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Science (New York, N.Y.)|January 21, 1994
Rational design of potent, bioavailable, nonpeptide cyclic ureas as HIV protease inhibitorsP Y Lam, P K Jadhav, C J Eyermann, et al.Academic Medicine : Journal of the Association of American Medical Colleges|November 13, 2009
Evaluating the quality of learning-team processes in medical education: development and validation of a new measureBritta M Thompson, Ruth E Levine, Frances Kennedy, et al.Journal of Medicinal Chemistry|May 23, 1998
Nonpeptide cyclic cyanoguanidines as HIV-1 protease inhibitors: synthesis, structure-activity relationships, and X-ray crystal structure studiesP K Jadhav, F J Woerner, P Y Lam, et al.Chemistry & Biology|April 1, 1996
Improved cyclic urea inhibitors of the HIV-1 protease: synthesis, potency, resistance profile, human pharmacokinetics and X-ray crystal structure of DMP 450C N Hodge, P E Aldrich, L T Bacheler, et al.Pageof 7