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	Elucidating structural and molecular mechanisms of beta-arrestin-biased agonism at GPCRs via MS-based proteomics
	Xiao, Kunhong; Sun, Jinpeng
刊名	CELLULAR SIGNALLING
	2017
卷号	41页码:56-64
关键词	7TMR GPCR Arrestin beta-Arrestin Biased agonism Biased agonist Mass spectrometry Proteomics Pharmacology Drug discovery
DOI	10.1016/j.cellsig.2017.09.013
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/4686076
专题	山东大学
作者单位	1.Univ Pittsburgh, Sch Med, Dept Pharmacol & Chem Biol, Pittsburgh, PA 15261 USA. 2.Univ Pittsburgh, Sch Med, Vasc Med
推荐引用方式 GB/T 7714	Xiao, Kunhong,Sun, Jinpeng. Elucidating structural and molecular mechanisms of beta-arrestin-biased agonism at GPCRs via MS-based proteomics[J]. CELLULAR SIGNALLING,2017,41:56-64.
APA	Xiao, Kunhong,&Sun, Jinpeng.(2017).Elucidating structural and molecular mechanisms of beta-arrestin-biased agonism at GPCRs via MS-based proteomics.CELLULAR SIGNALLING,41,56-64.
MLA	Xiao, Kunhong,et al."Elucidating structural and molecular mechanisms of beta-arrestin-biased agonism at GPCRs via MS-based proteomics".CELLULAR SIGNALLING 41(2017):56-64.

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