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PUBMED FOR HANDHELDS

Journal Abstract Search

288 related items for PubMed ID: 11134085

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  • 5. Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle.
    Toral-Ojeda I, Aldanondo G, Lasa-Elgarresta J, Lasa-Fernández H, Fernández-Torrón R, López de Munain A, Vallejo-Illarramendi A.
    Expert Rev Mol Med; 2016 Apr 08; 18():e7. PubMed ID: 27055500
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  • 6. Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain.
    Huebsch KA, Kudryashova E, Wooley CM, Sher RB, Seburn KL, Spencer MJ, Cox GA.
    Hum Mol Genet; 2005 Oct 01; 14(19):2801-11. PubMed ID: 16115818
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  • 8. Force impairment in calpain 3-deficient mice is not correlated with mechanical disruption.
    Fougerousse F, Gonin P, Durand M, Richard I, Raymackers JM.
    Muscle Nerve; 2003 May 01; 27(5):616-23. PubMed ID: 12707983
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  • 9. A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.
    Vissing J, Barresi R, Witting N, Van Ghelue M, Gammelgaard L, Bindoff LA, Straub V, Lochmüller H, Hudson J, Wahl CM, Arnardottir S, Dahlbom K, Jonsrud C, Duno M.
    Brain; 2016 Aug 01; 139(Pt 8):2154-63. PubMed ID: 27259757
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  • 11. Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families.
    Kawai H, Akaike M, Kunishige M, Inui T, Adachi K, Kimura C, Kawajiri M, Nishida Y, Endo I, Kashiwagi S, Nishino H, Fujiwara T, Okuno S, Roudaut C, Richard I, Beckmann JS, Miyoshi K, Matsumoto T.
    Muscle Nerve; 1998 Nov 01; 21(11):1493-501. PubMed ID: 9771675
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  • 13. Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3.
    Kramerova I, Kudryashova E, Ermolova N, Saenz A, Jaka O, López de Munain A, Spencer MJ.
    Hum Mol Genet; 2012 Jul 15; 21(14):3193-204. PubMed ID: 22505582
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  • 16. Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency.
    Ho M, Post CM, Donahue LR, Lidov HG, Bronson RT, Goolsby H, Watkins SC, Cox GA, Brown RH.
    Hum Mol Genet; 2004 Sep 15; 13(18):1999-2010. PubMed ID: 15254015
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  • 17. Deletion of murine SMN exon 7 directed to skeletal muscle leads to severe muscular dystrophy.
    Cifuentes-Diaz C, Frugier T, Tiziano FD, Lacène E, Roblot N, Joshi V, Moreau MH, Melki J.
    J Cell Biol; 2001 Mar 05; 152(5):1107-14. PubMed ID: 11238465
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  • 18. Pseudometabolic expression and phenotypic variability of calpain deficiency in two siblings.
    Pénisson-Besnier I, Richard I, Dubas F, Beckmann JS, Fardeau M.
    Muscle Nerve; 1998 Aug 05; 21(8):1078-80. PubMed ID: 9655129
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  • 19. Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A.
    Tagawa K, Taya C, Hayashi Y, Nakagawa M, Ono Y, Fukuda R, Karasuyama H, Toyama-Sorimachi N, Katsui Y, Hata S, Ishiura S, Nonaka I, Seyama Y, Arahata K, Yonekawa H, Sorimachi H, Suzuki K.
    Hum Mol Genet; 2000 May 22; 9(9):1393-402. PubMed ID: 10814721
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  • 20. Novel Missense CAPN3 Mutation Responsible for Adult-Onset Limb Girdle Muscular Dystrophy with Calves Hypertrophy.
    Rekik S, Sakka S, Ben Romdhan S, Farhat N, Baba Amer Y, Lehkim L, Authier FJ, Mhiri C.
    J Mol Neurosci; 2019 Dec 22; 69(4):563-569. PubMed ID: 31410652
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