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Journal Abstract Search

125 related items for PubMed ID: 8645562

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  • 2. Expression of laminin alpha1, alpha2, alpha4, and alpha5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice.
    Ringelmann B, Röder C, Hallmann R, Maley M, Davies M, Grounds M, Sorokin L.
    Exp Cell Res; 1999 Jan 10; 246(1):165-82. PubMed ID: 9882526
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  • 7. Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation.
    Miner JH, Li C, Mudd JL, Go G, Sutherland AE.
    Development; 2004 May 10; 131(10):2247-56. PubMed ID: 15102706
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  • 8. Merosin (laminin-2) localization in basal lamina of normal skeletal muscle fibers and changes in plasma membrane of merosin-deficient skeletal muscle fibers.
    Shibuya S, Wakayama Y, Inoue M, Kojima H, Oniki H.
    Med Electron Microsc; 2003 Dec 10; 36(4):213-20. PubMed ID: 16228654
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  • 9. 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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  • 10. Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles.
    Vilquin JT, Guérette B, Puymirat J, Yaffe D, Tomé FM, Fardeau M, Fiszman M, Schwartz K, Tremblay JP.
    Gene Ther; 1999 May 20; 6(5):792-800. PubMed ID: 10505103
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  • 11. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
    Smeyers P.
    Rev Neurol; 1999 May 20; 28(2):141-9. PubMed ID: 10101782
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  • 12. Laminin alpha1 chain improves laminin alpha2 chain deficient peripheral neuropathy.
    Gawlik KI, Li JY, Petersén A, Durbeej M.
    Hum Mol Genet; 2006 Sep 15; 15(18):2690-700. PubMed ID: 16893907
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  • 14. Prenatal diagnosis in laminin alpha2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers.
    Vainzof M, Richard P, Herrmann R, Jimenez-Mallebrera C, Talim B, Yamamoto LU, Ledeuil C, Mein R, Abbs S, Brockington M, Romero NB, Zatz M, Topaloglu H, Voit T, Sewry C, Muntoni F, Guicheney P, Tomé FM.
    Neuromuscul Disord; 2005 Oct 15; 15(9-10):588-94. PubMed ID: 16084089
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  • 15. Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice.
    Gawlik K, Miyagoe-Suzuki Y, Ekblom P, Takeda S, Durbeej M.
    Hum Mol Genet; 2004 Aug 15; 13(16):1775-84. PubMed ID: 15213105
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  • 20. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
    Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T.
    Biochem Biophys Res Commun; 2006 Apr 07; 342(2):489-502. PubMed ID: 16487936
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