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Mutations of optineurin in amyotrophic lateral sclerosis.
Maruyama H, Morino H, Ito H, Izumi Y, Kato H, Watanabe Y, Kinoshita Y, Kamada M, Nodera H, Suzuki H, Komure O, Matsuura S, Kobatake K, Morimoto N, Abe K, Suzuki N, Aoki M, Kawata A, Hirai T, Kato T, Ogasawara K, Hirano A, Takumi T, Kusaka H, Hagiwara K, Kaji R, Kawakami H. Maruyama H, et al. Nature. 2010 May 13;465(7295):223-6. doi: 10.1038/nature08971. Epub 2010 Apr 28. Nature. 2010. PMID: 20428114
Unique features of the CAG repeats in Machado-Joseph disease.
Kawakami H, Maruyama H, Nakamura S, Kawaguchi Y, Kakizuka A, Doyu M, Sobue G. Kawakami H, et al. Among authors: maruyama h. Nat Genet. 1995 Apr;9(4):344-5. doi: 10.1038/ng0495-344. Nat Genet. 1995. PMID: 7795637 No abstract available.
Cloning and expression of a rat brain basic helix-loop-helix factor.
Kawakami H, Maruyama H, Yasunami M, Ohkubo H, Hara H, Saida T, Nakanishi S, Nakamura S. Kawakami H, et al. Among authors: maruyama h. Biochem Biophys Res Commun. 1996 Apr 5;221(1):199-204. doi: 10.1006/bbrc.1996.0569. Biochem Biophys Res Commun. 1996. PMID: 8660336
[Molecular genetics of Machado-Joseph disease].
Kawakami H, Maruyama H, Nakamura S. Kawakami H, et al. Among authors: maruyama h. Nihon Rinsho. 1996 Mar;54(3):854-60. Nihon Rinsho. 1996. PMID: 8904248 Review. Japanese.
Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).
Matsuyama Z, Kawakami H, Maruyama H, Izumi Y, Komure O, Udaka F, Kameyama M, Nishio T, Kuroda Y, Nishimura M, Nakamura S. Matsuyama Z, et al. Among authors: maruyama h. Hum Mol Genet. 1997 Aug;6(8):1283-7. doi: 10.1093/hmg/6.8.1283. Hum Mol Genet. 1997. PMID: 9259274
Structure and regulation of the human NeuroD (BETA2/BHF1) gene.
Miyachi T, Maruyama H, Kitamura T, Nakamura S, Kawakami H. Miyachi T, et al. Among authors: maruyama h. Brain Res Mol Brain Res. 1999 Jun 8;69(2):223-31. doi: 10.1016/s0169-328x(99)00112-6. Brain Res Mol Brain Res. 1999. PMID: 10366743
1,952 results