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MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain.
Goodwin M, Mohan A, Batra R, Lee KY, Charizanis K, Fernández Gómez FJ, Eddarkaoui S, Sergeant N, Buée L, Kimura T, Clark HB, Dalton J, Takamura K, Weyn-Vanhentenryck SM, Zhang C, Reid T, Ranum LP, Day JW, Swanson MS. Goodwin M, et al. Among authors: dalton j. Cell Rep. 2015 Aug 18;12(7):1159-68. doi: 10.1016/j.celrep.2015.07.029. Epub 2015 Aug 6. Cell Rep. 2015. PMID: 26257173 Free PMC article.
Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.
Day JW, Ricker K, Jacobsen JF, Rasmussen LJ, Dick KA, Kress W, Schneider C, Koch MC, Beilman GJ, Harrison AR, Dalton JC, Ranum LP. Day JW, et al. Among authors: dalton jc. Neurology. 2003 Feb 25;60(4):657-64. doi: 10.1212/01.wnl.0000054481.84978.f9. Neurology. 2003. PMID: 12601109
Molecular genetics of spinocerebellar ataxia type 8 (SCA8).
Mosemiller AK, Dalton JC, Day JW, Ranum LP. Mosemiller AK, et al. Among authors: dalton jc. Cytogenet Genome Res. 2003;100(1-4):175-83. doi: 10.1159/000072852. Cytogenet Genome Res. 2003. PMID: 14526178 Review.
Insulin receptor splicing alteration in myotonic dystrophy type 2.
Savkur RS, Philips AV, Cooper TA, Dalton JC, Moseley ML, Ranum LP, Day JW. Savkur RS, et al. Among authors: dalton jc. Am J Hum Genet. 2004 Jun;74(6):1309-13. doi: 10.1086/421528. Epub 2004 Apr 26. Am J Hum Genet. 2004. PMID: 15114529 Free PMC article.
Cerebral and muscle MRI abnormalities in myotonic dystrophy.
Franc DT, Muetzel RL, Robinson PR, Rodriguez CP, Dalton JC, Naughton CE, Mueller BA, Wozniak JR, Lim KO, Day JW. Franc DT, et al. Neuromuscul Disord. 2012 Jun;22(6):483-91. doi: 10.1016/j.nmd.2012.01.003. Epub 2012 Jan 30. Neuromuscul Disord. 2012. PMID: 22290140 Free PMC article.
Spectrin mutations cause spinocerebellar ataxia type 5.
Ikeda Y, Dick KA, Weatherspoon MR, Gincel D, Armbrust KR, Dalton JC, Stevanin G, Dürr A, Zühlke C, Bürk K, Clark HB, Brice A, Rothstein JD, Schut LJ, Day JW, Ranum LP. Ikeda Y, et al. Among authors: dalton jc. Nat Genet. 2006 Feb;38(2):184-90. doi: 10.1038/ng1728. Epub 2006 Jan 22. Nat Genet. 2006. PMID: 16429157
SNP haplotype mapping in a small ALS family.
Krueger KA, Tsuji S, Fukuda Y, Takahashi Y, Goto J, Mitsui J, Ishiura H, Dalton JC, Miller MB, Day JW, Ranum LP. Krueger KA, et al. Among authors: dalton jc. PLoS One. 2009 May 25;4(5):e5687. doi: 10.1371/journal.pone.0005687. PLoS One. 2009. PMID: 19479031 Free PMC article.
Gene symbol: SCN8A. Disease: Ataxia. Accession #Hd0520.
Meisler MH, Trudeau MM, Dalton JC, Day JW, Ranum LP. Meisler MH, et al. Among authors: dalton jc. Hum Genet. 2006 Feb;118(6):776. Hum Genet. 2006. PMID: 17297687 No abstract available.
1,330 results