Papers associated with ncor2

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	Functional characterization of the mucus barrier on the Xenopus tropicalis skin surface., Dubaissi E, Rousseau K, Hughes GW, Ridley C, Grencis RK, Roberts IS, Thornton DJ., Proc Natl Acad Sci U S A. January 23, 2018; 115 (4): 726-731.
	Frogs model man: In vivo thyroid hormone signaling during development., Sachs LM, Buchholz DR., Genesis. January 1, 2017; 55 (1-2):
	Corepressor diversification by alternative mRNA splicing is species specific., Privalsky ML, Snyder CA, Goodson ML., BMC Evol Biol. October 19, 2016; 16 (1): 221.
	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):
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A, Nguyen TT, Aisaki K, Igarashi K, Kitajima S, Chandraratna RA, Kanno J, Blumberg B., Development. June 1, 2014; 141 (11): 2260-70.
	Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK, Bratoeva M, Mezentseva NV, Bernanke JM, Remond MC, Ramsdell AF, Eisenberg CA, Eisenberg LM., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.
	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.
	Thyroid disruption by Di-n-butyl phthalate (DBP) and mono-n-butyl phthalate (MBP) in Xenopus laevis., Shen O, Wu W, Du G, Liu R, Yu L, Sun H, Han X, Jiang Y, Shi W, Hu W, Song L, Xia Y, Wang S, Wang X., PLoS One. April 22, 2011; 6 (4): e19159.
	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.
	SMRT recruitment by PPARgamma is mediated by specific residues located in its carboxy-terminal interacting domain., Sutanto MM, Symons MS, Cohen RN., Mol Cell Endocrinol. October 19, 2006; 259 (1-2): 43-9.
	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.
	Xenopus embryos lacking specific isoforms of the corepressor SMRT develop abnormal heads., Malartre M, Short S, Sharpe C., Dev Biol. April 15, 2006; 292 (2): 333-43.
	SMRT has tissue-specific isoform profiles that include a form containing one CoRNR box., Short S, Malartre M, Sharpe C., Biochem Biophys Res Commun. September 2, 2005; 334 (3): 845-52.
	Alternative splicing generates multiple SMRT transcripts encoding conserved repressor domains linked to variable transcription factor interaction domains., Malartre M, Short S, Sharpe C., Nucleic Acids Res. September 1, 2004; 32 (15): 4676-86.
	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.
	Methylation gets SMRT. Functional insights into Rett syndrome., Vetter ML., Dev Cell. September 1, 2003; 5 (3): 359-60.
	A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos., Stancheva I, Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR., Mol Cell. August 1, 2003; 12 (2): 425-35.
	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.
	SHARP is a novel component of the Notch/RBP-Jkappa signalling pathway., Oswald F, Kostezka U, Astrahantseff K, Bourteele S, Dillinger K, Zechner U, Ludwig L, Wilda M, Hameister H, Knöchel W, Liptay S, Schmid RM., EMBO J. October 15, 2002; 21 (20): 5417-26.
	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.
	Active repression of RAR signaling is required for head formation., Koide T, Downes M, Chandraratna RA, Blumberg B, Umesono K., Genes Dev. August 15, 2001; 15 (16): 2111-21.
	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.
	A histone deacetylase corepressor complex regulates the Notch signal transduction pathway., Kao HY, Ordentlich P, Koyano-Nakagawa N, Tang Z, Downes M, Kintner CR, Evans RM, Kadesch T., Genes Dev. August 1, 1998; 12 (15): 2269-77.

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