Rapid ex vivo reverse genetics identifies the essential determinants of prion protein toxicity-Reference-Cited by-同舟云学术

Rapid ex vivo reverse genetics identifies the essential determinants of prion protein toxicity

Published:2022-11-03 Issue:2 Volume:33 Page:
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Reimann Regina R.¹^ORCID,Puzio Martina¹^ORCID,Rosati Antonella¹,Emmenegger Marc¹^ORCID,Schneider Bernard L.²^ORCID,Valdés Pamela²,Huang Danzhi³,Caflisch Amedeo³^ORCID,Aguzzi Adriano¹^ORCID

Affiliation:

1. Institute of Neuropathology University of Zurich Zurich Switzerland

2. Brain Mind Institute, Ecole Polytechnique Fédérale de Lausanne Lausanne Switzerland

3. Department of Biochemistry University of Zürich Zürich Switzerland

Funder

Human Frontier Science Program

Michael J. Fox Foundation

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Stavros Niarchos Foundation

Georg und Bertha Schwyzer-Winiker-Stiftung

H2020 European Research Council

Innosuisse - Schweizerische Agentur für Innovationsförderung

Michael J. Fox Foundation for Parkinson's Research

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bpa.13130

Reference63 articles.

1. NMR characterization of the full-length recombinant murine prion protein, m PrP(23-231)

2. Normal host prion protein necessary for scrapie-induced neurotoxicity

3. Anchorless Prion Protein Results in Infectious Amyloid Disease Without Clinical Scrapie

4. Depleting Neuronal PrP in Prion Infection Prevents Disease and Reverses Spongiosis

5. PrP is a central player in toxicity mediated by soluble aggregates of neurodegeneration-causing proteins

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