-
1
-
-
0022471697
-
Initial studies on the cellular pharmacology of 2′,3′-dideoxycytidine, an inhibitor of HTLV-III infectivity
-
Cooney, D. A., M. Dalal, H. Mitsuya, J. B. McMahon, M. Nadkarni, J. Balzarini, S. Broder, and D. G. Johns. Initial studies on the cellular pharmacology of 2′,3′-dideoxycytidine, an inhibitor of HTLV-III infectivity. Biochem. Pharmacol. 35:2065-2068 (1986).
-
(1986)
Biochem. Pharmacol.
, vol.35
, pp. 2065-2068
-
-
Cooney, D.A.1
Dalal, M.2
Mitsuya, H.3
McMahon, J.B.4
Nadkarni, M.5
Balzarini, J.6
Broder, S.7
Johns, D.G.8
-
2
-
-
0022996630
-
Phosphorylation of 3′-azido-3′-deoxythymidine and selective interaction of the 5′-triphosphate with human immunodeficiency virus reverse transcriptase
-
Furman, P. A., J. A. Fyfe, M. H. St. Clair, K. Weinhold, J. L. Rideout, G. A. Freeman, S. Nusinoff Lehrman, D. P. Bolognesi, S. Broder, H. Mitsuya, and D. W. Barry. Phosphorylation of 3′-azido-3′-deoxythymidine and selective interaction of the 5′-triphosphate with human immunodeficiency virus reverse transcriptase. Proc. Natl. Acad. Sci. USA 83:8333-8337 (1986).
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 8333-8337
-
-
Furman, P.A.1
Fyfe, J.A.2
St. Clair, M.H.3
Weinhold, K.4
Rideout, J.L.5
Freeman, G.A.6
Nusinoff Lehrman, S.7
Bolognesi, D.P.8
Broder, S.9
Mitsuya, H.10
Barry, D.W.11
-
3
-
-
0023656787
-
Initial studies on the cellular pharmacology of 2′,3′-dideoxyinosine, an inhibitor of HW infectivity
-
Ahluwalia, G., D. A. Cooney, H. Mitsuya, A. Fridland, K P. Flora, Z. Hao, M. Dalal, S. Broder, and D. G. Johns. Initial studies on the cellular pharmacology of 2′,3′-dideoxyinosine, an inhibitor of HW infectivity. Biochem. Pharmacol. 36:3797-3801 (1987).
-
(1987)
Biochem. Pharmacol.
, vol.36
, pp. 3797-3801
-
-
Ahluwalia, G.1
Cooney, D.A.2
Mitsuya, H.3
Fridland, A.4
Flora, K.P.5
Hao, Z.6
Dalal, M.7
Broder, S.8
Johns, D.G.9
-
4
-
-
0023475103
-
3′-Azido-3-deoxythymidine triphosphate as an inhibitor and substrate of purified human immunodeficiency virus reverse transcriptase
-
St. Clair, M. H., C. A. Richards, T. Spector, K. J. Weinhold, W. H. Miller, A. J. Langlois, and P. A. Furman. 3′-Azido-3-deoxythymidine triphosphate as an inhibitor and substrate of purified human immunodeficiency virus reverse transcriptase. Antimicrob. Agents Chemother. 31:1972-1977 (1987).
-
(1987)
Antimicrob. Agents Chemother.
, vol.31
, pp. 1972-1977
-
-
St. Clair, M.H.1
Richards, C.A.2
Spector, T.3
Weinhold, K.J.4
Miller, W.H.5
Langlois, A.J.6
Furman, P.A.7
-
5
-
-
0024592935
-
Differential patterns of intracellular metabolism of 2′,3′-didehydro-2′,3′-dideoxythymidine and 3′-azido-2′,3′-dideoxythymidine, two potent anti-human immunodeficiency virus compounds
-
Balzarini, J., P. Herdewijn, and E. De Clercq. Differential patterns of intracellular metabolism of 2′,3′-didehydro-2′,3′-dideoxythymidine and 3′-azido-2′,3′-dideoxythymidine, two potent anti-human immunodeficiency virus compounds. J. Biol. Chem. 264:6127-6133 (1989).
