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  1. 61
    Thermodynamic Stabilization of the Folded Domain of Prion Protein Inhibits Prion Infection in Vivo
    “... Prion diseases, or transmissible spongiform encephalopathies (TSEs), are associated...”
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    Article
  2. 62
    Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease.
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    Article
  3. 63
    Prion and Prion-Like Protein Strains: Deciphering the Molecular Basis of Heterogeneity in Neurodegeneration
    Subjects: “...prion...”
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    Article
  4. 64
    Importance of dimerization in aggregation and neurotoxicity of Prion and [alpha]-Synuclein in prion and Parkinson's diseases
    by Roostaee, Alireza
    Published 2015
    Subjects: “...Protease-resistant prion protein...”
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  5. 65
    Molecular genetic analysis of the prion protein gene locus in human prion disease
    by Mead, Simon Harvey
    Published 2003
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  6. 66
    Prion Protein Misfolding, Strains, and Neurotoxicity: An Update from Studies on Mammalian Prions
    “...Prion diseases, also known as transmissible spongiform encephalopathies (TSEs), are a group...”
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    Article
  7. 67
    The Way forward for the Origin of Life: Prions and Prion-Like Molecules First Hypothesis
    Subjects: “...prions...”
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    Article
  8. 68
    Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases
    “...) is an ultrasensitive prion amyloid seeding assay for diagnosis of sporadic Creutzfeldt–Jakob disease (CJD) but several...”
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    Article
  9. 69
    Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein.
    “...Prions are infectious agents causing fatal neurodegenerative diseases of humans and animals...”
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    Article
  10. 70
    A unifying model for the propagation of prion proteins in yeast brings insight into the [PSI+] prion.
    “...The use of yeast systems to study the propagation of prions and amyloids has emerged as a crucial...”
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    Article
  11. 71
    Structural evidence for the critical role of the prion protein hydrophobic region in forming an infectious prion.
    “...Prion or PrPSc is the proteinaceous infectious agent causing prion diseases in various mammalian...”
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    Article
  12. 72
    <i>C. elegans</i> Models to Study the Propagation of Prions and Prion-Like Proteins
    Subjects: “...prions...”
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    Article
  13. 73
    Ex vivo mammalian prions are formed of paired double helical prion protein fibrils
    Subjects: “...prion...”
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    Article
  14. 74
    An antipsychotic drug exerts anti-prion effects by altering the localization of the cellular prion protein.
    “...Prion diseases are neurodegenerative conditions characterized by the conformational conversion...”
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    Article
  15. 75
    Influence of Interspecies Transmission of Atypical Bovine Spongiform Encephalopathy Prions to Hamsters on Prion Characteristics
    Subjects: “...prion strain...”
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    Article
  16. 76
    Plasmacytoid dendritic cells sequester high prion titres at early stages of prion infection.
    “...In most transmissible spongiform encephalopathies prions accumulate in the lymphoreticular system...”
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    Article
  17. 77
    Manganese enhances prion protein survival in model soils and increases prion infectivity to cells.
    by Paul Davies, David R Brown
    Published 2009-10-01
    “...Prion diseases are considered to be transmissible. The existence of sporadic forms of prion...”
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    Article
  18. 78
    Ultraviolet-ozone treatment reduces levels of disease-associated prion protein and prion infectivity
    “... of fatal neurodegenerative diseases caused by novel infectious agents referred to as prions. Prions appear...”
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    Article
  19. 79
    Region-Specific Sialylation Pattern of Prion Strains Provides Novel Insight into Prion Neurotropism
    Subjects: “...prions...”
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    Article
  20. 80
    Targeting of prion-infected lymphoid cells to the central nervous system accelerates prion infection
    Subjects: “...prion...”
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    Article
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