Matsuura T - Search Results

1

Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10).

Almeida T, Alonso I, Martins S, Ramos EM, Azevedo L, Ohno K, Amorim A, Saraiva-Pereira ML, Jardim LB, Matsuura T, Sequeiros J, Silveira I. Almeida T, et al. Among authors: matsuura t. PLoS One. 2009;4(2):e4553. doi: 10.1371/journal.pone.0004553. Epub 2009 Feb 23. PLoS One. 2009. PMID: 19234597 Free PMC article.

2

Long-range PCR for the diagnosis of spinocerebellar ataxia type 10.

Kurosaki T, Matsuura T, Ohno K, Ueda S. Kurosaki T, et al. Among authors: matsuura t. Neurogenetics. 2008 May;9(2):151-2. doi: 10.1007/s10048-007-0117-x. Epub 2008 Jan 16. Neurogenetics. 2008. PMID: 18197441 No abstract available.

3

Alu-mediated acquisition of unstable ATTCT pentanucleotide repeats in the human ATXN10 gene.

Kurosaki T, Matsuura T, Ohno K, Ueda S. Kurosaki T, et al. Among authors: matsuura t. Mol Biol Evol. 2009 Nov;26(11):2573-9. doi: 10.1093/molbev/msp172. Epub 2009 Aug 3. Mol Biol Evol. 2009. PMID: 19651850

4

The unstable CCTG repeat responsible for myotonic dystrophy type 2 originates from an AluSx element insertion into an early primate genome.

Kurosaki T, Ueda S, Ishida T, Abe K, Ohno K, Matsuura T. Kurosaki T, et al. Among authors: matsuura t. PLoS One. 2012;7(6):e38379. doi: 10.1371/journal.pone.0038379. Epub 2012 Jun 19. PLoS One. 2012. PMID: 22723857 Free PMC article.

5

Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian families.

Saito T, Amakusa Y, Kimura T, Yahara O, Aizawa H, Ikeda Y, Day JW, Ranum LP, Ohno K, Matsuura T. Saito T, et al. Among authors: matsuura t. Neurogenetics. 2008 Feb;9(1):61-3. doi: 10.1007/s10048-007-0110-4. Epub 2007 Dec 5. Neurogenetics. 2008. PMID: 18057971

6

Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?

Matsuura T, Fang P, Pearson CE, Jayakar P, Ashizawa T, Roa BB, Nelson DL. Matsuura T, et al. Am J Hum Genet. 2006 Jan;78(1):125-9. doi: 10.1086/498654. Epub 2005 Nov 15. Am J Hum Genet. 2006. PMID: 16385455 Free PMC article.

7

FXTAS, SCA10, and SCA17 in American patients with movement disorders.

Seixas AI, Maurer MH, Lin M, Callahan C, Ahuja A, Matsuura T, Ross CA, Hisama FM, Silveira I, Margolis RL. Seixas AI, et al. Among authors: matsuura t. Am J Med Genet A. 2005 Jul 1;136(1):87-9. doi: 10.1002/ajmg.a.30761. Am J Med Genet A. 2005. PMID: 15889413 No abstract available.

8

[Molecular and genetic analysis of spinocerebellar ataxia type 10 (SCA10)].

Matsuura T. Matsuura T. Rinsho Shinkeigaku. 2008 Jan;48(1):1-10. doi: 10.5692/clinicalneurol.48.1. Rinsho Shinkeigaku. 2008. PMID: 18386626 Review. Japanese.

9

[Molecular and genetic analysis of spinocerebellar ataxia type 10 (SCA10)].

Matsuura T. Matsuura T. Rinsho Shinkeigaku. 2008 Nov;48(11):823-5. doi: 10.5692/clinicalneurol.48.823. Rinsho Shinkeigaku. 2008. PMID: 19198092 Review. Japanese.

10

Myotonic dystrophy type 2 is rare in the Japanese population.

Matsuura T, Minami N, Arahata H, Ohno K, Abe K, Hayashi YK, Nishino I. Matsuura T, et al. J Hum Genet. 2012 Mar;57(3):219-20. doi: 10.1038/jhg.2011.152. Epub 2012 Jan 19. J Hum Genet. 2012. PMID: 22258159 No abstract available.

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