Goto J - Search Results

1

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan.

Li M, Ishikawa K, Toru S, Tomimitsu H, Takashima M, Goto J, Takiyama Y, Sasaki H, Imoto I, Inazawa J, Toda T, Kanazawa I, Mizusawa H. Li M, et al. Among authors: goto j. J Hum Genet. 2003;48(3):111-8. doi: 10.1007/s100380300017. J Hum Genet. 2003. PMID: 12624721

2

Unstable transmission of the RS447 human megasatellite tandem repetitive sequence that contains the USP17 deubiquitinating enzyme gene.

Okada T, Gondo Y, Goto J, Kanazawa I, Hadano S, Ikeda JE. Okada T, et al. Among authors: goto j. Hum Genet. 2002 Apr;110(4):302-13. doi: 10.1007/s00439-002-0698-2. Epub 2002 Mar 16. Hum Genet. 2002. PMID: 11941478

3

Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.

Tachikawa M, Nagai Y, Nakamura K, Kobayashi K, Fujiwara T, Han HJ, Nakabayashi Y, Ichikawa Y, Goto J, Kanazawa I, Nakamura Y, Toda T. Tachikawa M, et al. Among authors: goto j. J Hum Genet. 2002;47(6):275-8. doi: 10.1007/s100380200039. J Hum Genet. 2002. PMID: 12111376

4

The genomic structure and expression of MJD, the Machado-Joseph disease gene.

Ichikawa Y, Goto J, Hattori M, Toyoda A, Ishii K, Jeong SY, Hashida H, Masuda N, Ogata K, Kasai F, Hirai M, Maciel P, Rouleau GA, Sakaki Y, Kanazawa I. Ichikawa Y, et al. Among authors: goto j. J Hum Genet. 2001;46(7):413-22. doi: 10.1007/s100380170060. J Hum Genet. 2001. PMID: 11450850

5

Sporadic ataxias in Japan--a population-based epidemiological study.

Tsuji S, Onodera O, Goto J, Nishizawa M; Study Group on Ataxic Diseases. Tsuji S, et al. Among authors: goto j. Cerebellum. 2008;7(2):189-97. doi: 10.1007/s12311-008-0028-x. Cerebellum. 2008. PMID: 18418674

6

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses.

Ishiura H, Takahashi Y, Hayashi T, Saito K, Furuya H, Watanabe M, Murata M, Suzuki M, Sugiura A, Sawai S, Shibuya K, Ueda N, Ichikawa Y, Kanazawa I, Goto J, Tsuji S. Ishiura H, et al. Among authors: goto j. J Hum Genet. 2014 Mar;59(3):163-72. doi: 10.1038/jhg.2013.139. Epub 2014 Jan 23. J Hum Genet. 2014. PMID: 24451228

7

Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease.

Masuda N, Goto J, Murayama N, Watanabe M, Kondo I, Kanazawa I. Masuda N, et al. Among authors: goto j. J Med Genet. 1995 Sep;32(9):701-5. doi: 10.1136/jmg.32.9.701. J Med Genet. 1995. PMID: 8544189 Free PMC article.

8

[Molecular genetics of Huntington's disease].

Goto J, Masuda N, Watanabe M, Kanazawa I. Goto J, et al. Rinsho Shinkeigaku. 1995 Dec;35(12):1529-31. Rinsho Shinkeigaku. 1995. PMID: 8752453 Japanese.

9

Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and spinocerebellar ataxia type 1.

Hashida H, Goto J, Kurisaki H, Mizusawa H, Kanazawa I. Hashida H, et al. Among authors: goto j. Ann Neurol. 1997 Apr;41(4):505-11. doi: 10.1002/ana.410410414. Ann Neurol. 1997. PMID: 9124808

10

Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1.

Ichikawa Y, Ishiura H, Mitsui J, Takahashi Y, Kobayashi S, Takuma H, Kanazawa I, Doi K, Yoshimura J, Morishita S, Goto J, Tsuji S. Ichikawa Y, et al. Among authors: goto j. J Neurol Sci. 2013 Aug 15;331(1-2):158-60. doi: 10.1016/j.jns.2013.05.018. Epub 2013 Jun 18. J Neurol Sci. 2013. PMID: 23786967

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