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Year | Number of Results |
---|---|
2000 | 1 |
2001 | 1 |
2004 | 1 |
2006 | 2 |
2013 | 1 |
2024 | 0 |
PubMed (cited) for id: 611150
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Page 1
Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability.
Eur J Hum Genet. 2013 Nov;21(11):1272-6. doi: 10.1038/ejhg.2013.32. Epub 2013 Feb 27.
Eur J Hum Genet. 2013.
PMID: 23443018
Free PMC article.
The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10.
Wakamiya M, Matsuura T, Liu Y, Schuster GC, Gao R, Xu W, Sarkar PS, Lin X, Ashizawa T.
Wakamiya M, et al.
Neurology. 2006 Aug 22;67(4):607-13. doi: 10.1212/01.wnl.0000231140.26253.eb.
Neurology. 2006.
PMID: 16924013
Item in Clipboard
Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10.
Alonso I, Jardim LB, Artigalas O, Saraiva-Pereira ML, Matsuura T, Ashizawa T, Sequeiros J, Silveira I.
Alonso I, et al.
Neurology. 2006 May 23;66(10):1602-4. doi: 10.1212/01.wnl.0000216266.30177.bb.
Neurology. 2006.
PMID: 16717236
No abstract available.
Item in Clipboard
Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10.
Matsuura T, Fang P, Lin X, Khajavi M, Tsuji K, Rasmussen A, Grewal RP, Achari M, Alonso ME, Pulst SM, Zoghbi HY, Nelson DL, Roa BB, Ashizawa T.
Matsuura T, et al.
Am J Hum Genet. 2004 Jun;74(6):1216-24. doi: 10.1086/421526. Epub 2004 May 4.
Am J Hum Genet. 2004.
PMID: 15127363
Free PMC article.
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Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.
Rasmussen A, Matsuura T, Ruano L, Yescas P, Ochoa A, Ashizawa T, Alonso E.
Rasmussen A, et al.
Ann Neurol. 2001 Aug;50(2):234-9. doi: 10.1002/ana.1081.
Ann Neurol. 2001.
PMID: 11506407
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Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T.
Matsuura T, et al.
Nat Genet. 2000 Oct;26(2):191-4. doi: 10.1038/79911.
Nat Genet. 2000.
PMID: 11017075
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