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Journal Abstract Search

391 related items for PubMed ID: 9731527

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  • 2. The third human FER-1-like protein is highly similar to dysferlin.
    Britton S, Freeman T, Vafiadaki E, Keers S, Harrison R, Bushby K, Bashir R.
    Genomics; 2000 Sep 15; 68(3):313-21. PubMed ID: 10995573
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  • 4. C. elegans dysferlin homolog fer-1 is expressed in muscle, and fer-1 mutations initiate altered gene expression of muscle enriched genes.
    Krajacic P, Hermanowski J, Lozynska O, Khurana TS, Lamitina T.
    Physiol Genomics; 2009 Dec 30; 40(1):8-14. PubMed ID: 19755517
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  • 6. Dysferlin protein analysis in limb-girdle muscular dystrophies.
    Vainzof M, Anderson LV, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RC, Passos-Bueno MR, Zatz M.
    J Mol Neurosci; 2001 Aug 30; 17(1):71-80. PubMed ID: 11665864
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  • 7. Genetic and physical mapping at the limb-girdle muscular dystrophy locus (LGMD2B) on chromosome 2p.
    Bashir R, Keers S, Strachan T, Passos-Bueno R, Zatz M, Weissenbach J, Le Paslier D, Meisler M, Bushby K.
    Genomics; 1996 Apr 01; 33(1):46-52. PubMed ID: 8617508
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  • 8. Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).
    Weiler T, Bashir R, Anderson LV, Davison K, Moss JA, Britton S, Nylen E, Keers S, Vafiadaki E, Greenberg CR, Bushby CR, Wrogemann K.
    Hum Mol Genet; 1999 May 01; 8(5):871-7. PubMed ID: 10196377
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  • 9. Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.
    Moreira ES, Wiltshire TJ, Faulkner G, Nilforoushan A, Vainzof M, Suzuki OT, Valle G, Reeves R, Zatz M, Passos-Bueno MR, Jenne DE.
    Nat Genet; 2000 Feb 01; 24(2):163-6. PubMed ID: 10655062
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  • 10. [Positional cloning of the gene for Miyoshi myopathy and limb-girdle muscular dystrophy].
    Aoki M, Arahata K, Brown RH.
    Rinsho Shinkeigaku; 1999 Dec 01; 39(12):1272-5. PubMed ID: 10791095
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  • 12. Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation.
    McNally EM, Ly CT, Rosenmann H, Mitrani Rosenbaum S, Jiang W, Anderson LV, Soffer D, Argov Z.
    Am J Med Genet; 2000 Apr 10; 91(4):305-12. PubMed ID: 10766988
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  • 13. Seven autosomal recessive limb-girdle muscular dystrophies in the Brazilian population: from LGMD2A to LGMD2G.
    Passos-Bueno MR, Vainzof M, Moreira ES, Zatz M.
    Am J Med Genet; 1999 Feb 19; 82(5):392-8. PubMed ID: 10069710
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  • 15. Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies.
    Pogue R, Anderson LV, Pyle A, Sewry C, Pollitt C, Johnson MA, Davison K, Moss JA, Mercuri E, Muntoni F, Bushby KM.
    Neuromuscul Disord; 2001 Jan 19; 11(1):80-7. PubMed ID: 11166169
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  • 19. Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy.
    Aoki M, Liu J, Richard I, Bashir R, Britton S, Keers SM, Oeltjen J, Brown HE, Marchand S, Bourg N, Beley C, McKenna-Yasek D, Arahata K, Bohlega S, Cupler E, Illa I, Majneh I, Barohn RJ, Urtizberea JA, Fardeau M, Amato A, Angelini C, Bushby K, Beckmann JS, Brown RH.
    Neurology; 2001 Jul 24; 57(2):271-8. PubMed ID: 11468312
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  • 20. Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).
    Anderson LV, Harrison RM, Pogue R, Vafiadaki E, Pollitt C, Davison K, Moss JA, Keers S, Pyle A, Shaw PJ, Mahjneh I, Argov Z, Greenberg CR, Wrogemann K, Bertorini T, Goebel HH, Beckmann JS, Bashir R, Bushby KM.
    Neuromuscul Disord; 2000 Dec 24; 10(8):553-9. PubMed ID: 11053681
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