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  1. 241
    Folding, Misfolding and Therapeutics in Prion Diseases
    by Spagnolli, Giovanni
    Published 2021
    “...Prion diseases are rare neurodegenerative disorders affecting humans and other animals, caused by a...”
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    Doctoral Thesis
  2. 242
    Correction: Fishing for Prion Protein Function.
    Published 2014-06-01
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    Article
  3. 243
    Yeast prions: protein aggregation is not enough.
    by Michael Y Sherman
    Published 2004-04-01
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    Article
  4. 244
    Changes in sympathetic activity in prion neuroinvasion
    Subjects: “...Prion disease...”
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    Article
  5. 245
    The metabolism of glycosaminoglycans is impaired in prion diseases
    Subjects: “...Prion diseases...”
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    Article
  6. 246
    Prion Diseases: What Is the Neurotoxic Molecule?
    by Roberto Chiesa, David A. Harris
    Published 2001-10-01
    “... of prions, the infectious agents responsible for transmissible spongiform encephalopathies. In contrast...”
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    Article
  7. 247
    Complement activation in human prion disease
    Subjects: “...Prion disease...”
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    Article
  8. 248
    PrPSc Prions: State of the Art
    Published 2018
    Subjects: “...Prion diseases...”
    Open Access: DOAB: description of the publication
    Open Access: DOAB, download the publication
    eBook
  9. 249
    Prions, protein homeostasis, and phenotypic diversity
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    Article
  10. 250
    PMCA-generated prions from the olfactory mucosa of patients with Fatal Familial Insomnia cause prion disease in mice
    Subjects: “...prion...”
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    Article
  11. 251
    Correction: Prion Protein Modulates Cellular Iron Uptake: A Novel Function with Implications for Prion Disease Pathogenesis
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    Article
  12. 252
    From Prions to Stress Granules: Defining the Compositional Features of Prion-Like Domains That Promote Different Types of Assemblies
    by Anastasia Fomicheva, Eric D. Ross
    Published 2021-01-01
    Subjects: “...prion...”
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    Article
  13. 253
    Medial Temporal Lobe Involvement in Human Prion Diseases: Implications for the Study of Focal Non Prion Neurodegenerative Pathology
    Subjects: “...human prion diseases...”
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    Article
  14. 254
    Molecular interactions between prions as seeds and recombinant prion proteins as substrates resemble the biological interspecies barrier in vitro.
    “...Prion diseases like Creutzfeldt-Jakob disease in humans, Scrapie in sheep or bovine spongiform...”
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    Article
  15. 255
    Peptide aptamer-mediated modulation of prion protein α-cleavage as treatment strategy for prion and other neurodegenerative diseases
    by Antonia N Klein, Erica Corda, Sabine Gilch
    Published 2018-01-01
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    Article
  16. 256
    Identification of Prion Disease-Related Somatic Mutations in the Prion Protein Gene (<i>PRNP)</i> in Cancer Patients
    by Yong-Chan Kim, Sae-Young Won, Byung-Hoon Jeong
    Published 2020-06-01
    Subjects: “...prion...”
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    Article
  17. 257
    Biological and biochemical characterization of mice expressing prion protein devoid of the octapeptide repeat region after infection with prions.
    “...Accumulating lines of evidence indicate that the N-terminal domain of prion protein (PrP...”
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    Article
  18. 258
    Disparate Modes of Evolution Shaped Modern Prion (PRNP) and Prion-Related Doppel (PRND) Variation in Domestic Cattle.
    “...Previous investigations aimed at determining whether the mammalian prion protein actually...”
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    Article
  19. 259
    Correction: Prion Protein Modulates Cellular Iron Uptake: A Novel Function with Implications for Prion Disease Pathogenesis.
    Get full text
    Article
  20. 260
    Evidence for varied aetiologies regulating the transmission of prion disease: implications for understanding the heritable basis of prion incubation times.
    “... disorders, triggered by abnormal folding of the endogenous prion protein molecule. The encoding gene is a...”
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    Article
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