Shiwu Zhang

State Key Laboratory Of Frigid Zone Cardiovascular Diseases, The Key Laboratory Of Myocardial Ischemia
Harbin, China

Last Updated: 09/26/2026

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Found 11 publications

Mitochondrial STING Governs Glycolytic Reprogramming in Diabetic Cardiomyopathy.

Mitochondrial STING Governs Glycolytic Reprogramming in Diabetic Cardiomyopathy.

Journal: Circulation research

Published: July 02, 2026

Translocation of SIRT6 promotes glycolysis reprogramming to exacerbate diabetic angiopathy.

Translocation of SIRT6 promotes glycolysis reprogramming to exacerbate diabetic angiopathy.

Journal: Redox biology

Published: May 26, 2025

Exogenous hydrogen sulfide enhances myogenic differentiation of C2C12 myoblasts under high palmitate stress.

Exogenous hydrogen sulfide enhances myogenic differentiation of C2C12 myoblasts under high palmitate stress.

Journal: Heliyon

Published: June 26, 2024

Impaired Iron-Sulfur Cluster Synthesis Induces Mitochondrial PARthanatos in Diabetic Cardiomyopathy.

Impaired Iron-Sulfur Cluster Synthesis Induces Mitochondrial PARthanatos in Diabetic Cardiomyopathy.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: June 17, 2024

Hydrogen sulfide improves endothelial barrier function by modulating the ubiquitination degradation of KLF4 through TRAF7 S-sulfhydration in diabetic aorta.

Hydrogen sulfide improves endothelial barrier function by modulating the ubiquitination degradation of KLF4 through TRAF7 S-sulfhydration in diabetic aorta.

Journal: Free radical biology & medicine

Published: December 04, 2023

Exogenous H2S initiating Nrf2/GPx4/GSH pathway through promoting Syvn1-Keap1 interaction in diabetic hearts.

Exogenous H2S initiating Nrf2/GPx4/GSH pathway through promoting Syvn1-Keap1 interaction in diabetic hearts.

Journal: Cell death discovery

Published: June 22, 2023

Exogenous H2 S promotes ubiquitin-mediated degradation of SREBP1 to alleviate diabetic cardiomyopathy via SYVN1 S-sulfhydration.

Exogenous H2 S promotes ubiquitin-mediated degradation of SREBP1 to alleviate diabetic cardiomyopathy via SYVN1 S-sulfhydration.

Journal: Journal of cachexia, sarcopenia and muscle

Published: April 02, 2023

Hydrogen sulfide regulates SERCA2a SUMOylation by S-Sulfhydration of SENP1 to ameliorate cardiac systole-diastole function in diabetic cardiomyopathy.

Hydrogen sulfide regulates SERCA2a SUMOylation by S-Sulfhydration of SENP1 to ameliorate cardiac systole-diastole function in diabetic cardiomyopathy.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: November 13, 2022

Hydrogen Sulfide Regulates SERCA2a Ubiquitylation via Muscle RING Finger-1 S-Sulfhydration to Affect Cardiac Contractility in db/db Mice.

Hydrogen Sulfide Regulates SERCA2a Ubiquitylation via Muscle RING Finger-1 S-Sulfhydration to Affect Cardiac Contractility in db/db Mice.

Journal: Cells

Published: September 22, 2022

Hydrogen sulphide reduced the accumulation of lipid droplets in cardiac tissues of db/db mice via Hrd1 S-sulfhydration.

Hydrogen sulphide reduced the accumulation of lipid droplets in cardiac tissues of db/db mice via Hrd1 S-sulfhydration.

Journal: Journal of cellular and molecular medicine

Published: July 17, 2020

Hydrogen sulphide ameliorating skeletal muscle atrophy in db/db mice via Muscle RING finger 1 S-sulfhydration.

Hydrogen sulphide ameliorating skeletal muscle atrophy in db/db mice via Muscle RING finger 1 S-sulfhydration.

Journal: Journal of cellular and molecular medicine

Published: February 21, 2020

Showing 1-11 of 11

Last Updated: 09/26/2026