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Journal of Biomolecular Screening|June 12, 2004
Affinity capillary electrophoresis for the screening of novel antimicrobial targetsL Michelle Lewis, Linda J Engle, William E Pierceall, et al.
Elife|January 10, 2018
Replication Study: Transcriptional amplification in tumor cells with elevated c-MycL Michelle Lewis, Meredith C Edwards, Zachary R Meyers, et al.
Channels (Austin, Tex.)|February 18, 2009
The Kir channel immunoglobulin domain is essential for Kir1.1 (ROMK) thermodynamic stability, trafficking and gatingKatherine Fallen, Sreedatta Banerjee, Jonathan Sheehan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 13, 2009
Small-molecule screen identifies inhibitors of the neuronal K-Cl cotransporter KCC2Eric Delpire, Emily Days, L Michelle Lewis, et al.
The Journal of Biological Chemistry|November 5, 2003
Transcription factor B contacts promoter DNA near the transcription start site of the archaeal transcription initiation complexMatthew B Renfrow, Nikolai Naryshkin, L Michelle Lewis, et al.
Tetrahedron Letters|November 18, 2011
MAOS ls for the general synthesis and lead optimization of 3,6-disubstituted-[1,2,4]triazolo[4,3-b]pyridazinesLeslie N Aldrich, Evan P Lebois, L Michelle Lewis, et al.
Molecular Pharmacology|August 27, 2009
High-throughput screening reveals a small-molecule inhibitor of the renal outer medullary potassium channel and Kir7.1L Michelle Lewis, Gautam Bhave, Brian A Chauder, et al.
Frontiers in Pharmacology|January 26, 2012
Discovery, characterization, and structure-activity relationships of an inhibitor of inward rectifier potassium (Kir) channels with preference for Kir2.3, Kir3.x, and Kir7.1Rene Raphemot, Daniel F Lonergan, Thuy T Nguyen, et al.
Molecular Pharmacology|October 8, 2010
Development of a selective small-molecule inhibitor of Kir1.1, the renal outer medullary potassium channelGautam Bhave, Brian A Chauder, Wen Liu, et al.
Bioorganic & Medicinal Chemistry Letters|January 8, 2008
Synthesis and SAR of selective muscarinic acetylcholine receptor subtype 1 (M1 mAChR) antagonistsL Michelle Lewis, Douglas Sheffler, Richard Williams, et al.
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