Qian Wang

发表

Role of the MAPKs/TGF-β1/TRAF6 signaling pathway in postoperative atrial fibrillation

Xiao-qing Chen, Xu Liu, Dao-liang Zhang, 2017, PloS one.

GATA5 loss-of-Function Mutations Underlie Tetralogy

Ruo-Gu Li, Ying-Jia Xu, Xing-yuan Liu, 2013 .

Determination of Chloramphenicol Residual in Freshwater Fish by HPLC

Y. Yang, Qian Wang, Qiao Wang, 2013 .

A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.

W. Fang, Ruo-Gu Li, Ying-Jia Xu, 2013, International journal of molecular medicine.

GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.

Lei Xu, Ruo-Gu Li, X. Qiu, 2014, International journal of molecular medicine.

GATA 5 loss-of-function mutations associated with congenital bicuspid aortic valve

Ruo-Gu Li, X. Qiu, Ying-Jia Xu, 2022 .

Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillation.

W. Fang, Ruo-Gu Li, Ying-Jia Xu, 2013, International journal of molecular medicine.

Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.

W. Fang, Ruo-Gu Li, Ying-Jia Xu, 2013, Molecular medicine reports.

A novel GATA 5 loss-of-function mutation underlies lone atrial fibrillation

W. Fang, Ruo-Gu Li, Ying-Jia Xu, 2022 .

Eplerenone inhibits atrial fibrosis in mutant TGF-β1 transgenic mice

Xiao-qing Chen, Wuchang Zhang, Q. Wang, 2016, Science China Life Sciences.

Repeat Catheter Ablation of Long-standing Persistent Atrial Fibrillation in Patients with a Total Atrial Fibrillation Duration of More Than 2 Years: Effects of the CHA2DS2-VASc Score and Estimated Glomerular Filtration Rate on the Outcomes.

Yi-Qing Yang, Qian Wang, Xu Liu, 2016, Internal medicine.

GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot

Ruo-Gu Li, Ying-Jia Xu, Xing-yuan Liu, 2012, International journal of medical sciences.

A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy.

Q. Wang, Yi-Qing Yang, Jia-hong Xu, 2014, International journal of molecular medicine.

Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation.

W. Fang, Yi-Qing Yang, Juan Wang, 2012, International journal of cardiology.

A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle

Q. Wang, Xing-yuan Liu, Yi-Qing Yang, 2018, Pediatric Cardiology.

A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect.

Qian Wang, Ri-tai Huang, S. Xue, 2017, European journal of medical genetics.

Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.

W. Fang, Ruo-Gu Li, Yi-Qing Yang, 2012, DNA and cell biology.

A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle

Xing-yuan Liu, Yi-Qing Yang, Wei Wang, 2018, Pediatric Cardiology.