順天堂大学 · 医学研究科/医学部 · 助教

研究关键词amyotrophic lateral sclerosis genetics・C9ORF72 repeat expansion・TDP-43 pathology・PINK1-mediated mitophagy・Parkinson disease mechanisms・myotonia congenita・neurodegenerative disease biomarkers・Creutzfeldt-Jakob disease imaging

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• Konno T, Tada M, Shiga A, Tsujino A, Eguchi H, Masuda-Suzukake M, Hasegawa M, Nishizawa M, Onodera O, Kakita A, Takahashi H. C9ORF72 repeat-associated non-ATG-translated polypeptides are distributed independently of TDP-43 in a Japanese patient with c9ALS.Neuropathol Appl Neurobiol. 2014 May2014
• Konno T, Shiga A, Tsujino A, Sugai A, Kato T, Kanai K, Yokoseki A, Eguchi H, Kuwabara S, Nishizawa M, Takahashi H, Onodera O. Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72. 2013 Apr;84(4):398-401. doi: 10.1136/jnnp-2012-302272.2012
• Hattori N, Eguchi H, Imaizumi M, Saiki S, Sato S, Nagamatsu S. The pathomechanisms of young-onset Parkinson's disease (PD), approach to the causes of PD form the mechanisms of insulin secretion system Rinsho Shinkeigaku. 2011 Nov;51(11):986-72011
• Tsujino A, Kaibara M, Hayashi H, Eguchi H, Nakayama S, Sato K, Fukuda T, Tateishi Y, Shirabe S, Taniyama K, Kawakami A. A CLCN1 mutation in dominant myotonia congenita impairs the increment of chloride conductance during repetitive depolarization. Neurosci Lett. 2011 Apr 25;494(2):155-60. Epub 2011 Mar 6.2011

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