Moseley ML - Search Results

1

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. Among authors: moseley ml. 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.

2

DM2 intronic expansions: evidence for CCUG accumulation without flanking sequence or effects on ZNF9 mRNA processing or protein expression.

Margolis JM, Schoser BG, Moseley ML, Day JW, Ranum LP. Margolis JM, et al. Among authors: moseley ml. Hum Mol Genet. 2006 Jun 1;15(11):1808-15. doi: 10.1093/hmg/ddl103. Epub 2006 Apr 19. Hum Mol Genet. 2006. PMID: 16624843

3

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

4

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. Among authors: moseley ml. 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.

5

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8).

Koob MD, Moseley ML, Schut LJ, Benzow KA, Bird TD, Day JW, Ranum LP. Koob MD, et al. Among authors: moseley ml. Nat Genet. 1999 Apr;21(4):379-84. doi: 10.1038/7710. Nat Genet. 1999. PMID: 10192387

6

SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance.

Moseley ML, Schut LJ, Bird TD, Koob MD, Day JW, Ranum LP. Moseley ML, et al. Hum Mol Genet. 2000 Sep 1;9(14):2125-30. doi: 10.1093/hmg/9.14.2125. Hum Mol Genet. 2000. PMID: 10958651

7

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: moseley ml. Neurology. 2000 Sep 12;55(5):649-57. doi: 10.1212/wnl.55.5.649. Neurology. 2000. PMID: 10980728

8

[Double the trouble: bidirectional expression of the SCA8 CAG/CTG expansion mutation - evidence for RNA and protein gain of function effects].

Ranum LP, Daughters RS, Tuttle DL, Gao W, Ikeda Y, Moseley ML, Ebner T, Swanson MS. Ranum LP, et al. Among authors: moseley ml. Rinsho Shinkeigaku. 2010 Nov;50(11):982-3. doi: 10.5692/clinicalneurol.50.982. Rinsho Shinkeigaku. 2010. PMID: 21921535 Japanese. No abstract available.

9

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA.

Koob MD, Benzow KA, Bird TD, Day JW, Moseley ML, Ranum LP. Koob MD, et al. Among authors: moseley ml. Nat Genet. 1998 Jan;18(1):72-5. doi: 10.1038/ng0198-72. Nat Genet. 1998. PMID: 9425905

10

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families.

Moseley ML, Benzow KA, Schut LJ, Bird TD, Gomez CM, Barkhaus PE, Blindauer KA, Labuda M, Pandolfo M, Koob MD, Ranum LP. Moseley ML, et al. Neurology. 1998 Dec;51(6):1666-71. doi: 10.1212/wnl.51.6.1666. Neurology. 1998. PMID: 9855520

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