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 6127-6133
-
-
Balzarini, J.1
Herdewijn, P.2
De Clercq, E.3
-
6
-
-
0025866982
-
Anti-human immunodeficiency virus type 1 activity and in vitro toxicity of 2′-deoxy-3′-thiacytidine (BCH-189), a novel heterocyclic nucleoside analog
-
Soudeyns, H , X.-J. Yao, Q. Gao, B. Belleau, J.-L. Kraus, N. Nguyen-Ba, B. Spira, and M. A. Wainberg. Anti-human immunodeficiency virus type 1 activity and in vitro toxicity of 2′-deoxy-3′-thiacytidine (BCH-189), a novel heterocyclic nucleoside analog. Antimicrob. Agents Chemother. 35:1386-1390 (1991).
-
(1991)
Antimicrob. Agents Chemother.
, vol.35
, pp. 1386-1390
-
-
Soudeyns, H.1
Yao, X.-J.2
Gao, Q.3
Belleau, B.4
Kraus, J.-L.5
Nguyen-Ba, N.6
Spira, B.7
Wainberg, M.A.8
-
7
-
-
0026541703
-
The separated enantiomers of 2′-deoxy-3′-thiacytidine (BCH 189) both inhibit human immunodeficiency virus replication in vitro
-
Coates, J. A. V., N. Cammack, H. J. Jenkinson, I. M. Mutton, B. A. Pearson, R. Storer, J. M. Cameron, and C. R. Penn. The separated enantiomers of 2′-deoxy-3′-thiacytidine (BCH 189) both inhibit human immunodeficiency virus replication in vitro. Antimicrob. Agents Chemother. 36:202-205 (1992).
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 202-205
-
-
Coates, J.A.V.1
Cammack, N.2
Jenkinson, H.J.3
Mutton, I.M.4
Pearson, B.A.5
Storer, R.6
Cameron, J.M.7
Penn, C.R.8
-
8
-
-
0026701167
-
In vitro toxicity of 2′,3′-dideoxy-3′-thiacytidine (BCH189/3TC), a new synthetic anti-HIV-1 nucleoside
-
Lisignoli, G., A. Facchini, L. Cattini, M. C. G. Monaco, A. Degrassi, and E. Mariani. In vitro toxicity of 2′,3′-dideoxy-3′-thiacytidine (BCH189/3TC), a new synthetic anti-HIV-1 nucleoside. Antiviral Chem. Chemother. 3:299-303 (1992).
-
(1992)
Antiviral Chem. Chemother.
, vol.3
, pp. 299-303
-
-
Lisignoli, G.1
Facchini, A.2
Cattini, L.3
Monaco, M.C.G.4
Degrassi, A.5
Mariani, E.6
-
9
-
-
7344264636
-
Activities of the four optical isomers of 2′,3′-dideoxy-3′-thiacytidine (BCH-189) against human immunodeficiency virus type 1 in human lymphocytes
-
Schinazi, R. F., C. K. Chu, A. Peck, A. McMillan, R. Mathis, D. Cannon, L.-S. Jeong, J. W. Beach, W.-B. Choi, S. Yeola, and D. C Liotta. Activities of the four optical isomers of 2′,3′-dideoxy-3′-thiacytidine (BCH-189) against human immunodeficiency virus type 1 in human lymphocytes. Antimicrob. Agents Chemother. 36:672-676 (1992).
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 672-676
-
-
Schinazi, R.F.1
Chu, C.K.2
Peck, A.3
McMillan, A.4
Mathis, R.5
Cannon, D.6
Jeong, L.-S.7
Beach, J.W.8
Choi, W.-B.9
Yeola, S.10
Liotta, D.C.11
-
10
-
-
0026471558
-
Comparison of cytotoxicity of the (-)- and (+)-enantiomer of 2′,3′-dideoxy-3′-thiacytidine in normal human hone marrow progenitor cells
-
Sommadossi, J.-P., R. F. Schinazi, C. K. Chu, and M.-Y. Xie. Comparison of cytotoxicity of the (-)- and (+)-enantiomer of 2′,3′-dideoxy-3′-thiacytidine in normal human hone marrow progenitor cells. Biochem. Pharmacol. 44:1921-1925 (1992).
-
(1992)
Biochem. Pharmacol.
, vol.44
, pp. 1921-1925
-
-
Sommadossi, J.-P.1
Schinazi, R.F.2
Chu, C.K.3
Xie, M.-Y.4
-
11
-
-
0028120730
-
HIV resistance to reverse transcriptase inhibitors
-
De Clercq, E. HIV resistance to reverse transcriptase inhibitors. Biochem. Pharmacol. 47:155-169 (1993)
-
(1993)
Biochem. Pharmacol.
