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PUBMED FOR HANDHELDS

Journal Abstract Search


297 related items for PubMed ID: 12609501

  • 1. Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice.
    Sasaoka T, Imamura M, Araishi K, Noguchi S, Mizuno Y, Takagoshi N, Hama H, Wakabayashi-Takai E, Yoshimoto-Matsuda Y, Nonaka I, Kaneko K, Yoshida M, Ozawa E.
    Neuromuscul Disord; 2003 Mar; 13(3):193-206. PubMed ID: 12609501
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  • 2. Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy.
    Durbeej M, Sawatzki SM, Barresi R, Schmainda KM, Allamand V, Michele DE, Campbell KP.
    Proc Natl Acad Sci U S A; 2003 Jul 22; 100(15):8910-5. PubMed ID: 12851463
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  • 4. Rescue of skeletal muscles of gamma-sarcoglycan-deficient mice with adeno-associated virus-mediated gene transfer.
    Cordier L, Hack AA, Scott MO, Barton-Davis ER, Gao G, Wilson JM, McNally EM, Sweeney HL.
    Mol Ther; 2000 Feb 22; 1(2):119-29. PubMed ID: 10933922
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  • 6. Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.
    Crosbie RH, Barresi R, Campbell KP.
    FASEB J; 2002 Nov 22; 16(13):1786-91. PubMed ID: 12409321
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  • 12. Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex.
    Barresi R, Moore SA, Stolle CA, Mendell JR, Campbell KP.
    J Biol Chem; 2000 Dec 08; 275(49):38554-60. PubMed ID: 10993904
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  • 15. Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2).
    Duggan DJ, Manchester D, Stears KP, Mathews DJ, Hart C, Hoffman EP.
    Neurogenetics; 1997 May 08; 1(1):49-58. PubMed ID: 10735275
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  • 17. epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex.
    Straub V, Ettinger AJ, Durbeej M, Venzke DP, Cutshall S, Sanes JR, Campbell KP.
    J Biol Chem; 1999 Sep 24; 274(39):27989-96. PubMed ID: 10488149
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  • 19. [The frequency of patients with adhalin deficiency in a muscular dystrophy patient population].
    Hayashi YK, Arahata K.
    Nihon Rinsho; 1997 Dec 24; 55(12):3165-8. PubMed ID: 9436429
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  • 20. Cell therapy of alpha-sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblasts.
    Sampaolesi M, Torrente Y, Innocenzi A, Tonlorenzi R, D'Antona G, Pellegrino MA, Barresi R, Bresolin N, De Angelis MG, Campbell KP, Bottinelli R, Cossu G.
    Science; 2003 Jul 25; 301(5632):487-92. PubMed ID: 12855815
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