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1 sence of the reverse-transcriptase inhibitor azidothymidine.
2 inhibitors have been approved for human use: azidothymidine; 2'3'-dideoxycytidine; 2'3'-dideoxyinosin
3 tudy to demonstrate the on-demand release of azidothymidine 5'-triphosphate, an anti-human immunodefi
5 found that pre-incubation of the cells with azidothymidine, a pro-oxidant drug, significantly improv
6 omal cell-derived factor-1 (for HIVIIIB), or azidothymidine added during the HIV pulse, as well as by
13 ilylated nucleoside scaffold derived from 3'-azidothymidine (AZT) consistently and selectively inhibi
14 bination of interferon alpha (IFN-alpha) and azidothymidine (AZT) induces apoptosis in PEL cell lines
17 replication inhibitors hydroxyurea (HU) and azidothymidine (AZT) was suppressed by alleles of dnaA t
19 ons to anti-HIV/AIDS pharmaceuticals such as azidothymidine (AZT), anti-malarial compounds and novel
22 as steeper in patients receiving zidovudine (azidothymidine [AZT], -3.64 g/dL vs. no AZT, -2.08 g/dL)
23 iency virus type 1 (HIV-1) to zidovudine (3'-azidothymidine; AZT) and appear to approximate the templ
24 lex formation, and primer terminated with 3'-azidothymidine formed dead-end complex with 25-fold elev
25 creased the cell toxicity of ganciclovir and azidothymidine in PEL cells but had no significant effec
26 M184V suppressed the excision of 3'-deoxy-3'-azidothymidine monophosphate (AZTMP) to a greater extent
27 EA (9-(2-phosphonylmethoxyethyl)adenine) and azidothymidine monophosphate from cells and, thus, with
28 e nucleoside reverse transcriptase inhibitor azidothymidine or the protease inhibitor indinavir to th
31 trains, and reverse transcriptase-resistant, azidothymidine-resistant, ddC/ddI-resistant, nivirapine-
33 in some patients receiving 2',3'-dideoxy-3'-azidothymidine therapy in combination with 2',3'-dideoxy
35 and the two nucleoside analog RT inhibitors (azidothymidine triphosphate or ddCTP), whereas two non-n
38 When the reverse transcriptase inhibitor azidothymidine was added to the DCs during exposure to H
40 the phosphorylated forms of ganciclovir and azidothymidine, we found that PEL cells exposed to hypox
41 ideoxyinosine, 2',3'-dideoxycytidine, and 3'-azidothymidine, which are known inhibitors of N1 or N2,
42 the accurate assessment of HIV inhibition by azidothymidine (zidovudine), dideoxycytidine (zalcytibin
43 vents, this study defines such a mutagen, 3'-azidothymidine [zidovudine (AZT)], used widely in the tr
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