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R. C. Becker (1), T. Povsic (2), M. G. Cohen (3, 4), C. P. Rusconi (5), B. Sullenger (6)
(1) Duke University Medical Center, Duke Clinical Research Institute, Durham, North Carolina, USA; (2) Division of Cardiology, Duke University Medical Center, Durham, North Carolina, USA; (3) Miller School of Medicine, University of Miami, Miami, Florida, USA; (4) Cardiac Catheterization Laboratory, University of Miami Hospital, Miami, Florida, USA; (5) Regado Biosciences, Inc, Durham, North Carolina, USA; (6) Department of Genetics, Center for Genetics and Cellular Therapies, Duke University Medical Center, Durham, North Carolina, USA
Antithrombotic therapy for the acute management of thrombotic disorders has been stimulated and guided actively by our current understanding of platelet biology, coagulation proteases, and vascular science. A translatable platform for coagulation, based soundly on biochemistry, enzymology and cellular events on platelets and tissue factor-baring cells, introduces fundamental constructs, mechanistic clarity, and an unparalleled opportunity for accelerating the development and clinical investigation of both disease- and patient-specific therapies. In the current review, we build upon and expand substantially our observations surrounding nucleic acids as antithrombotic agents.
anticoagulant therapy, Nucleic acids, RNA and DNA aptamers, protein-binding oligonucleotides
| 1. | A randomised double-blind dose-response study | |
G. Raskob (1), A. T. Cohen (2), B. I. Eriksson (3), D. Puskas (4), M. Shi (5), T. Bocanegra (5), J. I. Weitz (6) Thrombosis and Haemostasis 2010 104 3: 642-649 http://dx.doi.org/10.1160/TH10-02-0142 | ||
| 2. | ||
José Antonio Nieto1, Timoteo Camara1, Elena Gonzalez-Higueras1, Nuria Ruiz-Gimenez2, Ricardo Guijarro3, Pablo Javier Marchena4, Manuel Monreal5; for the RIETE Investigators* Thrombosis and Haemostasis 2008 100 5: 789-796 http://dx.doi.org/10.1160/TH08-06-0390 | ||