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Journal Abstract Search

412 related items for PubMed ID: 10093060

  • 1. Myotonic ADR-MDX mutant mice show less severe muscular dystrophy than MDX mice.
    Krämer R, Lochmüller H, Abicht A, Rüdel R, Brinkmeier H.
    Neuromuscul Disord; 1998 Dec; 8(8):542-50. PubMed ID: 10093060
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  • 2. Mutual interference of myotonia and muscular dystrophy in the mouse: a study on ADR-MDX double mutants.
    Heimann P, Augustin M, Wieneke S, Heising S, Jockusch H.
    Neuromuscul Disord; 1998 Dec; 8(8):551-60. PubMed ID: 10093061
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  • 3. 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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  • 4. Serum parvalbumin, an indicator of muscle disease in murine dystrophy and myotonia.
    Jockusch H, Friedrich G, Zippel M.
    Muscle Nerve; 1990 Jun 19; 13(6):551-5. PubMed ID: 2366828
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  • 5. Breeding of the gad-mdx mouse: influence of genetically induced denervation on dystrophic muscle fibers.
    Suh JG, Yamazaki A, Tomita T.
    Lab Anim Sci; 1994 Feb 19; 44(1):42-6. PubMed ID: 8007658
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  • 6. miR-146a deficiency does not aggravate muscular dystrophy in mdx mice.
    Bronisz-Budzyńska I, Chwalenia K, Mucha O, Podkalicka P, Karolina-Bukowska-Strakova, Józkowicz A, Łoboda A, Kozakowska M, Dulak J.
    Skelet Muscle; 2019 Aug 14; 9(1):22. PubMed ID: 31412923
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  • 7. Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers.
    Tutdibi O, Brinkmeier H, Rüdel R, Föhr KJ.
    J Physiol; 1999 Mar 15; 515 ( Pt 3)(Pt 3):859-68. PubMed ID: 10066910
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  • 8. 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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  • 10. Phenotype of dystrophinopathy in old mdx mice.
    Lefaucheur JP, Pastoret C, Sebille A.
    Anat Rec; 1995 May 15; 242(1):70-6. PubMed ID: 7604983
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  • 11. Increased plasma lipid levels exacerbate muscle pathology in the mdx mouse model of Duchenne muscular dystrophy.
    Milad N, White Z, Tehrani AY, Sellers S, Rossi FMV, Bernatchez P.
    Skelet Muscle; 2017 Sep 12; 7(1):19. PubMed ID: 28899419
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  • 13. The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy.
    Stedman HH, Sweeney HL, Shrager JB, Maguire HC, Panettieri RA, Petrof B, Narusawa M, Leferovich JM, Sladky JT, Kelly AM.
    Nature; 1991 Aug 08; 352(6335):536-9. PubMed ID: 1865908
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  • 14. Protein-Anchoring Therapy of Biglycan for Mdx Mouse Model of Duchenne Muscular Dystrophy.
    Ito M, Ehara Y, Li J, Inada K, Ohno K.
    Hum Gene Ther; 2017 May 08; 28(5):428-436. PubMed ID: 27485975
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  • 15. The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy.
    Hammers DW, Hart CC, Matheny MK, Wright LA, Armellini M, Barton ER, Sweeney HL.
    Sci Rep; 2020 Aug 21; 10(1):14070. PubMed ID: 32826942
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  • 16. Sub-physiological sarcoglycan expression contributes to compensatory muscle protection in mdx mice.
    Li D, Long C, Yue Y, Duan D.
    Hum Mol Genet; 2009 Apr 01; 18(7):1209-20. PubMed ID: 19131360
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  • 19. Comparative evolution of muscular dystrophy in diaphragm, gastrocnemius and masseter muscles from old male mdx mice.
    Muller J, Vayssiere N, Royuela M, Leger ME, Muller A, Bacou F, Pons F, Hugon G, Mornet D.
    J Muscle Res Cell Motil; 2001 Apr 01; 22(2):133-9. PubMed ID: 11519736
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