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Stringent comparative sequence analysis reveals SOX10 as a putative inhibitor of glial cell differentiation.

Gopinath C, Law WD, Rodríguez-Molina JF, Prasad AB, Song L, Crawford GE, Mullikin JC, Svaren J, Antonellis A.

BMC Genomics. 2016 Nov 7;17(1):887.


Upregulation of the Nr2f1-A830082K12Rik gene pair in murine neural crest cells results in a complex phenotype reminiscent of Waardenburg syndrome type 4.

Bergeron KF, Nguyen CM, Cardinal T, Charrier B, Silversides DW, Pilon N.

Dis Model Mech. 2016 Nov 1;9(11):1283-1293. Epub 2016 Sep 1.


SOX10 regulates an alternative promoter at the Charcot-Marie-Tooth disease locus MTMR2.

Fogarty EA, Brewer MH, Rodriguez-Molina JF, Law WD, Ma KH, Steinberg NM, Svaren J, Antonellis A.

Hum Mol Genet. 2016 Sep 15;25(18):3925-3936. doi: 10.1093/hmg/ddw233. Epub 2016 Jul 27.


Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new players.

Bondurand N, Southard-Smith EM.

Dev Biol. 2016 Sep 15;417(2):139-57. doi: 10.1016/j.ydbio.2016.06.042. Epub 2016 Jun 28. Review.


Regulation of SOX10 stability via ubiquitination-mediated degradation by Fbxw7α modulates melanoma cell migration.

Lv XB, Wu W, Tang X, Wu Y, Zhu Y, Liu Y, Cui X, Chu J, Hu P, Li J, Guo Q, Cai Z, Wu J, Hu K, Ouyang N.

Oncotarget. 2015 Nov 3;6(34):36370-82. doi: 10.18632/oncotarget.5639.


Genomic analysis reveals distinct mechanisms and functional classes of SOX10-regulated genes in melanocytes.

Fufa TD, Harris ML, Watkins-Chow DE, Levy D, Gorkin DU, Gildea DE, Song L, Safi A, Crawford GE, Sviderskaya EV, Bennett DC, Mccallion AS, Loftus SK, Pavan WJ.

Hum Mol Genet. 2015 Oct 1;24(19):5433-50. doi: 10.1093/hmg/ddv267. Epub 2015 Jul 23.


The transcription factors Ets1 and Sox10 interact during murine melanocyte development.

Saldana-Caboverde A, Perera EM, Watkins-Chow DE, Hansen NF, Vemulapalli M, Mullikin JC; NISC Comparative Sequencing Program, Pavan WJ, Kos L.

Dev Biol. 2015 Nov 15;407(2):300-12. doi: 10.1016/j.ydbio.2015.04.012. Epub 2015 Apr 23.


Haplotype-specific modulation of a SOX10/CREB response element at the Charcot-Marie-Tooth disease type 4C locus SH3TC2.

Brewer MH, Ma KH, Beecham GW, Gopinath C, Baas F, Choi BO, Reilly MM, Shy ME, Züchner S, Svaren J, Antonellis A.

Hum Mol Genet. 2014 Oct 1;23(19):5171-87. doi: 10.1093/hmg/ddu240. Epub 2014 May 15.


Developmental programming mediated by complementary roles of imprinted Grb10 in mother and pup.

Cowley M, Garfield AS, Madon-Simon M, Charalambous M, Clarkson RW, Smalley MJ, Kendrick H, Isles AR, Parry AJ, Carney S, Oakey RJ, Heisler LK, Moorwood K, Wolf JB, Ward A.

PLoS Biol. 2014 Feb 25;12(2):e1001799. doi: 10.1371/journal.pbio.1001799. eCollection 2014 Feb.


Epistatic and combinatorial effects of pigmentary gene mutations in the domestic pigeon.

Domyan ET, Guernsey MW, Kronenberg Z, Krishnan S, Boissy RE, Vickrey AI, Rodgers C, Cassidy P, Leachman SA, Fondon JW 3rd, Yandell M, Shapiro MD.

