Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Strammiello, Rosaria"'
Autor:
Notari, Silvio, Strammiello, Rosaria, Capellari, Sabina, Giese, Armin, Cescatti, Maura, Grassi, Jacques, Ghetti, Bernardino, Langeveld, Jan P.M. **, Zou, Wen-Quan, Gambetti, Pierluigi, Kretzschmar, Hans A., Parchi, Piero
Publikováno v:
In Journal of Biological Chemistry 7 November 2008 283(45):30557-30565
Autor:
Notari, Silvio, Capellari, Sabina, Langeveld, Jan, Giese, Armin, Strammiello, Rosaria, Gambetti, Pierluigi, Kretzschmar, Hans A, Parchi, Piero
Publikováno v:
In Laboratory Investigation November 2007 87(11):1103-1112
Autor:
Porcelli, Anna Maria, Scotlandi, Katia, Strammiello, Rosaria, Gislimberti, Gabriella, Baldini, Nicola, Rugolo, Michela *
Publikováno v:
In BBA - Molecular Cell Research 30 January 2002 1542(1-3):125-138
Autor:
Manara, Maria Cristina, Perbal, Bernard, Benini, Stefania, Strammiello, Rosaria, Cerisano, Vanessa, Perdichizzi, Stefania, Serra, Massimo, Astolfi, Annalisa, Bertoni, Franco, Alami, Jennifer, Yeger, Herman, Picci, Piero, Scotlandi, Katia
Publikováno v:
In The American Journal of Pathology 2002 160(3):849-859
Autor:
LODI, RAFFAELE, MANNERS, DAVID NEIL, MALUCELLI, EMIL, TESTA, CLAUDIA, RIZZO, GIOVANNI, CAPELLARI, SABINA, STRAMMIELLO, ROSARIA, PIERANGELI, GIULIA, CORTELLI, PIETRO, MONTAGNA, PASQUALE, BARBIROLI, BRUNO, TONON, CATERINA, PARCHI, PIERO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::19f7d5e6bee70d310d2faca41f9b110a
http://hdl.handle.net/11585/399297
http://hdl.handle.net/11585/399297
The differences in lesion profile among sporadic (s) CJD subtypes to date has been mainly characterized in terms of distribution of histopathological lesions and amount of PrPSc, although strain related differences in microglial response have also be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::b712957cdaaa8119bdeb8d1d5e1e5839
http://hdl.handle.net/11585/78310
http://hdl.handle.net/11585/78310
Autor:
C. Jansen, J. C. van Swieten, A. J. M. Rozemuller, PARCHI, PIERO, CAPELLARI, SABINA, CORRADO, PATRIZIA, STRAMMIELLO, ROSARIA
We have characterized the clinicopathological and PrPSc phenotype of a patient carrying a novel stop codon mutation at codon 227, in the C-terminal part of the prion protein gene (PRNP), resulting in a C-terminally truncated protein lacking the glyco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4094::9641c809b75ee8847d64653d7101714b
http://hdl.handle.net/11585/78308
http://hdl.handle.net/11585/78308
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