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PrPSc Proteins Summary

Description: Abnormal isoform of prion proteins (PRIONS) resulting from a posttranslational modification of the cellular prion protein (PRPC PROTEINS). PrPSc are disease-specific proteins seen in certain human and animal neurodegenerative diseases (PRION DISEASES).

Also Known As: HaSp 33-37; PrP (CJD); PrP (GSS); PrP 33-35; PrP-res Show All >>

Networked: 403 relevant articles (5 outcomes, 44 trials/studies) for this Bio-Agent

Key Diseases for which PrPSc Proteins is Relevant

  1. Scrapie : 2 outcomes 22 studies in 174 results
  2. Prion Diseases (Transmissible Spongiform Encephalopathies) : 1 outcome 7 studies in 115 results
  3. Creutzfeldt-Jakob Syndrome (Creutzfeldt-Jakob Disease) : 1 outcome 3 studies in 41 results
  4. Disease Susceptibility (Diathesis) : 1 outcome in 2 results
  5. Infection : 13 studies in 84 results
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Drugs Related to PrPSc Proteins

  1. Amphotericin B (Amphotericin)
  2. MS 8209
  3. PrPC Proteins
  4. PrPSc Proteins
  5. Prions
  6. Haemophilus influenzae type b-polysaccharide vaccine-diphtheria toxoid conjugate
  7. Soil
  8. Stainless Steel (Steel, Stainless)
  9. Peptide Fragments
  10. Nucleic Acids
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Therapies Related to PrPSc Proteins

  1. Surgical Instruments (Clip)
  2. Therapeutics
  3. Splenectomy
  4. Intraperitoneal Injections
  5. Hyperbaric Oxygenation

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