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1 uracil, 6-chlorouracil, 5-bromouracil, and 5-iodouracil.
5 2'-deoxy-1-beta-d-arabinofuranosyl-5-[(124)I]iodouracil) and the Cis-p53TKGFP reporter system, is suf
6 eting of [(125)I]2'-fluoro-2'-deoxy-beta-D-5-iodouracil-arabinofuranoside ([(125)I]FIAU) to tumors en
7 l/L) of (76)Br-FBAU and 2'-fluoro-2'-deoxy-5-iodouracil-beta-d-arabinofuranoside ((14)C-FIAU) was als
8 s 85 proteins formed UV photocrosslinks with iodouracil-containing RNA at the same rate as the wild-t
10 using single-stranded templates containing 5-iodouracil either before, in, or after the canonical 3'-
11 ne deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-iodouracil (FIAU) was toxic in trials for chronic hepati
12 ro-2'-deoxy-1-beta-D-beta-arabinofuranosyl-5-iodouracil (FIAU), (18)F-2'-fluoro-2'-deoxy-1-beta-D-bet
13 -fluoro-2'-deoxy-1-beta-D-arabinofuranosyl-5-iodouracil (FIAU), (18)F-labeled 9-[4-fluoro-3-(hydroxym
14 (2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-5-iodouracil (FIAU), beta-L-(-)-2',3'-dideoxy-3'-thiacytid
15 2-deoxy-2-fluoro-beta-D-arabino-furanosyl)-5-iodouracil (FIAU), is incorporated into DNA in cell cult
20 he product of primer synthesis, containing 5-iodouracil in the template generated the same apparent c
21 2'-deoxy-2'-fluoro-beta-d-arabinofuranosyl-5-iodouracil) permitted independent contemporaneous tracki
25 th the uracil analogues 5-fluorouracil and 5-iodouracil were over 20- to 30-fold higher than those ob
26 sly that incorporation of 5-bromouracil or 5-iodouracil within the UUUUUNU element abolishes terminat
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