Palmer SJ - Search Results

1

The role of GTF2IRD1 in the auditory pathology of Williams-Beuren Syndrome.

Canales CP, Wong AC, Gunning PW, Housley GD, Hardeman EC, Palmer SJ. Canales CP, et al. Among authors: palmer sj. Eur J Hum Genet. 2015 Jun;23(6):774-80. doi: 10.1038/ejhg.2014.188. Epub 2014 Sep 24. Eur J Hum Genet. 2015. PMID: 25248400 Free PMC article.

2

Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development.

Palmer SJ, Tay ES, Santucci N, Cuc Bach TT, Hook J, Lemckert FA, Jamieson RV, Gunnning PW, Hardeman EC. Palmer SJ, et al. Gene Expr Patterns. 2007 Feb;7(4):396-404. doi: 10.1016/j.modgep.2006.11.008. Epub 2006 Dec 1. Gene Expr Patterns. 2007. PMID: 17239664

3

Negative autoregulation of GTF2IRD1 in Williams-Beuren syndrome via a novel DNA binding mechanism.

Palmer SJ, Santucci N, Widagdo J, Bontempo SJ, Taylor KM, Tay ES, Hook J, Lemckert F, Gunning PW, Hardeman EC. Palmer SJ, et al. J Biol Chem. 2010 Feb 12;285(7):4715-24. doi: 10.1074/jbc.M109.086660. Epub 2009 Dec 9. J Biol Chem. 2010. PMID: 20007321 Free PMC article.

4

Mutation of Gtf2ird1 from the Williams-Beuren syndrome critical region results in facial dysplasia, motor dysfunction, and altered vocalisations.

Howard ML, Palmer SJ, Taylor KM, Arthurson GJ, Spitzer MW, Du X, Pang TY, Renoir T, Hardeman EC, Hannan AJ. Howard ML, et al. Among authors: palmer sj. Neurobiol Dis. 2012 Mar;45(3):913-22. doi: 10.1016/j.nbd.2011.12.010. Epub 2011 Dec 11. Neurobiol Dis. 2012. PMID: 22198572

5

GTF2IRD2 from the Williams-Beuren critical region encodes a mobile-element-derived fusion protein that antagonizes the action of its related family members.

Palmer SJ, Taylor KM, Santucci N, Widagdo J, Chan YK, Yeo JL, Adams M, Gunning PW, Hardeman EC. Palmer SJ, et al. J Cell Sci. 2012 Nov 1;125(Pt 21):5040-50. doi: 10.1242/jcs.102798. Epub 2012 Aug 16. J Cell Sci. 2012. PMID: 22899722 Free PMC article.

6

SUMOylation of GTF2IRD1 regulates protein partner interactions and ubiquitin-mediated degradation.

Widagdo J, Taylor KM, Gunning PW, Hardeman EC, Palmer SJ. Widagdo J, et al. Among authors: palmer sj. PLoS One. 2012;7(11):e49283. doi: 10.1371/journal.pone.0049283. Epub 2012 Nov 8. PLoS One. 2012. PMID: 23145142 Free PMC article.

7

The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulation.

Carmona-Mora P, Widagdo J, Tomasetig F, Canales CP, Cha Y, Lee W, Alshawaf A, Dottori M, Whan RM, Hardeman EC, Palmer SJ. Carmona-Mora P, et al. Among authors: palmer sj. Hum Genet. 2015 Oct;134(10):1099-115. doi: 10.1007/s00439-015-1591-0. Epub 2015 Aug 15. Hum Genet. 2015. PMID: 26275350

8

RNA-Seq analysis of Gtf2ird1 knockout epidermal tissue provides potential insights into molecular mechanisms underpinning Williams-Beuren syndrome.

Corley SM, Canales CP, Carmona-Mora P, Mendoza-Reinosa V, Beverdam A, Hardeman EC, Wilkins MR, Palmer SJ. Corley SM, et al. Among authors: palmer sj. BMC Genomics. 2016 Jun 13;17:450. doi: 10.1186/s12864-016-2801-4. BMC Genomics. 2016. PMID: 27295951 Free PMC article.

9

MusTRD can regulate postnatal fiber-specific expression.

Issa LL, Palmer SJ, Guven KL, Santucci N, Hodgson VR, Popovic K, Joya JE, Hardeman EC. Issa LL, et al. Among authors: palmer sj. Dev Biol. 2006 May 1;293(1):104-15. doi: 10.1016/j.ydbio.2006.01.019. Epub 2006 Feb 21. Dev Biol. 2006. PMID: 16494860 Free article.

10

hMusTRD1alpha1 represses MEF2 activation of the troponin I slow enhancer.

Polly P, Haddadi LM, Issa LL, Subramaniam N, Palmer SJ, Tay ES, Hardeman EC. Polly P, et al. Among authors: palmer sj. J Biol Chem. 2003 Sep 19;278(38):36603-10. doi: 10.1074/jbc.M212814200. Epub 2003 Jul 10. J Biol Chem. 2003. PMID: 12857748 Free article.

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