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Methods in Molecular Biology (Clifton, N.J.)|October 31, 2017
Challenges and Opportunities in Enabling High-Throughput, Miniaturized High Content ScreeningDebra Nickischer, Lisa Elkin, Normand Cloutier, et al.
Current Chemical Genomics and Translational Medicine|March 6, 2014
Establishing a High-content Analysis Method for Tubulin Polymerization to Evaluate Both the Stabilizing and Destabilizing Activities of CompoundsChi Shing Sum, Debra Nickischer, Ming Lei, et al.
Methods in Enzymology|November 18, 2006
Development and implementation of three mitogen-activated protein kinase (MAPK) signaling pathway imaging assays to provide MAPK module selectivity profiling for kinase inhibitors: MK2-EGFP translocation, c-Jun, and ERK activationDebra Nickischer, Carmen Laethem, Oscar J Trask, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 25, 2009
High-throughput automated confocal microscopy imaging screen of a kinase-focused library to identify p38 mitogen-activated protein kinase inhibitors using the GE InCell 3000 analyzerO Joseph Trask, Debra Nickischer, Audrey Burton, et al.
Methods in Enzymology|November 18, 2006
Generation and characterization of a stable MK2-EGFP cell line and subsequent development of a high-content imaging assay on the Cellomics ArrayScan platform to screen for p38 mitogen-activated protein kinase inhibitorsRhonda Gates Williams, Ramani Kandasamy, Debra Nickischer, et al.
Methods in Enzymology|November 18, 2006
Assay development and case history of a 32K-biased library high-content MK2-EGFP translocation screen to identify p38 mitogen-activated protein kinase inhibitors on the ArrayScan 3.1 imaging platformOscar J Trask, Audrey Baker, Rhonda Gates Williams, et al.
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