Sfoglia per Autore CALI', IGNAZIO
Classification of sporadic Creutzfeldt-Jakob disease revisited
2006-01-01 Cali, I; Castellani, R; Yuan, J; Al-Shekhlee, A; Cohen, Ml; Xiao, X; Moleres, Fj; Parchi, P; Zou, Wq; Gambetti, P
Insoluble Aggregates and Protease-resistant Conformers of Prion Protein in Uninfected Human Brains
2006-01-01 Yuan, Jue; Xiao, Xiangzhu; Mcgeehan, John; Dong, Zhiqian; Cali, Ignazio; Fujioka, Hisashi; Kong, Qingzhong; Kneale, Geoff; Gambetti, Pierluigi; Zou, Wen-Quan
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain.
2008-01-01 Kong, Qingzhong; Zheng, Mengjie; Casalone, Cristina; Qing, Liuting; Huang, Shenghai; Chakraborty, Bikram; Wang, Ping; Chen, Fusong; Cali, Ignazio; Corona, Cristiano; Martucci, Francesca; Iulini, Barbara; Acutis, Pierluigi; Wang, Lan; Liang, Jingjing; Wang, Meiling; Xinyi, Li; Monaco, Salvatore; Zanusso, Gianluigi; Zou, Wen-Quan; Caramelli, Maria; Gambetti, Pierluigi
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype
2009-01-01 Ghoshal, N; Cali, I; Perrin, Rj; Josephson, Sa; Sun, N; Gambetti, P; Morris, Jc
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics
2009-01-01 Cali, I; Castellani, R; Alshekhlee, A; Cohen, Y; Blevins, J; Yuan, J; Langeveld, Jp; Parchi, P; Safar, Jg; Zou, Wq; Gambetti, P
Variant Creutzfeldt-Jakob disease
2010-01-01 Notari, S; Xiao, X; Shimoji, M; Yuan, J; H, Bi; Cali, I; Kong, Q; Gambetti, P; W Q, Zou
Sporadic Creutzfeldt-Jakob disease
2010-01-01 Gambetti, P.; Puoti, G.; Cali, Ignazio; Kong, Q.; Zou, W. Q.
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States
2010-01-01 Notari, S; Moleres, Fj; Hunter, Sb; Belay, Ed; Schonberger, Lb; Cali, I; Parchi, P; Shieh, Wj; Brown, P; Zaki, S; Zou, Wq; Gambetti, P.
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease
2010-01-01 Tartaglia, Mc; Thai, Jn; See, T; Kuo, A; Harbaugh, R; Raudabaugh, B; Cali, I; Sattavat, M; Sanchez, H; Dearmond, Sj; Geschwind, Md
Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors
2010-01-01 Kim, Ji; Cali, I; Surewicz, K; Kong, Q; Raymond, Gj; Atarashi, R; Race, B; Qing, L; Gambetti, P; Caughey, B; Surewicz, Wk
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein
2010-01-01 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.
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report
2011-01-01 Moody, Km; Schonberger, Lb; Maddox, Ra; Zou, Wq; Cracco, L; Cali, I
Molecular biology and pathology of prion strains in sporadic human prion diseases
2011-01-01 Gambetti, P; Cali, I; Notari, S; Kong, Q; Zou, Wq; Surewicz, Wk
Co-occurrence of Distinct Types of Scrapie Prion Protein in Sporadic Creutzfeldt-Jakob Disease
2013-01-01 Cali, I; Puoti, G; Cracco, L; Iyer, S; J P, Langeveld; Kitamoto, T; Notari, S; W Q, Zou; Gambetti, P
Glycoform-selective prion formation in sporadic and familial forms of prion disease
2013-01-01 Xiao, X; Yuan, J; Haïk, S; Cali, I; Zhan, Y; Moudjou, M; B, Li; Laplanche, Jl; Laude, H; Langeveld, J; Gambetti, P; Kitamoto, T; Kong, Q; Brandel, Jp; Cobb, Ba; Petersen, Rb; Zou, Wq
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases
2013-01-01 Kim, Mo; Cali, I; Oehler, A; Fong, Jc; Wong, K; See, T; Katz, Js; Gambetti, P; Bettcher, Bm; Dearmond, Sj; Geschwind, Md
Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo
2013-01-01 Kong, Q; Mills, Jl; Kundu, B; X, Li; Qing, L; Surewicz, K; Cali, I; Huang, S; Zheng, M; Swietnicki, W; Sönnichsen, Fd; Gambetti, P; Surewicz, Wk
Protease-sensitive prions with 144-bp insertion mutations
2013-01-01 Xiao, X; Cali, I; Dong, Z; Puoti, G; Yuan, J; Qing, L; Wang, H; Kong, Q; Gambetti, P; Zou, Wq
Transmissibility and propagation of co-existing prions of sporadic Creutzfeldt-Jakob disease into humanized transgenic mice
2014-01-01 Cali, I; Zou, W; Cracco, L; A E, Hurley; Kitamoto, T; Kong, Q; Gambetti, P.
