Citations for
1ARID1B, MRD12
Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling.
Vasileiou G, Ekici AB, Uebe S, Zweier C, Hoyer J, Engels H, Behrens J, Reis A, Hadjihannas MV.
Am J Hum Genet 97(3):445-56. doi: 10.1016/j.ajhg.2015.08.002. 2015
2ARID1B
De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature.
Yu Y, Yao R, Wang L, Fan Y, Huang X, Hirschhorn J, Dauber A, Shen Y.
BMC Genomics 16(1):701. doi: 10.1186/s12864-015-1898-1. 2015
3ARID1B
ARID1B-mediated disorders: Mutations and possible mechanisms.
Sim JC, White SM, Lockhart PJ.
Intractable Rare Dis Res 4(1):17-23. doi: 10.5582/irdr.2014.01021. Review. 2015
4ARID1B, CSSSA1B
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability.
Mari F, Marozza A, Mencarelli MA, Lo Rizzo C, Fallerini C, Dosa L, Di Marco C, Carignani G, Baldassarri M, Cianci P, Vivarelli R, Vascotto M, Grosso S, Rubegni P, Caffarelli C, Pretegiani E, Fimiani M, Garavelli L, Cristofoli F, Vermeesch JR, Nuti R, Dotti MT, Balestri P, Hayek J, Selicorni A, Renieri A.
Brain Dev 37(5):527-36. doi: 10.1016/j.braindev.2014.08.009. Epub 2014 Sep 22. 2015
5ARID1A, ARID1B
Numerous BAF complex genes are mutated in Coffin-Siris syndrome.
Miyake N, Tsurusaki Y, Matsumoto N.
Am J Med Genet C Semin Med Genet m J Med Genet C Semin Med Genet. 2014 Jul 31. doi: 10.1002/ajmg.c.31406. [Epub ahead of print] 2014
6ARID1B, CSSSA1B
Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene.
Vals MA, Ňiglane-Shlik E, N§ukas M, Shor R, Peet A, Kals M, Kivistik PA, Metspalu A, Ňunap K.
Eur J Hum Genet 22(11):1327-9. doi: 10.1038/ejhg.2014.25. Epub 2014 Feb 26. 2014
7ARID1B
The ARID1B phenotype: what we have learned so far.
Santen GW, Clayton-Smith J; ARID1B-CSS consortium.
Am J Med Genet C Semin Med Genet 166C(3):276-89. doi: 10.1002/ajmg.c.31414. Epub 2014 Aug 28. Review. 2014
8ARID1B
ARID1B, a member of the human SWI/SNF chromatin remodeling complex, exhibits tumour-suppressor activities in pancreatic cancer cell lines.
Khursheed M, Kolla JN, Kotapalli V, Gupta N, Gowrishankar S, Uppin SG, Sastry RA, Koganti S, Sundaram C, Pollack JR, Bashyam MD.
Br J Cancer 108(10):2056-62. doi: 10.1038/bjc.2013.200. Epub 2013 May 9. 2013
9ARID1A, ARID1B, CSS, CSSSA1A, CSSSA1B, CSSSB1, CSSSCA2, CSSSCA4, CSSSCE1, SMARCA2, SMARCA4, SMARCB1, SMARCE1
Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome.
Tsurusaki Y, Okamoto N, Ohashi H, Kosho T, Imai Y, Hibi-Ko Y, Kaname T, Naritomi K, Kawame H, Wakui K, Fukushima Y, Homma T, Kato M, Hiraki Y, Yamagata T, Yano S, Mizuno S, Sakazume S, Ishii T, Nagai T, Shiina M, Ogata K, Ohta T, Niikawa N, Miyatake S, Okada I, Mizuguchi T, Doi H, Saitsu H, Miyake N, Matsumoto N.
Nat Genet at Genet. 2012 Mar 18. doi: 10.1038/ng.2219. [Epub ahead of print] 2012
10ARID1B, DEL6Q25
Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability.
Hoyer J, Ekici AB, Endele S, Popp B, Zweier C, Wiesener A, Wohlleber E, Dufke A, Rossier E, Petsch C, Zweier M, Gohring I, Zink AM, Rappold G, Schrock E, Wieczorek D, Riess O, Engels H, Rauch A, Reis A.
Am J Hum Genet 90(3):565-572. 2012
11ARID1B, CSS, CSSSA1B
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.
Santen GW, Aten E, Sun Y, Almomani R, Gilissen C, Nielsen M, Kant SG, Snoeck IN, Peeters EA, Hilhorst-Hofstee Y, Wessels MW, den Hollander NS, Ruivenkamp CA, van Ommen GJ, Breuning MH, den Dunnen JT, van Haeringen A, Kriek M.
Nat Genet at Genet. 2012 Mar 18. doi: 10.1038/ng.2217. [Epub ahead of print] 2012
12ARID1B, DEL6Q25, ZDHHC14
Delineation of the interstitial 6q25 microdeletion syndrome: Refinement of the critical causative region.
Michelson M, Ben-Sasson A, Vinkler C, Leshinsky-Silver E, Netzer I, Frumkin A, Kivity S, Lerman-Sagie T, Lev D.
Am J Med Genet A 158A(6):1395-9. doi: 10.1002/ajmg.a.35361. Epub 2012 May 14. 2012
13ARID1B, MRD12
Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability.
Hoyer J, Ekici AB, Endele S, Popp B, Zweier C, Wiesener A, Wohlleber E, Dufke A, Rossier E, Petsch C, Zweier M, G÷hring I, Zink AM, Rappold G, Schr÷ck E, Wieczorek D, Riess O, Engels H, Rauch A, Reis A.
