Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Joel F. Moake"'
Autor:
J. P. Girma, Armando Tripodi, M. E. Rick, Ulrich Budde, Kenneth D. Friedman, Martina Böhm, Veena Chantarangkul, Peter Turecek, Joel F. Moake, Miriam Galbusera, Jing-fei Dong, P. M. Mannucci, Jan-Dirk Studt
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 2(9)
Summary. Background: ADAMTS-13 is a von Willebrand factor (VFW)-cleaving protease. Its congenital or acquired deficiency is associated with thrombotic thrombocytopenic purpura (TTP) and more rarely with the hemolytic uremic syndrome. We report on a s
Publikováno v:
Blood. 104(1)
ADAMTS13 cleaves ultralarge and hyperreactive von Willebrand factor (ULVWF) freshly released from activated endothelial cells to smaller and less active forms. This process may be affected by the amount of ULVWF released and the processing capacity o
Autor:
Joel F. Moake, Aubrey Bernardo, Leticia Nolasco, Jody L. Whitelock, Jing-fei Dong, Miguel A. Cruz
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 2(3)
The metalloprotease ADAMTS-13 cleaves von Willebrand factor (VWF) at the Y842/M843 peptide bond located in the A2 domain. Measurement of ADAMTS-13 activity is a clinical utility for thrombotic diseases, but the current assays used for diagnostic and
Publikováno v:
Blood. 108:420-420
von Willebrand factor (VWF) shares a similar domain structure with many polymeric mucins, including the presence of D domains and a C-terminal cysteine knot, which allows these molecules to form polymeric structures that can reach immense sizes. Prec
Autor:
Li Liu, Jing-fei Dong, Hiuwan Choi, Joel F. Moake, Trung C. Nguyen, Angela L. Bergeron, Leticia Nolasco, Anne Liu, Patricia Mapua
Publikováno v:
Blood. 104:848-848
Von Willebrand factor (VWF) is synthesized and released from endothelial cells and megakaryocytes/platelets in a form that is ultra-large (UL) in size and hyper-reactive in functions, capable of spontaneously activating and aggregating platelets. Upo
Publikováno v:
Blood. 104:854-854
Thrombotic thrombocytopenic purpura (TTP) is characterized by severe thrombocytopenia, hemolytic anemia, and diffuse and non-focal neurological findings. Microthrombi found in these patients are predominantly composed of platelets and von Willebrand
Autor:
Li Liu, Changgeng Ruan, Bernardo Aubrey, Joel F. Moake, Huiwan Choi, Jing-fei Dong, Angila Bergeron, Leticia Nolasco
Publikováno v:
Blood. 104:3527-3527
The adhesion ligand von Willebrand factor (VWF) is synthesized and stored in vascular endothelial cells and megakaryocytes/platelets. These cells release VWF in response to similar stimulations. However, a longstanding observation stated that, unlike