| 1 | ARID3A, IFNA1
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| Human effector B lymphocytes express ARID3a and secrete interferon alpha.
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| Ward JM, Ratliff ML, Dozmorov MG, Wiley G, Guthridge JM, Gaffney PM, James JA, Webb CF.
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| J Autoimmun 75:130-140. doi: 10.1016/j.jaut.2016.08.003. Epub 2016 Aug 10.
2016
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| 2 | ARID3A, LIN28B
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| Lin28b promotes fetal B lymphopoiesis through the transcription factor Arid3a.
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| Zhou Y, Li YS, Bandi SR, Tang L, Shinton SA, Hayakawa K, Hardy RR.
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| J Exp Med 212(4):569-80. doi: 10.1084/jem.20141510. Epub 2015 Mar 9.
2015
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| 3 | ARID3A, CDKN1A, TP53
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| Cooperation between ARID3A and p53 in the transcriptional activation of p21WAF1 in response to DNA damage.
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| Lestari W, Ichwan SJ, Otsu M, Yamada S, Iseki S, Shimizu S, Ikeda MA.
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| Biochem Biophys Res Commun 417(2):710-6. doi: 10.1016/j.bbrc.2011.12.003. Epub 2011 Dec 8.
2012
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| 4 | ARID3A, ARID3B
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| The ARID family transcription factor bright is required for both hematopoietic stem cell and B lineage development.
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| Webb CF, Bryant J, Popowski M, Allred L, Kim D, Harriss J, Schmidt C, Miner CA, Rose K, Cheng HL, Griffin C, Tucker PW.
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| Mol Cell Biol 31(5):1041-53. Epub 2011 Jan 3.
2011
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| 5 | ARID3A, ARID3B, ARID3C
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| Characterization of a new ARID family transcription factor (Brightlike/ARID3C) that co-activates Bright/ARID3A-mediated immunoglobulin gene transcription.
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| Tidwell JA, Schmidt C, Heaton P, Wilson V, Tucker PW.
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| Mol Immunol ol Immunol. 2011 Sep 26. [Epub ahead of print]
2011
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| 6 | ARID3A
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| Loss of Bright/ARID3a function promotes developmental plasticity.
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| An G, Miner CA, Nixon JC, Kincade PW, Bryant J, Tucker PW, Webb CF.
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| Stem Cells 28(9):1560-7.
2010
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| 7 | ARID3A, BTK, GTF2I
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| Signalling of the BCR is regulated by a lipid rafts-localised transcription factor, Bright.
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| Schmidt C, Kim D, Ippolito GC, Naqvi HR, Probst L, Mathur S, Rosas-Acosta G, Wilson VG, Oldham AL, Poenie M, Webb CF, Tucker PW.
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| EMBO J 28(6):711-24. Epub 2009 Feb 12.
2009
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| 8 | ARID3A, ID1
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| Cross talk between Id1 and its interactive protein Dril1 mediate fibroblast responses to transforming growth factor-beta in pulmonary fibrosis.
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| Lin L, Zhou Z, Zheng L, Alber S, Watkins S, Ray P, Kaminski N, Zhang Y, Morse D.
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| Am J Pathol 173(2):337-46. Epub 2008 Jun 26.
2008
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| 9 | ARID3A
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| Bright/ARID3A contributes to chromatin accessibility of the immunoglobulin heavy chain enhancer.
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| Lin D, Ippolito GC, Zong RT, Bryant J, Koslovsky J, Tucker P.
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| Mol Cancer 6:23.
2007
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| 10 | ARID3A, ARID3B, ARID3C
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| REKLES is an ARID3-restricted multifunctional domain.
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| Kim D, Probst L, Das C, Tucker PW.
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| J Biol Chem 282(21):15768-77. Epub 2007 Mar 29.
2007
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| 11 | ARID3A, BTK, GTF2I
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| Induction of immunoglobulin heavy-chain transcription through the transcription factor Bright requires TFII-I.
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| Rajaiya J, Nixon JC, Ayers N, Desgranges ZP, Roy AL, Webb CF.
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| Mol Cell Biol 26(12):4758-68.
2006
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| 12 | ARID3A
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| A regulated nucleocytoplasmic shuttle contributes to Bright's function as a transcriptional activator of immunoglobulin genes.
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| Kim D, Tucker PW.
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| Mol Cell Biol 26(6):2187-201.
2006
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| 13 | ARID3A
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| Mutations in the DNA-binding domain of the transcription factor Bright act as dominant negative proteins and interfere with immunoglobulin transactivation.
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| Nixon JC, Rajaiya J, Webb CF.
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| J Biol Chem 279(50):52465-72. Epub 2004 Sep 27.
2004
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| 14 | ARID3A
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| A functional screen identifies hDRIL1 as an oncogene that rescues RAS-induced senescence.
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| Peeper DS, Shvarts A, Brummelkamp T, Douma S, Koh EY, Daley GQ, Bernards R.
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| Nat Cell Biol 4(2):148-53.
2002
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| 15 | ARID3A, ARID3B, BTBD1, BTBD2, HAPLN3, EXLD2P, HMG20A, HMG20B, SH3GL1, SH3GL2, TM6SF1, TM6SF2
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| Cloning of the novel gene TM6SF1 reveals conservation of clusters of paralogous genes between human chromosomes 15q24-->q26 and 19p13.3-->p12.
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| Carim-Todd L, Escarceller M, Estivill X, Sumoy L.
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| Cytogenet Cell Genet 90(3-4):255-260. 2000
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| 16 | ARID3A, ARID3C
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| ARID proteins come in from the desert.
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| Kortschak RD, Tucker PW, Saint R.
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| Trends Biochem Sci 25(6):294-9. Review. 2000
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| 17 | ARID3A
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| The human dead ringer/bright homolog, DRIL1 : cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers syndrome.
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| Kortschak RD, et al.
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| Genomics 51 : 288-292. 1998
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