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  1. 261
    Recombinant prion protein refolded with lipid and RNA has the biochemical hallmarks of a prion but lacks in vivo infectivity.
    “...During prion infection, the normal, protease-sensitive conformation of prion protein (PrP(C...”
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  2. 262
    Exploration of the main sites for the transformation of normal prion protein (PrPC) into pathogenic prion protein (PrPsc)
    Subjects: “...prion proteins...”
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    Article
  3. 263
    D159 and S167 are protective residues in the prion protein from dog and horse, two prion-resistant animals
    Subjects: “...Prion protein...”
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  4. 264
    Reversible symptoms and clearance of mutant prion protein in an inducible model of a genetic prion disease in Drosophila melanogaster
    by A. Murali, R.A. Maue, P.J. Dolph
    Published 2014-07-01
    Subjects: “...Clearance of misfolded prion protein...”
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  5. 265
    Prion protein post-translational modifications modulate heparan sulfate binding and limit aggregate size in prion disease
    “.... In prion disease, the N-linked glycans and GPI-anchor on the prion protein (PrP) impair fibril assembly...”
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  6. 266
    Mouse-hamster chimeric prion protein (PrP) devoid of N-terminal residues 23-88 restores susceptibility to 22L prions, but not to RML prions in PrP-knockout mice.
    “...Prion infection induces conformational conversion of the normal prion protein PrPC...”
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  7. 267
    Follicular dendritic cell-specific prion protein (PrP) expression alone is sufficient to sustain prion infection in the spleen.
    “...Prion diseases are characterised by the accumulation of PrP(Sc), an abnormally folded isoform...”
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  8. 268
    Deep conservation of prion-like composition in the eukaryotic prion-former Pub1/Tia1 family and its relatives
    by Wan-Chun Su, Paul M. Harrison
    Published 2020-04-01
    Subjects: “...Prion...”
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    Article
  9. 269
    Fatal transmissible amyloid encephalopathy: a new type of prion disease associated with lack of prion protein membrane anchoring.
    “...Prion diseases are fatal neurodegenerative diseases of humans and animals characterized by gray...”
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    Article
  10. 270
    Transmissibility of atypical scrapie in ovine transgenic mice: major effects of host prion protein expression and donor prion genotype.
    “... of the protease-resistant prion protein PrP(res) and the genetic factors involved in susceptibility to the disease...”
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    Article
  11. 271
    Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains.
    “...Prions propagate as multiple strains in a wide variety of mammalian species. The detection of all...”
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    Article
  12. 272
    The N-terminal sequence of prion protein consists an epitope specific to the abnormal isoform of prion protein (PrP(Sc)).
    “...The conformation of abnormal prion protein (PrP(Sc)) differs from that of cellular prion protein...”
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    Article
  13. 273
    The toxicity of a mutant prion protein is cell-autonomous, and can be suppressed by wild-type prion protein on adjacent cells.
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    Article
  14. 274
    Das zelluläre Prion-Protein als Mediator der Scrapie-Prion-Protein- und Amyloid Beta-induzierten Neurotoxizität
    by Resenberger, Ulrike
    Published 2012
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  15. 275
    Recent Advances in Understanding Mammalian Prion Structure: A Mini Review
    by Cassandra Terry, Jonathan D. F. Wadsworth
    Published 2019-07-01
    Subjects: “...prion disease...”
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    Article
  16. 276
    The mechanism of toxicity in HET-S/HET-s prion incompatibility.
    “...The HET-s protein from the filamentous fungus Podospora anserina is a prion involved in a cell...”
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    Article
  17. 277
    Regulation of embryonic cell adhesion by the prion protein.
    “...Prion proteins (PrPs) are key players in fatal neurodegenerative disorders, yet their physiological...”
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    Article
  18. 278
    Chronic wasting disease--prion disease in the wild.
    by Steve Bunk
    Published 2004-04-01
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  19. 279
    The mutational landscape of a prion-like domain
    “... to measure the toxicity of more than 50,000 mutations in the prion domain of TDP43, the authors conclude...”
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  20. 280
    Artificial strain of human prions created in vitro
    “...Synthetic prions have previously been generated from recombinant rodent PrP. Here the authors...”
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