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584 related items for PubMed ID: 9536261

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  • 4. Herpes simplex virus vector-mediated dystrophin gene transfer and expression in MDX mouse skeletal muscle.
    Akkaraju GR, Huard J, Hoffman EP, Goins WF, Pruchnic R, Watkins SC, Cohen JB, Glorioso JC.
    J Gene Med; 1999; 1(4):280-9. PubMed ID: 10738561
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  • 5. Autotransplantation in mdx mice of mdx myoblasts genetically corrected by an HSV-1 amplicon vector.
    Bujold M, Caron N, Camiran G, Mukherjee S, Allen PD, Tremblay JP, Wang Y.
    Cell Transplant; 2002; 11(8):759-67. PubMed ID: 12588108
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  • 6. Transient immunosuppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice.
    Lochmüller H, Petrof BJ, Pari G, Larochelle N, Dodelet V, Wang Q, Allen C, Prescott S, Massie B, Nalbantoglu J, Karpati G.
    Gene Ther; 1996 Aug; 3(8):706-16. PubMed ID: 8854096
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  • 7. Expression of human dystrophin following the transplantation of genetically modified mdx myoblasts.
    Moisset PA, Gagnon Y, Karpati G, Tremblay JP.
    Gene Ther; 1998 Oct; 5(10):1340-6. PubMed ID: 9930339
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  • 8. Expression of full-length human dystrophin cDNA in mdx mouse muscle by HVJ-liposome injection.
    Yanagihara I, Inui K, Dickson G, Turner G, Piper T, Kaneda Y, Okada S.
    Gene Ther; 1996 Jun; 3(6):549-53. PubMed ID: 8789805
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  • 9. Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) mice.
    Yang L, Lochmuller H, Luo J, Massie B, Nalbantoglu J, Karpati G, Petrof BJ.
    Gene Ther; 1998 Mar; 5(3):369-79. PubMed ID: 9614557
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  • 10. Genetic correction of dystrophin deficiency and skeletal muscle remodeling in adult MDX mouse via transplantation of retroviral producer cells.
    Fassati A, Wells DJ, Sgro Serpente PA, Walsh FS, Brown SC, Strong PN, Dickson G.
    J Clin Invest; 1997 Aug 01; 100(3):620-8. PubMed ID: 9239410
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  • 11. Full-length dystrophin gene transfer to the mdx mouse in utero.
    Reay DP, Bilbao R, Koppanati BM, Cai L, O'Day TL, Jiang Z, Zheng H, Watchko JF, Clemens PR.
    Gene Ther; 2008 Apr 01; 15(7):531-6. PubMed ID: 18273052
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  • 12. Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transfer.
    Cerletti M, Negri T, Cozzi F, Colpo R, Andreetta F, Croci D, Davies KE, Cornelio F, Pozza O, Karpati G, Gilbert R, Mora M.
    Gene Ther; 2003 May 01; 10(9):750-7. PubMed ID: 12704413
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  • 13. Ex vivo gene transfer to mature skeletal muscle by using adenovirus helper cells.
    Kimura S, Ikezawa M, Cao B, Kanda Y, Pruchnic R, Cummins J, Huard J, Miike T, Suzuki S.
    J Gene Med; 2004 Feb 01; 6(2):155-65. PubMed ID: 14978769
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  • 14. Restoration of dystrophin expression in mdx mice by intravascular injection of naked DNA containing full-length dystrophin cDNA.
    Liang KW, Nishikawa M, Liu F, Sun B, Ye Q, Huang L.
    Gene Ther; 2004 Jun 01; 11(11):901-8. PubMed ID: 14985786
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  • 15. Full-length dystrophin cDNA transfer into skeletal muscle of adult mdx mice by electroporation.
    Murakami T, Nishi T, Kimura E, Goto T, Maeda Y, Ushio Y, Uchino M, Sunada Y.
    Muscle Nerve; 2003 Feb 01; 27(2):237-41. PubMed ID: 12548532
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  • 16. Transfer of full-length Dmd to the diaphragm muscle of Dmd(mdx/mdx) mice through systemic administration of plasmid DNA.
    Liu F, Nishikawa M, Clemens PR, Huang L.
    Mol Ther; 2001 Jul 01; 4(1):45-51. PubMed ID: 11472105
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  • 17. Mini- and full-length dystrophin gene transfer induces the recovery of nitric oxide synthase at the sarcolemma of mdx4cv skeletal muscle fibers.
    Decrouy A, Renaud JM, Lunde JA, Dickson G, Jasmin BJ.
    Gene Ther; 1998 Jan 01; 5(1):59-64. PubMed ID: 9536265
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  • 18. Gene delivery to dystrophic muscle.
    Wells KE, McMahon J, Foster H, Ferrer A, Wells DJ.
    Methods Mol Biol; 2008 Jan 01; 423():421-31. PubMed ID: 18370219
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  • 19. Immune evasion by muscle-specific gene expression in dystrophic muscle.
    Hartigan-O'Connor D, Kirk CJ, Crawford R, Mulé JJ, Chamberlain JS.
    Mol Ther; 2001 Dec 01; 4(6):525-33. PubMed ID: 11735336
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  • 20. CTLA4Ig delivered by high-capacity adenoviral vector induces stable expression of dystrophin in mdx mouse muscle.
    Jiang Z, Schiedner G, Gilchrist SC, Kochanek S, Clemens PR.
    Gene Ther; 2004 Oct 01; 11(19):1453-61. PubMed ID: 15269713
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