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  1. 141
    Interaction networks of prion, prionogenic and prion-like proteins in budding yeast, and their role in gene regulation.
    by Djamel Harbi, Paul M Harrison
    Published 2014-01-01
    “...Prions are transmissible, propagating alternative states of proteins. Prions in budding yeast...”
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    Article
  2. 142
    Effects of solution chemistry and aging time on prion protein adsorption and replication of soil-bound prions.
    “...Prion interactions with soil may play an important role in the transmission of chronic wasting...”
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    Article
  3. 143
    Prion peptide uptake in microglial cells--the effect of naturally occurring autoantibodies against prion protein.
    “...In prion disease, a profound microglial activation that precedes neurodegeneration has been...”
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    Article
  4. 144
    Genesis of mammalian prions: from non-infectious amyloid fibrils to a transmissible prion disease.
    “...The transmissible agent of prion disease consists of a prion protein in its abnormal, β-sheet rich...”
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    Article
  5. 145
    From Seeds to Fibrils and Back: Fragmentation as an Overlooked Step in the Propagation of Prions and Prion-Like Proteins
    Subjects: “...prion diseases...”
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    Article
  6. 146
    Protease resistance of infectious prions is suppressed by removal of a single atom in the cellular prion protein.
    “...Resistance to proteolytic digestion has long been considered a defining trait of prions in tissues...”
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    Article
  7. 147
    Spontaneous variants of the [RNQ+] prion in yeast demonstrate the extensive conformational diversity possible with prion proteins.
    by Vincent J Huang, Kevin C Stein, Heather L True
    Published 2013-01-01
    “...Prion strains (or variants) are structurally distinct amyloid conformations arising from a single...”
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    Article
  8. 148
    Destabilizing polymorphism in cervid prion protein hydrophobic core determines prion conformation and conversion efficiency.
    “...Prion diseases are infectious neurodegenerative disorders of humans and animals caused by misfolded...”
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    Article
  9. 149
    Classical Bovine Spongiform Encephalopathy by Transmission of H-Type Prion in Homologous Prion Protein Context
    Subjects: “...prion strain...”
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    Article
  10. 150
    YEAST PRION PROTEIN Ure2p – A USEFUL MODEL FOR HUMAN PRION DISEASES.
    Subjects: “...Prion-Induced Disorders...”
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    Article
  11. 151
    Prion induction involves an ancient system for the sequestration of aggregated proteins and heritable changes in prion fragmentation
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    Article
  12. 152
    Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein
    “...Abstract Human familial prion diseases are associated with mutations at 34 different prion protein...”
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    Article
  13. 153
    Genetic predictions of prion disease susceptibility in carnivore species based on variability of the prion gene coding region.
    “...Mammalian species vary widely in their apparent susceptibility to prion diseases. For example...”
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    Article
  14. 154
    Quaternary structure of pathological prion protein as a determining factor of strain-specific prion replication dynamics.
    “...Prions are proteinaceous infectious agents responsible for fatal neurodegenerative diseases...”
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    Article
  15. 155
    Strain-Dependent Prion Infection in Mice Expressing Prion Protein with Deletion of Central Residues 91–106
    Subjects: “...prions...”
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    Article
  16. 156
    Oral Ingestion of Synthetically Generated Recombinant Prion Is Sufficient to Cause Prion Disease in Wild-Type Mice
    Subjects: “...prion...”
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    Article
  17. 157
    Double-Edge Sword of Sustained ROCK Activation in Prion Diseases through Neuritogenesis Defects and Prion Accumulation.
    “...In prion diseases, synapse dysfunction, axon retraction and loss of neuronal polarity precede...”
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    Article
  18. 158
    Insight From Animals Resistant to Prion Diseases: Deciphering the Genotype – Morphotype – Phenotype Code for the Prion Protein
    Subjects: “...prion disease...”
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    Article
  19. 159
    Prion protein modulates cellular iron uptake: a novel function with implications for prion disease pathogenesis.
    “...Converging evidence leaves little doubt that a change in the conformation of prion protein (PrP(C...”
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    Article
  20. 160
    Prion protein amino acid determinants of differential susceptibility and molecular feature of prion strains in mice and voles.
    “...The bank vole is a rodent susceptible to different prion strains from humans and various animal...”
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    Article
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