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10.1038/cr.2017.88

Existing drugs as broad-spectrum and potent inhibitors for Zika virus by targeting NS2B-NS3 interaction

引用

progenitor cells、clinical use、drug target

27

R3 ;R97

MB was partially supported by the NIH Biodefense and Emerging Infectious Disease training grant AI055429.CFQ was supported by the National Natural Science Foundation of China NSFC Excellent Young Scientist81522025;Innovative Research Group81621005;the National Key Research and Development Project of China2016YFD0500304;the National Science and Technology Major Project of China2017ZX09101005;the Newton Advanced Fellowship from the UK Academy of Medical SciencesNAF0031003;the NSFC 81661130162.BL was partially supported by a visiting scholarship sponsored by Guangdong Ocean University.FG was partially supported by a visiting scholarship sponsored by the China Scholarship Council.This work was partially supported by the Wadsworth Center flavivirus drug discovery seed;by NIH grant DA038446;by the Intramural Research Program of NCATS,NIH

2017-09-15(万方平台首次上网日期,不代表论文的发表时间)

共19页

1046-1064

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细胞研究(英文版)

1001-0602(Print);1748-7838(Onl

31-1568

27

2017,27(8)

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