Article
High-content phenotypic screen to identify small molecule enhancers of Parkin-dependent ubiquitination and mitophagy
2022-10-01
Abstract excerpt
<h4>ABSTRACT</h4> Mitochondrial dysfunction and aberrant mitochondrial homeostasis are key aspects of Parkinson’s disease (PD) pathophysiology. Mutations in PINK1 and Parkin proteins lead to autosomal recessive PD, suggesting that defective mitochondrial clearance via mitophagy is key in PD etiology. Accelerating the identification and/or removal of dysfunctional mitochondria could therefore provide a disease-mod...
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Identifiers and source
- Literature Corpus work
- 98bf37c6-765b-5dd0-9524-ac904953bad6
- DOI
- 10.1101/2022.09.30.509127