, vol.47
, pp. 155-169
-
-
De Clercq, E.1
-
12
-
-
0026077832
-
Viral resistance to human immunodeficiency virus type 1-specific pyridinone reverse transcriptase inhibitors
-
Nunberg, J. H., W. A. Schleif, E. J. Boots, J. A. O'Brien, J. C. Quintero, J. M. Hoffman, Jr., E. A. Emini, and M. E. Goldman. Viral resistance to human immunodeficiency virus type 1-specific pyridinone reverse transcriptase inhibitors. J. Virol. 65:4887-4892 (1991).
-
(1991)
J. Virol.
, vol.65
, pp. 4887-4892
-
-
Nunberg, J.H.1
Schleif, W.A.2
Boots, E.J.3
O'Brien, J.A.4
Quintero, J.C.5
Hoffman Jr., J.M.6
Emini, E.A.7
Goldman, M.E.8
-
13
-
-
0026318387
-
Human immunodeficiency virus type 1 mutants resistant to non-nucleoside inhibitors of reverse transcriptase arise in tissue culture
-
Richman, D., C.-K. Shih, I. Lowy, J. Rose, P. Prodanovich, S. Goff, and J. Griffin. Human immunodeficiency virus type 1 mutants resistant to non-nucleoside inhibitors of reverse transcriptase arise in tissue culture. Proc. Natl. Acad. Sci. USA 88:11241-11245 (1991).
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 11241-11245
-
-
Richman, D.1
Shih, C.-K.2
Lowy, I.3
Rose, J.4
Prodanovich, P.5
Goff, S.6
Griffin, J.7
-
14
-
-
0026579394
-
In vitro selection and molecular characterization of human immunodeficiency virus-1 resistant to non-nucleoside inhibitors of reverse transcriptase
-
Mellors, J. W., G E. Dutschman, G.-J. Im, E. Tramontano, S. R. Winkler, and Y.-C. Cheng. In vitro selection and molecular characterization of human immunodeficiency virus-1 resistant to non-nucleoside inhibitors of reverse transcriptase. Mol. Pharmacol. 41:446-451 (1992).
-
(1992)
Mol. Pharmacol.
, vol.41
, pp. 446-451
-
-
Mellors, J.W.1
Dutschman, G.E.2
Im, G.-J.3
Tramontano, E.4
Winkler, S.R.5
Cheng, Y.-C.6
-
15
-
-
0027363224
-
Knocking-out concentrations of HIV-1-specific inhibitors completely suppress HIV-1 infection and prevent the emergence of drug-resistant virus
-
Balzarini, J., A. Karlsson, M.-J. Pérez-Pérez, M.-J. Camarasa, and E. De Clercq. Knocking-out concentrations of HIV-1-specific inhibitors completely suppress HIV-1 infection and prevent the emergence of drug-resistant virus. Virology 196:576-585 (1993).
-
(1993)
Virology
, vol.196
, pp. 576-585
-
-
Balzarini, J.1
Karlsson, A.2
Pérez-Pérez, M.-J.3
Camarasa, M.-J.4
De Clercq, E.5
-
16
-
-
0027214433
-
Treatment of human immunodeficiency virus type 1 (HIV-1)-infected cells with combinations of HIV-1-specific inhibitors results in a different resistance pattern than does treatment with single-drug therapy
-
Balzarini, J., A. Karlsson, M.-J. Pérez-Pérez, M.-J. Camarasa, W. G. Tarpley, and E. De Clercq. Treatment of human immunodeficiency virus type 1 (HIV-1)-infected cells with combinations of HIV-1-specific inhibitors results in a different resistance pattern than does treatment with single-drug therapy. J. Virol. 67:5353-5359 (1993).
-
(1993)
J. Virol.
, vol.67
, pp. 5353-5359
-
-
Balzarini, J.1
Karlsson, A.2
Pérez-Pérez, M.-J.3
Camarasa, M.-J.4
Tarpley, W.G.5
De Clercq, E.6
-
17
-
-
0028285185
-
Human immunodeficiency virus 1 (HIV-1)-specific reverse transcriptase (RT) inhibitors may suppress the replication of specific drug-resistant (E138K) RT HIV-1 mutants or select for highly resistant (Y181C → C181I) RT HIV-1 mutants
-
Balzarini, J., A. Karlsson, V. V. Sardana, E. A. Emini, M.-J. Camarasa, and E. De Clercq. Human immunodeficiency virus 1 (HIV-1)-specific reverse transcriptase (RT) inhibitors may suppress the replication of specific drug-resistant (E138K) RT HIV-1 mutants or select for highly resistant (Y181C → C181I) RT HIV-1 mutants. Proc Natl. Acad. Sci USA 91:6599-6603 (1994).
