• Thumbnail for Major prion protein
    major prion protein (PrP) is encoded in the human body by the PRNP gene also known as CD230 (cluster of differentiation 230). Expression of the protein is...
    45 KB (5,140 words) - 15:04, 28 September 2024
  • Thumbnail for Prion
    A prion /ˈpriːɒn/ is a misfolded protein that induces misfolding in normal variants of the same protein, leading to cellular death. Prions are responsible...
    99 KB (10,732 words) - 04:10, 18 October 2024
  • Thumbnail for Transmissible spongiform encephalopathy
    animal with no prion protein mutation. Inherited TSE occurs in animals carrying a rare mutant prion allele, which expresses prion proteins that contort...
    40 KB (4,438 words) - 02:05, 19 October 2024
  • Thumbnail for Creutzfeldt–Jakob disease
    abnormal folding of a protein known as a prion. Infectious prions are misfolded proteins that can cause normally folded proteins to also become misfolded...
    70 KB (7,661 words) - 01:26, 20 October 2024
  • Thumbnail for Kuru (disease)
    Kuru (disease) (category Prions)
    of a host-encoded protein called prion (PrP). Prion proteins are encoded by the Prion Protein Gene (PRNP). The two forms of prion are designated as PrPc...
    33 KB (3,726 words) - 14:21, 4 October 2024
  • Thumbnail for Scrapie
    accumulation of prions in the central nervous system, and immunohistochemical staining and ELISA can also be used to demonstrate the protein. No treatment...
    43 KB (5,035 words) - 18:55, 18 October 2024
  • Thumbnail for Fungal prion
    A fungal prion is a prion that infects hosts which are fungi. Fungal prions are naturally occurring proteins that can switch between multiple, structurally...
    23 KB (2,738 words) - 01:44, 4 September 2024
  • Thumbnail for Prion pseudoknot
    The prion pseudoknot is predicted RNA pseudoknot structure found in prion protein mRNA. It has been suggested that this element has a possible effect...
    2 KB (182 words) - 19:56, 15 September 2024
  • Thumbnail for Variant Creutzfeldt–Jakob disease
    following the onset of symptoms is 13 months. It is caused by prions, which are misfolded proteins. Spread is believed to be primarily due to eating beef infected...
    45 KB (4,536 words) - 08:20, 13 October 2024
  • Thumbnail for Gerstmann–Sträussler–Scheinker syndrome
    encephalopathies (TSE) due to the causative role played by PRNP, the human prion protein. GSS was first reported by the Austrian physicians Josef Gerstmann,...
    14 KB (1,426 words) - 04:26, 21 June 2024