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208 related items for PubMed ID: 25447673

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Valosin-containing protein (VCP) is a novel IQ motif-containing GTPase activating protein 1 (IQGAP1)-interacting protein.
    Itoh N, Nagai T, Watanabe T, Taki K, Nabeshima T, Kaibuchi K, Yamada K.
    Biochem Biophys Res Commun; 2017 Dec 02; 493(4):1384-1389. PubMed ID: 28970065
    [Abstract] [Full Text] [Related]

  • 3. Valosin-Containing Protein (VCP)/p97 Oligomerization.
    Yu G, Bai Y, Zhang ZY.
    Subcell Biochem; 2024 Dec 02; 104():485-501. PubMed ID: 38963497
    [Abstract] [Full Text] [Related]

  • 4. 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 Dec 02; 11(10):e0164864. PubMed ID: 27768726
    [Abstract] [Full Text] [Related]

  • 5. Inclusion body myopathy, Paget's disease of the bone and fronto-temporal dementia: a disorder of autophagy.
    Ju JS, Weihl CC.
    Hum Mol Genet; 2010 Apr 15; 19(R1):R38-45. PubMed ID: 20410287
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 52(1):9-16. PubMed ID: 23000505
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 183(2):504-15. PubMed ID: 23747512
    [Abstract] [Full Text] [Related]

  • 9. Phenotypic variability in three families with valosin-containing protein mutation.
    Spina S, Van Laar AD, Murrell JR, Hamilton RL, Kofler JK, Epperson F, Farlow MR, Lopez OL, Quinlan J, DeKosky ST, Ghetti B.
    Eur J Neurol; 2013 Feb 15; 20(2):251-8. PubMed ID: 22900631
    [Abstract] [Full Text] [Related]

  • 10. Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone.
    Custer SK, Neumann M, Lu H, Wright AC, Taylor JP.
    Hum Mol Genet; 2010 May 01; 19(9):1741-55. PubMed ID: 20147319
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation.
    Shinjo SK, Oba-Shinjo SM, Lerario AM, Marie SKN.
    Clin Rheumatol; 2018 Apr 15; 37(4):1129-1136. PubMed ID: 29127544
    [Abstract] [Full Text] [Related]

  • 13. Pathogenic VCP/TER94 alleles are dominant actives and contribute to neurodegeneration by altering cellular ATP level in a Drosophila IBMPFD model.
    Chang YC, Hung WT, Chang YC, Chang HC, Wu CL, Chiang AS, Jackson GR, Sang TK.
    PLoS Genet; 2011 Feb 03; 7(2):e1001288. PubMed ID: 21304887
    [Abstract] [Full Text] [Related]

  • 14. Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease.
    Ju JS, Fuentealba RA, Miller SE, Jackson E, Piwnica-Worms D, Baloh RH, Weihl CC.
    J Cell Biol; 2009 Dec 14; 187(6):875-88. PubMed ID: 20008565
    [Abstract] [Full Text] [Related]

  • 15. [Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia].
    Hayashi Y.
    Rinsho Shinkeigaku; 2013 Dec 14; 53(11):947-50. PubMed ID: 24291843
    [Abstract] [Full Text] [Related]

  • 16. 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 14; 18(12):1131-43. PubMed ID: 24215292
    [Abstract] [Full Text] [Related]

  • 17. VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD.
    Tresse E, Salomons FA, Vesa J, Bott LC, Kimonis V, Yao TP, Dantuma NP, Taylor JP.
    Autophagy; 2010 Feb 14; 6(2):217-27. PubMed ID: 20104022
    [Abstract] [Full Text] [Related]

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  • 20. The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis.
    Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, Nguyen C, Mukherjee J, Caiozzo V, Martin B, Watts GD, Vesa J, Smith C, Kimonis VE.
    J Mol Neurosci; 2011 Nov 14; 45(3):522-31. PubMed ID: 21892620
    [Abstract] [Full Text] [Related]

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