-
(1994)
Proc Natl. Acad. Sci USA
, vol.91
, pp. 6599-6603
-
-
Balzarini, J.1
Karlsson, A.2
Sardana, V.V.3
Emini, E.A.4
Camarasa, M.-J.5
De Clercq, E.6
-
18
-
-
0028068907
-
Sensitivity of (138 Glu → lysine) mutated human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) to HIV-1-specific RT inhibitors
-
Balzarini, J., J.-P. Kleim, G. Riess, M.-J. Camarasa, E. De Clercq, and A. Karlsson. Sensitivity of (138 Glu → lysine) mutated human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) to HIV-1-specific RT inhibitors. Biochem. Biophys. Res. Commun. 201:1305-1312 (1994).
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.201
, pp. 1305-1312
-
-
Balzarini, J.1
Kleim, J.-P.2
Riess, G.3
Camarasa, M.-J.4
De Clercq, E.5
Karlsson, A.6
-
19
-
-
0026465275
-
Novel mutation in the human immunodeficiency virus type 1 reverse transcriptase gene that encodes cross-resistance to 2′,3′-dideoxyinosine and 2′,3′-dideoxycytidine
-
Gu, Z., Q. Gao, X. Li, M. A. Parniak, and M. A. Wainberg. Novel mutation in the human immunodeficiency virus type 1 reverse transcriptase gene that encodes cross-resistance to 2′,3′-dideoxyinosine and 2′,3′-dideoxycytidine J. Virol. 66:7128-7135 (1992).
-
(1992)
J. Virol.
, vol.66
, pp. 7128-7135
-
-
Gu, Z.1
Gao, Q.2
Li, X.3
Parniak, M.A.4
Wainberg, M.A.5
-
20
-
-
0027373308
-
High-level resistance to (-) enantiomeric 2′-deoxy-3′-thiacytidine in vitro is due to one amino acid substitution in the catalytic site of human immunodeficiency virus type 1 reverse transcriptase
-
Boucher, C. A. B., N. Cammack, P. Schipper, R. Schuurman, P. Rouse, M. A. Wainberg, and J. M. Cameron. High-level resistance to (-) enantiomeric 2′-deoxy-3′-thiacytidine in vitro is due to one amino acid substitution in the catalytic site of human immunodeficiency virus type 1 reverse transcriptase. Antimicrob. Agents Chemother. 37:2231-2234 (1993).
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 2231-2234
-
-
Boucher, C.A.B.1
Cammack, N.2
Schipper, P.3
Schuurman, R.4
Rouse, P.5
Wainberg, M.A.6
Cameron, J.M.7
-
21
-
-
0027155374
-
The same mutation that encodes low-level human immunodeficiency virus type 1 resistance to 2′:3′-dideoxyinosine and 2′,3′-dideoxycytidine confers high-level resistance to the (-) enantiomer of 2′,3′-dideoxy-3′-thiacytidine
-
Gao, Q., Z. Gu, M. A. Parniak, J. Cameron, N. Cammack, C. Boucher, and M. A. Wainberg. The same mutation that encodes low-level human immunodeficiency virus type 1 resistance to 2′:3′-dideoxyinosine and 2′,3′-dideoxycytidine confers high-level resistance to the (-) enantiomer of 2′,3′-dideoxy-3′-thiacytidine. Antimicrob. Agents Chemother. 37:1390-1392 (1993).
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 1390-1392
-
-
Gao, Q.1
Gu, Z.2
Parniak, M.A.3
Cameron, J.4
Cammack, N.5
Boucher, C.6
Wainberg, M.A.7
-
22
-
-
0027409698
-
Characterization of human immunodeficiency viruses resistant to oxathiolane-cytosine nucleosides
-
Schinazi, R. F., R. M. Lloyd, Jr., M.-H. Nguyen, D. L. Cannon, A. McMillan, N. Ilksoy, C. K. Chu, D. C. Liotta, H. Z. Bazmi, and J. W. Mellors. Characterization of human immunodeficiency viruses resistant to oxathiolane-cytosine nucleosides. Antimicrob. Agents Chemother. 37:875-881 (1993).
