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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

180 related items for PubMed ID: 10407857

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  • 3. A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy.
    Bies RD, Maeda M, Roberds SL, Holder E, Bohlmeyer T, Young JB, Campbell KP.
    J Mol Cell Cardiol; 1997 Dec; 29(12):3175-88. PubMed ID: 9441825
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  • 6. Dystrophin muscle enhancer 1 is implicated in the activation of non-muscle isoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathy.
    Bastianutto C, Bestard JA, Lahnakoski K, Broere D, De Visser M, Zaccolo M, Pozzan T, Ferlini A, Muntoni F, Patarnello T, Klamut HJ.
    Hum Mol Genet; 2001 Nov 01; 10(23):2627-35. PubMed ID: 11726549
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  • 8. X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene.
    Franz WM, Cremer M, Herrmann R, Grünig E, Fogel W, Scheffold T, Goebel HH, Kircheisen R, Kübler W, Voit T.
    Ann N Y Acad Sci; 1995 Mar 27; 752():470-91. PubMed ID: 7755293
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  • 10. Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
    Fanin M, Melacini P, Angelini C, Danieli GA.
    J Mol Cell Cardiol; 1999 Aug 27; 31(8):1501-8. PubMed ID: 10423348
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  • 11. Utrophin may be a precursor of dystrophin during skeletal muscle development.
    Lin S, Burgunder JM.
    Brain Res Dev Brain Res; 2000 Feb 07; 119(2):289-95. PubMed ID: 10675780
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  • 12. [Mutations of the dystrophin gene in dilated cardiomyopathy].
    Shiga N, Akita H, Yokoyama M.
    Nihon Rinsho; 2000 Jan 07; 58(1):123-7. PubMed ID: 10885299
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  • 15. Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.
    Muntoni F, Di Lenarda A, Porcu M, Sinagra G, Mateddu A, Marrosu G, Ferlini A, Cau M, Milasin J, Melis MA, Marrosu MG, Cianchetti C, Sanna A, Falaschi A, Camerini F, Giacca M, Mestroni L.
    Heart; 1997 Dec 07; 78(6):608-12. PubMed ID: 9470882
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  • 16. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
    Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M.
    Circulation; 1993 Jun 07; 87(6):1854-65. PubMed ID: 8504498
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  • 19. Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy.
    Fadic R, Sunada Y, Waclawik AJ, Buck S, Lewandoski PJ, Campbell KP, Lotz BP.
    N Engl J Med; 1996 Feb 08; 334(6):362-6. PubMed ID: 8538707
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  • 20. Utrophin and dystrophin-associated glycoproteins in normal and dystrophin deficient cardiac muscle.
    Rivier F, Robert A, Royuela M, Hugon G, Bonet-Kerrache A, Mornet D.
    J Muscle Res Cell Motil; 1999 Apr 08; 20(3):305-14. PubMed ID: 10471993
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