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Journal Abstract Search

609 related items for PubMed ID: 10525423

  • 1. Decreased myocardial nNOS, increased iNOS and abnormal ECGs in mouse models of Duchenne muscular dystrophy.
    Bia BL, Cassidy PJ, Young ME, Rafael JA, Leighton B, Davies KE, Radda GK, Clarke K.
    J Mol Cell Cardiol; 1999 Oct; 31(10):1857-62. PubMed ID: 10525423
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  • 5. iNOS expression in dystrophinopathies can be reduced by somatic gene transfer of dystrophin or utrophin.
    Louboutin JP, Rouger K, Tinsley JM, Halldorson J, Wilson JM.
    Mol Med; 2001 May; 7(5):355-64. PubMed ID: 11474581
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  • 8. Mini- and full-length dystrophin gene transfer induces the recovery of nitric oxide synthase at the sarcolemma of mdx4cv skeletal muscle fibers.
    Decrouy A, Renaud JM, Lunde JA, Dickson G, Jasmin BJ.
    Gene Ther; 1998 Jan; 5(1):59-64. PubMed ID: 9536265
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  • 9. 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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  • 11. Expression of full-length utrophin prevents muscular dystrophy in mdx mice.
    Tinsley J, Deconinck N, Fisher R, Kahn D, Phelps S, Gillis JM, Davies K.
    Nat Med; 1998 Dec 15; 4(12):1441-4. PubMed ID: 9846586
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  • 13. Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscle.
    Wells KE, Torelli S, Lu Q, Brown SC, Partridge T, Muntoni F, Wells DJ.
    Neuromuscul Disord; 2003 Jan 15; 13(1):21-31. PubMed ID: 12467729
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  • 14. An attempt of gene therapy in Duchenne muscular dystrophy: overexpression of utrophin in transgenic mdx mice.
    Gillis JM.
    Acta Neurol Belg; 2000 Sep 15; 100(3):146-50. PubMed ID: 11098286
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  • 15. Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions.
    Torelli S, Brown SC, Jimenez-Mallebrera C, Feng L, Muntoni F, Sewry CA.
    Neuropathol Appl Neurobiol; 2004 Oct 15; 30(5):540-5. PubMed ID: 15488030
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  • 17. Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strains.
    van Putten M, Kumar D, Hulsker M, Hoogaars WM, Plomp JJ, van Opstal A, van Iterson M, Admiraal P, van Ommen GJ, 't Hoen PA, Aartsma-Rus A.
    Neuromuscul Disord; 2012 May 15; 22(5):406-17. PubMed ID: 22284942
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  • 18. [Utrophin, a way to cure Duchenne muscle dystrophy].
    Gillis JM.
    Med Sci (Paris); 2004 Apr 15; 20(4):442-7. PubMed ID: 15124117
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  • 19. 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 15; 19(1):79-82. PubMed ID: 9590295
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  • 20. [Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy].
    Wang S, Shen D.
    Zhonghua Yi Xue Za Zhi; 2002 Feb 10; 82(3):155-7. PubMed ID: 11953148
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