Determination of minimal transcriptional signatures of compounds for target prediction.
Exploring drug combinations in genetic interaction network.
Quantitatively integrating molecular structure and bioactivity profile evidence into drug-target relationship analysis.
A comparative analysis of protein targets of withdrawn cardiovascular drugs in human and mouse.
Classification of scaffold-hopping approaches.
Mass spectrometry-based metabolomics to elucidate functions in marine organisms and ecosystems.
Comprehensive predictions of target proteins based on protein-chemical interaction using virtual screening and experimental verifications.
Systems analysis of inflammatory bowel disease based on comprehensive gene information.
Network systems biology for targeted cancer therapies.
Three ring posttranslational circuses: insertion of oxazoles, thiazoles, and pyridines into protein-derived frameworks.