-
1
-
-
37049188108
-
Suramin Protection of T Cells in vitro against Infectivity and Cytopathic Effect of HTLV-III
-
Mitsuya H, Popovic M, Yarchoan R, Matsushita S, Gallo RC, Broder S. Suramin Protection of T Cells in vitro against Infectivity and Cytopathic Effect of HTLV-III. Science 1984; 226: 172-4.
-
(1984)
Science
, vol.226
, pp. 172-174
-
-
Mitsuya, H.1
Popovic, M.2
Yarchoan, R.3
Matsushita, S.4
Gallo, R.C.5
Broder, S.6
-
2
-
-
0001707601
-
3′-Azido-3′-deoxythymidine (BW A509U): An antiviral agent that inhibits the infectivity and cytopathic effect of human T-lymphotropic virus type III/lymphadenopathy-associated virus in vitro
-
Mitsuya H, Weinhold KJ, Furman PA, St Clair MH, Lehrman SN, Gallo RC, et al. 3′-Azido-3′-deoxythymidine (BW A509U : an antiviral agent that inhibits the infectivity and cytopathic effect of human T-lymphotropic virus type III/lymphadenopathy-associated virus in vitro. Proc Nat Acad Sci USA 1985; 82: 7096-100.
-
(1985)
Proc. Nat. Acad. Sci. USA
, vol.82
, pp. 7096-7100
-
-
Mitsuya, H.1
Weinhold, K.J.2
Furman, P.A.3
St Clair, M.H.4
Lehrman, S.N.5
Gallo, R.C.6
-
3
-
-
0022404296
-
Infection of HTLV-III/LAV in HTLV-1-carrying cells MT-2 and MT-4 and application in a plaque assay
-
Harada S, Koyanagi Y, Yamamoto N. Infection of HTLV-III/LAV in HTLV-1-carrying cells MT-2 and MT-4 and application in a plaque assay. Science 1985; 229: 563-6.
-
(1985)
Science
, vol.229
, pp. 563-566
-
-
Harada, S.1
Koyanagi, Y.2
Yamamoto, N.3
-
4
-
-
0025186450
-
Molecular targets for AIDS therapy
-
Mitsuya H, Yarchoan R, Broder S. Molecular targets for AIDS therapy. Science 1990; 249:1533-44.
-
(1990)
Science
, vol.249
, pp. 1533-1544
-
-
Mitsuya, H.1
Yarchoan, R.2
Broder, S.3
-
5
-
-
0030869269
-
Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy
-
Gulick RM, Mellors JW, Havlir D, Eton JJ, Gonzalez C, McMahon D, et al. Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy. N Engl J Med 1997; 337: 734-9.
-
(1997)
N. Engl. J. Med.
, vol.337
, pp. 734-739
-
-
Gulick, R.M.1
Mellors, J.W.2
Havlir, D.3
Eton, J.J.4
Gonzalez, C.5
McMahon, D.6
-
6
-
-
0442268112
-
A controlled trial of two nucleoside analogues plus indinavir in persons with human immunodeficiency virus infection and CD4 cell counts of 200 per cubic millimeter or less
-
AIDS Clinical Trials Group 320 Study Team
-
Hammer SM, Squires KE, Hughes MD, Grimes JM, Demeter LM, Currier JS, et al. A controlled trial of two nucleoside analogues plus indinavir in persons with human immunodeficiency virus infection and CD4 cell counts of 200 per cubic millimeter or less. AIDS Clinical Trials Group 320 Study Team. N Engl J Med 1997; 337: 725-33.
-
(1997)
N. Engl. J. Med.
, vol.337
, pp. 725-733
-
-
Hammer, S.M.1
Squires, K.E.2
Hughes, M.D.3
Grimes, J.M.4
Demeter, L.M.5
Currier, J.S.6
-
7
-
-
2642709177
-
Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection
-
HIV Outpatient Study Investigators
-
Palella FJ, Delaney KM, Moorman AC, Loveless MO, Fuhrer J, Satten GA, et al. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. HIV Outpatient Study Investigators. N Engl J Med 1998 338: 853-60.
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 853-860
-
-
PaleOutpatientDelaney, K.M.1
Moorman, A.C.2
Loveless, M.O.3
Fuhrer, J.4
Satten, G.A.5
-
8
-
-
0032547101
-
HIV treatment failure: Testing for HIV resistance in clinical practice
-
Perrin L, Telenti A. HIV treatment failure: testing for HIV resistance in clinical practice. Science 1998; 280: 1871-3.
-
(1998)
Science
, vol.280
, pp. 1871-1873
-
-
Perrin, L.1
Telenti, A.2
-
9
-
-
0028952146
-
HIV population dynamics in vivo: Implications for genetic variation, pathogenesis, and therapy
-
Coffin JM. HIV population dynamics in vivo: implications for genetic variation, pathogenesis, and therapy. Science 1995; 267: 483-9.
-
(1995)
Science
, vol.267
, pp. 483-489
-
-
Coffin, J.M.1
-
10
-
-
10644289884
-
-
Coffin JM, Hughes SH, Varmus HE Eds, Cold Spring Harbor Laboratory Press
-
Vogt PK. In: Coffin JM, Hughes SH, Varmus HE Eds, Retroviruses. Cold Spring Harbor Laboratory Press. 1977; 1-25.
-
(1977)
Retroviruses
, pp. 1-25
-
-
Vogt, P.K.1
-
11
-
-
0030002637
-
HIV-1 entry cofactor: Functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor
-
Feng Y, Broder CC, Kennedy PE, Berger EA. HIV-1 entry cofactor: functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor. Science 1996; 272: 872.
-
(1996)
Science
, vol.272
, pp. 872
-
-
Feng, Y.1
Broder, C.C.2
Kennedy, P.E.3
Berger, E.A.4
-
12
-
-
15844389650
-
HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5
-
Dragic T, Litwin V, Allaway GP, Martin SR, Huang Y, Nagashima KA, et al. HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5. Nature 1996; 381: 667-73.
-
(1996)
Nature
, vol.381
, pp. 667-673
-
-
Dragic, T.1
Litwin, V.2
Allaway, G.P.3
Martin, S.R.4
Huang, Y.5
Nagashima, K.A.6
-
13
-
-
0034675998
-
HIV-1 membrane fusion: Targets of opportunity
-
Donis RW, Moore JP. HIV-1 membrane fusion: targets of opportunity. J Cell Biol 2000; 151: 179-14.
-
(2000)
J. Cell Biol.
, vol.151
-
-
Donis, R.W.1
Moore, J.P.2
-
14
-
-
0034120341
-
Membrane fusion mediated by coiled coils: A hypothesis
-
Bentz J. Membrane fusion mediated by coiled coils: a hypothesis. Biophys J 2000; 78: 886-900.
-
(2000)
Biophys. J.
, vol.78
, pp. 886-900
-
-
Bentz, J.1
-
15
-
-
0034675886
-
Evidence that the transition of HIV-1 gp41 into a six-helix bundle, not the bundle configuration, induces membrane fusion
-
Melikyan GB, Markosyan RM, Hemmati H, Delmedico MK, Lambert DM, Cohen FS. Evidence that the transition of HIV-1 gp41 into a six-helix bundle, not the bundle configuration, induces membrane fusion. J Cell Biol 2000; 151: 413-23.
-
(2000)
J. Cell Biol.
, vol.151
, pp. 413-423
-
-
Melikyan, G.B.1
Markosyan, R.M.2
Hemmati, H.3
Delmedico, M.K.4
Lambert, D.M.5
Cohen, F.S.6
-
16
-
-
0030962291
-
Atomic structure of the ectodomain from HIV-1 gp41
-
Weissenhorn W, Dessen A, Harrison SC, Skehel JJ, Wiley DC. Atomic structure of the ectodomain from HIV-1 gp41. Nature 1997; 387: 426-30.
-
(1997)
Nature
, vol.387
, pp. 426-430
-
-
Weissenhorn, W.1
Dessen, A.2
Harrison, S.C.3
Skehel, J.J.4
Wiley, D.C.5
-
18
-
-
0035036358
-
HIV fusion and its inhibition
-
LaBranche CC, Galasso G, Moore JM, Bolognesi DP, Hirsch MS, Hammer SM. HIV fusion and its inhibition. Antiviral Research 2001; 50: 95-115.
-
(2001)
Antiviral Research
, vol.50
, pp. 95-115
-
-
LaBranche, C.C.1
Galasso, G.2
Moore, J.M.3
Bolognesi, D.P.4
Hirsch, M.S.5
Hammer, S.M.6
-
19
-
-
0002296754
-
-
Coffin JM, Hughes SH, Varmus HE Eds, Cold Spring Harbor Laboratory Press
-
Telesnitsky A, Goff SP. In: Coffin JM, Hughes SH, Varmus HE Eds, Retroviruses. Cold Spring Harbor Laboratory Press, 1977; 121-160.
-
(1977)
Retroviruses
, pp. 121-160
-
-
Telesnitsky, A.1
Goff, S.P.2
-
20
-
-
0033813928
-
Retroviral integrase inhibitors year 2000: Update and perspectives
-
Pommier Y, Marchand C, Neamati N, Retroviral integrase inhibitors year 2000: update and perspectives. Antiviral Res 2000; 47: 139-48.
-
(2000)
Antiviral Res.
, vol.47
, pp. 139-148
-
-
Pommier, Y.1
Marchand, C.2
Neamati, N.3
-
21
-
-
0041488800
-
Small-molecule HIV-1 integrase inhibitors: The 2001 - 2002 update
-
Dayam R, Neamati N. Small-molecule HIV-1 integrase inhibitors: the 2001 - 2002 update. Curr Pharm Des 2003; 9: 1789-802.
-
(2003)
Curr. Pharm. Des.
, vol.9
, pp. 1789-1802
-
-
Dayam, R.1
Neamati, N.2
-
22
-
-
0034564471
-
HIV-1 integrase inhibitors: Past, present, and future
-
Neamati N, Marchand C, Pommier Y. HIV-1 integrase inhibitors: past, present, and future. Adv Pharmacol 2000; 49: 147-65.
-
(2000)
Adv. Pharmacol.
, vol.49
, pp. 147-165
-
-
Neamati, N.1
Marchand, C.2
Pommier, Y.3
-
23
-
-
10644265691
-
-
Coffin JM, Hughes. SH, Varmus HE Eds, Cold Spring Harbor Laboratory Press
-
Vogt VM. In: Coffin JM, Hughes. SH, Varmus HE Eds, Retroviruses. Cold Spring Harbor Laboratory Press. 1977; 27-69.
-
(1977)
Retroviruses
, pp. 27-69
-
-
Vogt, V.M.1
-
24
-
-
10644261011
-
-
Coffin JM, Hughes SH, Varmus HE Eds, Cold Spring Harbor Laboratory Press
-
Robinson AB, Graves BJ. In: Coffin JM, Hughes SH, Varmus HE Eds, Retroviruses. Cold Spring Harbor Laboratory Press. 1977; 205-261.
-
(1977)
Retroviruses
, pp. 205-261
-
-
Robinson, A.B.1
Graves, B.J.2
-
25
-
-
0031893416
-
Inhibition of acute-, latent-, and chronic-phase human immunodeficiency virus type 1 (HIV-1) replication by a bistriazoloacridone analog that selectively inhibits HIV-1 transcription
-
Turpin JA, Buckheit RW Jr, Derse D, Hollingshead M, Williamson K, Palamone C, et al. Inhibition of acute-, latent-, and chronic-phase human immunodeficiency virus type 1 (HIV-1) replication by a bistriazoloacridone analog that selectively inhibits HIV-1 transcription. Antimicrob Agents Chemother 1998; 42: 487-94.
-
(1998)
Antimicrob. Agents. Chemother.
, vol.42
, pp. 487-494
-
-
Turpin, J.A.1
Buckheit Jr., R.W.2
Derse, D.3
Hollingshead, M.4
Williamson, K.5
Palamone, C.6
-
26
-
-
0031866266
-
Inhibition of human immunodeficiency virus type 1 replication and cytokine production by fluoroquinoline derivatives
-
Baba M, Okamoto M, Kawamura M, Makino M, Higashida T, Takashi T, et al. Inhibition of human immunodeficiency virus type 1 replication and cytokine production by fluoroquinoline derivatives. Mol Pharmacol 1998; 53: 1097-103.
-
(1998)
Mol. Pharmacol.
, vol.53
, pp. 1097-1103
-
-
Baba, M.1
Okamoto, M.2
Kawamura, M.3
Makino, M.4
Higashida, T.5
Takashi, T.6
-
27
-
-
0001118596
-
-
Coffin JM, Hughes SH, Varmus HE Eds, Cold Spring Harbor Laboratory Press
-
Swanstrom R, Wills JW. In: Coffin JM, Hughes SH, Varmus HE Eds, Retroviruses. Cold Spring Harbor Laboratory Press. 1977; 263-334.
-
(1977)
Retroviruses
, pp. 263-334
-
-
Swanstrom, R.1
Wills, J.W.2
-
28
-
-
0033863969
-
Human immunodeficiency virus type 1 Vif protein is an integral component of an mRNP complex of viral RNA and could be involved in the viral RNA folding and packaging process
-
Zhang H, Pomerantz RJ, Dornadula G, Sun Y. Human immunodeficiency virus type 1 Vif protein is an integral component of an mRNP complex of viral RNA and could be involved in the viral RNA folding and packaging process. J Virol 2000; 74: 8252-61.
-
(2000)
J. Virol.
, vol.74
, pp. 8252-8261
-
-
Zhang, H.1
Pomerantz, R.J.2
Dornadula, G.3
Sun, Y.4
-
29
-
-
0038004471
-
The cytidine deaminase CEM15 induces hypermutation in newly synthesized HIV-1 DNA
-
Zhang H, Yang B, Pomerantz RJ, Zhang C, Arunachalam SC, Gao L. The cytidine deaminase CEM15 induces hypermutation in newly synthesized HIV-1 DNA. Nature 2003; 424: 94-8.
-
(2003)
Nature
, vol.424
, pp. 94-98
-
-
Zhang, H.1
Yang, B.2
Pomerantz, R.J.3
Zhang, C.4
Arunachalam, S.C.5
Gao, L.6
-
30
-
-
0242578406
-
Induction of APOBEC3G ubiquitination and degradation by an HIV-1 Vif-Cul5-SCF complex
-
Yu X, Yu Y, Liu B, Luo K, Kong W, Mao P, et al. Induction of APOBEC3G ubiquitination and degradation by an HIV-1 Vif-Cul5-SCF complex. Science 2003; 302: 1056-60.
