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The Journal of Biological Chemistry|October 14, 2005
ADAMTS13 substrate recognition of von Willebrand factor A2 domainSara Zanardelli, James T B Crawley, Chan K N Chan Kwo Chion, et al.
Blood|March 24, 2010
Activated protein C cofactor function of protein S: a critical role for Asp95 in the EGF1-like domainHelena M Andersson, Márcia J Arantes, James T B Crawley, et al.
Biophysical Journal|March 13, 2026
Mechanisms of thrombin inhibition by protein S and the TFPIα-fVshort-protein S complexAlexander G Ginsberg, Josefin Ahnström, James T B Crawley, et al.
Journal of Thrombosis and Haemostasis : JTH|November 23, 2007
Prevalence of the ADAMTS-13 missense mutation R1060W in late onset adult thrombotic thrombocytopenic purpuraR S Camilleri, H Cohen, I J Mackie, et al.
Arxiv|December 19, 2025
Mechanisms of thrombin inhibition by protein S and the TFPIα-fVshort-protein S complexAlexander G Ginsberg, Josefin Ahnström, James T B Crawley, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2014
Conformational activation of ADAMTS13Kieron South, Brenda M Luken, James T B Crawley, et al.
Blood|April 22, 2011
Activated protein C cofactor function of protein S: a novel role for a γ-carboxyglutamic acid residueJosefin Ahnström, Helena M Andersson, Kevin Canis, et al.
Blood Advances|November 3, 2021
Laminin G1 residues of protein S mediate its TFPI cofactor function and are competitively regulated by C4BPAdrienn Teraz-Orosz, Magdalena Gierula, Anastasis Petri, et al.
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