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Bodywide skipping of exons 45-55 in dystrophic mdx52 mice by systemic antisense delivery.
Aoki Y, Yokota T, Nagata T, Nakamura A, Tanihata J, Saito T, Duguez SM, Nagaraju K, Hoffman EP, Partridge T, Takeda S. Aoki Y, et al. Among authors: saito t. Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):13763-8. doi: 10.1073/pnas.1204638109. Epub 2012 Aug 6. Proc Natl Acad Sci U S A. 2012. PMID: 22869723 Free PMC article.
Treatable renal failure found in non-ambulatory Duchenne muscular dystrophy patients.
Motoki T, Shimizu-Motohashi Y, Komaki H, Mori-Yoshimura M, Oya Y, Takeshita E, Ishiyama A, Saito T, Nakagawa E, Sugai K, Murata M, Sasaki M. Motoki T, et al. Among authors: saito t. Neuromuscul Disord. 2015 Oct;25(10):754-7. doi: 10.1016/j.nmd.2015.07.006. Epub 2015 Jul 29. Neuromuscul Disord. 2015. PMID: 26298609
Novel mutation in HPRT1 causing a splicing error with multiple variations.
Baba S, Saito T, Yamada Y, Takeshita E, Nomura N, Yamada K, Wakamatsu N, Sasaki M. Baba S, et al. Among authors: saito t. Nucleosides Nucleotides Nucleic Acids. 2017 Jan 2;36(1):1-6. doi: 10.1080/15257770.2016.1163381. Epub 2016 Oct 18. Nucleosides Nucleotides Nucleic Acids. 2017. PMID: 27754763
Effects of systemic multiexon skipping with peptide-conjugated morpholinos in the heart of a dog model of Duchenne muscular dystrophy.
Echigoya Y, Nakamura A, Nagata T, Urasawa N, Lim KRQ, Trieu N, Panesar D, Kuraoka M, Moulton HM, Saito T, Aoki Y, Iversen P, Sazani P, Kole R, Maruyama R, Partridge T, Takeda S, Yokota T. Echigoya Y, et al. Among authors: saito t. Proc Natl Acad Sci U S A. 2017 Apr 18;114(16):4213-4218. doi: 10.1073/pnas.1613203114. Epub 2017 Apr 3. Proc Natl Acad Sci U S A. 2017. PMID: 28373570 Free PMC article.
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