-
1
-
-
0022495870
-
Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone
-
Adachi, A., et al. 1986. Production of acquired immunodeficiency syndrome-ssociated retrovirus in human and nonhuman cells transfected with an infectious molecular clone. J. Virol. 59:284-291. (Pubitemid 16013975)
-
(1986)
Journal of Virology
, vol.59
, Issue.2
, pp. 284-291
-
-
Adachi, A.1
Gendelman, H.E.2
Koenig, S.3
-
2
-
-
0035037383
-
Genotypic correlates of phenotypic resistance to efavirenz in virus isolates from patients failing nonnucleoside reverse transcriptase inhibitor therapy
-
Bacheler, L., et al. 2001. Genotypic correlates of phenotypic resistance to efavirenz in virus isolates from patients failing nonnucleoside reverse transcriptase inhibitor therapy. J. Virol. 75:4999-5008.
-
(2001)
J. Virol.
, vol.75
, pp. 4999-5008
-
-
Bacheler, L.1
-
3
-
-
0033840455
-
Human immunodeficiency virus type 1 mutations selected in patients failing efavirenz combination therapy
-
Bacheler, L. T., et al. 2000. Human immunodeficiency virus type 1 mutations selected in patients failing efavirenz combination therapy. Antimicrob. Agents Chemother. 44:2475-2484.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, pp. 2475-2484
-
-
Bacheler, L.T.1
-
4
-
-
0037303182
-
S-1360 Shionogi-GlaxoSmithKline
-
Billich, A. 2003. S-1360 Shionogi-GlaxoSmithKline. Curr. Opin. Investig. Drugs 4:206-209.
-
(2003)
Curr. Opin. Investig. Drugs
, vol.4
, pp. 206-209
-
-
Billich, A.1
-
5
-
-
33748774971
-
Synthesis and HIV-integrase strand transfer inhibition activity of 7-hydroxy[1,3]thiazolo[5,4-b]pyridin-5(4H)-ones
-
Boros, E. E., B. A. Johns, E. P. Garvey, C. S. Koble, and W. H. Miller. 2006. Synthesis and HIV-integrase strand transfer inhibition activity of 7-hydroxy[1,3]thiazolo[5,4-b]pyridin-5(4H)-ones. Bioorg. Med. Chem. Lett. 16:5668-5672.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 5668-5672
-
-
Boros, E.E.1
Johns, B.A.2
Garvey, E.P.3
Koble, C.S.4
Miller, W.H.5
-
6
-
-
0027373308
-
High-level resistance to (-) enantiomeric 2′-deoxy-3′- thiacytidine in vitro is due to one amino acid substitution in the catalytic site of human immunodeficiency virus type 1 reverse transcriptase
-
Boucher, C. A., et al. 1993. High-level resistance to (-) enantiomeric 2′-deoxy-3′-thiacytidine in vitro is due to one amino acid substitution in the catalytic site of human immunodeficiency virus type 1 reverse transcriptase. Antimicrob. Agents Chemother. 37:2231-2234.
-
(1993)
Antimicrob. Agents Chemother.
, vol.37
, pp. 2231-2234
-
-
Boucher, C.A.1
-
7
-
-
0030004944
-
Effects of zidovudine-selected human immunodeficiency virus type 1 reverse transcriptase amino acid substitutions on processive DNA synthesis and viral replication
-
Caliendo, A. M., et al. 1996. Effects of zidovudine-selected human immunodeficiency virus type 1 reverse transcriptase amino acid substitutions on processive DNA synthesis and viral replication. J. Virol. 70:2146-2153.
-
(1996)
J. Virol.
, vol.70
, pp. 2146-2153
-
-
Caliendo, A.M.1
-
8
-
-
65549085822
-
Characterization and structural analysis of HIV-1 integrase conservation
-
Ceccherini-Silberstein, F., et al. 2009. Characterization and structural analysis of HIV-1 integrase conservation. AIDS Rev. 11:17-29.
-
(2009)
AIDS Rev.
