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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.
Mutagenic roles of DNA "repair" proteins in antibody diversity and disease-associated trinucleotide repeat instability.
Slean MM, Panigrahi GB, Ranum LP, Pearson CE. Slean MM, et al. Among authors: ranum lp. DNA Repair (Amst). 2008 Jul 1;7(7):1135-54. doi: 10.1016/j.dnarep.2008.03.014. Epub 2008 May 16. DNA Repair (Amst). 2008. PMID: 18485833 Review.
Mutant β-III spectrin causes mGluR1α mislocalization and functional deficits in a mouse model of spinocerebellar ataxia type 5.
Armbrust KR, Wang X, Hathorn TJ, Cramer SW, Chen G, Zu T, Kangas T, Zink AN, Öz G, Ebner TJ, Ranum LP. Armbrust KR, et al. Among authors: ranum lp. J Neurosci. 2014 Jul 23;34(30):9891-904. doi: 10.1523/JNEUROSCI.0876-14.2014. J Neurosci. 2014. PMID: 25057192 Free PMC article.
Spinocerebellar ataxia type 5.
Dick KA, Ikeda Y, Day JW, Ranum LP. Dick KA, et al. Among authors: ranum lp. Handb Clin Neurol. 2012;103:451-9. doi: 10.1016/B978-0-444-51892-7.00028-0. Handb Clin Neurol. 2012. PMID: 21827906 Review.
In 1994, Ranum and colleagues identified a ten-generation American kindred with a relatively mild autosomal dominant form of spinocerebellar ataxia (Ranum et al., 1994). The mutation was mapped to the centromeric region of chromosome 11, and the disorder designated …
In 1994, Ranum and colleagues identified a ten-generation American kindred with a relatively mild autosomal dominant form of spinocer …
Dominant non-coding repeat expansions in human disease.
Dick KA, Margolis JM, Day JW, Ranum LPW. Dick KA, et al. Among authors: ranum lpw. Genome Dyn. 2006;1:67-83. doi: 10.1159/000092501. Genome Dyn. 2006. PMID: 18724054 Review.
Spinocerebellar ataxia type 20 is genetically distinct from spinocerebellar ataxia type 5.
Lorenzo DN, Forrest SM, Ikeda Y, Dick KA, Ranum LP, Knight MA. Lorenzo DN, et al. Among authors: ranum lp. Neurology. 2006 Dec 12;67(11):2084-5. doi: 10.1212/01.wnl.0000247662.05197.59. Neurology. 2006. PMID: 17159129 No abstract available.
Molecular genetics of spinocerebellar ataxia type 8 (SCA8).
Mosemiller AK, Dalton JC, Day JW, Ranum LP. Mosemiller AK, et al. Among authors: ranum lp. Cytogenet Genome Res. 2003;100(1-4):175-83. doi: 10.1159/000072852. Cytogenet Genome Res. 2003. PMID: 14526178 Review.
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: ranum lp. Neurology. 2003 Feb 25;60(4):657-64. doi: 10.1212/01.wnl.0000054481.84978.f9. Neurology. 2003. PMID: 12601109
Spinocerebellar ataxia type 8: clinical features in a large family.
Day JW, Schut LJ, Moseley ML, Durand AC, Ranum LP. Day JW, et al. Among authors: ranum lp. Neurology. 2000 Sep 12;55(5):649-57. doi: 10.1212/wnl.55.5.649. Neurology. 2000. PMID: 10980728
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
Orr HT, Chung MY, Banfi S, Kwiatkowski TJ Jr, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY. Orr HT, et al. Among authors: ranum lp. Nat Genet. 1993 Jul;4(3):221-6. doi: 10.1038/ng0793-221. Nat Genet. 1993. PMID: 8358429
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