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Journal Abstract Search

208 related items for PubMed ID: 24119107

  • 1. Cytokine profiling in patients with VCP-associated disease.
    Dec E, Rana P, Katheria V, Dec R, Khare M, Nalbandian A, Leu SY, Radom-Aizik S, Llewellyn K, BenMohamed L, Zaldivar F, Kimonis V.
    Clin Transl Sci; 2014 Feb; 7(1):29-32. PubMed ID: 24119107
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  • 3. 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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  • 4. 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; 183(2):504-15. PubMed ID: 23747512
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  • 5. 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; 1853(1):222-32. PubMed ID: 25447673
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  • 6. The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice?
    Clemen CS, Winter L, Strucksberg KH, Berwanger C, Türk M, Kornblum C, Florin A, Aguilar-Pimentel JA, Amarie OV, Becker L, Garrett L, Hans W, Moreth K, Neff F, Pingen L, Rathkolb B, Rácz I, Rozman J, Treise I, Fuchs H, Gailus-Durner V, de Angelis MH, Vorgerd M, Eichinger L, Schröder R.
    Biochem Biophys Res Commun; 2018 Sep 18; 503(4):2770-2777. PubMed ID: 30100055
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  • 7. Motor neuron involvement in multisystem proteinopathy: implications for ALS.
    Benatar M, Wuu J, Fernandez C, Weihl CC, Katzen H, Steele J, Oskarsson B, Taylor JP.
    Neurology; 2013 May 14; 80(20):1874-80. PubMed ID: 23635965
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  • 13. Inclusion body myopathy with Paget disease of bone and frontotemporal dementia linked to VCP p.Arg155Cys in a Korean family.
    Kim EJ, Park YE, Kim DS, Ahn BY, Kim HS, Chang YH, Kim SJ, Kim HJ, Lee HW, Seeley WW, Kim S.
    Arch Neurol; 2011 Jun 14; 68(6):787-96. PubMed ID: 21320982
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  • 14. [An advanced case of myopathy and dementia with a new mutation in the valosin-containing protein gene].
    Kamiyama T, Sengoku R, Sasaki M, Hayashi Y, Nishino I, Mochio S, Iguchi Y.
    Rinsho Shinkeigaku; 2013 Jun 14; 53(6):465-9. PubMed ID: 23782825
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  • 18. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia.
    Wang H, Wu S.
    Neuromuscul Disord; 2015 Mar 14; 25(3):273. PubMed ID: 25497399
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  • 20. Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels.
    Bartolome F, Wu HC, Burchell VS, Preza E, Wray S, Mahoney CJ, Fox NC, Calvo A, Canosa A, Moglia C, Mandrioli J, Chiò A, Orrell RW, Houlden H, Hardy J, Abramov AY, Plun-Favreau H.
    Neuron; 2013 Apr 10; 78(1):57-64. PubMed ID: 23498975
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