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Journal Abstract Search

800 related items for PubMed ID: 16476707

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  • 2. Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin.
    Rooney JE, Welser JV, Dechert MA, Flintoff-Dye NL, Kaufman SJ, Burkin DJ.
    J Cell Sci; 2006 Jun 01; 119(Pt 11):2185-95. PubMed ID: 16684813
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  • 4. Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy.
    Porter JD, Merriam AP, Leahy P, Gong B, Feuerman J, Cheng G, Khanna S.
    Hum Mol Genet; 2004 Feb 01; 13(3):257-69. PubMed ID: 14681298
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  • 6. Absence of integrin alpha 7 causes a novel form of muscular dystrophy.
    Mayer U, Saher G, Fässler R, Bornemann A, Echtermeyer F, von der Mark H, Miosge N, Pöschl E, von der Mark K.
    Nat Genet; 1997 Nov 01; 17(3):318-23. PubMed ID: 9354797
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  • 7. Constitutive properties, not molecular adaptations, mediate extraocular muscle sparing in dystrophic mdx mice.
    Porter JD, Merriam AP, Khanna S, Andrade FH, Richmonds CR, Leahy P, Cheng G, Karathanasis P, Zhou X, Kusner LL, Adams ME, Willem M, Mayer U, Kaminski HJ.
    FASEB J; 2003 May 01; 17(8):893-5. PubMed ID: 12670877
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  • 11. Levels of α7 integrin and laminin-α2 are increased following prednisone treatment in the mdx mouse and GRMD dog models of Duchenne muscular dystrophy.
    Wuebbles RD, Sarathy A, Kornegay JN, Burkin DJ.
    Dis Model Mech; 2013 Sep 01; 6(5):1175-84. PubMed ID: 23846963
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  • 15. Regulation of the cardiac sodium channel Nav1.5 by utrophin in dystrophin-deficient mice.
    Albesa M, Ogrodnik J, Rougier JS, Abriel H.
    Cardiovasc Res; 2011 Feb 01; 89(2):320-8. PubMed ID: 20952415
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  • 16. Myotendinous junction defects and reduced force transmission in mice that lack alpha7 integrin and utrophin.
    Welser JV, Rooney JE, Cohen NC, Gurpur PB, Singer CA, Evans RA, Haines BA, Burkin DJ.
    Am J Pathol; 2009 Oct 01; 175(4):1545-54. PubMed ID: 19729483
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  • 18. Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice.
    Rafael JA, Tinsley JM, Potter AC, Deconinck AE, Davies KE.
    Nat Genet; 1998 May 01; 19(1):79-82. PubMed ID: 9590295
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  • 19. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
    Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T.
    Biochem Biophys Res Commun; 2006 Apr 07; 342(2):489-502. PubMed ID: 16487936
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