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Inhibition of hepatitis C virus RNA replication by 2'-modified nucleoside analogs.
Carroll SS, Tomassini JE, Bosserman M, Getty K, Stahlhut MW, Eldrup AB, Bhat B, Hall D, Simcoe AL, LaFemina R, Rutkowski CA, Wolanski B, Yang Z, Migliaccio G, De Francesco R, Kuo LC, MacCoss M, Olsen DB. Carroll SS, et al. Among authors: hall d. J Biol Chem. 2003 Apr 4;278(14):11979-84. doi: 10.1074/jbc.M210914200. Epub 2003 Jan 27. J Biol Chem. 2003. PMID: 12554735 Free article.
Three-dimensional structure of a mutant HIV-1 protease displaying cross-resistance to all protease inhibitors in clinical trials.
Chen Z, Li Y, Schock HB, Hall D, Chen E, Kuo LC. Chen Z, et al. Among authors: hall d. J Biol Chem. 1995 Sep 15;270(37):21433-6. doi: 10.1074/jbc.270.37.21433. J Biol Chem. 1995. PMID: 7665551 Free article.
Analysis of mutational effects in the human immunodeficiency virus type-1 (HIV-1) provirus has revealed that as few as four amino acid side-chain substitutions in the HIV-1 protease (M46I/L63P/V82T/I84V) suffice to yield viral variants cross-resistant to a panel of protease inhib …
Analysis of mutational effects in the human immunodeficiency virus type-1 (HIV-1) provirus has revealed that as few as four amino acid side- …
Active human cytomegalovirus protease is a dimer.
Darke PL, Cole JL, Waxman L, Hall DL, Sardana MK, Kuo LC. Darke PL, et al. Among authors: hall dl. J Biol Chem. 1996 Mar 29;271(13):7445-9. doi: 10.1074/jbc.271.13.7445. J Biol Chem. 1996. PMID: 8631772 Free article.
4,284 results