Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Dehong Teng"'
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Rheumatoid arthritis (RA) is an autoimmune disease. The etiology of RA remains undetermined and the pathogenesis is complex. There remains a paucity of ideal therapeutic drugs and treatment strategies. The epigenetic modifications affect and regulate
Externí odkaz:
https://doaj.org/article/da563afed5644248b733d75b2582b7ce
Autor:
Shaohong Zang, Xiaorong Cai, Mengshan Chen, Dehong Teng, Fei Jing, Zhe Leng, Yingtang Zhou, Feng Lin
Publikováno v:
Nanomaterials, Vol 12, Iss 11, p 1931 (2022)
Photocatalytic water splitting is one of the promising approaches to solving environmental problems and energy crises. However, the sluggish 4e− transfer kinetics in water oxidation half-reaction restricts the 2e− reduction efficiency in photocat
Externí odkaz:
https://doaj.org/article/a0eb1a0dbab443ceb9b29f276ebfad55
Autor:
Dehong Teng, Jing Zhang, Xinzhi Luo, Fei Jing, Hengwei Wang, Jing Chen, Chao Yang, Shaohong Zang, Yingtang Zhou
Publikováno v:
Journal of Renewable Materials. 10:2378-2391
Autor:
Lin, Shaohong Zang, Xiaorong Cai, Mengshan Chen, Dehong Teng, Fei Jing, Zhe Leng, Yingtang Zhou, Feng
Publikováno v:
Nanomaterials; Volume 12; Issue 11; Pages: 1931
Photocatalytic water splitting is one of the promising approaches to solving environmental problems and energy crises. However, the sluggish 4e− transfer kinetics in water oxidation half-reaction restricts the 2e− reduction efficiency in photocat
Publikováno v:
2020 12th IEEE PES Asia-Pacific Power and Energy Engineering Conference (APPEEC).
A new generation of flexible AC transmission devices such as TCPST can effectively improve the transmission capacity of transmission lines. However, TCPST has been in the theoretical research stage, so there is an urgent need for a TCPST site selecti
Autor:
Chao, Yang, Yuan, Fang, Xiang, Luo, Dehong, Teng, Zhongqiu, Liu, Yingtang, Zhou, Guochao, Liao
Publikováno v:
Bioorganic Chemistry. 120:105596
Histone lysine specific demethylase 1 (LSD1) is a promising new therapeutic target for cancer therapy. Following the work on the discovery of natural LSD1 inhibitor higenamine, we herein performed further structure-based design, synthesis, and extens
Publikováno v:
Bioorganic Chemistry. 109:104723
Natural products are a rich source of lead compounds and have shown promise for epigenetic drug discovery. In this work, we discovered higenamine from our natural product library as a potent, selective and cellular active natural LSD1 inhibitor. Hige
Publikováno v:
2008 International Conference on Electrical Machines & Systems; 2008, p110-114, 5p