Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marina Algeri"'
Autor:
Fabrizio Tagliavini, Luisa Diomede, L. De Gioia, Marina Algeri, Gianluigi Forloni, Giorgio Giaccone, Nadia Angeretti, Mario Salmona, Orso Bugiani
Publikováno v:
Neurobiology of Disease, Vol 4, Iss 1, Pp 47-57 (1997)
Prion-related encephalopathies are characterized by astrogliosis and nerve cell degeneration and loss. These lesions might be the consequence of an interaction between the abnormal isoform of the cellular prion protein that accumulates in nervous tis
Autor:
Mario Salmona, Walter Luini, Roberto Chiesa, Marina Algeri, Luca De Gioia, Patricia M.-J. Lievens, Luisa Diomede, Gianluigi Forloni, Silvano Sozzani, Fabrizio Tagliavini, Orso Bugiani
Publikováno v:
Scopus-Elsevier
Prion-related encephalopathies are characterized by the intracerebral accumulation of an abnormal isoform of the cellular prion protein (PrPC) named scrapie prion protein (PrPSc). The pathological forms of this protein and its cellular precursor are
Autor:
Marina Algeri, Maurizio D'Incalci, Mario Salmona, Luigi Imperatori, Giovanna Damia, Edward J. Modest, Luisa Diomede
Publikováno v:
International journal of cancer. 59(4)
Autor:
Mario Salmona, Luisa Diomede, Marina Algeri, Orso Bugiani, Fabrizio Tagliavini, L. De Gioia, Gianluigi Forloni, T. Florio, G. Schettini
Publikováno v:
Journal of Neuropathology and Experimental Neurology. 54:449