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Journal Abstract Search

275 related items for PubMed ID: 8246011

  • 1. Abnormal localization of laminin subunits in muscular dystrophies.
    Hayashi YK, Engvall E, Arikawa-Hirasawa E, Goto K, Koga R, Nonaka I, Sugita H, Arahata K.
    J Neurol Sci; 1993 Oct; 119(1):53-64. PubMed ID: 8246011
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  • 2. Immunocytochemical analysis of dystrophin in congenital muscular dystrophy.
    Arikawa E, Ishihara T, Nonaka I, Sugita H, Arahata K.
    J Neurol Sci; 1991 Sep; 105(1):79-87. PubMed ID: 1795174
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  • 4. Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy.
    Ishii H, Hayashi YK, Nonaka I, Arahata K.
    Neuromuscul Disord; 1997 May; 7(3):191-7. PubMed ID: 9185184
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  • 5. Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining.
    Connolly AM, Pestronk A, Planer GJ, Yue J, Mehta S, Choksi R.
    Neurology; 1996 Mar; 46(3):810-14. PubMed ID: 8618688
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  • 7. Distribution of ten laminin chains in dystrophic and regenerating muscles.
    Patton BL, Connoll AM, Martin PT, Cunningham JM, Mehta S, Pestronk A, Miner JH, Sanes JR.
    Neuromuscul Disord; 1999 Oct; 9(6-7):423-33. PubMed ID: 10545049
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  • 9. [Expression of connective tissue growth factor in progressive muscular dystrophy].
    Sun GL, Yao F, Jiang HK, Li P, Kazuhiro H.
    Zhonghua Er Ke Za Zhi; 2005 Oct; 43(10):753-7. PubMed ID: 16255854
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  • 10. Abnormal expression of laminin beta 1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy.
    Li M, Dickson DW, Spiro AJ.
    Arch Neurol; 1997 Dec; 54(12):1457-61. PubMed ID: 9400354
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  • 11. 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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  • 12. Localization of laminin subunits in the central nervous system in Fukuyama congenital muscular dystrophy: an immunohistochemical investigation.
    Yamamoto T, Shibata N, Kanazawa M, Kobayashi M, Komori T, Ikeya K, Kondo E, Saito K, Osawa M.
    Acta Neuropathol; 1997 Aug 07; 94(2):173-9. PubMed ID: 9255393
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  • 13. Laminin abnormality in severe childhood autosomal recessive muscular dystrophy.
    Yamada H, Tomé FM, Higuchi I, Kawai H, Azibi K, Chaouch M, Roberds SL, Tanaka T, Fujita S, Mitsui T.
    Lab Invest; 1995 Jun 07; 72(6):715-22. PubMed ID: 7783429
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  • 14. Congenital muscular dystrophy with merosin deficiency.
    Tomé FM, Evangelista T, Leclerc A, Sunada Y, Manole E, Estournet B, Barois A, Campbell KP, Fardeau M.
    C R Acad Sci III; 1994 Apr 07; 317(4):351-7. PubMed ID: 8000914
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  • 15. Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy.
    Voit T, Sewry CA, Meyer K, Hermann R, Straub V, Muntoni F, Kahn T, Unsöld R, Helliwell TR, Appleton R.
    Neuropediatrics; 1995 Jun 07; 26(3):148-55. PubMed ID: 7477753
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  • 16. Fibronectin, laminin, type I, III and IV collagens in Duchenne's muscular dystrophy, congenital muscular dystrophies and congenital myopathies: an immunocytochemical study.
    Hantaï D, Labat-Robert J, Grimaud JA, Fardeau M.
    Connect Tissue Res; 1985 Jun 07; 13(4):273-81. PubMed ID: 3161692
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  • 17. 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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  • 19. Changes of laminin beta 2 chain expression in congenital muscular dystrophy.
    Cohn RD, Herrmann R, Wewer UM, Voit T.
    Neuromuscul Disord; 1997 Sep 01; 7(6-7):373-8. PubMed ID: 9327401
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