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Diagnostics (Basel, Switzerland)|August 26, 2022
Identification of SOX18 as a New Gene Predisposing to Congenital Heart DiseaseHong-Yu Shi, Meng-Shi Xie, Chen-Xi Yang, et al.Diagnostics (Basel, Switzerland)|January 10, 2026
Discovery of SOX5 as a New Causative Gene for Atrial FibrillationDao-Liang Zhang, Xing-Biao Qiu, Ning Li, et al.American Journal of Translational Research|March 14, 2023
A novel GJA5 variant associated with increased risk of essential hypertensionJuan Wang, Xue-Cheng Wang, Zhao-Hua Gu, et al.Genetics and Molecular Biology|December 11, 2020
A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valveWei-Feng Jiang, Ying-Jia Xu, Cui-Mei Zhao, et al.American Journal of Translational Research|February 7, 2024
Discovery of BMP10 as a new gene underpinning congenital heart defectsBin-Bin Dong, Yan-Jie Li, Xing-Yuan Liu, et al.Gene|April 14, 2018
GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valveYing-Jia Xu, Ruo-Min Di, Qi Qiao, et al.Genes|June 26, 2026
Rare Truncating HAND2 Variants Predispose to Atrial FibrillationHong Zhang, Xiao-Qing Hu, Ning Li, et al.International Heart Journal|May 6, 2021
SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial HypertensionTian-Ming Wang, Shan-Shan Wang, Ying-Jia Xu, et al.Journal of Geriatric Cardiology : JGC|October 18, 2013
Utility of 64-MSCT in assessing acute non-reperfused myocardial infarct sizeXin-Kai Qu, Wei-Yi Fang, Jian-Ding Ye, et al.Genetics and Molecular Biology|April 4, 2022
A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosusZun-Ping Ke, Gao-Feng Zhang, Yu-Han Guo, et al.Pageof 9