Early preclinical detection of prions in the skin of prion-infected animals von Wang, Zerui, Manca, Matteo, Foutz, Aaron, Camacho, Manuel V., Raymond, Gregory J., Race, Brent, Orru, Christina D., Yuan, Jue, Shen, Pingping, Li, Baiya, Lang, Yue, Dang, Johnny, Adornato, Alise, Williams, Katie, Maurer, Nicholas R., Gambetti, Pierluigi, Xu, Bin, Surewicz, Witold, Petersen, Robert B., Dong, Xiaoping, Appleby, Brian S., Caughey, Byron, Cui, Li, Kong, Qingzhong, Zou, Wen-Quan

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Amyloid fibrils from the N-terminal prion protein fragment are infectious von Choi, Jin-Kyu, Cali, Ignazio, Surewicz, Krystyna, Kong, Qingzhong, Gambetti, Pierluigi, Surewicz, Witold K.

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Novel Strain of the Chronic Wasting Disease Agent Isolated From Experimentally Inoculated Elk With LL132 Prion Protein von Moore, Jo, Tatum, Trudy, Hwang, Soyoun, Vrentas, Catherine, West Greenlee, M. Heather, Kong, Qingzhong, Nicholson, Eric, Greenlee, Justin

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Mammalian Prions Generated from Bacterially Expressed Prion Protein in the Absence of Any Mammalian Cofactors von Kim, Jae-Il, Cali, Ignazio, Surewicz, Krystyna, Kong, Qingzhong, Raymond, Gregory J., Atarashi, Ryuichiro, Race, Brent, Qing, Liuting, Gambetti, Pierluigi, Caughey, Byron, Surewicz, Witold K.

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Artificial strain of human prions created in vitro von Kim, Chae, Xiao, Xiangzhu, Chen, Shugui, Haldiman, Tracy, Smirnovas, Vitautas, Kofskey, Diane, Warren, Miriam, Surewicz, Krystyna, Maurer, Nicholas R., Kong, Qingzhong, Surewicz, Witold, Safar, Jiri G.

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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 von Ding, Mingxuan, Teruya, Kenta, Zhang, Weiguanliu, Lee, Hae Weon, Yuan, Jue, Oguma, Ayumi, Foutz, Aaron, Camacho, Manuel V., Mitchell, Marcus, Greenlee, Justin J., Kong, Qingzhong, Doh-ura, Katsumi, Cui, Li, Zou, Wen-Quan

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Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein von Zou, Wen-Quan, Puoti, Gianfranco, Xiao, Xiangzhu, Yuan, Jue, Qing, Liuting, Cali, Ignazio, Shimoji, Miyuki, Langeveld, Jan P.M., Castellani, Rudy, Notari, Silvio, Crain, Barbara, Schmidt, Robert E., Geschwind, Michael, DeArmond, Stephen J., Cairns, Nigel J., Dickson, Dennis, Honig, Lawrence, Torres, Juan Maria, Mastrianni, James, Capellari, Sabina, Giaccone, Giorgio, Belay, Ermias D., Schonberger, Lawrence B., Cohen, Mark, Perry, George, Kong, Qingzhong, Parchi, Piero, Tagliavini, Fabrizio, Gambetti, Pierluigi

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Molecular biology and pathology of prion strains in sporadic human prion diseases von Gambetti, Pierluigi, Cali, Ignazio, Notari, Silvio, Kong, Qingzhong, Zou, Wen-Quan, Surewicz, Witold K.

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A novel human disease with abnormal prion protein sensitive to protease von Gambetti, Pierluigi, Dong, Zhiqian, Yuan, Jue, Xiao, Xiangzhu, Zheng, Mengjie, Alshekhlee, Amer, Castellani, Rudy, Cohen, Mark, Barria, Marcelo A., Gonzalez-Romero, D., Belay, Ermias D., Schonberger, Lawrence B., Marder, Karen, Harris, Carrie, Burke, James R., Montine, Thomas, Wisniewski, Thomas, Dickson, Dennis W., Soto, Claudio, Hulette, Christine M., Mastrianni, James A., Kong, Qingzhong, Zou, Wen-Quan

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An Ex Vivo Brain Slice Culture Model of Chronic Wasting Disease: Implications for Disease Pathogenesis and Therapeutic Development von Kondru, Naveen, Manne, Sireesha, Kokemuller, Robyn, Greenlee, Justin, Greenlee, M. Heather West, Nichols, Tracy, Kong, Qingzhong, Anantharam, Vellareddy, Kanthasamy, Arthi, Halbur, Patrick, Kanthasamy, Anumantha G.

