| 1 | ARID1A, ARID1B, TNPO1
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| TNPO1-mediated nuclear import of ARID1B promotes tumor growth in ARID1A-deficient gynecologic cancer.
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| Yang B, Chen J, Li X, Zhang X, Hu L, Jiang S, Zhang Z, Teng Y.
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| Cancer Lett. Sep 1;515:14-27. doi: 10.1016/j.canlet.2021.05.016. Epub 2021 May 25 2021
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| 2 | ARID1B, MRD12
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| Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling.
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| Vasileiou G, Ekici AB, Uebe S, Zweier C, Hoyer J, Engels H, Behrens J, Reis A, Hadjihannas MV.
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| Am J Hum Genet 97(3):445-56. doi: 10.1016/j.ajhg.2015.08.002.
2015
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| 3 | ARID1B
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| De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature.
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| Yu Y, Yao R, Wang L, Fan Y, Huang X, Hirschhorn J, Dauber A, Shen Y.
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| BMC Genomics 16(1):701. doi: 10.1186/s12864-015-1898-1.
2015
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| 4 | ARID1B
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| ARID1B-mediated disorders: Mutations and possible mechanisms.
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| Sim JC, White SM, Lockhart PJ.
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| Intractable Rare Dis Res 4(1):17-23. doi: 10.5582/irdr.2014.01021. Review.
2015
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| 5 | ARID1B, CSSSA1B
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| Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability.
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| 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.
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| Brain Dev 37(5):527-36. doi: 10.1016/j.braindev.2014.08.009. Epub 2014 Sep 22. 2015
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| 6 | ARID1A, ARID1B
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| Numerous BAF complex genes are mutated in Coffin-Siris syndrome.
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| Miyake N, Tsurusaki Y, Matsumoto N.
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| 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
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| 7 | ARID1B, CSSSA1B
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| Coffin-Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene.
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| Vals MA, Õiglane-Shlik E, Nõukas M, Shor R, Peet A, Kals M, Kivistik PA, Metspalu A, Õunap K.
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| Eur J Hum Genet 22(11):1327-9. doi: 10.1038/ejhg.2014.25. Epub 2014 Feb 26. 2014
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| 8 | ARID1B
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| The ARID1B phenotype: what we have learned so far.
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| Santen GW, Clayton-Smith J; ARID1B-CSS consortium.
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| Am J Med Genet C Semin Med Genet 166C(3):276-89. doi: 10.1002/ajmg.c.31414. Epub 2014 Aug 28. Review.
2014
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| 9 | ARID1B
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| ARID1B, a member of the human SWI/SNF chromatin remodeling complex, exhibits tumour-suppressor activities in pancreatic cancer cell lines.
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| Khursheed M, Kolla JN, Kotapalli V, Gupta N, Gowrishankar S, Uppin SG, Sastry RA, Koganti S, Sundaram C, Pollack JR, Bashyam MD.
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| Br J Cancer 108(10):2056-62. doi: 10.1038/bjc.2013.200. Epub 2013 May 9.
2013
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| 10 | ARID1B, METTL4, ZPLD1
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| Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy.
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| Kobayashi D, Nishizawa D, Takasaki Y, Kasai S, Kakizawa T, Ikeda K, Fukuda K.
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| Mol Pain 9:34. doi: 10.1186/1744-8069-9-34.
2013
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| 11 | ARID1A, ARID1B, CSS, CSSSA1A, CSSSA1B, CSSSB1, CSSSCA2, CSSSCA4, CSSSCE1, SMARCA2, SMARCA4, SMARCB1, SMARCE1
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| Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome.
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| 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.
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| Nat Genet at Genet. 2012 Mar 18. doi: 10.1038/ng.2219. [Epub ahead of print] 2012
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| 12 | ARID1B, DEL6Q25
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| Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability.
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| 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.
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| Am J Hum Genet 90(3):565-572. 2012
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| 13 | ARID1B, CSS, CSSSA1B
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| Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.
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| 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.
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| Nat Genet at Genet. 2012 Mar 18. doi: 10.1038/ng.2217. [Epub ahead of print] 2012
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| 14 | ARID1B, MRD12
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| Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability.
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| Hoyer J, Ekici AB, Endele S, Popp B, Zweier C, Wiesener A, Wohlleber E, Dufke A, Rossier E, Petsch C, Zweier M, Göhring I, Zink AM, Rappold G, Schröck E, Wieczorek D, Riess O, Engels H, Rauch A, Reis A.
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| Am J Hum Genet 90(3):565-72. doi: 10.1016/j.ajhg.2012.02.007.
