Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ming Dao Chen"'
Publikováno v:
IEEE Access, Vol 6, Pp 49056-49066 (2018)
An eye tracking technology provides a faster and more intuitive interface to explore the learner psychology. In this paper, with the aim of assisting researcher to expand the knowledge of video lectures, we present an efficient system named VLEYE bas
Externí odkaz:
https://doaj.org/article/c0463f7b16724647aa05ee78c210ad4a
Autor:
Shuang-Xia Zhao, Wei Liu, Ming Zhan, Zhi-Yi Song, Shao-Ying Yang, Li-Qiong Xue, Chun-Ming Pan, Zhao-Hui Gu, Bing-Li Liu, Hai-Ning Wang, Liming Liang, Jun Liang, Xiao-Mei Zhang, Guo-Yue Yuan, Chang-Gui Li, Ming-Dao Chen, Jia-Lun Chen, Guan-Qi Gao, Huai-Dong Song, China Consortium for the Genetics of Autoimmune Thyroid Disease
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e57758 (2013)
To pinpoint the exact location of the etiological variant/s present at 1q21.1 harboring FCRL1-5 and CD5L genes, we carried out a refined association study in the entire FCRL region in 1,536 patients with Graves' disease (GD) and 1,516 sex-matched con
Externí odkaz:
https://doaj.org/article/4d47f18e24bb4837a4327b688e987d21
Publikováno v:
IEEE Access, Vol 6, Pp 49056-49066 (2018)
An eye tracking technology provides a faster and more intuitive interface to explore the learner psychology. In this paper, with the aim of assisting researcher to expand the knowledge of video lectures, we present an efficient system named VLEYE bas
Autor:
Bing Han, Huai-Dong Song, Bing-Li Liu, Yingli Lu, Chun-Ming Pan, Wei Liu, Jie Qiao, Li-Qiong Xue, Wan-Ling Wu, Li-Bo Chen, Ming-Dao Chen, Hui Zhu
Publikováno v:
Translational Research. 161:44-49
17α-hydroxylase/17,20-lyase deficiency (17OHD) is a rare autosomal recessive genetic disease that is characterized by low-renin hypertension, hypokalemia, and abnormal development of the genitalia. Mutations in the CYP17A1 gene account for this dise
Autor:
Guoyue Yuan, Ming-Dao Chen, Lianxi Li, Ling Yang, Dong Wang, Jue Jia, Chaoming Mao, Jingjing Ye, Jifang Wang, Sijing Dong, Liangliang Di, Ying Yang, Libin Zhou
Publikováno v:
Biochemical and Biophysical Research Communications. 424:462-468
Adipose tissue is now recognized to be an important endocrine organ, secreting a variety of adipokines that are involved in the regulation of energy metabolism, insulin resistance and metabolic syndrome. C-reactive protein (CRP) is considered as one
Autor:
Hui Zhu, Huai-Dong Song, Jie Qiao, Bing Han, He Jiang, Jiajun Wu, Bing-Li Liu, Wei Liu, Bo-Ren Jiang, Ming-Dao Chen, Ting Gu, Chun-Ming Pan, Wan-Ling Wu, Ying-Li Lu
Publikováno v:
European Journal of Endocrinology. 164:627-633
Background17α-Hydroxylase/17,20-lyase deficiency (17OHD) caused by a mutation in the CYP17A1 gene is characterized by hypertension, hypokalemia, and abnormal development of the genitalia. The majority of CYP17A1 mutations are located in the coding s
Autor:
Qin-Yun Ma, Jun-Hua Ma, Xiao-Na Zhang, Ming-Dao Chen, Fei Sun, Chun-Ming Pan, Huai-Dong Song, Ping Li, Huang-Ming Cao, He Jiang
Publikováno v:
Biochemical and Biophysical Research Communications. 390:1208-1213
Obesity is frequently associated with malfunctions of the hypothalamus-pituitary-adrenal (HPA) axis and hyperaldosteronism, but the mechanism underlying this association remains unclear. Since the adrenal glands are embedded in adipose tissue, direct
Autor:
Shuang-Xia Zhao, Jia-Lun Chen, Bing Han, Ming-Dao Chen, Jinfeng Tang, Kaixiang Cheng, Wan-Ling Wu, Jun Liang, Ying-Li Lu, Xia Chen, Jie Qiao, Huai-Dong Song, Bing-Li Liu, Fu-Guo Chen, Ying Ru, Yi-Xin Wu
Publikováno v:
Human Mutation. 30:E855-E865
Leydig cell hypoplasia (LCH) is a rare form of male pseudohermaphroditism caused by inactivating mutations in the luteinizing hormone receptor gene (LHCGR). The majority of LHCGR mutations are located in the coding sequence, resulting in impairment o
Autor:
Guoyue Yuan, Xiao Wang, Boren Jiang, Ying Yang, Hua Jing, Wenbin Shang, Li Shao, Libin Zhou, Jingfeng Tang, Ming-Dao Chen, Fengying Li
Publikováno v:
Endocrinology. 149:4510-4518
Berberine, a hypoglycemic agent, has recently been shown to activate AMP-activated protein kinase (AMPK) contributing to its beneficial metabolic effects in peripheral tissues. However, whether berberine exerts a regulatory effect on β-cells via AMP
Autor:
Ying Yang, Wei Wang, Wenbin Shang, Fengying Li, Wenli Lu, Jinfeng Tang, Libin Zhou, Ming-Dao Chen, Hua Jin, Qingyun Ma, Boren Jiang
Publikováno v:
Diabetes Research and Clinical Practice. 79:412-418
Visfatin was recently identified as an adipocytokine and has insulin mimetic properties, but its role in adolescents remains largely unknown. In this study, we examined the impact of adolescent obesity on circulating visfatin levels and the relations