284 results on '"Reverse transcriptase -- Research"'
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252. Chromosome replication process discovery may prove valuable in cancer diagnosis/treatment
253. The effectiveness of viral stimulators on the release of reverse transcriptase from monocytes of patients with breast cancer
254. Detection of a human intracisternal retroviral particle associated with CD4+ T-cell deficiency
255. Fifth mutation in human immunodeficiency virus type 1 reverse transcriptase contributes to the development of high-level resistance to zidovudine
256. Fluorimetric characterization of human immunodeficiency virus 1 (HIV-1) reverse transcriptase
257. Structure of the ribonuclease H domain of HIV-1 reverse transcriptase
258. Nevirapine binding domain from HIV-1 reverse transcriptase confers sensitivity to HIV-2 reverse transcriptase
259. Trials with non-nucleoside RT inhibitors halted due to resistance
260. Viral resistance to human immunodeficiency virus type 1-specific pyridinone reverse transcriptase inhibitors
261. Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 1. tricyclic pyridobenzo- and dipyridodiazepinones
262. Mutations in both the U5 region and the primer-binding site influence the selection of the tRNA used for the initiation of HIV-1 reverse transcription
263. Constitutive expression of HIV-1 reverse transcriptase heterodimer in a human cell line
264. Amino acid for HIV-1 reverse transcriptase identified
265. Fidelity of HIV-1 reverse transcriptase in vitro
266. Resistance of human immunodeficiency virus type 1 reverse transcriptase to TIBO derivatives induced by site-directed mutagenesis
267. The disposition of L-696,229, a potent and specific inhibitor of human immunodeficiency virus reverse transcriptase, in rats and rhesus monkeys
268. Metabolism of a new HIV-1 reverse transcriptase inhibitor, 3-2-(benzoxazol-2-YL)ethyl-5-ethyl-6-methylpyridin-2(1H)-one(L-696,229), in rat and liver slices
269. Kinetic characterization of a C-terminal mutant of HIV reverse transcriptase
270. Template/primer interactions with recombinant forms of HIV-1 reverse transcriptase
271. Identification of amino acid residues at the binding site of HIV-1 reverse transcriptase for the non-nucleoside inhibitor nevirapine
272. Fucoidan, a sulfated algal polysaccharide, inhibits recombinant HIV reverse transcriptase activity in vitro
273. Isolation and characterization of polynucleotide binding regions of recombinant HIV-1 reverse transcriptase
274. Comparison of the structures of HIV reverse transcriptase and that of the Klenow fragment of DNA pol I bound to duplex DNA
275. PCR-based gene assembly of HIV-1 reverse transcriptase
276. Active recombinant HIV-1 RNase H domain: cloning, expression, purification and characterization
277. Identification of amino acid residues at the binding site of HIV-1 reverse transcriptase for the non-nucleoside inhibitor nevirapine
278. Fucoidan, a sulfated algal polysaccharide, inhibits recombinant HIV reverse transcriptase activity in vitro
279. Nevirapine binding domain from HIV-1 reverse transcriptase confers sensitivity to HIV-2 reverse transcriptase
280. Psychotrine and its O-methyl ether are selective inhibitors of human immunodeficiency virus-1 reverse transcriptase
281. Finding opens way for new AIDS drugs
282. Resistance to ddI and sensitivity to AZT induced by a mutation in HIV-1 reverse transcriptase
283. The P15 carboxyl-terminal proteolysis product of the human immunodeficiency virus type 1 reverse transcriptase P66 has DNA polymerase activity
284. 2',5'-oligoadenylate-mediated inhibition of HIV-1 reverse transcriptase
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