-
(2003)
Science
, vol.302
, pp. 1056-1060
-
-
Yu, X.1
Yu, Y.2
Liu, B.3
Luo, K.4
Kong, W.5
Mao, P.6
-
31
-
-
0041589542
-
Death by deamination: A novel host restriction system for HIV-1
-
Goff SP. Death by deamination: a novel host restriction system for HIV-1. Cell 2003; 114: 281-3.
-
(2003)
Cell
, vol.114
, pp. 281-283
-
-
Goff, S.P.1
-
32
-
-
0026579208
-
The HIV-1 protease as a therapeutic target for AIDS
-
Debouck C. The HIV-1 protease as a therapeutic target for AIDS. AIDS Res Hum Retroviruses 1992; 8:153-64.
-
(1992)
AIDS Res. Hum. Retroviruses
, vol.8
, pp. 153-164
-
-
Debouck, C.1
-
33
-
-
0023189868
-
A structural model for the retroviral proteases
-
Pearl LH, Taylor WR. A structural model for the retroviral proteases. Nature 1987; 329: 351-4.
-
(1987)
Nature
, vol.329
, pp. 351-354
-
-
Pearl, L.H.1
Taylor, W.R.2
-
34
-
-
0022546859
-
HTLV-III gag protein is processed in yeast cells by the virus pol-protease
-
Kramer RA, Schaber MD, Skalka AM, Ganguly K, Wong-Staal F. Reddy EP. HTLV-III gag protein is processed in yeast cells by the virus pol-protease. Science 1986; 231: 15804.
-
(1986)
Science
, vol.231
, pp. 1580-1584
-
-
Kramer, R.A.1
Schaber, M.D.2
Skalka, A.M.3
Ganguly, K.4
Wong-Staal, F.5
Reddy, E.P.6
-
35
-
-
0023992802
-
An 11-kDa form of human immunodeficiency virus protease expressed in Escherichia coli is sufficient for enzymatic activity
-
Graves MC, Lim JJ, Heimer EP, Kramer RA. An 11-kDa form of human immunodeficiency virus protease expressed in Escherichia coli is sufficient for enzymatic activity. Proc Natl Acad Sci USA 1988; 85: 2449-53.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 2449-2453
-
-
Graves, M.C.1
Lim, J.J.2
Heimer, E.P.3
Kramer, R.A.4
-
36
-
-
0024063076
-
Active site mutagenesis of the AIDS virus protease and its alleviation by trans complementation
-
Le Grice SF, Mills J, Mous J. Active site mutagenesis of the AIDS virus protease and its alleviation by trans complementation. EMBO J 1988; 7: 2547-53.
-
(1988)
EMBO J.
, vol.7
, pp. 2547-2553
-
-
Le Grice, S.F.1
Mills, J.2
Mous, J.3
-
37
-
-
0005241362
-
Active human immunodeficiency virus protease is required for viral infectivity
-
Kohl NE, Emini EA, Schleif WA, Davis LJ, Heimbach JC, Dixon RA, et al. Active human immunodeficiency virus protease is required for viral infectivity. Proc Natl Acad Sci USA 1988; 85: 4686-90.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 4686-4690
-
-
Kohl, N.E.1
Emini, E.A.2
Schleif, W.A.3
Davis, L.J.4
Heimbach, J.C.5
Dixon, R.A.6
-
38
-
-
0345687956
-
Colinearity of reverse transcriptase inhibitor resistance mutations detected by population-based sequencing
-
Gonzales MJ, Johnson E, Dupnik KM, Imamichi T, Shafer RW. Colinearity of reverse transcriptase inhibitor resistance mutations detected by population-based sequencing. J Acquir Immune Defic Syndr 2003; 34: 398-402.
-
(2003)
J. Acquir. Immune Defic. Syndr.
, vol.34
, pp. 398-402
-
-
Gonzales, M.J.1
Johnson, E.2
Dupnik, K.M.3
Imamichi, T.4
Shafer, R.W.5
-
39
-
-
0026693137
-
Crystal structure at 3.5 A resolution of HIV-1 reverse transcriptase complexed with an inhibitor
-
Kohlstaedt LA, Wang J, Friedman JM, Rice PA, Steitz TA. Crystal structure at 3.5 A resolution of HIV-1 reverse transcriptase complexed with an inhibitor, Science 1992; 256: 1783-90.
-
(1992)
Science
, vol.256
, pp. 1783-1790
-
-
Kohlstaedt, L.A.1
Wang, J.2
Friedman, J.M.3
Rice, P.A.4
Steitz, T.A.5
-
40
-
-
0026572005
-
Structure of HIV-1 reverse transcriptase/DNA complex at 7 A resolution showing active site locations
-
Arnold E, Jacobo-Molina A, Nanni RG, Williams RE, Lu X, Ding J, et al. Structure of HIV-1 reverse transcriptase/DNA complex at 7 A resolution showing active site locations. Nature 1992; 357: 85-9.
-
(1992)
Nature
, vol.357
, pp. 85-89
-
-
Arnold, E.1
Jacobo-Molina, A.2
Nanni, R.G.3
Williams, R.E.4
Lu, X.5
Ding, J.6
-
41
-
-
0027318776
-
Crystal structure of human immunodeficiency virus type 1 reverse transcriptase complexed with double-stranded DNA at 3.0 A resolution shows bent DNA
-
Jacobo-Molina A, Ding J, Nanni RG, Lark AD, Lu X, Tantillo C, et al. Crystal structure of human immunodeficiency virus type 1 reverse transcriptase complexed with double-stranded DNA at 3.0 A resolution shows bent DNA. Porc Natl Acad Sci USA 1993, 90: 6320-4.
-
(1993)
Porc. Natl. Acad. Sci. USA
, vol.90
, pp. 6320-6324
-
-
Jacobo-Molina, A.1
Ding, J.2
Nanni, R.G.3
Lark, A.D.4
Lu, X.5
Tantillo, C.6
-
42
-
-
0001587762
-
Inhibition of the in vitro infectivity and cytopathic effect of human T-lymphotrophic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV) by 2′, 3′-dideoxynucleosides
-
Mitsuya H, Broder S. Inhibition of the in vitro infectivity and cytopathic effect of human T-lymphotrophic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV) by 2′, 3′-dideoxynucleosides. Proc Natl Acad Sci USA 1986; 83: 1911-5.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 1911-1915
-
-
Mitsuya, H.1
Broder, S.2
-
43
-
-
0023091963
-
Strategies for antiviral therapy in AIDS
-
Mitsuya H, Broder S. Strategies for antiviral therapy in AIDS. Nature 1987; 325: 773-8.
-
(1987)
Nature
, vol.325
, pp. 773-778
-
-
Mitsuya, H.1
Broder, S.2
-
44
-
-
0022996630
-
Phosphorylation of 3′-azido-3-deoxythymidine and Selective Interaction of the 5′-triphosphate with Human Immunodeficiency Virus Reverse Transcriptase
-
Furman PA, Fyfe JA, St Clair MH, Weinhold K, Rideout JL, Freeman GA, et al. Phosphorylation of 3′ -azido-3-deoxythymidine and Selective Interaction of the 5′ -triphosphate with Human Immunodeficiency Virus Reverse Transcriptase. Proc Natl Acad Sci USA 1986; 83: 8333-7.
-
(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
-
45
-
-
0023951483
-
Regulation of human thymidine kinase during the cell cycle
-
Sherley JL, Thomas JK. Regulation of human thymidine kinase during the cell cycle. J Biol Chem 1988; 263: 8350-8.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 8350-8358
-
-
Sherley, J.L.1
Thomas, J.K.2
-
46
-
-
0037229062
-
Actinomycin D induces high-level resistance to thymidine analogs in replication ofhuman immunodeficiency virus type 1 by interfering with host cell thymidine kinase expression
-
Imamichi T, Murphy MA, Adelsbergers JW, Yang J, Watkins CM, Berg SC, et al. Actinomycin D induces high-level resistance to thymidine analogs in replication ofhuman immunodeficiency virus type 1 by interfering with host cell thymidine kinase expression. J Virol 2003; 77: 1011-20.
-
(2003)
J. Virol.
, vol.77
, pp. 1011-1020
-
-
Imamichi, T.1
Murphy, M.A.2
Adelsbergers, J.W.3
Yang, J.4
Watkins, C.M.5
Berg, S.C.6
-
47
-
-
0027534661
-
Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phosphonates: Potent and selective in vitro and in vivo antiretrovirus activities of(R)-9-(2-phosphonomethoxypropyl)-2, 6-diaminopurine
-
Balzarini J, Holy A, Jindrich J, Naesens L, Snoeck R, Schols D, et al. Differential antiherpesvirus and antiretrovirus effects of the (S) and (R) enantiomers of acyclic nucleoside phosphonates: potent and selective in vitro and in vivo antiretrovirus activities of(R)-9-(2-phosphonomethoxypropyl)-2, 6-diaminopurine. Antimicrob Agents Chemother 1993; 37: 332-8.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 332-338
-
-
Balzarini, J.1
Holy, A.2
Jindrich, J.3
Naesens, L.4
Snoeck, R.5
Schols, D.6
-
48
-
-
0031430945
-
Metabolism and pharmacokinetics of novel oral prodrugs of 9-[(R)-2-(phosphonomethoxy)propyl]adenine (PMPA) in dogs
-
Shaw JP, Sueoko CM, Oliyai R, Lee WA, Arimilli MN, Kim CU, et al. Metabolism and pharmacokinetics of novel oral prodrugs of 9-[(R)-2-(phosphonomethoxy)propyl]adenine (PMPA) in dogs. Pharm Res 1997; 14: 1824-9.
-
(1997)
Pharm. Res.
, vol.14
, pp. 1824-1829
-
-
Shaw, J.P.1
Sueoko, C.M.2
Oliyai, R.3
Lee, W.A.4
Arimilli, M.N.5
Kim, C.U.6
-
49
-
-
0031916651
-
Anti-human immunodeficiency virus activity and cellular metabolism of a potential prodrug of the acyclic nucleoside phosphonate 9-R-(2-phosphonomethoxypropyl)adenine (PMPA), Bis(isopropyloxymethylcarbonyl)PMPA Antimicrob
-
Robbins BL, Srinivas RV, Kim C, Bischofberger N, Fridland A. Anti-human immunodeficiency virus activity and cellular metabolism of a potential prodrug of the acyclic nucleoside phosphonate 9-R-(2-phosphonomethoxypropyl)adenine (PMPA), Bis(isopropyloxymethylcarbonyl)PMPA. Antimicrob Agents Chemother 1998; 42: 612-7.
-
(1998)
Agents Chemother.
, vol.42
, pp. 612-617
-
-
Robbins, B.L.1
Srinivas, R.V.2
Kim, C.3
Bischofberger, N.4
Fridland, A.5
-
50
-
-
0027980948
-
Equal inhibition of the replication of human immunodeficiency virus in human T-cell culture by ddA bis(SATE)phosphotriester and 3′-azido-2′, 3′-dideoxythymidine
-
Perigaud C, Aubertin AM, Benzaria S, Pelicano H, Girardet JL, Maury G, et al. Equal inhibition of the replication of human immunodeficiency virus in human T-cell culture by ddA bis(SATE)phosphotriester and 3′-azido-2′, 3′ -dideoxythymidine. Biochem Pharmacol 1994; 48: 11-14.
-
(1994)
Biochem. Pharmacol.
, vol.48
, pp. 11-14
-
-
Perigaud, C.1
Aubertin, A.M.2
Benzaria, S.3
Pelicano, H.4
Girardet, J.L.5
Maury, G.6
-
51
-
-
0029946597
-
Mechanism of anti-HIV action of masked alaninyl d4T-MP derivatives
-
Balzarini J, Karlsson A, Aquaro S, Perno CF, Cahard D, Naesens L, et al. Mechanism of anti-HIV action of masked alaninyl d4T-MP derivatives. Proc Natl Acad Sci USA 1996; 93: 7295.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 7295
-
-
Balzarini, J.1
Karlsson, A.2
Aquaro, S.3
Perno, C.F.4
Cahard, D.5
Naesens, L.6
-
52
-
-
0030903443
-
Unique intracellular activation of the potent anti-human immunodeficiency virus agent _1592U89
-
Faletto MB, Miller WH, Garvey EP, St Clair MH, Daluge SM, Good SS. Unique intracellular activation of the potent anti-human immunodeficiency virus agent _1592U89. Antimicrob Agents Chemother 1997; 41: 1099-107.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1099-1107
-
-
Faletto, M.B.1
Miller, W.H.2
Garvey, E.P.3
St Clair, M.H.4
Daluge, S.M.5
Good, S.S.6
-
53
-
-
0023791782
-
Potent and selective activity of a new carbocyclic nucleoside analog (carbovir: NSC 614846) against human immunodeficiency virus in vitro
-
Vince R, Hua M, Brownell J, Daluge S, Lee F, Shannon WM, et al. Potent and selective activity of a new carbocyclic nucleoside analog (carbovir: NSC 614846) against human immunodeficiency virus in vitro. Biochem Biophys Res Commun 1988; 156: 1046-53.
-
(1988)
Biochem. Biophys. Res. Commun.
, vol.156
, pp. 1046-1053
-
-
Vince, R.1
Hua, M.2
Brownell, J.3
Daluge, S.4
Lee, F.5
Shannon, W.M.6
-
54
-
-
0026634744
-
A novel human phosphotransferase highly specific for adenosine
-
Garvey EP, Krenitsky TA. A novel human phosphotransferase highly specific for adenosine. Arch Biochem Biophys 1992; 296: 161-9.
-
(1992)
Arch. Biochem. Biophys.
, vol.296
, pp. 161-169
-
-
Garvey, E.P.1
Krenitsky, T.A.2
-
55
-
-
0026480950
-
Selective inhibition of human immunodeficiency viruses by racemates and enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1, 3-oxathiolan-5-yl[cytosine
-
Schinazi RF, McMillan A, Cannon D, Mathis R, Lloyd RM, Peck A, et al. Selective inhibition of human immunodeficiency viruses by racemates and enantiomers of cis-5-fluoro-1-[2-(hydroxymethyl)-1, 3-oxathiolan-5-yl[cytosine. Antimicrob Agents Chemother 1992; 36: 2423-31.
-
(1992)
Antimicrob. Agents Chemother.
, vol.36
, pp. 2423-2431
-
-
Schinazi, R.F.1
McMillan, A.2
Cannon, D.3
Mathis, R.4
Lloyd, R.M.5
Peck, A.6
-
56
-
-
0032829089
-
Mechanistic studies show that (-)-FTC-TP is a better inhibitor of HIV-1 reverse transcriptase than 3TC-TP
-
Feng JY, Shi J, Schinazi RF, Anderson KS. Mechanistic studies show that (-)-FTC-TP is a better inhibitor of HIV-1 reverse transcriptase than 3TC-TP. FASEB J 1999; 13: 1511-7.
-
(1999)
FASEB J.
