Jue Yuan

Concealment of epitope by reduction and alkylation in prion protein.

Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models.

Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.

Classification of sporadic Creutzfeldt-Jakob disease revisited.

Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains.

A novel human disease with abnormal prion protein sensitive to protease.

Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.

PrP conformational transitions alter species preference of a PrP-specific antibody.

Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.

Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain.

Insoluble cellular prion protein and its association with prion and Alzheimer diseases.

Characterization of spontaneously generated prion-like conformers in cultured cells.

Alkylating antitumor drug mechlorethamine conceals a structured PrP domain and inhibits in vitro prion amplification.