Issue Date | Title | Author(s) | Relation | scopus | WOS | Fulltext/Archive link |
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2003 | Molecular identification of combined homozygous and compound heterozygous mutations in the CYP21 gene in simple virilizing congenital adrenal hyperplasia in Taiwan | Wang, H. H.; Lee, H. H.; Wu, D. A.; Lee, Y. J.; Chung, B. C. ; Wang, T. R. | Acta Paediatr Taiwan 44, 339-342 | |||
2005 | Novel missense mutations, GCC [Ala306]- > GTC [Val] and ACG [Thr318]- > CCG [Pro], in the CYP11B1 gene cause steroid 11beta-hydroxylase deficiency in the Chinese | Lee, H. H.; Won, G. S.; Chao, H. T.; Lee, Y. J.; Chung, B. C. | Clinical Endocrinology 62, 418-422 | |||
1997 | Overexpression of mitogen-activated protein kinase kinase kinase reversed cAMP inhibition of NF-kappaB in T cells | Ho, H. Y.; Lee, H. H.; Lai, M. Z. | Eur J Immunol 27, 222-226 |