Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Zhang-Sheng Wang"'
Publikováno v:
In Engineering Structures 15 April 2024 305
Autor:
Xi Su, Yan Yan, Qiurong Li, Zeneng Wang, Min-Na Tang, Danbo Lu, Xiaofan Zhao, Zhi-Feng Yao, Jialu Hu, Chun Tang, Zhang-Sheng Wang
Publikováno v:
Engineering. 7:1715-1724
Gut microbiota community shift with coronary artery disease (CAD) has been reported in several limited cohorts during the past several years. However, whether the enriched or decreased microbiota taxa with CAD can be reproducible deserves further inv
Publikováno v:
Gong-kuang zidonghua, Vol 39, Iss 1, Pp 110-112 (2013)
In order to solve problem of personnel safety caused by manual operation mode of roadheader in underground tunneling face at present, a remote video monitoring system of underground tunneling face was designed based on wireless network transmission,
Externí odkaz:
https://doaj.org/article/e65d49ec6e0749949daf86f60a270499
Publikováno v:
Journal of Cellular Biochemistry. 121:3752-3763
Long noncoding RNAs (lncRNAs) are an emerging class of RNA species that could participate in some critical pathways and disease pathogenesis. However, the underlying molecular mechanism of lncRNAs in atrial fibrillation (AF) is still not fully unders
Autor:
Yi-Qing Yang, Xin-Hua Wang, Ying-Jia Xu, Xing-Biao Qiu, Ruo-Gu Li, Ruo-Min Di, Xiu-Mei Li, Ning Li, Zhang-Sheng Wang, Min Zhang, Qi Qiao, Xiao-Juan Guo
Publikováno v:
International Journal of Medical Sciences
Atrial fibrillation (AF), as the most common sustained cardiac arrhythmia, is associated with substantially increased morbidity and mortality. Aggregating evidence demonstrates that genetic defects play a crucial role in the pathogenesis of AF, espec
Autor:
Hua Liu, Xiu-Mei Li, Xin-Kai Qu, Min Zhang, Yi-Qing Yang, Ruo-Min Di, Ying-Jia Xu, Zhang-Sheng Wang, Qi Qiao, Xing-Biao Qiu, Ruo-Gu Li
Publikováno v:
European journal of medical genetics. 62(9)
As two members of the basic helix-loop-helix family of transcription factors, HAND1 and HAND2 are both required for the embryonic cardiogenesis and postnatal ventricular structural remodeling. Recently a HAND1 mutation has been reported to cause dila
Akademický článek
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