Xiangzhu Xiao

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

High-performance affinity chromatography with immobilization of protein A and L-histidine on molded monolith.

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.

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.

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

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.