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1 e hamster V79 cells were labeled with (131)I-iododeoxyuridine ((131)IdU), mixed with unlabeled cells,
5 il precursor is the halogenated nucleotide 5-iododeoxyuridine (5IdU), a cytotoxic and radiosensitizin
7 er proliferative defects, we have adapted an iododeoxyuridine and bromodeoxyuridine double labeling p
8 esidues in the enzyme by using end-labeled 5-iododeoxyuridine- and azidophenacyl-substituted oligonuc
10 eplication foci were labeled with BrdU and 5-iododeoxyuridine at the beginning of different cell cycl
11 (+/-z-VAD-fmk cotreatment) and by levels of iododeoxyuridine-DNA incorporation, is independent of BR
12 ty of BrdU with two other thymidine analogs, iododeoxyuridine (IdU) and chlorodeoxyuridine (CldU).
13 abeling of slow-cycling cells, mice received iododeoxyuridine (IdU) for 30 days, followed by a 40-day
15 the maximally tolerated doses (MTDs) of i.p. iododeoxyuridine (IdUrd) alone and in combination with i
16 t the halogenated thymidine (dThd) analogues iododeoxyuridine (IdUrd) and bromodeoxyuridine (BrdUrd)
17 o the halogenated thymidine (dThd) analogues iododeoxyuridine (IdUrd) and bromodeoxyuridine (BrdUrd)
18 f the halogenated thymidine (dThd) analogues iododeoxyuridine (IdUrd) and bromodeoxyuridine (BrdUrd),
20 (1 to 3%) but increases dramatically upon 5'-iododeoxyuridine (IUdR) treatment, (iv) lacZ expression
25 These values are compared with standard 5-iododeoxyuridine Tpot measures and volume doubling times
26 able to cross-link a forked substrate when 5-iododeoxyuridine was located within the duplex portion.
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