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Qing Zhong

Researcher at University of Texas Southwestern Medical Center

Publications -  54
Citations -  12965

Qing Zhong is an academic researcher from University of Texas Southwestern Medical Center. The author has contributed to research in topics: Autophagy & Autophagosome. The author has an hindex of 37, co-authored 48 publications receiving 11014 citations. Previous affiliations of Qing Zhong include University of California, Irvine & University of California, Berkeley.

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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.
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Molecular definitions of autophagy and related processes

Lorenzo Galluzzi, +62 more
- 03 Jul 2017 - 
TL;DR: A panel of leading experts in the field attempts here to define several autophagy‐related terms based on specific biochemical features to formulate recommendations that facilitate the dissemination of knowledge within and outside the field of autophagic research.
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Mule/ARF-BP1, a BH3-Only E3 Ubiquitin Ligase, Catalyzes the Polyubiquitination of Mcl-1 and Regulates Apoptosis

TL;DR: It is demonstrated that Mcl-1 is ubiquinated at five lysines, and Mule is a unique BH3-containing E3 ubiquitin ligase apical to Bcl-2 family proteins during DNA damage-induced apoptosis.
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Differential Regulation of Distinct Vps34 Complexes by AMPK in Nutrient Stress and Autophagy

TL;DR: It is shown that AMPK plays a key role in regulating different Vps34 complexes and Atg14L, an autophagy-essential gene present only in the proautophagy VPS34 complex, inhibits Vps 34 phosphorylation but increases Beclin1 phosphorylated by AMPK.
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Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response

TL;DR: It is shown that BRCA1 interacts in vitro and in vivo with hRad50, which forms a complex with hMre11 and p95/nibrin that is important for the cellular responses to DNA damage that are mediated by the h Rad50-hMre 11-p95 complex.