Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Samuel, Génier"'
Autor:
Christine Lavoie, Jade Degrandmaison, Véronique Blais, Jim Boulter, Jean-Luc Parent, Samuel Génier, Khaled Abdallah, Louis Gendron, Catherine M. Cahill, Francis Bergeron, Marie-Pier Lalumière
Publikováno v:
Proc Natl Acad Sci U S A
With over 30% of current medications targeting this family of proteins, G-protein–coupled receptors (GPCRs) remain invaluable therapeutic targets. However, due to their unique physicochemical properties, their low abundance, and the lack of highly
Autor:
Jade Degrandmaison, Samuel Picard, Louis Fréchette, Samuel Génier, Jean-Luc Parent, Chantal Binda, Steve Jean, Eric Marsault
Publikováno v:
J Biol Chem
Accumulating evidence indicates that G protein–coupled receptors (GPCRs) interact with Rab GTPases during their intracellular trafficking. How GPCRs recruit and activate the Rabs is unclear. Here, we report that depletion of endogenous L-type prost
Autor:
Louis, Fréchette, Chantal, Binda, Samuel, Génier, Jade, Degrandmaison, Marilou, Boisvert, Jean-Luc, Parent
Publikováno v:
Cellular signalling. 72
Mechanisms controlling the recycling of G protein-coupled receptors (GPCRs) remain largely unclear. We report that GGA3 (Golgi-associated, γ adaptin ear containing, ADP-ribosylation factor-binding protein 3) regulates the recycling and signaling of
Autor:
Jean-Luc Parent, Véronique Blais, Christine Lavoie, Samuel Génier, Louis Gendron, Jade Degrandmaison, Sébastien Grastilleur, Étienne St-Louis
Publikováno v:
Molecular and Cellular Neuroscience. 79:53-63
The delta opioid receptor (DOPr) is known to be mainly expressed in intracellular compartments. It remains unknown why DOPr is barely exported to the cell surface, but it seems that a substantial proportion of the immature receptor is trapped within
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1947
G protein-coupled receptors (GPCRs) contain highly hydrophobic domains that are subject to aggregation when exposed to the crowded environment of the cytoplasm. Many events can lead to protein aggregation such as mutations, endoplasmic reticulum (ER)
Publikováno v:
Methods in Molecular Biology ISBN: 9781493991204
G protein-coupled receptors (GPCRs) contain highly hydrophobic domains that are subject to aggregation when exposed to the crowded environment of the cytoplasm. Many events can lead to protein aggregation such as mutations, endoplasmic reticulum (ER)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ba0435c47070e011b76bfd8a2edff77
https://doi.org/10.1007/978-1-4939-9121-1_16
https://doi.org/10.1007/978-1-4939-9121-1_16
Autor:
Pascale Labrecque, Jean-Luc Parent, Terence E. Hébert, Samuel Génier, Pierrick Moreau, Jade Degrandmaison
Publikováno v:
Molecular Biology of the Cell
A direct and functional interaction between a subunit of the CCT/TCP-1 ring complex (TRiC) chaperonin complex and G protein–coupled receptor (GPCRs) is shown. Evidence is provided that distinct nascent GPCRs can undergo alternative folding pathways
Autor:
Pierre Lavigne, Samuel Génier, Esther Gauthier, Samuel Picard, Jean-Luc Parent, Danny Létourneau, Marilou Boisvert
Publikováno v:
Journal of Structural Biology. 212:107582
Rab4a is a small GTPase associated with endocytic compartments and a key regulator of early endosomes recycling. Gathering evidence indicates that its expression and activation are required for the development of metastases. Rab4a-intrinsic GTPase pr
Autor:
Samuel Génier, Jean-Luc Parent, Louis Fréchette, Marilou Boisvert, Chantal Binda, Jade Degrandmaison
Publikováno v:
Cellular Signalling. 72:109641
Mechanisms controlling the recycling of G protein-coupled receptors (GPCRs) remain largely unclear. We report that GGA3 (Golgi-associated, γ adaptin ear containing, ADP-ribosylation factor-binding protein 3) regulates the recycling and signaling of
Autor:
Jean-Luc Parent, Jason C. Young, Andréane Cartier, Jean-François Larrivée, Jana Stankova, Samuel Génier, Chantal Binda
Publikováno v:
The Journal of Cell Biology
The GPCR DP1 promotes the activity of L-PGDS, the enzyme that produces the DP1 agonist PGD2, while at the same time L-PGDS promotes the export and activity of DP1 in response to PGD2.
Export of newly synthesized G protein–coupled receptors (GP
Export of newly synthesized G protein–coupled receptors (GP