Q. Wu

Ligand specificity of human thrombomodulin. Equilibrium binding of human thrombin, meizothrombin, and factor Xa to recombinant thrombomodulin.

J. Sadler, S. Lentz, M. Tsiang, 1992, The Journal of biological chemistry.

Structure-function relationships of the thrombin-thrombomodulin interaction.

J. Sheehan, J. Sadler, S. Lentz, 1993, Haemostasis.

Enterokinase, the initiator of intestinal digestion, is a mosaic protease composed of a distinctive assortment of domains.

J. Sadler, Y. Kitamoto, D. McCourt, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Generation and characterization of mice deficient in hepsin, a hepatic transmembrane serine protease.

M. Halks-Miller, J. Morser, J. Sadler, 1998, The Journal of clinical investigation.

Activation-induced exposure of the thrombin anion-binding exosite. Interactions of recombinant mutant prothrombins with thrombomodulin and a thrombin exosite-specific antibody.

M. Aiach, V. Picard, J. Sadler, 1994, The Journal of biological chemistry.

Localization of the single-stranded DNA binding site in the thrombin anion-binding exosite.

J. Sadler, M. Tsiang, Qingyu Wu, 1992, The Journal of biological chemistry.

Single amino acid substitutions dissociate fibrinogen-clotting and thrombomodulin-binding activities of human thrombin.

J. Sheehan, J. Sadler, S. Lentz, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Incomplete embryonic lethality and fatal neonatal hemorrhage caused by prothrombin deficiency in mice.

K. Shim, J. Sadler, Xinglong Zheng, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Mutagenesis of thrombin selectively modulates inhibition by serpins heparin cofactor II and antithrombin III. Interaction with the anion-binding exosite determines heparin cofactor II specificity.

D. Tollefsen, J. Sheehan, J. Sadler, 1993, The Journal of biological chemistry.