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Summary Expression Phenotypes Gene Literature (26) GO Terms (7) Nucleotides (485) Proteins (79) Interactants (405) Wiki
XB-GENEPAGE-995847

Papers associated with chd4



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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.

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.

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.

Generation of superhelical torsion by ATP-dependent chromatin remodeling activities., Havas K, Flaus A, Phelan M, Kingston R, Wade PA, Lilley DM, Owen-Hughes T., Cell. December 22, 2000; 103 (7): 1133-42.

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.

Two highly related p66 proteins comprise a new family of potent transcriptional repressors interacting with MBD2 and MBD3., Brackertz M, Boeke J, Zhang R, Renkawitz R., J Biol Chem. October 25, 2002; 277 (43): 40958-66.

Nucleosome sliding induced by the xMi-2 complex does not occur exclusively via a simple twist-diffusion mechanism., Aoyagi S, Wade PA, Hayes JJ., J Biol Chem. August 15, 2003; 278 (33): 30562-8.

The SNF2 domain protein family in higher vertebrates displays dynamic expression patterns in Xenopus laevis embryos., Linder B, Cabot RA, Schwickert T, Rupp RA., Gene. February 4, 2004; 326 59-66.                                              

Developmental roles of the Mi-2/NURD-associated protein p66 in Drosophila., Kon C, Cadigan KM, da Silva SL, Nusse R., Genetics. April 1, 2005; 169 (4): 2087-100.

CHD4/Mi-2beta activity is required for the positioning of the mesoderm/neuroectoderm boundary in Xenopus., Linder B, Mentele E, Mansperger K, Straub T, Kremmer E, Rupp RA., Genes Dev. April 15, 2007; 21 (8): 973-83.            

Different Mi-2 complexes for various developmental functions in Caenorhabditis elegans., Passannante M, Marti CO, Pfefferli C, Moroni PS, Kaeser-Pebernard S, Puoti A, Hunziker P, Wicky C, Müller F., PLoS One. October 27, 2010; 5 (10): e13681.                

Localization of receptor site on insect sodium channel for depressant β-toxin BmK IT2., He H, Liu Z, Dong B, Zhang J, Shu X, Zhou J, Ji Y., PLoS One. January 7, 2011; 6 (1): e14510.            

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.      

CHD4 is a RanGTP-dependent MAP that stabilizes microtubules and regulates bipolar spindle formation., Yokoyama H, Nakos K, Santarella-Mellwig R, Rybina S, Krijgsveld J, Koffa MD, Mattaj IW., Curr Biol. December 16, 2013; 23 (24): 2443-51.                      

Purification of nuclear localization signal-containing proteins and its application to investigation of the mechanisms of the cell division cycle., Christodoulou A, Yokoyama H., Small GTPases. January 1, 2015; 6 (1): 20-7.      

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.                              

Id genes are essential for early heart formation., Cunningham TJ, Yu MS, McKeithan WL, Spiering S, Carrette F, Huang CT, Bushway PJ, Tierney M, Albini S, Giacca M, Mano M, Puri PL, Sacco A, Ruiz-Lozano P, Riou JF, Umbhauer M, Duester G, Mercola M, Colas AR., Genes Dev. July 1, 2017; 31 (13): 1325-1338.                

HELLS and CDCA7 comprise a bipartite nucleosome remodeling complex defective in ICF syndrome., Jenness C, Giunta S, Müller MM, Kimura H, Muir TW, Funabiki H., Proc Natl Acad Sci U S A. January 30, 2018; 115 (5): E876-E885.                                

A NuRD Complex from Xenopus laevis Eggs Is Essential for DNA Replication during Early Embryogenesis., Christov CP, Dingwell KS, Skehel M, Wilkes HS, Sale JE, Smith JC, Krude T., Cell Rep. February 27, 2018; 22 (9): 2265-2278.                        

