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Journal Abstract Search

167 related items for PubMed ID: 10937856

  • 1. Functional roles of dystrophin and of associated proteins. New insights for the sarcoglycans.
    Betto R, Biral D, Sandonà D.
    Ital J Neurol Sci; 1999 Dec; 20(6):371-9. PubMed ID: 10937856
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  • 2. Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.
    Matsumura K, Campbell KP.
    Muscle Nerve; 1994 Jan; 17(1):2-15. PubMed ID: 8264699
    [Abstract] [Full Text] [Related]

  • 3. Muscular dystrophies: diseases of the dystrophin-glycoprotein complex.
    Worton R.
    Science; 1995 Nov 03; 270(5237):755-6. PubMed ID: 7481760
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  • 4. Sarcoglycans in muscular dystrophy.
    Hack AA, Groh ME, McNally EM.
    Microsc Res Tech; 1995 Nov 03; 48(3-4):167-80. PubMed ID: 10679964
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  • 5. Sarcoglycan complex: a muscular supporter of dystroglycan-dystrophin interplay?
    Matsumura K, Saito F, Yamada H, Hase A, Sunada Y, Shimizu T.
    Cell Mol Biol (Noisy-le-grand); 1999 Sep 03; 45(6):751-62. PubMed ID: 10541473
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  • 6. Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex.
    Crosbie RH, Lebakken CS, Holt KH, Venzke DP, Straub V, Lee JC, Grady RM, Chamberlain JS, Sanes JR, Campbell KP.
    J Cell Biol; 1999 Apr 05; 145(1):153-65. PubMed ID: 10189375
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  • 8. 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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  • 11. 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 25; 11(2):197-207. PubMed ID: 11257478
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  • 12. Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle.
    Cohn RD, Mayer U, Saher G, Herrmann R, van der Flier A, Sonnenberg A, Sorokin L, Voit T.
    J Neurol Sci; 1999 Mar 01; 163(2):140-52. PubMed ID: 10371075
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  • 13. 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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  • 14. 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 01; 1(1):49-58. PubMed ID: 10735275
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  • 16. 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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  • 17. [Significance of merosin and sarcoglycan in manifestations of certain forms of muscular dystrophy].
    Medić S, Rakocević-Stojanović V.
    Srp Arh Celok Lek; 1998 Jul 22; 126(1-2):34-9. PubMed ID: 9525081
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  • 19. 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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