Cali I - Search Results

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: cali i. 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.

2

Classification of sporadic Creutzfeldt-Jakob disease revisited.

Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P. Cali I, et al. Brain. 2006 Sep;129(Pt 9):2266-77. doi: 10.1093/brain/awl224. Brain. 2006. PMID: 16923954

3

Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains.

Yuan J, Xiao X, McGeehan J, Dong Z, Cali I, Fujioka H, Kong Q, Kneale G, Gambetti P, Zou WQ. Yuan J, et al. Among authors: cali i. J Biol Chem. 2006 Nov 17;281(46):34848-58. doi: 10.1074/jbc.M602238200. Epub 2006 Sep 20. J Biol Chem. 2006. PMID: 16987816 Free article.

4

Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions.

Yuan J, Dong Z, Guo JP, McGeehan J, Xiao X, Wang J, Cali I, McGeer PL, Cashman NR, Bessen R, Surewicz WK, Kneale G, Petersen RB, Gambetti P, Zou WQ. Yuan J, et al. Among authors: cali i. Cell Mol Life Sci. 2008 Feb;65(4):631-43. doi: 10.1007/s00018-007-7478-z. Cell Mol Life Sci. 2008. PMID: 18193391 Free PMC article.

5

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.

6

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.

Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, Langeveld JP, Parchi P, Safar JG, Zou WQ, Gambetti P. Cali I, et al. Brain. 2009 Oct;132(Pt 10):2643-58. doi: 10.1093/brain/awp196. Epub 2009 Sep 4. Brain. 2009. PMID: 19734292 Free PMC article.

7

Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States.

Notari S, Moleres FJ, Hunter SB, Belay ED, Schonberger LB, Cali I, Parchi P, Shieh WJ, Brown P, Zaki S, Zou WQ, Gambetti P. Notari S, et al. Among authors: cali i. PLoS One. 2010 Jan 19;5(1):e8765. doi: 10.1371/journal.pone.0008765. PLoS One. 2010. PMID: 20098730 Free PMC article.

8

Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors.

Kim JI, Cali I, Surewicz K, Kong Q, Raymond GJ, Atarashi R, Race B, Qing L, Gambetti P, Caughey B, Surewicz WK. Kim JI, et al. Among authors: cali i. J Biol Chem. 2010 May 7;285(19):14083-7. doi: 10.1074/jbc.C110.113464. Epub 2010 Mar 19. J Biol Chem. 2010. PMID: 20304915 Free PMC article.

9

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.

10

Molecular biology and pathology of prion strains in sporadic human prion diseases.

Gambetti P, Cali I, Notari S, Kong Q, Zou WQ, Surewicz WK. Gambetti P, et al. Among authors: cali i. Acta Neuropathol. 2011 Jan;121(1):79-90. doi: 10.1007/s00401-010-0761-3. Epub 2010 Nov 7. Acta Neuropathol. 2011. PMID: 21058033 Free PMC article. Review.

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