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Journal Abstract Search

298 related items for PubMed ID: 18334986

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  • 2. Delivery of AAV2/9-microdystrophin genes incorporating helix 1 of the coiled-coil motif in the C-terminal domain of dystrophin improves muscle pathology and restores the level of α1-syntrophin and α-dystrobrevin in skeletal muscles of mdx mice.
    Koo T, Malerba A, Athanasopoulos T, Trollet C, Boldrin L, Ferry A, Popplewell L, Foster H, Foster K, Dickson G.
    Hum Gene Ther; 2011 Nov; 22(11):1379-88. PubMed ID: 21453126
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  • 4. Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy.
    Church JE, Trieu J, Chee A, Naim T, Gehrig SM, Lamon S, Angelini C, Russell AP, Lynch GS.
    Exp Physiol; 2014 Apr; 99(4):675-87. PubMed ID: 24443351
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  • 7. Stable micro-dystrophin gene transfer using an integrating adeno-retroviral hybrid vector ameliorates the dystrophic pathology in mdx mouse muscle.
    Roberts ML, Wells DJ, Graham IR, Fabb SA, Hill VJ, Duisit G, Yuasa K, Takeda S, Cosset FL, Dickson G.
    Hum Mol Genet; 2002 Jul 15; 11(15):1719-30. PubMed ID: 12095914
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  • 8. Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice.
    Ebihara S, Guibinga GH, Gilbert R, Nalbantoglu J, Massie B, Karpati G, Petrof BJ.
    Physiol Genomics; 2000 Sep 08; 3(3):133-44. PubMed ID: 11015608
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  • 9. Adeno-associated virus vector gene transfer and sarcolemmal expression of a 144 kDa micro-dystrophin effectively restores the dystrophin-associated protein complex and inhibits myofibre degeneration in nude/mdx mice.
    Fabb SA, Wells DJ, Serpente P, Dickson G.
    Hum Mol Genet; 2002 Apr 01; 11(7):733-41. PubMed ID: 11929846
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  • 13. Lentiviral Micro-dystrophin Gene Treatment into Late-stage mdx Mice for Duchenne Muscular Dystrophy Disease.
    Eren SA, Tastan C, Karadeniz KB, Turan RD, Cakirsoy D, Kancagi DD, Yilmaz SU, Oztatlici M, Oztatlici H, Ozer S, Tumentemur G, Baykal AT, Ovali E.
    Curr Gene Ther; 2023 Apr 01; 23(4):304-315. PubMed ID: 37032509
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  • 14. Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy.
    Ahmad A, Brinson M, Hodges BL, Chamberlain JS, Amalfitano A.
    Hum Mol Genet; 2000 Oct 12; 9(17):2507-15. PubMed ID: 11030755
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  • 15. 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 12; 15(7):531-6. PubMed ID: 18273052
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  • 16. Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene.
    Koppanati BM, Li J, Reay DP, Wang B, Daood M, Zheng H, Xiao X, Watchko JF, Clemens PR.
    Gene Ther; 2010 Nov 12; 17(11):1355-62. PubMed ID: 20535217
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  • 17. Long-term functional adeno-associated virus-microdystrophin expression in the dystrophic CXMDj dog.
    Koo T, Okada T, Athanasopoulos T, Foster H, Takeda S, Dickson G.
    J Gene Med; 2011 Sep 12; 13(9):497-506. PubMed ID: 22144143
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  • 18. Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice.
    Burkin DJ, Wallace GQ, Nicol KJ, Kaufman DJ, Kaufman SJ.
    J Cell Biol; 2001 Mar 19; 152(6):1207-18. PubMed ID: 11257121
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  • 19. Isometric resistance training increases strength and alters histopathology of dystrophin-deficient mouse skeletal muscle.
    Lindsay A, Larson AA, Verma M, Ervasti JM, Lowe DA.
    J Appl Physiol (1985); 2019 Feb 01; 126(2):363-375. PubMed ID: 30571283
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  • 20. Restoration of all dystrophin protein interactions by functional domains in trans does not rescue dystrophy.
    Gardner KL, Kearney JA, Edwards JD, Rafael-Fortney JA.
    Gene Ther; 2006 May 01; 13(9):744-51. PubMed ID: 16307000
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