| Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
| 2006 | A novel compound heterozygous mutation of K494_V495 deletion plus R496L and D487_F489 deletion in extreme C-terminus of cytochrome P450c17 causes 17alpha-hydroxylase deficiency | Lee, L. S.; Shu, W. J.; Wu, C. M.; Hsieh, C. H.; Chen, S. M.; Hu, C. J.; Chen, W. Y.; Chung, B. C. | Mol Cell Endocrinol 249, 16-20 | | | |
| 2005 | Identification of novel HLA-A*0201-restricted CD8+ T-cell epitopes on hepatitis delta virus | Huang, Y. H.; Tao, M. H.; Hu, C. P.; Shu, W. J.; Wu, J. C. | J Gen Virol 85, 3089-3098 | | | |
