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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

312 related articles for article (PubMed ID: 19208399)

  • 41. Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations.
    Forman MS; Mackenzie IR; Cairns NJ; Swanson E; Boyer PJ; Drachman DA; Jhaveri BS; Karlawish JH; Pestronk A; Smith TW; Tu PH; Watts GD; Markesbery WR; Smith CD; Kimonis VE
    J Neuropathol Exp Neurol; 2006 Jun; 65(6):571-81. PubMed ID: 16783167
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 43. One family, one gene and three phenotypes: A novel VCP (valosin-containing protein) mutation associated with myopathy with rimmed vacuoles, amyotrophic lateral sclerosis and frontotemporal dementia.
    Abrahao A; Abath Neto O; Kok F; Zanoteli E; Santos B; Pinto WB; Barsottini OG; Oliveira AS; Pedroso JL
    J Neurol Sci; 2016 Sep; 368():352-8. PubMed ID: 27538664
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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; 11(10):e0164864. PubMed ID: 27768726
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Radiological features of Paget disease of bone associated with VCP myopathy.
    Farpour F; Tehranzadeh J; Donkervoort S; Smith C; Martin B; Vanjara P; Osann K; Kimonis VE
    Skeletal Radiol; 2012 Mar; 41(3):329-37. PubMed ID: 21643886
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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; 69(6):699-707. PubMed ID: 38551101
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A case report comparing clinical, imaging and neuropsychological assessment findings in twins discordant for the VCP p.R155C mutation.
    Surampalli A; Gold BT; Smith C; Castellani RJ; Khare M; Yu H; Nguyen C; Lan M; Wencel M; Wigal S; Caiozzo V; Kimonis V
    Neuromuscul Disord; 2015 Feb; 25(2):177-83. PubMed ID: 25582679
    [TBL] [Abstract][Full Text] [Related]  

  • 50. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 51. 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; 7(2):e1001288. PubMed ID: 21304887
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [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; 53(6):465-9. PubMed ID: 23782825
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Characterization of the Asian myopathy patients with VCP mutations.
    Shi Z; Hayashi YK; Mitsuhashi S; Goto K; Kaneda D; Choi YC; Toyoda C; Hieda S; Kamiyama T; Sato H; Wada M; Noguchi S; Nonaka I; Nishino I
    Eur J Neurol; 2012 Mar; 19(3):501-9. PubMed ID: 22040362
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts.
    Vesa J; Su H; Watts GD; Krause S; Walter MC; Martin B; Smith C; Wallace DC; Kimonis VE
    Neuromuscul Disord; 2009 Nov; 19(11):766-72. PubMed ID: 19828315
    [TBL] [Abstract][Full Text] [Related]  

  • 55. VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder.
    Kimonis VE; Fulchiero E; Vesa J; Watts G
    Biochim Biophys Acta; 2008 Dec; 1782(12):744-8. PubMed ID: 18845250
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. 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; 187(6):875-88. PubMed ID: 20008565
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Multilocular Paget's disease in IBMPFD syndrome. A case report with 14-year follow-up].
    Zajonz D; Langsieb C; Chavdarova L; Kellermann S; Baum P; Wickenhauser C; von Salis-Soglio G; Prietzel T
    Orthopade; 2012 Jun; 41(6):482-7. PubMed ID: 22699758
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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; 179(2):93-103. PubMed ID: 22728077
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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; 493(4):1384-1389. PubMed ID: 28970065
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.