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 | | | |
2006 | Promoter region methylation and reduced expression of thrombospondin-1 after oxygen-glucose deprivation in murine cerebral endothelial cells | Hu, C. J.; Chen, S. D.; Yang, D. Y.; Lin, T. N.; Chen, C. M.; Huang, T. H. M.; Hsu, C. Y. | Journal of Cerebral Blood Flow and Metabolism 26(12), 1519-1526 | | | |