Structure-function analysis of β-arrestin Kurtz reveals a critical role of receptor interactions in downregulation of GPCR signaling in vivo.

MLA

Chai, Fei, et al. “Structure-Function Analysis of β-Arrestin Kurtz Reveals a Critical Role of Receptor Interactions in Downregulation of GPCR Signaling in Vivo.” Developmental Biology, vol. 455, no. 2, Nov. 2019, pp. 409–19. EBSCOhost, https://doi.org/10.1016/j.ydbio.2019.07.013.

APA

Chai, F., Xu, W., Musoke, T., Tarabelsi, G., Assaad, S., Freedman, J., Peterson, R., Piotrowska, K., Byrnes, J., Rogers, S., & Veraksa, A. (2019). Structure-function analysis of β-arrestin Kurtz reveals a critical role of receptor interactions in downregulation of GPCR signaling in vivo. Developmental Biology, 455(2), 409–419. https://doi.org/10.1016/j.ydbio.2019.07.013

Chicago

Chai, Fei, Wenjian Xu, Timothy Musoke, George Tarabelsi, Steven Assaad, Jason Freedman, Rachel Peterson, et al. 2019. “Structure-Function Analysis of β-Arrestin Kurtz Reveals a Critical Role of Receptor Interactions in Downregulation of GPCR Signaling in Vivo.” Developmental Biology 455 (2): 409–19. doi:10.1016/j.ydbio.2019.07.013.