Ito C - Search Results

1

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.

Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T. Satake W, et al. Among authors: ito c. Nat Genet. 2009 Dec;41(12):1303-7. doi: 10.1038/ng.485. Epub 2009 Nov 15. Nat Genet. 2009. PMID: 19915576

2

Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.

Mizuta I, Satake W, Nakabayashi Y, Ito C, Suzuki S, Momose Y, Nagai Y, Oka A, Inoko H, Fukae J, Saito Y, Sawabe M, Murayama S, Yamamoto M, Hattori N, Murata M, Toda T. Mizuta I, et al. Among authors: ito c. Hum Mol Genet. 2006 Apr 1;15(7):1151-8. doi: 10.1093/hmg/ddl030. Epub 2006 Feb 24. Hum Mol Genet. 2006. PMID: 16500997

3

Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.

Satake W, Mizuta I, Suzuki S, Nakabayashi Y, Ito C, Watanabe M, Takeda A, Hasegawa K, Sakoda S, Yamamoto M, Hattori N, Murata M, Toda T. Satake W, et al. Among authors: ito c. Neuroreport. 2007 Jun 11;18(9):937-40. doi: 10.1097/WNR.0b013e328133265b. Neuroreport. 2007. PMID: 17515805

4

YY1 binds to α-synuclein 3'-flanking region SNP and stimulates antisense noncoding RNA expression.

Mizuta I, Takafuji K, Ando Y, Satake W, Kanagawa M, Kobayashi K, Nagamori S, Shinohara T, Ito C, Yamamoto M, Hattori N, Murata M, Kanai Y, Murayama S, Nakagawa M, Toda T. Mizuta I, et al. Among authors: ito c. J Hum Genet. 2013 Nov;58(11):711-9. doi: 10.1038/jhg.2013.90. Epub 2013 Sep 12. J Hum Genet. 2013. PMID: 24026176

5

Temporal requirement of dystroglycan glycosylation during brain development and rescue of severe cortical dysplasia via gene delivery in the fetal stage.

Sudo A, Kanagawa M, Kondo M, Ito C, Kobayashi K, Endo M, Minami Y, Aiba A, Toda T. Sudo A, et al. Among authors: ito c. Hum Mol Genet. 2018 Apr 1;27(7):1174-1185. doi: 10.1093/hmg/ddy032. Hum Mol Genet. 2018. PMID: 29360985 Free PMC article.

6

Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression.

Kanagawa M, Yu CC, Ito C, Fukada S, Hozoji-Inada M, Chiyo T, Kuga A, Matsuo M, Sato K, Yamaguchi M, Ito T, Ohtsuka Y, Katanosaka Y, Miyagoe-Suzuki Y, Naruse K, Kobayashi K, Okada T, Takeda S, Toda T. Kanagawa M, et al. Among authors: ito t, ito c. Hum Mol Genet. 2013 Aug 1;22(15):3003-15. doi: 10.1093/hmg/ddt157. Epub 2013 Apr 4. Hum Mol Genet. 2013. PMID: 23562821

7

Contribution of dysferlin deficiency to skeletal muscle pathology in asymptomatic and severe dystroglycanopathy models: generation of a new model for Fukuyama congenital muscular dystrophy.

Kanagawa M, Lu Z, Ito C, Matsuda C, Miyake K, Toda T. Kanagawa M, et al. Among authors: ito c. PLoS One. 2014 Sep 8;9(9):e106721. doi: 10.1371/journal.pone.0106721. eCollection 2014. PLoS One. 2014. PMID: 25198651 Free PMC article.

8

Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression.

Ohtsuka Y, Kanagawa M, Yu CC, Ito C, Chiyo T, Kobayashi K, Okada T, Takeda S, Toda T. Ohtsuka Y, et al. Among authors: ito c. Sci Rep. 2015 Feb 9;5:8316. doi: 10.1038/srep08316. Sci Rep. 2015. PMID: 25661440 Free PMC article.

9

Partial tandem duplication of GRIA3 in a male with mental retardation.

Chiyonobu T, Hayashi S, Kobayashi K, Morimoto M, Miyanomae Y, Nishimura A, Nishimoto A, Ito C, Imoto I, Sugimoto T, Jia Z, Inazawa J, Toda T. Chiyonobu T, et al. Among authors: ito c. Am J Med Genet A. 2007 Jul 1;143A(13):1448-55. doi: 10.1002/ajmg.a.31798. Am J Med Genet A. 2007. PMID: 17568425

10

Hsp40 gene therapy exerts therapeutic effects on polyglutamine disease mice via a non-cell autonomous mechanism.

Popiel HA, Takeuchi T, Fujita H, Yamamoto K, Ito C, Yamane H, Muramatsu S, Toda T, Wada K, Nagai Y. Popiel HA, et al. Among authors: ito c. PLoS One. 2012;7(11):e51069. doi: 10.1371/journal.pone.0051069. Epub 2012 Nov 30. PLoS One. 2012. PMID: 23226463 Free PMC article.

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