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129 related items for PubMed ID: 2363122
1. Development of MDL 28,050, a small stable antithrombin agent based on a functional domain of the leech protein, hirudin. Krstenansky JL, Broersma RJ, Owen TJ, Payne MH, Yates MT, Mao SJ. Thromb Haemost; 1990 Apr 12; 63(2):208-14. PubMed ID: 2363122 [Abstract] [Full Text] [Related]
2. Allosteric changes of thrombin catalytic site induced by interaction of bothrojaracin with anion-binding exosites I and II. Monteiro RQ, Rapôso JG, Wisner A, Guimarães JA, Bon C, Zingali RB. Biochem Biophys Res Commun; 1999 Sep 07; 262(3):819-22. PubMed ID: 10471408 [Abstract] [Full Text] [Related]
3. Probing the distance between the two binding sites of hirudin for its interaction with the active site and the fibrin(ogen)-binding site of alpha-thrombin. Wagner U, Schmitz T, Otte M, Dodt J. Biomed Biochim Acta; 1991 Sep 07; 50(4-6):707-10. PubMed ID: 1801747 [Abstract] [Full Text] [Related]
5. Rational design of true hirudin mimetics: synthesis and characterization of multisite-directed alpha-thrombin inhibitors. Lombardi A, Nastri F, Della Morte R, Rossi A, De Rosa A, Staiano N, Pedone C, Pavone V. J Med Chem; 1996 May 10; 39(10):2008-17. PubMed ID: 8642559 [Abstract] [Full Text] [Related]
6. Hirudin as alternative anticoagulant--a historical review. Markwardt F. Semin Thromb Hemost; 2002 Oct 10; 28(5):405-14. PubMed ID: 12420235 [Abstract] [Full Text] [Related]
7. The C-terminal binding domain of hirullin P18. Antithrombin activity and comparison to hirudin peptides. Krstenansky JL, Owen TJ, Yates MT, Mao SJ. FEBS Lett; 1990 Sep 03; 269(2):425-9. PubMed ID: 2401369 [Abstract] [Full Text] [Related]
8. Comparison of hirudin and hirudin PA C-terminal fragments and related analogs as antithrombin agents. Krstenansky JL, Owen TJ, Yates MT, Mao SJ. Thromb Res; 1988 Oct 15; 52(2):137-41. PubMed ID: 3194888 [Abstract] [Full Text] [Related]
9. [Recent developments in the biochemistry of hirudins]. Walsmann P. Folia Haematol Int Mag Klin Morphol Blutforsch; 1989 Oct 15; 116(6):821-30. PubMed ID: 2483699 [Abstract] [Full Text] [Related]
10. A screening procedure to evaluate the anticoagulant activity and the kinetic behaviour of direct thrombin inhibitors. Rupin A, Mennecier P, de Nanteuil G, Laubie M, Verbeuren TJ. Thromb Res; 1995 May 01; 78(3):217-25. PubMed ID: 7631302 [Abstract] [Full Text] [Related]
11. Electrostatic steering and ionic tethering in the formation of thrombin-hirudin complexes: the role of the thrombin anion-binding exosite-I. Myles T, Le Bonniec BF, Betz A, Stone SR. Biochemistry; 2001 Apr 24; 40(16):4972-9. PubMed ID: 11305913 [Abstract] [Full Text] [Related]
12. Covalent linkage of streptokinase to recombinant hirudin: a novel thrombolytic agent with antithrombotic properties. Phaneuf MD, Ozaki CK, Johnstone MT, Loza JP, Quist WC, LoGerfo FW. Thromb Haemost; 1994 Apr 24; 71(4):481-7. PubMed ID: 8052967 [Abstract] [Full Text] [Related]
13. Effect of new synthetic heparin mimetics on whole blood thrombin generation in vivo and in vitro in rats. Hérault JP, Bernat A, Gaich C, Herbert M. Thromb Haemost; 2002 Feb 24; 87(2):238-44. PubMed ID: 11858483 [Abstract] [Full Text] [Related]
14. Domains specifying thrombin-receptor interaction. Vu TK, Wheaton VI, Hung DT, Charo I, Coughlin SR. Nature; 1991 Oct 17; 353(6345):674-7. PubMed ID: 1717851 [Abstract] [Full Text] [Related]
18. Interaction of hirudin with thrombin: identification of a minimal binding domain of hirudin that inhibits clotting activity. Mao SJ, Yates MT, Owen TJ, Krstenansky JL. Biochemistry; 1988 Oct 18; 27(21):8170-3. PubMed ID: 3233202 [Abstract] [Full Text] [Related]
20. In-depth study of tripeptide-based alpha-ketoheterocycles as inhibitors of thrombin. Effective utilization of the S1' subsite and its implications to structure-based drug design. Costanzo MJ, Almond HR, Hecker LR, Schott MR, Yabut SC, Zhang HC, Andrade-Gordon P, Corcoran TW, Giardino EC, Kauffman JA, Lewis JM, de Garavilla L, Haertlein BJ, Maryanoff BE. J Med Chem; 2005 Mar 24; 48(6):1984-2008. PubMed ID: 15771442 [Abstract] [Full Text] [Related] Page: [Next] [New Search]