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Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.
Matsuo M, Masumura T, Nishio H, Nakajima T, Kitoh Y, Takumi T, Koga J, Nakamura H. Matsuo M, et al. J Clin Invest. 1991 Jun;87(6):2127-31. doi: 10.1172/JCI115244. J Clin Invest. 1991. PMID: 2040695 Free PMC article.
The consensus sequences at the 5' and 3' splice sites of exon 19 were unaltered (Matsuo, M., et al. 1990. Biochem. Biophys. Res. Commun. 170:963-967). ...
The consensus sequences at the 5' and 3' splice sites of exon 19 were unaltered (Matsuo, M., et al. 1990. Biochem. Biophys. Re …
[Mutation detection by PCR-TGGE].
Shirakawa T, Nishiyama K, Matsuo M. Shirakawa T, et al. Among authors: matsuo m. Rinsho Byori. 1995 Jul;43(7):679-85. Rinsho Byori. 1995. PMID: 7674540 Japanese.
Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in dystrophin Kobe.
Takeshima Y, Nishio H, Sakamoto H, Nakamura H, Matsuo M. Takeshima Y, et al. Among authors: matsuo m. J Clin Invest. 1995 Feb;95(2):515-20. doi: 10.1172/JCI117693. J Clin Invest. 1995. PMID: 7860733 Free PMC article.
Molecular analysis of dystrophin Kobe showed that exon 19 of the dystrophin gene bearing 52-bp deletion was skipped during splicing, although the known consensus sequences at the 5' and 3' splice sites of exon 19 were maintained (Matsuo, M., T. Masumura, H. Nishio, …
Molecular analysis of dystrophin Kobe showed that exon 19 of the dystrophin gene bearing 52-bp deletion was skipped during splicing, althoug …
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