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Amyloid fibrils from the N-terminal prion protein fragment are infectious.
Choi JK, Cali I, Surewicz K, Kong Q, Gambetti P, Surewicz WK. Choi JK, et al. Among authors: cali i. Proc Natl Acad Sci U S A. 2016 Nov 29;113(48):13851-13856. doi: 10.1073/pnas.1610716113. Epub 2016 Nov 14. Proc Natl Acad Sci U S A. 2016. PMID: 27849581 Free PMC article.
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain.
Kong Q, Zheng M, Casalone C, Qing L, Huang S, Chakraborty B, Wang P, Chen F, Cali I, Corona C, Martucci F, Iulini B, Acutis P, Wang L, Liang J, Wang M, Li X, Monaco S, Zanusso G, Zou WQ, Caramelli M, Gambetti P. Kong Q, et al. Among authors: cali i. J Virol. 2008 Apr;82(7):3697-701. doi: 10.1128/JVI.02561-07. Epub 2008 Jan 30. J Virol. 2008. PMID: 18234793 Free PMC article.
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.
Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, Shimoji M, Langeveld JP, Castellani R, Notari S, Crain B, Schmidt RE, Geschwind M, Dearmond SJ, Cairns NJ, Dickson D, Honig L, Torres JM, Mastrianni J, Capellari S, Giaccone G, Belay ED, Schonberger LB, Cohen M, Perry G, Kong Q, Parchi P, Tagliavini F, Gambetti P. Zou WQ, et al. Among authors: cali i. Ann Neurol. 2010 Aug;68(2):162-72. doi: 10.1002/ana.22094. Ann Neurol. 2010. PMID: 20695009 Free PMC article.
339 results