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Journal Abstract Search

198 related items for PubMed ID: 4058470

  • 1. Protein degradation in cultured skeletal muscle from Duchenne muscular dystrophy patients.
    Neville HE, Harrold S.
    Muscle Nerve; 1985; 8(3):253-7. PubMed ID: 4058470
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  • 3. Single skinned muscle fibers in Duchenne muscular dystrophy generate normal force.
    Horowits R, Dalakas MC, Podolsky RJ.
    Ann Neurol; 1990 Jun; 27(6):636-41. PubMed ID: 2360800
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  • 5. Branched-chain ketoacids reduce muscle protein degradation in Duchenne muscular dystrophy.
    Stewart PM, Walser M, Drachman DB.
    Muscle Nerve; 1982 Mar; 5(3):197-201. PubMed ID: 7088016
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  • 7. Increased rates of myofibrillar protein breakdown in muscle-wasting diseases.
    Warnes DM, Tomas FM, Ballard FJ.
    Muscle Nerve; 1981 Mar; 4(1):62-6. PubMed ID: 7231447
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  • 8. Platelet-derived growth factor and its receptors are related to the progression of human muscular dystrophy: an immunohistochemical study.
    Zhao Y, Haginoya K, Sun G, Dai H, Onuma A, Iinuma K.
    J Pathol; 2003 Sep; 201(1):149-59. PubMed ID: 12950028
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  • 9. Mechanism of muscle wasting in myotonic dystrophy.
    Griggs RC, Jozefowicz R, Kingston W, Nair KS, Herr BE, Halliday D.
    Ann Neurol; 1990 May; 27(5):505-12. PubMed ID: 2360792
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  • 11. Impaired muscle differentiation in explant cultures of Duchenne muscular dystrophy.
    Jasmin G, Tautu C, Vanasse M, Brochu P, Simoneau R.
    Lab Invest; 1984 Feb; 50(2):197-207. PubMed ID: 6694359
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  • 12. Degradation of individual intracellular proteins analyzed by two-dimensional gel electrophoresis and computerized video densitometry.
    Rodemann HP.
    Electrophoresis; 1990 Mar; 11(3):228-31. PubMed ID: 2344852
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  • 14. Proteins of muscle subcellular fractions in Duchenne progressive muscular dystrophy stained with "stains-all" cationic carbocyanine dye and with Coomassie Blue.
    Niebroj-Dobosz I, Kornguth S, Schutta H, Siegel FL, Hausmanowa-Petrusewicz I.
    Muscle Nerve; 1989 Apr; 12(4):273-80. PubMed ID: 2770780
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  • 15. Ion channels in a skeletal muscle cell line from a Duchenne muscular dystrophy patient.
    Caviedes R, Caviedes P, Liberona JL, Jaimovich E.
    Muscle Nerve; 1994 Sep; 17(9):1021-8. PubMed ID: 7520531
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  • 18. Biochemistry of muscle membranes in Duchenne muscular dystrophy.
    Rowland LP.
    Muscle Nerve; 1980 Sep; 3(1):3-20. PubMed ID: 6445503
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  • 19. An autoradiographic study of muscular dystrophy, motor neuron disease and Charcot-Marie-Tooth disease.
    Monckton G, Marusyk H.
    Can J Neurol Sci; 1977 Feb; 4(1):25-9. PubMed ID: 837261
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  • 20. Immunochemical study of connectin (titin) in neuromuscular diseases using a monoclonal antibody: connectin is degraded extensively in Duchenne muscular dystrophy.
    Matsumura K, Shimizu T, Nonaka I, Mannen T.
    J Neurol Sci; 1989 Nov; 93(2-3):147-56. PubMed ID: 2592979
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