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Justine Paradis
Justine Paradis
Verified email at ucsd.edu
Title
Cited by
Cited by
Year
A new inhibitor of the β-arrestin/AP2 endocytic complex reveals interplay between GPCR internalization and signalling
A Beautrait, JS Paradis, B Zimmerman, J Giubilaro, L Nikolajev, ...
Nature communications 8 (1), 15054, 2017
1422017
Receptor sequestration in response to β-arrestin-2 phosphorylation by ERK1/2 governs steady-state levels of GPCR cell-surface expression
JS Paradis, S Ly, É Blondel-Tepaz, JA Galan, A Beautrait, MGH Scott, ...
Proceedings of the National Academy of Sciences 112 (37), E5160-E5168, 2015
532015
Synthetic Lethal Screens Reveal Cotargeting FAK and MEK as a Multimodal Precision Therapy for GNAQ-Driven Uveal Melanoma
JS Paradis, M Acosta, R Saddawi-Konefka, A Kishore, S Lubrano, ...
Clinical Cancer Research 27 (11), 3190-3200, 2021
472021
A biosensor to monitor dynamic regulation and function of tumour suppressor PTEN in living cells
E Lima-Fernandes, S Misticone, C Boularan, JS Paradis, H Enslen, ...
Nature communications 5 (1), 4431, 2014
272014
NF45 and NF90 regulate mitotic gene expression by competing with staufen-mediated mRNA decay
S Nourreddine, G Lavoie, J Paradis, KB El Kadhi, A Meant, L Aubert, ...
Cell reports 31 (7), 2020
222020
The RanBP2/RanGAP1-SUMO complex gates β-arrestin2 nuclear entry to regulate the Mdm2-p53 signaling axis
E Blondel-Tepaz, M Leverve, B Sokrat, JS Paradis, M Kosic, K Saha, ...
Oncogene 40 (12), 2243-2257, 2021
122021
Establishment of a novel cancer cell line derived from vulvar carcinoma associated with lichen sclerosus exhibiting a fibroblast-dependent tumorigenic potential
H Dongre, N Rana, S Fromreide, S Rajthala, IB Engelsen, J Paradis, ...
Experimental Cell Research 386 (1), 111684, 2020
102020
A new inhibitor of the beta-arrestin/AP2 endocytic complex reveals interplay between GPCR internalization and signalling. Nat Commun 8: 15054
A Beautrait, JS Paradis, B Zimmerman, J Giubilaro, L Nikolajev, ...
doi. org/10.1038/ncomms15054, 2017
92017
Computationally designed GPCR quaternary structures bias signaling pathway activation
JS Paradis, X Feng, B Murat, RE Jefferson, B Sokrat, M Szpakowska, ...
Nature communications 13 (1), 6826, 2022
82022
Synergistic antitumor efficacy of the dual RAF/MEK inhibitor VS-6766 with FAK inhibition for treatment of RAS-dependent solid tumors
S Coma, M Musteanu, JS Paradis, JS Gutkind, M Barbacid, JA Pachter
Cancer Research 81 (13), 2021
32021
Correction: Synthetic Lethal Screens Reveal Cotargeting FAK and MEK as a Multimodal Precision Therapy for GNAQ-Driven Uveal Melanoma
JS Paradis, M Acosta, R Saddawi-Konefka, A Kishore, S Lubrano, ...
Clinical Cancer Research 27 (16), 4664-4664, 2021
22021
Gαs is dispensable for β-arrestin coupling but dictates GRK selectivity and is predominant for gene expression regulation by β2-adrenergic receptor
V Burghi, JS Paradis, A Officer, SR Adame-Garcia, X Wu, ESF Matthees, ...
Journal of Biological Chemistry 299 (11), 2023
2023
Anticancer treatment for uveal melanoma
J Gutkind, D Schlaepfer, J Paradis, A Kishore, M Acosta, N Arang
US Patent 11,679,113, 2023
2023
Computationally designed GPCR quaternary structures bias signaling pathway activation
R Jefferson, X Feng, P Barth, J Paradis, M Bouvier, A Chevigne, ...
Protein Science 30, 51-51, 2021
2021
FAK and MEK co-targeting: A new multimodal precision therapy for GNAQ-driven uveal melanoma
JS Paradis, M Acosta, N Arang, R Saddawi-Konefka, A Kishore, T Sugase, ...
Cancer Research 80 (16_Supplement), 6406-6406, 2020
2020
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