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Summary Expression Phenotypes Gene Literature (79) GO Terms (16) Nucleotides (159) Proteins (57) Interactants (595) Wiki
XB--481105

Papers associated with hdac3



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Xenopus HDm, a maternally expressed histone deacetylase, belongs to an ancient family of acetyl-metabolizing enzymes., Ladomery M, Lyons S, Sommerville J., Gene. October 1, 1997; 198 (1-2): 275-80.        

A multiple subunit Mi-2 histone deacetylase from Xenopus laevis cofractionates with an associated Snf2 superfamily ATPase., Wade PA, Jones PL, Vermaak D, Wolffe AP., Curr Biol. July 2, 1998; 8 (14): 843-6.

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.

Maternal histone deacetylase is accumulated in the nuclei of Xenopus oocytes as protein complexes with potential enzyme activity., Ryan J, Llinas AJ, White DA, Turner BM, Sommerville J., J Cell Sci. July 1, 1999; 112 ( Pt 14) 2441-52.

Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation., Wade PA, Gegonne A, Jones PL, Ballestar E, Aubry F, Wolffe AP., Nat Genet. September 1, 1999; 23 (1): 62-6.

Functional analysis of the SIN3-histone deacetylase RPD3-RbAp48-histone H4 connection in the Xenopus oocyte., Vermaak D, Wade PA, Jones PL, Shi YB, Wolffe AP., Mol Cell Biol. September 1, 1999; 19 (9): 5847-60.

Histone deacetylase activity is required for the induction of the MyoD muscle cell lineage in Xenopus., Steinbac OC, Wolffe AP, Rupp RA., Biol Chem. January 1, 2000; 381 (9-10): 1013-6.

Transient depletion of xDnmt1 leads to premature gene activation in Xenopus embryos., Stancheva I, Meehan RR., Genes Dev. February 1, 2000; 14 (3): 313-27.                    

ATP-Dependent histone octamer mobilization and histone deacetylation mediated by the Mi-2 chromatin remodeling complex., Guschin D, Wade PA, Kikyo N, Wolffe AP., Biochemistry. May 9, 2000; 39 (18): 5238-45.

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.

Histone acetylation is a checkpoint in FGF-stimulated mesoderm induction., Xu RH, Peng Y, Fan J, Yan D, Yamagoe S, Princler G, Sredni D, Ozato K, Kung HF., Dev Dyn. August 1, 2000; 218 (4): 628-35.

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.

Multiple stage-dependent roles for histone deacetylases during amphibian embryogenesis: implications for the involvement of extracellular matrix remodeling., Damjanovski S, Sachs LM, Shi YB, Shi YB., Int J Dev Biol. October 1, 2000; 44 (7): 769-76.                    

Competitive recruitment of CBP and Rb-HDAC regulates UBF acetylation and ribosomal transcription., Pelletier G, Stefanovsky VY, Faubladier M, Hirschler-Laszkiewicz I, Savard J, Rothblum LI, Côté J, Moss T., Mol Cell. November 1, 2000; 6 (5): 1059-66.

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.

Nrarp is a novel intracellular component of the Notch signaling pathway., Lamar E, Deblandre G, Wettstein D, Gawantka V, Pollet N, Niehrs C, Kintner C., Genes Dev. August 1, 2001; 15 (15): 1885-99.                        

Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen., Phiel CJ, Zhang F, Huang EY, Guenther MG, Lazar MA, Klein PS., J Biol Chem. September 28, 2001; 276 (39): 36734-41.              

An essential role of histone deacetylases in postembryonic organ transformations in Xenopus laevis., Sachs LM, Amano T, Shi YB., Int J Mol Med. December 1, 2001; 8 (6): 595-601.

RNA helicase p54 (DDX6) is a shuttling protein involved in nuclear assembly of stored mRNP particles., Smillie DA, Sommerville J., J Cell Sci. January 15, 2002; 115 (Pt 2): 395-407.                  

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.

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.

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.

Active repression by unliganded retinoid receptors in development: less is sometimes more., Weston AD, Blumberg B, Underhill TM., J Cell Biol. April 28, 2003; 161 (2): 223-8.

Methylation gets SMRT. Functional insights into Rett syndrome., Vetter ML., Dev Cell. September 1, 2003; 5 (3): 359-60.

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.

Nuclear import and activity of histone deacetylase in Xenopus oocytes is regulated by phosphorylation., Smillie DA, Llinas AJ, Ryan JT, Kemp GD, Sommerville J., J Cell Sci. April 1, 2004; 117 (Pt 9): 1857-66.

Regulation of tissue-specific and extracellular matrix-related genes by a class I histone deacetylase., Whetstine JR, Ceron J, Ladd B, Dufourcq P, Reinke V, Shi Y., Mol Cell. May 13, 2005; 18 (4): 483-90.

Association of valproate-induced teratogenesis with histone deacetylase inhibition in vivo., Gurvich N, Berman MG, Wittner BS, Gentleman RC, Klein PS, Green JB., FASEB J. July 1, 2005; 19 (9): 1166-8.

