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Journal Abstract Search


676 related items for PubMed ID: 12797117

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  • 6. Terminal antisense oligonucleotide modifications can enhance induced exon skipping.
    Gebski BL, Errington SJ, Johnsen RD, Fletcher S, Wilton SD.
    Neuromuscul Disord; 2005 Oct; 15(9-10):622-9. PubMed ID: 16084084
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  • 9. Characterization of a complex Duchenne muscular dystrophy-causing dystrophin gene inversion and restoration of the reading frame by induced exon skipping.
    Madden HR, Fletcher S, Davis MR, Wilton SD.
    Hum Mutat; 2009 Jan; 30(1):22-8. PubMed ID: 18570328
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  • 12. By-passing the nonsense mutation in the 4 CV mouse model of muscular dystrophy by induced exon skipping.
    Mitrpant C, Fletcher S, Iversen PL, Wilton SD.
    J Gene Med; 2009 Jan; 11(1):46-56. PubMed ID: 19006096
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  • 13. Exploring the frontiers of therapeutic exon skipping for Duchenne muscular dystrophy by double targeting within one or multiple exons.
    Aartsma-Rus A, Kaman WE, Weij R, den Dunnen JT, van Ommen GJ, van Deutekom JC.
    Mol Ther; 2006 Sep; 14(3):401-7. PubMed ID: 16753346
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  • 14. Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy.
    Takeshima Y, Yagi M, Wada H, Ishibashi K, Nishiyama A, Kakumoto M, Sakaeda T, Saura R, Okumura K, Matsuo M.
    Pediatr Res; 2006 May; 59(5):690-4. PubMed ID: 16627883
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  • 17. Rescue of dystrophic muscle through U7 snRNA-mediated exon skipping.
    Goyenvalle A, Vulin A, Fougerousse F, Leturcq F, Kaplan JC, Garcia L, Danos O.
    Science; 2004 Dec 03; 306(5702):1796-9. PubMed ID: 15528407
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  • 20. Optimizing RNA/ENA chimeric antisense oligonucleotides using in vitro splicing.
    Takeshima Y, Yagi M, Matsuo M.
    Methods Mol Biol; 2012 Dec 03; 867():131-41. PubMed ID: 22454059
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