BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

403 related articles for article (PubMed ID: 15772339)

  • 1. The disulfide isomerase Grp58 is a protective factor against prion neurotoxicity.
    Hetz C; Russelakis-Carneiro M; Wälchli S; Carboni S; Vial-Knecht E; Maundrell K; Castilla J; Soto C
    J Neurosci; 2005 Mar; 25(11):2793-802. PubMed ID: 15772339
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Protein disulfide isomerase regulates endoplasmic reticulum stress and the apoptotic process during prion infection and PrP mutant-induced cytotoxicity.
    Wang SB; Shi Q; Xu Y; Xie WL; Zhang J; Tian C; Guo Y; Wang K; Zhang BY; Chen C; Gao C; Dong XP
    PLoS One; 2012; 7(6):e38221. PubMed ID: 22685557
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prion disease is accelerated in mice lacking stress-induced heat shock protein 70 (HSP70).
    Mays CE; Armijo E; Morales R; Kramm C; Flores A; Tiwari A; Bian J; Telling GC; Pandita TK; Hunt CR; Soto C
    J Biol Chem; 2019 Sep; 294(37):13619-13628. PubMed ID: 31320473
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Caspase-12 and endoplasmic reticulum stress mediate neurotoxicity of pathological prion protein.
    Hetz C; Russelakis-Carneiro M; Maundrell K; Castilla J; Soto C
    EMBO J; 2003 Oct; 22(20):5435-45. PubMed ID: 14532116
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Utility of RNAi-mediated prnp gene silencing in neuroblastoma cells permanently infected by prions: potentials and limitations.
    Kim Y; Han B; Titlow W; Mays CE; Kwon M; Ryou C
    Antiviral Res; 2009 Nov; 84(2):185-93. PubMed ID: 19748523
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Endoplasmic Reticulum Chaperone GRP78/BiP Modulates Prion Propagation in vitro and in vivo.
    Park KW; Eun Kim G; Morales R; Moda F; Moreno-Gonzalez I; Concha-Marambio L; Lee AS; Hetz C; Soto C
    Sci Rep; 2017 Mar; 7():44723. PubMed ID: 28333162
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Protein-disulfide Isomerase ERp57 Regulates the Steady-state Levels of the Prion Protein.
    Torres M; Medinas DB; Matamala JM; Woehlbier U; Cornejo VH; Solda T; Andreu C; Rozas P; Matus S; Muñoz N; Vergara C; Cartier L; Soto C; Molinari M; Hetz C
    J Biol Chem; 2015 Sep; 290(39):23631-45. PubMed ID: 26170458
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prion Protein Devoid of the Octapeptide Repeat Region Delays Bovine Spongiform Encephalopathy Pathogenesis in Mice.
    Hara H; Miyata H; Das NR; Chida J; Yoshimochi T; Uchiyama K; Watanabe H; Kondoh G; Yokoyama T; Sakaguchi S
    J Virol; 2018 Jan; 92(1):. PubMed ID: 29046443
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular mechanisms of neurotoxicity of pathological prion protein.
    Castilla J; Hetz C; Soto C
    Curr Mol Med; 2004 Jun; 4(4):397-403. PubMed ID: 15354870
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Calnexin inhibits thermal aggregation and neurotoxicity of prion protein.
    Wang W; Chen R; Luo K; Wu D; Huang L; Huang T; Xiao G
    J Cell Biochem; 2010 Oct; 111(2):343-9. PubMed ID: 20506117
    [TBL] [Abstract][Full Text] [Related]  

  • 11. ERp57 as a novel cellular factor controlling prion protein biosynthesis: Therapeutic potential of protein disulfide isomerases.
    Sepulveda M; Rozas P; Hetz C; Medinas DB
    Prion; 2016; 10(1):50-6. PubMed ID: 26864548
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Disease-related prion protein forms aggresomes in neuronal cells leading to caspase activation and apoptosis.
    Kristiansen M; Messenger MJ; Klöhn PC; Brandner S; Wadsworth JD; Collinge J; Tabrizi SJ
    J Biol Chem; 2005 Nov; 280(46):38851-61. PubMed ID: 16157591
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prion-Associated Neurodegeneration Causes Both Endoplasmic Reticulum Stress and Proteasome Impairment in a Murine Model of Spontaneous Disease.
    Otero A; Betancor M; Eraña H; Fernández Borges N; Lucas JJ; Badiola JJ; Castilla J; Bolea R
    Int J Mol Sci; 2021 Jan; 22(1):. PubMed ID: 33466523
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein.
    Stewart RS; Piccardo P; Ghetti B; Harris DA
    J Neurosci; 2005 Mar; 25(13):3469-77. PubMed ID: 15800202
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prion infection of muscle cells in vitro.
    Dlakic WM; Grigg E; Bessen RA
    J Virol; 2007 May; 81(9):4615-24. PubMed ID: 17314174
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Aggresome formation by mutant prion proteins: the unfolding role of proteasomes in familial prion disorders.
    Mishra RS; Bose S; Gu Y; Li R; Singh N
    J Alzheimers Dis; 2003 Feb; 5(1):15-23. PubMed ID: 12590162
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Infection by ME7 prion is not modified in transgenic mice expressing the yeast chaperone Hsp104 in neurons.
    Dandoy-Dron F; Bogdanova A; Beringue V; Bailly Y; Tovey MG; Laude H; Dron M
    Neurosci Lett; 2006 Sep; 405(3):181-5. PubMed ID: 16884849
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Correlative studies support lipid peroxidation is linked to PrP(res) propagation as an early primary pathogenic event in prion disease.
    Brazier MW; Lewis V; Ciccotosto GD; Klug GM; Lawson VA; Cappai R; Ironside JW; Masters CL; Hill AF; White AR; Collins S
    Brain Res Bull; 2006 Jan; 68(5):346-54. PubMed ID: 16377442
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autophagy induction by trehalose counteracts cellular prion infection.
    Aguib Y; Heiseke A; Gilch S; Riemer C; Baier M; Schätzl HM; Ertmer A
    Autophagy; 2009 Apr; 5(3):361-9. PubMed ID: 19182537
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Involvement of mitochondria in endoplasmic reticulum stress-induced apoptotic cell death pathway triggered by the prion peptide PrP(106-126).
    Ferreiro E; Costa R; Marques S; Cardoso SM; Oliveira CR; Pereira CM
    J Neurochem; 2008 Feb; 104(3):766-76. PubMed ID: 17995926
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.