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Journal Abstract Search

194 related items for PubMed ID: 9804081

  • 1. Proteasomes in distal myopathy with rimmed vacuoles.
    Kumamoto T, Fujimoto S, Nagao S, Masuda T, Sugihara R, Ueyama H, Tsuda T.
    Intern Med; 1998 Sep; 37(9):746-52. PubMed ID: 9804081
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  • 2. The ubiquitin-proteasome pathway in distal myopathy with rimmed vacuoles.
    Jimi T, Wakayama Y.
    Intern Med; 1998 Sep; 37(9):722-3. PubMed ID: 9804076
    [No Abstract] [Full Text] [Related]

  • 3. Proteasome expression in the skeletal muscles of patients with muscular dystrophy.
    Kumamoto T, Fujimoto S, Ito T, Horinouchi H, Ueyama H, Tsuda T.
    Acta Neuropathol; 2000 Dec; 100(6):595-602. PubMed ID: 11078210
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  • 4. Increased lysosome-related proteins in the skeletal muscles of distal myopathy with rimmed vacuoles.
    Kumamoto T, Ito T, Horinouchi H, Ueyama H, Toyoshima I, Tsuda T.
    Muscle Nerve; 2000 Nov; 23(11):1686-93. PubMed ID: 11054746
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  • 5. Role of ubiquitin-proteasome proteolysis in muscle fiber destruction in experimental chloroquine-induced myopathy.
    Kimura N, Kumamoto T, Oniki T, Nomura M, Nakamura K, Abe Y, Hazama Y, Ueyama H.
    Muscle Nerve; 2009 Apr; 39(4):521-8. PubMed ID: 19296457
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  • 14. [A case of acute quadriplegic myopathy].
    Horinouchi H, Kumamoto T, Fujimoto S, Ueyama H, Sannomiya K, Tsuda T.
    Rinsho Shinkeigaku; 2000 Jun; 40(6):586-90. PubMed ID: 11086398
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  • 15. Abnormal increases of lysosomal cysteinine proteinases in rimmed vacuoles in the skeletal muscle.
    Ii K, Hizawa K, Nonaka I, Sugita H, Kominami E, Katunuma N.
    Am J Pathol; 1986 Feb; 122(2):193-8. PubMed ID: 3511718
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  • 16. A Gne knockout mouse expressing human V572L mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
    Malicdan MC, Noguchi S, Nonaka I, Hayashi YK, Nishino I.
    Hum Mol Genet; 2007 Jan 15; 16(2):115-28. PubMed ID: 17164266
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  • 17. A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
    Malicdan MC, Noguchi S, Nonaka I, Hayashi YK, Nishino I.
    Hum Mol Genet; 2007 Nov 15; 16(22):2669-82. PubMed ID: 17704511
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  • 19. Down-regulation of genes in the lysosomal and ubiquitin-proteasome proteolytic pathways in calpain-3-deficient muscle.
    Combaret L, Béchet D, Claustre A, Taillandier D, Richard I, Attaix D.
    Int J Biochem Cell Biol; 2003 May 15; 35(5):676-84. PubMed ID: 12672459
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