Takeda S - Search Results

1

Current status of pharmaceutical and genetic therapeutic approaches to treat DMD.

Pichavant C, Aartsma-Rus A, Clemens PR, Davies KE, Dickson G, Takeda S, Wilton SD, Wolff JA, Wooddell CI, Xiao X, Tremblay JP. Pichavant C, et al. Among authors: takeda s. Mol Ther. 2011 May;19(5):830-40. doi: 10.1038/mt.2011.59. Epub 2011 Apr 5. Mol Ther. 2011. PMID: 21468001 Free PMC article. Review.

2

Effective restoration of dystrophin-associated proteins in vivo by adenovirus-mediated transfer of truncated dystrophin cDNAs.

Yuasa K, Miyagoe Y, Yamamoto K, Nabeshima Y, Dickson G, Takeda S. Yuasa K, et al. Among authors: takeda s. FEBS Lett. 1998 Mar 27;425(2):329-36. doi: 10.1016/s0014-5793(98)00251-8. FEBS Lett. 1998. PMID: 9559674 Free article.

3

Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene.

Sakamoto M, Yuasa K, Yoshimura M, Yokota T, Ikemoto T, Suzuki M, Dickson G, Miyagoe-Suzuki Y, Takeda S. Sakamoto M, et al. Among authors: takeda s. Biochem Biophys Res Commun. 2002 May 17;293(4):1265-72. doi: 10.1016/S0006-291X(02)00362-5. Biochem Biophys Res Commun. 2002. PMID: 12054513

4

Stable micro-dystrophin gene transfer using an integrating adeno-retroviral hybrid vector ameliorates the dystrophic pathology in mdx mouse muscle.

Roberts ML, Wells DJ, Graham IR, Fabb SA, Hill VJ, Duisit G, Yuasa K, Takeda S, Cosset FL, Dickson G. Roberts ML, et al. Among authors: takeda s. Hum Mol Genet. 2002 Jul 15;11(15):1719-30. doi: 10.1093/hmg/11.15.1719. Hum Mol Genet. 2002. PMID: 12095914

5

Adeno-associated virus vector-mediated gene transfer into dystrophin-deficient skeletal muscles evokes enhanced immune response against the transgene product.

Yuasa K, Sakamoto M, Miyagoe-Suzuki Y, Tanouchi A, Yamamoto H, Li J, Chamberlain JS, Xiao X, Takeda S. Yuasa K, et al. Among authors: takeda s. Gene Ther. 2002 Dec;9(23):1576-88. doi: 10.1038/sj.gt.3301829. Gene Ther. 2002. PMID: 12424610

6

AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype.

Yoshimura M, Sakamoto M, Ikemoto M, Mochizuki Y, Yuasa K, Miyagoe-Suzuki Y, Takeda S. Yoshimura M, et al. Among authors: takeda s. Mol Ther. 2004 Nov;10(5):821-8. doi: 10.1016/j.ymthe.2004.07.025. Mol Ther. 2004. PMID: 15509500 Free article.

7

Expansion of revertant fibers in dystrophic mdx muscles reflects activity of muscle precursor cells and serves as an index of muscle regeneration.

Yokota T, Lu QL, Morgan JE, Davies KE, Fisher R, Takeda S, Partridge TA. Yokota T, et al. Among authors: takeda s. J Cell Sci. 2006 Jul 1;119(Pt 13):2679-87. doi: 10.1242/jcs.03000. Epub 2006 Jun 6. J Cell Sci. 2006. PMID: 16757519

8

Transduction efficiency and immune response associated with the administration of AAV8 vector into dog skeletal muscle.

Ohshima S, Shin JH, Yuasa K, Nishiyama A, Kira J, Okada T, Takeda S. Ohshima S, et al. Among authors: takeda s. Mol Ther. 2009 Jan;17(1):73-80. doi: 10.1038/mt.2008.225. Epub 2008 Oct 21. Mol Ther. 2009. PMID: 18941441 Free PMC article.

9

In-frame dystrophin following exon 51-skipping improves muscle pathology and function in the exon 52-deficient mdx mouse.

Aoki Y, Nakamura A, Yokota T, Saito T, Okazawa H, Nagata T, Takeda S. Aoki Y, et al. Among authors: takeda s. Mol Ther. 2010 Nov;18(11):1995-2005. doi: 10.1038/mt.2010.186. Epub 2010 Sep 7. Mol Ther. 2010. PMID: 20823833 Free PMC article.

10

The status of exon skipping as a therapeutic approach to duchenne muscular dystrophy.

Lu QL, Yokota T, Takeda S, Garcia L, Muntoni F, Partridge T. Lu QL, et al. Among authors: takeda s. Mol Ther. 2011 Jan;19(1):9-15. doi: 10.1038/mt.2010.219. Epub 2010 Oct 26. Mol Ther. 2011. PMID: 20978473 Free PMC article. Review.

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