2018 | Adaptable Small Ligand of CYP1 Enzymes for Use in Understanding the Structural Features Determining Isoform Selectivity | 최선; 이윤지 | Article |
2021 | Discovery of Benzopyridone-Based Transient Receptor Potential Vanilloid 1 Agonists and Antagonists and the Structural Elucidation of Their Activity Shift | 최선; 이윤지 | Article |
2008 | FAK/SRC PATHWAY PLAYS A KEY ROLE IN FARNESIFEROL C INDUCED ANTIANGIOGENIC AND ANTITUMOR ACTIVITIES | 최선; 이윤지 | Meeting Abstract |
2019 | Importance of protein dynamics in the structure-based drug discovery of class A G protein-coupled receptors (GPCRs) | 최선; 이윤지 | Article |
2021 | N-terminus-independent activation of c-Src via binding to a tetraspan(in) TM4SF5 in hepatocellular carcinoma is abolished by the TM4SF5 C-terminal peptide application | 최선; 이윤지 | Article |
2009 | Non-vanillyl resiniferatoxin analogues as potent and metabolically stable transient receptor potential vanilloid 1 agonists | 최선; 이윤지 | Article |
2018 | Recent Advances in Structure-Based Drug Design Targeting Class A G Protein-Coupled Receptors Utilizing Crystal Structures and Computational Simulations | 최선; 이윤지 | Article |
2021 | Subtle Chemical Changes Cross the Boundary between Agonist and Antagonist: New A(3) Adenosine Receptor Homology Models and Structural Network Analysis Can Predict This Boundary | 최선; Pankaz Kumar Sharma; 이윤지 | Article |
2016 | Ultraslow Water-Mediated Transmembrane Interactions Regulate the Activation of A(2A) Adenosine Receptor | 최선; 이윤지 | Article |
2018 | Understanding G protein-coupled receptor allostery via molecular dynamics simulations: Implications for drug discovery | 최선; 이윤지 | Book Chapter |