Papers associated with ncor1

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	A phospho-dependent mechanism involving NCoR and KMT2D controls a permissive chromatin state at Notch target genes., Oswald F, Rodriguez P, Giaimo BD, Antonello ZA, Mira L, Mittler G, Thiel VN, Collins KJ, Tabaja N, Cizelsky W, Rothe M, Kühl SJ, Kühl SJ, Kühl M, Ferrante F, Hein K, Kovall RA, Dominguez M, Borggrefe T., Nucleic Acids Res. June 2, 2016; 44 (10): 4703-20.
	Short linear motif acquisition, exon formation and alternative splicing determine a pathway to diversity for NCoR-family co-repressors., Short S, Peterkin T, Guille M, Patient R, Sharpe C., Open Biol. August 1, 2015; 5 (8):
	Epigenetic regulation of thyroid hormone-induced adult intestinal stem cell development during anuran metamorphosis., Sun G, Fu L, Shi YB., Cell Biosci. November 28, 2014; 4 73.
	The development of the adult intestinal stem cells: Insights from studies on thyroid hormone-dependent amphibian metamorphosis., Shi YB, Hasebe T, Fu L, Fujimoto K, Ishizuya-Oka A., Cell Biosci. September 6, 2011; 1 (1): 30.
	Molecular and genetic studies suggest that thyroid hormone receptor is both necessary and sufficient to mediate the developmental effects of thyroid hormone., Das B, Matsuda H, Fujimoto K, Sun G, Matsuura K, Shi YB, Shi YB., Gen Comp Endocrinol. September 1, 2010; 168 (2): 174-80.
	A role of unliganded thyroid hormone receptor in postembryonic development in Xenopus laevis., Sato Y, Buchholz DR, Paul BD, Shi YB, Shi YB., Mech Dev. July 1, 2007; 124 (6): 476-88.
	A feed-forward repression mechanism anchors the Sin3/histone deacetylase and N-CoR/SMRT corepressors on chromatin., Vermeulen M, Walter W, Le Guezennec X, Kim J, Edayathumangalam RS, Lasonder E, Luger K, Roeder RG, Logie C, Berger SL, Stunnenberg HG., Mol Cell Biol. July 1, 2006; 26 (14): 5226-36.
	Recruitment of N-CoR/SMRT-TBLR1 corepressor complex by unliganded thyroid hormone receptor for gene repression during frog development., Tomita A, Buchholz DR, Shi YB., Mol Cell Biol. April 1, 2004; 24 (8): 3337-46.
	In vitro targeting reveals intrinsic histone tail specificity of the Sin3/histone deacetylase and N-CoR/SMRT corepressor complexes., Vermeulen M, Carrozza MJ, Lasonder E, Workman JL, Logie C, Stunnenberg HG., Mol Cell Biol. March 1, 2004; 24 (6): 2364-72.
	Fusion protein of retinoic acid receptor alpha with promyelocytic leukemia protein or promyelocytic leukemia zinc finger protein recruits N-CoR-TBLR1 corepressor complex to repress transcription in vivo., Tomita A, Buchholz DR, Obata K, Shi YB, Shi YB., J Biol Chem. August 15, 2003; 278 (33): 30788-95.
	N-CoR-HDAC corepressor complexes: roles in transcriptional regulation by nuclear hormone receptors., Jones PL, Shi YB., Curr Top Microbiol Immunol. January 1, 2003; 274 237-68.
	Specific targeting and constitutive association of histone deacetylase complexes during transcriptional repression., Li J, Lin Q, Wang W, Wade P, Wong J., Genes Dev. March 15, 2002; 16 (6): 687-92.
	Multiple N-CoR complexes contain distinct histone deacetylases., Jones PL, Sachs LM, Rouse N, Wade PA, Shi YB, Shi YB., J Biol Chem. March 23, 2001; 276 (12): 8807-11.
	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. August 15, 2000; 19 (16): 4342-50.
	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, Shi YB, Wolffe AP., EMBO J. August 1, 2000; 19 (15): 4074-90.

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