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Akademický článek
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Autor:
Meng-Long Li, Yu-Jia Ren
Publikováno v:
Proceedings of the 4th Annual International Conference on Social Science and Contemporary Humanity Development (SSCHD 2018).
Autor:
Meng-Long Li, Yu-Jia Ren
Publikováno v:
DEStech Transactions on Social Science, Education and Human Science.
Autor:
Yu-Jia Ren, Peng-Fei Wang, Hai-Liang Zhu, Hai-Bin Gong, Zhong-Chang Wang, Ai-Qin Jiang, Han-Yue Qiu, Xin Zhang
Publikováno v:
RSC Advances. 5:21445-21454
A series of dihydropyridine containing thiazolinone derivatives (4a–4r) have been designed, synthesized and their biological activities evaluated as potential EGFR and HER-2 kinase inhibitors and in tumor cell antiproliferation. The synthesized com
Autor:
Xi Li, Hai-Liang Zhu, Li-Rong Zhang, Hui Zhang, Na-Na Peng, Man Xing, Yu-Jia Ren, Ting-Ting Zhao, Gao-Qi Liu, Xian-Hui Yang
Publikováno v:
Medicinal Chemistry Research. 23:3274-3286
A series of pyrazolyl-acylhydrazone derivatives (1e–20e) have been designed and synthesized and their biologic activities were also evaluated for telomerase inhibition and tumor cell antiproliferation. Among all the compounds, 12e showed the most p
Autor:
Peng-Cheng Lv, Xian-Hui Yang, Man Xing, Yu-Shun Yang, Hai-Liang Zhu, Ting-Ting Zhao, Yu-Jia Ren, Wei-Ming Zhang
Publikováno v:
RSC Adv.. 4:37197-37207
A series of pyrazole derivatives (1e–30e) has been designed and synthesized, and their biological activities were evaluated for EGFR and HER-2 inhibition and tumor cell antiproliferation. Among the compounds synthesized, compound 30e exhibited exce
Publikováno v:
Advanced Materials Research. :375-378
Objective The paper is designed to launch teaching researches on the network curriculum of Fundamental Nursing that based on implicit theories. Method 180 students of nursing major are randomly assigned into the experimental group and the contrast gr
Autor:
Yu-Jia Ren, Zhong-Chang Wang, Peng-Fei Wang, Hai-Liang Zhu, Hai-Bin Gong, Ai-Qin Jiang, Xin Zhang, Han-Yue Qiu
Publikováno v:
ChemInform. 46
Compound (IIIe) is found to exhibit high antiproliferative activity against B16-F10, HeLa, and MCF-7 in vitro.