Kurosaki T - Search Results

1

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. Mol Biol Evol. 2009 Nov;26(11):2573-9. doi: 10.1093/molbev/msp172. Epub 2009 Aug 3. Mol Biol Evol. 2009. PMID: 19651850

2

The neuronal POU transcription factor Brn-2 interacts with Jab1, a gene involved in the onset of neurodegenerative diseases.

Huang YT, Iwamoto K, Kurosaki T, Nasu M, Ueda S. Huang YT, et al. Among authors: kurosaki t. Neurosci Lett. 2005 Jul 1-8;382(1-2):175-8. doi: 10.1016/j.neulet.2005.03.008. Epub 2005 Apr 2. Neurosci Lett. 2005. PMID: 15911144

3

Evolutionary scenario for acquisition of CAG repeats in human SCA1 gene.

Kurosaki T, Ninokata A, Wang L, Ueda S. Kurosaki T, et al. Gene. 2006 May 24;373:23-7. doi: 10.1016/j.gene.2005.12.017. Epub 2006 Feb 23. Gene. 2006. PMID: 16497448

4

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

Kurosaki T, Matsuura T, Ohno K, Ueda S. Kurosaki T, et al. 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.

5

Comparative genetics of the poly-Q tract of ataxin-1 and its binding protein PQBP-1.

Kurosaki T, Gojobori J, Ueda S. Kurosaki T, et al. Biochem Genet. 2012 Apr;50(3-4):309-17. doi: 10.1007/s10528-011-9473-1. Epub 2011 Oct 1. Biochem Genet. 2012. PMID: 21964520

6

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. PLoS One. 2012;7(6):e38379. doi: 10.1371/journal.pone.0038379. Epub 2012 Jun 19. PLoS One. 2012. PMID: 22723857 Free PMC article.

7

Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy.

Matsuura T, Kurosaki T, Omote Y, Minami N, Hayashi YK, Nishino I, Abe K. Matsuura T, et al. Among authors: kurosaki t. J Hum Genet. 2013 Aug;58(8):564-5. doi: 10.1038/jhg.2013.33. Epub 2013 May 16. J Hum Genet. 2013. PMID: 23677060 No abstract available.

8

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: kurosaki t. Neurobiol Dis. 2014 Sep;69:200-5. doi: 10.1016/j.nbd.2014.05.026. Epub 2014 May 27. Neurobiol Dis. 2014. PMID: 24878509

9

Publisher Correction: NMD-degradome sequencing reveals ribosome-bound intermediates with 3'-end non-templated nucleotides.

Kurosaki T, Miyoshi K, Myers JR, Maquat LE. Kurosaki T, et al. Nat Struct Mol Biol. 2018 Nov;25(11):1059. doi: 10.1038/s41594-018-0153-2. Nat Struct Mol Biol. 2018. PMID: 30353197

10

Rules that govern UPF1 binding to mRNA 3' UTRs.

Kurosaki T, Maquat LE. Kurosaki T, et al. Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3357-62. doi: 10.1073/pnas.1219908110. Epub 2013 Feb 12. Proc Natl Acad Sci U S A. 2013. PMID: 23404710 Free PMC article.

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