Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Sanhu Gou"'
Publikováno v:
ACS Omega, Vol 6, Iss 33, Pp 21359-21367 (2021)
Externí odkaz:
https://doaj.org/article/cbade83963b540688ac96435594f773d
Publikováno v:
Micromachines, Vol 14, Iss 2, p 350 (2023)
In this paper, silver nanoparticles (AgNPs) were successfully green-synthesized for the first time using Hedysarum polysaccharide (HPS) as a reducing agent, stabilizer, and modifier (HPS-AgNP). Thiamazole could induce the aggregation of HPS-AgNPs in
Externí odkaz:
https://doaj.org/article/a2d4f47fe6d044dfa5348e6ba0193999
Autor:
Chao Zhong, Yuewen Zhu, Ningyi Zhu, Tianqi Liu, Sanhu Gou, Fangyan Zhang, JIa Yao, Junqiu Xie, Jingman Ni
Publikováno v:
International Journal of Medical Microbiology, Vol 310, Iss 5, Pp 151433- (2020)
Due to the rise of antibiotic-resistant bacteria around the world, AMPs (antimicrobial peptides), depending on non-specific membrane mechanism and low tendency to develop bacterial resistance, attract widespread attentions as novel antimicrobial alte
Externí odkaz:
https://doaj.org/article/54b623b09eda4cfa8def978f8a4a15a6
Autor:
Linlin Chang, Xiaoyan Wu, Kaixin Ran, Yali Tian, Xu Ouyang, Hui Liu, Sanhu Gou, Yun Zhang, Jingman Ni
Publikováno v:
ACS Omega. 8:7536-7545
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ec95b0d57fd20daf358948d7b703110
https://doi.org/10.1021/acsomega.2c06766
https://doi.org/10.1021/acsomega.2c06766
Autor:
Beibei Li, Xu Ouyang, Zufang Ba, Yinyin Yang, Jingying Zhang, Hui Liu, Tianyue Zhang, Fangyan Zhang, Yun Zhang, Sanhu Gou, Jingman Ni
Publikováno v:
Journal of Medicinal Chemistry. 65:5625-5641
The emergence of multidrug-resistant bacteria has dramatically increased the lethality, level of resistance, and difficulty of treatment. In this study, a series of new antimicrobial peptides (AMPs) based on the β-hairpin structure with the template
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bf01fcbe9f06069f1eb73775b1f7102
https://doi.org/10.1021/acs.jmedchem.1c02140
https://doi.org/10.1021/acs.jmedchem.1c02140
Publikováno v:
Advanced Powder Technology. 32:3540-3549
A colorimetric assay based on the oriented TA-AuNPs-PEG-FITC for rapid and sensitive PABA detection was proposed. Initially, the negatively charged TA modified on the surface of AuNPs enabled rapid binding to PABA due to the electrostatic interaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9beb6ff6feebca4917facefecd10bf95
https://doi.org/10.1016/j.apt.2021.08.011
https://doi.org/10.1016/j.apt.2021.08.011
Autor:
Xu Ouyang, Beibei Li, Yinyin Yang, Zufang Ba, Jingying Zhang, Tianyue Zhang, Linlin Chang, Fangyan Zhang, Yun Zhang, Hui Liu, Sanhu Gou, Jingman Ni
Publikováno v:
Journal of medicinal chemistry. 65(20)
Nonselective toxicity of antimicrobial peptides (AMPs) needs to be solved urgently for their application. Temporin-PE (T-PE, FLPIVAKLLSGLL-NH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bc8cca6f08f16e8a465b4b03422f931
https://pubmed.ncbi.nlm.nih.gov/36148510
https://pubmed.ncbi.nlm.nih.gov/36148510
Publikováno v:
ACS Omega, Vol 6, Iss 33, Pp 21359-21367 (2021)
ACS Omega
ACS Omega
Dendrimeric antimicrobial peptides or lipopeptides have strong transmembrane ability and antibacterial activity. To obtain some ideal antimicrobial peptides, anoplin, a natural antimicrobial peptide with weak antimicrobial activity, was modified by C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c684c55f35ae4d278fd63d27bccb45a
https://doaj.org/article/cbade83963b540688ac96435594f773d
https://doaj.org/article/cbade83963b540688ac96435594f773d
Autor:
Fangyan Zhang, Ping Yang, Wenbo Mao, Chao Zhong, Jingying Zhang, Linlin Chang, Xiaoyan Wu, Hui Liu, Yun Zhang, Sanhu Gou, Jingman Ni
Publikováno v:
Acta biomaterialia. 154
The increasingly severe bacterial resistance worldwide pushes people to discover and design potential antibacterial drugs unavoidably. In this work, a series of short, mirror-symmetric peptides were designed and successfully synthesized, centered on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e7cb9af7d117e8504ef54b61931c687
https://pubmed.ncbi.nlm.nih.gov/36241015
https://pubmed.ncbi.nlm.nih.gov/36241015
Publikováno v:
Journal of Drug Targeting. 29:651-659
Anticancer peptides have received widespread attention as alternative antitumor therapeutics due to their unique action mode. However, the systemic toxicity hampers their successful utilisation in tumour therapy. Here, the tumour acidic environment w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7315802bd5a23208320144efb6dd0083
https://doi.org/10.1080/1061186x.2021.1873351
https://doi.org/10.1080/1061186x.2021.1873351