Gerald W. Shipps

Synthesis and screening of small molecule libraries active in binding to DNA (diversityycombinatorial chemistryyureasygel-shift assayyDNA binding)

Julius Rebek, Gerald W. Shipps, K Ent E. Pryor, 1997 .

Discovery and Characterization of Orthosteric and Allosteric Muscarinic M2 Acetylcholine Receptor Ligands by Affinity Selection-Mass Spectrometry

Michael R. Ziebell, Gerald W. Shipps, M. Ziebell, 2006, Journal of biomolecular screening.

An affinity selection–mass spectrometry method for the identification of small molecule ligands from self-encoded combinatorial libraries: Discovery of a novel antagonist of E. coli dihydrofolate reductase

Patrick J. Curran, Gerald W. Shipps, E. Wintner, 2004 .

Inhibitors of hepatitis C virus polymerase: synthesis and characterization of novel 2-oxy-6-fluoro-N-((S)-1-hydroxy-3-phenylpropan-2-yl)-benzamides.

Sony Agrawal, Charles A. Lesburg, Gerald W. Shipps, 2010, Bioorganic & medicinal chemistry letters.

Structure-based design and optimization of 2-aminothiazole-4-carboxamide as a new class of CHK1 inhibitors.

Gerald W. Shipps, T. Fischmann, W. Seghezzi, 2013, Bioorganic & medicinal chemistry letters.