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Journal Abstract Search

255 related items for PubMed ID: 11371436

  • 1. Mutations in calpain 3 associated with limb girdle muscular dystrophy: analysis by molecular modeling and by mutation in m-calpain.
    Jia Z, Petrounevitch V, Wong A, Moldoveanu T, Davies PL, Elce JS, Beckmann JS.
    Biophys J; 2001 Jun; 80(6):2590-6. PubMed ID: 11371436
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  • 2. Limb-girdle muscular dystrophy type 2A can result from accelerated autoproteolytic inactivation of calpain 3.
    Garnham CP, Hanna RA, Chou JS, Low KE, Gourlay K, Campbell RL, Beckmann JS, Davies PL.
    Biochemistry; 2009 Apr 21; 48(15):3457-67. PubMed ID: 19226146
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  • 3. Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A.
    Ono Y, Shimada H, Sorimachi H, Richard I, Saido TC, Beckmann JS, Ishiura S, Suzuki K.
    J Biol Chem; 1998 Jul 03; 273(27):17073-8. PubMed ID: 9642272
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  • 4. Calpainopathy-a survey of mutations and polymorphisms.
    Richard I, Roudaut C, Saenz A, Pogue R, Grimbergen JE, Anderson LV, Beley C, Cobo AM, de Diego C, Eymard B, Gallano P, Ginjaar HB, Lasa A, Pollitt C, Topaloglu H, Urtizberea JA, de Visser M, van der Kooi A, Bushby K, Bakker E, Lopez de Munain A, Fardeau M, Beckmann JS.
    Am J Hum Genet; 1999 Jun 03; 64(6):1524-40. PubMed ID: 10330340
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  • 5. Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3.
    Jenne DE, Kley RA, Vorgerd M, Schröder JM, Weis J, Reimann H, Albrecht B, Nürnberg P, Thiele H, Müller CR, Meng G, Witt CC, Labeit S.
    Biol Chem; 2005 Jan 03; 386(1):61-7. PubMed ID: 15843148
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  • 6. New aspect of the research on limb-girdle muscular dystrophy 2A: a molecular biologic and biochemical approach to pathology.
    Ono Y, Sorimachi H, Suzuki K.
    Trends Cardiovasc Med; 1999 Jul 03; 9(5):114-8. PubMed ID: 10639725
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  • 7. 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. 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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  • 10. 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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  • 11. Molecular analysis of p94 and its application to diagnosis of limb girdle muscular dystrophy type 2A.
    Sorimachi H, Ono Y, Suzuki K.
    Methods Mol Biol; 2000 Dec 23; 144():75-84. PubMed ID: 10818750
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  • 12. Skeletal muscle-specific calpain, p94, and connectin/titin: their physiological functions and relationship to limb-girdle muscular dystrophy type 2A.
    Sorimachi H, Ono Y, Suzuki K.
    Adv Exp Med Biol; 2000 Dec 23; 481():383-95; discussion 395-7. PubMed ID: 10987085
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  • 13. Pathophysiology of limb girdle muscular dystrophy type 2A: hypothesis and new insights into the IkappaBalpha/NF-kappaB survival pathway in skeletal muscle.
    Baghdiguian S, Richard I, Martin M, Coopman P, Beckmann JS, Mangeat P, Lefranc G.
    J Mol Med (Berl); 2001 Jun 23; 79(5-6):254-61. PubMed ID: 11485017
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  • 15. An eccentric calpain, CAPN3/p94/calpain-3.
    Ono Y, Ojima K, Shinkai-Ouchi F, Hata S, Sorimachi H.
    Biochimie; 2016 Mar 23; 122():169-87. PubMed ID: 26363099
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  • 20. Limb girdle muscular dystrophy type 2A in India: a study based on semi-quantitative protein analysis, with clinical and histopathological correlation.
    Pathak P, Sharma MC, Sarkar C, Jha P, Suri V, Mohd H, Singh S, Bhatia R, Gulati S.
    Neurol India; 2010 Mar 23; 58(4):549-54. PubMed ID: 20739790
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