| 1 | SATB2, UPF3B
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| Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene.
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| Leoyklang P, Suphapeetiporn K, Srichomthong C, Tongkobpetch S, Fietze S, Dorward H, Cullinane AR, Gahl WA, Huizing M, Shotelersuk V.
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| Hum Genet 132(12):1383-93. doi: 10.1007/s00439-013-1345-9. Epub 2013 Aug 8.
2013
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| 2 | SATB2, SKI
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| Protooncogene Ski cooperates with the chromatin-remodeling factor Satb2 in specifying callosal neurons.
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| Baranek C, Dittrich M, Parthasarathy S, Bonnon CG, Britanova O, Lanshakov D, Boukhtouche F, Sommer JE, Colmenares C, Tarabykin V, Atanasoski S.
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| Proc Natl Acad Sci U S A. 109(9):3546-51 2012
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| 3 | SATB1, SATB2
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| Satb1 and Satb2 are dispensable for X chromosome inactivation in mice.
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| Nechanitzky R, Dávila A, Savarese F, Fietze S, Grosschedl R.
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| Dev Cell 23(4):866-71. doi: 10.1016/j.devcel.2012.09.018.
2012
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| 4 | SATB1, SATB2
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| SATB homeobox proteins regulate trophoblast stem cell renewal and differentiation.
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| Asanoma K, Kubota K, Chakraborty D, Renaud SJ, Wake N, Fukushima K, Soares MJ, Rumi MA.
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| J Biol Chem 287(3):2257-68. doi: 10.1074/jbc.M111.287128. Epub 2011 Nov 28.
2012
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| 5 | DEL2Q32, SATB2
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| Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.
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| Balasubramanian M, Smith K, Basel-Vanagaite L, Feingold MF, Brock P, Gowans GC, Vasudevan PC, Cresswell L, Taylor EJ, Harris CJ, Friedman N, Moran R, Feret H, Zackai EH, Theisen A, Rosenfeld JA, Parker MJ.
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| J Med Genet 48(5):290-8. Epub 2011 Feb 22.
2011
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| 6 | SATB2, SP7
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| Osteoblast-specific transcription factor Osterix (Osx) is an upstream regulator of Satb2 during bone formation.
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| Tang W, Li Y, Osimiri L, Zhang C.
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| J Biol Chem 286(38):32995-3002. Epub 2011 Aug 2.
2011
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| 7 | SATB2, TP63
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| Special AT-rich binding protein-2 (SATB2) differentially affects disease-causing p63 mutant proteins.
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| Chung J, Grant RI, Kaplan DR, Irwin MS.
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| J Biol Chem 286(47):40671-80. doi: 10.1074/jbc.M111.271189. Epub 2011 Sep 29.
2011
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| 8 | NANOG, SATB1, SATB2
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| Satb1 and Satb2 regulate embryonic stem cell differentiation and Nanog expression.
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| Savarese F, Dávila A, Nechanitzky R, De La Rosa-Velazquez I, Pereira CF, Engelke R, Takahashi K, Jenuwein T, Kohwi-Shigematsu T, Fisher AG, Grosschedl R.
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| Genes Dev 23(22):2625-38.PMID: 19933152 2009
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| 9 | DEL2Q32, SATB2
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| Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.
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| Rosenfeld JA, Ballif BC, Lucas A, Spence EJ, Powell C, Aylsworth AS, Torchia BA, Shaffer LG.
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| PLoS One 4(8):e6568.PMID: 19668335 2009
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| 10 | SATB1, SATB2
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| The mRNA expression of SATB1 and SATB2 in human breast cancer.
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| Patani N, Jiang W, Mansel R, Newbold R, Mokbel K.
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| Cancer Cell Int 9:18.PMID: 19642980 2009
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| 11 | SATB2
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| Toriello-Carey syndrome in a patient with a de novo balanced translocation [46,XY,t(2;14)(q33;q22)] interrupting SATB2.
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| Tegay DH, Chan KK, Leung L, Wang C, Burkett S, Stone G, Stanyon R, Toriello HV, Hatchwell E.
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| Clin Genet 75(3):259-64.PMID: 19170718 2009
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| 12 | DEL2Q32, SATB2
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| 4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate.
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| Urquhart J, Black GC, Clayton-Smith J.
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| Eur J Med Genet 52(6):454-7. Epub 2009 Jul 1.PMID: 19576302 2009
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| 13 | SATB2
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| SATB2 interacts with chromatin-remodeling molecules in differentiating cortical neurons.
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| Gyorgy AB, Szemes M, de Juan Romero C, Tarabykin V, Agoston DV.
