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Biochemical Pharmacology|May 19, 2009
X-ray structure breakthroughs in the GPCR transmembrane regionSid Topiol, Michael SabioBioorganic & Medicinal Chemistry Letters|February 5, 2008
Use of the X-ray structure of the Beta2-adrenergic receptor for drug discoverySid Topiol, Michael SabioBioorganic & Medicinal Chemistry Letters|December 27, 2015
7TM X-ray structures for class C GPCRs as new drug-discovery tools. 1. mGluR5Sid Topiol, Michael SabioExpert Opinion on Drug Discovery|July 28, 2015
The role of experimental and computational structural approaches in 7TM drug discoverySid Topiol, Michael SabioBioorganic & Medicinal Chemistry Letters|October 3, 2008
Use of the X-ray structure of the beta2-adrenergic receptor for drug discovery. Part 2: Identification of active compoundsMichael Sabio, Kenneth Jones, Sid TopiolNeuropharmacology|August 14, 2010
Exploration of structure-based drug design opportunities for mGluRsSid Topiol, Michael Sabio, Michelle UbertiChemical Biology & Drug Design|November 26, 2022
Design and biological characterization of a series of dual mechanism ERK1/2 inhibitors with a Triazolopyridinone coreSajedeh Lotfaliansaremi, Stephen Cornwell, Candice Casillas, et al.Cancer Research|May 6, 2004
Depletion of methionine aminopeptidase 2 does not alter cell response to fumagillin or bengamidesSunkyu Kim, Kenneth LaMontagne, Michael Sabio, et al.Bioorganic & Medicinal Chemistry Letters|February 5, 2003
1,4-Diazepane-2-ones as novel inhibitors of LFA-1Sompong Wattanasin, Rainer Albert, Claus Ehrhardt, et al.Assay and Drug Development Technologies|December 19, 2008
Development of an aequorin luminescence calcium assay for high-throughput screening using a plate reader, the LumiLuxVeena Menon, Arun Ranganathn, Vincent H Jorgensen, et al.Pageof 2