Prion Diseases
Author:
Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-97-4480-0_11
Reference105 articles.
1. Adrover M, Pauwels K, Prigent S, de Chiara C, Xu Z, Chapuis C, Pastore A, Rezaei H (2010) Prion fibrillization is mediated by a native structural element that comprises helices H2 and H3*. J Biol Chem 285:21004. https://doi.org/10.1074/jbc.M110.111815
2. Alper T, Cramp WA, Haig DA, Clarke MC (1967) Does the agent of scrapie replicate without nucleic acid? Nature 214:764–766
3. Animal TSEs (Prion Diseases)—Minnesota Dept. of Health (n.d.) [WWW Document]. https://www.health.state.mn.us/diseases/tses/animal.html. Accessed 24 Mar 2021
4. Asante EA, Smidak M, Grimshaw A, Houghton R, Tomlinson A, Jeelani A, Jakubcova T, Hamdan S, Richard-Londt A, Linehan JM, Brandner S, Alpers M, Whitfield J, Mead S, Wadsworth JDF, Collinge J (2015) A naturally occurring variant of the human prion protein completely prevents prion disease. Nature 522:478. https://doi.org/10.1038/nature14510
5. Baltaci SB, Mogulkoc R, Baltaci AK (2019) Molecular mechanisms of early and late LTP. Neurochem Res 44:281–296. https://doi.org/10.1007/s11064-018-2695-4
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