Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Lin-ping Wang"'
Autor:
Yi Zhou, Lin Zhao, Zenglei Zhang, Xu Meng, Qiu-jing Cai, Xiao-lei Zhao, Lin-ping Wang, Ai-hua Hu, Xian-liang Zhou
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background For adolescents, abnormal dipping patterns in blood pressure (BP) are associated with early-onset organ damage and a higher risk of cardiovascular disorders in adulthood. Obesity is one of the most common reasons for abnormal BP d
Externí odkaz:
https://doaj.org/article/3b0543d327774282b40f503b7cc25960
Publikováno v:
Frontiers in Psychology, Vol 12 (2021)
This research offers a theoretical model to measure the impact of social media usage on social capital in the agricultural system of China. Furthermore, this research also investigates the relationship between agricultural policies related to entrepr
Externí odkaz:
https://doaj.org/article/41ed393177e14e5781c8d2ceec6f81d1
Publikováno v:
Frontiers in Psychology, Vol 12 (2021)
Social capital, which is derived from psychological research, has an important value in the construction of network relationships in enterprises. It influences the direction and tendency of network connections in start-up enterprises and has graduall
Externí odkaz:
https://doaj.org/article/64d2d7ab66704932b72f039bdd1d4ff5
Autor:
Hui Tang, Ji Zheng, Xuan Bai, Ke-Lin Yue, Jian-Hua Liang, Dan-Yang Li, Lin-Ping Wang, Jin-Li Wang, Qiang Guo
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Angiogenesis and the tumor microenvironment (TME) play important roles in tumorigenesis. Forkhead box Q1 (FOXQ1) is a well-established oncogene in multiple tumors, including colorectal cancer (CRC); however, whether FOXQ1 contributes to angiogenesis
Externí odkaz:
https://doaj.org/article/9e39274a04124a8790b15a18d8387a94
Autor:
Kun-Qi Yang, Chao-Xia Lu, Ying Zhang, Yan-Kun Yang, Jia-Cheng Li, Tian Lan, Xu Meng, Peng Fan, Tao Tian, Lin-Ping Wang, Ya-Xin Liu, Xue Zhang, Xian-Liang Zhou
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract PRKAG2 syndrome is a rare autosomal dominant inherited disorder that is characterized by cardiac hypertrophy, ventricular pre-excitation and conduction system abnormalities. There is little knowledge in cardiovascular magnetic resonance (CMR
Externí odkaz:
https://doaj.org/article/5acc6955e994498e811bcbc02fa0346f
Autor:
Shi-Meng, Xu, Bao-Long, Pan, Dan, Gao, Yun-Wei, Zhang, Jia-Ping, Huan, Xiao, Han, Jing, Song, Lin-Ping, Wang, Hui-Fang, Zhang, Qiao, Niu, Xiao-Ting, Lu
Publikováno v:
NeuroToxicology. 91:282-289
To explore the effects of occupational aluminum exposure on workers' cognitive function and blood glucose concentration, and to analyze whether blood glucose concentration can mediate the cognitive changes caused by aluminum.Our study recruited 375 w
Autor:
Yang Sun, Ya-Xin Liu, Wei-Xian Yang, Ran-Xu Zhao, Chaoxia Lu, Tao Tian, Lin-Ping Wang, Ying Zhang, Yan Xiao, Xianliang Zhou, Tian-Jie Wang
Publikováno v:
The American Journal of the Medical Sciences. 362:260-267
Background The prevalence of Fabry disease (FD) in Chinese patients with hypertrophic cardiomyopathy (HCM) is unclear. We aimed to evaluate the prevalence, clinical characteristics, and outcomes of FD in Chinese patients with HCM. Methods Of 217 pati
Publikováno v:
Computational Biology and Chemistry. 104:107862
Autor:
Tao Tian, Xianliang Zhou, Fang Luo, Jun Cai, Lin-Ping Wang, Di Zhang, Kun-Qi Yang, Peng Fan, Huimin Zhang, Xue-Ying Liu, Ying Lou, Wenjun Ma, Lei Song, Yi-Ting Lu, Ya-Xin Liu
Publikováno v:
Endocrine
Purpose Apparent mineralocorticoid excess (AME) is an ultrarare autosomal recessive disorder resulting from deficiency of 11β-hydroxysteroid dehydrogenase type 2 (11βHSD2) caused by mutations in HSD11B2. The purpose of this study was to identify no
Autor:
Fang Luo, Peng Fan, Tao Tian, Kun‑Qi Yang, Di Zhang, Xian‑Liang Zhou, Ya‑Xin Liu, Lin‑Ping Wang
Publikováno v:
Molecular Medicine Reports
Progressive cardiac conduction defect (PCCD) is an inherited autosomal dominant cardiac disorder characterized by an age‑dependent cardiac electrical conduction block. Several genes have been associated with the genetic pathogenesis of PCCD. The pr