Nucleosome-CHD4 chromatin remodeler structure maps human disease mutations., Farnung L, Ochmann M, Cramer P., Elife. June 16, 2020; 9                       

Characterization of axolotl lampbrush chromosomes by fluorescence in situ hybridization and immunostaining., Keinath MC, Davidian A, Timoshevskiy V, Timoshevskaya N, Gall JG., Exp Cell Res. April 15, 2021; 401 (2): 112523.            

A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB, Willsey HR, Xu Y, Xu Y, Mei Y, Dea J, Wang S, Curtis C, Sempou E, Khokha MK, Chi NC, Willsey AJ, Fisch KM, Ideker T., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.            

The H2A.Z and NuRD associated protein HMG20A controls early head and heart developmental transcription programs., Herchenröther A, Gossen S, Friedrich T, Reim A, Daus N, Diegmüller F, Leers J, Sani HM, Gerstner S, Schwarz L, Stellmacher I, Szymkowiak LV, Nist A, Stiewe T, Borggrefe T, Mann M, Mackay JP, Bartkuhn M, Borchers A, Lan J, Hake SB., Nat Commun. January 28, 2023; 14 (1): 472.                                                    

The Gene Ontology knowledgebase in 2023., Gene Ontology Consortium, Aleksander SA, Balhoff J, Carbon S, Cherry JM, Drabkin HJ, Ebert D, Feuermann M, Gaudet P, Harris NL, Hill DP, Lee R, Mi H, Moxon S, Mungall CJ, Muruganugan A, Mushayahama T, Sternberg PW, Thomas PD, Van Auken K, Ramsey J, Siegele DA, Chisholm RL, Fey P, Aspromonte MC, Nugnes MV, Quaglia F, Tosatto S, Giglio M, Nadendla S, Antonazzo G, Attrill H, Dos Santos G, Marygold S, Strelets V, Tabone CJ, Thurmond J, Zhou P, Ahmed SH, Asanitthong P, Luna Buitrago D, Erdol MN, Gage MC, Ali Kadhum M, Li KYC, Long M, Michalak A, Pesala A, Pritazahra A, Saverimuttu SCC, Su R, Thurlow KE, Lovering RC, Logie C, Oliferenko S, Blake J, Christie K, Corbani L, Dolan ME, Drabkin HJ, Hill DP, Ni L, Sitnikov D, Smith C, Cuzick A, Seager J, Cooper L, Elser J, Jaiswal P, Gupta P, Jaiswal P, Naithani S, Lera-Ramirez M, Rutherford K, Wood V, De Pons JL, Dwinell MR, Hayman GT, Kaldunski ML, Kwitek AE, Laulederkind SJF, Tutaj MA, Vedi M, Wang SJ, D'Eustachio P, Aimo L, Axelsen K, Bridge A, Hyka-Nouspikel N, Morgat A, Aleksander SA, Cherry JM, Engel SR, Karra K, Miyasato SR, Nash RS, Skrzypek MS, Weng S, Wong ED, Bakker E, Berardini TZ, Reiser L, Auchincloss A, Axelsen K, Argoud-Puy G, Blatter MC, Boutet E, Breuza L, Bridge A, Casals-Casas C, Coudert E, Estreicher A, Livia Famiglietti M, Feuermann M, Gos A, Gruaz-Gumowski N, Hulo C, Hyka-Nouspikel N, Jungo F, Le Mercier P, Lieberherr D, Masson P, Morgat A, Pedruzzi I, Pourcel L, Poux S, Rivoire C, Sundaram S, Bateman A, Bowler-Barnett E, Bye-A-Jee H, Denny P, Ignatchenko A, Ishtiaq R, Lock A, Lussi Y, Magrane M, Martin MJ, Orchard S, Raposo P, Speretta E, Tyagi N, Warner K, Zaru R, Diehl AD, Lee R, Chan J, Diamantakis S, Raciti D, Zarowiecki M, Fisher M, Fisher M, James-Zorn C, Ponferrada V, Zorn A, Ramachandran S, Ruzicka L, Westerfield M., Genetics. May 4, 2023; 224 (1):       

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