2012
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| 15 | ARID1B, DEL6Q25, ZDHHC14
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| Delineation of the interstitial 6q25 microdeletion syndrome: refinement of the critical causative region
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| Michelson M, Ben-Sasson A, Vinkler C, Leshinsky-Silver E, Netzer I, Frumkin A, Kivity S, Lerman-Sagie T, Lev D.
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| Am J Med Genet A. Jun;158A(6):1395-9. doi: 10.1002/ajmg.a.35361. Epub 2012 May 14. 2012
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| 16 | ARID1B, DEL6Q25
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| Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B.
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| 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.
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| Clin Genet lin Genet. 2011 Jul 29. doi: 10.1111/j.1399-0004.2011.01755.x. [Epub ahead of print]
2011
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| 17 | ARID1A, ARID1B
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| Dynamics of expression of ARID1A and ARID1B subunits in mouse embryos and in cells during the cell cycle.
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| Flores-Alcantar A, Gonzalez-Sandoval A, Escalante-Alcalde D, Lomelí H.
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| Cell Tissue Res 345(1):137-48. doi: 10.1007/s00441-011-1182-x. Epub 2011 Jun 7.
2011
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| 18 | ARID1A, ARID1B
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| Mammalian SWI/SNF--a subunit BAF250/ARID1 is an E3 ubiquitin ligase that targets histone H2B.
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| Li XS, Trojer P, Matsumura T, Treisman JE, Tanese N.
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| Mol Cell Biol 30(7):1673-88. Epub 2010 Jan 19.
2010
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| 19 | ARID1B, SH3BGRL2, TSPYL1, ZHX2
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| Expression of new red cell-related genes in erythroid differentiation.
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| De Andrade T, Moreira L, Duarte A, Lanaro C, De Albuquerque D, Saad S, Costa F.
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| Biochem Genet 48(1-2):164-71. Epub 2009 Nov 26.PMID: 19941055 2010
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| 20 | ARID1A, ARID1B
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| Variations in the composition of mammalian SWI/SNF chromatin remodelling complexes.
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| Ryme J, Asp P, Böhm S, Cavellán E, Farrants AK.
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| J Cell Biochem 108(3):565-76.PMID: 19650111 2009
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| 21 | ARID1B, TSPYL1, ZHX2
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| Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster.
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| de Andrade TG, Peterson KR, Cunha AF, Moreira LS, Fattori A, Saad ST, Costa FF.
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| Blood Cells Mol Dis 37(2):82-90. Epub 2006 Sep 6.PMID: 16952470 2006
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| 22 | ARID1A, ARID1B
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| The p270 (ARID1A/SMARCF1) subunit of mammalian SWI/SNF-related complexes is essential for normal cell cycle arrest.
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| Nagl NG Jr, Patsialou A, Haines DS, Dallas PB, Beck GR Jr, Moran E.
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| Cancer Res 65(20):9236-44. 2005
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| 23 | ARID1A, ARID1B
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| Two related ARID family proteins are alternative subunits of human SWI/SNF complexes.
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| Wang X, Nagl NG, Wilsker D, Van Scoy M, Pacchione S, Yaciuk P, Dallas PB, Moran E.
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| Biochem J 383(Pt 2):319-25. 2004
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| 24 | ARID1B, ARID1A
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| Novel SWI/SNF chromatin-remodeling complexes contain a mixed-lineage leukemia chromosomal translocation partner.
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| Nie Z, Yan Z, Chen EH, Sechi S, Ling C, Zhou S, Xue Y, Yang D, Murray D, Kanakubo E, Cleary ML, Wang W.
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| Mol Cell Biol 23(8):2942-52. 2003
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| 25 | ARID1B
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| Ischemia induces early expression of a new transcription factor (6A3-5) in kidney vascular smooth muscle cells: studies in rat and human renal pathology.
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| Garin G, Badid C, McGregor B, Vincent M, Guerret S, Zibara K, Hurlstone A, Laville M, McGregor JL.
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| Am J Pathol 163(6):2485-94. 2003
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| 26 | ARID1B, SMARCA4
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| Cloning and characterization of hELD/OSA1, a novel BRG1 interacting protein.
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| Hurlstone AF, Olave IA, Barker N, van Noort M, Clevers H.
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| Biochem J 364(Pt 1):255-64. 2002
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| 27 | AARS2, 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, KIAA1191, KIAA1217, KIAA1274, LCHN, LMBR1L, LRFN2, LRRC47, MACF1, MAP7D1, MIER2, MTA3, MYO5B, MYOF, MYORG, 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, ZBTB21, ZBTB47, ZC4H2, ZNF490, ZNF644, ZNF777
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| Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain.
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| Hirosawa M, Nagase T, Ishikawa K, Kikuno R, Nomura N, Ohara O.
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| DNA Res 6(5):329-36. 1999
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