Jean Luc Galzi
Affiliations: | Université de Strasbourg |
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"Jean Luc Galzi"Mean distance: 8.31 | S | N | B | C | P |
Parents
Sign in to add mentorMaurice Goeldner | grad student | Université de Strasbourg | |
Jean-Pierre Changeux | post-doc | Université de Strasbourg |
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Publications
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Lecat S, Belemnaba L, Galzi JL, et al. (2015) Neuropeptide Y receptor mediates activation of ERK1/2 via transactivation of the IGF receptor. Cellular Signalling. 27: 1297-304 |
Daval SB, Kellenberger E, Bonnet D, et al. (2013) Exploration of the orthosteric/allosteric interface in human M1 muscarinic receptors by bitopic fluorescent ligands. Molecular Pharmacology. 84: 71-85 |
Galzi JL, Ilien B. (2012) [G protein-coupled receptors: allosteric regulators of cell metabolism]. MéDecine Sciences : M/S. 28: 852-7 |
Daval SB, Valant C, Bonnet D, et al. (2012) Fluorescent derivatives of AC-42 to probe bitopic orthosteric/allosteric binding mechanisms on muscarinic M1 receptors. Journal of Medicinal Chemistry. 55: 2125-43 |
Lecat S, Ouédraogo M, Cherrier T, et al. (2011) Contribution of a tyrosine-based motif to cellular trafficking of wild-type and truncated NPY Y(1) receptors. Cellular Signalling. 23: 228-38 |
De Mota N, Iturrioz X, Alvear R, et al. (2010) The apelin receptor: from ligand discovery to physiological role. Regulatory Peptides. 164: 26 |
Iturrioz X, Alvear-Perez R, De Mota N, et al. (2010) Identification and pharmacological properties of E339-3D6, the first nonpeptidic apelin receptor agonist. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 24: 1506-17 |
Ilien B, Glasser N, Clamme JP, et al. (2009) Pirenzepine promotes the dimerization of muscarinic M1 receptors through a three-step binding process. The Journal of Biological Chemistry. 284: 19533-43 |
Ouedraogo M, Lecat S, Rochdi MD, et al. (2008) Distinct motifs of neuropeptide Y receptors differentially regulate trafficking and desensitization. Traffic (Copenhagen, Denmark). 9: 305-24 |
Maillet EL, Pellegrini N, Valant C, et al. (2007) A novel, conformation-specific allosteric inhibitor of the tachykinin NK2 receptor (NK2R) with functionally selective properties. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 21: 2124-34 |