Generation of a new infectious recombinant prion: a model to understand Gerstmann–Sträussler–Scheinker syndrome-Reference-Cited by-同舟云学术

Generation of a new infectious recombinant prion: a model to understand Gerstmann–Sträussler–Scheinker syndrome

Published:2017-08-29 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Elezgarai Saioa R.,Fernández-Borges Natalia,Eraña Hasier,Sevillano Alejandro M.,Charco Jorge M.^ORCID,Harrathi Chafik,Saá Paula^ORCID,Gil David,Kong Qingzhong^ORCID,Requena Jesús R.,Andréoletti Olivier,Castilla Joaquín^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-09489-3.pdf

Reference77 articles.

1. Aguzzi, A. Prion diseases of humans and farm animals: epidemiology, genetics, and pathogenesis. J Neurochem 97, 1726–1739 (2006).

2. Prusiner, S. B. Novel proteinaceous infectious particles cause scrapie. Science 216, 136–144 (1982).

3. Collinge, J. Molecular neurology of prion disease. J Neurol Neurosurg Psychiatry 76, 906–919 (2005).

4. Imran, M. & Mahmood, S. An overview of human prion diseases. Virol J 8, 559 (2011).

5. Gambetti, P., Kong, Q., Zou, W., Parchi, P. & Chen, S. G. Sporadic and familial CJD: classification and characterisation. Br Med Bull 66, 213–239 (2003).

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