These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

484 related items for PubMed ID: 27226613

  • 1. Pathogenic Mutations in the Valosin-containing Protein/p97(VCP) N-domain Inhibit the SUMOylation of VCP and Lead to Impaired Stress Response.
    Wang T, Xu W, Qin M, Yang Y, Bao P, Shen F, Zhang Z, Xu J.
    J Biol Chem; 2016 Jul 01; 291(27):14373-14384. PubMed ID: 27226613
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Valosin-Containing Protein (VCP)/p97 Oligomerization.
    Yu G, Bai Y, Zhang ZY.
    Subcell Biochem; 2024 Jan 15; 104():485-501. PubMed ID: 38963497
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Interaction between salt-inducible kinase 2 (SIK2) and p97/valosin-containing protein (VCP) regulates endoplasmic reticulum (ER)-associated protein degradation in mammalian cells.
    Yang FC, Lin YH, Chen WH, Huang JY, Chang HY, Su SH, Wang HT, Chiang CY, Hsu PH, Tsai MD, Tan BC, Lee SC.
    J Biol Chem; 2013 Nov 22; 288(47):33861-33872. PubMed ID: 24129571
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97.
    Ritson GP, Custer SK, Freibaum BD, Guinto JB, Geffel D, Moore J, Tang W, Winton MJ, Neumann M, Trojanowski JQ, Lee VM, Forman MS, Taylor JP.
    J Neurosci; 2010 Jun 02; 30(22):7729-39. PubMed ID: 20519548
    [Abstract] [Full Text] [Related]

  • 8. 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 02; 18(12):1131-43. PubMed ID: 24215292
    [Abstract] [Full Text] [Related]

  • 9. AAA ATPase p97/valosin-containing protein interacts with gp78, a ubiquitin ligase for endoplasmic reticulum-associated degradation.
    Zhong X, Shen Y, Ballar P, Apostolou A, Agami R, Fang S.
    J Biol Chem; 2004 Oct 29; 279(44):45676-84. PubMed ID: 15331598
    [Abstract] [Full Text] [Related]

  • 10. The role of the N-domain in the ATPase activity of the mammalian AAA ATPase p97/VCP.
    Niwa H, Ewens CA, Tsang C, Yeung HO, Zhang X, Freemont PS.
    J Biol Chem; 2012 Mar 09; 287(11):8561-70. PubMed ID: 22270372
    [Abstract] [Full Text] [Related]

  • 11. 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 09; 45(4):773-82. PubMed ID: 23333620
    [Abstract] [Full Text] [Related]

  • 12. 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 09; 6(2):217-27. PubMed ID: 20104022
    [Abstract] [Full Text] [Related]

  • 13. Valosin-containing protein (p97) is a regulator of endoplasmic reticulum stress and of the degradation of N-end rule and ubiquitin-fusion degradation pathway substrates in mammalian cells.
    Wójcik C, Rowicka M, Kudlicki A, Nowis D, McConnell E, Kujawa M, DeMartino GN.
    Mol Biol Cell; 2006 Nov 09; 17(11):4606-18. PubMed ID: 16914519
    [Abstract] [Full Text] [Related]

  • 14. Structural basis for ovarian tumor domain-containing protein 1 (OTU1) binding to p97/valosin-containing protein (VCP).
    Kim SJ, Cho J, Song EJ, Kim SJ, Kim HM, Lee KE, Suh SW, Kim EE.
    J Biol Chem; 2014 May 02; 289(18):12264-74. PubMed ID: 24610782
    [Abstract] [Full Text] [Related]

  • 15. Derlin-1 regulates mutant VCP-linked pathogenesis and endoplasmic reticulum stress-induced apoptosis.
    Liang CJ, Chang YC, Chang HC, Wang CK, Hung YC, Lin YE, Chan CC, Chen CH, Chang HY, Sang TK.
    PLoS Genet; 2014 Sep 02; 10(9):e1004675. PubMed ID: 25255315
    [Abstract] [Full Text] [Related]

  • 16. Valosin-Containing Protein (VCP)/p97: A Prognostic Biomarker and Therapeutic Target in Cancer.
    Costantini S, Capone F, Polo A, Bagnara P, Budillon A.
    Int J Mol Sci; 2021 Sep 21; 22(18):. PubMed ID: 34576340
    [Abstract] [Full Text] [Related]

  • 17. Valosin-containing Protein (VCP)/p97 Segregase Mediates Proteolytic Processing of Cockayne Syndrome Group B (CSB) in Damaged Chromatin.
    He J, Zhu Q, Wani G, Sharma N, Wani AA.
    J Biol Chem; 2016 Apr 01; 291(14):7396-408. PubMed ID: 26826127
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Regulation of ER-associated degradation via p97/VCP-interacting motif.
    Ballar P, Fang S.
    Biochem Soc Trans; 2008 Oct 01; 36(Pt 5):818-22. PubMed ID: 18793143
    [Abstract] [Full Text] [Related]

  • 20. 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]

    Page: [Next] [New Search]
    of 25.