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Journal Abstract Search

220 related items for PubMed ID: 15337777

  • 1. Sorting of a nonmuscle tropomyosin to a novel cytoskeletal compartment in skeletal muscle results in muscular dystrophy.
    Kee AJ, Schevzov G, Nair-Shalliker V, Robinson CS, Vrhovski B, Ghoddusi M, Qiu MR, Lin JJ, Weinberger R, Gunning PW, Hardeman EC.
    J Cell Biol; 2004 Aug 30; 166(5):685-96. PubMed ID: 15337777
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  • 2. A cytoskeletal tropomyosin can compromise the structural integrity of skeletal muscle.
    Kee AJ, Gunning PW, Hardeman EC.
    Cell Motil Cytoskeleton; 2009 Sep 30; 66(9):710-20. PubMed ID: 19530183
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  • 3. Tropomyosin 4 defines novel filaments in skeletal muscle associated with muscle remodelling/regeneration in normal and diseased muscle.
    Vlahovich N, Schevzov G, Nair-Shaliker V, Ilkovski B, Artap ST, Joya JE, Kee AJ, North KN, Gunning PW, Hardeman EC.
    Cell Motil Cytoskeleton; 2008 Jan 30; 65(1):73-85. PubMed ID: 17968984
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  • 4. Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity.
    Rajan S, Ahmed RP, Jagatheesan G, Petrashevskaya N, Boivin GP, Urboniene D, Arteaga GM, Wolska BM, Solaro RJ, Liggett SB, Wieczorek DF.
    Circ Res; 2007 Jul 20; 101(2):205-14. PubMed ID: 17556658
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  • 5. Myofiber adaptational response to exercise in a mouse model of nemaline myopathy.
    Nair-Shalliker V, Kee AJ, Joya JE, Lucas CA, Hoh JF, Hardeman EC.
    Muscle Nerve; 2004 Oct 20; 30(4):470-80. PubMed ID: 15372535
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  • 6. An alphaTropomyosin mutation alters dimer preference in nemaline myopathy.
    Corbett MA, Akkari PA, Domazetovska A, Cooper ST, North KN, Laing NG, Gunning PW, Hardeman EC.
    Ann Neurol; 2005 Jan 20; 57(1):42-9. PubMed ID: 15562513
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  • 7. Tropomyosin isoforms: divining rods for actin cytoskeleton function.
    Gunning PW, Schevzov G, Kee AJ, Hardeman EC.
    Trends Cell Biol; 2005 Jun 20; 15(6):333-41. PubMed ID: 15953552
    [Abstract] [Full Text] [Related]

  • 8. A novel role for non-muscle gamma-actin in skeletal muscle sarcomere assembly.
    Lloyd CM, Berendse M, Lloyd DG, Schevzov G, Grounds MD.
    Exp Cell Res; 2004 Jul 01; 297(1):82-96. PubMed ID: 15194427
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  • 10. Dystrophin deficiency in canine X-linked muscular dystrophy in Japan (CXMDJ) alters myosin heavy chain expression profiles in the diaphragm more markedly than in the tibialis cranialis muscle.
    Yuasa K, Nakamura A, Hijikata T, Takeda S.
    BMC Musculoskelet Disord; 2008 Jan 09; 9():1. PubMed ID: 18182116
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  • 12. Plectin defects in epidermolysis bullosa simplex with muscular dystrophy.
    McMillan JR, Akiyama M, Rouan F, Mellerio JE, Lane EB, Leigh IM, Owaribe K, Wiche G, Fujii N, Uitto J, Eady RA, Shimizu H.
    Muscle Nerve; 2007 Jan 09; 35(1):24-35. PubMed ID: 16967486
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  • 13. Divergent regulation of the sarcomere and the cytoskeleton.
    Schevzov G, Fath T, Vrhovski B, Vlahovich N, Rajan S, Hook J, Joya JE, Lemckert F, Puttur F, Lin JJ, Hardeman EC, Wieczorek DF, O'Neill GM, Gunning PW.
    J Biol Chem; 2008 Jan 04; 283(1):275-283. PubMed ID: 17951248
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  • 14. Cap disease due to mutation of the beta-tropomyosin gene (TPM2).
    Clarke NF, Domazetovska A, Waddell L, Kornberg A, McLean C, North KN.
    Neuromuscul Disord; 2009 May 04; 19(5):348-51. PubMed ID: 19345583
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