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Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990
Sequence-specific interaction of Tat protein and Tat peptides with the transactivation-responsive sequence element of human immunodeficiency virus type 1 in vitroM G Cordingley, R L LaFemina, P L Callahan, et al.
Journal of Translational Medicine|September 3, 2014
CD160 isoforms and regulation of CD4 and CD8 T-cell responsesMohamed El-Far, Charles Pellerin, Louise Pilote, et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems|October 13, 2011
Cross-species absorption, metabolism, distribution and pharmacokinetics of BI 201335, a potent HCV genotype 1 NS3/4A protease inhibitorJianmin Duan, Chan-Loi Yong, Michel Garneau, et al.
Bioorganic & Medicinal Chemistry Letters|January 27, 2004
Novel nevirapine-like inhibitors with improved activity against NNRTI-resistant HIV: 8-heteroarylthiomethyldipyridodiazepinone derivativesC Yoakim, P R Bonneau, R Déziel, et al.
Journal of Medicinal Chemistry|November 14, 2014
Discovery of BI 207524, an indole diamide NS5B thumb pocket 1 inhibitor with improved potency for the potential treatment of chronic hepatitis C virus infectionPierre L Beaulieu, Paul C Anderson, Richard Bethell, et al.
Journal of Medicinal Chemistry|August 19, 2010
Discovery of a potent and selective noncovalent linear inhibitor of the hepatitis C virus NS3 protease (BI 201335)Montse Llinàs-Brunet, Murray D Bailey, Nathalie Goudreau, et al.
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