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Journal Abstract Search

176 related items for PubMed ID: 10508505

  • 1. Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B.
    Bittner RE, Anderson LV, Burkhardt E, Bashir R, Vafiadaki E, Ivanova S, Raffelsberger T, Maerk I, Höger H, Jung M, Karbasiyan M, Storch M, Lassmann H, Moss JA, Davison K, Harrison R, Bushby KM, Reis A.
    Nat Genet; 1999 Oct; 23(2):141-2. PubMed ID: 10508505
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  • 2. Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation.
    Vafiadaki E, Reis A, Keers S, Harrison R, Anderson LV, Raffelsberger T, Ivanova S, Hoger H, Bittner RE, Bushby K, Bashir R.
    Neuroreport; 2001 Mar 05; 12(3):625-9. PubMed ID: 11234777
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  • 4. Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding.
    Wenzel K, Carl M, Perrot A, Zabojszcza J, Assadi M, Ebeling M, Geier C, Robinson PN, Kress W, Osterziel KJ, Spuler S.
    Hum Mutat; 2006 Jun 05; 27(6):599-600. PubMed ID: 16705711
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  • 7. Dysferlin-deficient muscular dystrophy: gadofluorine M suitability at MR imaging in a mouse model.
    Schmidt S, Vieweger A, Obst M, Mueller S, Gross V, Gutberlet M, Steinbrink J, Taubert S, Misselwitz B, Luedemann L, Spuler S.
    Radiology; 2009 Jan 05; 250(1):87-94. PubMed ID: 19001151
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  • 9. Expression profiling with progression of dystrophic change in dysferlin-deficient mice (SJL).
    Suzuki N, Aoki M, Hinuma Y, Takahashi T, Onodera Y, Ishigaki A, Kato M, Warita H, Tateyama M, Itoyama Y.
    Neurosci Res; 2005 May 05; 52(1):47-60. PubMed ID: 15811552
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  • 10. Dysferlin and the plasma membrane repair in muscular dystrophy.
    Bansal D, Campbell KP.
    Trends Cell Biol; 2004 Apr 05; 14(4):206-13. PubMed ID: 15066638
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  • 12. The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titin.
    Garvey SM, Rajan C, Lerner AP, Frankel WN, Cox GA.
    Genomics; 2002 Feb 05; 79(2):146-9. PubMed ID: 11829483
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  • 14. The sarcolemma in the Large(myd) mouse.
    Reed PW, Mathews KD, Mills KA, Bloch RJ.
    Muscle Nerve; 2004 Nov 05; 30(5):585-95. PubMed ID: 15389724
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  • 15. Characterisation of the dysferlin skeletal muscle promoter.
    Foxton RM, Laval SH, Bushby KM.
    Eur J Hum Genet; 2004 Feb 05; 12(2):127-31. PubMed ID: 14560310
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  • 16. Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy.
    Sinnreich M, Therrien C, Karpati G.
    Neurology; 2006 Apr 11; 66(7):1114-6. PubMed ID: 16606933
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  • 17. The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.
    von der Hagen M, Laval SH, Cree LM, Haldane F, Pocock M, Wappler I, Peters H, Reitsamer HA, Hoger H, Wiedner M, Oberndorfer F, Anderson LV, Straub V, Bittner RE, Bushby KM.
    Neuromuscul Disord; 2005 Dec 11; 15(12):863-77. PubMed ID: 16288871
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  • 18. Genetic manipulation of dysferlin expression in skeletal muscle: novel insights into muscular dystrophy.
    Millay DP, Maillet M, Roche JA, Sargent MA, McNally EM, Bloch RJ, Molkentin JD.
    Am J Pathol; 2009 Nov 11; 175(5):1817-23. PubMed ID: 19834057
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  • 19. 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 11; 8(3):297-302. PubMed ID: 7874173
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