subcutaneous prophylaxis of hemophilia A/B (HA/HB) with or without inhibitors. Breakthrough bleeds while on concizumab prophylaxis
Autor:
Peter Thygesen, A. Henriksen, Haisun Zhu, Mette B. Hermit, Laust Bruun Johnsen, Per Jr Greisen, Søren Lund, Henrik Rahbek-Nielsen, Stine Kjellev, Kasper Lamberth, Henrik Østergaard, Eva Johansson, Thomas Lindebo Holm, Jais Rose Bjelke, Prafull S. Gandhi, Carsten Dan Ley, Daniel Elenius Madsen, Nikolai Lorenzen, Lisbeth Moreau Andersen, Zhiru Yang, Gustav Røder, Jacob Lund, Mette Loftager, Bjarne Gram Hansen, Amalie Carnbring Bonde, Rong Zhou, Ida Hilden, Thomas Egebjerg, Karina Thorn, Morten Grønbech Rasch, Xun Li, Fabian Stavenuiter
Publikováno v:
Blood
Østergaard and colleagues report the development of a potent bispecific antibody, Mim8, which binds both activated factor IX and factor X, mimicking the propagation of coagulation by activated factor VIII. They detail biophysical, in vitro, and in v
Publikováno v:
Haemophilia. 23:769-776
Aims Concizumab, a humanized monoclonal antibody against tissue factor pathway inhibitor (TFPI), is being developed as a subcutaneously (s.c.) administered treatment for haemophilia. It demonstrated a concentration-dependent procoagulant effect in fu
Autor:
Susan A. Maroney, Joan Cox Gill, Ida Hilden, Alan E. Mast, Peter Thyregod, Nicholas D. Martinez, Paul E. R. Ellery
Publikováno v:
Haemophilia
Introduction Tissue factor pathway inhibitor (TFPI) is a naturally occurring anticoagulant found in plasma, where it circulates bound to lipoproteins, factor V (FV) or Protein S (PS), and in platelets. Therapeutic agents targeting TFPI are under deve
Autor:
Brian Lauritzen, Ida Hilden
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 25(6)
Autor:
Donald F. Brophy, Heidi L. Holmberg, Thomas Egebjerg, Helle Demuth, Mari Enoksson, Jens Buchardt, Thomas N. Krogh, Mette S Jensen, Marianne Kjalke, Erika J. Martin, Mads Kjelgaard-Hansen, Ida Hilden, Annika Sanfridson
Publikováno v:
Journal of thrombosis and haemostasis : JTHREFERENCES. 18(1)
Background Recombinant factor VIIa (rFVIIa) enhances thrombin generation in a platelet-dependent manner; however, rFVIIa binds activated platelets with relatively low affinity. Triggering receptor expressed on myeloid cells (TREM)-like transcript (TL
Autor:
Kristoffer W. Balling, Brian Lauritzen, Janne Olling, Mads Bjelke, Cecilia Augustsson, Ida Hilden, Anne Charlotte Hegelund, Kristin L. Abel
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 17(3)
Essentials Hemophilia patients on concizumab prophylaxis may need rFVIIa to treat breakthrough bleeds. Effect and safety of concizumab + rFVIIa were tested in vitro and in vivo. Concizumab + rFVIIa had no additive effects on bleeding in hemophilic ra
Autor:
Mette Loftager, Susan A. Maroney, Ida Hilden, Alan E. Mast, Paul E. R. Ellery, Nicholas D. Martinez, Ken Sejling
Publikováno v:
Research and practice in thrombosis and haemostasis
Background Plasma Tissue Factor Pathway Inhibitor (TFPI) circulates bound to factor V (fV) and Protein S (PS). Estrogen therapy decreases plasma TFPI and PS. TFPI, fV, and PS circulate within platelets, and are released upon activation to modulate th
Publikováno v:
Journal of Thrombosis and Haemostasis. 13:2041-2052
SummaryBackground Conventional coagulation factor assays are associated with certain limitations, as they do not always reflect the clinical heterogeneity of bleeding in hemophilic patients or correctly reflect the individual patient response to trea