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1 ly and specific infectivity as early as 24 h posttransfection.
2 US-Res and wild-type bacmids at early stages posttransfection.
3 rogressively decreased and was lost by day 7 posttransfection.
4 level of RNA was established at 3 to 4 days posttransfection.
5 of only 8% per cell generation over 24 days posttransfection.
6 s but diminished to low levels beyond 8 days posttransfection.
7 time points ranging from 2 weeks to 6 months posttransfection.
8 pfu) of virus per ml of supernatant at 48 hr posttransfection.
9 modified per antigenome during 6 to 13 days posttransfection.
10 generated infectious IPNV particles 10 days posttransfection.
11 ells) than progenitors at the peak of 3 days posttransfection.
12 oduction from progenitors as late as 5 weeks posttransfection.
13 between 2 and 10 h and the other after 26 h posttransfection.
15 experiments, were identical at 4 and 8 days posttransfection and in the wild type and the L-HDAg-def
16 level at the early time points (1 to 2 days posttransfection) but then lose this capability at later
17 lymph nodes of two lambs sacrificed 9 months posttransfection, but no macroscopic or histological SPA
18 peared in the transfected cultures 2-3 weeks posttransfection; cloned transformants showed anchorage
19 se lung elicited peak expression at days 1-4 posttransfection, followed by a gradual return to baseli
20 lost precipitously from cells during 2 weeks posttransfection (>25% rate of loss per cell generation)
24 t the Rluc signal that occurred at 2 to 10 h posttransfection reflects viral translation of the input
25 and very late genes was lower at later times posttransfection relative to the results seen with wild-
27 nalysis of the replicated HDV-L RNA at day 1 posttransfection showed that it had undergone multiple n
29 imately 12 h following transfection; by 24 h posttransfection, the overall levels of luciferase activ
32 e supernatants, collected approximately 36 h posttransfection, were passed onto fresh ST cells where
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