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Journal Abstract Search

358 related items for PubMed ID: 16569668

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  • 2. Expression of a NOS transgene in dystrophin-deficient muscle reduces muscle membrane damage without increasing the expression of membrane-associated cytoskeletal proteins.
    Tidball JG, Wehling-Henricks M.
    Mol Genet Metab; 2004 Aug; 82(4):312-20. PubMed ID: 15308129
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  • 11. 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; 17(8):893-5. PubMed ID: 12670877
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  • 14. The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma.
    Lapidos KA, Kakkar R, McNally EM.
    Circ Res; 2004 Apr 30; 94(8):1023-31. PubMed ID: 15117830
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  • 17. 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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  • 18. Downstream utrophin enhancer is required for expression of utrophin in skeletal muscle.
    Tanihata J, Suzuki N, Miyagoe-Suzuki Y, Imaizumi K, Takeda S.
    J Gene Med; 2008 Jun 15; 10(6):702-13. PubMed ID: 18338831
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  • 20. CAPON expression in skeletal muscle is regulated by position, repair, NOS activity, and dystrophy.
    Ségalat L, Grisoni K, Archer J, Vargas C, Bertrand A, Anderson JE.
    Exp Cell Res; 2005 Jan 15; 302(2):170-9. PubMed ID: 15561099
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