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Journal of the American Heart Association|November 8, 2021
Loss of Endothelial Hypoxia Inducible Factor-Prolyl Hydroxylase 2 Induces Cardiac Hypertrophy and FibrosisZhiyu Dai, Jianding Cheng, Bin Liu, et al.
Cardiogenetics|December 10, 2013
LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotypeJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.
Forensic Science International. Genetics|April 26, 2024
Targeted genetic analysis in a cohort of sporadic death from spontaneous rupture of thoracic aortic dissection in Han Chinese populationQianhao Zhao, Nan Zhou, Qiuping Wu, et al.
Journal of the American Heart Association|January 8, 2018
Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han PopulationLei Huang, Kuo-Ho Wu, Liyong Zhang, et al.
Theranostics|March 21, 2020
Distinct cardiac energy metabolism and oxidative stress adaptations between obese and non-obese type 2 diabetes mellitusXinghui Li, Yandi Wu, Jingjing Zhao, et al.
Mayo Clinic Proceedings|October 7, 2016
Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern ChinaLiyong Zhang, David J Tester, Di Lang, et al.
Circulation. Arrhythmia and Electrophysiology|December 17, 2009
Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium currentJianding Cheng, David W Van Norstrand, Argelia Medeiros-Domingo, et al.
Metabolism: Clinical and Experimental|December 22, 2022
Hepatocyte Ninjurin2 promotes hepatic stellate cell activation and liver fibrosis through the IGF1R/EGR1/PDGF-BB signaling pathwayYifan Wang, Pengyun Wang, Yubing Yu, et al.
Nature Communications|March 2, 2023
Retinol dehydrogenase 10 reduction mediated retinol metabolism disorder promotes diabetic cardiomyopathy in male miceYandi Wu, Tongsheng Huang, Xinghui Li, et al.
Forensic Science, Medicine, and Pathology|August 12, 2024
Characterization of a novel SCN5A mutation associated with long QT syndrome and arrhythmogenic right ventricular cardiomyopathy in a familyRui Li, Da Zheng, Chunxi Lin, et al.
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