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Updated: Mar 3, 2026

The Use of Primary Human Fibroblasts for Monitoring Mitochondrial Phenotypes in the Field of Parkinson's Disease
Published on: October 3, 2012
PINK1-Based Screen Shines Light on Autophagy Enhancers for Parkinson's Disease
Dominik Haddad1, Ken Nakamura2
1Gladstone Institute of Neurological Disease, San Francisco, CA 94158, USA.
Abstract:
In this issue of Cell Chemical Biology, Zhang et al. (2017) report a zebrafish model of Parkinson's disease (PD), incorporating the PD-protein PINK1 and rotenone, a toxin linked to PD. Using it as a drug-screening platform, they identify trifluoperazine and other piperazine phenothiazines as protective compounds that enhance autophagy independent of PINK1.
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