, vol.11
, pp. 17-29
-
-
Ceccherini-Silberstein, F.1
-
9
-
-
0030899871
-
Human immunodeficiency virus type 1 coreceptors participate in postentry stages in the virus replication cycle and function in simian immunodeficiency virus infection
-
Chackerian, B., E. M. Long, P. A. Luciw, and J. Overbaugh. 1997. Human immunodeficiency virus type 1 coreceptors participate in postentry stages in the virus replication cycle and function in simian immunodeficiency virus infection. J. Virol. 71:3932-3939.
-
(1997)
J. Virol.
, vol.71
, pp. 3932-3939
-
-
Chackerian, B.1
Long, E.M.2
Luciw, P.A.3
Overbaugh, J.4
-
10
-
-
78349311194
-
In-vitro phenotypic susceptibility of HIV-2 clinical isolates to the integrase inhibitor S/GSK1349572
-
Charpentier, C., et al. 2010. In-vitro phenotypic susceptibility of HIV-2 clinical isolates to the integrase inhibitor S/GSK1349572. AIDS 24:2753-2755.
-
(2010)
AIDS
, vol.24
, pp. 2753-2755
-
-
Charpentier, C.1
-
11
-
-
47949114939
-
Subgroup and resistance analyses of raltegravir for resistant HIV-1 infection
-
Cooper, D. A., et al. 2008. Subgroup and resistance analyses of raltegravir for resistant HIV-1 infection. N. Engl. J. Med. 359:355-365.
-
(2008)
N. Engl. J. Med.
, vol.359
, pp. 355-365
-
-
Cooper, D.A.1
-
12
-
-
0028283770
-
5-Chloro-2′,3′-dideoxy-3′-fluorouridine (935U83), a selective anti-human immunodeficiency virus agent with an improved metabolic and toxicological profile
-
Daluge, S. M., et al. 1994. 5-Chloro-2′,3′-dideoxy-3′- fluorouridine (935U83), a selective anti-human immunodeficiency virus agent with an improved metabolic and toxicological profile. Antimicrob. Agents Chemother. 38:1590-1603.
-
(1994)
Antimicrob. Agents Chemother.
, vol.38
, pp. 1590-1603
-
-
Daluge, S.M.1
-
13
-
-
33748113778
-
Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatmentnaive and treatment- experienced patients
-
DeJesus, E., et al. 2006. Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatmentnaive and treatment-experienced patients. J. Acquir. Immune Defic. Syndr. 43:1-5.
-
(2006)
J. Acquir. Immune Defic. Syndr.
, vol.43
, pp. 1-5
-
-
DeJesus, E.1
-
14
-
-
33846916481
-
A potent and orally active HIV-1 integrase inhibitor
-
Egbertson, M. S., et al. 2007. A potent and orally active HIV-1 integrase inhibitor. Bioorg. Med. Chem. Lett. 17:1392-1398.
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 1392-1398
-
-
Egbertson, M.S.1
-
15
-
-
40549145842
-
The naphthyridinone GSK364735 is a novel, potent human immunodeficiency virus type 1 integrase inhibitor and antiretroviral
-
Garvey, E. P., et al. 2008. The naphthyridinone GSK364735 is a novel, potent human immunodeficiency virus type 1 integrase inhibitor and antiretroviral. Antimicrob. Agents Chemother. 52:901-908.
-
(2008)
Antimicrob. Agents Chemother.
, vol.52
, pp. 901-908
-
-
Garvey, E.P.1
-
16
-
-
0022404296
-
Infection of HTLV-III/LAV in HTLV-I-carrying cells MT-2 and MT-4 and application in a plaque assay
-
Harada, S., Y. Koyanagi, and N. Yamamoto. 1985. Infection of HTLV-III/LAV in HTLV-I-carrying cells MT-2 and MT-4 and application in a plaque assay. Science 229:563-566. (Pubitemid 16239336)
-
(1985)
Science
, vol.229
, Issue.4713
, pp. 563-566
-
-
Harada, S.1
Koyanagi, Y.2
Yamamoto, N.3
-
17
-
-
0034723439
-
Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells
-
Hazuda, D. J., et al. 2000. Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells. Science 287:646-650.
