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Inorganic Chemistry|September 11, 1996
Nucleophilic Addition of CH, NH, and OH Bonds to the Phosphadiazonium Cation and Interpretation of (31)P Chemical Shifts at Dicoordinate Phosphorus CentersNeil Burford, T. Stanley Cameron, Jason A. C. Clyburne, et al.Journal of the American Chemical Society|November 21, 2002
Transformations between monomeric, dimeric, and trimeric phosphazanes: oligomerizing NP analogues of olefinsNeil Burford, T Stanley Cameron, Korey D Conroy, et al.Journal of Biomolecular Screening|May 3, 2014
Integrating High-Content Analysis into a Multiplexed Screening Approach to Identify and Characterize GPCR AgonistsYingjie Zhu, John Watson, Mengjie Chen, et al.Journal of Laboratory Automation|February 24, 2012
Design of an automated enhanced-throughput platform for functional characterization of positive allosteric modulator-induced leftward shifts in apparent agonist potency in vitroAdam Hendricson, Michele Matchett, Meredith Ferrante, et al.Bioorganic & Medicinal Chemistry Letters|February 7, 2006
Inhibitors of human mitotic kinesin Eg5: characterization of the 4-phenyl-tetrahydroisoquinoline lead seriesChristine M Tarby, Robert F Kaltenbach, Tram Huynh, et al.Bioorganic & Medicinal Chemistry Letters|March 11, 2015
The discovery of potent agonists for GPR88, an orphan GPCR, for the potential treatment of CNS disordersYingzhi Bi, Carolyn D Dzierba, Cynthia Fink, et al.Analytical Biochemistry|June 6, 2009
Assessing compound binding to the Eg5 motor domain using a thermal shift assayPatricia A McDonnell, Joseph Yanchunas, John A Newitt, et al.Bioorganic & Medicinal Chemistry Letters|February 19, 2015
Design, synthesis, and evaluation of phenylglycinols and phenyl amines as agonists of GPR88Carolyn D Dzierba, Yingzhi Bi, Bireshwar Dasgupta, et al.Pageof 10