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Heart and Vessels|November 4, 2018
ISL1 loss-of-function mutation contributes to congenital heart defectsLan Ma, Juan Wang, Li Li, et al.European Journal of Medical Genetics|July 4, 2012
GATA6 loss-of-function mutation in atrial fibrillationYi-Qing Yang, Li Li, Juan Wang, et al.Molecular Medicine Reports|May 29, 2015
Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathyXin-Kai Qu, Fang Yuan, Ruo-Gu Li, et al.Molecular Therapy. Nucleic Acids|July 1, 2026
Milk-derived extracellular vesicles loaded with miR-146a-5p as a novel therapeutic strategy for allergic airway inflammationChan-Gu Li, Qi Sun, Tian Tian, et al.International Journal of Molecular Medicine|February 6, 2019
NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valveJuan Wang, Pradhan Abhinav, Ying-Jia Xu, et al.International Journal of Molecular Medicine|August 15, 2014
GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathyLei Xu, Lan Zhao, Fang Yuan, et al.Pediatric Cardiology|April 11, 2015
A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart DiseaseYun Pan, Zha-Gen Wang, Xing-Yuan Liu, et al.Molecular Medicine Reports|March 6, 2017
Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular blockYing-Jia Xu, Xing-Biao Qiu, Fang Yuan, et al.Journal of Geriatric Cardiology : JGC|January 21, 2016
Efficacy and safety of a novel multi-electrode radiofrequency ablation catheter for renal sympathetic denervation in pigsQian Gan, Xin-Kai Qu, Kai-Zheng Gong, et al.G3 (Bethesda, Md.)|February 12, 2016
A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary StenosisYu-Min Sun, Jun Wang, Xing-Biao Qiu, et al.Pageof 17