Wen-Quan Zou
Affiliations: | Case Western Reserve University, Cleveland Heights, OH, United States |
Website:
http://www.case.edu/med/pathology/faculty/zou.htmlGoogle:
"Wen-Quan Zou"Mean distance: 106866
Cross-listing: Neuropathology Tree
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Publications
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| Zhang W, Orrú CD, Foutz A, et al. (2024) Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseases. Acta Neuropathologica. 147: 17 |
| Jeong MJ, Wang Z, Zou WQ, et al. (2023) The first report of polymorphisms of the prion protein gene () in Pekin ducks (). Frontiers in Veterinary Science. 10: 1273050 |
| Myers RR, John A, Zhang W, et al. (2023) Y225A induces long-range conformational changes in human prion protein that are protective in Drosophila. The Journal of Biological Chemistry. 104881 |
| Wood AR, Foliaki ST, Groveman BR, et al. (2022) Hereditary E200K mutation within the prion protein gene alters human iPSC derived cardiomyocyte function. Scientific Reports. 12: 15788 |
| Wang Z, Qin K, Camacho MV, et al. (2021) Generation of human chronic wasting disease in transgenic mice. Acta Neuropathologica Communications. 9: 158 |
| Trichka J, Zou WQ. (2021) Modulation of Neuroinflammation by the Gut Microbiota in Prion and Prion-Like Diseases. Pathogens (Basel, Switzerland). 10 |
| Ding M, Teruya K, Zhang W, et al. (2021) Decrease in Skin Prion-Seeding Activity of Prion-Infected Mice Treated with a Compound Against Human and Animal Prions: a First Possible Biomarker for Prion Therapeutics. Molecular Neurobiology |
| Zhang W, Xiao X, Ding M, et al. (2021) Further Characterization of Glycoform-Selective Prions of Variably Protease-Sensitive Prionopathy. Pathogens (Basel, Switzerland). 10 |
| Shen P, Dang J, Wang Z, et al. (2020) Characterization of Anchorless Human PrP With Q227X Stop Mutation Linked to Gerstmann-Sträussler-Scheinker Syndrome In Vivo and In Vitro. Molecular Neurobiology |
| Foliaki ST, Groveman BR, Yuan J, et al. (2020) Pathogenic Prion Protein Isoforms Are Not Present in Cerebral Organoids Generated from Asymptomatic Donors Carrying the E200K Mutation Associated with Familial Prion Disease. Pathogens (Basel, Switzerland). 9 |