| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2006 | A simple electrostatic switch important in the activation of type I protein kinase A by cyclic AMP | Vigil, D.; Lin, J. -H.; Sotriffer, C. A.; Pennypacker, J. K.; McCammon, J. A.; Taylor, S. S. | Protein Science 15, 113-121 | | | |
| 2002 | Bridging implicit and explicit solvent approaches for membrane electrostatics | Lin, J. -H; Baker, N. A.; McCammon, J. A. | Biophysical Journal 83, 1374-1379 | | | |
| 2002 | Computational drug design acommodating receptor flexibility: The relaxed complex scheme | Lin, J. -H; Perryman, A. L.; Schames, J. R.; McCammon, J. A. | J. Am. Chem. Soc 124, 5632-5633 | | | |
| 2004 | HIV-1 protease molecular dynamics of a wild-type and of the V82F/I84V mutant: Possible contributions to drug resistance and a potential new drug target site for drugs | Perryman, A. L.; Lin, J. -H.; McCammon, J. A. | Protein Science 13, 1108-1123 | | | |
| 2006 | Increased membrane affinity of the C1 domain of protein kinase Cdelta components for the lack of involvement of its C2 Domain in membrane recruitment | Giorgione, J. R.; Lin, J. -H.; McCammon, J. A.; Newton, A. C. | J. Biol. Chem 281, 1660-1669 | | | |
| 2006 | Optimization and computational evaluation of a series of potential active site inhibitors of the V82F/I84V drug-resistant mutant of HIV-1 protease: an application of the relaxed complex method of structure-based drug design | Perryman, A. L.; Lin, J. -H.; McCammon, J. A. | Chemical Biology & Drug Design 67(5), 336-345 | | | |
| 2006 | Restrained molecular dynamics of HIV-1 protease: Validating a new target for drug design | Perryman, A. L.; Lin, J. -H.; McCammon, J. A. | Biopolymers 82, 272-284 | | | |
