A novel KLF13 mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve

por Abhinav, Pradhan, Zhang, Gao-Feng, Zhao, Cui-Mei, Xu, Ying-Jia, Wang, Juan, Yang, Yi-Qing
Publicado 2022

A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve

por Jiang, Wei-Feng, Xu, Ying-Jia, Zhao, Cui-Mei, Wang, Xin-Hua, Qiu, Xing-Biao, Liu, Xu, Wu, Shao-Hui, Yang, Yi-Qing
Publicado 2020

PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

por Zhao, Cui-Mei, Peng, Lu-Ying, Li, Li, Liu, Xing-Yuan, Wang, Juan, Zhang, Xian-Ling, Yuan, Fang, Li, Ruo-Gu, Qiu, Xing-Biao, Yang, Yi-Qing
Publicado 2015

miR-218 Involvement in Cardiomyocyte Hypertrophy Is Likely through Targeting REST

por Liu, Jing-Jing, Zhao, Cui-Mei, Li, Zhi-Gang, Wang, Yu-Mei, Miao, Wei, Wu, Xiu-Juan, Wang, Wen-Jing, Liu, Chang, Wang, Duo, Wang, Kang, Li, Li, Peng, Lu-Ying
Publicado 2016