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Journal Abstract Search

520 related items for PubMed ID: 9215691

  • 1. Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.
    Metzinger L, Blake DJ, Squier MV, Anderson LV, Deconinck AE, Nawrotzki R, Hilton-Jones D, Davies KE.
    Hum Mol Genet; 1997 Jul; 6(7):1185-91. PubMed ID: 9215691
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  • 2. 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; 1(1):49-58. PubMed ID: 10735275
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  • 3. Dystrobrevin dynamics in muscle-cell signalling: a possible target for therapeutic intervention in Duchenne muscular dystrophy?
    Blake DJ.
    Neuromuscul Disord; 2002 Oct; 12 Suppl 1():S110-7. PubMed ID: 12206805
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  • 6. 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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  • 7. Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in gamma- or delta-sarcoglycan-deficient mice.
    Porter JD, Merriam AP, Hack AA, Andrade FH, McNally EM.
    Neuromuscul Disord; 2001 Mar 22; 11(2):197-207. PubMed ID: 11257478
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  • 12. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12.
    Lim LE, Duclos F, Broux O, Bourg N, Sunada Y, Allamand V, Meyer J, Richard I, Moomaw C, Slaughter C.
    Nat Genet; 1995 Nov 22; 11(3):257-65. PubMed ID: 7581448
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  • 13. Cellular and molecular properties of alpha-dystrobrevin in skeletal muscle.
    Enigk RE, Maimone MM.
    Front Biosci; 2001 Jan 01; 6():D53-64. PubMed ID: 11145920
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  • 14. Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.
    Araishi K, Sasaoka T, Imamura M, Noguchi S, Hama H, Wakabayashi E, Yoshida M, Hori T, Ozawa E.
    Hum Mol Genet; 1999 Sep 01; 8(9):1589-98. PubMed ID: 10441321
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  • 16. Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects.
    Handa V, Mital A, Gupta M, Goyle S.
    Neurol India; 2001 Mar 01; 49(1):19-24. PubMed ID: 11303236
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  • 18. Assembly of the sarcoglycan complex. Insights for muscular dystrophy.
    Holt KH, Campbell KP.
    J Biol Chem; 1998 Dec 25; 273(52):34667-70. PubMed ID: 9856984
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