-
(2000)
Science
, vol.287
, pp. 646-650
-
-
Hazuda, D.J.1
-
18
-
-
35648950291
-
Resistance to the HIV-integrase inhibitor raltegravir: Analysis of protocol 005, a phase 2 study in patients with triple-class resistant HIV-1 infection
-
Hazuda, D. J., M. D. Miller, B. Y. Nguyen, and J. Zhao. 2007. Resistance to the HIV-integrase inhibitor raltegravir: analysis of protocol 005, a phase 2 study in patients with triple-class resistant HIV-1 infection. XVI Int. HIV Drug Resist. Workshop, Barbados, West Indies. http://www.natap.org/2007/ResisWksp/ ResisWksp-37.htm.
-
(2007)
XVI Int. HIV Drug Resist. Workshop, Barbados, West Indies
-
-
Hazuda, D.J.1
Miller, M.D.2
Nguyen, B.Y.3
Zhao, J.4
-
19
-
-
0030957788
-
Effects of drugs on 2′,3′-dideoxy-2′,3′- didehydrothymidine phosphorylation in vitro
-
Hoggard, P. G., S. Kewn, M. G. Barry, S. H. Khoo, and D. J. Back. 1997. Effects of drugs on 2′,3′-dideoxy-2′,3′- didehydrothymidine phosphorylation in vitro. Antimicrob. Agents Chemother. 41:1231-1236.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1231-1236
-
-
Hoggard, P.G.1
Kewn, S.2
Barry, M.G.3
Khoo, S.H.4
Back, D.J.5
-
20
-
-
0033544335
-
Small amino acid changes in the V3 loop of human immunodeficiency virus type 2 determines the coreceptor usage for CXCR4 and CCR5
-
Isaka, Y., et al. 1999. Small amino acid changes in the V3 loop of human immunodeficiency virus type 2 determines the coreceptor usage for CXCR4 and CCR5. Virology 264:237-243.
-
(1999)
Virology
, vol.264
, pp. 237-243
-
-
Isaka, Y.1
-
21
-
-
0034977702
-
Phenotypic analysis of the sensitivity of HIV-1 to inhibitors of the reverse transcriptase, protease, and integrase using a self-inactivating virus vector system
-
Jármy, G., M. Heinkelein, B. Weissbrich, C. Jassoy, and A. Rethwilm. 2001. Phenotypic analysis of the sensitivity of HIV-1 to inhibitors of the reverse transcriptase, protease, and integrase using a self-inactivating virus vector system. J. Med. Virol. 64:223-231.
-
(2001)
J. Med. Virol.
, vol.64
, pp. 223-231
-
-
Jármy, G.1
Heinkelein, M.2
Weissbrich, B.3
Jassoy, C.4
Rethwilm, A.5
-
22
-
-
62949153971
-
Preclinical evaluation of GS-9160, a novel inhibitor of human immunodeficiency virus type 1 integrase
-
Jones, G. S., et al. 2009. Preclinical evaluation of GS-9160, a novel inhibitor of human immunodeficiency virus type 1 integrase. Antimicrob. Agents Chemother. 53:1194-1203.
-
(2009)
Antimicrob. Agents Chemother.
, vol.53
, pp. 1194-1203
-
-
Jones, G.S.1
-
23
-
-
0034909925
-
Identification of genotypic changes in human immunodeficiency virus protease that correlate with reduced susceptibility to the protease inhibitor lopinavir among viral isolates from protease inhibitor-experienced patients
-
Kempf, D. J., et al. 2001. Identification of genotypic changes in human immunodeficiency virus protease that correlate with reduced susceptibility to the protease inhibitor lopinavir among viral isolates from protease inhibitor-experienced patients. J. Virol. 75:7462-7469.
