Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Minyu Liu"'
Autor:
Minyu Liu
Publikováno v:
Mobile Information Systems. 2022:1-8
In recent years, with the continuous development of science and Internet technology, people’s lifestyles are changing dramatically, especially with the development of information technology, which has contributed to the transformation of digital li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f5565a75b17148fa4355294e25288b9
https://doi.org/10.1155/2022/7870724
https://doi.org/10.1155/2022/7870724
Autor:
Ying Peng, Huanhuan Qi, Qingqing Chang, Yu Zhang, Weiyi Liu, Minyu Liu, Quanhai Liu, Guangji Wang, Jianguo Sun
Publikováno v:
Molecules, Vol 24, Iss 11, p 2082 (2019)
GC20, a novel soluble bis-chelated gold(I)−diphosphine compound, has been reported as a promising anticancer candidate. Assessing the pharmacokinetic properties of GC20 is critical for its medicinal evaluation. First, a sensitive and specific liqui
Externí odkaz:
https://doaj.org/article/8a00698ff1a54f26930a22c0d92f3e41
Traffic flow prediction is an important part of smart transportation. The goal is to predict future traffic conditions based on historical data recorded by sensors and the traffic network. As the city continues to build, parts of the transportation n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0288c6648cdac5d65abc0d9cc18922ba
Autor:
Huang Xiaoling, Tong Wu, Minyu Liu, Yu Pengxia, Yifang Deng, Jintao Zhang, Quanhai Liu, Dong Yuqiong
Publikováno v:
International Immunopharmacology. 66:236-241
Many studies confirmed that the over-activation of RAF-MEK-ERK signaling pathway plays a central role in human cancers. To avoid drug resistance during cancer treatment, many researchers focused on the study of the downstream therapeutic target of RA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9497f9b1aa59015d5714c939cbf69795
https://doi.org/10.1016/j.intimp.2018.11.031
https://doi.org/10.1016/j.intimp.2018.11.031
Publikováno v:
Food Quality and Preference. 62:106-110
The objective of the present study determined cross-modal sensory interactions between volatile stimuli elicited by 3-isobutyl-2-methoxypyrazine (IBMP) and orange extract, and the astringent stimulus aluminium ammonium sulphate dodecahydrate (alum).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0367ab8ac47c7112d55e85e917dd3bfa
https://doi.org/10.1016/j.foodqual.2017.07.002
https://doi.org/10.1016/j.foodqual.2017.07.002
Autor:
Quanhai Liu, Huang Xiaoling, Zhen Zhang, Peng-Xia Yu, Minyu Liu, Mei Su, Wang Guoping, Yifang Deng
Publikováno v:
Chinese journal of natural medicines. 16(8)
Farnesoid X receptor (FXR) is a member of the nuclear receptor superfamily of ligand-activated transcription factors. As a metabolic regulator, FXR plays key roles in bile acid and cholesterol metabolism and lipid and glucose homeostasis. Therefore,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04aabd04c769b9781c8a29786bcbeed9
https://pubmed.ncbi.nlm.nih.gov/30197122
https://pubmed.ncbi.nlm.nih.gov/30197122
Autor:
Ming Yin, Haiyan Sun, Yifang Deng, Ying Liu, Yong-Xiang Wang, Minyu Liu, Wei-xia Xiong, Fei Li, Quanhai Liu, Geng-Hui Chen, Lin Xiao, Zhen Zhang, Huang Xiaoling
Publikováno v:
Chinese Journal of Natural Medicines. 12:768-776
Aim JS-38 (mitothiolore), a synthetic version of a metabolite isolated from Xenorhabdus sp., was evaluated for its anti-tumor and white blood cell (WBC) elevating activities. Method These anti-proliferative activities were assessed in vitro using a p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d9840d35600d843b58bf27bf6974b6c
https://doi.org/10.1016/s1875-5364(14)60117-5
https://doi.org/10.1016/s1875-5364(14)60117-5
Autor:
Wei-xia Xiong, Li Cai, Quanhai Liu, Dong Yuqiong, Ying Liu, Minyu Liu, Lin Xiao, Ming Yin, Yu-long Yao
Publikováno v:
Acta Pharmacologica Sinica. 35:1302-1310
To investigate the anticancer effects of S115, a novel heteroaromatic thiosemicarbazone compound in vitro and in vivo.The anti-proliferative action of S115 was analyzed in 12 human and mouse cancer cell lines using MTT assay. Autograft and xenograft
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90b2ee93a8a991c6c5716fe6927580e
https://doi.org/10.1038/aps.2014.71
https://doi.org/10.1038/aps.2014.71
Publikováno v:
Journal of Chemical Information and Modeling. 52:2730-2740
To discover novel tubulin inhibitors, we performed structure-based virtual screening against the colchicine binding pocket. In combination with a hierarchical docking and scoring procedure, the structural information of an additional subpocket in col
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b02e9c9f06d23bb87fecfe6d63a45e1b
https://doi.org/10.1021/ci300302c
https://doi.org/10.1021/ci300302c
A soluble bis-chelated gold(I) diphosphine compound with strong anticancer activity and low toxicity
Publikováno v:
Journal of medicinal chemistry. 56(4)
Gold-containing compounds have shown anticancer potential, but their clinical applications have been severely limited by poor stability and high toxicity in vivo. Here, we report a novel soluble bis-chelated gold(I)–diphosphine compound (GC20) with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::816ad1b5d6e2a7fb88b6c73671629090
https://pubmed.ncbi.nlm.nih.gov/23362983
https://pubmed.ncbi.nlm.nih.gov/23362983