, vol.13
, pp. 1511-1517
-
-
Feng, J.Y.1
Shi, J.2
Schinazi, R.F.3
Anderson, K.S.4
-
57
-
-
0031430945
-
Metabolism and pharmacokinetics of novel oral prodrugs of 9-[(R)-2-(phosphonomethoxy)propyl]adenine (PMPA) in dogs
-
Shaw JP, Sueoko CM, Oliyai R, Lee WA, Arimilli MN, Kim CU, et al. Metabolism and pharmacokinetics of novel oral prodrugs of 9-[(R)-2-(phosphonomethoxy)propyl]adenine (PMPA) in dogs. Pharm Res 1997; 14: 1824-9.
-
(1997)
Pharm. Res.
, vol.14
, pp. 1824-1829
-
-
Shaw, J.P.1
Sueoko, C.M.2
Oliyai, R.3
Lee, W.A.4
Arimilli, M.N.5
Kim, C.U.6
-
58
-
-
0032573488
-
Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: Implications for drug resistance
-
Huang H, Chopra R, Verdine GL, Harrison S. Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: implications for drug resistance. Science 1998; 282: 1669-75.
-
(1998)
Science
, vol.282
, pp. 1669-1675
-
-
Huang, H.1
Chopra, R.2
Verdine, G.L.3
Harrison, S.4
-
59
-
-
0001113422
-
Mutations in retroviral genes associated with drug resistance; 1999-2000
-
Schinazi RF, Larder BA, Mellors JW. Mutations in retroviral genes associated with drug resistance; 1999-2000. Int Antiviral News 2000; 7: 46-69.
-
(2000)
Int. Antiviral News
, vol.7
, pp. 46-69
-
-
Schinazi, R.F.1
Larder, B.A.2
Mellors, J.W.3
-
60
-
-
0028057581
-
Identification of a mutation at codon 65 in the IKKK motif of reverse transcriptase that encodes human immunodeficiency virus resistance to 2′, 3′-dideoxycytidine and 2′, 3′-dideoxy-3′-thiacytidine
-
Gu Z, Gao Q, Fang H, Salomon H, Parniak MA, Goldberg E, et al. Identification of a mutation at codon 65 in the IKKK motif of reverse transcriptase that encodes human immunodeficiency virus resistance to 2′, 3′-dideoxycytidine and 2′, 3′-dideoxy-3′-thiacytidine. Antimicrob Agents Chemother 1994; 38: 275-81.
-
(1994)
Antimicrob. Agents Chemother.
, vol.38
, pp. 275-281
-
-
Gu, Z.1
Gao, Q.2
Fang, H.3
Salomon, H.4
Parniak, M.A.5
Goldberg, E.6
-
61
-
-
0028031833
-
Resistance to 2′, 3′-dideoxycytidine conferred by a mutation in codon 65 of the human immunodeficiency virus type 1 reverse transcriptase
-
Zhang D, Caliendo AM, Eron JJ, DeVore KM, Kaplan JC, Hirsch MS, et al. Resistance to 2′, 3′-dideoxycytidine conferred by a mutation in codon 65 of the human immunodeficiency virus type 1 reverse transcriptase. Antimicrob Agents Chemother 1994; 38: 282-7.
-
(1994)
Antimicrob. Agents Chemother.
, vol.38
, pp. 282-287
-
-
Zhang, D.1
Caliendo, A.M.2
Eron, J.J.3
DeVore, K.M.4
Kaplan, J.C.5
Hirsch, M.S.6
-
62
-
-
0030945276
-
Combination of mutations in human immunodeficiency virus type 1 reverse trariscriptase required for resistance to the carbocyclic nucleoside 1592U89
-
Tisdale M, Alnadaf T, Cousens D. Combination of mutations in human immunodeficiency virus type 1 reverse trariscriptase required for resistance to the carbocyclic nucleoside 1592U89. Antimicrob Agents Chemother 1997; 41: 1094-8.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1094-1098
-
-
Tisdale, M.1
Alnadaf, T.2
Cousens, D.3
-
63
-
-
20644436472
-
In vitro selection and characterization of HIV-1 with reduced susceptibility to PMPA
-
Wainberg MA, Miller MD, Quan Y, Salomon H, Mulato AS, Lamy PD, et al. In vitro selection and characterization of HIV-1 with reduced susceptibility to PMPA. Antivir Ther 1999; 4: 87-94.
-
(1999)
Antivir. Ther.
, vol.4
, pp. 87-94
-
-
Wainberg, M.A.1
Miller, M.D.2
Quan, Y.3
Salomon, H.4
Mulato, A.S.5
Lamy, P.D.6
-
64
-
-
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, Kemp SD, Parry NR, Larder BA. 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 1993; 90: 5653-6.
-
(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
-
65
-
-
0027409698
-
Characterization of human immunodeficiency viruses resistant to oxathiolane-cytosine nucleosides
-
Schinazi RF, Lloyd RM Jr, Nguyen MH, Cannon DL, McMillan A, Ilksoy N, Chu CK, et al. Characterization of human immunodeficiency viruses resistant to oxathiolane-cytosine nucleosides. Antimicrob Agents Chemother 1993; 37: 875-81.
-
(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
-
66
-
-
0027155374
-
The same mutation that encodes low-level human immunodeficiency virus type 1 resistance to 2′, 3′ -dideoxymosine and 2′, 3′-dideoxycytidine confers high-level resistance to the (-) enantiomer of 2′, 3′-dideoxy-3′ -thiacytidine
-
Gao Q, Gu Z, Parniak MA, Cameron J, Cammack N, Boucher C, et al. The same mutation that encodes low-level human immunodeficiency virus type 1 resistance to 2′, 3′ -dideoxymosine and 2′, 3′-dideoxycytidine confers high-level resistance to the (-) enantiomer of 2′, 3′-dideoxy-3′ -thiacytidine. Antimicrob Agents Chemother 1993; 37: 1390-2.
-
(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
-
67
-
-
0029843986
-
Significance of amino acid variation at human immunodeficiency virus type 1 reverse transcriptase residue 210 for zidovudine susceptibility
-
Harrigan PR, Kinghorn I, Bloor S. Kemp SD, Najera I, Kolili A, et al. Significance of amino acid variation at human immunodeficiency virus type 1 reverse transcriptase residue 210 for zidovudine susceptibility. J Virol 1996; 70: 5930-4.
-
(1996)
J. Virol.
, vol.70
, pp. 5930-5934
-
-
Harrigan, P.R.1
Kinghorn, I.2
Bloor, S.3
Kemp, S.D.4
Najera, I.5
Kolili, A.6
-
68
-
-
10244227943
-
An in vivo mutation from leucine to tryptophan at position 210 in human immunodeficiency virus type 1 reverse transcriptase contributes to high-level resistance to 3′-azido-3′ -deoxythymidine
-
Hooker DJ, Tachedjian G, Solomon AE, Gurusinghe AD, Land S, Birch C, et al. An in vivo mutation from leucine to tryptophan at position 210 in human immunodeficiency virus type 1 reverse transcriptase contributes to high-level resistance to 3′-azido-3′-deoxythymidine. J Virol 1996; 70: 8010-8.
-
(1996)
J. Virol.
, vol.70
, pp. 8010-8018
-
-
Hooker, D.J.1
Tachedjian, G.2
Solomon, A.E.3
Gurusinghe, A.D.4
Land, S.5
Birch, C.6
-
69
-
-
0026565278
-
Fifth mutation in human immunodeficiency virus type 1 reverse transcriptase contributes to the development of high-level resistance to zidovudine
-
Kellam P, Boucher CA, Larder BA. Fifth mutation in human immunodeficiency virus type 1 reverse transcriptase contributes to the development of high-level resistance to zidovudine. Proc Natl Acad Sci USA 1992; 89: 1934-8.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 1934-1938
-
-
Kellam, P.1
Boucher, C.A.2
Larder, B.A.3
-
70
-
-
0024310253
-
Multiple mutations in HIV-1 reverse transcriptase confer high-level resistance to zidovudine (AZT)
-
Larder BA, Kemp SD. Multiple mutations in HIV-1 reverse transcriptase confer high-level resistance to zidovudine (AZT). Science 1989; 246: 1155-8.
-
(1989)
Science
, vol.246
, pp. 1155-1158
-
-
Larder, B.A.1
Kemp, S.D.2
-
71
-
-
0025138304
-
Susceptibilities of zidovudine-susceptible and -resistant human immunodeficiency virus isolates to antiviral agents determined by using a quantitative plaque reduction assay
-
Larder BA, Chesebro B, Richman DD. Susceptibilities of zidovudine-susceptible and -resistant human immunodeficiency virus isolates to antiviral agents determined by using a quantitative plaque reduction assay. Antimicrob Agents Chemother 1990; 34: 436-41.
-
(1990)
Antimicrob. Agents Chemother.
, vol.34
, pp. 436-441
-
-
Larder, B.A.1
Chesebro, B.2
Richman, D.D.3
-
72
-
-
0027988547
-
Genotypic and phenotypic analysis of human immunodeficiency virus type 1 isolates from patients on prolonged stavudine therapy
-
Lin PF, Samanta H, Rose RE, Patick AK, Trimble J, Bechtold CM, et al. Genotypic and phenotypic analysis of human immunodeficiency virus type 1 isolates from patients on prolonged stavudine therapy. J Infect Dis 1994; 170: 1157-64.
-
(1994)
J. Infect. Dis.
, vol.170
, pp. 1157-1164
-
-
Lin, P.F.1
Samanta, H.2
Rose, R.E.3
Patick, A.K.4
Trimble, J.5
Bechtold, C.M.6
-
73
-
-
0028332029
-
Novel mutation (V75T) in human immunodeficiency virus type 1 reverse transcriptase confers resistance to 2′, 3′ -didehydro-2′, 3′-dideoxythymidine in cell culture. Antimicrob
-
Lacey SF, Larder BA. Novel mutation (V75T) in human immunodeficiency virus type 1 reverse transcriptase confers resistance to 2′, 3′-didehydro-2′, 3′-dideoxythymidine in cell culture. Antimicrob. Agents Chemother 1994; 38: 1428-32.
-
(1994)
Agents Chemother.
, vol.38
, pp. 1428-1432
-
-
Lacey, S.F.1
Larder, B.A.2
-
74
-
-
0032898472
-
Stavudine resistance: An update on susceptibility following prolonged therapy
-
Lin PF, Gonzalez CJ, Griffith B, Friedland Gs, Calvez V, Ferchal F, et al. Stavudine resistance: an update on susceptibility following prolonged therapy. Antivir Ther 1999; 4: 21-8.
-
(1999)
Antivir. Ther.
, vol.4
, pp. 21-28
-
-
Lin, P.F.1
Gonzalez, C.J.2
Griffith, B.3
Friedland, Gs.4
Calvez, V.5
Ferchal, F.6
-
75
-
-
0033165851
-
A mechanism of AZT resistance: An increase in nucleotide-dependent primer unblocking by mutant HIV-1 reverse transcriptase
-
Meyer PR, Matsuura SE, Mian AM, Scott WA. A mechanism of AZT resistance: an increase in nucleotide-dependent primer unblocking by mutant HIV-1 reverse transcriptase. Mol Cell 1999; 4: 35-43.
-
(1999)
Mol. Cell
, vol.4
, pp. 35-43
-
-
Meyer, P.R.1
Matsuura, S.E.2
Mian, A.M.3
Scott, W.A.4
-
76
-
-
0032506055
-
Phenotypic mechanism of HIV-1 resistance to 3′-azido-3′-deoxythymidine (AZT): Increased polymerization processivity and enhanced sensitivity to pyrophospliate of the mutant viral reverse transcriptase
-
Arion D, Kaushik N, McCormick S, Borkow G, Parniak MA. Phenotypic mechanism of HIV-1 resistance to 3′-azido-3′-deoxythymidine (AZT): increased polymerization processivity and enhanced sensitivity to pyrophospliate of the mutant viral reverse transcriptase. Biochemistry 1998; 37: 15908-17.
-
(1998)
Biochemistry
, vol.37
, pp. 15908-15917
-
-
Arion, D.1
Kaushik, N.2
McCormick, S.3
Borkow, G.4
Parniak, M.A.5
-
77
-
-
0032506228
-
Unblocking of chain-terminated primer by HIV-1 reverse transcriptase through a nucleotide-dependent mechanism
-
Meyer PR, Matsuura SE, So AG, Scott WA. Unblocking of chain-terminated primer by HIV-1 reverse transcriptase through a nucleotide-dependent mechanism. Proc Natl Acad Sci USA 1998: 95: 13471-6.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13471-13476
-
-
Meyer, P.R.1
Matsuura, S.E.2
So, A.G.3
Scott, W.A.4
-
78
-
-
0034425841
-
Differential removal of thymidine nucleofide analogues from blocked DNA chains by human immunodeficiency virus reverse transcriptase in the presence of physiological concentrations of 2′ -deoxynucleoside triphosphates
-
Meyer PR, Matsuura SE, Schinazi RE, So AG, Scott WA. Differential removal of thymidine nucleofide analogues from blocked DNA chains by human immunodeficiency virus reverse transcriptase in the presence of physiological concentrations of 2′-deoxynucleoside triphosphates. Antimicrob. Agents Chemother 2000; 44: 3465-72.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, pp. 3465-3472
-
-
Meyer, P.R.1
Matsuura, S.E.2
Schinazi, R.E.3
So, A.G.4
Scott, W.A.5
-
79
-
-
0035984790
-
ATP-dependent removal of nucleoside reverse transcriptase inhibitors by human immunodeficiency virus type 1 reverse transcriptase
-
Naeger LK, Margot NA, Miller MD. ATP-dependent removal of nucleoside reverse transcriptase inhibitors by human immunodeficiency virus type 1 reverse transcriptase. Antimicrob. Agents Chemother 2002; 46: 2179-84.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 2179-2184
-
-
Naeger, L.K.1
Margot, N.A.2
Miller, M.D.3
-
80
-
-
0034963036
-
Biochemical mechanism of human immunodeficiency virus type 1 reverse transcriptase resistance to stavudine
-
Lennerstrand J, Stammers DK, Larder BA. Biochemical mechanism of human immunodeficiency virus type 1 reverse transcriptase resistance to stavudine. Antimicrob Agents Chemother 2001; 45: 2144-6.