-
(2001)
J. Virol.
, vol.75
, pp. 7462-7469
-
-
Kempf, D.J.1
-
24
-
-
53249087908
-
Selection of diverse and clinically relevant integrase inhibitor-resistant human immunodeficiency virus type 1 mutants
-
Kobayashi, M., et al. 2008. Selection of diverse and clinically relevant integrase inhibitor-resistant human immunodeficiency virus type 1 mutants. Antiviral Res. 80:213-222.
-
(2008)
Antiviral Res.
, vol.80
, pp. 213-222
-
-
Kobayashi, M.1
-
25
-
-
70350166248
-
Potent antiviral activity of S/GSK1349572, a next generation integrase inhibitor (INI), in INI-naïve HIV-1-infected patients
-
abstr. TUAB105
-
Lalezari, J., et al. 2009. Potent antiviral activity of S/GSK1349572, a next generation integrase inhibitor (INI), in INI-naïve HIV-1-infected patients, abstr. TUAB105. Fifth Int. AIDS Soc. Conf. HIV Pathogenesis, Treatment and Prevention, Cape Town, South Africa.
-
(2009)
Fifth Int. AIDS Soc. Conf. HIV Pathogenesis, Treatment and Prevention, Cape Town, South Africa
-
-
Lalezari, J.1
-
26
-
-
34447263572
-
Natural polymorphism of the HIV-1 integrase gene and mutations associated with integrase inhibitor resistance
-
Lataillade, M., J. Chiarella, and M. J. Kozal. 2007. Natural polymorphism of the HIV-1 integrase gene and mutations associated with integrase inhibitor resistance. Antivir. Ther. 12:563-570.
-
(2007)
Antivir. Ther.
, vol.12
, pp. 563-570
-
-
Lataillade, M.1
Chiarella, J.2
Kozal, M.J.3
-
27
-
-
79953184825
-
Elvitegravir (GS-9137/JTK-303), an HIV-1 integrase inhibitor, has additive to synergistic interactions with other antiretroviral drugs in vitro
-
abstr. MOPEA052
-
Ledford, R., N. Margot, M. Miller, and D. McColl. 2007. Elvitegravir (GS-9137/JTK-303), an HIV-1 integrase inhibitor, has additive to synergistic interactions with other antiretroviral drugs in vitro, abstr. MOPEA052. Fourth Int. AIDS Soc. Conf. HIV Pathogenesis, Treatment and Prevention, Sydney, Australia. http://www.ias2007.org/pag/Abstracts.aspx?SID=153&AID=4041.
-
(2007)
Fourth Int. AIDS Soc. Conf. HIV Pathogenesis, Treatment and Prevention, Sydney, Australia
-
-
Ledford, R.1
Margot, N.2
Miller, M.3
McColl, D.4
-
28
-
-
62549166235
-
Quasispecies variant dynamics during emergence of resistance to raltegravir in HIV-1-infected patients
-
Malet, I., et al. 2009. Quasispecies variant dynamics during emergence of resistance to raltegravir in HIV-1-infected patients. J. Antimicrob. Chemother. 63:795-804.
-
(2009)
J. Antimicrob. Chemother.
, vol.63
, pp. 795-804
-
-
Malet, I.1
-
29
-
-
51549116289
-
Comparison of raltegravir and elvitegravir on HIV-1 integrase catalytic reactions and on a series of drug-resistant integrase mutants
-
Marinello, J., et al. 2008. Comparison of raltegravir and elvitegravir on HIV-1 integrase catalytic reactions and on a series of drug-resistant integrase mutants. Biochemistry 47:9345-9354.
-
(2008)
Biochemistry
, vol.47
, pp. 9345-9354
-
-
Marinello, J.1
-
30
-
-
35349021681
-
Rapid onset and durable antiretroviral effect of raltegravir (MK-0518), a novel HIV-1 integrase inhibitor, as part of combination ART in treatment of HIV-1 infected patients: 48-week data
-
abstr. TUPAB104
-
Markowitz, M., et al. 2007. Rapid onset and durable antiretroviral effect of raltegravir (MK-0518), a novel HIV-1 integrase inhibitor, as part of combination ART in treatment of HIV-1 infected patients: 48-week data, abstr. TUPAB104. Fourth Int. AIDS Soc. Conf. HIV Pathogenesis, Treatment and Prevention, Sydney, Australia. http://www.ias2007.org/pag/Abstracts.aspx?SID= 48&AID=3027.
