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Journal Abstract Search


334 related items for PubMed ID: 28104817

  • 1. Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy.
    Hofhuis J, Bersch K, Büssenschütt R, Drzymalski M, Liebetanz D, Nikolaev VO, Wagner S, Maier LS, Gärtner J, Klinge L, Thoms S.
    J Cell Sci; 2017 Mar 01; 130(5):841-852. PubMed ID: 28104817
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  • 2. Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle.
    Klinge L, Harris J, Sewry C, Charlton R, Anderson L, Laval S, Chiu YH, Hornsey M, Straub V, Barresi R, Lochmüller H, Bushby K.
    Muscle Nerve; 2010 Feb 01; 41(2):166-73. PubMed ID: 20082313
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  • 7. Dysferlin interacts with affixin (beta-parvin) at the sarcolemma.
    Matsuda C, Kameyama K, Tagawa K, Ogawa M, Suzuki A, Yamaji S, Okamoto H, Nishino I, Hayashi YK.
    J Neuropathol Exp Neurol; 2005 Apr 01; 64(4):334-40. PubMed ID: 15835269
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  • 10. Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretch.
    Waddell LB, Lemckert FA, Zheng XF, Tran J, Evesson FJ, Hawkes JM, Lek A, Street NE, Lin P, Clarke NF, Landstrom AP, Ackerman MJ, Weisleder N, Ma J, North KN, Cooper ST.
    J Neuropathol Exp Neurol; 2011 Apr 01; 70(4):302-13. PubMed ID: 21412170
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  • 11. Dysferlin and the plasma membrane repair in muscular dystrophy.
    Bansal D, Campbell KP.
    Trends Cell Biol; 2004 Apr 01; 14(4):206-13. PubMed ID: 15066638
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  • 12. 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 01; 10(8):553-9. PubMed ID: 11053681
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  • 14. Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes.
    Nguyen K, Bassez G, Krahn M, Bernard R, Laforêt P, Labelle V, Urtizberea JA, Figarella-Branger D, Romero N, Attarian S, Leturcq F, Pouget J, Lévy N, Eymard B.
    Arch Neurol; 2007 Aug 01; 64(8):1176-82. PubMed ID: 17698709
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  • 15. 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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  • 16. [Dysferlin expression in limb-girdle muscular dystrophy and Miyoshi myopathy: analysis of 45 cases].
    Ren SC, Yan CZ, Li MX, Liu SP, Wu JL, Zhao YY, Li W, Li DN.
    Zhonghua Yi Xue Za Zhi; 2007 Jun 05; 87(21):1486-90. PubMed ID: 17785089
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  • 17. Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane.
    Kerr JP, Ziman AP, Mueller AL, Muriel JM, Kleinhans-Welte E, Gumerson JD, Vogel SS, Ward CW, Roche JA, Bloch RJ.
    Proc Natl Acad Sci U S A; 2013 Dec 17; 110(51):20831-6. PubMed ID: 24302765
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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 17; 175(5):1817-23. PubMed ID: 19834057
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  • 20. Sarcolemmal proteins and the spectrum of limb-girdle muscular dystrophies.
    Bönnemann CG, Finkel RS.
    Semin Pediatr Neurol; 2002 Jun 17; 9(2):81-99. PubMed ID: 12139001
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