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, pp. 2144-2146
-
-
Lennerstrand, J.1
Stammers, D.K.2
Larder, B.A.3
-
81
-
-
0033621167
-
Lamivudine 3TC resistance in HIV-1 reverse transcriptase involves steric hindrance with beta-branched amino acids
-
Sarafianos SG, Das K, Clark AD Jr, Ding J, Boyer PL, Hughes SH, et al. Lamivudine 3TC resistance in HIV-1 reverse transcriptase involves steric hindrance with beta-branched amino acids. Proc Natl Acad Sci USA 1999; 96: 10027-32.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 10027-10032
-
-
Sarafianos, S.G.1
Das, K.2
Clark Jr., A.D.3
Ding, J.4
Boyer, P.L.5
Hughes, S.H.6
-
82
-
-
0036888501
-
Interactions of enantiomers of 2′, 3′-didehydro-2′, 3′-dideoxy-fluorocytidine with wild type and M184V mutant HIV-1 reverse transcriptase
-
Ray AS, Murakami E. Peterson CN, Shi J, Schinazi RE, Anderson KS. Interactions of enantiomers of 2′, 3′-didehydro-2′, 3′-dideoxy-fluorocytidine with wild type and M184V mutant HIV-1 reverse transcriptase. Antiviral Res 2002; 56: 189-205.
-
(2002)
Antiviral Res.
, vol.56
, pp. 189-205
-
-
Ray, A.S.1
Murakami, E.2
Peterson, C.N.3
Shi, J.4
Schinazi, R.E.5
Anderson, K.S.6
-
83
-
-
0033587620
-
Mechanistic studies examining the efficiency and fidelity of DNA synthesis by the 3TC-resistant mutant (184V) of HIV-1 reverse transcriptase
-
Feng JY, Anderson KS. Mechanistic studies examining the efficiency and fidelity of DNA synthesis by the 3TC-resistant mutant (184V) of HIV-1 reverse transcriptase. Biochemistry 1999; 38: 9440-8.
-
(1999)
Biochemistry
, vol.38
, pp. 9440-9448
-
-
Feng, J.Y.1
Anderson, K.S.2
-
84
-
-
0142100752
-
The M184V mutation in the reverse transcriptase of human immunodeficiency virus type 1 impairs rescue ofchain-terminated DNA synthesis
-
Gotte M, Arion D, Parniak MA, Wainberg MA. The M184V mutation in the reverse transcriptase of human immunodeficiency virus type 1 impairs rescue ofchain-terminated DNA synthesis. J Virol 2000; 74: 3579-85.
-
(2000)
J. Virol.
, vol.74
, pp. 3579-3585
-
-
Gotte, M.1
Arion, D.2
Parniak, M.A.3
Wainberg, M.A.4
-
85
-
-
0034616958
-
The role of steric hindrance in 3TC resistance of human immunodeficiency virus type-1 reverse transcriptase
-
Gao HQ, Boyer PL, Sarafianos SG, Arnold E, Hughes SH. The role of steric hindrance in 3TC resistance of human immunodeficiency virus type-1 reverse transcriptase. J Mol Biol 2000; 300: 403-18.
-
(2000)
J. Mol. Biol.
, vol.300
, pp. 403-418
-
-
Gao, H.Q.1
Boyer, P.L.2
Sarafianos, S.G.3
Arnold, E.4
Hughes, S.H.5
-
86
-
-
0242317289
-
Studies of molecular mechanism of tenofovir against 3TC- and AZT-resistance mutant HIV-1 reverse transcriptase
-
Chong Y, Akula N, Chu CK. Studies of molecular mechanism of tenofovir against 3TC- and AZT-resistance mutant HIV-1 reverse transcriptase. Bioorg Med Chem Lett 2003; 13: 4019-22.
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 4019-4022
-
-
Chong, Y.1
Akula, N.2
Chu, C.K.3
-
87
-
-
0037175023
-
Mechanistic studies to understand the progressive development of resistance in human immunodeficiency virus type 1 reverse transcriptase to abacavir
-
Ray AS, Basavapathruni A, Anderson KS. Mechanistic studies to understand the progressive development of resistance in human immunodeficiency virus type 1 reverse transcriptase to abacavir. J Biol Chem 2002; 277: 40479-90.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 40479-40490
-
-
Ray, A.S.1
Basavapathruni, A.2
Anderson, K.S.3
-
88
-
-
0028940084
-
Emergence of human immunodeficiency virus type 1 variants with resistance to multiple dideoxynucleosides in patients receiving therapy with dideoxyiiucleosides
-
Shirasaka T, Kavlick MF, Ueno T, Gan WY, Kojima E, Alcaide ML, et al. Emergence of human immunodeficiency virus type 1 variants with resistance to multiple dideoxynucleosides in patients receiving therapy with dideoxyiiucleosides. Proc Natl Acad Sci USA 1995; 92: 2398-402.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 2398-2402
-
-
Shirasaka, T.1
Kavlick, M.F.2
Ueno, T.3
Gan, W.Y.4
Kojima, E.5
Alcaide, M.L.6
-
89
-
-
0031948662
-
Altered drug sensitivity, fitness, and evolution of human immunodeficiency virus type 1 with pol gene mutations conferring multi-dideoxynucleoside resistance
-
Maeda Y, Venzon DJ, Mitsuya H. Altered drug sensitivity, fitness, and evolution of human immunodeficiency virus type 1 with pol gene mutations conferring multi-dideoxynucleoside resistance. J Infect Dis 1998; 17: 1207-13.
-
(1998)
J. Infect. Dis.
, vol.17
, pp. 1207-1213
-
-
Maeda, Y.1
Venzon, D.J.2
Mitsuya, H.3
-
90
-
-
0033064963
-
Comparative fitness of multi-dideoxynucleoside-resistant human immunodeficiency virus type 1 (HIV-1) in an In vitro competitive HIV-1 replication assay
-
Kosalaraksa P, Kavlick ME, Maroun V, Le R, Mitsuya H. Comparative fitness of multi-dideoxynucleoside-resistant human immunodeficiency virus type 1 (HIV-1) in an In vitro competitive HIV-1 replication assay. J Virol 1999; 73: 5356-63.
-
(1999)
J. Virol.
, vol.73
, pp. 5356-5363
-
-
Kosalaraksa, P.1
Kavlick, M.E.2
Maroun, V.3
Le, R.4
Mitsuya, H.5
-
91
-
-
0030048748
-
Multidrug-resistant human immunodeficiency virus type 1 strains resulting from combination antiretroviral therapy
-
Iversen AK, Shafer RW, Wehrly K, Winters MA, Mullins JI, Chesebro B, et al. Multidrug-resistant human immunodeficiency virus type 1 strains resulting from combination antiretroviral therapy. J Virol 1996; 70: 1086-90.
-
(1996)
J. Virol.
, vol.70
, pp. 1086-1090
-
-
Iversen, A.K.1
Shafer, R.W.2
Wehrly, K.3
Winters, M.A.4
Mullins, J.I.5
Chesebro, B.6
-
92
-
-
0033819048
-
Evidence of a role for the Q151L mutation and the viral background in development of multiple dideoxynucleoside-resistant human immunodeficiency virus type 1
-
Garcia-Lerma JG, Gerrish PJ, Wright AC, Qari SH, Heneine W. Evidence of a role for the Q151L mutation and the viral background in development of multiple dideoxynucleoside-resistant human immunodeficiency virus type 1. J Virol 2000; 74: 9339-46.
-
(2000)
J. Virol.
, vol.74
, pp. 9339-9346
-
-
Garcia-Lerma, J.G.1
Gerrish, P.J.2
Wright, A.C.3
Qari, S.H.4
Heneine, W.5
-
93
-
-
0036829992
-
The molecular mechanism of multidrug resistance by the Q151M human immunodeficiency virus type 1 reverse transcriptase and its suppression using alpha-boranophosphate nucleotide analogues
-
Deval J, Selmi B, Boretto J, Egloff MP, Guerreiro C, Sarfati S, et al. The molecular mechanism of multidrug resistance by the Q151M human immunodeficiency virus type 1 reverse transcriptase and its suppression using alpha-boranophosphate nucleotide analogues. J Biol Chem 2002; 277: 42097-104.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 42097-42104
-
-
Deval, J.1
Selmi, B.2
Boretto, J.3
Egloff, M.P.4
Guerreiro, C.5
Sarfati, S.6
-
94
-
-
0032533207
-
A 6-basepair insert in the reverse transcriptase gene of human immunodeficiency virus type 1 confers resistance to multiple nucleoside inhibitors
-
Winters MA, Coolley KL, Girard YA, Levee DJ, Hamdan H, Shafer RW, et al. A 6-basepair insert in the reverse transcriptase gene of human immunodeficiency virus type 1 confers resistance to multiple nucleoside inhibitors. J Clin Invest 1998; 102: 1769-75.
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 1769-1775
-
-
Winters, M.A.1
Coolley, K.L.2
Girard, Y.A.3
Levee, D.J.4
Hamdan, H.5
Shafer, R.W.6
-
95
-
-
0033986107
-
High-level resistance to 3′-azido-3′-deoxythimidine due to a deletion in the reverse transcriptase gene of human immunodeficiency virus type 1
-
Imamichi T, Sinha T, Imamichi H, Zhang YM, Metcalf JA, Falloon J, et al. High-level resistance to 3′-azido-3′-deoxythimidine due to a deletion in the reverse transcriptase gene of human immunodeficiency virus type 1. J Virol 2000; 74: 1023-8.
-
(2000)
J. Virol.
, vol.74
, pp. 1023-1028
-
-
Imamichi, T.1
Sinha, T.2
Imamichi, H.3
Zhang, Y.M.4
Metcalf, J.A.5
Falloon, J.6
-
96
-
-
0034469498
-
Relative replication fitness of a high-level 3′-azido-3′-deoxythymidine-resistant variant of human immunodeficiency virus type 1 possessing an amino acid deletion at codon 67 and a novel substitution (Thr-->Gly) at codon 69
-
Imamichi T, Berg SC, Imamichi H, Lopez JC, Metcalf JA, Falloon J, et al. Relative replication fitness of a high-level 3′-azido-3′-deoxythymidine-resistant variant of human immunodeficiency virus type 1 possessing an amino acid deletion at codon 67 and a novel substitution (Thr-->Gly) at codon 69. J Virol 2000; 74: 10958-64.
-
(2000)
J. Virol.
, vol.74
, pp. 10958-10964
-
-
Imamichi, T.1
Berg, S.C.2
Imamichi, H.3
Lopez, J.C.4
Metcalf, J.A.5
Falloon, J.6
-
97
-
-
0035088519
-
Amino acid deletion at codon 67 and Thr-to-Gly change at codon 69 of human immunodeficiency virus type 1 reverse transcriptase confer novel drug resistance profiles
-
Imamichi T, Murphy MA, Imamichi H, Lane HC. Amino acid deletion at codon 67 and Thr-to-Gly change at codon 69 of human immunodeficiency virus type 1 reverse transcriptase confer novel drug resistance profiles. J Virol 2001; 75: 3988-92.
-
(2001)
J. Virol.
, vol.75
, pp. 3988-3992
-
-
Imamichi, T.1
Murphy, M.A.2
Imamichi, H.3
Lane, H.C.4
-
98
-
-
0036720770
-
Nucleoside analog resistance caused by insertions in the fingers of human immunodeficiency virus type 1 reverse transcriplase involves ATP-mediated excision
-
Boyer PL, Sarafianos SG, Arnold E, Hughes SH. Nucleoside analog resistance caused by insertions in the fingers of human immunodeficiency virus type 1 reverse transcriplase involves ATP-mediated excision. J Virol 2002; 76: 9143-51.
-
(2002)
J. Virol.
, vol.76
, pp. 9143-9151
-
-
Boyer, P.L.1
Sarafianos, S.G.2
Arnold, E.3
Hughes, S.H.4
-
99
-
-
0037334586
-
Effects of dipeptide insertions between codons 69 and 70 of human immunodeficiency virus type 1 reverse transcriptase on primer unblocking, deoxynucleoside triphosphate inhibition, and DNA chain elongation
-
Meyer PR, Lennerstrand J, Matsuura SE, Larder BA, Scott WA. Effects of dipeptide insertions between codons 69 and 70 of human immunodeficiency virus type 1 reverse transcriptase on primer unblocking, deoxynucleoside triphosphate inhibition, and DNA chain elongation. J Virol 2003; 77: 3871-7.
-
(2003)
J. Virol.
, vol.77
, pp. 3871-3877
-
-
Meyer, P.R.1
Lennerstrand, J.2
Matsuura, S.E.3
Larder, B.A.4
Scott, W.A.5
-
100
-
-
85088600873
-
Role of a dipeptide insertion between codons 69 and 70 of HIV-1 reverse transcriptase in the mechanism of AZT resistance
-
Mas A, Patera M, Briones C, Soriano V, Martinez MA, Domingo E, et al. Role of a dipeptide insertion between codons 69 and 70 of HIV-1 reverse transcriptase in the mechanism of AZT resistance. EMBO J 2000; 19: 575-61.
-
(2000)
EMBO J.
, vol.19
, pp. 575-661
-
-
Mas, A.1
Patera, M.2
Briones, C.3
Soriano, V.4
Martinez, M.A.5
Domingo, E.6
-
101
-
-
0036406111
-
Multidrug-resistant HIV-1 reverse transcriptase: Involvement of ribonucleotide-dependent phosphorolysis in cross-resistance to nucleoside analogue inhibitors
-
Mas A, Vazquez-Alvarez BM, Domingo E, Menendez-Arias L. Multidrug-resistant HIV-1 reverse transcriptase: involvement of ribonucleotide-dependent phosphorolysis in cross-resistance to nucleoside analogue inhibitors. J Mol Biol 2002; 323: 181-97.
-
(2002)
J. Mol. Biol.
, vol.323
, pp. 181-197
-
-
Mas, A.1
Vazquez-Alvarez, B.M.2
Domingo, E.3
Menendez-Arias, L.4
-
102
-
-
0028947588
-
High resolution structures of HIV-1 RT from four RT-inhibitor complexes
-
Ren J, Esnouf R, Garman E, Somers D, Ross C, Kirby I, et al. High resolution structures of HIV-1 RT from four RT-inhibitor complexes. Nat Struct Biol 1995; 2: 293-302.
-
(1995)
Nat. Struct. Biol.
, vol.2
, pp. 293-302
-
-
Ren, J.1
Esnouf, R.2
Garman, E.3
Somers, D.4
Ross, C.5
Kirby, I.6
-
103
-
-
0026077832
-
Viral resistance to human immunodeficiency virus type 1-specific pyridinone reverse transcriptase inhibitors
-
Nunberg JH, Schleif WA, Boots EJ, O'Brien JA, Quintero JC, Hoffman JM, et al. Viral resistance to human immunodeficiency virus type 1-specific pyridinone reverse transcriptase inhibitors. J Virol 1991; 65: 4887-92.
-
(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, J.M.6
-
104
-
-
0027957791
-
Nevirapine resistance mutations of human immunodeficiency virus type 1 selected during therapy
-
Richman DD, Havlir D, Corbeil J, Looney D, Ignacio C, Spector SA, et al. Nevirapine resistance mutations of human immunodeficiency virus type 1 selected during therapy. J Virol 1994; 68: 1660-6.