-
(2007)
Fourth Int. AIDS Soc. Conf. HIV Pathogenesis, Treatment and Prevention, Sydney, Australia
-
-
Markowitz, M.1
-
31
-
-
33845366857
-
Antiretroviral activity, pharmacokinetics, and tolerability of MK-0518, a novel inhibitor of HIV-1 integrase, dosed as monotherapy for 10 days in treatment-naive HIV-1-infected individuals
-
Markowitz, M., et al. 2006. Antiretroviral activity, pharmacokinetics, and tolerability of MK-0518, a novel inhibitor of HIV-1 integrase, dosed as monotherapy for 10 days in treatment-naive HIV-1-infected individuals. J. Acquir. Immune Defic. Syndr. 43:509-515.
-
(2006)
J. Acquir. Immune Defic. Syndr.
, vol.43
, pp. 509-515
-
-
Markowitz, M.1
-
32
-
-
35648940077
-
Resistance and cross-resistance to first generation integrase inhibitors: Insights from a phase 2 study of elvitegravir (GS-9137)
-
abstr. 9
-
McColl, D. J., et al. 2007. Resistance and cross-resistance to first generation integrase inhibitors: insights from a phase 2 study of elvitegravir (GS-9137), abstr. 9. XVI Int. HIV Drug Resist. Workshop, Bridgetown, Barbados. http://www.natap.org/2007/ResisWksp/ResisWksp-43.htm.
-
(2007)
XVI Int. HIV Drug Resist. Workshop, Bridgetown, Barbados
-
-
McColl, D.J.1
-
33
-
-
73849124557
-
Pharmacokinetics and safety of S/GSK1349572, a nextgeneration HIV integrase inhibitor, in healthy volunteers
-
Min, S., et al. 2010. Pharmacokinetics and safety of S/GSK1349572, a nextgeneration HIV integrase inhibitor, in healthy volunteers. Antimicrob. Agents Chemother. 54:254-258.
-
(2010)
Antimicrob. Agents Chemother.
, vol.54
, pp. 254-258
-
-
Min, S.1
-
34
-
-
58149459588
-
Secondary mutations in viruses resistant to HIV-1 integrase inhibitors that restore viral infectivity and replication kinetics
-
Nakahara, K., et al. 2009. Secondary mutations in viruses resistant to HIV-1 integrase inhibitors that restore viral infectivity and replication kinetics. Antiviral Res. 81:141-146.
-
(2009)
Antiviral Res.
, vol.81
, pp. 141-146
-
-
Nakahara, K.1
-
35
-
-
0033022106
-
Highly drug-resistant HIV-1 clinical isolates are cross-resistant to many antiretroviral compounds in current clinical development
-
Palmer, S., R. W. Shafer, and T. C. Merigan. 1999. Highly drug-resistant HIV-1 clinical isolates are cross-resistant to many antiretroviral compounds in current clinical development. AIDS 13:661-667.
-
(1999)
AIDS
, vol.13
, pp. 661-667
-
-
Palmer, S.1
Shafer, R.W.2
Merigan, T.C.3
-
36
-
-
0029092503
-
In vitro selection and characterization of human immunodeficiency virus type 1 (HIV-1) isolates with reduced sensitivity to hydroxyethylamino sulfonamide inhibitors of HIV-1 aspartyl protease
-
Partaledis, J. A., et al. 1995. In vitro selection and characterization of human immunodeficiency virus type 1 (HIV-1) isolates with reduced sensitivity to hydroxyethylamino sulfonamide inhibitors of HIV-1 aspartyl protease. J. Virol. 69:5228-5235.
