Kawakami H - Search Results

1

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. Among authors: kawakami h. Nature. 2010 May 13;465(7295):223-6. doi: 10.1038/nature08971. Epub 2010 Apr 28. Nature. 2010. PMID: 20428114

2

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. Nat Genet. 1995 Apr;9(4):344-5. doi: 10.1038/ng0495-344. Nat Genet. 1995. PMID: 7795637 No abstract available.

3

Reevaluation of the exact CAG repeat length in hereditary cerebellar ataxias using highly denaturing conditions and long PCR.

Maruyama H, Kawakami H, Nakamura S. Maruyama H, et al. Among authors: kawakami h. Hum Genet. 1996 May;97(5):591-5. doi: 10.1007/BF02281866. Hum Genet. 1996. PMID: 8655136

4

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. Biochem Biophys Res Commun. 1996 Apr 5;221(1):199-204. doi: 10.1006/bbrc.1996.0569. Biochem Biophys Res Commun. 1996. PMID: 8660336

5

[Molecular genetics of Machado-Joseph disease].

Kawakami H, Maruyama H, Nakamura S. Kawakami H, et al. Nihon Rinsho. 1996 Mar;54(3):854-60. Nihon Rinsho. 1996. PMID: 8904248 Review. Japanese.

6

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: kawakami h. Hum Mol Genet. 1997 Aug;6(8):1283-7. doi: 10.1093/hmg/6.8.1283. Hum Mol Genet. 1997. PMID: 9259274

7

A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA(Leu)(UUR) 3254C-to-G.

Kawarai T, Kawakami H, Kozuka K, Izumi Y, Matsuyama Z, Watanabe C, Kohriyama T, Nakamura S. Kawarai T, et al. Among authors: kawakami h. Neurology. 1997 Aug;49(2):598-600. doi: 10.1212/wnl.49.2.598. Neurology. 1997. PMID: 9270605

8

No association between apolipoprotein E alleles and olivopontocerebellar atrophy.

Toji H, Kawakami H, Kawarai T, Nakayama T, Komure O, Kuno S, Nakamura S. Toji H, et al. Among authors: kawakami h. J Neurol Sci. 1998 Jun 11;158(1):110-2. doi: 10.1016/s0022-510x(98)00099-9. J Neurol Sci. 1998. PMID: 9667788

9

Apolipoprotein E promoter polymorphism and sporadic Alzheimer's disease in a Japanese population.

Toji H, Maruyama H, Sasaki K, Nakamura S, Kawakami H. Toji H, et al. Among authors: kawakami h. Neurosci Lett. 1999 Jan 4;259(1):56-8. doi: 10.1016/s0304-3940(98)00855-6. Neurosci Lett. 1999. PMID: 10027555

10

Spinocerebellar ataxia type 6 in relation to CAG repeat length.

Kaseda Y, Kawakami H, Matsuyama Z, Kumagai R, Toji M, Komure O, Nishimura M, Izumi Y, Udaka F, Kameyama M, Nishio T, Sunohara N, Kuroda Y, Nakamura S. Kaseda Y, et al. Among authors: kawakami h. Acta Neurol Scand. 1999 Apr;99(4):209-12. doi: 10.1111/j.1600-0404.1999.tb07348.x. Acta Neurol Scand. 1999. PMID: 10225349

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