-
(1994)
J. Virol.
, vol.68
, pp. 1660-1666
-
-
Richman, D.D.1
Havlir, D.2
Corbeil, J.3
Looney, D.4
Ignacio, C.5
Spector, S.A.6
-
105
-
-
0026579394
-
In vitro selection and molecular characterization of human immunodeficiency virus-1 resistant to non-nucleoside inhibitors of reverse transcriptase
-
Mellors JW, Dutschman GE, Im GJ, Tramontano E, Winkler SR, Cheng YC. In vitro selection and molecular characterization of human immunodeficiency virus-1 resistant to non-nucleoside inhibitors of reverse transcriptase. Mol Pharmacol 1992; 41: 446-51.
-
(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
-
106
-
-
0026318387
-
Human immunodeficiency virus type 1 mutants resistant to nonnucleoside inhibitors of reverse transcriptase arise in tissue culture
-
Richman D, Shih CK, Lowy I, Rose J, Prodanovich P, Goff S, et al. Human immunodeficiency virus type 1 mutants resistant to nonnucleoside inhibitors of reverse transcriptase arise in tissue culture. Proc Natl Acad Sci USA 1991; 88: 11241-5.
-
(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
-
107
-
-
0034435564
-
Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase
-
Ren J, Milton J, Weaver KL, Short SA, Stuart DI, Stammers DK. Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase. Structure 2000; 8: 1089-94.
-
(2000)
Structure
, vol.8
, pp. 1089-1094
-
-
Ren, J.1
Milton, J.2
Weaver, K.L.3
Short, S.A.4
Stuart, D.I.5
Stammers, D.K.6
-
108
-
-
0028785708
-
L-743, 726 (DMP-266): A novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase
-
Young SD, Britcher SF, Tran LO, Payne LS, Lumma WC, Lyle TA, et al. L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase. Antimicrob Agents Chemother 1995; 39: 2602-5.
-
(1995)
Antimicrob. Agents Chemother.
, vol.39
, pp. 2602-2605
-
-
Young, S.D.1
Britcher, S.F.2
Tran, L.O.3
Payne, L.S.4
Lumma, W.C.5
Lyle, T.A.6
-
109
-
-
0036229823
-
Structural basis for the inhibitory efficacy of efavirenz (DMP-266), MSC194 and PNU142721 towards the HIV-1 RT K103N mutant
-
Lindberg J, Sigurdsson S, Lowgren S, Andersson HO, Sahlberg C, Noreen R, et al. Structural basis for the inhibitory efficacy of efavirenz (DMP-266), MSC194 and PNU142721 towards the HIV-1 RT K103N mutant. Eur J Biochem 2002; 269: 1670-7.
-
(2002)
Eur. J. Biochem.
, vol.269
, pp. 1670-1677
-
-
Lindberg, J.1
Sigurdsson, S.2
Lowgren, S.3
Andersson, H.O.4
Sahlberg, C.5
Noreen, R.6
-
110
-
-
0032786364
-
Expanded-spectrum nonnucleoside reverse transcriptase inhibitors inhibit clinically relevant mutant variants of human immunodeficiency virus type 1
-
Corbett JW, Ko SS, Rodgers JD, Jeffrey S, Bacheler LT, Klabe RM, et al. Expanded-spectrum nonnucleoside reverse transcriptase inhibitors inhibit clinically relevant mutant variants of human immunodeficiency virus type 1. Antimicrob Agents Chemother 1999; 43: 2893-7.
-
(1999)
Antimicrob. Agents Chemother.
, vol.43
, pp. 2893-2897
-
-
Corbett, J.W.1
Ko, S.S.2
Rodgers, J.D.3
Jeffrey, S.4
Bacheler, L.T.5
Klabe, R.M.6
-
111
-
-
0034128898
-
Inhibition of clinically relevant mutant variants of HIV-1 by quinazolinone non-nucleoside reverse transcriptase inhibitors
-
Corbett JW, Ko SS, Rodgers JD, Gearhart LA, Magnus NA, Bacheler LT, et al. Inhibition of clinically relevant mutant variants of HIV-1 by quinazolinone non-nucleoside reverse transcriptase inhibitors. J Med Chem 2000; 43: 2019-30.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2019-2030
-
-
Corbett, J.W.1
Ko, S.S.2
Rodgers, J.D.3
Gearhart, L.A.4
Magnus, N.A.5
Bacheler, L.T.6
-
112
-
-
0031805095
-
S-1153 inhibits replication of known drug-resistant strains of human immunodeficiency virus type 1
-
Fujiwara T, Sato A, el-Farrash M, Miki S, Abe K, Isaka Y, et al. S-1153 inhibits replication of known drug-resistant strains of human immunodeficiency virus type 1. Antimicrob Agents Chemother 1998; 42: 1340-5.
-
(1998)
Antimicrob. Agents Chemother.
, vol.42
, pp. 1340-1345
-
-
Fujiwara, T.1
Sato, A.2
el-Farrash, M.3
Miki, S.4
Abe, K.5
Isaka, Y.6
-
113
-
-
0035139222
-
SJ-3366, a unique and highly potent nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1 (HIV-1) that also inhibits HIV-2
-
Buckheit RW Jr, Watson K, Fliakas-Boltz V, Russell J, Loftus TL, Osterling MC, et al. SJ-3366, a unique and highly potent nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1 (HIV-1) that also inhibits HIV-2. Antimicrob Agents Chemother 2001; 45: 393-400.
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, pp. 393-400
-
-
Buckheit Jr., R.W.1
Watson, K.2
Fliakas-Boltz, V.3
Russell, J.4
Loftus, T.L.5
Osterling, M.C.6
-
114
-
-
0027218692
-
-
Richardson CC, Abelson JN, Meister A, Walsh CT. Eds, Annual Review Inc
-
Wlodawer A, Erickson JW. In: Richardson CC, Abelson JN, Meister A, Walsh CT. Eds, Ann Rev Biochem. Annual Review Inc., 1993; 62: 543-583.
-
(1993)
Ann. Rev. Biochem.
, vol.62
, pp. 543-583
-
-
Wlodawer, A.1
Erickson, J.W.2
-
115
-
-
0024392730
-
Human immunodeficiency virus-like particles produced by a vaccinia virus expression vector
-
Karacostas V, Nagashima K, Gonda MA, Moss B. Human immunodeficiency virus-like particles produced by a vaccinia virus expression vector. Proc Natl Acad Sci USA 1989; 8: 8964-7.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.8
, pp. 8964-8967
-
-
Karacostas, V.1
Nagashima, K.2
Gonda, M.A.3
Moss, B.4
-
116
-
-
0025268321
-
Rational design of peptide-based HIV proteinase inhibitors
-
Roberts NA, Martin JA, Kinchigton D, Broadhurst AV, Craig JC, Duncan IB, et al. Rational design of peptide-based HIV proteinase inhibitors. Science 1990; 248: 358-61.
-
(1990)
Science
, vol.248
, pp. 358-361
-
-
Roberts, N.A.1
Martin, J.A.2
Kinchigton, D.3
Broadhurst, A.V.4
Craig, J.C.5
Duncan, I.B.6
-
117
-
-
0026579208
-
The HIV-1 protease as a therapeutic target for AIDS
-
Debouck C. The HIV-1 protease as a therapeutic target for AIDS. AIDS Res Hum Retroviruses 1992; 8: 153-64.
-
(1992)
AIDS Res. Hum. Retroviruses
, vol.8
, pp. 153-164
-
-
Debouck, C.1
-
118
-
-
15444377672
-
Ordered accumulation of mutations in HIV protease confers resistance to ritonavir
-
Molla A, Korneyeva M, Gao Q, Vasavanonda S, Schipper PJ, Mo HM, et al. Ordered accumulation of mutations in HIV protease confers resistance to ritonavir. Nat Med 1996; 2: 760-6.
-
(1996)
Nat. Med.
, vol.2
, pp. 760-766
-
-
Molla, A.1
Korneyeva, M.2
Gao, Q.3
Vasavanonda, S.4
Schipper, P.J.5
Mo, H.M.6
-
119
-
-
0028945211
-
Structural basis of drug resistance for the V82A mutant of HIV-1 proteinase
-
Baldwin ET, Bhat TN, Liu B, Pattabiraman N, Erickson JW. Structural basis of drug resistance for the V82A mutant of HIV-1 proteinase. Nat Struct Biol 1995; 2: 244-9.
-
(1995)
Nat. Struct. Biol.
, vol.2
, pp. 244-249
-
-
Baldwin, E.T.1
Bhat, T.N.2
Liu, B.3
Pattabiraman, N.4
Erickson, J.W.5
-
120
-
-
0029644939
-
Structure of HIV-1 protease with KNI-272, a tight-binding transition-state analog containing allophenylnorstatine
-
Baldwin ET, Bhat TN, Gulnik S, Liu B, Topol IA, Kiso Y, et al. Structure of HIV-1 protease with KNI-272, a tight-binding transition-state analog containing allophenylnorstatine. Structure 1995; 3: 581-90.
-
(1995)
Structure
, vol.3
, pp. 581-590
-
-
Baldwin, E.T.1
Bhat, T.N.2
Gulnik, S.3
Liu, B.4
Topol, I.A.5
Kiso, Y.6
-
121
-
-
0028958868
-
Flap opening in HIV-1 protease simulated by 'activated' molecular dynamics
-
Collins JR, Burt SK, Erickson JW. Flap opening in HIV-1 protease simulated by 'activated' molecular dynamics. Nat Struct Biol 1995; 2: 334-8.
-
(1995)
Nat. Struct. Biol.
, vol.2
, pp. 334-338
-
-
Collins, J.R.1
Burt, S.K.2
Erickson, J.W.3
-
122
-
-
0033778181
-
Crystal structure of an in vivo HIV-1 protease mutant in complex with saquinavir: Insights into the mechanisms of drug resistance
-
Hong L, Zhang XC, Hartsuck JA, Tang J. Crystal structure of an in vivo HIV-1 protease mutant in complex with saquinavir: insights into the mechanisms of drug resistance. Protein Sci 2000; 9: 1898-904.
-
(2000)
Protein Sci.
, vol.9
, pp. 1898-1904
-
-
Hong, L.1
Zhang, X.C.2
Hartsuck, J.A.3
Tang, J.4
-
123
-
-
0030769354
-
Drug resistance during indinavir therapy is caused by mutations in the protease gene and in its Gag substrate cleavage sites
-
Zhang YM, Imamichi H, Imamichi T, Lane HC, Falloon J, Vasudevachari MB, et al. Drug resistance during indinavir therapy is caused by mutations in the protease gene and in its Gag substrate cleavage sites. J Virol 1997; 71: 6662-70.
-
(1997)
J. Virol.
, vol.71
, pp. 6662-6670
-
-
Zhang, Y.M.1
Imamichi, H.2
Imamichi, T.3
Lane, H.C.4
Falloon, J.5
Vasudevachari, M.B.6
-
124
-
-
0031015475
-
Impaired fitness of human immunodeficiency virus type 1 variants with high-level resistance to protease inhibitors
-
Croteau G, Doyon L, Thibeault D, McKercher G, Pilote L, Lamarre D. Impaired fitness of human immunodeficiency virus type 1 variants with high-level resistance to protease inhibitors. J Virol 1997; 71: 1089-96.
-
(1997)
J. Virol.
, vol.71
, pp. 1089-1096
-
-
Croteau, G.1
Doyon, L.2
Thibeault, D.3
McKercher, G.4
Pilote, L.5
Lamarre, D.6
-
125
-
-
0031846317
-
Resistance-associated loss of viral fitness in human immunodeficiency virus type 1: Phenotypic analysis of protease and gag coevolution in protease inhibitor-treated patients
-
Mammano F, Petit C, Clavel F. Resistance-associated loss of viral fitness in human immunodeficiency virus type 1: phenotypic analysis of protease and gag coevolution in protease inhibitor-treated patients. J Virol 1998; 72: 7632-7.
-
(1998)
J. Virol.
, vol.72
, pp. 7632-7637
-
-
Mammano, F.1
Petit, C.2
Clavel, F.3
-
126
-
-
0031946007
-
Loss of viral fitness associated with multiple Gag and Gag-Pol processing defects in human immunodeficiency virus type 1 variants selected for resistance to protease inhibitors in vivo
-
Zennou V, Mammano F, Paulous S, Mathez D, Clavel F. Loss of viral fitness associated with multiple Gag and Gag-Pol processing defects in human immunodeficiency virus type 1 variants selected for resistance to protease inhibitors in vivo. J Virol 1998; 72: 3300-6.
-
(1998)
J. Virol.
, vol.72
, pp. 3300-3306
-
-
Zennou, V.1
Mammano, F.2
Paulous, S.3
Mathez, D.4
Clavel, F.5
-
127
-
-
0032928065
-
Replicative fitness of protease inhibitor-resistant mutants of human immunodeficiency virus type 1
-
Martinez-Picado J, Savara AV, Sutton L, D'Aquila RT. Replicative fitness of protease inhibitor-resistant mutants of human immunodeficiency virus type 1. J Virol 1999; 73: 3744-52.
-
(1999)
J. Virol.
, vol.73
, pp. 3744-3752
-
-
Martinez-Picado, J.1
Savara, A.V.2
Sutton, L.3
D'Aquila, R.T.4
-
128
-
-
0032804864
-
Increased fitness of drug resistant HIV-1 protease as a result of acquisition of compensatory mutations during suboptimal therapy
-
Nijhuis M, Schuurman R, de Jong D, Erickson J, Gustchina E, Albert J, et al. Increased fitness of drug resistant HIV-1 protease as a result of acquisition of compensatory mutations during suboptimal therapy. AIDS 1999; 13: 2349-59.
-
(1999)
AIDS
, vol.13
, pp. 2349-2359
-
-
Nijhuis, M.1
Schuurman, R.2
de Jong, D.3
Erickson, J.4
Gustchina, E.5
Albert, J.6
-
130
-
-
0033834920
-
Virological and immunological characteristics of HIV treatment failure
-
Kaufmann D, Munoz M, Bleiber G, Fleury S, Lotti B, Martinez R, et al. Virological and immunological characteristics of HIV treatment failure. AIDS 2000; 14: 1767-74.
-
(2000)
AIDS
, vol.14
, pp. 1767-1774
-
-
Kaufmann, D.1
Munoz, M.2
Bleiber, G.3
Fleury, S.4
Lotti, B.5
Martinez, R.6
-
131
-
-
0034492631
-
Altered viral fitness of HIV-1 following failure of protease inhibitor-based therapy
-
Picchio GR, Valdez H, Sabbe R, Landay AL, Kuritzkes DR, Lederman MM, Mosier DE. Altered viral fitness of HIV-1 following failure of protease inhibitor-based therapy. J Acquir Immune Defic Syndr 2000; 25; 289-95.
