scispace - formally typeset
C

Chenyao Wang

Researcher at Cleveland Clinic Lerner Research Institute

Publications -  25
Citations -  588

Chenyao Wang is an academic researcher from Cleveland Clinic Lerner Research Institute. The author has contributed to research in topics: Phosphorylation & Medicine. The author has an hindex of 9, co-authored 15 publications receiving 329 citations. Previous affiliations of Chenyao Wang include Cleveland Clinic & Chinese Academy of Sciences.

Papers
More filters
Journal ArticleDOI

AMPK regulates autophagy by phosphorylating BECN1 at threonine 388

TL;DR: It is shown that AMP-activated protein kinase (AMPK) regulates autophagy by phosphorylating BECN1 at Thr388, uncovering a novel mechanism of Autophagy regulation.
Journal ArticleDOI

Phosphorylation of ULK1 affects autophagosome fusion and links chaperone-mediated autophagy to macroautophagy

TL;DR: A late role for ULK in auotophagosome–lysosome fusion is demonstrated and the significance of the mutual regulation of macroautophagy and CMA in maintaining the balance of autophagy is revealed.
Journal ArticleDOI

Tyrosine phosphorylation activates 6-phosphogluconate dehydrogenase and promotes tumor growth and radiation resistance

TL;DR: It is shown that activation of EGFR induces phosphorylation of this enzyme at Y481 to activate the pentose phosphate pathway, which consequently reduces ROS and accelerates DNA synthesis to promote tumor growth and radioresistance.
Journal ArticleDOI

PAQR3 controls autophagy by integrating AMPK signaling to enhance ATG14L‐associated PI3K activity

TL;DR: PAQR3 can not only enhance the capacity of pro‐autophagy class III PI3K due to its scaffold function, but also integrate AMPK signal to activation of ATG14L‐linked VPS34 complex upon glucose starvation.
Journal ArticleDOI

CRTH2 promotes endoplasmic reticulum stress‐induced cardiomyocyte apoptosis through m‐calpain

TL;DR: It is demonstrated that CRTH2 disruption markedly improved cardiac recovery in mice postmyocardial infarction and doxorubicin challenge by suppressing cardiomyocyte apoptosis, suggesting thatCRTH2 inhibition has therapeutic potential for ischemic cardiopathy.