Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Fengtao Cai"'
Autor:
Fengtao Cai, Chenfen Zhou, Na Jiao, Xinling Liang, Zhiming Ye, Wei Chen, Qiongqiong Yang, Hui Peng, Ying Tang, Chaoqun Niu, Guoping Zhao, Zefeng Wang, Guoqing Zhang, Xueqing Yu
Publikováno v:
Microbiology Spectrum, Vol 11, Iss 5 (2023)
Externí odkaz:
https://doaj.org/article/6db20a7b8ef743dc94301b0a5a7206a6
Autor:
Fengtao Cai, Chenfen Zhou, Na Jiao, Xinling Liang, Zhiming Ye, Wei Chen, Qiongqiong Yang, Hui Peng, Ying Tang, Chaoqun Niu, Guoping Zhao, Zefeng Wang, Guoqing Zhang, Xueqing Yu
Publikováno v:
Microbiology Spectrum, Vol 11, Iss 3 (2023)
ABSTRACT IgA nephropathy (IgAN) is reportedly associated with microbial dysbiosis. However, the microbiome dysregulation of IgAN patients across multiple niches remains unclear. To gain a systematic understanding of microbial dysbiosis, we conducted
Externí odkaz:
https://doaj.org/article/b5d6d2b85539418e9c6f563c7fe3c4e2
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2019)
Matrine, an alkaloid compound isolated from the medicinal plant Sophora flavescens, inhibits many types of cancer proliferation. However, the precise mechanism of the matrine antihuman chronic myeloid leukemia remains unclear. In this study, we showe
Externí odkaz:
https://doaj.org/article/95e18124705248bba518e73631572a80
Autor:
Jinqin Chen, Li Liang, Huying Ning, Fengtao Cai, Zhuguo Liu, Longxiao Zhang, Liangyi Zhou, Qiuyun Dai
Publikováno v:
Marine Drugs, Vol 16, Iss 4, p 112 (2018)
α-Conotoxins (α-CTxs) are small peptides composed of 11 to 20 amino acid residues with two disulfide bridges. Most of them potently and selectively target nicotinic acetylcholine receptor (nAChR) subtypes, and a few were found to inhibit the GABAB
Externí odkaz:
https://doaj.org/article/46615dcfcbfe440b89f3956c0c9bb41f
Autor:
Fengtao, Cai, Ning, Xu, Zhuguo, Liu, Rong, Ding, Shuo, Yu, Mingxin, Dong, Shuo, Wang, Jintao, Shen, Han-Shen, Tae, David J, Adams, Xuerong, Zhang, Qiuyun, Dai
Publikováno v:
Journal of medicinal chemistry. 61(22)
α-Conotoxins exhibiting analgesic activity, such as Vc1.1, have been shown to inhibit α9α10 nicotinic acetylcholine receptors (nAChRs) and GABA
Autor:
Qiuyun Dai, Zhuguo Liu, Huying Ning, Jinqin Chen, Liangyi Zhou, Longxiao Zhang, Fengtao Cai, Li Liang
Publikováno v:
Marine Drugs, Vol 16, Iss 4, p 112 (2018)
Marine Drugs; Volume 16; Issue 4; Pages: 112
Marine Drugs
Marine Drugs; Volume 16; Issue 4; Pages: 112
Marine Drugs
α-Conotoxins (α-CTxs) are small peptides composed of 11 to 20 amino acid residues with two disulfide bridges. Most of them potently and selectively target nicotinic acetylcholine receptor (nAChR) subtypes, and a few were found to inhibit the GABAB