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Results: 1-25 | 26-32 |
Results: 26-32/32
TREATMENT OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1)-INFECTED CELLS WITH COMBINATIONS OF HIV-1-SPECIFIC INHIBITORS RESULTS IN A DIFFERENT RESISTANCE PATTERN THAN DOES TREATMENT WITH SINGLE-DRUG THERAPY
Authors: BALZARINI J KARLSSON A PEREZPEREZ MJ CAMARASA MJ TARPLEY WG DECLERCQ E
Citation: J. Balzarini et al., TREATMENT OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1)-INFECTED CELLS WITH COMBINATIONS OF HIV-1-SPECIFIC INHIBITORS RESULTS IN A DIFFERENT RESISTANCE PATTERN THAN DOES TREATMENT WITH SINGLE-DRUG THERAPY, Journal of virology, 67(9), 1993, pp. 5353-5359
INHIBITORS OF THE PROTEASE FROM HUMAN-IMMUNODEFICIENCY-VIRUS - SYNTHESIS, ENZYME-INHIBITION, AND ANTIVIRAL ACTIVITY OF A SERIES OF COMPOUNDS CONTAINING THE DIHYDROXYETHYLENE TRANSITION-STATE ISOSTERE
Authors: THAISRIVONGS S TURNER SR STROHBACH JW TENBRINK RE TARPLEY WG MCQUADE TJ HEINRIKSON RL TOMASSELLI AG HUI JO HOWE WJ
Citation: S. Thaisrivongs et al., INHIBITORS OF THE PROTEASE FROM HUMAN-IMMUNODEFICIENCY-VIRUS - SYNTHESIS, ENZYME-INHIBITION, AND ANTIVIRAL ACTIVITY OF A SERIES OF COMPOUNDS CONTAINING THE DIHYDROXYETHYLENE TRANSITION-STATE ISOSTERE, Journal of medicinal chemistry, 36(8), 1993, pp. 941-952
BIS(HETEROARYL)PIPERAZINE (BHAP) REVERSE-TRANSCRIPTASE INHIBITORS - STRUCTURE-ACTIVITY-RELATIONSHIPS OF NOVEL SUBSTITUTED INDOLE ANALOGS AND THE IDENTIFICATION OF ]-4-[3-[(1-METHYLETHYL)AMINO]-PYRIDINYL]PIPERAZINE MONOMETHANESULFONATE (U-90152S), A 2ND-GENERATION CLINICAL CANDIDATE
Authors: ROMERO DL MORGE RA GENIN MJ BILES C BUSSO M RESNICK L ALTHAUS IW REUSSER F THOMAS RC TARPLEY WG
Citation: Dl. Romero et al., BIS(HETEROARYL)PIPERAZINE (BHAP) REVERSE-TRANSCRIPTASE INHIBITORS - STRUCTURE-ACTIVITY-RELATIONSHIPS OF NOVEL SUBSTITUTED INDOLE ANALOGS AND THE IDENTIFICATION OF ]-4-[3-[(1-METHYLETHYL)AMINO]-PYRIDINYL]PIPERAZINE MONOMETHANESULFONATE (U-90152S), A 2ND-GENERATION CLINICAL CANDIDATE, Journal of medicinal chemistry, 36(10), 1993, pp. 1505-1508
INHIBITION OF THE PROTEASE OF HUMAN-IMMUNODEFICIENCY-VIRUS BLOCKS REPLICATION AND INFECTIVITY OF THE VIRUS IN CHRONICALLY INFECTED MACROPHAGES
Authors: PERNO CF BERGAMINI A PESCE CD MILANESE G CAPOZZI M AQUARO S THAISRIVONGS S TARPLEY WG ZON G DAGOSTINI C ROCCHI G GARACI E CALIO R
Citation: Cf. Perno et al., INHIBITION OF THE PROTEASE OF HUMAN-IMMUNODEFICIENCY-VIRUS BLOCKS REPLICATION AND INFECTIVITY OF THE VIRUS IN CHRONICALLY INFECTED MACROPHAGES, The Journal of infectious diseases, 168(5), 1993, pp. 1148-1156
INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPLICATION IN-VITRO BY THE BISHETEROARYLPIPERZINE ATEVIRDINE (U-87201E) IN COMBINATION WITH ZIDOVUDINE OR DIDANOSINE
Authors: CAMPBELL TB YOUNG RK ERON JJ DAQUILA RT TARPLEY WG KURITZKES DR
Citation: Tb. Campbell et al., INHIBITION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REPLICATION IN-VITRO BY THE BISHETEROARYLPIPERZINE ATEVIRDINE (U-87201E) IN COMBINATION WITH ZIDOVUDINE OR DIDANOSINE, The Journal of infectious diseases, 168(2), 1993, pp. 318-326
THE QUINOLINE U-78036 IS A POTENT INHIBITOR OF HIV-1 REVERSE-TRANSCRIPTASE
Authors: ALTHAUS IW GONZALES AJ CHOU JJ ROMERO DL DEIBEL MR CHOU KC KEZDY FJ RESNICK L BUSSO ME SO AG DOWNEY KM THOMAS RC ARISTOFF PA TARPLEY WG REUSSER F
Citation: Iw. Althaus et al., THE QUINOLINE U-78036 IS A POTENT INHIBITOR OF HIV-1 REVERSE-TRANSCRIPTASE, The Journal of biological chemistry, 268(20), 1993, pp. 4875-4880
KINETIC-STUDIES WITH THE NONNUCLEOSIDE HIV-1 REVERSE-TRANSCRIPTASE INHIBITOR-U-88204E
Authors: ALTHAUS IW CHOU JJ GONZALES AJ DEIBEL MR CHOU KC KEZDY FJ ROMERO DL PALMER JR THOMAS RC ARISTOFF PA TARPLEY WG REUSSER F
Citation: Iw. Althaus et al., KINETIC-STUDIES WITH THE NONNUCLEOSIDE HIV-1 REVERSE-TRANSCRIPTASE INHIBITOR-U-88204E, Biochemistry, 32(26), 1993, pp. 6548-6554
Risultati: 1-25 | 26-32 |