Stephane A Laporte

Affiliations: 
McGill University, Montreal, QC, Canada 
Area:
GPCR
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"Stephane Laporte"
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Publications

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Baidya M, Chaturvedi M, Dwivedi-Agnihotri H, et al. (2022) Allosteric modulation of GPCR-induced β-arrestin trafficking and signaling by a synthetic intrabody. Nature Communications. 13: 4634
Sedki D, Cho A, Cao Y, et al. (2022) Prostaglandin F2α and angiotensin II type 1 receptors exhibit differential cognate G protein coupling regulation. The Journal of Biological Chemistry. 102294
Pandey S, Kumari P, Baidya M, et al. (2021) Intrinsic bias at non-canonical, β-arrestin-coupled seven transmembrane receptors. Molecular Cell
Free RB, Cuoco CA, Xie B, et al. (2021) Pharmacological characterization of the imipridone anti-cancer drug ONC201 reveals a negative allosteric mechanism of action at the D dopamine receptor. Molecular Pharmacology
Giubilaro J, Schuetz DA, Stepniewski TM, et al. (2021) Discovery of a dual Ras and ARF6 inhibitor from a GPCR endocytosis screen. Nature Communications. 12: 4688
Baidya M, Kumari P, Dwivedi-Agnihotri H, et al. (2020) Key phosphorylation sites in GPCRs orchestrate the contribution of β-Arrestin 1 in ERK1/2 activation. Embo Reports. e49886
Cao Y, Kumar S, Namkung Y, et al. (2020) Angiotensin II type 1 receptor variants alter endosomal receptor-β-arrestin complex stability and MAPK activation. The Journal of Biological Chemistry
Gagnon L, Cao Y, Cho A, et al. (2019) Genetic code expansion and photocross-linking identify different β-arrestin binding modes to the angiotensin II type 1 receptor. The Journal of Biological Chemistry
Cao Y, Namkung Y, Laporte SA. (2019) Methods to Monitor the Trafficking of β-Arrestin/G Protein-Coupled Receptor Complexes Using Enhanced Bystander BRET. Methods in Molecular Biology (Clifton, N.J.). 1957: 59-68
Wright SC, Cañizal MCA, Benkel T, et al. (2018) FZD is a Gα-coupled receptor that exhibits the functional hallmarks of prototypical GPCRs. Science Signaling. 11
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