Characterization of Truncated Forms of Abnormal Prion Protein in Creutzfeldt-Jakob Disease

Documenti analoghi

• Analysis of Conformational Stability of Abnormal Prion Protein Aggregates across the Spectrum of Creutzfeldt-Jakob Disease Prions
  di: Cescatti, Maura, et al.
  Pubblicazione: (2016)
• Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrP(Sc) types: an updated classification
  di: Parchi, Piero, et al.
  Pubblicazione: (2009)
• Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease
  di: Parchi, Piero, et al.
  Pubblicazione: (2010)
• Detection of prions in skin punch biopsies of Creutzfeldt–Jakob disease patients
  di: Mammana, Angela, et al.
  Pubblicazione: (2020)
• Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics
  di: Cali, Ignazio, et al.
  Pubblicazione: (2009)