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ABSTRACT:
SUBMITTER: Uchiyama K
PROVIDER: S-EPMC8584212 | biostudies-literature | 2021 Oct
REPOSITORIES: biostudies-literature
Uchiyama Keiji K Hara Hideyuki H Chida Junji J Pasiana Agriani Dini AD Imamura Morikazu M Mori Tsuyoshi T Takatsuki Hanae H Atarashi Ryuichiro R Sakaguchi Suehiro S
International journal of molecular sciences 20211029 21
Prion diseases are a group of fatal neurodegenerative disorders caused by accumulation of proteinaceous infectious particles, or prions, which mainly consist of the abnormally folded, amyloidogenic prion protein, designated PrP<sup>Sc</sup>. PrP<sup>Sc</sup> is produced through conformational conversion of the cellular isoform of prion protein, PrP<sup>C</sup>, in the brain. To date, no effective therapies for prion diseases have been developed. In this study, we incidentally noticed that mouse ...[more]