Am J Hum Genet 90(3):565-72. doi: 10.1016/j.ajhg.2012.02.007. 2012
14ARID1B, DEL6Q25
Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B.
Halgren C, Kjaergaard S, Bak M, Hansen C, El-Schich Z, Anderson C, Henriksen K, Hjalgrim H, Kirchhoff M, Bijlsma E, Nielsen M, den Hollander N, Ruivenkamp C, Isidor B, Le Caignec C, Zannolli R, Mucciolo M, Renieri A, Mari F, Anderlid BM, Andrieux J, Dieux A, Tommerup N, Bache I.
Clin Genet lin Genet. 2011 Jul 29. doi: 10.1111/j.1399-0004.2011.01755.x. [Epub ahead of print] 2011
15ARID1A, ARID1B
Dynamics of expression of ARID1A and ARID1B subunits in mouse embryos and in cells during the cell cycle.
Flores-Alcantar A, Gonzalez-Sandoval A, Escalante-Alcalde D, LomelÝ H.
Cell Tissue Res 345(1):137-48. doi: 10.1007/s00441-011-1182-x. Epub 2011 Jun 7. 2011
16ARID1A, ARID1B
Mammalian SWI/SNF--a subunit BAF250/ARID1 is an E3 ubiquitin ligase that targets histone H2B.
Li XS, Trojer P, Matsumura T, Treisman JE, Tanese N.
Mol Cell Biol 30(7):1673-88. Epub 2010 Jan 19. 2010
17ARID1B, SH3BGRL2, TSPYL1, ZHX2
Expression of new red cell-related genes in erythroid differentiation.
De Andrade T, Moreira L, Duarte A, Lanaro C, De Albuquerque D, Saad S, Costa F.
Biochem Genet 48(1-2):164-71. Epub 2009 Nov 26.PMID: 19941055 2010
18ARID1A, ARID1B
Variations in the composition of mammalian SWI/SNF chromatin remodelling complexes.
Ryme J, Asp P, B÷hm S, Cavellßn E, Farrants AK.
J Cell Biochem 108(3):565-76.PMID: 19650111 2009
19ARID1B, TSPYL1, ZHX2
Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster.
de Andrade TG, Peterson KR, Cunha AF, Moreira LS, Fattori A, Saad ST, Costa FF.
Blood Cells Mol Dis 37(2):82-90. Epub 2006 Sep 6.PMID: 16952470 2006
20ARID1A, ARID1B
The p270 (ARID1A/SMARCF1) subunit of mammalian SWI/SNF-related complexes is essential for normal cell cycle arrest.
Nagl NG Jr, Patsialou A, Haines DS, Dallas PB, Beck GR Jr, Moran E.
Cancer Res 65(20):9236-44. 2005
21ARID1A, ARID1B
Two related ARID family proteins are alternative subunits of human SWI/SNF complexes.
Wang X, Nagl NG, Wilsker D, Van Scoy M, Pacchione S, Yaciuk P, Dallas PB, Moran E.
Biochem J 383(Pt 2):319-25. 2004
22ARID1B, ARID1A
Novel SWI/SNF chromatin-remodeling complexes contain a mixed-lineage leukemia chromosomal translocation partner.
Nie Z, Yan Z, Chen EH, Sechi S, Ling C, Zhou S, Xue Y, Yang D, Murray D, Kanakubo E, Cleary ML, Wang W.
Mol Cell Biol 23(8):2942-52. 2003
23ARID1B
Ischemia induces early expression of a new transcription factor (6A3-5) in kidney vascular smooth muscle cells: studies in rat and human renal pathology.
Garin G, Badid C, McGregor B, Vincent M, Guerret S, Zibara K, Hurlstone A, Laville M, McGregor JL.
Am J Pathol 163(6):2485-94. 2003
24ARID1B, SMARCA4
Cloning and characterization of hELD/OSA1, a novel BRG1 interacting protein.
Hurlstone AF, Olave IA, Barker N, van Noort M, Clevers H.
Biochem J 364(Pt 1):255-64. 2002
25AARS2, ADAMTSL3, AHRR, AMIGO1, ANKFY1, ARHGAP31, ARID1A, ARID1B, ASAP1, ASB1, BACE1, BIRC6, BRPF3, C14orf118, CASKIN2, CCPG1, CD2BP2, CNOT6, COG6, CPAMD8, DCDC2, DLG3, ERBIN, ERGIC1, FAM190B, FAM63B, FBXO40, FILIP1, FSTL5, FZR1, GALNTL1, GATAD2B, GDA, GMEB2, GNPTAB, GRID1, GRIPAP1, HECTD1, HEG1, HHATL, INTU, IPO9, ISY1, KCNH3, KIAA1143, KIAA1161, KIAA1191, KIAA1217, KIAA1274, LCHN, LMBR1L, LRFN2, LRRC47, MACF1, MAP7D1, MIER2, MTA3, MYO5B, MYOF, NDFIP2, NDRG2, NELFB, NLGN4X, NLN, OGDHL, PAIP2B, PAK7, PECR, PLEKHG1, PLEKHH1, PNKD, PNMAL2, PPP1R9A, PRDM10, REXO1, RIMKLB, RNF150, SGPL1, SHROOM4, SLC39A10, SLC45A4, SRGAP2, STK36, SULF2, TBC1D24, TLE4, TMCC3, TPCN1, TRMT6, TTC7A, TTC7B, USP31, ZBTB47, ZC4H2, ZNF295, ZNF490, ZNF644, ZNF777
Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain.
Hirosawa M, Nagase T, Ishikawa K, Kikuno R, Nomura N, Ohara O.
DNA Res 6(5):329-36. 1999