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Journal Abstract Search

415 related items for PubMed ID: 28322724

  • 21. The Cure VCP Scientific Conference 2021: Molecular and clinical insights into neurodegeneration and myopathy linked to multisystem proteinopathy-1 (MSP-1).
    Johnson MA, Klickstein JA, Khanna R, Gou Y, Cure VCP Disease Research Consortium, Raman M.
    Neurobiol Dis; 2022 Jul; 169():105722. PubMed ID: 35405261
    [Abstract] [Full Text] [Related]

  • 22. Characteristics of VCP mutation-associated cardiomyopathy.
    Wang SC, Smith CD, Lombardo DM, Kimonis V.
    Neuromuscul Disord; 2021 Aug; 31(8):701-705. PubMed ID: 34244020
    [Abstract] [Full Text] [Related]

  • 23. Valosin-containing protein and neurofibromin interact to regulate dendritic spine density.
    Wang HF, Shih YT, Chen CY, Chao HW, Lee MJ, Hsueh YP.
    J Clin Invest; 2011 Dec; 121(12):4820-37. PubMed ID: 22105171
    [Abstract] [Full Text] [Related]

  • 24. 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]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. 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 15; 64():8-10. PubMed ID: 30955949
    [Abstract] [Full Text] [Related]

  • 27. 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]

  • 28. 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]

  • 29. Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.
    Weihl CC, Pestronk A, Kimonis VE.
    Neuromuscul Disord; 2009 May 14; 19(5):308-15. PubMed ID: 19380227
    [Abstract] [Full Text] [Related]

  • 30. 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]

  • 31. Cross-sectional study of patients with VCP multisystem proteinopathy 1 using dual-energy x-ray absorptiometry.
    Columbres RCA, Luu V, Nguyen M, Kimonis V.
    Muscle Nerve; 2024 Jun 15; 69(6):699-707. PubMed ID: 38551101
    [Abstract] [Full Text] [Related]

  • 32. Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice.
    Weihl CC, Miller SE, Hanson PI, Pestronk A.
    Hum Mol Genet; 2007 Apr 15; 16(8):919-28. PubMed ID: 17329348
    [Abstract] [Full Text] [Related]

  • 33. 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 15; 7(1):29-32. PubMed ID: 24119107
    [Abstract] [Full Text] [Related]

  • 34. 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 15; 179(2):93-103. PubMed ID: 22728077
    [Abstract] [Full Text] [Related]

  • 35. 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]

  • 36. 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 10; 15(8):911-22. PubMed ID: 20604808
    [Abstract] [Full Text] [Related]

  • 37. Generation, Analyzing and in-vivo Drug Treatment of Drosophila Models with IBMPFD.
    Zhang T, Hay BA, Guo M.
    Bio Protoc; 2020 May 20; 10(10):e3621. PubMed ID: 33659294
    [Abstract] [Full Text] [Related]

  • 38. Pathological consequences of VCP mutations on human striated muscle.
    Hübbers CU, Clemen CS, Kesper K, Böddrich A, Hofmann A, Kämäräinen O, Tolksdorf K, Stumpf M, Reichelt J, Roth U, Krause S, Watts G, Kimonis V, Wattjes MP, Reimann J, Thal DR, Biermann K, Evert BO, Lochmüller H, Wanker EE, Schoser BG, Noegel AA, Schröder R.
    Brain; 2007 Feb 20; 130(Pt 2):381-93. PubMed ID: 16984901
    [Abstract] [Full Text] [Related]

  • 39. 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 20; 186(6):1623-34. PubMed ID: 27106764
    [Abstract] [Full Text] [Related]

  • 40. 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]

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