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Page 1
Generation of human chronic wasting disease in transgenic mice.
Wang Z, Qin K, Camacho MV, Cali I, Yuan J, Shen P, Greenlee J, Kong Q, Mastrianni JA, Zou WQ. Wang Z, et al. Among authors: mastrianni ja. Acta Neuropathol Commun. 2021 Sep 26;9(1):158. doi: 10.1186/s40478-021-01262-y. Acta Neuropathol Commun. 2021. PMID: 34565488 Free PMC article.
A novel human disease with abnormal prion protein sensitive to protease.
Gambetti P, Dong Z, Yuan J, Xiao X, Zheng M, Alshekhlee A, Castellani R, Cohen M, Barria MA, Gonzalez-Romero D, Belay ED, Schonberger LB, Marder K, Harris C, Burke JR, Montine T, Wisniewski T, Dickson DW, Soto C, Hulette CM, Mastrianni JA, Kong Q, Zou WQ. Gambetti P, et al. Among authors: mastrianni ja. Ann Neurol. 2008 Jun;63(6):697-708. doi: 10.1002/ana.21420. Ann Neurol. 2008. PMID: 18571782 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. Ann Neurol. 2010 Aug;68(2):162-72. doi: 10.1002/ana.22094. Ann Neurol. 2010. PMID: 20695009 Free PMC article.
Early Delivery of Misfolded PrP from ER to Lysosomes by Autophagy.
Cortes CJ, Qin K, Norstrom EM, Green WN, Bindokas VP, Mastrianni JA. Cortes CJ, et al. Among authors: mastrianni ja. Int J Cell Biol. 2013;2013:560421. doi: 10.1155/2013/560421. Epub 2013 Dec 17. Int J Cell Biol. 2013. PMID: 24454378 Free PMC article.
Impaired transmissibility of atypical prions from genetic CJDG114V.
Cali I, Mikhail F, Qin K, Gregory C, Solanki A, Martinez MC, Zhao L, Appleby B, Gambetti P, Norstrom E, Mastrianni JA. Cali I, et al. Among authors: mastrianni ja. Neurol Genet. 2018 Aug 7;4(4):e253. doi: 10.1212/NXG.0000000000000253. eCollection 2018 Aug. Neurol Genet. 2018. PMID: 30109268 Free PMC article.
A novel PRNP-G131R variant associated with familial prion disease.
Alshaikh JT, Qin K, Zhao L, Mastrianni JA. Alshaikh JT, et al. Among authors: mastrianni ja. Neurol Genet. 2020 Jun 5;6(4):e454. doi: 10.1212/NXG.0000000000000454. eCollection 2020 Aug. Neurol Genet. 2020. PMID: 32637633 Free PMC article. No abstract available.
59 results