Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions

por Guo, Yu-Han, Yang, Yi-Qing
Publicado 2022

Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation

por Gu, Jian-Yun, Xu, Jia-Hong, Yu, Hong, Yang, Yi-Qing
Publicado 2012

Induction of differentiation of human stem cells ex vivo: Toward large-scale platelet production

por Lei, Xiao-Hua, Yang, Yi-Qing, Ma, Chi-Yuan, Duan, En-Kui
Publicado 2019

Increased gestational palmitic acid predisposes offspring to congenital heart disease

por Lv, Yang, Gao, Ri-Feng, Yang, Chen-Xi, Xu, Ying-Jia, Yang, Yi-Qing
Publicado 2023

Mutation spectrum of GATA4 associated with congenital atrial septal defects

por Yang, Yi-Qing, Wang, Juan, Liu, Xing-Yuan, Chen, Xiao-Zhong, Zhang, Wei, Wang, Xiao-Zhou
Publicado 2013

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

GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot

por Wei, Dong, Bao, Han, Liu, Xing-Yuan, Zhou, Ning, Wang, Qian, Li, Ruo-Gu, Xu, Ying-Jia, Yang, Yi-Qing
Publicado 2012

Novel GATA4 mutations in patients with congenital ventricular septal defects

por Yang, Yi-Qing, Wang, Juan, Liu, Xing-Yuan, Chen, Xiao-Zhong, Zhang, Wei, Wang, Xiao-Zhou, Liu, Xu, Fang, Wei-Yi
Publicado 2012

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

por Xie, Wen-Hui, Chang, Cheng, Xu, Ying-Jia, Li, Ruo-Gu, Qu, Xin-Kai, Fang, Wei-Yi, Liu, Xu, Yang, Yi-Qing
Publicado 2013

PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

por Qiu, Xing-Biao, Xu, Ying-Jia, Li, Ruo-Gu, Xu, Lei, Liu, Xu, Fang, Wei-Yi, Yang, Yi-Qing, Qu, Xin-Kai
Publicado 2014

SMAD1 Loss-of-Function Variant Responsible for Congenital Heart Disease

por Wang, Zhi, Qiao, Xiao-Hui, Xu, Ying-Jia, Liu, Xing-Yuan, Huang, Ri-Tai, Xue, Song, Qiu, Hai-Yan, 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

Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

por Shi, Hong-Yu, Xie, Meng-Shi, Yang, Chen-Xi, Huang, Ri-Tai, Xue, Song, Liu, Xing-Yuan, Xu, Ying-Jia, Yang, Yi-Qing
Publicado 2022

Association of angiotensin-converting enzyme gene I/D and CYP11B2 gene −344T/C polymorphisms with lone atrial fibrillation and its recurrence after catheter ablation

por ZHANG, XIAN-LING, WU, LI-QUN, LIU, XU, YANG, YI-QING, TAN, HONG-WEI, WANG, XIN-HUA, ZHOU, LI, JIANG, WEI-FENG, LI, ZHENG
Publicado 2012

MEF2C loss-of-function mutation contributes to congenital heart defects

por Qiao, Xiao-Hui, Wang, Fei, Zhang, Xian-Ling, Huang, Ri-Tai, Xue, Song, Wang, Juan, Qiu, Xing-Biao, Liu, Xing-Yuan, Yang, Yi-Qing
Publicado 2017

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy

por Li, Ning, Xu, Ying-Jia, Shi, Hong-Yu, Yang, Chen-Xi, Guo, Yu-Han, Li, Ruo-Gu, Qiu, Xing-Biao, Yang, Yi-Qing, Zhang, Min
Publicado 2021

A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus

por Ke, Zun-Ping, Zhang, Gao-Feng, Guo, Yu-Han, Sun, Yu-Min, Wang, Jun, Li, Ning, Qiu, Xing-Biao, Xu, Ying-Jia, Yang, Yi-Qing
Publicado 2022

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

Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy

por Gu, Jia-Ning, Yang, Chen-Xi, Ding, Yuan-Yuan, Qiao, Qi, Di, Ruo-Min, Sun, Yu-Min, Wang, Jun, Yang, Ling, Xu, Ying-Jia, Yang, Yi-Qing
Publicado 2023

KLF13 Loss‐of‐Function Mutations Underlying Familial Dilated Cardiomyopathy

por Guo, Yu‐Han, Wang, Jun, Guo, Xiao‐Juan, Gao, Ri‐Feng, Yang, Chen‐Xi, Li, Li, Sun, Yu‐Min, Qiu, Xing‐Biao, Xu, Ying‐Jia, Yang, Yi‐Qing
Publicado 2022