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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

121 related items for PubMed ID: 8070559

  • 41.
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  • 42. Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice.
    Nguyen HH, Jayasinha V, Xia B, Hoyte K, Martin PT.
    Proc Natl Acad Sci U S A; 2002 Apr 16; 99(8):5616-21. PubMed ID: 11960016
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  • 43. Deficiency of alpha-dystroglycan in muscle-eye-brain disease.
    Kano H, Kobayashi K, Herrmann R, Tachikawa M, Manya H, Nishino I, Nonaka I, Straub V, Talim B, Voit T, Topaloglu H, Endo T, Yoshikawa H, Toda T.
    Biochem Biophys Res Commun; 2002 Mar 15; 291(5):1283-6. PubMed ID: 11883957
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  • 46. 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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  • 47. Dystrophin-deficient muscular dystrophy in a Weimaraner.
    Baltzer WI, Calise DV, Levine JM, Shelton GD, Edwards JF, Steiner JM.
    J Am Anim Hosp Assoc; 2007 Mar 19; 43(4):227-32. PubMed ID: 17615404
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  • 53. Dystrophin, utrophin and beta-dystroglycan expression in skeletal muscle from patients with Becker muscular dystrophy.
    Kawajiri M, Mitsui T, Kawai H, Kobunai T, Tsuchihashi T, Saito S.
    J Neuropathol Exp Neurol; 1996 Aug 19; 55(8):896-903. PubMed ID: 8759779
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  • 54. WW and EF hand domains of dystrophin-family proteins mediate dystroglycan binding.
    Chung W, Campanelli JT.
    Mol Cell Biol Res Commun; 1999 Aug 19; 2(3):162-71. PubMed ID: 10662592
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  • 56. Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy.
    Matsumura K, Tomé FM, Collin H, Azibi K, Chaouch M, Kaplan JC, Fardeau M, Campbell KP.
    Nature; 1992 Sep 24; 359(6393):320-2. PubMed ID: 1406935
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  • 57. Effects of an immunosuppressive treatment in the GRMD dog model of Duchenne muscular dystrophy.
    Barthélémy I, Uriarte A, Drougard C, Unterfinger Y, Thibaud JL, Blot S.
    PLoS One; 2012 Sep 24; 7(11):e48478. PubMed ID: 23185260
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  • 58. Muscular dystrophy in a dog resembling human becker muscular dystrophy.
    Baroncelli AB, Abellonio F, Pagano TB, Esposito I, Peirone B, Papparella S, Paciello O.
    J Comp Pathol; 2014 May 24; 150(4):429-33. PubMed ID: 24529507
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  • 59. 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 24; 10(9):750-7. PubMed ID: 12704413
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  • 60. Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses.
    Côté PD, Moukhles H, Lindenbaum M, Carbonetto S.
    Nat Genet; 1999 Nov 24; 23(3):338-42. PubMed ID: 10610181
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