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Journal Abstract Search

224 related items for PubMed ID: 25497399

  • 1. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia.
    Wang H, Wu S.
    Neuromuscul Disord; 2015 Mar; 25(3):273. PubMed ID: 25497399
    [No Abstract] [Full Text] [Related]

  • 2. Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia.
    Peyer AK, Kinter J, Hench J, Frank S, Fuhr P, Thomann S, Fischmann A, Kneifel S, Camaño P, López de Munain A, Sinnreich M, Renaud S.
    Neuromuscul Disord; 2013 Feb; 23(2):149-54. PubMed ID: 23140793
    [Abstract] [Full Text] [Related]

  • 3. [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 Feb; 53(6):465-9. PubMed ID: 23782825
    [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
    [Abstract] [Full Text] [Related]

  • 5. 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; 20(2):251-8. PubMed ID: 22900631
    [Abstract] [Full Text] [Related]

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

  • 7. A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
    Fanganiello RD, Kimonis VE, Côrte CC, Nitrini R, Passos-Bueno MR.
    Braz J Med Biol Res; 2011 Apr; 44(4):374-80. PubMed ID: 21412659
    [Abstract] [Full Text] [Related]

  • 8. Distal myopathy and rapidly progressive dementia associated with a novel mutation in the VCP gene: Expanding inclusion body myopathy with early-onset Paget disease and frontotemporal dementia spectrum.
    Falcão de Campos C, de Carvalho M.
    J Clin Neurosci; 2019 Jun; 64():8-10. PubMed ID: 30955949
    [Abstract] [Full Text] [Related]

  • 9. [A patient with familial amyotrophic lateral sclerosis associated with a new valosin-containing protein (VCP) gene mutation].
    Segawa M, Hoshi A, Naruse H, Kuroda M, Bujo H, Ugawa Y.
    Rinsho Shinkeigaku; 2015 Jun; 55(12):914-20. PubMed ID: 26511028
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

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

  • 12. The Myoblast C2C12 Transfected with Mutant Valosin-Containing Protein Exhibits Delayed Stress Granule Resolution on Oxidative Stress.
    Rodriguez-Ortiz CJ, Flores JC, Valenzuela JA, Rodriguez GJ, Zumkehr J, Tran DN, Kimonis VE, Kitazawa M.
    Am J Pathol; 2016 Jun 14; 186(6):1623-34. PubMed ID: 27106764
    [Abstract] [Full Text] [Related]

  • 13. 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 14; 37(4):1129-1136. PubMed ID: 29127544
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. 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 10; 1853(1):222-32. PubMed ID: 25447673
    [Abstract] [Full Text] [Related]

  • 17. 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 10; 7(1):29-32. PubMed ID: 24119107
    [Abstract] [Full Text] [Related]

  • 18. Clinical Reasoning: Progressive proximal weakness in a 56-year-old man with bone pain.
    Torabi T, Huttner A, Nowak RJ, Roy B.
    Neurology; 2019 Nov 19; 93(21):939-944. PubMed ID: 31740511
    [No Abstract] [Full Text] [Related]

  • 19. 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 19; 68(6):787-96. PubMed ID: 21320982
    [Abstract] [Full Text] [Related]

  • 20. 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 19; 45(4):773-82. PubMed ID: 23333620
    [Abstract] [Full Text] [Related]

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