Histone deacetylase activity is necessary for chromosome condensation during meiotic maturation in Xenopus laevis., Magnaghi-Jaulin L, Jaulin C., Chromosome Res. January 1, 2006; 14 (3): 319-32.

Molecular and developmental analyses of thyroid hormone receptor function in Xenopus laevis, the African clawed frog., Buchholz DR, Paul BD, Fu L, Shi YB, Shi YB., Gen Comp Endocrinol. January 1, 2006; 145 (1): 1-19.

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.              

Inhibition of histone deacetylase as a new mechanism of teratogenesis., Menegola E, Di Renzo F, Broccia ML, Giavini E., Birth Defects Res C Embryo Today. December 1, 2006; 78 (4): 345-53.

FoxN3 is required for craniofacial and eye development of Xenopus laevis., Schuff M, Rössner A, Wacker SA, Donow C, Gessert S, Knöchel W., Dev Dyn. January 1, 2007; 236 (1): 226-39.                            

Characterization of histone lysine-specific demethylase in relation to thyroid hormone-regulated anuran metamorphosis., Chen W, Obara M, Ishida Y, Suzuki K, Yoshizato K., Dev Growth Differ. May 1, 2007; 49 (4): 325-34.          

Role for histone deacetylase 1 in human tumor cell proliferation., Senese S, Zaragoza K, Minardi S, Muradore I, Ronzoni S, Passafaro A, Bernard L, Draetta GF, Alcalay M, Seiser C, Chiocca S., Mol Cell Biol. July 1, 2007; 27 (13): 4784-95.

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.              

Oct25 represses transcription of nodal/activin target genes by interaction with signal transducers during Xenopus gastrulation., Cao Y, Siegel D, Oswald F, Knöchel W., J Biol Chem. December 5, 2008; 283 (49): 34168-77.                

The Xenopus Bowline/Ripply family proteins negatively regulate the transcriptional activity of T-box transcription factors., Hitachi K, Danno H, Tazumi S, Aihara Y, Uchiyama H, Okabayashi K, Kondow A, Asashima M., Int J Dev Biol. January 1, 2009; 53 (4): 631-9.                    

Transport by SLC5A8 with subsequent inhibition of histone deacetylase 1 (HDAC1) and HDAC3 underlies the antitumor activity of 3-bromopyruvate., Thangaraju M, Karunakaran SK, Itagaki S, Gopal E, Elangovan S, Prasad PD, Ganapathy V., Cancer. October 15, 2009; 115 (20): 4655-66.

A DNAJB chaperone subfamily with HDAC-dependent activities suppresses toxic protein aggregation., Hageman J, Rujano MA, van Waarde MA, Kakkar V, Dirks RP, Govorukhina N, Oosterveld-Hut HM, Lubsen NH, Kampinga HH., Mol Cell. February 12, 2010; 37 (3): 355-69.              

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.        

Effect of Inhibiting Histone Deacetylase with Short-Chain Carboxylic Acids and Their Hydroxamic Acid Analogs on Vertebrate Development and Neuronal Chromatin., Fass DM, Shah R, Ghosh B, Hennig K, Norton S, Zhao WN, Reis SA, Klein PS, Mazitschek R, Maglathlin RL, Lewis TA, Haggarty SJ., ACS Med Chem Lett. October 8, 2010; 2 (1): 39-42.

HDAC activity is required during Xenopus tail regeneration., Tseng AS, Carneiro K, Lemire JM, Levin M., PLoS One. January 1, 2011; 6 (10): e26382.              

Affinity-based enrichment strategies to assay methyl-CpG binding activity and DNA methylation in early Xenopus embryos., Bogdanović O, Veenstra GJ., BMC Res Notes. May 6, 2011; 4 300.      

Histone deacetylase activity is necessary for left-right patterning during vertebrate development., Carneiro K, Donnet C, Rejtar T, Karger BL, Barisone GA, Díaz E, Kortagere S, Lemire JM, Levin M., BMC Dev Biol. May 20, 2011; 11 29.              

Role of SLC5A8, a plasma membrane transporter and a tumor suppressor, in the antitumor activity of dichloroacetate., Babu E, Ramachandran S, CoothanKandaswamy V, Elangovan S, Prasad PD, Ganapathy V, Thangaraju M., Oncogene. September 22, 2011; 30 (38): 4026-37.            

Histone deacetylases are required for amphibian tail and limb regeneration but not development., Taylor AJ, Beck CW., Mech Dev. January 1, 2012; 129 (9-12): 208-18.            

The LIM adaptor protein LMO4 is an essential regulator of neural crest development., Ochoa SD, Salvador S, LaBonne C., Dev Biol. January 15, 2012; 361 (2): 313-25.              

SUMOylated SoxE factors recruit Grg4 and function as transcriptional repressors in the neural crest., Lee PC, Taylor-Jaffe KM, Nordin KM, Prasad MS, Lander RM, LaBonne C., J Cell Biol. September 3, 2012; 198 (5): 799-813.              

Unliganded thyroid hormone receptor regulates metamorphic timing via the recruitment of histone deacetylase complexes., Shi YB., Curr Top Dev Biol. January 1, 2013; 105 275-97.

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