Ueno S - Search Results

1

Step Numbers and Hoehn-Yahr Stage after Six Years.

Kataoka H, Tanaka N, Kiriyama T, Eura N, Ikeda M, Izumi T, Furiya Y, Sugie K, Ueno S. Kataoka H, et al. Among authors: ueno s. Eur Neurol. 2018;79(3-4):118-124. doi: 10.1159/000487331. Epub 2018 Feb 22. Eur Neurol. 2018. PMID: 29471292

2

Expression of the costimulatory molecule BB-1 and its receptors in patients with scleroderma-polymyositis overlap syndrome.

Murata KY, Sugie K, Takamure M, Ueno S. Murata KY, et al. Among authors: ueno s. J Neurol Sci. 2002 Dec 15;205(1):65-70. doi: 10.1016/s0022-510x(02)00309-x. J Neurol Sci. 2002. PMID: 12409186

3

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: ueno s. Neurosci Lett. 2004 Aug 12;366(2):120-5. doi: 10.1016/j.neulet.2004.05.034. Neurosci Lett. 2004. PMID: 15276230

4

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: ueno s. 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

5

Effect of humanin on decreased ATP levels of human lymphocytes harboring A3243G mutant mitochondrial DNA.

Kariya S, Hirano M, Furiya Y, Ueno S. Kariya S, et al. Among authors: ueno s. Neuropeptides. 2005 Apr;39(2):97-101. doi: 10.1016/j.npep.2004.11.004. Neuropeptides. 2005. PMID: 15752543

6

Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent.

Kariya S, Hirano M, Furiya Y, Sugie K, Ueno S. Kariya S, et al. Among authors: ueno s. Acta Neuropathol. 2005 Apr;109(4):367-72. doi: 10.1007/s00401-004-0965-5. Epub 2005 Mar 10. Acta Neuropathol. 2005. PMID: 15759134

7

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: ueno s. J Mol Neurosci. 2005;25(2):165-9. doi: 10.1385/JMN:25:2:165. J Mol Neurosci. 2005. PMID: 15784964

8

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: ueno s. 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

9

Alpha-1-antichymotrypsin gene polymorphism and susceptibility to multiple system atrophy (MSA).

Furiya Y, Hirano M, Kurumatani N, Nakamuro T, Matsumura R, Futamura N, Ueno S. Furiya Y, et al. Among authors: ueno s. Brain Res Mol Brain Res. 2005 Aug 18;138(2):178-81. doi: 10.1016/j.molbrainres.2005.04.011. Brain Res Mol Brain Res. 2005. PMID: 15907346

10

Autophagic vacuoles with sarcolemmal features delineate Danon disease and related myopathies.

Sugie K, Noguchi S, Kozuka Y, Arikawa-Hirasawa E, Tanaka M, Yan C, Saftig P, von Figura K, Hirano M, Ueno S, Nonaka I, Nishino I. Sugie K, et al. Among authors: ueno s. J Neuropathol Exp Neurol. 2005 Jun;64(6):513-22. doi: 10.1093/jnen/64.6.513. J Neuropathol Exp Neurol. 2005. PMID: 15977643

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