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Prion protein localizes at the ciliary base during neural and cardiovascular development, and its depletion affects α-tubulin post-translational modifications

Although conversion of the cellular form of the prion protein (PrP(C)) into a misfolded isoform is the underlying cause of prion diseases, understanding PrP(C) physiological functions has remained challenging. PrP(C) depletion or overexpression alters the proliferation and differentiation properties...

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Библиографические подробности
Опубликовано в: :Sci Rep
Главные авторы: Halliez, Sophie, Martin-Lannerée, Séverine, Passet, Bruno, Hernandez-Rapp, Julia, Castille, Johan, Urien, Céline, Chat, Sophie, Laude, Hubert, Vilotte, Jean-Luc, Mouillet-Richard, Sophie, Béringue, Vincent
Формат: Artigo
Язык:Inglês
Опубликовано: Nature Publishing Group 2015
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4683536/
https://ncbi.nlm.nih.gov/pubmed/26679898
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep17146
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