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A drug resistance mutation in the inhibitor binding pocket of human immunodeficiency virus type 1 reverse transcriptase impairs DNA synthesis and RNA degradation. [electronic resource] by
- Fan, N
- Rank, K B
- Slade, D E
- Poppe, S M
- Evans, D B
- Kopta, L A
- Olmsted, R A
- Thomas, R C
- Tarpley, W G
- Sharma, S K
Producer: 19960910
In:
Biochemistry vol. 35
Availability: No items available.
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Antiviral activity of the dihydropyrone PNU-140690, a new nonpeptidic human immunodeficiency virus protease inhibitor. [electronic resource] by
- Poppe, S M
- Slade, D E
- Chong, K T
- Hinshaw, R R
- Pagano, P J
- Markowitz, M
- Ho, D D
- Mo, H
- Gorman, R R
- Dueweke, T J
- Thaisrivongs, S
- Tarpley, W G
Producer: 19970821
In:
Antimicrobial agents and chemotherapy vol. 41
Availability: No items available.
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7.
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(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes. [electronic resource] by
- Olmsted, R A
- Slade, D E
- Kopta, L A
- Poppe, S M
- Poel, T J
- Newport, S W
- Rank, K B
- Biles, C
- Morge, R A
- Dueweke, T J
- Yagi, Y
- Romero, D L
- Thomas, R C
- Sharma, S K
- Tarpley, W G
Producer: 19960723
In:
Journal of virology vol. 70
Availability: No items available.
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8.
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Structure-based design of HIV protease inhibitors: sulfonamide-containing 5,6-dihydro-4-hydroxy-2-pyrones as non-peptidic inhibitors. [electronic resource] by
- Thaisrivongs, S
- Skulnick, H I
- Turner, S R
- Strohbach, J W
- Tommasi, R A
- Johnson, P D
- Aristoff, P A
- Judge, T M
- Gammill, R B
- Morris, J K
- Romines, K R
- Chrusciel, R A
- Hinshaw, R R
- Chong, K T
- Tarpley, W G
- Poppe, S M
- Slade, D E
- Lynn, J C
- Horng, M M
- Tomich, P K
- Seest, E P
- Dolak, L A
- Howe, W J
- Howard, G M
- Watenpaugh, K D
Producer: 19961210
In:
Journal of medicinal chemistry vol. 39
Availability: No items available.
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