Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Rongcheng Zhang"'
Autor:
Zhongqi Zhang, Tianmiao Zhang, Rongcheng Zhang, Xiaonian Zhu, Xiaoyan Wu, Shengkui Tan, Zhiyuan Jian
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
Background and objectivesColorectal cancer remains an important public health problem in the context of the COVID-19 (Corona virus disease 2019) pandemic. The decline in detection rates and delayed diagnosis of the disease necessitate the exploration
Externí odkaz:
https://doaj.org/article/0163dcd375964da99abf8258529de575
Publikováno v:
Sensors, Vol 24, Iss 13, p 4064 (2024)
In this paper, we investigate a cell-free massive multiple-input multiple-output (CF-mMIMO) system with a reconfigurable intelligent surface (RIS) carried by an unmanned aerial vehicle (UAV), called the UAV-RIS. Compared with the RIS located on the g
Externí odkaz:
https://doaj.org/article/c01b96fe7b764c548ee35833b6bcffd1
Publikováno v:
Future Science OA, Vol 9, Iss 9 (2023)
In recent years, many studies have attempted to clarify the formation, structure and biological function of migrasomes, which are defined as specialized organelles formed by the tips and intersections of Retraction Fibrils during cell migration. It h
Externí odkaz:
https://doaj.org/article/21a9d1ef7bcb4e1282ba0a9482b11bca
Autor:
Yunhao Wang, Genjiang Zheng, Xiaoxing Xie, Wei Yu, Jianxi Wang, Fazhi Zang, Chen Yang, Qiangqiang Xiao, Rongcheng Zhang, Leixin Wei, Xiaodong Wu, Lei Liang, Peng Cao, Chen Xu, Jing Li, Bo Hu, Tao Zhang, Jinglei Wu, Huajiang Chen
Publikováno v:
Journal of Nanobiotechnology, Vol 21, Iss 1, Pp 1-18 (2023)
Abstract Intervertebral disc degeneration (IDD) has been identified as one of the predominant factors leading to persistent low back pain and disability in middle-aged and elderly people. Dysregulation of Prostaglandin E2 (PGE2) can cause IDD, while
Externí odkaz:
https://doaj.org/article/90e91fc4ac5a4e69b7ac88f0d7c3685f
Autor:
Bin Sun, Huiqiao Wu, Jiajia Lu, Rongcheng Zhang, Xiaolong Shen, Yifei Gu, Changgui Shi, Ying Zhang, Wen Yuan
Publikováno v:
Journal of Orthopaedic Translation, Vol 38, Iss , Pp 175-189 (2023)
Objective: Osteogenesis imperfecta (OI) is a congenital disorder characterized by muscle defect and skeletal fragility, and no cure is yet available. Crosstalk between bone and muscle has become a new coming focus of therapeutic strategy in OI. Irisi
Externí odkaz:
https://doaj.org/article/8b9dbb987f7349d8af7fb3abcd923686
Autor:
Xinke Zhao, Rongcheng Zhang, Hugang Jiang, Kai Liu, Chengxu Ma, Ming Bai, Tao An, Younan Yao, Xinqiang Wang, Ming Wang, Yingdong Li, Yuhui Zhang, Jian Zhang
Publikováno v:
BMC Endocrine Disorders, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background In patients with established HF, low triiodothyronine syndrome (LT3S) is commonly present, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) is a useful marker for predicting death. This study was aimed to evaluate the pro
Externí odkaz:
https://doaj.org/article/f9d33374a621416c89a6c8a036d816d5
Publikováno v:
ESC Heart Failure, Vol 7, Iss 6, Pp 3582-3592 (2020)
Abstract Aims This study was to determine the cost‐effectiveness of dapagliflozin in heart failure with reduced ejection fraction (HFrEF) patients in China from a perspective of health care payers. Methods and results We built a Markov model to per
Externí odkaz:
https://doaj.org/article/34143fc9762143c0be1d7859dc404799
Autor:
Shengkui Tan, Xin Song, Chenchen Zhang, Yishu Sun, Jiaxi Zhang, Zhongqi Zhang, Rongcheng Zhang, Tianmiao Zhang, Xiaonian Zhu, Hongzhuan Tan
Publikováno v:
Journal of Immunology Research, Vol 2022 (2022)
Tetraspanins (TSPANs) play crucial roles in cell adhesion, migration, and metastasis of human cancer. However, there is no study in revealing the aspects of TSPAN9 traits and its functions in hepatocellular carcinoma (HCC) prognosis. Our study is the
Externí odkaz:
https://doaj.org/article/938291bca013404cba418bde8236c103
Autor:
Qiangqiang Xiao, Yao Chen, Jianxi Wang, Fazhi Zang, Yunhao Wang, Genjiang Zheng, Kunyu Yang, Rongcheng Zhang, Bo Hu, Huajiang Chen
Publikováno v:
Medical Physics.
Autor:
Changgui Shi, Bin Sun, Huiqiao Wu, Rongcheng Zhang, Lecheng Wu, Lei Guo, Changwei Li, Yanhai Xi, Wen Yuan, Ying Zhang, Guohua Xu
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral ResearchReferences. 38(1)
Osteogenesis imperfecta (OI) is a genetic disorder caused by mutations of type I collagen-related genes, and excessive transforming growth factor-beta (TGF-β) signaling is a common mechanism. TGF-β/Smad signaling has inhibitory effects on osteoblas