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Zixu Mao

Researcher at Emory University

Publications -  53
Citations -  12734

Zixu Mao is an academic researcher from Emory University. The author has contributed to research in topics: Autophagy & Chaperone-mediated autophagy. The author has an hindex of 28, co-authored 50 publications receiving 10947 citations.

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Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Regulation of Neuronal Survival Factor MEF2D by Chaperone-Mediated Autophagy

TL;DR: It is found that chaperone-mediated autophagy regulated the activity of myocyte enhancer factor 2D (MEF2D), a transcription factor required for neuronal survival, and dysregulation of this pathway is associated with Parkinson's disease.
Journal ArticleDOI

Alternative Mitochondrial Electron Transfer as a Novel Strategy for Neuroprotection

TL;DR: Methylene blue functions as an alternative electron carrier, which accepts electrons from NADH and transfers them to cytochrome c and bypasses complex I/III blockage, and indicates that rerouting mitochondrial electron transfer by MB or similar molecules provides a novel strategy for neuroprotection against both chronic and acute neurological diseases involving mitochondrial dysfunction.
Journal ArticleDOI

Calpain-regulated p35/cdk5 plays a central role in dopaminergic neuron death through modulation of the transcription factor myocyte enhancer factor 2.

TL;DR: Evidence is provided that calpain-p35-p25/cdk5-mediated inactivation of MEF2 plays a critical role in dopaminergic loss in vivo, and that “cdk 5 phosphorylation site mutant” ofMEF2D provides neuroprotection in an MPTP mouse model of PD.