BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

282 related articles for article (PubMed ID: 18845250)

  • 1. 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]  

  • 2. Valosin-containing protein gene mutations: clinical and neuropathologic features.
    Guyant-Maréchal L; Laquerrière A; Duyckaerts C; Dumanchin C; Bou J; Dugny F; Le Ber I; Frébourg T; Hannequin D; Campion D
    Neurology; 2006 Aug; 67(4):644-51. PubMed ID: 16790606
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.
    Kimonis VE; Mehta SG; Fulchiero EC; Thomasova D; Pasquali M; Boycott K; Neilan EG; Kartashov A; Forman MS; Tucker S; Kimonis K; Mumm S; Whyte MP; Smith CD; Watts GD
    Am J Med Genet A; 2008 Mar; 146A(6):745-57. PubMed ID: 18260132
    [TBL] [Abstract][Full Text] [Related]  

  • 4. TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.
    Neumann M; Mackenzie IR; Cairns NJ; Boyer PJ; Markesbery WR; Smith CD; Taylor JP; Kretzschmar HA; Kimonis VE; Forman MS
    J Neuropathol Exp Neurol; 2007 Feb; 66(2):152-7. PubMed ID: 17279000
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy.
    Guinto JB; Ritson GP; Taylor JP; Forman MS
    Acta Neuropathol; 2007 Jul; 114(1):55-61. PubMed ID: 17457594
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.
    Watts GD; Wymer J; Kovach MJ; Mehta SG; Mumm S; Darvish D; Pestronk A; Whyte MP; Kimonis VE
    Nat Genet; 2004 Apr; 36(4):377-81. PubMed ID: 15034582
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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; 19(5):308-15. PubMed ID: 19380227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 45(3):522-31. PubMed ID: 21892620
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His.
    van der Zee J; Pirici D; Van Langenhove T; Engelborghs S; Vandenberghe R; Hoffmann M; Pusswald G; Van den Broeck M; Peeters K; Mattheijssens M; Martin JJ; De Deyn PP; Cruts M; Haubenberger D; Kumar-Singh S; Zimprich A; Van Broeckhoven C
    Neurology; 2009 Aug; 73(8):626-32. PubMed ID: 19704082
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 15(8):911-22. PubMed ID: 20604808
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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(2):189-99. PubMed ID: 16321991
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 19(9):1741-55. PubMed ID: 20147319
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
    Watts GD; Thomasova D; Ramdeen SK; Fulchiero EC; Mehta SG; Drachman DA; Weihl CC; Jamrozik Z; Kwiecinski H; Kaminska A; Kimonis VE
    Clin Genet; 2007 Nov; 72(5):420-6. PubMed ID: 17935506
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 16(8):919-28. PubMed ID: 17329348
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

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

  • 20. A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.
    Djamshidian A; Schaefer J; Haubenberger D; Stogmann E; Zimprich F; Auff E; Zimprich A
    Muscle Nerve; 2009 Mar; 39(3):389-91. PubMed ID: 19208399
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.