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 875-881
-
-
Schinazi, R.F.1
Lloyd Jr., R.M.2
Nguyen, M.-H.3
Cannon, D.L.4
McMillan, A.5
Ilksoy, N.6
Chu, C.K.7
Liotta, D.C.8
Bazmi, H.Z.9
Mellors, J.W.10
-
23
-
-
0027285372
-
Rapid in vitro selection of human immunodeficiency virus type 1 resistant to 3′-thiacytidine inhibitors due to a mutation in the YMDD region of reverse transcriptase
-
Tisdale, M., S. D. Kemp, N. R. Parry, and B. A. Larder. Rapid in vitro selection of human immunodeficiency virus type 1 resistant to 3′-thiacytidine inhibitors due to a mutation in the YMDD region of reverse transcriptase. Proc. Natl Acad. Sci. USA 90:5653-5656 (1993).
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 5653-5656
-
-
Tisdale, M.1
Kemp, S.D.2
Parry, N.R.3
Larder, B.A.4
-
24
-
-
0026771409
-
3′-Spiro nucleosides, a new class of specific human immunodeficiency virus type 1 inhibitors: Synthesis and antiviral activity of [2′:5′-bis-O-(tert-butyldimethylsilyl)-β-D-xylo- And -ribofuranose]-3′-spiro-5′-[4′-amino-1′,2′- oxathiole 2′,2′-dioxide] (TSAO) pyrimidine nucleosides
-
Camarasa, M.-J., M.-J. Pérez-Pérez, A. San-Felix, J. Balzarini, and E. De Clercq. 3′-Spiro nucleosides, a new class of specific human immunodeficiency virus type 1 inhibitors: synthesis and antiviral activity of [2′:5′-bis-O-(tert-butyldimethylsilyl)-β-D-xylo- and -ribofuranose]-3′-spiro-5′-[4′-amino-1′,2′- oxathiole 2′,2′-dioxide] (TSAO) pyrimidine nucleosides. J. Med. Chem. 35:2721-2727 (1992).
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2721-2727
-
-
Camarasa, M.-J.1
Pérez-Pérez, M.-J.2
San-Felix, A.3
Balzarini, J.4
De Clercq, E.5
-
25
-
-
0026737678
-
TSAO analogues: Stereospecific synthesis and anti-HIV-1 activity of 1-[2′,5′-bis-O-(tert-butyldimethyl)-β-D-ribofuranosyl]-3′ -spiro-5′-(4′-amino-1′,2′-oxathiole 2′,2′-dioxide) pyrimidine and pyrimidine-modified nucleosides
-
Pérez-Pérez, M. J., A. San-Félix, J. Balzarini, E. De Clercq, and M. J. Camarasa. TSAO analogues: stereospecific synthesis and anti-HIV-1 activity of 1-[2′,5′-bis-O-(tert-butyldimethyl)-β-D-ribofuranosyl]-3′ -spiro-5′-(4′-amino-1′,2′-oxathiole 2′,2′-dioxide) pyrimidine and pyrimidine-modified nucleosides. J. Med. Chem. 35:2988-2995 (1992).
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2988-2995
-
-
Pérez-Pérez, M.J.1
San-Félix, A.2
Balzarini, J.3
De Clercq, E.4
Camarasa, M.J.5
-
26
-
-
0026650693
-
Synthesis of [1-[2′,5′-bis-O-(t-butyldimethylsilyl)-β-D-xylo- And β-D-ribofuranosyl]thymine]-3′-spiro-5′-[4′-amino-1′ ,2′-oxathiole-2′,2′-dioxide] (TSAO): Novel types of specific anti-HIV agents
-
Pérez-Pérez, M.-J., A. San-Félix, M.-J. Camarasa, J. Balzarini, and E. De Clercq. Synthesis of [1-[2′,5′-bis-O-(t-butyldimethylsilyl)-β-D-xylo- and β-D-ribofuranosyl]thymine]-3′-spiro-5′-[4′-amino-1′ ,2′-oxathiole-2′,2′-dioxide] (TSAO): novel types of specific anti-HIV agents. Tetrahedron Lett. 33:3029-3032 (1992).
