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Feng Gao

Researcher at Chinese Academy of Sciences

Publications -  74
Citations -  9411

Feng Gao is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Protein structure & Verticillium dahliae. The author has an hindex of 29, co-authored 72 publications receiving 7591 citations. Previous affiliations of Feng Gao include Soochow University (Suzhou) & China Agricultural University.

Papers
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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.
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky, +2983 more
- 08 Feb 2021 - 
TL;DR: In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
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Streptococcal toxic shock syndrome caused by Streptococcus suis serotype 2.

Jiaqi Tang, +26 more
- 11 Apr 2006 - 
TL;DR: Clinical and pathological characterization of the human patients revealed the hallmarks of typical STSS, which to date had only been associated with GAS infection, and multiple lines of evidence confirmed that highly virulent strains of SS2 were the causative agents of both outbreaks.
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Parkin mono-ubiquitinates Bcl-2 and regulates autophagy.

Dong Chen, +6 more
- 03 Dec 2010 - 
TL;DR: This work identifies the Bcl-2, an anti-apoptotic and autophagy inhibitory protein, as a substrate for parkin and provides evidence that parkin mono-ubiquitinates B cl-2 and regulates Autophagy via Bcl1, while overexpression of parkin enhances the interactions between Bcl2 and Beclin 1.
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The mitochondrial protein BNIP3L is the substrate of PARK2 and mediates mitophagy in PINK1/PARK2 pathway

Feng Gao, +6 more
- 22 Jan 2015 - 
TL;DR: It is demonstrated that BNIP3L, as a substrate of PARK2, promotes mitophagy in the PINK1/PARK2 pathway associated with PD pathogenesis.