-
(2000)
J. Acquir. Immune Defic. Syndr.
, vol.25
, pp. 289-295
-
-
Picchio, G.R.1
Valdez, H.2
Sabbe, R.3
Landay, A.L.4
Kuritzkes, D.R.5
Lederman, M.M.6
Mosier, D.E.7
-
132
-
-
0034632745
-
HIV type 1 protease cleavage site mutations and viral fitness: Implications for drug susceptibility phenotyping assays
-
Robinson LH, Myers RE, Snowden BW, Tisdale M, Blair ED. HIV type 1 protease cleavage site mutations and viral fitness: implications for drug susceptibility phenotyping assays. AIDS Res Hum Retroviruses 2000; 16: 1149-56.
-
(2000)
AIDS Res. Hum. Retroviruses
, vol.16
, pp. 1149-1156
-
-
Robinson, L.H.1
Myers, R.E.2
Snowden, B.W.3
Tisdale, M.4
Blair, E.D.5
-
133
-
-
0035104646
-
Individual contributions of mutant protease and reverse transcriptase to viral infectivity, replication, and protein maturation of antiretroviral drug-resistant human immunodeficiency virus type 1
-
Bleiber G, Munoz M, Ciuffi A, Meylan P, Telentj A. Individual contributions of mutant protease and reverse transcriptase to viral infectivity, replication, and protein maturation of antiretroviral drug-resistant human immunodeficiency virus type 1. J Virol 2001; 75: 3291-300.
-
(2001)
J. Virol.
, vol.75
, pp. 3291-3300
-
-
Bleiber, G.1
Munoz, M.2
Ciuffi, A.3
Meylan, P.4
Telentj, A.5
-
134
-
-
0031849665
-
In vitro selection and characterization of human immunodeficiency virus type 1 variants with increased resistance to ABT-378, a novel protease inhibitor
-
Carrillo A, Stewart KD, Sham HL, Norbeck DW, Kohlbrenner WE, Leonard JM, et al. In vitro selection and characterization of human immunodeficiency virus type 1 variants with increased resistance to ABT-378, a novel protease inhibitor. J Virol 1998; 72: 7532-41.
-
(1998)
J. Virol.
, vol.72
, pp. 7532-7541
-
-
Carrillo, A.1
Stewart, K.D.2
Sham, H.L.3
Norbeck, D.W.4
Kohlbrenner, W.E.5
Leonard, J.M.6
-
135
-
-
0029899093
-
Second locus involved in human immunodeficiency virus type 1 resistance to protease inhibitors
-
Doyon L, Croteau G, Thibeault D, Poulin F, Pilote L, Lamarre D. Second locus involved in human immunodeficiency virus type 1 resistance to protease inhibitors. J Virol 1996; 70: 3763-9.
-
(1996)
J. Virol.
, vol.70
, pp. 3763-3769
-
-
Doyon, L.1
Croteau, G.2
Thibeault, D.3
Poulin, F.4
Pilote, L.5
Lamarre, D.6
-
136
-
-
0031748806
-
Novel Gag-Pol frameshift site in human immunodeficiency virus type 1 variants resistant to protease inhibitors
-
Doyon L, Payant C, Brakier-Gingras L, Lamarre D. Novel Gag-Pol frameshift site in human immunodeficiency virus type 1 variants resistant to protease inhibitors. J Virol 1998; 72: 6146-50.
-
(1998)
J. Virol.
, vol.72
, pp. 6146-6150
-
-
Doyon, L.1
Payant, C.2
Brakier-Gingras, L.3
Lamarre, D.4
-
137
-
-
0028943992
-
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
-
Condra JH, Schleif WA, Blahy OM, Gabryelski LJ, Graham DJ, Quintero J, et al. In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors. Nature 1995 374: 569-71.
-
(1995)
Nature
, vol.374
, pp. 569-571
-
-
Condra, J.H.1
Schleif, W.A.2
Blahy, O.M.3
Gabryelski, L.J.4
Graham, D.J.5
Quintero, J.6
-
138
-
-
7344249601
-
HIV protease genotype and viral sensitivity to HIV protease inhibitors following saquinavir therapy
-
Craig C, Race E, Sheldon J, Whittaker L, Gilbert S, Moffatt A, et al. HIV protease genotype and viral sensitivity to HIV protease inhibitors following saquinavir therapy. AIDS 1998; 12: 1611-8.
-
(1998)
AIDS
, vol.12
, pp. 1611-1618
-
-
Craig, C.1
Race, E.2
Sheldon, J.3
Whittaker, L.4
Gilbert, S.5
Moffatt, A.6
-
139
-
-
0033033234
-
HIV RNA and CD4 cell count response to protease inhibitor therapy in an urban AIDS clinic: Response to both initial and salvage therapy
-
Decks SG, Hecht FM, Swanson M, Elbeik T, Loftus R, Cohen PT, et al. HIV RNA and CD4 cell count response to protease inhibitor therapy in an urban AIDS clinic: response to both initial and salvage therapy. AIDS 1999; 13: F35-43.
-
(1999)
AIDS
, vol.13
-
-
Decks, S.G.1
Hecht, F.M.2
Swanson, M.3
Elbeik, T.4
Loftus, R.5
Cohen, P.T.6
-
140
-
-
0032889457
-
Constrained evolution of human immunodeficiency virus type 1 protease during sequential therapy with two distinct protease inhibitors
-
Dulioust A, Paulous S, Guillemot L, Delavalle AM, Bone F, Clavel F. Constrained evolution of human immunodeficiency virus type 1 protease during sequential therapy with two distinct protease inhibitors. J Virol 1999; 73: 850-4.
-
(1999)
J. Virol.
, vol.73
, pp. 850-854
-
-
Dulioust, A.1
Paulous, S.2
Guillemot, L.3
Delavalle, A.M.4
Bone, F.5
Clavel, F.6
-
141
-
-
0032842750
-
Salvage therapy with regimens containing ritonavir and saquinavir in extensively pretreated HIV-infected patients
-
Fatkenheuer G, Hoetelmans RM, Hunn N, Schwenk A, Franzen C, Reiser M, et al. Salvage therapy with regimens containing ritonavir and saquinavir in extensively pretreated HIV-infected patients. AIDS 1999; 13:1485-9.
-
(1999)
AIDS
, vol.13
, pp. 1485-1489
-
-
Fatkenheuer, G.1
Hoetelmans, R.M.2
Hunn, N.3
Schwenk, A.4
Franzen, C.5
Reiser, M.6
-
142
-
-
0032568248
-
Resistance and cross-resistance with saquinavir and other HIV protease inhibitors: Theory and practice
-
Roberts NA, Craig JC, Sheldon J. Resistance and cross-resistance with saquinavir and other HIV protease inhibitors: theory and practice. AIDS 1998; 12: 453-60.
-
(1998)
AIDS
, vol.12
, pp. 453-460
-
-
Roberts, N.A.1
Craig, J.C.2
Sheldon, J.3
-
143
-
-
0031949563
-
Human immunodeficiency virus type 1 protease genotypes and in vitro protease inhibitor susceptibilities of isolates from individuals who were switched to other protease inhibitors after long-term saquinavir treatment
-
Winters MA, Schapiro JM, Lawrence J, Merigan TC, Human immunodeficiency virus type 1 protease genotypes and in vitro protease inhibitor susceptibilities of isolates from individuals who were switched to other protease inhibitors after long-term saquinavir treatment. J Virol 1998; 72: 5303-6.
-
(1998)
J. Virol.
, vol.72
, pp. 5303-5306
-
-
Winters, M.A.1
Schapiro, J.M.2
Lawrence, J.3
Merigan, T.C.4
-
145
-
-
0031596029
-
Nucleoside analog 1592U89 and human immunodeficiency virus protease inhibitor 141W94 are synergistic in vitro
-
Drusano GL, D'Argenio DZ, Symonds W, Bilello PA, McDowell J, Sadler B, et al. Nucleoside analog 1592U89 and human immunodeficiency virus protease inhibitor 141W94 are synergistic in vitro. Antimicrob Agents Chemother 1998; 42: 2153-9.
-
(1998)
Antimicrob. Agents Chemother.
, vol.42
, pp. 2153-2159
-
-
Drusano, G.L.1
D'Argenio, D.Z.2
Symonds, W.3
Bilello, P.A.4
McDowell, J.5
Sadler, B.6
-
146
-
-
0033022106
-
Highly drug-resistant HIV-1 clinical isolates are cross-resistant to many antiretroviral compounds in current clinical development
-
Palmer S, Shafer RW, Merigan TC. Highly drug-resistant HIV-1 clinical isolates are cross-resistant to many antiretroviral compounds in current clinical development. AIDS 1999; 13: 661-7.
-
(1999)
AIDS
, vol.13
, pp. 661-667
-
-
Palmer, S.1
Shafer, R.W.2
Merigan, T.C.3
-
147
-
-
0032899327
-
Treatment with amprenavir alone or amprenavir with zidovudine and lamivudine in adults with human immunodeficiency virus infection
-
AIDS Clinical Trials Group 347 Study Team
-
Murphy RL, Gulick RM, DeGruttola V, D'Aquila RT, Eron JJ, Sommadossi JP, Currier JS, et al. Treatment with amprenavir alone or amprenavir with zidovudine and lamivudine in adults with human immunodeficiency virus infection. AIDS Clinical Trials Group 347 Study Team. J Infect Dis 1999; 179: 808-16.
-
(1999)
J. Infect. Dis.
, vol.179
, pp. 808-816
-
-
Murphy, R.L.1
Gulick, R.M.2
DeGruttola, V.3
D'Aquila, R.T.4
Eron, J.J.5
Sommadossi, J.P.6
Currier, J.S.7
-
148
-
-
0032824724
-
Phenotypic changes in drug susceptibility associated with failure of human immunodeficiency virus type 1 (HIV-1) triple combination therapy
-
Parkin NT, Lie YS, Hellmann N, Markowitz M, Bonhoeffer S, Ho DD, et al. Phenotypic changes in drug susceptibility associated with failure of human immunodeficiency virus type 1 (HIV-1) triple combination therapy. J Infect Dis 1999; 180: 865-70.
-
(1999)
J. Infect. Dis.
, vol.180
, pp. 865-870
-
-
Parkin, N.T.1
Lie, Y.S.2
Hellmann, N.3
Markowitz, M.4
Bonhoeffer, S.5
Ho, D.D.6
-
149
-
-
0033743891
-
Low level of cross-resistance to amprenavir (141W94) in samples from patients pretreated with other protease inhibitors
-
Schmidt B, Kom K, Moschik B, Paatz C, Uberla K, Walter H. Low level of cross-resistance to amprenavir (141W94) in samples from patients pretreated with other protease inhibitors. Antimicrob Agents Chemother2000;44:3213-6.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, pp. 3213-3216
-
-
Schmidt, B.1
Kom, K.2
Moschik, B.3
Paatz, C.4
Uberla, K.5
Walter, H.6
-
150
-
-
0037379517
-
Activities of atazanavir (BMS-232632) against a large panel of human immunodeficiency virus type 1 clinical isolates resistant to one or more approved protease inhibitors
-
Colonno RJ, Thiry A, Limoli K, Parkin N. Activities of atazanavir (BMS-232632) against a large panel of human immunodeficiency virus type 1 clinical isolates resistant to one or more approved protease inhibitors. Antimicrob Agents Chemother 2003; 47: 1324-33.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 1324-1333
-
-
Colonno, R.J.1
Thiry, A.2
Limoli, K.3
Parkin, N.4
-
151
-
-
0033844808
-
In vitro resistance profile of the human immunodeficiency virus type 1 protease inhibitor BMS-232632
-
Gong YF, Robinson BS, Rose RE, Deminie C, Spicer TP, Stock D, et al. In vitro resistance profile of the human immunodeficiency virus type 1 protease inhibitor BMS-232632. Antimicrob Agents Chemother 2000; 44: 2319-26.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, pp. 2319-2326
-
-
Gong, Y.F.1
Robinson, B.S.2
Rose, R.E.3
Deminie, C.4
Spicer, T.P.5
Stock, D.6
-
152
-
-
0031788930
-
ABT-378, a highly potent inhibitor of the human immunodeficiency virus protease
-
Sham HL, Kempf DJ, Molla A, Marsh KC, Kumar GN, Chen CM, et al. ABT-378, a highly potent inhibitor of the human immunodeficiency virus protease. Antimicrob Agents Chemother 1998; 42: 3218-24.
-
(1998)
Antimicrob. Agents Chemother.
, vol.42
, pp. 3218-3224
-
-
Sham, H.L.1
Kempf, D.J.2
Molla, A.3
Marsh, K.C.4
Kumar, G.N.5
Chen, C.M.6
-
153
-
-
0032566902
-
Human serum attenuates tile activity of protease inhibitors toward wild-type and mutant human immunodeficiency virus
-
Molla A, Vasavanonda S, Kumar G, Sham HL, Johnson M, Grabowski B, et al. Human serum attenuates tile activity of protease inhibitors toward wild-type and mutant human immunodeficiency virus. Virology 1998; 250: 255-62.
-
(1998)
Virology
, vol.250
, pp. 255-262
-
-
Molla, A.1
Vasavanonda, S.2
Kumar, G.3
Sham, H.L.4
Johnson, M.5
Grabowski, B.6
-
154
-
-
0031035968
-
Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir
-
Kempf DJ, Marsh KC, Kumar G, Rodrigues AD, Denissen JF, McDonald E, et al. Pharmacokinetic enhancement of inhibitors of the human immunodeficiency virus protease by coadministration with ritonavir. Antimicrob Agents Chemother 1997; 41: 654-60.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 654-660
-
-
Kempf, D.J.1
Marsh, K.C.2
Kumar, G.3
Rodrigues, A.D.4
Denissen, J.F.5
McDonald, E.6
-
155
-
-
0033931167
-
BMS-232632, a highly potent human immunodeficiency virus protease inhibitor that can be used in combination with other available antiretroviral agents
-
Robinson BS, Riccardi KA, Gong YF, Guo Q, Stock DA, Blair WS, et al. BMS-232632, a highly potent human immunodeficiency virus protease inhibitor that can be used in combination with other available antiretroviral agents. Antimicrob Agents Chemother 2000; 44: 2093-9.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, pp. 2093-2099
-
-
Robinson, B.S.1
Riccardi, K.A.2
Gong, Y.F.3
Guo, Q.4
Stock, D.A.5
Blair, W.S.6
-
156
-
-
0027220895
-
Peptidomimetic HIV protease inhibitors: Phosphate prodrugs with improved biological activities
-
Chong KT, Ruwart MJ, Hinshaw RR, Wilkinson KF, Rush BD, Yancey MF, et al. Peptidomimetic HIV protease inhibitors: phosphate prodrugs with improved biological activities. J Med Chem 1993; 36: 2575-7.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2575-2577
-
-
Chong, K.T.1
Ruwart, M.J.2
Hinshaw, R.R.3
Wilkinson, K.F.4
Rush, B.D.5
Yancey, M.F.6
-
157
-
-
0028986487
-
Targeting HIV-1 protease: A test of drug-design methodologies
-
West ML, Fairlie DP. Targeting HIV-1 protease: a test of drug-design methodologies. Trend. Pharmaco Sci 1995; 16: 67-75.
