Prion gene paralogs are dispensable for early zebrafish development and have nonadditive roles in seizure susceptibility-Reference-Cited by-同舟云学术

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Prion gene paralogs are dispensable for early zebrafish development and have nonadditive roles in seizure susceptibility

Published:2018-08 Issue:32 Volume:293 Page:12576-12592
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Leighton Patricia L.A.,Kanyo Richard,Neil Gavin J.,Pollock Niall M.,Allison W. Ted

Funder

Alberta Innovates | Alberta Innovates Bio Solutions (AI Bio)

Alberta Innovates | Alberta Innovates - Health Solutions (AIHS)

Alzheimer Society (Société Alzheimer)

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference81 articles.

1. Protein misfolding in prion and prion-like diseases: reconsidering a required role for protein loss–of–function;Leighton;J. Alzheimers Dis,2016

2. Reduced abundance and subverted functions of proteins in prion-like diseases: gained functions fascinate but lost functions affect aetiology;Allison;Int. J. Mol. Sci,2017

3. Differential toxicity of antibodies to the prion protein;Reimann;PLoS Pathog,2016

4. Cellular prion protein as a therapeutic target in Alzheimer's disease;Laurén;J. Alzheimers Dis,2014

5. Cellular prion protein binds laminin and mediates neuritogenesis;Graner;Mol. Brain Res,2000

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