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Items: 1 to 20 of 356

1.

Phosphorylation of thyroid hormone receptor-associated nuclear receptor corepressor holocomplex by the DNA-dependent protein kinase enhances its histone deacetylase activity.

Jeyakumar M, Liu XF, Erdjument-Bromage H, Tempst P, Bagchi MK.

J Biol Chem. 2007 Mar 30;282(13):9312-22. Epub 2007 Jan 22.

2.

Very strong correlation between dominant negative activities of mutant thyroid hormone receptors and their binding avidity for corepressor SMRT.

Matsushita A, Misawa H, Andoh S, Natsume H, Nishiyama K, Sasaki S, Nakamura H.

J Endocrinol. 2000 Dec;167(3):493-503.

3.

A novel mechanism of thyroid hormone-dependent negative regulation by thyroid hormone receptor, nuclear receptor corepressor (NCoR), and GAGA-binding factor on the rat cD44 promoter.

Kim SW, Ho SC, Hong SJ, Kim KM, So EC, Christoffolete M, Harney JW.

J Biol Chem. 2005 Apr 15;280(15):14545-55. Epub 2005 Jan 27.

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Differences between the silencing-related properties of the extreme carboxyl-terminal regions of thyroid hormone receptors alpha 1 and beta 1.

Nishiyama K, Matsushita A, Natsume H, Mikami T, Genma R, Sasaki S, Nakamura H.

J Endocrinol. 2000 Nov;167(2):219-27.

8.
9.

The retinoid X receptor binding to the thyroid hormone receptor: relationship with cofactor binding and transcriptional activity.

Tagami T, Yamamoto H, Moriyama K, Sawai K, Usui T, Shimatsu A, Naruse M.

J Mol Endocrinol. 2009 May;42(5):415-28. doi: 10.1677/JME-08-0153. Epub 2009 Feb 11.

PMID:
19211732
10.

Multiple N-CoR complexes contain distinct histone deacetylases.

Jones PL, Sachs LM, Rouse N, Wade PA, Shi YB.

J Biol Chem. 2001 Mar 23;276(12):8807-11. Epub 2001 Jan 19.

11.

Targeting of N-CoR and histone deacetylase 3 by the oncoprotein v-erbA yields a chromatin infrastructure-dependent transcriptional repression pathway.

Urnov FD, Yee J, Sachs L, Collingwood TN, Bauer A, Beug H, Shi YB, Wolffe AP.

EMBO J. 2000 Aug 1;19(15):4074-90.

12.

The nuclear receptor corepressors NCoR and SMRT decrease peroxisome proliferator-activated receptor gamma transcriptional activity and repress 3T3-L1 adipogenesis.

Yu C, Markan K, Temple KA, Deplewski D, Brady MJ, Cohen RN.

J Biol Chem. 2005 Apr 8;280(14):13600-5. Epub 2005 Feb 3.

13.

Both corepressor proteins SMRT and N-CoR exist in large protein complexes containing HDAC3.

Li J, Wang J, Wang J, Nawaz Z, Liu JM, Qin J, Wong J.

EMBO J. 2000 Aug 15;19(16):4342-50.

15.

Coactivator and corepressor complexes in nuclear receptor function.

Xu L, Glass CK, Rosenfeld MG.

Curr Opin Genet Dev. 1999 Apr;9(2):140-7. Review.

PMID:
10322133
16.

The functional relationship between co-repressor N-CoR and SMRT in mediating transcriptional repression by thyroid hormone receptor alpha.

Choi KC, Oh SY, Kang HB, Lee YH, Haam S, Kim HI, Kim K, Ahn YH, Kim KS, Yoon HG.

Biochem J. 2008 Apr 1;411(1):19-26.

PMID:
18052923
17.

IkappaB kinase alpha-mediated derepression of SMRT potentiates acetylation of RelA/p65 by p300.

Hoberg JE, Popko AE, Ramsey CS, Mayo MW.

Mol Cell Biol. 2006 Jan;26(2):457-71.

18.

Modulation of thyroid hormone receptor silencing function by co-repressors and a synergizing transcription factor.

Lutz M, Baniahmad A, Renkawitz R.

Biochem Soc Trans. 2000;28(4):386-9. Review.

PMID:
10961925
19.
20.

The nuclear corepressors recognize distinct nuclear receptor complexes.

Cohen RN, Putney A, Wondisford FE, Hollenberg AN.

Mol Endocrinol. 2000 Jun;14(6):900-14.

PMID:
10847591

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