Direct and Differential Interaction of β-Arrestins with the Intracellular Domains of Different Opioid Receptors
Bo Cen(Medical University of South Carolina), Gang Pei(Tongji University), Lan Ma(State Key Laboratory of Medical Neurobiology), Ying Xiong(Shanghai Medical College of Fudan University)
Cited by 7
Related Papers
Nuclear cGAS suppresses DNA repair and promotes tumorigenesis
|Nature|2018|661
β-Arrestin2 Is Critically Involved in CXCR4-mediated Chemotaxis, and This Is Mediated by Its Enhancement of p38 MAPK Activation
|Journal of Biological Chemistry|2002|381
β-arrestin signaling and regulation of transcription
|Journal of Cell Science|2007|257
High-throughput synergy screening identifies microbial metabolites as combination agents for the treatment of fungal infections
|Proceedings of the National Academy of Sciences|2007|254
A Point Mutation That Confers Constitutive Activity to CXCR4 Reveals That T140 Is an Inverse Agonist and That AMD3100 and ALX40-4C Are Weak Partial Agonists
|Journal of Biological Chemistry|2002|254