Decrease in pathology and progression of scrapie after immunisation with synthetic prion protein peptides in hamsters

Author:

Magri Giuliana,Clerici Mario,Dall’Ara Paola,Biasin Mara,Caramelli Maria,Casalone Cristina,Giannino Maria Laura,Longhi Renato,Piacentini Luca,Bella Silvia Della,Gazzuola Paola,Martino Piera Anna,Bella Silvia Della,Pollera Claudia,Puricelli Maria,Servida Francesco,Crescio Ines,Boasso Adriano,Ponti Wilma,Poli Giorgio

Publisher

Elsevier BV

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,General Veterinary,General Immunology and Microbiology,Molecular Medicine

Reference43 articles.

1. Molecular biology and pathogenesis of prion disease;Prusiner;Trends Biochem Sci,1998

2. Prion diseases of humans and animals: their causes and molecular basis;Collinge;Annu Rev Neurosci,2001

3. Microglia and prion disease;Brown;Microsc Res Tech,2001

4. A model for the mechanism of astrogliosis in prion disease;Hafiz;Mol Cell Neurosci,2000

5. Molecular analysis of prion protein (PrP) and glial fibrillary acidic protein (GFAP) transcripts in experimental Creuzfeldt–Jakob disease in mice;Kordek;Acta Neurobiol Exp,1997

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