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Journal Abstract Search

228 related items for PubMed ID: 19759562

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  • 3. Effective rescue of dystrophin improves cardiac function in dystrophin-deficient mice by a modified morpholino oligomer.
    Wu B, Moulton HM, Iversen PL, Jiang J, Li J, Li J, Spurney CF, Sali A, Guerron AD, Nagaraju K, Doran T, Lu P, Xiao X, Lu QL.
    Proc Natl Acad Sci U S A; 2008 Sep 30; 105(39):14814-9. PubMed ID: 18806224
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  • 4. In vivo delivery of naked antisense oligos in aged mdx mice: analysis of dystrophin restoration in skeletal and cardiac muscle.
    Vitiello L, Bassi N, Campagnolo P, Zaccariotto E, Occhi G, Malerba A, Pigozzo S, Reggiani C, Ausoni S, Zaglia T, Gamba P, Baroni MD, Ditadi AP.
    Neuromuscul Disord; 2008 Aug 30; 18(8):597-605. PubMed ID: 18602263
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  • 5. Induction of dystrophin expression by exon skipping in mdx mice following intramuscular injection of antisense oligonucleotides complexed with PEG-PEI copolymers.
    Williams JH, Sirsi SR, Latta DR, Lutz GJ.
    Mol Ther; 2006 Jul 30; 14(1):88-96. PubMed ID: 16488666
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  • 6. 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 30; 11(1):46-56. PubMed ID: 19006096
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  • 10. Towards a therapeutic inhibition of dystrophin exon 23 splicing in mdx mouse muscle induced by antisense oligoribonucleotides (splicomers): target sequence optimisation using oligonucleotide arrays.
    Graham IR, Hill VJ, Manoharan M, Inamati GB, Dickson G.
    J Gene Med; 2004 Oct 30; 6(10):1149-58. PubMed ID: 15386737
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  • 11. Peptide-morpholino conjugate: a promising therapeutic for Duchenne muscular dystrophy.
    Moulton HM, Wu B, Jearawiriyapaisarn N, Sazani P, Lu QL, Kole R.
    Ann N Y Acad Sci; 2009 Sep 30; 1175():55-60. PubMed ID: 19796077
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  • 12. 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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  • 14. Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles.
    Floyd SS, Clemens PR, Ontell MR, Kochanek S, Day CS, Yang J, Hauschka SD, Balkir L, Morgan J, Moreland MS, Feero GW, Epperly M, Huard J.
    Gene Ther; 1998 Jan 03; 5(1):19-30. PubMed ID: 9536261
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  • 15. In vivo comparison of 2'-O-methyl phosphorothioate and morpholino antisense oligonucleotides for Duchenne muscular dystrophy exon skipping.
    Heemskerk HA, de Winter CL, de Kimpe SJ, van Kuik-Romeijn P, Heuvelmans N, Platenburg GJ, van Ommen GJ, van Deutekom JC, Aartsma-Rus A.
    J Gene Med; 2009 Mar 03; 11(3):257-66. PubMed ID: 19140108
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  • 18. 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.
    Gene Ther; 2002 Dec 03; 9(23):1576-88. PubMed ID: 12424610
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  • 19. Dosing regimen has a significant impact on the efficiency of morpholino oligomer-induced exon skipping in mdx mice.
    Malerba A, Thorogood FC, Dickson G, Graham IR.
    Hum Gene Ther; 2009 Sep 03; 20(9):955-65. PubMed ID: 19469709
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