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Pharmacological Reviews|September 26, 2019
Harnessing Ion-Binding Sites for GPCR PharmacologyBarbara Zarzycka, Saheem A Zaidi, Bryan L Roth, et al.
Molecular Pharmacology|April 16, 2005
Molecular determinants for the interaction of the valvulopathic anorexigen norfenfluramine with the 5-HT2B receptorVincent Setola, Malgorzata Dukat, Richard A Glennon, et al.
Bioorganic & Medicinal Chemistry Letters|September 2, 2006
Interaction of N1-unsubstituted and N1-benzenesulfonyltryptamines at h5-HT6 receptorsRenata Kolanos, Małgorzata Dukat, Bryan L Roth, et al.
ACS Medicinal Chemistry Letters|September 19, 2019
β-Fluorofentanyls Are pH-Sensitive Mu Opioid Receptor AgonistsRicardo Rosas, Xi-Ping Huang, Bryan L Roth, et al.
Bioorganic & Medicinal Chemistry Letters|September 7, 2005
Synthesis of potent and selective serotonin 5-HT1B receptor ligandsYiyun Huang, Sung-A Bae, Bryan L Roth, et al.
Physiology (Bethesda, Md.)|December 17, 2008
Engineered GPCRs as tools to modulate signal transductionYing Pei, Sarah C Rogan, Feng Yan, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 14, 2022
TRUPATH: An Open-Source Biosensor Platform for Interrogating the GPCR TransduceromeJeffrey F DiBerto, Reid H J Olsen, Bryan L Roth
Biochemistry|September 10, 2003
Identification of two serine residues essential for agonist-induced 5-HT2A receptor desensitizationJohn A Gray, Beth A Compton-Toth, Bryan L Roth
Molecular Biosystems|June 10, 2010
A chemical-genetic approach for precise spatio-temporal control of cellular signalingShuyun Dong, John A Allen, Martilias Farrell, et al.
European Journal of Pharmacology|February 27, 2004
SK&F 83822 distinguishes adenylyl cyclase from phospholipase C-coupled dopamine D1-like receptors: behavioural topographyGerard J O'Sullivan, Bryan L Roth, Anthony Kinsella, et al.
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