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Page 1
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.
Moreira MC, Klur S, Watanabe M, Németh AH, Le Ber I, Moniz JC, Tranchant C, Aubourg P, Tazir M, Schöls L, Pandolfo M, Schulz JB, Pouget J, Calvas P, Shizuka-Ikeda M, Shoji M, Tanaka M, Izatt L, Shaw CE, M'Zahem A, Dunne E, Bomont P, Benhassine T, Bouslam N, Stevanin G, Brice A, Guimarães J, Mendonça P, Barbot C, Coutinho P, Sequeiros J, Dürr A, Warter JM, Koenig M. Moreira MC, et al. Among authors: shizuka ikeda m. Nat Genet. 2004 Mar;36(3):225-7. doi: 10.1038/ng1303. Epub 2004 Feb 8. Nat Genet. 2004. PMID: 14770181 Free article.
Presynaptic inhibition of cerebellar GABAergic transmission by glutamate decarboxylase autoantibodies in progressive cerebellar ataxia.
Takenoshita H, Shizuka-Ikeda M, Mitoma H, Song S, Harigaya Y, Igeta Y, Yaguchi M, Ishida K, Shoji M, Tanaka M, Mizusawa H, Okamoto K. Takenoshita H, et al. Among authors: shizuka ikeda m. J Neurol Neurosurg Psychiatry. 2001 Mar;70(3):386-9. doi: 10.1136/jnnp.70.3.386. J Neurol Neurosurg Psychiatry. 2001. PMID: 11181864 Free PMC article.
Generation of amyloid beta protein from a presenilin-1 and betaAPP complex.
Shizuka-Ikeda M, Matsubara E, Ikeda M, Kanai M, Tomidokoro Y, Ikeda Y, Watanabe M, Kawarabayashi T, Harigaya Y, Okamoto K, Maruyama K, Castaño EM, St George-Hyslop P, Shoji M. Shizuka-Ikeda M, et al. Biochem Biophys Res Commun. 2002 Mar 29;292(2):571-8. doi: 10.1006/bbrc.2002.6681. Biochem Biophys Res Commun. 2002. PMID: 11906199
Soluble Abeta homeostasis in AD and DS: impairment of anti-amyloidogenic protection by lipoproteins.
Matsubara E, Sekijima Y, Tokuda T, Urakami K, Amari M, Shizuka-Ikeda M, Tomidokoro Y, Ikeda M, Kawarabayashi T, Harigaya Y, Ikeda S, Murakami T, Abe K, Otomo E, Hirai S, Frangione B, Ghiso J, Shoji M. Matsubara E, et al. Among authors: shizuka ikeda m. Neurobiol Aging. 2004 Aug;25(7):833-41. doi: 10.1016/j.neurobiolaging.2003.10.004. Neurobiol Aging. 2004. PMID: 15212837 Clinical Trial.
Genetic analysis of the cystatin C gene in familial and sporadic ALS patients.
Watanabe M, Jackson M, Ikeda M, Mizushima K, Amari M, Takatama M, Hirai S, Ikeda Y, Shizuka-Ikeda M, Okamoto K. Watanabe M, et al. Among authors: shizuka ikeda m. Brain Res. 2006 Feb 16;1073-1074:20-4. doi: 10.1016/j.brainres.2005.12.046. Epub 2006 Jan 26. Brain Res. 2006. PMID: 16443201
Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype.
Takahashi T, Aoki M, Tateyama M, Kondo E, Mizuno T, Onodera Y, Takano R, Kawai H, Kamakura K, Mochizuki H, Shizuka-Ikeda M, Nakagawa M, Yoshida Y, Akanuma J, Hoshino K, Saito H, Nishizawa M, Kato S, Saito K, Miyachi T, Yamashita H, Kawai M, Matsumura T, Kuzuhara S, Ibi T, Sahashi K, Nakai H, Kohnosu T, Nonaka I, Arahata K, Brown RH Jr, Saito H, Itoyama Y. Takahashi T, et al. Among authors: shizuka ikeda m. Neurology. 2003 Jun 10;60(11):1799-804. doi: 10.1212/01.wnl.0000068333.43005.12. Neurology. 2003. PMID: 12796534