Justine Paradis
Affiliations: | Molecular Biology | Université de Montréal, Montréal, Canada |
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| Burghi V, Paradis JS, Officer A, et al. (2023) Gαs is dispensable for β-arrestin coupling but dictates GRK selectivity and is predominant for gene expression regulation by β2-adrenergic receptor. The Journal of Biological Chemistry. 299: 105293 |
| Paradis JS, Feng X, Murat B, et al. (2022) Computationally designed GPCR quaternary structures bias signaling pathway activation. Nature Communications. 13: 6826 |
| Blondel-Tepaz E, Leverve M, Sokrat B, et al. (2021) The RanBP2/RanGAP1-SUMO complex gates β-arrestin2 nuclear entry to regulate the Mdm2-p53 signaling axis. Oncogene |
| Nourreddine S, Lavoie G, Paradis J, et al. (2020) NF45 and NF90 Regulate Mitotic Gene Expression by Competing with Staufen-Mediated mRNA Decay. Cell Reports. 31: 107660 |
| Beautrait A, Paradis JS, Zimmerman B, et al. (2017) A new inhibitor of the β-arrestin/AP2 endocytic complex reveals interplay between GPCR internalization and signalling. Nature Communications. 8: 15054 |
| Paradis JS, Ly S, Blondel-Tepaz É, et al. (2015) Receptor sequestration in response to β-arrestin-2 phosphorylation by ERK1/2 governs steady-state levels of GPCR cell-surface expression. Proceedings of the National Academy of Sciences of the United States of America. 112: E5160-8 |
| Lima-Fernandes E, Misticone S, Boularan C, et al. (2014) A biosensor to monitor dynamic regulation and function of tumour suppressor PTEN in living cells. Nature Communications. 5: 4431 |