Transmissibility and propagation of PrPSc from sCJDMM1-2 in humanized transgenic mice
2014-01-01 Cali, I; W Q, Zou; Cracco, L; Kitamoto, T; Kong, Q; Gambetti, P
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Classification of sporadic Creutzfeldt-Jakob disease revisited | 1-gen-2006 | Cali, I; Castellani, R; Yuan, J; Al-Shekhlee, A; Cohen, Ml; Xiao, X; Moleres, Fj; Parchi, P; Zou, Wq; Gambetti, P | |
Insoluble Aggregates and Protease-resistant Conformers of Prion Protein in Uninfected Human Brains | 1-gen-2006 | Yuan, Jue; Xiao, Xiangzhu; Mcgeehan, John; Dong, Zhiqian; Cali, Ignazio; Fujioka, Hisashi; Kong, Qingzhong; Kneale, Geoff; Gambetti, Pierluigi; Zou, Wen-Quan | |
Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. | 1-gen-2008 | Kong, Qingzhong; Zheng, Mengjie; Casalone, Cristina; Qing, Liuting; Huang, Shenghai; Chakraborty, Bikram; Wang, Ping; Chen, Fusong; Cali, Ignazio; Corona, Cristiano; Martucci, Francesca; Iulini, Barbara; Acutis, Pierluigi; Wang, Lan; Liang, Jingjing; Wang, Meiling; Xinyi, Li; Monaco, Salvatore; Zanusso, Gianluigi; Zou, Wen-Quan; Caramelli, Maria; Gambetti, Pierluigi | |
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype | 1-gen-2009 | Ghoshal, N; Cali, I; Perrin, Rj; Josephson, Sa; Sun, N; Gambetti, P; Morris, Jc | |
Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics | 1-gen-2009 | Cali, I; Castellani, R; Alshekhlee, A; Cohen, Y; Blevins, J; Yuan, J; Langeveld, Jp; Parchi, P; Safar, Jg; Zou, Wq; Gambetti, P | |
Variant Creutzfeldt-Jakob disease | 1-gen-2010 | Notari, S; Xiao, X; Shimoji, M; Yuan, J; H, Bi; Cali, I; Kong, Q; Gambetti, P; W Q, Zou | |
Sporadic Creutzfeldt-Jakob disease | 1-gen-2010 | Gambetti, P.; Puoti, G.; Cali, Ignazio; Kong, Q.; Zou, W. Q. | |
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States | 1-gen-2010 | Notari, S; Moleres, Fj; Hunter, Sb; Belay, Ed; Schonberger, Lb; Cali, I; Parchi, P; Shieh, Wj; Brown, P; Zaki, S; Zou, Wq; Gambetti, P. | |
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease | 1-gen-2010 | Tartaglia, Mc; Thai, Jn; See, T; Kuo, A; Harbaugh, R; Raudabaugh, B; Cali, I; Sattavat, M; Sanchez, H; Dearmond, Sj; Geschwind, Md | |
Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors | 1-gen-2010 | Kim, Ji; Cali, I; Surewicz, K; Kong, Q; Raymond, Gj; Atarashi, R; Race, B; Qing, L; Gambetti, P; Caughey, B; Surewicz, Wk | |
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein | 1-gen-2010 | 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. | |
Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report | 1-gen-2011 | Moody, Km; Schonberger, Lb; Maddox, Ra; Zou, Wq; Cracco, L; Cali, I | |
Molecular biology and pathology of prion strains in sporadic human prion diseases | 1-gen-2011 | Gambetti, P; Cali, I; Notari, S; Kong, Q; Zou, Wq; Surewicz, Wk | |
Co-occurrence of Distinct Types of Scrapie Prion Protein in Sporadic Creutzfeldt-Jakob Disease | 1-gen-2013 | Cali, I; Puoti, G; Cracco, L; Iyer, S; J P, Langeveld; Kitamoto, T; Notari, S; W Q, Zou; Gambetti, P | |
Glycoform-selective prion formation in sporadic and familial forms of prion disease | 1-gen-2013 | Xiao, X; Yuan, J; Haïk, S; Cali, I; Zhan, Y; Moudjou, M; B, Li; Laplanche, Jl; Laude, H; Langeveld, J; Gambetti, P; Kitamoto, T; Kong, Q; Brandel, Jp; Cobb, Ba; Petersen, Rb; Zou, Wq | |
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases | 1-gen-2013 | Kim, Mo; Cali, I; Oehler, A; Fong, Jc; Wong, K; See, T; Katz, Js; Gambetti, P; Bettcher, Bm; Dearmond, Sj; Geschwind, Md | |
Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo | 1-gen-2013 | Kong, Q; Mills, Jl; Kundu, B; X, Li; Qing, L; Surewicz, K; Cali, I; Huang, S; Zheng, M; Swietnicki, W; Sönnichsen, Fd; Gambetti, P; Surewicz, Wk | |
Protease-sensitive prions with 144-bp insertion mutations | 1-gen-2013 | Xiao, X; Cali, I; Dong, Z; Puoti, G; Yuan, J; Qing, L; Wang, H; Kong, Q; Gambetti, P; Zou, Wq | |
Transmissibility and propagation of co-existing prions of sporadic Creutzfeldt-Jakob disease into humanized transgenic mice | 1-gen-2014 | Cali, I; Zou, W; Cracco, L; A E, Hurley; Kitamoto, T; Kong, Q; Gambetti, P. | |
Transmissibility and propagation of PrPSc from sCJDMM1-2 in humanized transgenic mice | 1-gen-2014 | Cali, I; W Q, Zou; Cracco, L; Kitamoto, T; Kong, Q; Gambetti, P |
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