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Journal Abstract Search

265 related items for PubMed ID: 8202529

  • 21. Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain gene.
    Besse S, Allamand V, Vilquin JT, Li Z, Poirier C, Vignier N, Hori H, Guénet JL, Guicheney P.
    Neuromuscul Disord; 2003 Mar; 13(3):216-22. PubMed ID: 12609503
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  • 22. Reduced fatigue in diaphragm muscle of merosin-deficient DY/DY dystrophic mice.
    van Lunteren E, Moyer M.
    Respiration; 2003 Mar; 70(6):636-42. PubMed ID: 14732796
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  • 24. Differential labelling of laminin alpha 2 in muscle and neural tissue of dy/dy mice: are there isoforms of the laminin alpha 2 chain?
    Sewry CA, Uziyel Y, Torelli S, Buchanan S, Sorokin L, Cohen J, Watt DJ.
    Neuropathol Appl Neurobiol; 1998 Feb; 24(1):66-72. PubMed ID: 9549731
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  • 25. Overexpression of the cytotoxic T cell (CT) carbohydrate inhibits muscular dystrophy in the dyW mouse model of congenital muscular dystrophy 1A.
    Xu R, Chandrasekharan K, Yoon JH, Camboni M, Martin PT.
    Am J Pathol; 2007 Jul; 171(1):181-99. PubMed ID: 17591965
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  • 26. Animal models of muscular dystrophies.
    Nonaka I.
    Lab Anim Sci; 1998 Feb; 48(1):8-17. PubMed ID: 9517883
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  • 27. Partial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantation.
    Vilquin JT, Kinoshita I, Roy B, Goulet M, Engvall E, Tomé F, Fardeau M, Tremblay JP.
    J Cell Biol; 1996 Apr; 133(1):185-97. PubMed ID: 8601607
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  • 28. Potent pro-inflammatory and pro-fibrotic molecules, osteopontin and galectin-3, are not major disease modulators of laminin α2 chain-deficient muscular dystrophy.
    Gawlik KI, Holmberg J, Svensson M, Einerborg M, Oliveira BM, Deierborg T, Durbeej M.
    Sci Rep; 2017 Mar 10; 7():44059. PubMed ID: 28281577
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  • 29. Transgenic overexpression of the α7 integrin reduces muscle pathology and improves viability in the dy(W) mouse model of merosin-deficient congenital muscular dystrophy type 1A.
    Doe JA, Wuebbles RD, Allred ET, Rooney JE, Elorza M, Burkin DJ.
    J Cell Sci; 2011 Jul 01; 124(Pt 13):2287-97. PubMed ID: 21652631
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  • 30. Pathological changes in levels of three small stress proteins, alphaB crystallin, HSP 27 and p20, in the hindlimb muscles of dy mouse.
    Sakuma K, Watanabe K, Totsuka T, Kato K.
    Biochim Biophys Acta; 1998 Mar 05; 1406(2):162-8. PubMed ID: 9573353
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  • 32. Structure and function of basement membranes.
    Engvall E.
    Int J Dev Biol; 1995 Oct 05; 39(5):781-7. PubMed ID: 8645562
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  • 33. Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models.
    Kuang W, Xu H, Vachon PH, Liu L, Loechel F, Wewer UM, Engvall E.
    J Clin Invest; 1998 Aug 15; 102(4):844-52. PubMed ID: 9710454
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  • 35. Overexpression of mini-agrin in skeletal muscle increases muscle integrity and regenerative capacity in laminin-alpha2-deficient mice.
    Bentzinger CF, Barzaghi P, Lin S, Ruegg MA.
    FASEB J; 2005 Jun 15; 19(8):934-42. PubMed ID: 15923403
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  • 36. Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophies.
    Hodges BL, Hayashi YK, Nonaka I, Wang W, Arahata K, Kaufman SJ.
    J Cell Sci; 1997 Nov 15; 110 ( Pt 22)():2873-81. PubMed ID: 9427295
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  • 40. An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.
    Moll J, Barzaghi P, Lin S, Bezakova G, Lochmüller H, Engvall E, Müller U, Ruegg MA.
    Nature; 2001 Sep 20; 413(6853):302-7. PubMed ID: 11565031
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