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Glycans are not necessary to maintain the pathobiological features of bovine spongiform encephalopathy von Otero, Alicia, Barrio, Tomás, Eraña, Hasier, Charco, Jorge M, Betancor, Marina, Díaz-Domínguez, Carlos M, Marín, Belén, Andréoletti, Olivier, Torres, Juan M, Kong, Qingzhong, Badiola, Juan J, Bolea, Rosa, Castilla, Joaquín

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Transmission characteristics of variably protease-sensitive prionopathy von Notari, Silvio, Xiao, Xiangzhu, Espinosa, Juan Carlos, Cohen, Yvonne, Qing, Liuting, Aguilar-Calvo, Patricia, Kofskey, Diane, Cali, Ignazio, Cracco, Laura, Kong, Qingzhong, Torres, Juan Maria, Zou, Wenquan, Gambetti, Pierluigi

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Generation of human chronic wasting disease in transgenic mice von Wang, Zerui, Qin, Kefeng, Camacho, Manuel V, Cali, Ignazio, Yuan, Jue, Shen, Pingping, Greenlee, Justin, Kong, Qingzhong, Mastrianni, James A, Zou, Wen-Quan

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Characterization of Anchorless Human PrP With Q227X Stop Mutation Linked to Gerstmann-Sträussler-Scheinker Syndrome In Vivo and In Vitro von Shen, Pingping, Dang, Johnny, Wang, Zerui, Zhang, Weiguanliu, Yuan, Jue, Lang, Yue, Ding, Mingxuan, Mitchell, Marcus, Kong, Qingzhong, Feng, Jiachun, Rozemuller, Annemiek J. M., Cui, Li, Petersen, Robert B., Zou, Wen-Quan

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Prion protein (PrP) knock-out mice show altered iron metabolism: a functional role for PrP in iron uptake and transport von Singh, Ajay, Kong, Qingzhong, Luo, Xiu, Petersen, Robert B, Meyerson, Howard, Singh, Neena

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A minimally invasive biomarker for sensitive and accurate diagnosis of Parkinson's disease von Wang, Zerui, Gilliland, Tricia, Kim, Hyun Jo, Gerasimenko, Maria, Sajewski, Kailey, Camacho, Manuel V, Bebek, Gurkan, Chen, Shu G, Gunzler, Steven A, Kong, Qingzhong

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Publisher Correction: Early preclinical detection of prions in the skin of prion-infected animals von Wang, Zerui, Manca, Matteo, Foutz, Aaron, Camacho, Manuel V., Raymond, Gregory J., Race, Brent, Orru, Christina D., Yuan, Jue, Shen, Pingping, Li, Baiya, Lang, Yue, Dang, Johnny, Adornato, Alise, Williams, Katie, Maurer, Nicholas R., Gambetti, Pierluigi, Xu, Bin, Surewicz, Witold, Petersen, Robert B., Dong, Xiaoping, Appleby, Brian S., Caughey, Byron, Cui, Li, Kong, Qingzhong, Zou, Wen-Quan

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Change in the characteristics of ferritin induces iron imbalance in prion disease affected brains von Singh, Ajay, Qing, Liuting, Kong, Qingzhong, Singh, Neena

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Small Protease Sensitive Oligomers of PrPSc in Distinct Human Prions Determine Conversion Rate of PrPC von Kim, Chae, Haldiman, Tracy, Surewicz, Krystyna, Cohen, Yvonne, Chen, Wei, Blevins, Janis, Sy, Man-Sun, Cohen, Mark, Kong, Qingzhong, Telling, Glenn C., Surewicz, Witold K., Safar, Jiri G.

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CWD prions remain infectious after passage through the digestive system of coyotes (Canis latrans) von Nichols, Tracy A, Fischer, Justin W, Spraker, Terry R, Kong, Qingzhong, VerCauteren, Kurt C

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