Prion

Combining autophagy stimulators and cellulose ethers for therapy against prion disease

In vitro generation of tau aggregates conformationally distinct from parent tau seeds of Alzheimer’s brain

Amyloid properties of the yeast cell wall protein Toh1 and its interaction with prion proteins Rnq1 and Sup35

Clinicopathological findings of an MM2-cortical-type sporadic Creutzfeldt-Jakob disease patient with cortical blindness during a course of glaucoma and age-related macular degeneration

Use of faecal volatile organic compound analysis for ante-mortem discrimination between CWD-positive, -negative exposed, and -known negative white-tailed deer (Odocoileus virginianus)

Enrichment of miR-126 enhances the effects of endothelial progenitor cell–derived microvesicles on modulating MC3T3-E1 cell function via Erk1/2-Bcl-2 signalling pathway

Clinical features and genetic characteristics of two Chinese pedigrees with fatal family insomnia

Deciphering the BSE-type specific cell and tissue tropisms of atypical (H and L) and classical BSE

Axonal changes in experimental prion diseases recapitulate those following constriction of postganglionic branches of the superior cervical ganglion: a comparison 40 years later

A case of V180I genetic Creutzfeldt-Jakob disease presenting with conspicuous facial mimicry

Rodent models allow BSE discrimination of goat prions and reveal geographical differences in the biological properties of scrapie

Sensitivity and specificity evaluation of multiple neurodegenerative proteins for Creutzfeldt-Jakob disease diagnosis using a deep-learning approach

Sodium hydroxide treatment effectively inhibits PrPCWD replication in farm soil

Michael Ter-Avanesyan (1949-2018) – Advent of the scientist

Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report

Significant enhanced expressions of aquaporin-1, -4 and -9 in the brains of various prion diseases

Michael Ter-Avanesyan (1949-2018) - life in science

An autopsied case of MM1-type sporadic Creutzfeldt-Jakob disease with pathology of Wernicke encephalopathy

THERPA v2: an update of a small molecule database related to prion protein regulation and prion disease progression

The worst is yet to come: probable sporadic Creutzfeldt–Jakob disease in a well-controlled HIV patient

Prion-dependent proteome remodeling in response to environmental stress is modulated by prion variant and genetic background

The insomnia phenotype in genetic Creutzfeldt–Jakob disease based on the E200K mutation