Roberts RG - Search Results

1

Profound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat.

Böhm SV, Constantinou P, Tan S, Jin H, Roberts RG. Böhm SV, et al. Among authors: roberts rg. BMC Biol. 2009 Dec 4;7:85. doi: 10.1186/1741-7007-7-85. BMC Biol. 2009. PMID: 19961569 Free PMC article.

2

The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms.

Jin H, Tan S, Hermanowski J, Böhm S, Pacheco S, McCauley JM, Greener MJ, Hinits Y, Hughes SM, Sharpe PT, Roberts RG. Jin H, et al. Among authors: roberts rg. BMC Genomics. 2007 Jan 17;8:19. doi: 10.1186/1471-2164-8-19. BMC Genomics. 2007. PMID: 17233888 Free PMC article.

3

Schistosome dystrophin and dystrobrevin proteins contain large insertions.

Tan S, Johnston DA, Roberts RG. Tan S, et al. Among authors: roberts rg. Biochem Biophys Res Commun. 2007 Oct 26;362(3):700-6. doi: 10.1016/j.bbrc.2007.08.063. Epub 2007 Aug 24. Biochem Biophys Res Commun. 2007. PMID: 17764661

4

Dystrobrevin and dystrophin family gene expression in zebrafish.

Böhm S, Jin H, Hughes SM, Roberts RG, Hinits Y. Böhm S, et al. Among authors: roberts rg. Gene Expr Patterns. 2008 Jan;8(2):71-8. doi: 10.1016/j.modgep.2007.10.004. Epub 2007 Oct 24. Gene Expr Patterns. 2008. PMID: 18042440 Free PMC article.

5

Expression of members of the dystrophin, dystrobrevin, and dystrotelin superfamily.

Böhm SV, Roberts RG. Böhm SV, et al. Among authors: roberts rg. Crit Rev Eukaryot Gene Expr. 2009;19(2):89-108. doi: 10.1615/critreveukargeneexpr.v19.i2.10. Crit Rev Eukaryot Gene Expr. 2009. PMID: 19392646 Review.

6

Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene.

King K, Bagnall R, Fisher SA, Sheikh F, Cuthbert A, Tan S, Mundy NI, Rosenstiel P, Schreiber S, Mathew CG, Roberts RG. King K, et al. Among authors: roberts rg. Genomics. 2007 Oct;90(4):493-501. doi: 10.1016/j.ygeno.2007.07.009. Epub 2007 Aug 24. Genomics. 2007. PMID: 17719742 Free article.

7

Heterozygous deletion of a 2-Mb region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities.

Frost AR, Böhm SV, Sewduth RN, Josifova D, Ogilvie CM, Izatt L, Roberts RG. Frost AR, et al. Among authors: roberts rg. Eur J Hum Genet. 2010 Jul;18(7):852-5. doi: 10.1038/ejhg.2010.28. Epub 2010 Mar 17. Eur J Hum Genet. 2010. PMID: 20234391 Free PMC article.

8

Nesprin-2 epsilon: a novel nesprin isoform expressed in human ovary and Ntera-2 cells.

Lam le T, Böhm SV, Roberts RG, Morris GE. Lam le T, et al. Among authors: roberts rg. Biochem Biophys Res Commun. 2011 Aug 26;412(2):291-5. doi: 10.1016/j.bbrc.2011.07.085. Epub 2011 Jul 28. Biochem Biophys Res Commun. 2011. PMID: 21820406

9

Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardation.

Jin H, Gardner RJ, Viswesvaraiah R, Muntoni F, Roberts RG. Jin H, et al. Among authors: roberts rg. Eur J Hum Genet. 2000 Feb;8(2):87-94. doi: 10.1038/sj.ejhg.5200415. Eur J Hum Genet. 2000. PMID: 10757639

10

Structural evolution of the BRCA1 genomic region in primates.

Jin H, Selfe J, Whitehouse C, Morris JR, Solomon E, Roberts RG. Jin H, et al. Among authors: roberts rg. Genomics. 2004 Dec;84(6):1071-82. doi: 10.1016/j.ygeno.2004.08.019. Genomics. 2004. PMID: 15533724

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