-
(1995)
J. Virol.
, vol.69
, pp. 5228-5235
-
-
Partaledis, J.A.1
-
37
-
-
0024993530
-
A three-dimensional model to analyze drug-drug interactions
-
Prichard, M. N., and C. Shipman, Jr. 1990. A three-dimensional model to analyze drug-drug interactions. Antiviral Res. 14:181-205.
-
(1990)
Antiviral Res.
, vol.14
, pp. 181-205
-
-
Prichard, M.N.1
Shipman Jr., C.2
-
38
-
-
77951225696
-
Integrase inhibitors: Why do we need a new drug class for HIV therapy?
-
Rockstroh, J. K. 2009. Integrase inhibitors: why do we need a new drug class for HIV therapy? Eur. J. Med. Res. 14(Suppl. 3):1-3.
-
(2009)
Eur. J. Med. Res.
, vol.14
, Issue.SUPPL. 3
, pp. 1-3
-
-
Rockstroh, J.K.1
-
39
-
-
0037378801
-
Interactions of 1263W94 with other antiviral agents in inhibition of human cytomegalovirus replication
-
Selleseth, D. W., et al. 2003. Interactions of 1263W94 with other antiviral agents in inhibition of human cytomegalovirus replication. Antimicrob. Agents Chemother. 47:1468-1471.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 1468-1471
-
-
Selleseth, D.W.1
-
40
-
-
0027285372
-
Rapid in vitro selection of human immunodeficiency virus type 1 resistant to 3′-thiacytidine inhibitors due to a mutation in the YMDD region of reverse transcriptase
-
Tisdale, M., S. D. Kemp, N. R. Parry, and B. A. Larder. 1993. 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. U. S. A. 90:5653-5656.
-
(1993)
Proc. Natl. Acad. Sci. U. S. A.
, vol.90
, pp. 5653-5656
-
-
Tisdale, M.1
Kemp, S.D.2
Parry, N.R.3
Larder, B.A.4
-
41
-
-
0022039941
-
Testing the statistical certainty of a response to increasing doses of a drug
-
Tukey, J. W., J. L. Ciminera, and J. F. Heyse. 1985. Testing the statistical certainty of a response to increasing doses of a drug. Biometrics 41:295-301.
-
(1985)
Biometrics
, vol.41
, pp. 295-301
-
-
Tukey, J.W.1
Ciminera, J.L.2
Heyse, J.F.3
-
42
-
-
73549088975
-
S/GSK1349572: A next generation integrase inhibitor with activity against integrase inhibitor-resistant clinical isolates from patients experiencing virologic failure while on raltegravir therapy
-
abstr. WEPEA098
-
Underwood, M., B. Johns, A. Sato, T. Fujiwara, and W. Spreen. 2009. S/GSK1349572: a next generation integrase inhibitor with activity against integrase inhibitor-resistant clinical isolates from patients experiencing virologic failure while on raltegravir therapy, abstr. WEPEA098. Fifth Int. AIDS Soc. Conf. HIV Pathogenesis, Treatment and Prevention, Cape Town, South Africa. http://www.ias2009.org/pag/PDF/2051.pdf.
-
(2009)
Fifth Int. AIDS Soc. Conf. HIV Pathogenesis, Treatment and Prevention, Cape Town, South Africa
-
-
Underwood, M.1
Johns, B.2
Sato, A.3
Fujiwara, T.4
Spreen, W.5
-
43
-
-
34248199833
-
The HIV integrase inhibitor GS-9137 demonstrates potent antiretroviral activity in treatment-experienced patients
-
abstr. 143LB
-
Zolopa, A. R., et al. 2007. The HIV integrase inhibitor GS-9137 demonstrates potent antiretroviral activity in treatment-experienced patients, abstr. 143LB. Fourteenth Conf. Retrovir. Opportunistic Infect., Los Angeles, CA. http://www.retroconference.org/2007/Abstracts/30571.htm.
-
(2007)
Fourteenth Conf. Retrovir. Opportunistic Infect., Los Angeles, CA
-
-
Zolopa, A.R.1
|