Chiyo T - Search Results

1

Improvement of cardiac fibrosis in dystrophic mice by rAAV9-mediated microdystrophin transduction.

Shin JH, Nitahara-Kasahara Y, Hayashita-Kinoh H, Ohshima-Hosoyama S, Kinoshita K, Chiyo T, Okada H, Okada T, Takeda S. Shin JH, et al. Among authors: chiyo t. Gene Ther. 2011 Sep;18(9):910-9. doi: 10.1038/gt.2011.36. Epub 2011 Mar 31. Gene Ther. 2011. PMID: 21451578

2

Robust Long-term Transduction of Common Marmoset Neuromuscular Tissue With rAAV1 and rAAV9.

Okada H, Ishibashi H, Hayashita-Kinoh H, Chiyo T, Nitahara-Kasahara Y, Baba Y, Watanabe S, Takeda S, Okada T. Okada H, et al. Among authors: chiyo t. Mol Ther Nucleic Acids. 2013 May 28;2(5):e95. doi: 10.1038/mtna.2013.21. Mol Ther Nucleic Acids. 2013. PMID: 23715217 Free PMC article.

3

Dystrophic mdx mice develop severe cardiac and respiratory dysfunction following genetic ablation of the anti-inflammatory cytokine IL-10.

Nitahara-Kasahara Y, Hayashita-Kinoh H, Chiyo T, Nishiyama A, Okada H, Takeda S, Okada T. Nitahara-Kasahara Y, et al. Among authors: chiyo t. Hum Mol Genet. 2014 Aug 1;23(15):3990-4000. doi: 10.1093/hmg/ddu113. Epub 2014 Mar 21. Hum Mol Genet. 2014. PMID: 24659498

4

Intra-amniotic rAAV-mediated microdystrophin gene transfer improves canine X-linked muscular dystrophy and may induce immune tolerance.

Hayashita-Kinoh H, Yugeta N, Okada H, Nitahara-Kasahara Y, Chiyo T, Okada T, Takeda S. Hayashita-Kinoh H, et al. Among authors: chiyo t. Mol Ther. 2015 Apr;23(4):627-37. doi: 10.1038/mt.2015.5. Epub 2015 Jan 14. Mol Ther. 2015. PMID: 25586688 Free PMC article.

5

Improved transduction of canine X-linked muscular dystrophy with rAAV9-microdystrophin via multipotent MSC pretreatment.

Hayashita-Kinoh H, Guillermo PH, Nitahara-Kasahara Y, Kuraoka M, Okada H, Chiyo T, Takeda S, Okada T. Hayashita-Kinoh H, et al. Among authors: chiyo t. Mol Ther Methods Clin Dev. 2020 Nov 17;20:133-141. doi: 10.1016/j.omtm.2020.11.003. eCollection 2021 Mar 12. Mol Ther Methods Clin Dev. 2020. PMID: 33426145 Free PMC article.

6

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: chiyo t. Sci Rep. 2015 Feb 9;5:8316. doi: 10.1038/srep08316. Sci Rep. 2015. PMID: 25661440 Free PMC article.

7

Neuromuscular disease. DOK7 gene therapy benefits mouse models of diseases characterized by defects in the neuromuscular junction.

Arimura S, Okada T, Tezuka T, Chiyo T, Kasahara Y, Yoshimura T, Motomura M, Yoshida N, Beeson D, Takeda S, Yamanashi Y. Arimura S, et al. Among authors: chiyo t. Science. 2014 Sep 19;345(6203):1505-8. doi: 10.1126/science.1250744. Science. 2014. PMID: 25237101

8

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: chiyo t. 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

9

Specific inhibition of tumor cells by oncogenic EGFR specific silencing by RNA interference.

Takahashi M, Chiyo T, Okada T, Hohjoh H. Takahashi M, et al. Among authors: chiyo t. PLoS One. 2013 Aug 8;8(8):e73214. doi: 10.1371/journal.pone.0073214. eCollection 2013. PLoS One. 2013. PMID: 23951344 Free PMC article.

10

Supplemental Treatment for Huntington's Disease with miR-132 that Is Deficient in Huntington's Disease Brain.

Fukuoka M, Takahashi M, Fujita H, Chiyo T, Popiel HA, Watanabe S, Furuya H, Murata M, Wada K, Okada T, Nagai Y, Hohjoh H. Fukuoka M, et al. Among authors: chiyo t. Mol Ther Nucleic Acids. 2018 Jun 1;11:79-90. doi: 10.1016/j.omtn.2018.01.007. Epub 2018 Feb 2. Mol Ther Nucleic Acids. 2018. PMID: 29858092 Free PMC article.

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