Michel Bouvier spends much of his time researching Receptor, Cell biology, G protein-coupled receptor, Biochemistry and Signal transduction. Michel Bouvier combines subjects such as Endocrinology and Function with his study of Receptor. He has included themes like Molecular biology, Biogenesis and Mutant in his Cell biology study.
His Arrestin study in the realm of G protein-coupled receptor interacts with subjects such as Energy transfer. Michel Bouvier works mostly in the field of Biochemistry, limiting it down to topics relating to Biophysics and, in certain cases, Förster resonance energy transfer. His Signal transduction study incorporates themes from Internalization and Signalling.
His primary areas of study are Receptor, Cell biology, G protein-coupled receptor, Signal transduction and Biochemistry. His Receptor research incorporates elements of Endocrinology and Pharmacology. His Cell biology study combines topics in areas such as 5-HT5A receptor, Internalization and Endocytosis.
His G protein-coupled receptor study combines topics from a wide range of disciplines, such as Biophysics, Computational biology, Function and G protein. His Signal transduction research is multidisciplinary, incorporating perspectives in HEK 293 cells and Effector. His work on Enzyme-linked receptor as part of general Biochemistry study is frequently connected to Palmitoylation, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
Michel Bouvier mostly deals with G protein-coupled receptor, Receptor, Cell biology, Signal transduction and G protein. His studies deal with areas such as Computational biology, Endocytosis and Effector as well as G protein-coupled receptor. Michel Bouvier interconnects Cell signaling, Neuroscience and Drug discovery in the investigation of issues within Receptor.
His Cell biology research integrates issues from HEK 293 cells and Internalization. His biological study spans a wide range of topics, including Thrombin and Membrane protein. His G protein study combines topics from a wide range of disciplines, such as Intrinsic activity, Angiotensin II and Drug development.
His primary scientific interests are in Receptor, G protein-coupled receptor, Cell biology, Signal transduction and G protein. His Receptor research includes elements of Heart failure, Pharmacology and Monocyte. In general G protein-coupled receptor, his work in Functional selectivity is often linked to Ligand linking many areas of study.
His Cell biology research incorporates elements of Tissue homeostasis and Cell fusion. His Signal transduction research is multidisciplinary, relying on both HEK 293 cells and Effector. His study in G protein is interdisciplinary in nature, drawing from both Hormone and Ghrelin.
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Detection of beta 2-adrenergic receptor dimerization in living cells using bioluminescence resonance energy transfer (BRET).
Stephane Angers;Ali Salahpour;Eric Joly;Sandrine Hilairet.
Proceedings of the National Academy of Sciences of the United States of America (2000)
A Peptide Derived from a β2-Adrenergic Receptor Transmembrane Domain Inhibits Both Receptor Dimerization and Activation
Terence E. Hebert;Serge Moffett;Jean-Pierre Morello;Thomas P. Loisel.
Journal of Biological Chemistry (1996)
Roles of G-protein-coupled receptor dimerization.
Sonia Terrillon;Michel Bouvier.
EMBO Reports (2004)
Oligomerization of G-protein-coupled transmitter receptors
Nature Reviews Neuroscience (2001)
Palmitoylation of the human beta 2-adrenergic receptor. Mutation of Cys341 in the carboxyl tail leads to an uncoupled nonpalmitoylated form of the receptor.
B F O'Dowd;M Hnatowich;M G Caron;R J Lefkowitz.
Journal of Biological Chemistry (1989)
Dimerization: an emerging concept for G protein-coupled receptor ontogeny and function.
Stephane Angers;Ali Salahpour;Michel Bouvier.
Annual Review of Pharmacology and Toxicology (2002)
Pharmacological chaperones rescue cell-surface expression and function of misfolded V2 vasopressin receptor mutants
Jean-Pierre Morello;Ali Salahpour;André Laperrière;Virginie Bernier.
Journal of Clinical Investigation (2000)
Cross-talk between cellular signalling pathways suggested by phorbol-ester-induced adenylate cyclase phosphorylation.
Takaaki Yoshimasa;Takaaki Yoshimasa;David R. Sibley;Michel Bouvier;Robert J. Lefkowitz.
β-Arrestin-mediated activation of MAPK by inverse agonists reveals distinct active conformations for G protein-coupled receptors
Mounia Azzi;Pascale G. Charest;Stéphane Angers;Guy Rousseau.
Proceedings of the National Academy of Sciences of the United States of America (2003)
Quantitative Assessment of β1- and β2-Adrenergic Receptor Homo- and Heterodimerization by Bioluminescence Resonance Energy Transfer
Jean-François Mercier;Ali Salahpour;Stéphane Angers;Andreas Breit.
Journal of Biological Chemistry (2002)
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