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1 e hamster V79 cells were labeled with (131)I-iododeoxyuridine ((131)IdU), mixed with unlabeled cells,
2  succinimidyl ester) and labeled with (131)I-iododeoxyuridine ((131)IdU).
3 ed the photoactivated cross-linking moiety 5-iododeoxyuridine (5-IdUrd).
4                                            5-Iododeoxyuridine/5-chlorodeoxyuridine pulse-labeling exp
5 il precursor is the halogenated nucleotide 5-iododeoxyuridine (5IdU), a cytotoxic and radiosensitizin
6 th chlorodeoxyuridine and pulse-labeled with iododeoxyuridine 8 h before tumor removal.
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
9 x were analyzed using bromodeoxy-uridine and iododeoxyuridine as isosteric analogues of thymine.
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
14 d-catalyzed Suzuki-Miyaura cross-coupling to iododeoxyuridine (IdU) in DNA is described.
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),
19                                            5-Iododeoxyuridine (IUdR) and caffeine are recognized as p
20 (1 to 3%) but increases dramatically upon 5'-iododeoxyuridine (IUdR) treatment, (iv) lacZ expression
21                                              Iododeoxyuridine (IUdR) uptake and retention was imaged
22 nt (MMR(-)) HCT116 colon cancer cells with 5-iododeoxyuridine (IUdR).
23                 The emphasis of radiolabeled iododeoxyuridine (*IUdR) research at our institution to
24          The fraction of myocytes labeled by iododeoxyuridine ranged from 2.5% to 46%, and similar va
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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