Zobrazeno 1 - 10
of 10
pro vyhledávání: '"T. J. Dueweke"'
Autor:
D D Ho, P J Pagano, K T Chong, W. G. Tarpley, T J Dueweke, D E Slade, rd R R Gorman, S M Poppe, M Markowitz, S Thaisrivongs, R. R. Hinshaw, H Mo
Publikováno v:
Antimicrobial Agents and Chemotherapy. 41:1058-1063
PNU-140690 is a member of a new class of nonpeptidic human immunodeficiency virus (HIV) protease inhibitors (sulfonamide-containing 5,6-dihydro-4-hydroxy-2-pyrones) discovered by structure-based design. PNU-140690 has excellent potency against a vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df736ec299e4d25ad33f97274f0768a6
https://doi.org/10.1128/aac.41.5.1058
https://doi.org/10.1128/aac.41.5.1058
Autor:
T J Poel, Richard C. Thomas, K B Rank, R A Morge, S W Newport, Y Yagi, C Biles, T J Dueweke, D. L. Romero, R A Olmsted, L A Kopta, S K Sharma, D E Slade, W. G. Tarpley, S M Poppe
Publikováno v:
Journal of Virology. 70:3698-3705
The (alkylamino)piperidine bis(heteroaryl)piperizines (AAP-BHAPs) are a new class of human immunodeficiency virus type 1 (HIV-1)-specific inhibitors which were identified by targeted screening of recombinant reverse transcriptase (RT) enzymes carryin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::612cc6a32e010235b307f7e0c1f8b224
https://doi.org/10.1128/jvi.70.6.3698-3705.1996
https://doi.org/10.1128/jvi.70.6.3698-3705.1996
Autor:
K. W. Nuorala, K. S. Krieger, S. M. Poppe, D. J. Crampton, K. A. Re, R. K. Patel, T. J. Dueweke, W. G. Tarpley, L. K. Wathen
Publikováno v:
Journal of Clinical Laboratory Analysis. 10:262-268
A quantitative human immunodeficiency virus type 1 (HIV-1) RNA polymerase chain reaction assay has been validated analytically and clinically in > 13,000 samples. The assay is highly reproducible with intra- and inter-assay precision of 16% and 19%,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d8c87803009d644b6efb65b9c80ac94
https://doi.org/10.1002/(sici)1098-2825(1996)10:5<262::aid-jcla6>3.0.co
https://doi.org/10.1002/(sici)1098-2825(1996)10:5<262::aid-jcla6>3.0.co
Autor:
Mariano Busso, Donna Lee Romero, T J Dueweke, Kathleen M. Downey, S. M. Swaney, Lionel Resnick, S M Poppe, Fritz Reusser, Antero G. So, Irene W. Althaus
Publikováno v:
Antimicrobial Agents and Chemotherapy. 37:1127-1131
Bisheteroarylpiperazines are potent inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT). We describe a novel bisheteroarylpiperazine, U-90152 [1-(5-methanesulfonamido-1H-indol-2-yl-carbonyl)-4-[3-(1-methyl eth yl-amin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5071316058796b443c9e591414b0d9af
https://doi.org/10.1128/aac.37.5.1127
https://doi.org/10.1128/aac.37.5.1127
Publikováno v:
Journal of Biological Chemistry. 267:27-30
The bisheteroarylpiperazines (BHAPs) are potent inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) and specifically block HIV-1 replication (Romero, D. L., Busso, M., Tan, C.-K., Reusser, F., Palmer, J. R., Poppe, S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::671bb9be8aca97a8a014c4533e619044
https://doi.org/10.1016/s0021-9258(18)48451-7
https://doi.org/10.1016/s0021-9258(18)48451-7
Autor:
W. G. Tarpley, J. Q. Zhao, S M Poppe, I. S. Y. Chen, T J Dueweke, Mario Stevenson, S. M. Swaney, T. Pushkarskaya
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 90(10)
Several nonnucleoside inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) have been described, including Nevirapine, thiobenzimidazolone (TIBO) derivatives, pyridinone derivatives such as L-697,661, and the bis(hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aad357fc0ee363cdf6a79598ee994af4
https://pubmed.ncbi.nlm.nih.gov/7685109
https://pubmed.ncbi.nlm.nih.gov/7685109
Publikováno v:
The Journal of biological chemistry. 267(1)
The bisheteroarylpiperazines (BHAPs) are potent inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) and specifically block HIV-1 replication (Romero, D. L., Busso, M., Tan, C.-K., Reusser, F., Palmer, J. R., Poppe, S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1883317f387e92e8c2dc41d3319b4c3c
https://pubmed.ncbi.nlm.nih.gov/1370445
https://pubmed.ncbi.nlm.nih.gov/1370445
Autor:
T J, Dueweke, R B, Gennis
Publikováno v:
The Journal of biological chemistry. 265(8)
The aerobic respiratory chain of Escherichia coli contains two terminal oxidases: the cytochrome d complex and the cytochrome o complex. Each of these enzymes catalyzes the oxidation of ubiquinol-8 within the cytoplasmic membrane and the reduction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bcb9adcc9c35d4a3a85d4037d4200414
https://pubmed.ncbi.nlm.nih.gov/1689724
https://pubmed.ncbi.nlm.nih.gov/1689724
Publikováno v:
Journal of Biological Chemistry. 263:13130-13137
The cytochrome d terminal oxidase complex is a component of the aerobic respiratory chain of Escherichia coli. This enzyme catalyzes the oxidation of ubiquinol-8 within the cytoplasmic membrane and the reduction of molecular oxygen to water along wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d32e68485bc2ba76f51d47e333862f1
https://doi.org/10.1016/s0021-9258(18)37681-6
https://doi.org/10.1016/s0021-9258(18)37681-6
Publikováno v:
The Journal of biological chemistry. 263(26)
The cytochrome d terminal oxidase complex is a component of the aerobic respiratory chain of Escherichia coli. This enzyme catalyzes the oxidation of ubiquinol-8 within the cytoplasmic membrane and the reduction of molecular oxygen to water along wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::940e0926c6fe5bccd2c8dcf3c92d2ba2
https://pubmed.ncbi.nlm.nih.gov/3138232
https://pubmed.ncbi.nlm.nih.gov/3138232