메뉴 건너뛰기




Volumn 55, Issue 2, 2011, Pages 813-821

In vitro antiretroviral properties of S/GSK1349572, a next-generation HIV integrase inhibitor

Author keywords

[No Author keywords available]

Indexed keywords

ABACAVIR; ADEFOVIR; AMPRENAVIR; ANTIRETROVIRUS AGENT; EFAVIRENZ; ELVITEGRAVIR; ENFUVIRTIDE; INTEGRASE INHIBITOR; LAMIVUDINE; LOPINAVIR; MARAVIROC; NEVIRAPINE; RALTEGRAVIR; S GSK 1349572; STAVUDINE; UNCLASSIFIED DRUG;

EID: 78751697293     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.01209-10     Document Type: Article
Times cited : (354)

References (43)
  • 1
    • 0022495870 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 26
    • 34447263572 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.