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Journal Abstract Search

530 related items for PubMed ID: 33982338

  • 21.
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  • 23. Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice.
    Phelps SF, Hauser MA, Cole NM, Rafael JA, Hinkle RT, Faulkner JA, Chamberlain JS.
    Hum Mol Genet; 1995 Aug; 4(8):1251-8. PubMed ID: 7581361
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  • 27. 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; 11(19):1453-61. PubMed ID: 15269713
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  • 28. 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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  • 30. Cell transplantation-mediated dystrophin supplementation efficacy in Duchenne muscular dystrophy mouse motor function improvement demonstrated by enhanced skeletal muscle fatigue tolerance.
    Bourgeois Yoshioka CK, Takenaka-Ninagawa N, Goto M, Miki M, Watanabe D, Yamamoto M, Aoyama T, Sakurai H.
    Stem Cell Res Ther; 2024 Sep 19; 15(1):313. PubMed ID: 39300595
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  • 31. Micro-dystrophin cDNA ameliorates dystrophic phenotypes when introduced into mdx mice as a transgene.
    Sakamoto M, Yuasa K, Yoshimura M, Yokota T, Ikemoto T, Suzuki M, Dickson G, Miyagoe-Suzuki Y, Takeda S.
    Biochem Biophys Res Commun; 2002 May 17; 293(4):1265-72. PubMed ID: 12054513
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  • 33. 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 17; 10(9):750-7. PubMed ID: 12704413
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  • 34. [Current status and perspective of gene therapy on dystrophic animal model].
    Takeda S.
    Rinsho Shinkeigaku; 2004 Nov 17; 44(11):911-3. PubMed ID: 15651329
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  • 35. Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression.
    Teichmann MD, Wegner FV, Fink RH, Chamberlain JS, Launikonis BS, Martinac B, Friedrich O.
    PLoS One; 2008 Nov 17; 3(11):e3644. PubMed ID: 18982068
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  • 36. Muscle specific kinase protects dystrophic mdx mouse muscles from eccentric contraction-induced loss of force-producing capacity.
    Trajanovska S, Ban J, Huang J, Gregorevic P, Morsch M, Allen DG, Phillips WD.
    J Physiol; 2019 Sep 17; 597(18):4831-4850. PubMed ID: 31340406
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  • 37. Cardiac expression of a mini-dystrophin that normalizes skeletal muscle force only partially restores heart function in aged Mdx mice.
    Bostick B, Yue Y, Long C, Marschalk N, Fine DM, Chen J, Duan D.
    Mol Ther; 2009 Feb 17; 17(2):253-61. PubMed ID: 19066599
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  • 38. Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice.
    Ito K, Kimura S, Ozasa S, Matsukura M, Ikezawa M, Yoshioka K, Ueno H, Suzuki M, Araki K, Yamamura K, Miwa T, Dickson G, Thomas GD, Miike T.
    Hum Mol Genet; 2006 Jul 15; 15(14):2266-75. PubMed ID: 16777842
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  • 40. Systemic microdystrophin gene delivery improves skeletal muscle structure and function in old dystrophic mdx mice.
    Gregorevic P, Blankinship MJ, Allen JM, Chamberlain JS.
    Mol Ther; 2008 Apr 15; 16(4):657-64. PubMed ID: 18334986
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