Wen-Quan Zou

Department of Pathology, Case Western Reserve University School of Medicine

Affiliated withCase Western Reserve University School of Medicine

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 7	2012

Other Publications

Article	Year
Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form. The Journal of biological chemistry\| PubMed ID: 12161431	2002
A prion protein epitope selective for the pathologically misfolded conformation. Nature medicine\| PubMed ID: 12778138	2003
Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease. The Journal of biological chemistry\| PubMed ID: 12917418	2003
Antibody to DNA detects scrapie but not normal prion protein. Proceedings of the National Academy of Sciences of the United States of America\| PubMed ID: 14734804	2004
Concealment of epitope by reduction and alkylation in prion protein. Biochemical and biophysical research communications\| PubMed ID: 15596149	2005
Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine. The Journal of neuroscience : the official journal of the Society for Neuroscience\| PubMed ID: 15601934	2004
From microbes to prions the final proof of the prion hypothesis. Cell\| PubMed ID: 15851020	2005
Variant Creutzfeldt-Jakob disease death, United States. Emerging infectious diseases\| PubMed ID: 16229761	2005
Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD. The American journal of pathology\| PubMed ID: 16314483	2005
A prion disease--possible Gerstmann-Straussler-Scheinker disease: a case report. Journal of computer assisted tomography\| PubMed ID: 16365589	2006
Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain : a journal of neurology\| PubMed ID: 16923954	2006
Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains. The Journal of biological chemistry\| PubMed ID: 16987816	2006
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. Journal of virology\| PubMed ID: 18234793	2008
A novel human disease with abnormal prion protein sensitive to protease. Annals of neurology\| PubMed ID: 18571782	2008
Sporadic fatal insomnia masquerading as a paraneoplastic cerebellar syndrome. Archives of neurology\| PubMed ID: 18625868	2008
Creutzfeldt-Jakob disease in recipients of corneal transplants. Cornea\| PubMed ID: 18650677	2008
Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. The Journal of biological chemistry\| PubMed ID: 18753138	2008
Toxic effects of intracerebral PrP antibody administration during the course of BSE infection in mice. Prion\| PubMed ID: 19164902	2007
Variant Creutzfeldt-Jakob disease: French versus British. Annals of neurology\| PubMed ID: 19334065	2009
Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease. The American journal of pathology\| PubMed ID: 19349373	2009
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. Brain : a journal of neurology\| PubMed ID: 19734292	2009
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States. PloS one\| PubMed ID: 20098730	2010
PrP conformational transitions alter species preference of a PrP-specific antibody. The Journal of biological chemistry\| PubMed ID: 20194495	2010
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Annals of neurology\| PubMed ID: 20695009	2010
Sequence-dependent prion protein misfolding and neurotoxicity. The Journal of biological chemistry\| PubMed ID: 20817727	2010
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. Brain : a journal of neurology\| PubMed ID: 20823086	2010
Molecular biology and pathology of prion strains in sporadic human prion diseases. Acta neuropathologica\| PubMed ID: 21058033	2011
Amyloid-beta42 interacts mainly with insoluble prion protein in the Alzheimer brain. The Journal of biological chemistry\| PubMed ID: 21393248	2011
Variably protease-sensitive prionopathy: a novel disease of the prion protein. Journal of molecular neuroscience : MN\| PubMed ID: 21584652	2011
Insoluble cellular prion protein and its association with prion and Alzheimer diseases. Prion\| PubMed ID: 21847014	2011
Pulling rabbits to reveal the secrets of the prion protein. Communicative & integrative biology\| PubMed ID: 21980555	2011
Characterization of spontaneously generated prion-like conformers in cultured cells. Aging\| PubMed ID: 21990137	2011
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report. BMC neurology\| PubMed ID: 22040318	2011
Alkylating antitumor drug mechlorethamine conceals a structured PrP domain and inhibits in vitro prion amplification. Journal of toxicology and environmental health. Part A\| PubMed ID: 22043910	2011
Cellular prion protein is essential for oligomeric amyloid-Î²-induced neuronal cell death. Human molecular genetics\| PubMed ID: 22100763	2012
Creutzfeldt-Jakob disease with unusually extensive neuropathology in a child treated with native human growth hormone. Clinical neuropathology\| PubMed ID: 22551916	2012
Sporadic fatal insomnia with clinical, laboratory, and genetic findings. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia\| PubMed ID: 22717776	2012