G蛋白偶联受体
NADPH氧化酶
细胞生物学
受体
蛋白质亚单位
信号转导
活性氧
生物
细胞信号
生物化学
化学
基因
作者
Andreas Petry,Agnes Görlach
标识
DOI:10.1089/ars.2018.7525
摘要
As GPCRs are one of the most popular classes of investigational drug targets, further detailing of G protein-coupled mechanisms in the activation mechanism of NADPH oxidases as well as better understanding of the link between newly identified NADPH oxidase interaction partners and GPCR signaling will provide new opportunities for improved efficiency and decreased off target effects of therapies targeting GPCRs.
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