Wen-Quan Zou

Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form.

A prion protein epitope selective for the pathologically misfolded conformation.

Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease.

Antibody to DNA detects scrapie but not normal prion protein.

Concealment of epitope by reduction and alkylation in prion protein.

Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine.

From microbes to prions the final proof of the prion hypothesis.

Variant Creutzfeldt-Jakob disease death, United States.

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

A prion disease--possible Gerstmann-Straussler-Scheinker disease: a case report.

Classification of sporadic Creutzfeldt-Jakob disease revisited.

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

Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain.

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

Sporadic fatal insomnia masquerading as a paraneoplastic cerebellar syndrome.

Creutzfeldt-Jakob disease in recipients of corneal transplants.

Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease.

Toxic effects of intracerebral PrP antibody administration during the course of BSE infection in mice.

Variant Creutzfeldt-Jakob disease: French versus British.

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.

Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.

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

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

Sequence-dependent prion protein misfolding and neurotoxicity.

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.

Molecular biology and pathology of prion strains in sporadic human prion diseases.

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

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

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

Pulling rabbits to reveal the secrets of the prion protein.

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

Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report.

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

Cellular prion protein is essential for oligomeric amyloid-β-induced neuronal cell death.

Creutzfeldt-Jakob disease with unusually extensive neuropathology in a child treated with native human growth hormone.

Sporadic fatal insomnia with clinical, laboratory, and genetic findings.