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  1. 121
    por Davies, Paul, Brown, David R.
    Publicado 2009
    “…Prion diseases are considered to be transmissible. …”
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    Manganese Enhances Prion Protein Survival in Model Soils and Increases Prion Infectivity to Cells
  2. 122
    “…Chronic wasting disease (CWD) is a prion disease that affects free-ranging and captive cervids, including mule deer, white-tailed deer, Rocky Mountain elk and moose. …”
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    Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein
  3. 123
    “…In most transmissible spongiform encephalopathies prions accumulate in the lymphoreticular system (LRS) long before they are detectable in the central nervous system. …”
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    Plasmacytoid Dendritic Cells Sequester High Prion Titres at Early Stages of Prion Infection
  4. 124
    “…BACKGROUND: Prions, composed of a misfolded protein designated PrP(Sc), are infectious agents causing fatal neurodegenerative diseases. …”
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    Targeting of prion-infected lymphoid cells to the central nervous system accelerates prion infection
  5. 125
    por Mabbott, Neil A.
    Publicado 2012
    “…Prion diseases are subacute neurodegenerative diseases that affect humans and a range of domestic and free-ranging animal species. …”
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    Prion pathogenesis and secondary lymphoid organs (SLO): Tracking the SLO spread of prions to the brain
  6. 126
    “…Mammalian prions, transmissible agents causing lethal neurodegenerative diseases, are composed of assemblies of misfolded cellular prion protein (PrP) (1). …”
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    A naturally occurring variant of the human prion protein completely prevents prion disease
  7. 127
    “…Mammalian prions are hypothesized to be fibrillar or amyloid forms of prion protein (PrP), but structures observed to date have not been definitively correlated with infectivity and the three-dimensional structure of infectious prions has remained obscure. …”
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    Ex vivo mammalian prions are formed of paired double helical prion protein fibrils
  8. 128
    “…Prion diseases are neurodegenerative conditions characterized by the conformational conversion of the cellular prion protein (PrP(C)), an endogenous membrane glycoprotein of uncertain function, into PrP(Sc), a pathological isoform that replicates by imposing its abnormal folding onto PrP(C) molecules. …”
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    An antipsychotic drug exerts anti-prion effects by altering the localization of the cellular prion protein
  9. 129
    “…Prion or PrP(Sc) is the proteinaceous infectious agent causing prion diseases in various mammalian species. …”
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    Structural evidence for the critical role of the prion protein hydrophobic region in forming an infectious prion
  10. 130
    “…Mammalian prions are unconventional infectious agents that invade and replicate in an organism by recruiting a normal form of a prion protein (PrP(C)) and converting it into misfolded, disease-associated state referred to as PrP(Sc). …”
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    Region-Specific Sialylation Pattern of Prion Strains Provides Novel Insight into Prion Neurotropism
  11. 131
    “…Further, Western blot analysis demonstrated that PrP(res) banding patterns of the H-BSE prion were indistinguishable from those of the C-BSE prion in TgHaNSE mice. …”
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    Influence of Interspecies Transmission of Atypical Bovine Spongiform Encephalopathy Prions to Hamsters on Prion Characteristics
  12. 132
    “…Prions are transmissible agents causing lethal neurodegenerative diseases that are composed of aggregates of misfolded cellular prion protein (PrP(Sc)). …”
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    Isolation of infectious, non-fibrillar and oligomeric prions from a genetic prion disease
  13. 133
    “…The use of yeast systems to study the propagation of prions and amyloids has emerged as a crucial aspect of the global endeavor to understand those mechanisms. …”
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    A unifying model for the propagation of prion proteins in yeast brings insight into the [PSI(+)] prion
  14. 134
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    Erratum to: Porcine Prion Protein as a Paradigm of Limited Susceptibility to Prion Strain Propagation
  15. 135
    “…Corruption of cellular prion protein (PrP(C)) function(s) at the plasma membrane of neurons is at the root of prion diseases, such as Creutzfeldt-Jakob disease and its variant in humans, and Bovine Spongiform Encephalopathies, better known as mad cow disease, in cattle. …”
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    Loss of prion protein control of glucose metabolism promotes neurodegeneration in model of prion diseases
  16. 136
    “…Prion replication is believed to be the cause of the neurotoxicity that arises during prion disease pathogenesis. …”
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    Prion disease modelled in Drosophila
  17. 137
    “…Prions cause fatal and transmissible neurodegenerative disease. …”
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    The Expanding Universe of Prion Diseases
  18. 138
    por Wells, William A.
    Publicado 2002
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    An unlikely culprit in prion diseases
  19. 139
    “…Some of the early events following scrapie infection take place in the lymphoreticular system (LRS) and result in significant replication of prions in lymphoid organs. The identity of the cells in the LRS that produce prions and their role in neuroinvasion are still unknown. …”
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    Studies on Prion Replication in Spleen
  20. 140
    por Leslie, Mitch
    Publicado 2008
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    Prions show their good side
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