| - | A Global Targeting Strategy for acquisition of selective src-kinase inhibitor : from consensus sequence to bivalent ligand | Hah Jung Mi |
| - | Acquisition of selective Src Kinase Inhibitor based on Consensus peptide substrate assay | Hah Jung Mi; David Lawrence |
| - | Acquisition of selective Src Kinase Inhibitor via a Global Targeting Strategy | Hah Jung Mi |
| - | Asymetric 10-Membered Bislactam Synthesis for Peptidomimetic Template and Its Application to Kinase Inhibition | Sim Tae Bo; Choi Hwan Geun; SON JUNG BEOM; Ham Young Jin; Hah Jung Mi; Kangkook Lee |
| - | Correlation between Quantum Mechanical/Molecular Mechanical (QM/MM) Docking Performance and Binding Site Classification | chung, Jae Yoon; Hah Jung Mi; 조은성 |
| - | Effective 3D Boundary Condition Script for Fragment Based Virtual Screening | chung, Jae Yoon; Art Cho; Hah Jung Mi |
| - | Enantioseletive Total Synthesis of Natural Product, L-783277 | Sim Tae Bo; SON JUNG BEOM; Hah Jung Mi; Park Dong Sik |
| - | Hologram and Receptor-Guided 3D QSAR Models for Potent JNK3 Inhibitors | JEONG, JAE YOON; 조은성; Hah Jung Mi |
| - | HOLOGRAM AND RECEPTOR-GUIDED 3D QSAR MODELS FOR POTENT JNK3 INHIBITORS | Hah Jung Mi |
| - | The Chiral Synthesis of the Lucentamycins A-D Core, 3-Methyl -4-Ethylideneproline | Yu Hana; Choi Hwan Geun; Hah Jung Mi; Sim Tae Bo |
| - | Total Synthesis of Putative Lucentamycin A and Its Analogues by Rh-Catalyzed Diastereoselective Cycloisomerization of 1,6-Enyne | Ham Young Jin; Choi Hwan Geun; Yu Hana; Hah Jung Mi; Sim Tae Bo |
