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Journal Abstract Search

380 related items for PubMed ID: 25877298

  • 1. CAPN3-mediated processing of C-terminal titin replaced by pathological cleavage in titinopathy.
    Charton K, Sarparanta J, Vihola A, Milic A, Jonson PH, Suel L, Luque H, Boumela I, Richard I, Udd B.
    Hum Mol Genet; 2015 Jul 01; 24(13):3718-31. PubMed ID: 25877298
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  • 2. Interactions with M-band titin and calpain 3 link myospryn (CMYA5) to tibial and limb-girdle muscular dystrophies.
    Sarparanta J, Blandin G, Charton K, Vihola A, Marchand S, Milic A, Hackman P, Ehler E, Richard I, Udd B.
    J Biol Chem; 2010 Sep 24; 285(39):30304-15. PubMed ID: 20634290
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  • 3. 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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  • 4. Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function.
    Unger A, Beckendorf L, Böhme P, Kley R, von Frieling-Salewsky M, Lochmüller H, Schröder R, Fürst DO, Vorgerd M, Linke WA.
    Acta Neuropathol Commun; 2017 Sep 15; 5(1):72. PubMed ID: 28915917
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  • 8. 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 15; 79(2):146-9. PubMed ID: 11829483
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  • 9. Titin splicing regulates cardiotoxicity associated with calpain 3 gene therapy for limb-girdle muscular dystrophy type 2A.
    Lostal W, Roudaut C, Faivre M, Charton K, Suel L, Bourg N, Best H, Smith JE, Gohlke J, Corre G, Li X, Elbeck Z, Knöll R, Deschamps JY, Granzier H, Richard I.
    Sci Transl Med; 2019 Nov 27; 11(520):. PubMed ID: 31776291
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  • 10. Atypical phenotypes in titinopathies explained by second titin mutations.
    Evilä A, Vihola A, Sarparanta J, Raheem O, Palmio J, Sandell S, Eymard B, Illa I, Rojas-Garcia R, Hankiewicz K, Negrão L, Löppönen T, Nokelainen P, Kärppä M, Penttilä S, Screen M, Suominen T, Richard I, Hackman P, Udd B.
    Ann Neurol; 2014 Feb 27; 75(2):230-40. PubMed ID: 24395473
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  • 15. The N- and C-terminal autolytic fragments of CAPN3/p94/calpain-3 restore proteolytic activity by intermolecular complementation.
    Ono Y, Shindo M, Doi N, Kitamura F, Gregorio CC, Sorimachi H.
    Proc Natl Acad Sci U S A; 2014 Dec 23; 111(51):E5527-36. PubMed ID: 25512505
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  • 16. Mutations of CAPN3 in Korean patients with limb-girdle muscular dystrophy.
    Shin JH, Kim HS, Lee CH, Kim CM, Park KH, Kim DS.
    J Korean Med Sci; 2007 Jun 23; 22(3):463-9. PubMed ID: 17596655
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  • 17. Biophysical characterization of naturally occurring titin M10 mutations.
    Rudloff MW, Woosley AN, Wright NT.
    Protein Sci; 2015 Jun 23; 24(6):946-55. PubMed ID: 25739468
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  • 18. PLEIAD/SIMC1/C5orf25, a novel autolysis regulator for a skeletal-muscle-specific calpain, CAPN3, scaffolds a CAPN3 substrate, CTBP1.
    Ono Y, Iemura S, Novak SM, Doi N, Kitamura F, Natsume T, Gregorio CC, Sorimachi H.
    J Mol Biol; 2013 Aug 23; 425(16):2955-72. PubMed ID: 23707407
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  • 19. Muscle-specific calpain-3 is phosphorylated in its unique insertion region for enrichment in a myofibril fraction.
    Ojima K, Ono Y, Hata S, Noguchi S, Nishino I, Sorimachi H.
    Genes Cells; 2014 Nov 23; 19(11):830-41. PubMed ID: 25252031
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  • 20. Myopathies caused by homozygous titin mutations: limb-girdle muscular dystrophy 2J and variations of phenotype.
    Pénisson-Besnier I, Hackman P, Suominen T, Sarparanta J, Huovinen S, Richard-Crémieux I, Udd B.
    J Neurol Neurosurg Psychiatry; 2010 Nov 23; 81(11):1200-2. PubMed ID: 20571043
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