Furiya Y - Search Results

1

Novel splice variants increase molecular diversity of aprataxin, the gene responsible for early-onset ataxia with ocular motor apraxia and hypoalbuminemia.

Hirano M, Nishiwaki T, Kariya S, Furiya Y, Kawahara M, Ueno S. Hirano M, et al. Among authors: furiya y. Neurosci Lett. 2004 Aug 12;366(2):120-5. doi: 10.1016/j.neulet.2004.05.034. Neurosci Lett. 2004. PMID: 15276230

2

Loss of function mechanism in aprataxin-related early-onset ataxia.

Hirano M, Furiya Y, Kariya S, Nishiwaki T, Ueno S. Hirano M, et al. Among authors: furiya y. Biochem Biophys Res Commun. 2004 Sep 17;322(2):380-6. doi: 10.1016/j.bbrc.2004.07.135. Biochem Biophys Res Commun. 2004. PMID: 15325241

3

Cytoprotective effect of novel histone deacetylase inhibitors against polyglutamine toxicity.

Kariya S, Hirano M, Uesato S, Nagai Y, Nagaoka Y, Furiya Y, Asai H, Fujikake N, Toda T, Ueno S. Kariya S, et al. Among authors: furiya y. Neurosci Lett. 2006 Jan 16;392(3):213-5. doi: 10.1016/j.neulet.2005.09.019. Epub 2005 Sep 30. Neurosci Lett. 2006. PMID: 16199124

4

DNA single-strand break repair is impaired in aprataxin-related ataxia.

Hirano M, Yamamoto A, Mori T, Lan L, Iwamoto TA, Aoki M, Shimada K, Furiya Y, Kariya S, Asai H, Yasui A, Nishiwaki T, Imoto K, Kobayashi N, Kiriyama T, Nagata T, Konishi N, Itoyama Y, Ueno S. Hirano M, et al. Among authors: furiya y. Ann Neurol. 2007 Feb;61(2):162-74. doi: 10.1002/ana.21078. Ann Neurol. 2007. PMID: 17315206

5

Short half-lives of ataxia-associated aprataxin proteins in neuronal cells.

Hirano M, Asai H, Kiriyama T, Furiya Y, Iwamoto T, Nishiwaki T, Yamamoto A, Mori T, Ueno S. Hirano M, et al. Among authors: furiya y. Neurosci Lett. 2007 May 29;419(2):184-7. doi: 10.1016/j.neulet.2007.04.044. Epub 2007 Apr 25. Neurosci Lett. 2007. PMID: 17485165

6

Humanin attenuates apoptosis induced by DRPLA proteins with expanded polyglutamine stretches.

Kariya S, Hirano M, Nagai Y, Furiya Y, Fujikake N, Toda T, Ueno S. Kariya S, et al. Among authors: furiya y. J Mol Neurosci. 2005;25(2):165-9. doi: 10.1385/JMN:25:2:165. J Mol Neurosci. 2005. PMID: 15784964

7

Lack of association between polymorphic microsatellites of the VMAT2 gene and Parkinson's disease in Japan.

Kariya S, Hirano M, Takahashi N, Furiya Y, Ueno S. Kariya S, et al. Among authors: furiya y. J Neurol Sci. 2005 May 15;232(1-2):91-4. doi: 10.1016/j.jns.2005.02.005. J Neurol Sci. 2005. PMID: 15850588

8

ALADINI482S causes selective failure of nuclear protein import and hypersensitivity to oxidative stress in triple A syndrome.

Hirano M, Furiya Y, Asai H, Yasui A, Ueno S. Hirano M, et al. Among authors: furiya y. Proc Natl Acad Sci U S A. 2006 Feb 14;103(7):2298-303. doi: 10.1073/pnas.0505598103. Epub 2006 Feb 7. Proc Natl Acad Sci U S A. 2006. PMID: 16467144 Free PMC article.

9

Restoration of nuclear-import failure caused by triple A syndrome and oxidative stress.

Kiriyama T, Hirano M, Asai H, Ikeda M, Furiya Y, Ueno S. Kiriyama T, et al. Among authors: furiya y. Biochem Biophys Res Commun. 2008 Oct 3;374(4):631-4. doi: 10.1016/j.bbrc.2008.07.088. Epub 2008 Jul 26. Biochem Biophys Res Commun. 2008. PMID: 18662670

10

Protein kinase C gamma, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin.

Asai H, Hirano M, Shimada K, Kiriyama T, Furiya Y, Ikeda M, Iwamoto T, Mori T, Nishinaka K, Konishi N, Udaka F, Ueno S. Asai H, et al. Among authors: furiya y. Hum Mol Genet. 2009 Oct 1;18(19):3533-43. doi: 10.1093/hmg/ddp298. Epub 2009 Jun 26. Hum Mol Genet. 2009. PMID: 19561170

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