Author:
Balzarini J.,Brouwer W.G.,Felauer E.E.,De Clercq E.,Karlsson A.
Reference19 articles.
1. Highly specific inhibition of human immunodeficiency virus type 1 by a novel 6-substituted acyclouridine derivative;Baba;Biochem. Biophys. Res. Commun.,1989
2. Oxathiin carboxanilide, a potent inhibitor of human immunodeficiency virus reproduction;Bader,1991
3. 2′,5′-Bis-O-(tert-butyldimethylsilyl)-3′-spiro-5″-(4″-amino-1″,2″-oxathiole-2″,2″-dioxide)pyrimidine (TSAO) nucleoside analogues: highly selective inhibitors of human immunodeficiency virus type 1 that are targeted at the viral reverse transcriptase;Balzarini,1992
4. HIV-1-specific reverse transcriptase inhibitors show differential activity against HIV-1-mutant strains containing different amino acid substitutions in the reverse transcriptase;Balzarini;Virology,1993
5. Treatment of HIV-1-infected cells by combinations of HIV-1-specific inhibitors results in a different resistance pattern than with single drug therapy;Balzarini;J. Virol.,1993
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