Can China’s vehicular emissions regulation reduce air pollution?—a quasi-natural experiment based on the latest National Vehicular Emissions Standard (stage-VI)

por Liu, Xing-yuan, Xu, Ling-xia, Wu, Xiao-qing, Wen, Hong-xing
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

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

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

Functional metabolomics discover pentose and glucuronate interconversion pathways as promising targets for Yang Huang syndrome treatment with Yinchenhao Tang

por Sun, Hui, Zhang, Ai-hua, Song, Qi, Fang, Heng, Liu, Xing-yuan, Su, Jing, Yang, Le, Yu, Meng-die, Wang, Xi-jun
Publicado 2018

Serum metabolomics strategy for understanding the therapeutic effects of Yin-Chen-Hao-Tang against Yanghuang syndrome

por Liu, Xing-yuan, Zhang, Ai-hua, Fang, Heng, Li, Meng-xi, Song, Qi, Su, Jing, Yu, Meng-die, Yang, Le, Wang, Xi-jun
Publicado 2018

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

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

Short-term effects of air pollution on respiratory diseases among young children in Wuhan city, China

por Huang, Zeng-Hui, Liu, Xing-Yuan, Zhao, Tong, Jiao, Kui-Zhuang, Ma, Xu-Xi, Ren, Zhan, Qiu, Yun-Fei, Liao, Jing-Ling, Ma, Lu
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

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

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