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AIDS (London, England)|December 1, 1996
Effectiveness of 3TC in HIV clinical trials may be due in part to the M184V substitution in 3TC-resistant HIV-1 reverse transcriptaseM A Wainberg, M Hsu, Z Gu, et al.The Biochemical Journal|May 5, 2000
Mutational analysis of Lys65 of HIV-1 reverse transcriptaseN Sluis-Cremer, D Arion, N Kaushik, et al.The Journal of Biological Chemistry|May 15, 1993
Monoclonal antibody-mediated inhibition of HIV-1 reverse transcriptase polymerase activity. Interaction with a possible deoxynucleoside triphosphate binding domainJ Wu, E Amandoron, X Li, et al.Biochemistry|April 4, 1995
Carboxanilide derivative non-nucleoside inhibitors of HIV-1 reverse transcriptase interact with different mechanistic forms of the enzymeR S Fletcher, K Syed, S Mithani, et al.Journal of Virology|January 1, 1992
In vitro selection of variants of human immunodeficiency virus type 1 resistant to 3'-azido-3'-deoxythymidine and 2',3'-dideoxyinosineQ Gao, Z X Gu, M A Parniak, et al.Journal of Molecular Biology|June 6, 1998
Endogenous reverse transcriptase assays reveal synergy between combinations of the M184V and other drug resistance-conferring mutations in interactions with nucleoside analog triphosphatesY Quan, Z Gu, X Li, et al.Biochemical and Biophysical Research Communications|June 30, 1992
Variable tRNA content in HIV-1IIIBM Jiang, J Mak, M A Wainberg, et al.Archives of Virology|January 1, 1994
Generation of multiple drug resistance by sequential in vitro passage of the human immunodeficiency virus type 1Q Gao, Z Gu, H Salomon, et al.Biochemistry|February 24, 2000
Human immunodeficiency virus type 1 reverse transcriptase dimer destabilization by 1-[Spiro[4"-amino-2",2" -dioxo-1",2" -oxathiole-5",3'-[2', 5'-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]]]-3-ethylthy mineN Sluis-Cremer, G I Dmitrienko, J Balzarini, et al.Protein Expression and Purification|August 1, 1993
Expression, purification, and RNA-binding properties of HIV-1 p15gag nucleocapsid proteinX Li, Z Gu, R Geleziunas, et al.Pageof 8