Yao Wu

发表

The expression profile analysis of NKX2-5 knock-out embryonic mice to explore the pathogenesis of congenital heart disease.

Weicheng Chen, Xiaojing Ma, Guoying Huang, 2015, Journal of cardiology.

Functional analysis of HECA variants identified in congenital heart disease in the Chinese population

Wei Sheng, Ping Li, Yao Wu, 2022, Journal of clinical laboratory analysis.

Generation of a Urine-Derived Ips Cell Line from a Patient with a Ventricular Septal Defect and Heart Failure and the Robust Differentiation of These Cells to Cardiomyocytes via Small Molecules

Jin Xu, Weicheng Chen, Fang Liu, 2018, Cellular Physiology and Biochemistry.

Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot

Duan Ma, Hui-jun Wang, Ping Zhang, 2014, Journal of Translational Medicine.

DNA sequencing of TGFβ2 in sporadic patients with tetralogy of Fallot.

Duan Ma, Hui-jun Wang, Jing Zhang, 2012, Experimental and therapeutic medicine.

LINE-1 methylation status and its association with tetralogy of fallot in infants

Duan Ma, Hui-jun Wang, Ping Zhang, 2012, BMC Medical Genomics.

Uric acid and sphingomyelin enhance autophagy in iPS cell-originated cardiomyocytes through lncRNA MEG3/miR-7-5p/EGFR axis

Weicheng Chen, Guoying Huang, Junxiang Wen, 2019, Artificial cells, nanomedicine, and biotechnology.

Expression of Cx43-related microRNAs in patients with tetralogy of Fallot

Duan Ma, Hui-jun Wang, Xiao-jing Ma, 2014, World Journal of Pediatrics.

Expression of Cx 43-related microRNAs in patients with tetralogy of Fallot

Duan Ma, Hui-jun Wang, Wen-can Li, 2022 .

MicroRNA deregulation in right ventricular outflow tract myocardium in nonsyndromic tetralogy of fallot.

Duan Ma, Jin Zhang, Hui-jun Wang, 2013, The Canadian journal of cardiology.

Roles of miR-1-1 and miR-181c in ventricular septal defects.

Duan Ma, Yingying Meng, Jin Zhang, 2013, International journal of cardiology.