Ohno K - 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: ohno k. 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: ohno k. 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: ohno k. 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: ohno k. 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: ohno k. Neurogenetics. 2008 Feb;9(1):61-3. doi: 10.1007/s10048-007-0110-4. Epub 2007 Dec 5. Neurogenetics. 2008. PMID: 18057971

6

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. Among authors: ohno k. 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.

7

Human branch point consensus sequence is yUnAy.

Gao K, Masuda A, Matsuura T, Ohno K. Gao K, et al. Among authors: ohno k. Nucleic Acids Res. 2008 Apr;36(7):2257-67. doi: 10.1093/nar/gkn073. Epub 2008 Feb 19. Nucleic Acids Res. 2008. PMID: 18285363 Free PMC article.

8

hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome.

Masuda A, Shen XM, Ito M, Matsuura T, Engel AG, Ohno K. Masuda A, et al. Among authors: ohno k. Hum Mol Genet. 2008 Dec 15;17(24):4022-35. doi: 10.1093/hmg/ddn305. Epub 2008 Sep 20. Hum Mol Genet. 2008. PMID: 18806275 Free PMC article.

9

LDB3 splicing abnormalities are specific to skeletal muscles of patients with myotonic dystrophy type 1 and alter its PKC binding affinity.

Yamashita Y, Matsuura T, Kurosaki T, Amakusa Y, Kinoshita M, Ibi T, Sahashi K, Ohno K. Yamashita Y, et al. Among authors: ohno k. Neurobiol Dis. 2014 Sep;69:200-5. doi: 10.1016/j.nbd.2014.05.026. Epub 2014 May 27. Neurobiol Dis. 2014. PMID: 24878509

10

Clinical and genetic analysis of the first known Asian family with myotonic dystrophy type 2.

Nakayama T, Nakamura H, Oya Y, Kimura T, Imahuku I, Ohno K, Nishino I, Abe K, Matsuura T. Nakayama T, et al. Among authors: ohno k. J Hum Genet. 2014 Mar;59(3):129-33. doi: 10.1038/jhg.2013.133. Epub 2014 Jan 16. J Hum Genet. 2014. PMID: 24430576 Free PMC article.

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