Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dao Wu Wang"'
Autor:
Jingchun Yang, Peng Chen, Xiaolei Xu, Hon Chi Lee, Yigang Li, Dao Wu Wang, David J. Tester, John R. Giudicessi, Yonghe Ding, Dao Wen Wang, Michael J. Ackerman, Kunli Jiao, Kai Jiang, Tong Lu
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Background Sorbs2b (sorbin and SH3 domain‐containing 2b) was recently identified as a cardiomyopathy gene from a zebrafish mutagenesis screen. However, cardiac functions of its mammalian ortholog remain elusive. Methods and Results We conducted a d
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Background Autosomal dominant hypertension with brachydactyly type E syndrome caused by pathogenic variants in the PDE3A gene was first reported in 2015. To date, there are only a few reports of this kind of syndrome. Other patients still lack a gene
Publikováno v:
Cardiology. 145(10)
Brugada syndrome (BrS) is a known cause of sudden cardiac death (SCD) characterized by abnormal electrocardiograms and fatal arrhythmias. The variants in KCND3 encoding the KV4.3 potassium-channel (the α-subunit of the Ito) have seldom been reported
Autor:
Hon Chi Lee, Xiaolei Xu, Dao Wu Wang, Tong D Lu, Yigang Li, Dao Wen Wang, Yonghe Ding, David J. Tester, Jingchun Yang, Michael J. Ackerman, Peng Chen, Kai Jiang, Kunli Jiao
BACKGROUNDArrhythogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy characterized by right ventricular remodeling and ventricular arrhythmia. To date, 16 ARVC causative genes have been identified from human genetic studies,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96e1282e11e0c5ab104085e7e14cd81b
Autor:
Dao Wen Wang, Dao Wu Wang, Zongzhe Li, Jin Huang, Hu Ding, Hong Wang, Jinzhao Zhao, Chen Chen
Publikováno v:
Journal of Translational Medicine
Background Rapidly determining the complex genetic basis of Hypertrophic cardiomyopathy (HCM) is vital to better understanding and optimally managing this common polygenetic cardiovascular disease. Methods A rapid custom Ion-amplicon-resequencing ass
Autor:
Shi-Wei, Yang, Yan, Chen, Jun, Li, Jie, Yin, Yu-Ming, Qin, Gregor, Andelfinger, Dao-Wu, Wang, Ke-Jiang, Cao
Publikováno v:
Zhonghua xin xue guan bing za zhi. 41(4)
Restrictive cardiomyopathy (RCM) is rare in children, and little is known about the molecular basis of RCM. The aim of this study was to investigate the clinical and myopathological characteristics and to detect mutations on cardiac sarcomere protein