Gaétan Guillemette

Research

Ligands Biaisés Récepteur Gpcr Signalisation Intracellulaire Structure/Fonction

Latest papers

Memantine potentiates agonist-induced Ca2+ responses in HEK 293 cells.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2008
Protein kinase C decreases the apparent affinity of the inositol 1,4,5-trisphosphate receptor type 3 in RINm5F cells.
Cell calcium · 2007 · senior author
Protein kinase C phosphorylates the inositol 1,4,5-trisphosphate receptor type 2 and decreases the mobilization of Ca2+in pancreatoma AR4-2J cells.
The Journal of endocrinology · 2007 · senior author

All 6 publications

Latest funding

Bases moléculaires de la fonction du récepteur AT1 de l'angiotensineII
CIHR · 2014 · Nominated PI
$663,696

All 1 grants and awards

6 publications.

01

Memantine potentiates agonist-induced Ca2+ responses in HEK 293 cells.

Blanchard AP, Guillemette G, Boulay G

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology2008

DOI: 10.1159/000149798 PMID: 18769047

02

Protein kinase C decreases the apparent affinity of the inositol 1,4,5-trisphosphate receptor type 3 in RINm5F cells.

Caron AZ, Chaloux B, Arguin G, Guillemette G

Cell calcium2007Senior author

DOI: 10.1016/j.ceca.2007.01.002 PMID: 17320950

03

Protein kinase C phosphorylates the inositol 1,4,5-trisphosphate receptor type 2 and decreases the mobilization of Ca2+in pancreatoma AR4-2J cells.

Arguin G, Regimbald-Dumas Y, Fregeau MO, Caron AZ, Guillemette G

The Journal of endocrinology2007Senior author

DOI: 10.1677/joe-06-0179 PMID: 17332533

04

S-nitrosylation of cysteine 289 of the AT1 receptor decreases its binding affinity for angiotensin II.

Leclerc PC, Lanctot PM, Auger-Messier M, Escher E, Leduc R, Guillemette G

British journal of pharmacology2006Senior author

DOI: 10.1038/sj.bjp.0706725 PMID: 16565729

05

The constitutively active N111G-AT1 receptor for angiotensin II modifies the morphology and cytoskeletal organization of HEK-293 cells.

Auger-Messier M, Turgeon ES, Leduc R, Escher E, Guillemette G

Experimental cell research2005Senior author

DOI: 10.1016/j.yexcr.2005.04.015 PMID: 15896777

06

Expression of a truncated form of inositol 1,4,5-trisphosphate receptor type III in the cytosol of DT40 triple inositol 1,4,5-trisphosphate receptor-knockout cells.

Guillemette J, Caron AZ, Regimbald-Dumas Y, Arguin G, Mignery GA, Boulay G, Guillemette G

Cell calcium2005Senior author

DOI: 10.1016/j.ceca.2004.03.005 PMID: 15589990

Bases moléculaires de la fonction du récepteur AT1 de l'angiotensineII

Nominated PICIHR2014Operating Grant

Principal investigators: Guillemette, Gaétan

Keywords: Ligands Biaisés; Récepteur Gpcr; Signalisation Intracellulaire; Structure/Fonction

$663,696

From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.

Frequent collaborators

Pharmacologie
Pharmacologie - Physiologie
Physiology and Pharmacology

Co-authors at Université de Sherbrooke, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.

Mannix Auger-Messier

Pharmacologie - Physiologie

2 shared papers, latest 2006

Richard Leduc

Physiology and Pharmacology

2 shared papers, latest 2006

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Subject: Prospective PhD student: Ligands Biaisés Dear Professor Guillemette, My name is [your name], and I am a [your current degree or role] at [your institution]. I am applying for a PhD position starting in [term and year]. I read your paper "Memantine potentiates agonist-induced Ca2+ responses in HEK 293 cells." (2008), and it connects closely to my own work on [your research topic]. [One or two sentences on what you did and what you learned.] Are you accepting new PhD students for [term and year]? I have attached my CV and transcripts, and I would be glad to talk at a time that suits you. Thank you for your time. Kind regards, [your name]