Curr Biol. 2014 Feb 17;24(4):459-64. doi: 10.1016/j.cub.2014.01.020. Epub 2014 Feb 6.


From remote enhancers to gene regulation: charting the genome's regulatory landscapes.

Symmons O, Spitz F.

Philos Trans R Soc Lond B Biol Sci. 2013 May 6;368(1620):20120358. doi: 10.1098/rstb.2012.0358. Print 2013. Review.


Integration of ChIP-seq and machine learning reveals enhancers and a predictive regulatory sequence vocabulary in melanocytes.

Gorkin DU, Lee D, Reed X, Fletez-Brant C, Bessling SL, Loftus SK, Beer MA, Pavan WJ, McCallion AS.

Genome Res. 2012 Nov;22(11):2290-301. doi: 10.1101/gr.139360.112. Epub 2012 Sep 27.


Screening of MITF and SOX10 regulatory regions in Waardenburg syndrome type 2.

Baral V, Chaoui A, Watanabe Y, Goossens M, Attie-Bitach T, Marlin S, Pingault V, Bondurand N.

PLoS One. 2012;7(7):e41927. doi: 10.1371/journal.pone.0041927. Epub 2012 Jul 27.


Genome-wide analysis of EGR2/SOX10 binding in myelinating peripheral nerve.

Srinivasan R, Sun G, Keles S, Jones EA, Jang SW, Krueger C, Moran JJ, Svaren J.

Nucleic Acids Res. 2012 Aug;40(14):6449-60. doi: 10.1093/nar/gks313. Epub 2012 Apr 9.


Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4.

Bondurand N, Fouquet V, Baral V, Lecerf L, Loundon N, Goossens M, Duriez B, Labrune P, Pingault V.

Eur J Hum Genet. 2012 Sep;20(9):990-4. doi: 10.1038/ejhg.2012.29. Epub 2012 Feb 29.


Distal enhancers upstream of the Charcot-Marie-Tooth type 1A disease gene PMP22.

Jones EA, Brewer MH, Srinivasan R, Krueger C, Sun G, Charney KN, Keles S, Antonellis A, Svaren J.

Hum Mol Genet. 2012 Apr 1;21(7):1581-91. doi: 10.1093/hmg/ddr595. Epub 2011 Dec 15.


SOX10 regulates expression of the SH3-domain kinase binding protein 1 (Sh3kbp1) locus in Schwann cells via an alternative promoter.

Hodonsky CJ, Kleinbrink EL, Charney KN, Prasad M, Bessling SL, Jones EA, Srinivasan R, Svaren J, McCallion AS, Antonellis A.

Mol Cell Neurosci. 2012 Feb;49(2):85-96. doi: 10.1016/j.mcn.2011.10.004. Epub 2011 Oct 19.


An iterative genetic and dynamical modelling approach identifies novel features of the gene regulatory network underlying melanocyte development.

Greenhill ER, Rocco A, Vibert L, Nikaido M, Kelsh RN.

PLoS Genet. 2011 Sep;7(9):e1002265. doi: 10.1371/journal.pgen.1002265. Epub 2011 Sep 1.


Transcription factor Sox10 orchestrates activity of a neural crest-specific enhancer in the vicinity of its gene.

Wahlbuhl M, Reiprich S, Vogl MR, Bösl MR, Wegner M.

Nucleic Acids Res. 2012 Jan;40(1):88-101. doi: 10.1093/nar/gkr734. Epub 2011 Sep 9.


SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer.

Prasad MK, Reed X, Gorkin DU, Cronin JC, McAdow AR, Chain K, Hodonsky CJ, Jones EA, Svaren J, Antonellis A, Johnson SL, Loftus SK, Pavan WJ, McCallion AS.

BMC Dev Biol. 2011 Jun 14;11:40. doi: 10.1186/1471-213X-11-40.

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