-
(1995)
Trend. Pharmaco. Sci.
, vol.16
, pp. 67-75
-
-
West, M.L.1
Fairlie, D.P.2
-
158
-
-
0033047131
-
Structure-based discovery of Tipranavir disodium (PNU-140690E): A potent, orally bioavailable, nonpeptidic HIV protease inhibitor
-
Thaisrivongs S, Strohbach JW. Structure-based discovery of Tipranavir disodium (PNU-140690E): a potent, orally bioavailable, nonpeptidic HIV protease inhibitor. Biopolymers 1999; 51: 51-8.
-
(1999)
Biopolymers
, vol.51
, pp. 51-58
-
-
Thaisrivongs, S.1
Strohbach, J.W.2
-
159
-
-
0034934689
-
Metabolic complications associated with antiretroviral therapy
-
Jain RG, Furfine ES, Pedneault L, White AJ, Lenhard JM. Metabolic complications associated with antiretroviral therapy. Antiviral Res 2001; 51: 151-77.
-
(2001)
Antiviral Res.
, vol.51
, pp. 151-177
-
-
Jain, R.G.1
Furfine, E.S.2
Pedneault, L.3
White, A.J.4
Lenhard, J.M.5
-
160
-
-
0035882329
-
Osteonecrosis in patients infected with human immunodeficiency virus: A case-control study
-
Glesby MJ, Hoover DR, Vaamonde CM. Osteonecrosis in patients infected with human immunodeficiency virus: a case-control study. J Infect Dis 2001; 184: 519-23.
-
(2001)
J. Infect. Dis.
, vol.184
, pp. 519-523
-
-
Glesby, M.J.1
Hoover, D.R.2
Vaamonde, C.M.3
-
161
-
-
0035985004
-
Investigating the cellular targets of HIV protease inhibitors: Implications for metabolic disorders and improvements in drug therapy
-
Murata H, Hruz PW, Mueckler M. Investigating the cellular targets of HIV protease inhibitors: implications for metabolic disorders and improvements in drug therapy. Curr Drug Targets Infect Disord 2002; 2: 1-8.
-
(2002)
Curr. Drug Targets Infect. Disord.
, vol.2
, pp. 1-8
-
-
Murata, H.1
Hruz, P.W.2
Mueckler, M.3
-
162
-
-
0037350147
-
Effects of HIV protease inhibitor therapy on lipid metabolism
-
Hui DY, Effects of HIV protease inhibitor therapy on lipid metabolism. Prog Lipid Res 2003; 42: 81-92.
-
(2003)
Prog. Lipid Res.
, vol.42
, pp. 81-92
-
-
Hui, D.Y.1
-
163
-
-
0036652048
-
HIV-1, HAART and bone metabolism
-
Borderi M, Farneti B, Tampellini L, Giuliani R, Verucchi G, Vescini F, et al. HIV-1, HAART and bone metabolism. New Microbiol 2002; 25: 375-84.
-
(2002)
New Microbiol.
, vol.25
, pp. 375-384
-
-
Borderi, M.1
Farneti, B.2
Tampellini, L.3
Giuliani, R.4
Verucchi, G.5
Vescini, F.6
-
165
-
-
0028028221
-
Structure-based design of HIV protease inhibitors: 4-hydroxycoumarins and 4-hydroxy-2-pyrones as non-peptidic inhibitors
-
Thaisrivongs S, Tomich PK, Watenpaugh KD, Chong KT, Howe WJ, Yang CP, et al. Structure-based design of HIV protease inhibitors: 4-hydroxycoumarins and 4-hydroxy-2-pyrones as non-peptidic inhibitors. J Med Chem 1994; 37: 3200-4.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3200-3204
-
-
Thaisrivongs, S.1
Tomich, P.K.2
Watenpaugh, K.D.3
Chong, K.T.4
Howe, W.J.5
Yang, C.P.6
-
166
-
-
0029621821
-
Structure-based design of sulfonamide-substituted non-peptidic HIV protease inhibitors
-
Skulnick HI, Johnson PD, Howe WJ, Tomich PK, Chong KT, Watenpaugh KD, et al. Structure-based design of sulfonamide-substituted non-peptidic HIV protease inhibitors. J Med Chem 1995; 38: 4968-71.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4968-4971
-
-
Skulnick, H.I.1
Johnson, P.D.2
Howe, W.J.3
Tomich, P.K.4
Chong, K.T.5
Watenpaugh, K.D.6
-
167
-
-
9544235162
-
Cyclic HIV protease inhibitors: Synthesis, conformational analysis, P2/P2′ structure-activity relationship, and molecular recognition of cyclic ureas
-
Lam PY, Ru Y, Jadhav PK, Aldrich PE, DeLucca GV, Eyermann CJ, et al. Cyclic HIV protease inhibitors: synthesis, conformational analysis, P2/P2′ structure-activity relationship, and molecular recognition of cyclic ureas. J Med Chem 1996; 39: 3514-25.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3514-3525
-
-
Lam, P.Y.1
Ru, Y.2
Jadhav, P.K.3
Aldrich, P.E.4
DeLucca, G.V.5
Eyermann, C.J.6
-
168
-
-
0030113025
-
Improved cyclic urea inhibitors of the HIV-1 protease: Synthesis, potency, resistance profile, human pharmacokinetics and X-ray crystal structure of DMP 450
-
Hodge CN, Aldrich PE, Bacheler LT, Chang CH, Eyermann CJ, Garber S, et al. Improved cyclic urea inhibitors of the HIV-1 protease: synthesis, potency, resistance profile, human pharmacokinetics and X-ray crystal structure of DMP 450. Chem Biol 1996; 3: 301-14.
-
(1996)
Chem. Biol.
, vol.3
, pp. 301-314
-
-
Hodge, C.N.1
Aldrich, P.E.2
Bacheler, L.T.3
Chang, C.H.4
Eyermann, C.J.5
Garber, S.6
-
169
-
-
14444267317
-
Nonpeptide cyclic cyanoguanidines as HIV-1 protease inhibitors: Synthesis, structure-activity relationships, and X-ray crystal structure studies
-
Jadhav PK, Woerner FJ, Lam PY, Hodge CN, Eyermann CJ, Man HW, et al. Nonpeptide cyclic cyanoguanidines as HIV-1 protease inhibitors: synthesis, structure-activity relationships, and X-ray crystal structure studies. J Med Chem 1998; 41: 1446-55.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1446-1455
-
-
Jadhav, P.K.1
Woerner, F.J.2
Lam, P.Y.3
Hodge, C.N.4
Eyermann, C.J.5
Man, H.W.6
-
170
-
-
15144353143
-
New aza-dipeptide analogues as potent and orally absorbed HIV-1 protease inhibitors: Candidates for clinical development
-
Bold G, Fassler A, Capraro HG, Cozens R, Klimkait T, Lazdins J, et al. New aza-dipeptide analogues as potent and orally absorbed HIV-1 protease inhibitors: candidates for clinical development. J Med Chem 1998; 41: 3387-401.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 3387-3401
-
-
Bold, G.1
Fassler, A.2
Capraro, H.G.3
Cozens, R.4
Klimkait, T.5
Lazdins, J.6
-
171
-
-
12944322516
-
Tipranavir (PNU-140690): A potent, orally bioavailable nonpeptidic HIV protease inhibitor of the 5, 6-dihydro-4-hydroxy-2-pyrone sulfonamide class
-
Turner SR, Strohbach JW, Tommasi RA, Aristoft PA, Johnson PD, Skulnick HL et al. Tipranavir (PNU-140690): a potent, orally bioavailable nonpeptidic HIV protease inhibitor of the 5, 6-dihydro-4-hydroxy-2-pyrone sulfonamide class. J Med Chem 1998; 41: 3467-76.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 3467-3476
-
-
Turner, S.R.1
Strohbach, J.W.2
Tommasi, R.A.3
Aristoft, P.A.4
Johnson, P.D.5
Skulnick, H.L.6
-
172
-
-
13044254785
-
JE-2147: A dipeptide protease inhibitor (PI) that potently inhibits multi-PI-resistant HIV-1
-
Yoshimura K, Kato R. Yusa K, Kavlick MF, Maroun V, Nguyen A, et al. JE-2147: a dipeptide protease inhibitor (PI) that potently inhibits multi-PI-resistant HIV-1. Proc Natl Acad Sci USA 1999; 96: 8675-80.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 8675-8680
-
-
Yoshimura, K.1
Kato, R.2
Yusa, K.3
Kavlick, M.F.4
Maroun, V.5
Nguyen, A.6
-
173
-
-
10744226241
-
Novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI) UIC-94017 (TMC114) with potent activity against multi-PI-resistant human immunodeficiency virus in vitro
-
Koh Y, Nakata H, Maeda K. Ogata H, Bilcer G, Devasamudram T, et al. Novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI) UIC-94017 (TMC114) with potent activity against multi-PI-resistant human immunodeficiency virus in vitro. Antimicrob Agents Chemother 2003; 47: 3123-9.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 3123-3129
-
-
Koh, Y.1
Nakata, H.2
Maeda, K.3
Ogata, H.4
Bilcer, G.5
Devasamudram, T.6
-
174
-
-
0036145503
-
A potent human immunodeficiency virus type 1 protease inhibitor, UIC-94003 (TMC-126), and selection of a novel (A28S) mutation in the protease active site
-
Yoshimura K, Kato R, Kavlick MF, Nguyen A, Maroun V, Maeda K, Hussain KA, et al. A potent human immunodeficiency virus type 1 protease inhibitor, UIC-94003 (TMC-126), and selection of a novel (A28S) mutation in the protease active site. J Virol 2002; 76: 1349-58.
-
(2002)
J. Virol.
, vol.76
, pp. 1349-1358
-
-
Yoshimura, K.1
Kato, R.2
Kavlick, M.F.3
Nguyen, A.4
Maroun, V.5
Maeda, K.6
Hussain, K.A.7
-
175
-
-
0034769881
-
DPC 681 and DPC 684: Potent, selective inhibitors of human immunodeficiency virus protease active against clinically relevant mutant variants
-
Kaltenbach RF 3rd, Trainor G, Getman D, Harris G, Garber S, Cordova B, et al. DPC 681 and DPC 684: potent, selective inhibitors of human immunodeficiency virus protease active against clinically relevant mutant variants. Antimicrob Agents Chemother 2001; 45: 3021-8.
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, pp. 3021-3028
-
-
Kaltenbach III, R.F.1
Trainor, G.2
Getman, D.3
Harris, G.4
Garber, S.5
Cordova, B.6
-
176
-
-
0030895692
-
Antiviral activity of the dihydropyrone PNU-140690, a new nonpeptidic human immunodeficiency virus protease inhibitor
-
Poppe SM, Slade DE, Chong KT, Hinshaw RR, Pagano PJ, Markowitz M, et al. Antiviral activity of the dihydropyrone PNU-140690, a new nonpeptidic human immunodeficiency virus protease inhibitor. Antimicrob Agents Chemother 1997; 41: 1058-63.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1058-1063
-
-
Poppe, S.M.1
Slade, D.E.2
Chong, K.T.3
Hinshaw, R.R.4
Pagano, P.J.5
Markowitz, M.6
-
177
-
-
0034623020
-
Tipranavir inhibits broadly protease inhibitor-resistant HIV-1 clinical samples
-
Larder BA, Hertogs K. Bloor S, van den Eynde CH, DeCian W, Wang Y, et al. Tipranavir inhibits broadly protease inhibitor-resistant HIV-1 clinical samples. AIDS 2000; 14: 1943-8.
-
(2000)
AIDS
, vol.14
, pp. 1943-1948
-
-
Larder, B.A.1
Hertogs, K.2
Bloor, S.3
van den Eynde, C.H.4
DeCian, W.5
Wang, Y.6
-
178
-
-
0037043652
-
Antiretroviral-drug resistance among patients recently infected with HIV
-
Little SJ, Holte S, Routy JP, Daar ES, Markowitz M, Collier AC, et al. Antiretroviral-drug resistance among patients recently infected with HIV. N Engl J Med 2002; 347: 385-94.
-
(2002)
N. Engl. J. Med.
, vol.347
, pp. 385-394
-
-
Little, S.J.1
Holte, S.2
Routy, J.P.3
Daar, E.S.4
Markowitz, M.5
Collier, A.C.6
-
179
-
-
0034673154
-
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 mine
-
Sluis-Cremer N, Dmitrienko GI, Balzarini J, Camarasa MJ, Parniak MA. 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 mine. Biochemistry 2000; 39: 1427-33.
-
(2000)
Biochemistry
, vol.39
, pp. 1427-1433
-
-
Sluis-Cremer, N.1
Dmitrienko, G.I.2
Balzarini, J.3
Camarasa, M.J.4
Parniak, M.A.5
-
180
-
-
16944362355
-
Azodicarbonamide inhibits HIV-1 replication by targeting the nucleocapsid protein
-
Rice WG, Turpin JA, Huang M, Clanton D, Buckheit RW Jr, Covell DG, et al. Azodicarbonamide inhibits HIV-1 replication by targeting the nucleocapsid protein. Nat Med 1997; 3: 341-5.
-
(1997)
Nat. Med.
, vol.3
, pp. 341-345
-
-
Rice, W.G.1
Turpin, J.A.2
Huang, M.3
Clanton, D.4
Buckheit Jr., R.W.5
Covell, D.G.6
-
181
-
-
0344671562
-
Multiple effects of an anti-human immunodeficiency virus nucleocapsid inhibitor on virus morphology and replication
-
Berthoux L, Pechoux C, Darlix JL. Multiple effects of an anti-human immunodeficiency virus nucleocapsid inhibitor on virus morphology and replication. J Virol 1999; 73: 10000-9.
