Peptidomics analysis of plasma in patients with ankylosing spondylitis

por Zhang, Guo-ning, Xu, Ying-jia, Jin, Lei
Publicado 2023

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

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

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

Utility of 64-MSCT in assessing acute non-reperfused myocardial infarct size

por Qu, Xin-Kai, Fang, Wei-Yi, Ye, Jian-Ding, Guan, Shao-Feng, Li, Ruo-Gu, Xu, Ying-Jia, Shen, Yan, Zhang, Min, Liu, Hua
Publicado 2013

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

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

m(6)A demethylase ALKBH5 attenuates doxorubicin-induced cardiotoxicity via posttranscriptional stabilization of Rasal3

por Gao, Ri-Feng, Yang, Kun, Qu, Ya-Nan, Wei, Xiang, Shi, Jia-Ran, Lv, Chun-Yu, Zhao, Yong-Chao, Sun, Xiao-Lei, Xu, Ying-Jia, Yang, Yi-Qing
Publicado 2023

Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias

por Li, Yan-Jie, Wang, Juan, Ye, Willy G., Liu, Xing-Yuan, Li, Li, Qiu, Xing-Biao, Chen, Honghong, Xu, Ying-Jia, Yang, Yi-Qing, Bai, Donglin, Huang, Ri-Tai
Publicado 2023

PITX2c Loss-of-Function Mutations Responsible for Congenital Atrial Septal Defects

por Yuan, Fang, Zhao, Lan, Wang, Juan, Zhang, Wei, Li, Xin, Qiu, Xing-Biao, Li, Ruo-Gu, Xu, Ying-Jia, Xu, Lei, Qu, Xing-Kai, Fang, Wei-Yi, Yang, Yi-Qing
Publicado 2013

Efficacy and safety of a novel multi-electrode radiofrequency ablation catheter for renal sympathetic denervation in pigs

por Gan, Qian, Qu, Xin-Kai, Gong, Kai-Zheng, Guan, Shao-Feng, Han, Wen-Zheng, Dai, Jin-Jie, Li, Ruo-Gu, Zhang, Min, Liu, Hua, Xu, Ying-Jia, Zhang, You-Jun, Fang, Wei-Yi
Publicado 2015

Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation

por Wang, Zhan-Cheng, Ji, Wen-Hui, Ruan, Chang-Wu, Liu, Xing-Yuan, Qiu, Xing-Biao, Yuan, Fang, Li, Ruo-Gu, Xu, Ying-Jia, Liu, Xu, Huang, Ru-Tai, Xue, Song, Yang, Yi-Qing
Publicado 2016

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

por Sun, Yu-Min, Wang, Jun, Qiu, Xing-Biao, Yuan, Fang, Li, Ruo-Gu, Xu, Ying-Jia, Qu, Xin-Kai, Shi, Hong-Yu, Hou, Xu-Min, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing
Publicado 2016