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1 ly and specific infectivity as early as 24 h posttransfection.
2 rogressively decreased and was lost by day 7 posttransfection.
3  level of RNA was established at 3 to 4 days posttransfection.
4  of only 8% per cell generation over 24 days posttransfection.
5 US-Res and wild-type bacmids at early stages posttransfection.
6 time points ranging from 2 weeks to 6 months posttransfection.
7 pfu) of virus per ml of supernatant at 48 hr posttransfection.
8  modified per antigenome during 6 to 13 days posttransfection.
9  generated infectious IPNV particles 10 days posttransfection.
10 s but diminished to low levels beyond 8 days posttransfection.
11 became detectable in culture medium at day 4 posttransfection.
12 ells) than progenitors at the peak of 3 days posttransfection.
13 oduction from progenitors as late as 5 weeks posttransfection.
14  between 2 and 10 h and the other after 26 h posttransfection.
15                                   By 18 days posttransfection, a variety of different deltaAg stainin
16  experiments, were identical at 4 and 8 days posttransfection and in the wild type and the L-HDAg-def
17  level at the early time points (1 to 2 days posttransfection) but then lose this capability at later
18 lymph nodes of two lambs sacrificed 9 months posttransfection, but no macroscopic or histological SPA
19 peared in the transfected cultures 2-3 weeks posttransfection; cloned transformants showed anchorage
20 se lung elicited peak expression at days 1-4 posttransfection, followed by a gradual return to baseli
21 lost precipitously from cells during 2 weeks posttransfection (>25% rate of loss per cell generation)
22 the differences in the polymerase complexes, posttransfection/infection treatment with the compound r
23  every cell line tested for at least 50 days posttransfection/infection.
24  considerable gene silencing even after 96 h posttransfection; it showed that our modification could
25                                      By 72 h posttransfection, more than 50% of ie2-transfected cells
26                          However, at 3 weeks posttransfection of 221 cells, a variant of g123 emerged
27  transfection efficiency, time of processing posttransfection, or method of transfection.
28 lture supernatants approximately 4 to 9 days posttransfection reaching maximum titers during the foll
29 t the Rluc signal that occurred at 2 to 10 h posttransfection reflects viral translation of the input
30 and very late genes was lower at later times posttransfection relative to the results seen with wild-
31 replicon, while the Rluc activity after 26 h posttransfection represents RNA replication.
32 nalysis of the replicated HDV-L RNA at day 1 posttransfection showed that it had undergone multiple n
33                                      At 24 h posttransfection, the extent of repair assayed by measur
34 imately 12 h following transfection; by 24 h posttransfection, the overall levels of luciferase activ
35                                   At 30 days posttransfection, VEGF-transfected animals had more angi
36 ces were noted between ACH and ACH.p12(I) in posttransfection viral antigen production.
37 e supernatants, collected approximately 36 h posttransfection, were passed onto fresh ST cells where