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PUBMED FOR HANDHELDS

Journal Abstract Search

396 related items for PubMed ID: 18974005

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  • 5. 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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  • 6. 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 24; 19(11):830-41. PubMed ID: 25252031
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  • 8. 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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  • 9. 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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  • 10. Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
    Groen EJ, Charlton R, Barresi R, Anderson LV, Eagle M, Hudson J, Koref MS, Straub V, Bushby KM.
    Brain; 2007 Dec 23; 130(Pt 12):3237-49. PubMed ID: 18055493
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  • 11. A muscle-specific calpain, CAPN3, forms a homotrimer.
    Hata S, Doi N, Shinkai-Ouchi F, Ono Y.
    Biochim Biophys Acta Proteins Proteom; 2020 Jul 23; 1868(7):140411. PubMed ID: 32200007
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  • 12. Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway.
    Kramerova I, Kudryashova E, Venkatraman G, Spencer MJ.
    Hum Mol Genet; 2005 Aug 01; 14(15):2125-34. PubMed ID: 15961411
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  • 14. Mutational Spectrum of CAPN3 with Genotype-Phenotype Correlations in Limb Girdle Muscular Dystrophy Type 2A/R1 (LGMD2A/LGMDR1) Patients in India.
    Pathak P, Sharma MC, Jha P, Sarkar C, Faruq M, Jha P, Suri V, Bhatia R, Singh S, Gulati S, Husain M.
    J Neuromuscul Dis; 2021 Aug 01; 8(1):125-136. PubMed ID: 33337384
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  • 15. Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A).
    Kramerova I, Beckmann JS, Spencer MJ.
    Biochim Biophys Acta; 2007 Feb 01; 1772(2):128-44. PubMed ID: 16934440
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  • 16. Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations.
    Lasa-Elgarresta J, Mosqueira-Martín L, Naldaiz-Gastesi N, Sáenz A, López de Munain A, Vallejo-Illarramendi A.
    Int J Mol Sci; 2019 Sep 13; 20(18):. PubMed ID: 31540302
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  • 17. Failure to up-regulate transcription of genes necessary for muscle adaptation underlies limb girdle muscular dystrophy 2A (calpainopathy).
    Kramerova I, Ermolova N, Eskin A, Hevener A, Quehenberger O, Armando AM, Haller R, Romain N, Nelson SF, Spencer MJ.
    Hum Mol Genet; 2016 Jun 01; 25(11):2194-2207. PubMed ID: 27005420
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  • 19. Compound heterozygous CAPN3 variants identified in a family with limb-girdle muscular dystrophy recessive 1.
    Zhang C, Zheng X, Lu D, Xu L, Che F, Liu S.
    Mol Med Rep; 2021 Jun 01; 23(6):. PubMed ID: 33899113
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  • 20. 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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