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 3029-3032
-
-
Pérez-Pérez, M.-J.1
San-Félix, A.2
Camarasa, M.-J.3
Balzarini, J.4
De Clercq, E.5
-
27
-
-
0029079399
-
Suppression of the breakthrough of human immunodeficiency virus type 1 (HIV-1) in cell culture by thiocarboxanilide derivatives when used individually or in combination with other HIV-1-specific inhibitors (i.e., TSAO derivatives)
-
Balzarini, J., M.-J. Pérez-Pérez, S. Vélazquez, A. San-Félix, M.-J. Camarasa, E. De Clercq, and A. Karlsson. Suppression of the breakthrough of human immunodeficiency virus type 1 (HIV-1) in cell culture by thiocarboxanilide derivatives when used individually or in combination with other HIV-1-specific inhibitors (i.e., TSAO derivatives). Proc. Natl. Acad. Sci. USA 92:5470-5474 (1995).
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 5470-5474
-
-
Balzarini, J.1
Pérez-Pérez, M.-J.2
Vélazquez, S.3
San-Félix, A.4
Camarasa, M.-J.5
De Clercq, E.6
Karlsson, A.7
-
28
-
-
0028940526
-
Oxathiin carboxanilide derivatives, a class of non-nucleoside HIV-1-specific reverse transcriptase inhibitors (NNETIs) that are active against mutant HIV-1 strains resistant to other NNRTIs
-
Balzarini, J., H. Jonckheere, W. A. Harrison, D. C. Dao, J. Anné, E. De Clercq, and A. Karlsson. Oxathiin carboxanilide derivatives, a class of non-nucleoside HIV-1-specific reverse transcriptase inhibitors (NNETIs) that are active against mutant HIV-1 strains resistant to other NNRTIs. Antiviral Chem. Chemother. 6:169-178 (1995).
-
(1995)
Antiviral Chem. Chemother.
, vol.6
, pp. 169-178
-
-
Balzarini, J.1
Jonckheere, H.2
Harrison, W.A.3
Dao, D.C.4
Anné, J.5
De Clercq, E.6
Karlsson, A.7
-
29
-
-
0029011342
-
Activity of various thiocarboxanilide derivatives against wild-type and several mutant human immunodeficiency virus type 1 strains
-
Balzarini, J., W. G. Brouwer, E. E. Felauer, E. De Clercq, and A. Karlsson. Activity of various thiocarboxanilide derivatives against wild-type and several mutant human immunodeficiency virus type 1 strains. Antiviral Res. 27:219-236 (1995).
-
(1995)
Antiviral Res.
, vol.27
, pp. 219-236
-
-
Balzarini, J.1
Brouwer, W.G.2
Felauer, E.E.3
De Clercq, E.4
Karlsson, A.5
-
30
-
-
0029028067
-
Potential mechanism for sustained antiretroviral efficacy of AZT-3TC combination therapy
-
Larder, B. A., S. D. Kemp, and P. R. Harrigan. Potential mechanism for sustained antiretroviral efficacy of AZT-3TC combination therapy. Science (Washington D. C.) 269:696-699 (1995).
-
(1995)
Science (Washington D. C.)
, vol.269
, pp. 696-699
-
-
Larder, B.A.1
Kemp, S.D.2
Harrigan, P.R.3
-
31
-
-
13344272723
-
Mutational analysis of the saquinavir high dose monotherapy study
-
Sardinia, Italy
-
Schapiro, J. M., M. Winters, and T. C. Merigan. Mutational analysis of the saquinavir high dose monotherapy study, in Abstracts of the Fourth International Workshop on. HIV Drug-Resistance. Sardinia, Italy, 73 (1995).
-
(1995)
Abstracts of the Fourth International Workshop On. HIV Drug-Resistance
, vol.73
-
-
Schapiro, J.M.1
Winters, M.2
Merigan, T.C.3
-
32
-
-
13344254338
-
Factors determining sustained antiviral response to nevirapine
-
Sardinia, Italy
-
Havlir, D. V., V. A. Johnson, D. B. Hall, P. A. Robinson, C. B. Overbay, and D. D. Richman. Factors determining sustained antiviral response to nevirapine, in Abstracts of the Fourth International Workshop on HTV Drug-Resistance. Sardinia, Italy, 22 (1995).
-
(1995)
Abstracts of the Fourth International Workshop on HTV Drug-Resistance
, vol.22
-
-
Havlir, D.V.1
Johnson, V.A.2
Hall, D.B.3
Robinson, P.A.4
Overbay, C.B.5
Richman, D.D.6
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