Showing results (41-50 of 83) with videos related to
Sort By:
Pageof 9
Gene|December 15, 2015
PITX2 loss-of-function mutation contributes to tetralogy of FallotYu-Min Sun, Jun Wang, Xing-Biao Qiu, et al.Journal of the American Heart Association|November 8, 2022
KLF13 Loss-of-Function Mutations Underlying Familial Dilated CardiomyopathyYu-Han Guo, Jun Wang, Xiao-Juan Guo, et al.Iscience|March 6, 2023
m6A demethylase ALKBH5 attenuates doxorubicin-induced cardiotoxicity via posttranscriptional stabilization of Rasal3Ri-Feng Gao, Kun Yang, Ya-Nan Qu, et al.Clinical Chemistry and Laboratory Medicine|November 19, 2015
HAND1 loss-of-function mutation associated with familial dilated cardiomyopathyYi-Meng Zhou, Xiao-Yong Dai, Xing-Biao Qiu, et al.Clinical Chemistry and Laboratory Medicine|February 8, 2021
Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathyQi Qiao, Cui-Mei Zhao, Chen-Xi Yang, et al.Diagnostics (Basel, Switzerland)|March 13, 2025
Chromosomal Location and Identification of TBX20 as a New Gene Responsible for Familial Bicuspid Aortic ValveYan-Jie Li, Su Zou, Yi-Zhe Bian, et al.Diagnostics (Basel, Switzerland)|November 9, 2024
Identification and Functional Investigation of SOX4 as a Novel Gene Underpinning Familial Atrial FibrillationWei-Feng Jiang, Yu-Min Sun, Xing-Biao Qiu, et al.European Journal of Medical Genetics|January 19, 2023
VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathyHong-Yu Shi, Meng-Shi Xie, Yu-Han Guo, et al.Biology|March 29, 2023
Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and ArrhythmiasYan-Jie Li, Juan Wang, Willy G Ye, et al.International Heart Journal|September 6, 2019
A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right VentricleZhi Wang, Hao-Ming Song, Fei Wang, et al.Pageof 9