Characterization of Soft Amyloid Cores in Human Prion-Like Proteins
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-09714-z.pdf
Reference78 articles.
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2. Ventura, S. et al. Short amino acid stretches can mediate amyloid formation in globular proteins: the Src homology 3 (SH3) case. Proc. Natl. Acad. Sci. USA 101, 7258–7263 (2004).
3. Rousseau, F., Serrano, L. & Schymkowitz, J. W. How evolutionary pressure against protein aggregation shaped chaperone specificity. J Mol Biol 355, 1037–1047 (2006).
4. Aguzzi, A. & Calella, A. M. Prions: protein aggregation and infectious diseases. Physiological reviews 89, 1105–1152 (2009).
5. Sikorska, B. & Liberski, P. P. Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease. Sub-cellular biochemistry 65, 457–496 (2012).
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