Sylvain Armando
Affiliations: | Biochemistry and Molecular Medicine | Université de Montréal, Montréal, Canada |
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| 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 |
| 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 |
| Schrage R, Schmitz AL, Gaffal E, et al. (2015) The experimental power of FR900359 to study Gq-regulated biological processes. Nature Communications. 6: 10156 |
| Namkung Y, Radresa O, Armando S, et al. (2015) Quantifying biased signaling in GPCRs using BRET-based biosensors. Methods (San Diego, Calif.) |
| Armando S, Quoyer J, Lukashova V, et al. (2014) The chemokine CXC4 and CC2 receptors form homo- and heterooligomers that can engage their signaling G-protein effectors and βarrestin. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 28: 4509-23 |
| Quoyer J, Janz JM, Luo J, et al. (2013) Pepducin targeting the C-X-C chemokine receptor type 4 acts as a biased agonist favoring activation of the inhibitory G protein. Proceedings of the National Academy of Sciences of the United States of America. 110: E5088-97 |
| Yagi H, Tan W, Dillenburg-Pilla P, et al. (2011) A synthetic biology approach reveals a CXCR4-G13-Rho signaling axis driving transendothelial migration of metastatic breast cancer cells. Science Signaling. 4: ra60 |
| Martel C, Dugré-Brisson S, Boulay K, et al. (2010) Multimerization of Staufen1 in live cells. Rna (New York, N.Y.). 16: 585-97 |
| Busillo JM, Armando S, Sengupta R, et al. (2010) Site-specific phosphorylation of CXCR4 is dynamically regulated by multiple kinases and results in differential modulation of CXCR4 signaling. The Journal of Biological Chemistry. 285: 7805-17 |