Ribosomal profiling during prion disease uncovers progressive translational derangement in glia but not in neurons.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
22 09 2020
Historique:
received: 10 09 2020
accepted: 16 09 2020
pubmed: 23 9 2020
medline: 2 3 2021
entrez: 22 9 2020
Statut: epublish

Résumé

Prion diseases are caused by PrP

Identifiants

pubmed: 32960170
doi: 10.7554/eLife.62911
pii: 62911
pmc: PMC7527237
doi:
pii:

Substances chimiques

Recombinant Fusion Proteins 0
Ribosomal Proteins 0
Green Fluorescent Proteins 147336-22-9

Banques de données

GEO
['GSE149805']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : H2020 Marie Skłodowska-Curie Actions
ID : 706138
Pays : International
Organisme : H2020 European Research Council
ID : 670958
Pays : International
Organisme : Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschungf
ID : 179040
Pays : International
Organisme : Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
ID : 183563
Pays : International

Informations de copyright

© 2020, Scheckel et al.

Déclaration de conflit d'intérêts

CS, MI, PS, AA No competing interests declared

Références

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Auteurs

Claudia Scheckel (C)

Institute of Neuropathology, University of Zurich, Zurich, Switzerland.

Marigona Imeri (M)

Institute of Neuropathology, University of Zurich, Zurich, Switzerland.

Petra Schwarz (P)

Institute of Neuropathology, University of Zurich, Zurich, Switzerland.

Adriano Aguzzi (A)

Institute of Neuropathology, University of Zurich, Zurich, Switzerland.

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Classifications MeSH