Etiology of a genetically complex seizure disorder in Celf4 mutant mice von Wagnon, J. L., Mahaffey, C. L., Sun, W., Yang, Y., Chao, H.‐T., Frankel, W. N.

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Effects of estrogen on cognition, mood, and cerebral blood flow in AD: a controlled study von Wang, P N, Liao, S Q, Liu, R S, Liu, C Y, Chao, H T, Lu, S R, Yu, H Y, Wang, S J, Liu, H C

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Platelet‐activating factor‐acetylhydrolase A379V (exon 11) gene polymorphism is an independent and functional risk factor for premature myocardial infarction von LIU, P.‐Y., LI, Y.‐H., WU, H.‐L., CHAO, T.‐H., TSAI, L.‐M., LIN, L.‐J., SHI, G.‐Y., CHEN, J.‐H.

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Mitochondrial deoxyribonucleic acid 4977-bp deletion is associated with diminished fertility and motility of human sperm von Kao, S, Chao, H T, Wei, Y H

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Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa von KAO, S.-H, CHAO, H.-T, WEI, Y.-H

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Risk Factors Contributing to Early Occurrence of Port Site Metastases of Laparoscopic Surgery for Malignancy von Wang, Peng-Hui, Yuan, Chiou-Chung, Lin, Grace, Ng, Heung-Tat, Chao, Hsiang-Tai

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High prevalence of incidental brain findings in primary dysmenorrhoea von Li, W.C., Tu, C.H., Chao, H.T., Yeh, T.C., Chen, L.F., Hsieh, J.C.

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Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia von Lee, H H, Chao, H T, Ng, H T, Choo, K B

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Port Site Metastasis after Laparoscopic-Assisted Vaginal Hysterectomy for Endometrial Cancer: Possible Mechanisms and Prevention von Wang, Peng-Hui, Yen, Ming-Shyen, Yuan, Chiou-Chung, Chao, Kuan-Chong, Ng, Heung-Tat, Lee, Wen-Ling, Chao, Hsiang-Tai

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Stromelysin‐1 promoter 5A/6A polymorphism is an independent genetic prognostic risk factor and interacts with smoking cessation after index premature myocardial infarction von LIU, P.‐Y., LI, Y.‐H., TSAI, W.‐C., TSAI, L.‐M., CHAO, T.‐H., WU, H.‐L., CHEN, J.‐H.

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Role of BMK1 in regulation of growth factor-induced cellular responses von Kato, Y, Chao, T H, Hayashi, M, Tapping, R I, Lee, J D

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A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib von Chauhan, Dharminder, Catley, Laurence, Li, Guilan, Podar, Klaus, Hideshima, Teru, Velankar, Mugdha, Mitsiades, Constantine, Mitsiades, Nicolas, Yasui, Hiroshi, Letai, Anthony, Ovaa, Huib, Berkers, Celia, Nicholson, Benjamin, Chao, Ta-Hsiang, Neuteboom, Saskia T.C., Richardson, Paul, Palladino, Michael A., Anderson, Kenneth C.

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Structure−Activity Relationship Studies of Salinosporamide A (NPI-0052), a Novel Marine Derived Proteasome Inhibitor von Macherla, Venkat R, Mitchell, Scott S, Manam, Rama Rao, Reed, Katherine A, Chao, Ta-Hsiang, Nicholson, Benjamin, Deyanat-Yazdi, Gordafaried, Mai, Bao, Jensen, Paul R, Fenical, William F, Neuteboom, Saskia T. C, Lam, Kin S, Palladino, Michael A, Potts, Barbara C. M

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Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese von LEE, H.-H, CHAO, H.-T, LEE, Y.-J, SHU, S.-G, CHAO, M.-C, KUO, J.-M, CHUNG, B.-C

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A Combined Cross-sectional and Longitudinal Study of Predicting Metabolic Syndrome and Cardiovascular Disease by Using Haemoglobin in the Elderly von Chao, T-H, Hu, Y-H, Liang, P-C, Kuo, S-W, Wu, D-A

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G-33a mutation in the promoter region of thrombomodulin gene and its association with coronary artery disease and plasma soluble thrombomodulin levels von Li, Yi-Heng, Chen, Jyh-Hong, Wu, Hua-Lin, Shi, Guey-Yueh, Huang, Huey-Chun, Chao, Ting-Hsing, Tsai, Wei-Chuan, Tsai, Liang-Miin, Guo, How-Ran, Wu, Wen-Shiann, Chen, Zhih-Cherng

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Gonadotropin-releasing hormone-agonist as a neoadjuvant therapy for Sertoli–Leydig cell tumors of the ovary von Chao, H.T., Wang, P.H., Lin, H.D.

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Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese von LEE, H.-H, KUO, J.-M, CHAO, H.-T, LEE, Y.-J, CHANG, J.-G, TSAI, C.-H, CHUNG, B.-C

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Association Between FRAX Without BMD and Incidence of Falls in Middle-Aged and Old People: An Epidemiological Cohort Survey von Ou, L.-C, Chang, Y.-F, Chang, C.-S, Chiu, C.-J, Chao, T.-H, Lin, R.-M, Sun, Z.-J, Wu, C.-H

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Analysis of the Chimeric CYP21P/CYP21 Gene in Steroid 21-Hydroxylase Deficiency von Lee, Hsien-Hsiung, Chang, Jan-Gowth, Tsai, Chang-Hai, Tsai, Fuu-Jen, Chao, Hsiang-Tai, Chung, Bon-chu

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