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Journal Abstract Search

470 related items for PubMed ID: 12736199

  • 1. Dystroglycan glycosylation and its role in matrix binding in skeletal muscle.
    Martin PT.
    Glycobiology; 2003 Aug; 13(8):55R-66R. PubMed ID: 12736199
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  • 4. Towards an understanding of the dystrophin-glycoprotein complex: linkage between the extracellular matrix and the membrane cytoskeleton in muscle fibers.
    Ohlendieck K.
    Eur J Cell Biol; 1996 Jan; 69(1):1-10. PubMed ID: 8825019
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  • 5. Ultrastructural localization of adhalin, alpha-dystroglycan and merosin in normal and dystrophic muscle.
    Cullen MJ, Walsh J, Roberds SL, Campbell KP.
    Neuropathol Appl Neurobiol; 1996 Feb; 22(1):30-7. PubMed ID: 8866780
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  • 7. Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations.
    Huizing M, Rakocevic G, Sparks SE, Mamali I, Shatunov A, Goldfarb L, Krasnewich D, Gahl WA, Dalakas MC.
    Mol Genet Metab; 2004 Mar; 81(3):196-202. PubMed ID: 14972325
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  • 8. Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.
    Moore SA, Saito F, Chen J, Michele DE, Henry MD, Messing A, Cohn RD, Ross-Barta SE, Westra S, Williamson RA, Hoshi T, Campbell KP.
    Nature; 2002 Jul 25; 418(6896):422-5. PubMed ID: 12140559
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  • 10. Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.
    Longman C, Brockington M, Torelli S, Jimenez-Mallebrera C, Kennedy C, Khalil N, Feng L, Saran RK, Voit T, Merlini L, Sewry CA, Brown SC, Muntoni F.
    Hum Mol Genet; 2003 Nov 01; 12(21):2853-61. PubMed ID: 12966029
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  • 12. [Dystroglycan linkage and muscular dystrophy].
    Shimizu T.
    Rinsho Shinkeigaku; 2002 Nov 01; 42(11):1091-4. PubMed ID: 12784674
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  • 13. The WW domain of dystrophin requires EF-hands region to interact with beta-dystroglycan.
    Rentschler S, Linn H, Deininger K, Bedford MT, Espanel X, Sudol M.
    Biol Chem; 1999 Apr 01; 380(4):431-42. PubMed ID: 10355629
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  • 14. Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.
    Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP.
    Nature; 2002 Jul 25; 418(6896):417-22. PubMed ID: 12140558
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  • 15. 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 25; 45(6):751-62. PubMed ID: 10541473
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  • 16. Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy.
    Saito F, Blank M, Schröder J, Manya H, Shimizu T, Campbell KP, Endo T, Mizutani M, Kröger S, Matsumura K.
    FEBS Lett; 2005 Apr 25; 579(11):2359-63. PubMed ID: 15848172
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  • 17. Dystroglycan and muscular dystrophies related to the dystrophin-glycoprotein complex.
    Sciandra F, Bozzi M, Bianchi M, Pavoni E, Giardina B, Brancaccio A.
    Ann Ist Super Sanita; 2003 Apr 25; 39(2):173-81. PubMed ID: 14587215
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  • 18. Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses.
    Côté PD, Moukhles H, Lindenbaum M, Carbonetto S.
    Nat Genet; 1999 Nov 25; 23(3):338-42. PubMed ID: 10610181
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  • 19. Localization of phospho-beta-dystroglycan (pY892) to an intracellular vesicular compartment in cultured cells and skeletal muscle fibers in vivo.
    Sotgia F, Bonuccelli G, Bedford M, Brancaccio A, Mayer U, Wilson MT, Campos-Gonzalez R, Brooks JW, Sudol M, Lisanti MP.
    Biochemistry; 2003 Jun 17; 42(23):7110-23. PubMed ID: 12795607
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  • 20. The role of dystroglycan, a novel receptor of laminin and agrin, in cell differentiation.
    Matsumura K, Yamada H, Saito F, Sunada Y, Shimizu T.
    Histol Histopathol; 1997 Jan 17; 12(1):195-203. PubMed ID: 9046055
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