Transport of Prions in the Peripheral Nervous System: Pathways, Cell Types, and Mechanisms
Prion diseases are transmissible protein misfolding disorders that occur in animals and humans where the endogenous prion protein, PrP<sup>C</sup>, undergoes a conformational change into self-templating aggregates termed PrP<sup>Sc</sup>. Formation of PrP<sup>Sc</sup...
主要な著者: | , , |
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フォーマット: | 論文 |
言語: | English |
出版事項: |
MDPI AG
2022-03-01
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シリーズ: | Viruses |
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オンライン・アクセス: | https://www.mdpi.com/1999-4915/14/3/630 |