BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 20625431)

  • 1. Paradoxical role of prion protein aggregates in redox-iron induced toxicity.
    Das D; Luo X; Singh A; Gu Y; Ghosh S; Mukhopadhyay CK; Chen SG; Sy MS; Kong Q; Singh N
    PLoS One; 2010 Jul; 5(7):e11420. PubMed ID: 20625431
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Change in the characteristics of ferritin induces iron imbalance in prion disease affected brains.
    Singh A; Qing L; Kong Q; Singh N
    Neurobiol Dis; 2012 Mar; 45(3):930-8. PubMed ID: 22182691
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Abnormal brain iron homeostasis in human and animal prion disorders.
    Singh A; Isaac AO; Luo X; Mohan ML; Cohen ML; Chen F; Kong Q; Bartz J; Singh N
    PLoS Pathog; 2009 Mar; 5(3):e1000336. PubMed ID: 19283067
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prion protein modulates cellular iron uptake: a novel function with implications for prion disease pathogenesis.
    Singh A; Mohan ML; Isaac AO; Luo X; Petrak J; Vyoral D; Singh N
    PLoS One; 2009; 4(2):e4468. PubMed ID: 19212444
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Modulation of proteinase K-resistant prion protein in cells and infectious brain homogenate by redox iron: implications for prion replication and disease pathogenesis.
    Basu S; Mohan ML; Luo X; Kundu B; Kong Q; Singh N
    Mol Biol Cell; 2007 Sep; 18(9):3302-12. PubMed ID: 17567949
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Changed iron regulation in scrapie-infected neuroblastoma cells.
    Fernaeus S; Hälldin J; Bedecs K; Land T
    Brain Res Mol Brain Res; 2005 Feb; 133(2):266-73. PubMed ID: 15710243
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease.
    Singh N; Haldar S; Tripathi AK; McElwee MK; Horback K; Beserra A
    Antioxid Redox Signal; 2014 Jul; 21(3):471-84. PubMed ID: 24512387
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prion Protein-Hemin Interaction Upregulates Hemoglobin Synthesis: Implications for Cerebral Hemorrhage and Sporadic Creutzfeldt-Jakob Disease.
    Tripathi AK; Singh N
    J Alzheimers Dis; 2016; 51(1):107-21. PubMed ID: 26836195
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prion protein modulates iron transport in the anterior segment: Implications for ocular iron homeostasis and prion transmission.
    Ashok A; Karmakar S; Chandel R; Ravikumar R; Dalal S; Kong Q; Singh N
    Exp Eye Res; 2018 Oct; 175():1-13. PubMed ID: 29859760
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Iron content of ferritin modulates its uptake by intestinal epithelium: implications for co-transport of prions.
    Bhupanapadu Sunkesula SR; Luo X; Das D; Singh A; Singh N
    Mol Brain; 2010 Apr; 3():14. PubMed ID: 20429907
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Uptake and degradation of protease-sensitive and -resistant forms of abnormal human prion protein aggregates by human astrocytes.
    Choi YP; Head MW; Ironside JW; Priola SA
    Am J Pathol; 2014 Dec; 184(12):3299-307. PubMed ID: 25280631
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes.
    Zanusso G; Farinazzo A; Prelli F; Fiorini M; Gelati M; Ferrari S; Righetti PG; Rizzuto N; Frangione B; Monaco S
    J Biol Chem; 2004 Sep; 279(37):38936-42. PubMed ID: 15247220
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
    Cassard H; Huor A; Espinosa JC; Douet JY; Lugan S; Aron N; Vilette D; Delisle MB; Marín-Moreno A; Peran P; Beringue V; Torres JM; Ironside JW; Andreoletti O
    mBio; 2020 Jun; 11(3):. PubMed ID: 32546613
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.
    Zanusso G; Fiorini M; Ferrari S; Meade-White K; Barbieri I; Brocchi E; Ghetti B; Monaco S
    J Biol Chem; 2014 Feb; 289(8):4870-81. PubMed ID: 24398683
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Engineering a murine cell line for the stable propagation of hamster prions.
    Bourkas MEC; Arshad H; Al-Azzawi ZAM; Halgas O; Shikiya RA; Mehrabian M; Schmitt-Ulms G; Bartz JC; Watts JC
    J Biol Chem; 2019 Mar; 294(13):4911-4923. PubMed ID: 30705093
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A brain aggregate model gives new insights into the pathobiology and treatment of prion diseases.
    Bajsarowicz K; Ahn M; Ackerman L; Dearmond BN; Carlson G; DeArmond SJ
    J Neuropathol Exp Neurol; 2012 May; 71(5):449-66. PubMed ID: 22507918
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Endogenous prion protein conversion is required for prion-induced neuritic alterations and neuronal death.
    Cronier S; Carimalo J; Schaeffer B; Jaumain E; Béringue V; Miquel MC; Laude H; Peyrin JM
    FASEB J; 2012 Sep; 26(9):3854-61. PubMed ID: 22661006
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Upregulation of brain hepcidin in prion diseases.
    Chaudhary S; Ashok A; Wise AS; Rana NA; McDonald D; Kritikos AE; Kong Q; Singh N
    Prion; 2021 Dec; 15(1):126-137. PubMed ID: 34224321
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Attempts to convert the cellular prion protein into the scrapie isoform in cell-free systems.
    Raeber AJ; Borchelt DR; Scott M; Prusiner SB
    J Virol; 1992 Oct; 66(10):6155-63. PubMed ID: 1356161
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.