Zobrazeno 1 - 10
of 151
pro vyhledávání: '"D, Callas"'
Publikováno v:
Seminars in Thrombosis and Hemostasis. 21:076-079
Autor:
Demetra D. Callas, Jawed Fareed
Publikováno v:
Thrombosis Research. 83:463-468
Autor:
Demetra D. Callas, Jawed Fareed
Publikováno v:
Thrombosis Research. 83:97-102
Autor:
Demetra D. Callas, Jawed Fareed
Publikováno v:
Thrombosis Research. 78:457-460
Several synthetic and recombinant antithrombin agents are currently developed for anticoagulation during thrombolytic therapy. Many of these agents are designed to inhibit thrombin at the active site. This active site is similar in enzymes belonging
Publikováno v:
Expert Opinion on Investigational Drugs. 4:389-412
During the past decade, many significant developments in the clinical management of thrombotic and vascular disorders have occurred. In particular, several newer approaches for the prophylactic and therapeutic management of such disorders as venous t
Publikováno v:
Seminars in Thrombosis and Hemostasis. 21:166-176
An exposure of blood to tissue factor (TF) activates the coagulation system by the extrinsic pathway and may cause clot formation. Recombinant TF (r-TF) has been produced and subsequently reconstituted into phospholipid vesicles. The aim of these stu
Publikováno v:
Seminars in Thrombosis and Hemostasis. 21:177-183
Site-directed thrombin inhibitors are being currently assessed clinically for their antithrombotic efficacy. Although these agents are claimed to be specific and direct thrombin inhibitors, their mechanism of inhibition varies. The objective of these
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 1:114-124
Site-directed synthetic and recombinant antithrombin agents are widely used to prevent reocclusion during thrombolytic therapy in acute myocardial infarction and other vascular occlusive disorders. However, minimal studies have been conducted to exam
Publikováno v:
Thrombosis Research. 74:193-205
Newly developed synthetic and recombinant thrombin inhibitors possess strong anticoagulant effects. Despite these effects, interactions of these agents with enzymes in the fibrinolytic network result in the modulation of such proteases as t-PA, u-PA
Publikováno v:
Thrombosis Research. 69:369-376
Recently, a new chemically modified derivative of heparin (Suleparoide®, Syntex Laboratories Buenos Aires, Argentina) was introduced for the prophylaxis of thrombosis and treatment of vascular disorders. This agent is claimed to contain a depolymeri