Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Wei-Xin Zhang"'
Publikováno v:
Cancer Cell International, Vol 24, Iss 1, Pp 1-14 (2024)
Abstract Extensive exploration of the molecular subtypes of triple-negative breast cancer (TNBC) is critical for advancing precision medicine. Notably, the luminal androgen receptor (LAR) subtype has attracted attention for targeted treatment combini
Externí odkaz:
https://doaj.org/article/54ec87f0885247739ab300baf78b0ca1
Autor:
Wei‐xin Zhang, Qian Wu, Chuan‐liang Sun, Dao‐kuo Ge, Jing Cao, Wan‐jie Liang, Ying‐jun Yin, Hong Li, Hong‐xin Cao, Wen‐yu Zhang, Bai‐ming Li, Yu‐kai Xin
Publikováno v:
Food and Energy Security, Vol 13, Iss 1, Pp n/a-n/a (2024)
Abstract Lateral roots, including adventitious roots, are the main component of rapeseed roots with support, absorb, and synthesis functions and their morphological parameters directly affecting the plant's aboveground growth and yield. Root biomass,
Externí odkaz:
https://doaj.org/article/71b4745c58be4501b5f395dc250d0107
Autor:
Guang-Xi Yu, Ying Hu, Wei-Xin Zhang, Xin-Yi Tian, Sai-Yang Zhang, Yan Zhang, Shuo Yuan, Jian Song
Publikováno v:
Molecules, Vol 27, Iss 15, p 4996 (2022)
[1,2,4]Triazolo[1,5-a]pyrimidine and indole skeletons are widely used to design anticancer agents. Therefore, in this work, a series of [1,2,4]triazolo[1,5-a]pyrimidine indole derivatives were designed and synthesized by the molecular hybridization s
Externí odkaz:
https://doaj.org/article/df1d6f0c375545b48f306b2cc78d8810
Publikováno v:
Microbial Cell Factories, Vol 18, Iss 1, Pp 1-13 (2019)
Abstract Background Structurally stable α-galactosidases are of great interest for various biotechnological applications. More thermophilic α-galactosidases with high activity and structural stability have therefore to be mined and characterized. O
Externí odkaz:
https://doaj.org/article/14e97dc7cf4b48d78f3c428fe37aea4c
Autor:
Jin-Chao Shi, Wei-Ling Shi, Yan-Rong Zhou, Xiu-Lan Chen, Yu-Zhong Zhang, Xia Zhang, Wei-Xin Zhang, Xiao-Yan Song
Publikováno v:
Frontiers in Microbiology, Vol 11 (2020)
The biocontrol fungus Trichoderma longibrachiatum SMF2 secretes a large quantity of peptaibols that have been shown to have a range of biological activities and therefore great application values. However, the mechanism of the regulatory expression o
Externí odkaz:
https://doaj.org/article/46a3f11eb3ba44f6a7b472c6d5a27819
Autor:
Bai-Cheng Zhou, Xiu-Lan Chen, Xi-Ying Zhang, Wei-Xin Zhang, Cai-Yun Sun, Xiao-Yan Song, Sheng Dong, Hui-Lin Zhao, Yong-Sheng Yue, Ping-Yi Li, Bing Guo, Yu-Zhong Zhang
Publikováno v:
Marine Drugs, Vol 11, Iss 4, Pp 1173-1187 (2013)
Marine xylanases are rather less studied compared to terrestrial xylanases. In this study, a new xylanase gene, xynB, was cloned from the marine bacterium, Glaciecola mesophila KMM241, and expressed in Escherichia coli. xynB encodes a multi-domain xy
Externí odkaz:
https://doaj.org/article/10ff013d83e44ea1bd554c98c8220b25
Autor:
Huiqin Guo1,2, Wei-Xin Zhang2, Qiu-yan Zhang3, Meng Li2, Hai-Yun Wang2, Di Li2, Jiabin Liu2, Zhenjian Zhuo4, Jing He2 hejing198374@gmail.com, Lei Miao2 miaolei@gzhmu.edu.cn, Huimin Xia1,2 xia-huimin@foxmail.com
Publikováno v:
Journal of Cancer. 2023, Vol. 14 Issue 18, p3496-3507. 12p.
Discovery of novel tranylcypromine-based derivatives as LSD1 inhibitors for gastric cancer treatment
Autor:
Qi-Sheng Ma, Yi-Fan Zhang, Cheng-Yang Li, Wei-Xin Zhang, Lu Yuan, Jin-Bo Niu, Jian Song, Sai-Yang Zhang, Hong-Min Liu
Publikováno v:
European Journal of Medicinal Chemistry. 251:115228
Publikováno v:
OncoTargets and therapy
Weixin Zhang,1 ChunMiao Xu,2 Jianyu Guo,3 Limei Guo,2 Hongliang Huo,4 Huan Wang5 1Department of Nursing, Qiqihar Medical University, Qiqihar, 161000, China; 2Department of Nursing of Medicine and Surgery, Qiqihar Medical University, Qiqihar, 161000,
Autor:
Jian Song, Sheng-Hui Wang, Chun-Hong Song, Wei-Xin Zhang, Jun-Xia Zhu, Xin-Yi Tian, Xiang-Jing Fu, Yan Xu, Cheng-Yun Jin, Sai-Yang Zhang
Publikováno v:
European Journal of Medicinal Chemistry. 240:114583
Novel N-benzylarylamide saderivatives were designed and synthesized, and their antiproliferative activities were explored. Some of 51 target compounds exhibited potent inhibitory activities against MGC-803, HCT-116 and KYSE450 cells with IC