280 related articles for article (PubMed ID: 12665583)
1. Isotype-restricted corepressor recruitment: a constitutively closed helix 12 conformation in retinoic acid receptors beta and gamma interferes with corepressor recruitment and prevents transcriptional repression.
Farboud B; Hauksdottir H; Wu Y; Privalsky ML
Mol Cell Biol; 2003 Apr; 23(8):2844-58. PubMed ID: 12665583
[TBL] [Abstract][Full Text] [Related]
2. Retinoic acid receptors beta and gamma do not repress, but instead activate target gene transcription in both the absence and presence of hormone ligand.
Hauksdottir H; Farboud B; Privalsky ML
Mol Endocrinol; 2003 Mar; 17(3):373-85. PubMed ID: 12554770
[TBL] [Abstract][Full Text] [Related]
3. Retinoic acid receptor-alpha is stabilized in a repressive state by its C-terminal, isotype-specific F domain.
Farboud B; Privalsky ML
Mol Endocrinol; 2004 Dec; 18(12):2839-53. PubMed ID: 15331758
[TBL] [Abstract][Full Text] [Related]
4. Characterization of receptor interaction and transcriptional repression by the corepressor SMRT.
Li H; Leo C; Schroen DJ; Chen JD
Mol Endocrinol; 1997 Dec; 11(13):2025-37. PubMed ID: 9415406
[TBL] [Abstract][Full Text] [Related]
5. The specificity of interactions between nuclear hormone receptors and corepressors is mediated by distinct amino acid sequences within the interacting domains.
Cohen RN; Brzostek S; Kim B; Chorev M; Wondisford FE; Hollenberg AN
Mol Endocrinol; 2001 Jul; 15(7):1049-61. PubMed ID: 11435607
[TBL] [Abstract][Full Text] [Related]
6. SMRT corepressor interacts with PLZF and with the PML-retinoic acid receptor alpha (RARalpha) and PLZF-RARalpha oncoproteins associated with acute promyelocytic leukemia.
Hong SH; David G; Wong CW; Dejean A; Privalsky ML
Proc Natl Acad Sci U S A; 1997 Aug; 94(17):9028-33. PubMed ID: 9256429
[TBL] [Abstract][Full Text] [Related]
7. H11-H12 loop retinoic acid receptor mutants exhibit distinct trans-activating and trans-repressing activities in the presence of natural or synthetic retinoids.
Lefebvre B; Mouchon A; Formstecher P; Lefebvre P
Biochemistry; 1998 Jun; 37(26):9240-9. PubMed ID: 9649304
[TBL] [Abstract][Full Text] [Related]
8. Involvement of SMRT corepressor in transcriptional repression by the vitamin D receptor.
Kim JY; Son YL; Lee YC
Mol Endocrinol; 2009 Feb; 23(2):251-64. PubMed ID: 19098224
[TBL] [Abstract][Full Text] [Related]
9. Interactions that determine the assembly of a retinoid X receptor/corepressor complex.
Ghosh JC; Yang X; Zhang A; Lambert MH; Li H; Xu HE; Chen JD
Proc Natl Acad Sci U S A; 2002 Apr; 99(9):5842-7. PubMed ID: 11972046
[TBL] [Abstract][Full Text] [Related]
10. Identification and characterization of a functional zebrafish smrt corepressor (ncor2).
Linney E; Perz-Edwards A; Kelley B
Gene; 2011 Oct; 486(1-2):31-6. PubMed ID: 21767619
[TBL] [Abstract][Full Text] [Related]
11. Molecular determinants of nuclear receptor-corepressor interaction.
Perissi V; Staszewski LM; McInerney EM; Kurokawa R; Krones A; Rose DW; Lambert MH; Milburn MV; Glass CK; Rosenfeld MG
Genes Dev; 1999 Dec; 13(24):3198-208. PubMed ID: 10617569
[TBL] [Abstract][Full Text] [Related]
12. A nuclear hormone receptor corepressor mediates transcriptional silencing by receptors with distinct repression domains.
Zamir I; Harding HP; Atkins GB; Hörlein A; Glass CK; Rosenfeld MG; Lazar MA
Mol Cell Biol; 1996 Oct; 16(10):5458-65. PubMed ID: 8816459
[TBL] [Abstract][Full Text] [Related]
13. Cell-specific inhibition of retinoic acid receptor-alpha silencing by the AF2/tau c activation domain can be overcome by the corepressor SMRT, but not by N-CoR.
Baniahmad A; Dressel U; Renkawitz R
Mol Endocrinol; 1998 Apr; 12(4):504-12. PubMed ID: 9544986
[TBL] [Abstract][Full Text] [Related]
14. Characterization of the repressor function of the nuclear orphan receptor retinoid receptor-related testis-associated receptor/germ cell nuclear factor.
Yan Z; Jetten AM
J Biol Chem; 2000 Nov; 275(45):35077-85. PubMed ID: 10940306
[TBL] [Abstract][Full Text] [Related]
15. Retinoid isomers differ in the ability to induce release of SMRT corepressor from retinoic acid receptor-alpha.
Hong SH; Privalsky ML
J Biol Chem; 1999 Jan; 274(5):2885-92. PubMed ID: 9915825
[TBL] [Abstract][Full Text] [Related]
16. Gene silencing by chicken ovalbumin upstream promoter-transcription factor I (COUP-TFI) is mediated by transcriptional corepressors, nuclear receptor-corepressor (N-CoR) and silencing mediator for retinoic acid receptor and thyroid hormone receptor (SMRT).
Shibata H; Nawaz Z; Tsai SY; O'Malley BW; Tsai MJ
Mol Endocrinol; 1997 Jun; 11(6):714-24. PubMed ID: 9171235
[TBL] [Abstract][Full Text] [Related]
17. Synthetic retinoids dissociate coactivator binding from corepressor release.
Zechel C
J Recept Signal Transduct Res; 2002; 22(1-4):31-61. PubMed ID: 12503607
[TBL] [Abstract][Full Text] [Related]
18. Corepressor SMRT functions as a coactivator for thyroid hormone receptor T3Ralpha from a negative hormone response element.
Berghagen H; Ragnhildstveit E; Krogsrud K; Thuestad G; Apriletti J; Saatcioglu F
J Biol Chem; 2002 Dec; 277(51):49517-22. PubMed ID: 12388540
[TBL] [Abstract][Full Text] [Related]
19. Active repression of RAR signaling is required for head formation.
Koide T; Downes M; Chandraratna RA; Blumberg B; Umesono K
Genes Dev; 2001 Aug; 15(16):2111-21. PubMed ID: 11511542
[TBL] [Abstract][Full Text] [Related]
20. A unique secondary-structure switch controls constitutive gene repression by retinoic acid receptor.
le Maire A; Teyssier C; Erb C; Grimaldi M; Alvarez S; de Lera AR; Balaguer P; Gronemeyer H; Royer CA; Germain P; Bourguet W
Nat Struct Mol Biol; 2010 Jul; 17(7):801-7. PubMed ID: 20543827
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
