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Plos Pathogens|February 4, 2021
Evidence for distinct mechanisms of small molecule inhibitors of filovirus entryAdam Schafer, Rui Xiong, Laura Cooper, et al.
SLAS Discovery : Advancing Life Sciences R & D|May 3, 2025
Development of a high-throughput TR-FRET assay to identify inhibitors of the FAK-paxillin protein-protein interactionRukayat Aromokeye, Martha Ackerman-Berrier, Rosa Del Carmen Araujo, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 27, 2020
Mixed lineage kinase 3 inhibition induces T cell activation and cytotoxicitySandeep Kumar, Sunil Kumar Singh, Navin Viswakarma, et al.
BMC Neuroscience|October 21, 2015
Re-engineering a neuroprotective, clinical drug as a procognitive agent with high in vivo potency and with GABAA potentiating activity for use in dementiaJia Luo, Sue H Lee, Lawren VandeVrede, et al.
ACS Infectious Diseases|May 5, 2021
Probing the Surface of a Parasite Drug Target Thioredoxin Glutathione Reductase Using Small Molecule FragmentsFrancesca Fata, Ilaria Silvestri, Matteo Ardini, et al.
Free Radical Biology & Medicine|December 25, 2019
Ectopic suicide inhibition of thioredoxin glutathione reductaseIlaria Silvestri, Haining Lyu, Francesca Fata, et al.
Journal of Medicinal Chemistry|July 10, 2013
Design, synthesis, and optimization of novel epoxide incorporating peptidomimetics as selective calpain inhibitorsIsaac T Schiefer, Subhasish Tapadar, Vladislav Litosh, et al.
Cancer Prevention Research (Philadelphia, Pa.)|October 15, 2011
Hops (Humulus lupulus) inhibits oxidative estrogen metabolism and estrogen-induced malignant transformation in human mammary epithelial cells (MCF-10A)L P Hemachandra, P Madhubhani, R Chandrasena, et al.
Oncogene|February 22, 2023
TrkA expression directs the anti-neoplastic activity of MLK3 inhibitors in triple-negative breast cancerRakesh Sathish Nair, Sandeep Kumar, Subhasis Das, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
In search of nonlipogenic ABCA1 inducers (NLAI): precision coregulator TR-FRET identifies diverse signatures for LXR ligandsMegan S Laham, Martha Ackerman-Berrier, Fahmida Alam, et al.
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