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Mechanisms of prion protein assembly into amyloid.
Authors: Stoehr, J.; Weinmann, N.; Wille, H.; Kaimann, T.; Nagel-Steger, L.; Brinkmann, E.; Panza, G.; Prusiner, S. B.; Eigen, M.; Riesner, D.
Date of Publication (YYYY-MM-DD): 2008-02-19
Title of Journal: Proceedings of the National Academy of Sciences of the United States of America
Volume: 105
Issue / Number: 7
Start Page: 2409
End Page: 2414
Document Type: Article
ID: 416115.0
The polysaccharide scaffold of PrP 27-30 is a common compound of natural prions and consists of alpha-linked polyglucose
Authors: Dumpitak, C.; Beekes, M.; Weinmann, N.; Metzger, S.; Winklhofer, K. F.; Tatzelt, J.; Riesner, D.
Date of Publication (YYYY-MM-DD): 2005-11
Title of Journal: Biological Chemistry
Volume: 386
Issue / Number: 11
Start Page: 1149
End Page: 1155
Document Type: Article
ID: 265736.0
The structural transition of the prion protein into its pathogenic conformation is induced by unmasking hydrophobic sites
Authors: Leffers, K. W.; Schell, J.; Jansen, K.; Lucassen, R.; Kaimann, T.; Nagel-Steger, L.; Tatzelt, J.; Riesner, D.
Date of Publication (YYYY-MM-DD): 2004-11-26
Title of Journal: Journal of Molecular Biology
Volume: 344
Issue / Number: 3
Start Page: 839
End Page: 853
Document Type: Article
ID: 222090.0
Entries: 1-3  
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