Cryo-EM structure of an amyloid fibril formed by full-length human prion protein
Author:
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Structural Biology
Link
http://www.nature.com/articles/s41594-020-0441-5.pdf
Reference38 articles.
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2. Prusiner, S. B. Molecular biology and pathogenesis of prion diseases. Trends Biochem. Sci. 21, 482–487 (1996).
3. Scheckel, C. & Aguzzi, A. Prions, prionoids and protein misfolding disorders. Nat. Rev. Genet. 19, 405–418 (2018).
4. Watts, J. C., Bourkas, M. E. C. & Arshad, H. The function of the cellular prion protein in health and disease. Acta Neuropathol. 135, 159–178 (2018).
5. Kim, M.-O., Takada, L. T., Wong, K., Forner, S. A. & Geschwind, M. D. Genetic PrP prion diseases. Cold Spring Harb. Perspect. Biol. 10, a033134 (2018).
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