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Biochemical Pharmacology|October 3, 2013
Identification of transmembrane domain 3, 4 & 5 residues that contribute to the formation of the ligand-binding pocket of the urotensin-II receptorXavier Sainsily, Jérôme Cabana, Philip E Boulais, et al.
The Journal of Biological Chemistry|March 12, 2009
The second transmembrane domain of the human type 1 angiotensin II receptor participates in the formation of the ligand binding pocket and undergoes integral pivoting movement during the process of receptor activationIvana Domazet, Brian J Holleran, Stéphane S Martin, et al.
Molecular Pharmacology|March 27, 2015
Characterization of Angiotensin II Molecular Determinants Involved in AT1 Receptor Functional SelectivityIvana Domazet, Brian J Holleran, Alexandra Richard, et al.
Biochemical Pharmacology|May 12, 2009
Identification of transmembrane domain 6 & 7 residues that contribute to the binding pocket of the urotensin II receptorBrian J Holleran, Ivana Domazet, Marie-Eve Beaulieu, et al.
Biochemical Pharmacology|April 24, 2018
Angiotensin II cyclic analogs as tools to investigate AT1R biased signaling mechanismsDavid St-Pierre, Jérôme Cabana, Brian J Holleran, et al.
ACS Chemical Neuroscience|January 8, 2019
N-Guanidyl and C-Tetrazole Leu-Enkephalin Derivatives: Efficient Mu and Delta Opioid Receptor Agonists with Improved Pharmacological PropertiesJean-Louis Beaudeau, Véronique Blais, Brian J Holleran, et al.
The Journal of Biological Chemistry|September 24, 2009
The fifth transmembrane domain of angiotensin II Type 1 receptor participates in the formation of the ligand-binding pocket and undergoes a counterclockwise rotation upon receptor activationIvana Domazet, Stéphane S Martin, Brian J Holleran, et al.
Organic Letters|April 4, 2017
Synthesis and Evaluation of a 64Cu-Conjugate, a Selective δ-Opioid Receptor Positron Emission Tomography Imaging AgentAzadeh Pirisedigh, Véronique Blais, Samia Ait-Mohand, et al.
The Journal of Organic Chemistry|April 15, 2026
Trifluoromethylthio and Trifluoromethyl Functionalization of Endomorphin-1 Enhances its Hydrophobicity and Plasma Stability while Preserving its Affinity for the μ-Opioid ReceptorJure Gregorc, Jolien De Neve, Karine Guitot, et al.
International Journal of Molecular Sciences|March 10, 2022
Monitoring TRPC7 Conformational Changes by BRET Following GPCR ActivationCécile Pétigny, Audrey-Ann Dumont, Hugo Giguère, et al.
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