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1 (TH) triiodothyronine through regioselective deiodination.
2 sistent with Dio3 selectivity for inner ring deiodination.
3  as well as differences in susceptibility to deiodination.
4  that cannot be fully explained by increased deiodination.
5  did those in wild-type mice, independent of deiodination.
6 ibenzothiophene also undergoes photochemical deiodination.
7  thyroxine and 3,3', 5-triiodothyronine by 5-deiodination.
8 o melanin containing tissue with low in vivo deiodination; [(123)I]20 and [(123)I]53 in particular di
9  consistent with Hg-induced disruption of T4 deiodination, a mechanism of toxicity that may cause exc
10 ructurally elucidated, including products of deiodination, aliphatic chain oxidation, as well as dime
11  for proton transfer to the substrate during deiodination and a Prx-related mechanism for subsequent
12                                      Ensuing deiodination and desilylation proceed quantitatively to
13                                              Deiodination and oxidative side chain degradation were f
14             The TPs resulted from successive deiodinations and deacetylations.
15 ically active 27-kDa selenoprotein decreased deiodination by approximately 50%, and > 95% of the LLC-
16 rials for further transformations, including deiodination, C-N bond installation, epoxide synthesis,
17                                    Reductive deiodination combined with oxidative degradation provide
18 ory protein complex supports rapid cycles of deiodination, conjugation to ubiquitin, and enzyme react
19 se TG, T3 is formed de novo independently of deiodination from T4 We found that upon iodination in vi
20 (125)I]iodo-1,2,3-triazoles are resistant to deiodination in vivo, both as small molecular probes and
21 ues is a poor technique suffering from rapid deiodination in vivo.
22 owed inhibition of both outer and inner ring deiodination (O and IRD) of T3 and 3,3'-T2 formation fro
23         This enzyme promotes a net reductive deiodination of 3-iodotyrosine to form iodide and tyrosi
24 ctor operated in a continuous mode, complete deiodination of diatrizoate was achieved at an applied c
25 erved in our experiments are consistent with deiodination of labeled knob by dehalogenases in hepatoc
26          These enzymes also catalyze further deiodination of T3 and rT3 to produce a variety of di- a
27 um nanoparticles was examined as a means for deiodination of the common ICM diatrizoate.
28  responsible for iodide salvage by reductive deiodination of the iodotyrosine derivatives formed as b
29                                          The deiodination of thyroid hormones in extrathyroidal tissu
30    A notable exception is the iodination and deiodination of thyroid hormones.
31 meric enzyme in the brain that catalyzes the deiodination of thyroxine (T4) to its active metabolite,
32      Thus, the connective tissue may control deiodination of thyroxine and release of T3 to confer a
33      Type 2 deiodinase (D2) catalyzes the 5'-deiodination of thyroxine to form 3,5,3'-triiodothyronin
34 mbrane protein that catalyzes the outer ring deiodination of thyroxine.
35 thyronine (rT3) by the outer- and inner-ring deiodination pathways, respectively.
36 e deiodinases indicates that tissue-specific deiodination plays a much broader role than once thought
37 atoms (chalcogen bond) are important for the deiodination reactions.
38 riiodothyronine (T3), and hepatic outer ring deiodination (T4-ORD).
39 oval of diatrizoate and enabled its complete deiodination to 3,5-diacetamidobenzoic acid.
40                                    Reductive deiodination to methyl groups is achieved by hydrogenati
41 ity of T3 present is generated locally by T4 deiodination via the type 2 deiodinase (D2); this pathwa