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Journal Abstract Search

192 related items for PubMed ID: 22728077

  • 1. Rescue of growth defects of yeast cdc48 mutants by pathogenic IBMPFD-VCPs.
    Takata T, Kimura Y, Ohnuma Y, Kawawaki J, Kakiyama Y, Tanaka K, Kakizuka A.
    J Struct Biol; 2012 Aug; 179(2):93-103. PubMed ID: 22728077
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  • 2. Different dynamic movements of wild-type and pathogenic VCPs and their cofactors to damaged mitochondria in a Parkin-mediated mitochondrial quality control system.
    Kimura Y, Fukushi J, Hori S, Matsuda N, Okatsu K, Kakiyama Y, Kawawaki J, Kakizuka A, Tanaka K.
    Genes Cells; 2013 Dec; 18(12):1131-43. PubMed ID: 24215292
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  • 3. Enhanced ATPase activities as a primary defect of mutant valosin-containing proteins that cause inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
    Manno A, Noguchi M, Fukushi J, Motohashi Y, Kakizuka A.
    Genes Cells; 2010 Aug; 15(8):911-22. PubMed ID: 20604808
    [Abstract] [Full Text] [Related]

  • 4. A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.
    Gu JM, Ke YH, Yue H, Liu YJ, Zhang Z, Zhang H, Hu WW, Wang C, He JW, Hu YQ, Li M, Fu WZ, Zhang ZL.
    Bone; 2013 Jan; 52(1):9-16. PubMed ID: 23000505
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  • 5. Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation.
    Weihl CC, Dalal S, Pestronk A, Hanson PI.
    Hum Mol Genet; 2006 Jan 15; 15(2):189-99. PubMed ID: 16321991
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  • 6. A unique IBMPFD-related P97/VCP mutation with differential binding pattern and subcellular localization.
    Erzurumlu Y, Kose FA, Gozen O, Gozuacik D, Toth EA, Ballar P.
    Int J Biochem Cell Biol; 2013 Apr 15; 45(4):773-82. PubMed ID: 23333620
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  • 7. Proteomic analysis of a drosophila IBMPFD model reveals potential pathogenic mechanisms.
    Chan HT, Lee TR, Huang SH, Lee HY, Sang TK, Chan HL, Lyu PC.
    Mol Biosyst; 2012 Jun 15; 8(6):1730-41. PubMed ID: 22481368
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  • 9. IBMPFD Disease-Causing Mutant VCP/p97 Proteins Are Targets of Autophagic-Lysosomal Degradation.
    Bayraktar O, Oral O, Kocaturk NM, Akkoc Y, Eberhart K, Kosar A, Gozuacik D.
    PLoS One; 2016 Jun 15; 11(10):e0164864. PubMed ID: 27768726
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  • 12. Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy.
    Guinto JB, Ritson GP, Taylor JP, Forman MS.
    Acta Neuropathol; 2007 Jul 15; 114(1):55-61. PubMed ID: 17457594
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  • 13. Valosin-Containing Protein (VCP)/p97 Oligomerization.
    Yu G, Bai Y, Zhang ZY.
    Subcell Biochem; 2024 Jul 15; 104():485-501. PubMed ID: 38963497
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  • 16. Valosin-containing protein gene mutations: clinical and neuropathologic features.
    Guyant-Maréchal L, Laquerrière A, Duyckaerts C, Dumanchin C, Bou J, Dugny F, Le Ber I, Frébourg T, Hannequin D, Campion D.
    Neurology; 2006 Aug 22; 67(4):644-51. PubMed ID: 16790606
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  • 17. Nucleocytoplasmic shuttling of valosin-containing protein (VCP/p97) regulated by its N domain and C-terminal region.
    Song C, Wang Q, Song C, Lockett SJ, Colburn NH, Li CC, Wang JM, Rogers TJ.
    Biochim Biophys Acta; 2015 Jan 22; 1853(1):222-32. PubMed ID: 25447673
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  • 18. Neuronal-specific overexpression of a mutant valosin-containing protein associated with IBMPFD promotes aberrant ubiquitin and TDP-43 accumulation and cognitive dysfunction in transgenic mice.
    Rodriguez-Ortiz CJ, Hoshino H, Cheng D, Liu-Yescevitz L, Blurton-Jones M, Wolozin B, LaFerla FM, Kitazawa M.
    Am J Pathol; 2013 Aug 22; 183(2):504-15. PubMed ID: 23747512
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  • 19. Recent advances in p97/VCP/Cdc48 cellular functions.
    Yamanaka K, Sasagawa Y, Ogura T.
    Biochim Biophys Acta; 2012 Jan 22; 1823(1):130-7. PubMed ID: 21781992
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