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| Eur J Neurosci 27(4):865-73.PMID: 18333962 2008
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| 14 | SATB2
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| SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation.
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| Dobreva G, Chahrour M, Dautzenberg M, Chirivella L, Kanzler B, Farinas I, Karsenty G, Grosschedl R.
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| Cell 125(5):971-86. 2006
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| 15 | DEL2Q32, SATB2
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| Satb2 Haploinsufficiency Phenocopies 2q32-q33 Deletions, whereas Loss Suggests a Fundamental Role in the Coordination of Jaw Development.
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| Britanova O, Depew MJ, Schwark M, Thomas BL, Miletich I, Sharpe P, Tarabykin V.
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| Am J Hum Genet 79(4):668-78. Epub 2006 Aug 30. 2006
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| 16 | TGFA, SATB2, OFC2, OFC7
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| Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.
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| Beaty TH, Hetmanski JB, Fallin MD, Park JW, Sull JW, McIntosh I, Liang KY, Vanderkolk CA, Redett RJ, Boyadjiev SA, Jabs EW, Chong SS, Cheah FS, Wu-Chou YH, Chen PK, Chiu YF, Yeow V, Ng IS, Cheng J, Huang S, Ye X, Wang H, Ingersoll R, Scott AF.
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| Hum Genet 120(4):501-18. Epub 2006 Sep 5. 2006
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| 17 | SATB1, SATB2
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| Novel transcription factor Satb2 interacts with matrix attachment region DNA elements in a tissue-specific manner and demonstrates cell-type-dependent expression in the developing mouse CNS.
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| Britanova O, Akopov S, Lukyanov S, Gruss P, Tarabykin V.
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| Eur J Neurosci 21(3):658-68.PMID: 15733084 2005
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| 18 | FOXE1, HTAT, IRF6, MSX1, NECTIN1, OFC2, OFC5, OFC6, OFC6, SATB2, SCD5, TP63
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| Genetics of cleft lip and palate: syndromic genes contribute to the incidence of non-syndromic clefts.
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| Stanier P, Moore GE.
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| Hum Mol Genet 13 Spec No 1:R73-81. Epub 2004 Jan 13. 2004
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| 19 | DEL2Q32, OFC7, SATB2
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| Identification of SATB2 as the cleft palate gene on 2q32-q33.
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| FitzPatrick DR, Carr IM, McLaren L, Leek JP, Wightman P, Williamson K, Gautier P, McGill N, Hayward C, Firth H, Markham AF, Fantes JA, Bonthron DT.
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| Hum Mol Genet 12(19):2491-501. Epub 2003 Jul 29. 2003
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| 20 | SATB2
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| SUMO modification of a novel MAR-binding protein, SATB2, modulates immunoglobulin mu gene expression.
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| Dobreva G, Dambacher J, Grosschedl R.
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| Genes Dev. 17(24):3048-61. 2003
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| 21 | DEL2Q32,SATB2, PRS, OFC7
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| Pierre Robin sequence and interstitial deletion 2q32.3-q33.2.
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| Houdayer C, Portnoi MF, Vialard F, Soupre V, Crumiere C, Taillemite JL, Couderc R, Vazquez MP, Bahuau M.
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| Am J Med Genet 102(3):219-26. 2001
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| 22 | ABI2, AOX1, BMPR2, CASP10, CASP8, CD28, CFLAR, CLK1, CTLA4, DAZAP2, MAGI2, ORC2, PPH1, PSMA2, SATB2, SUMO1, TRAK2
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| A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension.
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| Machado RD, Pauciulo MW, Fretwell N, Veal C, Thomson JR, Vilarino Guell C, Aldred M, Brannon CA, Trembath RC, Nichols WC.
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| Genomics 68(2):220-8. 2000
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| 23 | AAK1, ANKRD26, ARHGEF4, CEP131, CEP164, DOCK9, DOLK, DOPEY1, EPN2, GARNL4, HIC2, KIAA1033, KIAA1109, LIMCH1, LMTK2, MYT1, NLGN1, OTUD4, PDZRN3, PITRM1, PLCH1, PLCL2, PPM1E, RAP140, RBM16, RNF44, SAMD4A, SAPS1, SATB2, SLC8A2, SMG5, SON, SULF1, SV2C, SYNPO, TBC1D2B, TRAK1, TRIM33, TRIM35, TTC28, USP2, USP22, USP24, WDTC1, ZC3H4, ZFR2, ZNF507
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| Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
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| Kikuno R, Nagase T, Ishikawa K, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O.
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| DNA Res 6(3):197-205. 1999
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