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1 as well as differences in susceptibility to deiodination.
2 that cannot be fully explained by increased deiodination.
3 did those in wild-type mice, independent of deiodination.
4 ibenzothiophene also undergoes photochemical deiodination.
5 thyroxine and 3,3', 5-triiodothyronine by 5-deiodination.
6 o melanin containing tissue with low in vivo deiodination; [(123)I]20 and [(123)I]53 in particular di
7 consistent with Hg-induced disruption of T4 deiodination, a mechanism of toxicity that may cause exc
8 ructurally elucidated, including products of deiodination, aliphatic chain oxidation, as well as dime
9 for proton transfer to the substrate during deiodination and a Prx-related mechanism for subsequent
13 ically active 27-kDa selenoprotein decreased deiodination by approximately 50%, and > 95% of the LLC-
15 ory protein complex supports rapid cycles of deiodination, conjugation to ubiquitin, and enzyme react
16 se TG, T3 is formed de novo independently of deiodination from T4 We found that upon iodination in vi
17 (125)I]iodo-1,2,3-triazoles are resistant to deiodination in vivo, both as small molecular probes and
19 owed inhibition of both outer and inner ring deiodination (O and IRD) of T3 and 3,3'-T2 formation fro
21 ctor operated in a continuous mode, complete deiodination of diatrizoate was achieved at an applied c
22 erved in our experiments are consistent with deiodination of labeled knob by dehalogenases in hepatoc
25 responsible for iodide salvage by reductive deiodination of the iodotyrosine derivatives formed as b
27 meric enzyme in the brain that catalyzes the deiodination of thyroxine (T4) to its active metabolite,
32 e deiodinases indicates that tissue-specific deiodination plays a much broader role than once thought
37 ity of T3 present is generated locally by T4 deiodination via the type 2 deiodinase (D2); this pathwa
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