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Journal Abstract Search

190 related items for PubMed ID: 7874173

  • 1. Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene.
    Xu H, Wu XR, Wewer UM, Engvall E.
    Nat Genet; 1994 Nov; 8(3):297-302. PubMed ID: 7874173
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  • 2. A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination.
    Patton BL, Wang B, Tarumi YS, Seburn KL, Burgess RW.
    J Cell Sci; 2008 May 15; 121(Pt 10):1593-604. PubMed ID: 18430779
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  • 3. New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin.
    Cox GA, Phelps SF, Chapman VM, Chamberlain JS.
    Nat Genet; 1993 May 15; 4(1):87-93. PubMed ID: 8099842
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  • 4. 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 15; 6(5):792-800. PubMed ID: 10505103
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  • 5. Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice.
    Sunada Y, Bernier SM, Utani A, Yamada Y, Campbell KP.
    Hum Mol Genet; 1995 Jun 15; 4(6):1055-61. PubMed ID: 7655459
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  • 6. Synaptic plasticity in the dy2J mouse model of laminin alpha2-deficient congenital muscular dystrophy.
    Anderson JL, Head SI, Morley JW.
    Brain Res; 2005 Apr 25; 1042(1):23-8. PubMed ID: 15823249
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  • 7. Gene expression profiling of diaphragm muscle in alpha2-laminin (merosin)-deficient dy/dy dystrophic mice.
    van Lunteren E, Moyer M, Leahy P.
    Physiol Genomics; 2006 Mar 13; 25(1):85-95. PubMed ID: 16368874
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  • 9. Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse.
    Xu H, Christmas P, Wu XR, Wewer UM, Engvall E.
    Proc Natl Acad Sci U S A; 1994 Jun 07; 91(12):5572-6. PubMed ID: 8202529
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  • 13. 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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  • 15. 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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  • 18. Cloning of the laminin alpha 3 chain gene (LAMA3) and identification of a homozygous deletion in a patient with Herlitz junctional epidermolysis bullosa.
    Vidal F, Baudoin C, Miquel C, Galliano MF, Christiano AM, Uitto J, Ortonne JP, Meneguzzi G.
    Genomics; 1995 Nov 20; 30(2):273-80. PubMed ID: 8586427
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  • 19. Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa.
    Pulkkinen L, Christiano AM, Airenne T, Haakana H, Tryggvason K, Uitto J.
    Nat Genet; 1994 Mar 20; 6(3):293-7. PubMed ID: 8012393
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  • 20. 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 20; 13(3):216-22. PubMed ID: 12609503
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