Regulation of Receptor Fate by Ubiquitination of Activated β2-Adrenergic Receptor and β-Arrestin
By Sudha K. Shenoy, P. McDonald, T. Kohout, R. J. Lefkowitz. Science, 2001
661 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/8bd72ae54b19cfbd1006fdd9102ada5edffb16d7
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- R. J. Lefkowitz
- Éric Reiter
- Sudha K. Shenoy
- Seungkirl Ahn
- S. Rajagopal
- A. Shukla
- Kunhong Xiao
- S. Artavanis-Tsakonas
Citations in the corpus
- GRKs and β-arrestins: roles in receptor silencing, trafficking and signaling (2006, background): “b-arrestins bind mouse double minute 2 protein, a negative regulator of P53 and an E3 ubiquitin ligase [ 32 ].”
- Mechanisms underlying acute protection from cardiac ischemia-reperfusion injury. (2008, background): “Mdm2 is also recruited to a β arrestin signaling complex (82, 227), and the β arrestin signaling complex appears to be involved in the protection afforded by preconditioning (256).”
- Distinct Phosphorylation Sites on the β2-Adrenergic Receptor Establish a Barcode That Encodes Differential Functions of β-Arrestin (2011, methodology): “HEK293 cells stably transfected with FLAG-tagged b2ARs have been previously described (13, 36).”