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Bioorganic & Medicinal Chemistry Letters|March 8, 2011
Discovery of 3-aryl-5-acylpiperazinyl-pyrazoles as antagonists to the NK3 receptorHamid R Hoveyda, Marie-Odile Roy, Sebastien Blanc, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2005
Synthesis and structure-activity relationships of novel poly(ADP-ribose) polymerase-1 inhibitorsMing Tao, Chung Ho Park, Ron Bihovsky, et al.
Assay and Drug Development Technologies|December 3, 2011
Comparison of two homogeneous cell-based kinase assays for JAK2 V617F: SureFire pSTAT5 and GeneBLAzer fluorescence resonance energy transfer assaysJie Qian, Jennifer L Mason, Beverly P Holskin, et al.
Assay and Drug Development Technologies|June 14, 2012
Comparison of LanthaScreen Eu kinase binding assay and surface plasmon resonance method in elucidating the binding kinetics of focal adhesion kinase inhibitorsJennifer L Mason, Chrysanthe Spais, Jean Husten, et al.
Assay and Drug Development Technologies|December 8, 2010
Modification of CellSensor irf1-bla TF-1 and irf1-bla HEL assays for direct comparison of wild-type JAK2 and JAK2 V617F inhibitionJennifer L Mason, Beverly P Holskin, Kristen A Murray, et al.
Assay and Drug Development Technologies|March 21, 2012
Time-resolved fluorescence resonance energy transfer as a versatile tool in the development of homogeneous cellular kinase assaysLisa Saville, Chrysanthe Spais, Jennifer L Mason, et al.
Bioorganic & Medicinal Chemistry Letters|January 24, 2012
Wake-promoting agents: search for next generation modafinil: part IDerek Dunn, Greg Hostetler, Mohamed Iqbal, et al.
Bioorganic & Medicinal Chemistry Letters|February 21, 2012
Wake-promoting agents: search for next generation modafinil: part IIDerek Dunn, Greg Hostetler, Mohamed Iqbal, et al.
Neuropharmacology|September 25, 2015
3-(1'-Cyclobutylspiro[4H-1,3-benzodioxine-2,4'-piperidine]-6-yl)-5,5-dimethyl-1,4-dihydropyridazin-6-one (CEP-32215), a new wake-promoting histamine H3 antagonist/inverse agonistRobert L Hudkins, John A Gruner, Rita Raddatz, et al.
Biochemical Pharmacology|July 20, 2010
Glycine transporter (GlyT1) inhibitors with reduced residence time increase prepulse inhibition without inducing hyperlocomotion in DBA/2 miceKarla Kopec, Dorothy G Flood, Maciej Gasior, et al.
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