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1 hment rates were over 150-fold compared with random screening.
2 fore enriched the hit rate by 1700-fold over random screening.
3 the model performs significantly better than random screening.
4 cially available molecules is preferred over random screening.
5 le could offer pivotal guidance to otherwise random screenings.
6  alga Cymopolia barbata was weakly active in random screening against PR.
7                                              Random screening and covalent selection of phage-display
8 s enrichment is greater than that found with random screening and docking to three-dimensional struct
9  were from known compounds (59%) followed by random screening approaches (21%).
10 vious efforts to develop AS inhibitors using random screening approaches, and that all of the ionizab
11 e by computation rather than immunization or random screening approaches.
12  1% of possible variants while outperforming random screening by 77%.
13 rically, most antibiotics were discovered by random screening campaigns, but over the past 20 years,
14            Most approaches to date depend on random screening, enrichment, and serendipity.
15                                        Using random screening for genetic suppressor elements, we sou
16 ts were discovered through optimization of a random screening hit, a p-(alpha-methylbenzyloxy)cinnami
17 g both site-directed mutagenesis and in vivo random screening in the yeast three-hybrid binding assay
18 m of 3- to 4-fold enrichment in actives over random screening is observed even though the actives ide
19       Given this observation, we performed a random screening of a chemical library and identified 3
20 human cytomegalovirus protease identified by random screening of a chemical library was 1,4-dihydro-7
21 ces that matched two cDNA clones obtained by random screening of a peppermint-oil gland cDNA library.
22                             Via large-scale, random screening of a portion of the receptorome, we hav
23 found a full-length clone coding for Isac by random screening of a salivary gland cDNA library.
24                 Natural product discovery by random screening of broth extracts derived from cultured
25 e structural analogs, FPL 55712 analogs, and random screening of corporate compound banks.
26 rkable compounds for medicinal chemists from random screening of large chemical libraries.
27                                              Random screening of Y. pseudotuberculosis transposon ins
28                                            A random screening on a panel of representative proteolyti
29 y be traced to a lead compound identified by random screening that was initially modified by incorpor
30 and least similar hit-to-clinical pairs from random screening were examined to provide perspective on