| 2007 | Synthesis, cytotoxicity, topoisomerase II inhibition, and DNA cross-linking study of new xanthone analogues | 권영주 | Meeting Abstract |
| 2007 | P-glycoprotein inhibitory activity of two phenolic compounds, (-)-syringaresinol and tricin from Sasa borealis | 서은경; 이화정; 권영주; 한아름 | Article |
| 2007 | Pharmacokinetics of doxazosin gastrointestinal therapeutic system after multiple administration in Korean healthy volunteers | 곽혜선 | Article |
| 2007 | Mycophenolic acid inhibits oleic acid-induced vascular smooth muscle cell activation by inhibiting cellular reactive oxygen species | 하헌주 | Article |
| 2007 | Design, docking, and synthesis of novel indeno[1,2-c]isoquinolines for the development of antitumor agents as topoisomerase I inhibitors | 이상국; 권영주 | Article |
| 2007 | Radical approach to diabetic nephropathy | 하헌주 | Conference Paper |
| 2007 | Histone deacetylase inhibitors: A novel class of therapeutic agents in diabetic nephropathy | 하헌주 | Conference Paper |
| 2007 | Kidney International: Introduction | 하헌주 | Conference Paper |
| 2007 | Mechanisms of epithelial-mesenchymal transition of peritoneal mesothelial cells during peritoneal dialysis | 하헌주 | Review |
| 2007 | Polyproline-rod approach to isolating protein targets of bioactive small molecules: Isolation of a new target of indomethacin | 권영주 | Article |
| 2006 | Improvement of interfacial protein stability by CHAPS | 김길수; 사홍기 | Article |
| 2006 | Homology modeling and molecular docking study of translationally controlled tumor protein and artemisinin | 김춘미 | Article |
| 2006 | Synthesis and antifungal activity of 6-hydroxycinnolines | 유충규 | Article |
| 2006 | Development of new microencapsulation techniques useful for the preparation of PLGA microspheres | 사홍기 | Article |
| 2006 | MEDI 104-Synthesis, structure-activity relationships, and mechanism of action of novel indirubin derivatives as potent anti-proliferative agents with CDK2 inhibitory activities | 이상국 | Meeting Abstract |
| 2006 | Orthogonal activation of the reengineered A3 adenosine receptor (neoceptor) using tailored nucleoside agonists | 정낙신 | Article |
| 2006 | Synthesis and structure-activity relationships of novel indirubin derivatives as potent anti-proliferative agents with CDK2 inhibitory activities | 이상국 | Article |
| 2006 | Structure-activity relationships of 2-chloro-N6-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2006 | Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5′-ribofuran-uronamide moiety | 정낙신 | Article |
| 2006 | Synthesis of novel l-N-MCd4T as a potent anti-HIV agent | 정낙신 | Article |
