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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2004 1
2006 3
2009 1
2020 0
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6 results
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Page 1
RNA-mediated neuromuscular disorders.
Ranum LP, Cooper TA. Ranum LP, et al. Annu Rev Neurosci. 2006;29:259-77. doi: 10.1146/annurev.neuro.29.051605.113014. Annu Rev Neurosci. 2006. PMID: 16776586 Review.
Dominant non-coding repeat expansions in human disease.
Dick KA, Margolis JM, Day JW, Ranum LPW. Dick KA, et al. Genome Dyn. 2006;1:67-83. doi: 10.1159/000092501. Genome Dyn. 2006. PMID: 18724054 Review.
Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.
Ikeda Y, Dalton JC, Moseley ML, Gardner KL, Bird TD, Ashizawa T, Seltzer WK, Pandolfo M, Milunsky A, Potter NT, Shoji M, Vincent JB, Day JW, Ranum LP. Ikeda Y, et al. Am J Hum Genet. 2004 Jul;75(1):3-16. doi: 10.1086/422014. Epub 2004 May 19. Am J Hum Genet. 2004. PMID: 15152344 Free PMC article.
Dominantly inherited, non-coding microsatellite expansion disorders.
Ranum LP, Day JW. Ranum LP, et al. Curr Opin Genet Dev. 2002 Jun;12(3):266-71. doi: 10.1016/s0959-437x(02)00297-6. Curr Opin Genet Dev. 2002. PMID: 12076668 Review.
RNA gain-of-function in spinocerebellar ataxia type 8.
Daughters RS, Tuttle DL, Gao W, Ikeda Y, Moseley ML, Ebner TJ, Swanson MS, Ranum LP. Daughters RS, et al. PLoS Genet. 2009 Aug;5(8):e1000600. doi: 10.1371/journal.pgen.1000600. Epub 2009 Aug 14. PLoS Genet. 2009. PMID: 19680539 Free PMC article.
Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.
Moseley ML, Zu T, Ikeda Y, Gao W, Mosemiller AK, Daughters RS, Chen G, Weatherspoon MR, Clark HB, Ebner TJ, Day JW, Ranum LP. Moseley ML, et al. Nat Genet. 2006 Jul;38(7):758-69. doi: 10.1038/ng1827. Epub 2006 Jun 25. Nat Genet. 2006. PMID: 16804541