-
(1999)
J. Virol.
, vol.73
, pp. 10000-10009
-
-
Berthoux, L.1
Pechoux, C.2
Darlix, J.L.3
-
182
-
-
0038799984
-
Synthesis, resolution, and determination of the absolute configuration of the enantiomers of cis-4, 5-dihydroxy-1, 2-dithiane 1, 1-dioxide, an HIV-INCp7 inhibitor
-
Mayasundari A, Rice WG, Diminnie JB, Baker DC. Synthesis, resolution, and determination of the absolute configuration of the enantiomers of cis-4, 5-dihydroxy-1, 2-dithiane 1, 1-dioxide, an HIV-INCp7 inhibitor. Bioorg Med Chem 2003; 11: 3215-9.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 3215-3219
-
-
Mayasundari, A.1
Rice, W.G.2
Diminnie, J.B.3
Baker, D.C.4
-
183
-
-
0024999408
-
Illimaquinone, a selective inhibitor of the RNase H activity of human immunodeficiency virus type 1 reverse transcriptase
-
Loya S, Tal R, Kashman Y, Hizi A. Illimaquinone, a selective inhibitor of the RNase H activity of human immunodeficiency virus type 1 reverse transcriptase. Antimicrob Agents Chemother 1990; 34: 2009-12.
-
(1990)
Antimicrob. Agents Chemother.
, vol.34
, pp. 2009-2012
-
-
Loya, S.1
Tal, R.2
Kashman, Y.3
Hizi, A.4
-
184
-
-
0036221012
-
Inhibitory effects of quinones on RNase H activity associated with HIV-1 reverse transcriptase
-
Min BS, Miyashiro H, Hattori M. Inhibitory effects of quinones on RNase H activity associated with HIV-1 reverse transcriptase. Phytother Res 2002; 16: S57-62.
-
(2002)
Phytother. Res.
, vol.16
-
-
Min, B.S.1
Miyashiro, H.2
Hattori, M.3
-
185
-
-
0027956796
-
Synthesis of naphthalenesulfonic acid small molecules as selective inhibitors of the DNA polymerase and ribonuclease H activities of HIV-1 reverse transcriptase
-
Mohan P, Loya S, Avidan O, Verma S, Dhindsa GS, Wong MF, et al. Synthesis of naphthalenesulfonic acid small molecules as selective inhibitors of the DNA polymerase and ribonuclease H activities of HIV-1 reverse transcriptase. J Med Chem 1994; 37: 2513-9.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2513-2519
-
-
Mohan, P.1
Loya, S.2
Avidan, O.3
Verma, S.4
Dhindsa, G.S.5
Wong, M.F.6
-
186
-
-
0031000566
-
Inhibition of the ribonuclease H and DNA polymerase activities of HIV-1 reverse transcriptase by N-(4-tert-butylbenzoyl)-2-hydroxy-1-naphthaldehyde hydrazone
-
Borkow G, Fletcher RS, Barnard J, Arion D, Motakis D, Dmitrienko GI, et al. nhibition of the ribonuclease H and DNA polymerase activities of HIV-1 reverse transcriptase by N-(4-tert-butylbenzoyl)-2-hydroxy-1-naphthaldehyde hydrazone. Biochemistry 1997; 36: 3179-85.
-
(1997)
Biochemistry
, vol.36
, pp. 3179-3185
-
-
Borkow, G.1
Fletcher, R.S.2
Barnard, J.3
Arion, D.4
Motakis, D.5
Dmitrienko, G.I.6
-
187
-
-
0036076157
-
Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors
-
Sluis-Cremer N, Arion D, Parniak MA. Destabilization of the HIV-1 reverse transcriptase dimer upon interaction with N-acyl hydrazone inhibitors. Mol Pharmacol 2002; 62: 398-405.
-
(2002)
Mol. Pharmacol.
, vol.62
, pp. 398-405
-
-
Sluis-Cremer, N.1
Arion, D.2
Parniak, M.A.3
-
188
-
-
0032847978
-
Inhibitors of DNA strand transfer reactions catalyzed by HIV-1 reverse transcriptase
-
Gabbara S, Davis WR, Hupe L, Hupe D, Peliska JA. Inhibitors of DNA strand transfer reactions catalyzed by HIV-1 reverse transcriptase. Biochemistry 1999; 38: 13070-6.
-
(1999)
Biochemistry
, vol.38
, pp. 13070-13076
-
-
Gabbara, S.1
Davis, W.R.2
Hupe, L.3
Hupe, D.4
Peliska, J.A.5
-
189
-
-
0034700290
-
Inhibition of HIV-1 reverse transcriptase-catalyzed DNA strand transfer reactions by 4-chlorophenylhydrazone of mesoxalic acid
-
Davis WR, Tomsho J, Nikam S, Cook EM, Somand D, Peliska JA. Inhibition of HIV-1 reverse transcriptase-catalyzed DNA strand transfer reactions by 4-chlorophenylhydrazone of mesoxalic acid. Biochemistry 2000; 39: 14279-91.
-
(2000)
Biochemistry
, vol.39
, pp. 14279-14291
-
-
Davis, W.R.1
Tomsho, J.2
Nikam, S.3
Cook, E.M.4
Somand, D.5
Peliska, J.A.6
-
190
-
-
0037474193
-
Inhibition of HIV-1 ribonuclease H by a novel diketo acid, 4-[5-(benzoylamino)thien-2-y1]-2, 4-dioxobutanoic acid
-
Shaw-Reid CA, Munshi V, Graham P, Wolfe A, Witmer M, Danzeisen R, et al. Inhibition of HIV-1 ribonuclease H by a novel diketo acid, 4-[5-(benzoylamino)thien-2-y1]-2, 4-dioxobutanoic acid. J Biol Chem 2003; 278: 2777-80.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 2777-2780
-
-
Shaw-Reid, C.A.1
Munshi, V.2
Graham, P.3
Wolfe, A.4
Witmer, M.5
Danzeisen, R.6
-
191
-
-
0028967421
-
The glucocorticoid receptor type II complex is a target of the HIV-1 vpr gene product
-
Refaeli Y, Levy DN, Weiner DB. The glucocorticoid receptor type II complex is a target of the HIV-1 vpr gene product. Proc Natl Acad Sci USA 1995; 92: 362-5.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 362-365
-
-
Refaeli, Y.1
Levy, D.N.2
Weiner, D.B.3
-
192
-
-
0032584088
-
HIV-1 Vpr interacts with a human 34-kDa mov34 homologue, a cellular factor linked to the G2/M phase transition of the mammalian cell cycle
-
Mahalingam S, Ayyavoo V, Patel M, Kieber-Emmons T, Kao GD, Muschel RJ, et al. HIV-1 Vpr interacts with a human 34-kDa mov34 homologue, a cellular factor linked to the G2/M phase transition of the mammalian cell cycle. Proc Natl Acad Sci USA 1998; 95: 3419-24.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 3419-3424
-
-
Mahalingam, S.1
Ayyavoo, V.2
Patel, M.3
Kieber-Emmons, T.4
Kao, G.D.5
Muschel, R.J.6
-
193
-
-
0028239060
-
The Vpr protein of human immunodeficiency virus type 1 influences nuclear localization of viral nucleic acids in nondividing host cells
-
Heinzinger NK, Bukinsky MI, Haggerty SA, Ragland AM, Kewalramani V, Lee MA, et al. The Vpr protein of human immunodeficiency virus type 1 influences nuclear localization of viral nucleic acids in nondividing host cells. Proc Natl Acad Sci USA 1994; 91: 7311-5.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 7311-7315
-
-
Heinzinger, N.K.1
Bukinsky, M.I.2
Haggerty, S.A.3
Ragland, A.M.4
Kewalramani, V.5
Lee, M.A.6
-
194
-
-
0029917395
-
Nuclear import and cell cycle arrest functions of the HIV-1 Vpr protein are encoded by two separate genes in HIV-2/SIV(SM)
-
Fletcher TM 3rd, Brichacek B, Sharova N, Newman MA, Stivahtis G, Sharp PM, et al. Nuclear import and cell cycle arrest functions of the HIV-1 Vpr protein are encoded by two separate genes in HIV-2/SIV(SM). EMBO J 1996; 15: 6155-65.
-
(1996)
EMBO J.
, vol.15
, pp. 6155-6165
-
-
Fletcher III, T.M.1
Brichacek, B.2
Sharova, N.3
Newman, M.A.4
Stivahtis, G.5
Sharp, P.M.6
-
195
-
-
18844468523
-
Viral protein R regulates nuclear import of the HIV-1 pre-integration complex
-
Popov S, Rexach M, Zybarth G, Reding N, Lee MA, Ratner L. et al. Viral protein R regulates nuclear import of the HIV-1 pre-integration complex. EMBO J 1998; 17: 909-17.
-
(1998)
EMBO J.
, vol.17
, pp. 909-917
-
-
Popov, S.1
Rexach, M.2
Zybarth, G.3
Reding, N.4
Lee, M.A.5
Ratner, L.6
-
196
-
-
0037043699
-
Isolation of a human gene that inhibits HIV-1 infection and is suppressed by the viral Vif protein
-
Sheehy AM, Gaddis NC, Choi JD, Malim MH. Isolation of a human gene that inhibits HIV-1 infection and is suppressed by the viral Vif protein. Nature 2002; 418: 646-50.
-
(2002)
Nature
, vol.418
, pp. 646-650
-
-
Sheehy, A.M.1
Gaddis, N.C.2
Choi, J.D.3
Malim, M.H.4
-
197
-
-
0344413641
-
The antiretroviral enzyme APOBEC3G is degraded by the proteasome in response to HIV-1 Vif
-
Sheehy AM, Gaddis NC, Malim MH. The antiretroviral enzyme APOBEC3G is degraded by the proteasome in response to HIV-1 Vif. Nat Med 2003; 9: 1404-7.
-
(2003)
Nat. Med.
, vol.9
, pp. 1404-1407
-
-
Sheehy, A.M.1
Gaddis, N.C.2
Malim, M.H.3
-
198
-
-
0032491180
-
Actinomycin D inhibition of DNA strand transfer reactions catalyzed by HIV-1 reverse transcriptase
-
Davis WR, Gabbara S, Hupe D, Peliska JA. Actinomycin D inhibition of DNA strand transfer reactions catalyzed by HIV-1 reverse transcriptase. Biochemistry 1998; 37: 14213-21.
-
(1998)
Biochemistry
, vol.37
, pp. 14213-14221
-
-
Davis, W.R.1
Gabbara, S.2
Hupe, D.3
Peliska, J.A.4
-
199
-
-
0031926679
-
Actinomycin D inhibits human immunodeficiency virus type 1 minus-strand transfer in in vitro and endogenous reverse transcriptase assays
-
Guo J, Wu T, Bess J, Henderson LE, Levin JG. Actinomycin D inhibits human immunodeficiency virus type 1 minus-strand transfer in in vitro and endogenous reverse transcriptase assays. J Virol 1998; 72: 6716-24.
-
(1998)
J. Virol.
, vol.72
, pp. 6716-6724
-
-
Guo, J.1
Wu, T.2
Bess, J.3
Henderson, L.E.4
Levin, J.G.5
-
201
-
-
0030852009
-
Differential inhibition of cytochrome P450 isoforms by the protease inhibitors, ritonavir, saquinavir and indinavir
-
Eagling VA, Back DJ, Barry MG. Differential inhibition of cytochrome P450 isoforms by the protease inhibitors, ritonavir, saquinavir and indinavir. Br J Clin Pharmacol 1997; 44: 190-4.
-
(1997)
Br. J. Clin. Pharmacol.
, vol.44
, pp. 190-194
-
-
Eagling, V.A.1
Back, D.J.2
Barry, M.G.3
-
202
-
-
0031896882
-
Active apical secretory efflux of the HIV protease inhibitors saquinavir and ritonavir in Caco-2 cell monolayers
-
Alsenz J, Steffen H, Alex R. Active apical secretory efflux of the HIV protease inhibitors saquinavir and ritonavir in Caco-2 cell monolayers. Pharm Res 1998; 15: 423-8.
-
(1998)
Pharm. Res.
, vol.15
, pp. 423-428
-
-
Alsenz, J.1
Steffen, H.2
Alex, R.3
-
203
-
-
0032518290
-
The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors
-
Kim RB, Fromm MF, Wandel C, Leake B, Wood AJ, Roden DM, et al. The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors. J Clin Invest 1998; 101: 289-94.
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 289-294
-
-
Kim, R.B.1
Fromm, M.F.2
Wandel, C.3
Leake, B.4
Wood, A.J.5
Roden, D.M.6
-
204
-
-
0030001001
-
Clinical trials of P-glycoproteiin reversal in solid tumors
-
Ferry DR, Traunecker H, Kerr DJ. Clinical trials of P-glycoproteiin reversal in solid tumors. Eur J Cancer 1996; 32A: 1070-81.
-
(1996)
Eur. J. Cancer
, vol.32 A
, pp. 1070-1081
-
-
Ferry, D.R.1
Traunecker, H.2
Kerr, D.J.3
-
205
-
-
0029939665
-
Experimental reversal of P-glycoprotein-mediated multidrug resistance by pharmacological chemo sensitisers
-
Ford JM. Experimental reversal of P-glycoprotein-mediated multidrug resistance by pharmacological chemo sensitisers. Fur J Cancer 1996; 32: 991-1001.
-
(1996)
Eur. J. Cancer
, vol.32
, pp. 991-1001
-
-
Ford, J.M.1
-
206
-
-
0036104758
-
Non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors: Past, present, and future perspectives
-
Campiani G, Ramunno A, Maga G, Nacci V, Fattorusso C, Catalanotti B, et al. Non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors: past, present, and future perspectives. Curr Pharm Design 2002; 8(8): 615-57.
-
(2002)
Curr. Pharm. Design
, vol.8
, Issue.8
, pp. 615-657
-
-
Campiani, G.1
Ramunno, A.2
Maga, G.3
Nacci, V.4
Fattorusso, C.5
Catalanotti, B.6
-
207
-
-
0036231063
-
Trends in the design of nucleoside analogues as anti-HIV drugs
-
el Kouni MH. Trends in the design of nucleoside analogues as anti-HIV drugs. Curr Pharm Design 2002; 8(8): 581-93.
-
(2002)
Curr. Pharm. Design
, vol.8
, Issue.8
, pp. 581-593
-
-
el Kouni, M.H.1
-
208
-
-
0036223082
-
Inhibitors of HIV-1 reverse transcriptase and integrase: Classical and emerging therapeutical approaches
-
Tarrago-Litvak L, Andreola ML, Fournier M, Nevinsky GA, Parissi V, de Soultrait VR, et al. Inhibitors of HIV-1 reverse transcriptase and integrase: classical and emerging therapeutical approaches. Curr Pharm Design 2002; 8(8): 595-614.
-
(2002)
Curr. Pharm. Design
, vol.8
, Issue.8
, pp. 595-614
-
-
Tarrago-Litvak, L.1
Andreola, M.L.2
Fournier, M.3
Nevinsky, G.A.4
Parissi, V.5
de Soultrait, V.R.6
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