Area of research
Biochemistry · Physiology
Research interest
Research interests include Diabetic cardiomyopathy, Internal medicine, Endocrinology, Cell biology, Heart failure, and KEAP1.
Translocation of SIRT6 promotes glycolysis reprogramming to exacerbate diabetic angiopathy
Hydrogen sulfide improves endothelial barrier function by modulating the ubiquitination degradation of KLF4 through TRAF7 S-sulfhydration in diabetic aorta
Impaired Iron–Sulfur Cluster Synthesis Induces Mitochondrial PARthanatos in Diabetic Cardiomyopathy
Exogenous hydrogen sulfide enhances myogenic differentiation of C2C12 myoblasts under high palmitate stress
Exogenous H2S initiating Nrf2/GPx4/GSH pathway through promoting Syvn1-Keap1 interaction in diabetic hearts
Exogenous H<sub>2</sub>S promotes ubiquitin‐mediated degradation of SREBP1 to alleviate diabetic cardiomyopathy via SYVN1 S‐sulfhydration
Hydrogen sulfide regulates SERCA2a SUMOylation by S-Sulfhydration of SENP1 to ameliorate cardiac systole-diastole function in diabetic cardiomyopathy
Hydrogen Sulfide Regulates SERCA2a Ubiquitylation via Muscle RING Finger-1 S-Sulfhydration to Affect Cardiac Contractility in db/db Mice