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PUBMED FOR HANDHELDS

Journal Abstract Search


135 related items for PubMed ID: 8736932

  • 21. Disrupted mechanical stability of the dystrophin-glycoprotein complex causes severe muscular dystrophy in sarcospan transgenic mice.
    Peter AK, Miller G, Crosbie RH.
    J Cell Sci; 2007 Mar 15; 120(Pt 6):996-1008. PubMed ID: 17311848
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  • 22. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.
    Higuchi I, Yamada H, Fukunaga H, Iwaki H, Okubo R, Nakagawa M, Osame M, Roberds SL, Shimizu T, Campbell KP.
    J Clin Invest; 1994 Aug 15; 94(2):601-6. PubMed ID: 8040315
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  • 23. The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin.
    Hayashi YK, Mizuno Y, Yoshida M, Nonaka I, Ozawa E, Arahata K.
    Neurology; 1995 Mar 15; 45(3 Pt 1):551-4. PubMed ID: 7898714
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  • 25. Use of western immunoblot for evaluation of myocardial dystrophin, alpha-sarcoglycan, and beta-dystroglycan in dogs with idiopathic dilated cardiomyopathy.
    Spier AW, Meurs KM, Coovert DD, Lehmkuhl LB, O'Grady MR, Freeman LM, Burghes AH, Towbin JA.
    Am J Vet Res; 2001 Jan 15; 62(1):67-71. PubMed ID: 11197563
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  • 26. Increased expression of dystrophin, beta-dystroglycan and adhalin in denervated rat muscles.
    Biral D, Senter L, Salviati G.
    J Muscle Res Cell Motil; 1996 Oct 15; 17(5):523-32. PubMed ID: 8906620
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  • 29. Normal expression of adhalin and merosin in ovine congenital progressive muscular dystrophy.
    Johnsen RD, Laing NG, Huxtable CR, Kakulas BA.
    Aust Vet J; 1997 Mar 15; 75(3):215-6. PubMed ID: 9088516
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  • 33. Sarcoglycans in muscular dystrophy.
    Hack AA, Groh ME, McNally EM.
    Microsc Res Tech; 1997 Mar 15; 48(3-4):167-80. PubMed ID: 10679964
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  • 37. Inhibition of dystroglycan binding to laminin disrupts the PI3K/AKT pathway and survival signaling in muscle cells.
    Langenbach KJ, Rando TA.
    Muscle Nerve; 2002 Nov 15; 26(5):644-53. PubMed ID: 12402286
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  • 38. [Severe childhood autosomal recessive muscular dystrophy].
    Matsumura K, Shimizu T.
    Rinsho Shinkeigaku; 1995 Dec 15; 35(12):1422-4. PubMed ID: 8752417
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  • 40. Nitric oxide synthase (NOS) in mouse skeletal muscle development and differentiated myoblasts.
    Blottner D, Lück G.
    Cell Tissue Res; 1998 May 15; 292(2):293-302. PubMed ID: 9560472
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