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1 e thyroid hormone (3,5, 3'-triiodothyronine; T3) receptor.
2 acts and was absent in CV-1 cells which lack T3-receptors.
3                                            A T3 receptor-alpha region containing the DNA binding doma
4 BX1a and PBX1b specifically bind the nuclear T3 receptor-alpha, and this interaction is enhanced by t
5 n of the chicken (c) or rat thyroid hormone (T3) receptor-alpha (T3Ralpha) decreased the T3-dependent
6 iated by the heterodimer of thyroid hormone (T3) receptor and 9-cis retinoid acid receptor (TR-RXR) i
7 r nuclear receptors, PP-activated receptors, T3 receptors, and retinoid X receptors.
8                           This TRE binds the T3 receptor as well as other nuclear proteins.
9 showed that co-transfected RXRalpha, but not T3 receptor beta1 (TRbeta1), abrogated the inhibitory ef
10                                          Two T3 receptor genes, Tr alpha and Tr beta are differential
11 one acetylase become co-repressors of the RA/T3 receptors in the presence of their respective ligands
12                                      Nuclear T3-receptors may be necessary for this T3-induced respon
13                                Thus, RA- and T3 receptor-mediated teratogenic effects in Xenopus embr
14                             Thyroid hormone (T3) receptors (T3Rs) are ligand-modulated transcription
15 his article, we report that thyroid hormone (T3) receptors (T3Rs), but not the closely related member
16 se A, and inhibited by overexpression of the T3 receptor; these results indicate involvement of the c
17 orphosis in the intestine via binding of the T3 receptor to the c-Myc promoter.
18 at PBX-MEIS1 complexes interact with nuclear T3 receptors to enhance T3 regulation of malic enzyme tr
19 d a direct interaction between P450R-TRE and T3 receptors TR alpha1 and TR beta1 was demonstrated by
20             We show that the heterodimers of T3 receptor (TR) and 9-cis-retinoic acid receptor bind t
21 ffects were mediated by interactions between T3 receptor (TR) and estrogen receptor (ER).
22 ecific bZip protein p45/NF-E2 interacts with T3 receptor (TR) and RA receptor (RAR) but not retinoid
23 complex 3) and another contained the nuclear T3 receptor (TR) and RXR (complex 4).
24 expression, and Dot1L in turn functions as a T3 receptor (TR) coactivator to promote vertebrate devel
25 s, the T3REs bound retinoid X receptor (RXR)-T3 receptor (TR) heterodimers and non-RXR/TR factors pre
26                           The role that each T3 receptor (TR) isotype, alpha and beta, plays in metam
27 esses prolactin (PRL) and Pit-1, but not the T3 receptor (TR) or GH, was used as a control.
28 cally bound the alpha-isoform of the nuclear T3 receptor (TR), and the presence of T3 enhanced this i
29 n kinase A (PKA) and thyroid hormone (T3) in T3 receptor (TR)-mediated transcription.
30 diated through transcriptional regulation by T3 receptor (TR).
31      Gene activation by the thyroid hormone (T3) receptor (TR) involves the recruitment of specific c
32 igated the role of PRMT1 in thyroid hormone (T3) receptor (TR)-mediated transcription in vivo during
33                                         This T3 receptor (TRbeta)-binding site differed considerably
34 tes rat liver S14 gene transcription through T3 receptors (TRbeta) binding distal thyroid hormone res
35                     T3 action is mediated by T3 receptors (TRs) that bind to T3 response elements (T3
36 regulating target gene transcription through T3 receptors (TRs).

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