Epigenetic regulation of COX‑2 expression by DNA hypomethylation via NF‑κB activation in ketamine‑induced ulcerative cystitis von Chuang, Shu‑Mien, Lu, Jian‑He, Lin, Kun‑Ling, Long, Cheng‑Yu, Lee, Yung‑Chin, Hsiao, Hui‑Pin, Tsai, Chia‑Chun, Wu, Wen‑Jeng, Yang, Hui‑Jun, Juan, Yung‑Shun

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Syndromic ciliopathy: a taiwanese single-center study von Pan, Yu-Wen, Ou, Tsung-Ying, Chou, Yen-Yin, Kuo, Pao-Lin, Hsiao, Hui-Pin, Chiu, Pao-Chin, Lin, Ju-Li, Lo, Fu-Sung, Wang, Chung-Hsing, Chen, Peng-Chieh, Tsai, Meng-Che

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Altered Pattern of Macrophage Polarization as a Biomarker for Severity of Childhood Asthma von Kuo, Chang-Hung, Tsai, Mei-Lan, Li, Chung-Hsiang, Hsiao, Hui-Pin, Chao, Mei-Chyn, Lee, Ming-Sheng, Lin, Yi-Ching, Hung, Chih-Hsing

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Congenital generalized lipodystrophy in Taiwan von Hsu, Rai-Hseng, Lin, Wei-De, Chao, Mei-Chyn, Hsiao, Hui-Pin, Wong, Siew-Lee, Chiu, Pao-Chin, Chu, Shao-Yin, Ke, Yu-Yuan, Lau, Beng-Huat, Chien, Yin-Hsiu, Hwu, Wuh-Liang, Tsai, Fuu-Jen, Wang, Chung-Hsing, Lee, Ni-Chung

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Effects of Cushing Disease on Bone Mineral Density in a Pediatric Population von Lodish, Maya B., MD, Hsiao, Hui-Pin, MD, Serbis, Anastasios, MD, Sinaii, Ninet, PhD, MPH, Rothenbuhler, Anya, MD, Keil, Margaret F., CRNP, Boikos, Sosipatros A., MD, Reynolds, James C., MD, Stratakis, Constantine A., MD, DSc

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Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome von Lin, Hsiang-Yu, Lee, Chung-Lin, Fran, Sisca, Tu, Ru-Yi, Chang, Ya-Hui, Niu, Dau-Ming, Chang, Chia-Ying, Chiu, Pao Chin, Chou, Yen-Yin, Hsiao, Hui-Pin, Yang, Chia-Feng, Tsai, Meng-Che, Chu, Tzu-Hung, Chuang, Chih-Kuang, Lin, Shuan-Pei

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Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese von Wu, Yi-Lei, Hwang, Daw-Yang, Hsiao, Hui-Pin, Ting, Wei-Hsin, Huang, Chi-Yu, Tsai, Wen-Yu, Chen, Hung-Chun, Chao, Mei-Chyn, Lo, Fu-Sung, Tsai, Jeng-Daw, Yang, Stone, Shih, Shin-Lin, Lin, Shuan-Pei, Lin, Chiung-Ling, Lee, Yann-Jinn

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Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome von Lin, Hsiang-Yu, Lee, Chung-Lin, Fran, Sisca, Tu, Ru-Yi, Chang, Ya-Hui, Niu, Dau-Ming, Chang, Chia-Ying, Chiu, Pao-Chin, Chou, Yen-Yin, Hsiao, Hui-Pin, Tsai, Meng-Che, Chao, Mei-Chyn, Tsai, Li-Ping, Yang, Chia-Feng, Su, Pen-Hua, Pan, Yu-Wen, Lee, Chen-Hao, Chu, Tzu-Hung, Chuang, Chih-Kuang, Lin, Shuan-Pei

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1,2,3,4,6 penta-O-galloyl-β-D-glucose ameliorates high-fat diet-induced nonalcoholic fatty liver disease and maintains the expression of genes involved in lipid homeostasis in mice... von Kant, Rajni, Lu, Chung-Kuang, Nguyen, Hien Minh, Hsiao, Hui-Hua, Chen, Chao-Ju, Hsiao, Hui-Pin, Lin, Kai-Jay, Fang, Cheng-Chieh, Yen, Chia-Hung

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Clinical and Genetic Heterogeneity, Overlap with Other Tumor Syndromes, and Atypical Glucocorticoid Hormone Secretion in Adrenocorticotropin-Independent Macronodular Adrenal Hyperp... von Hsiao, Hui-Pin, Kirschner, Lawrence S., Bourdeau, Isabelle, Keil, Margaret F., Boikos, Sosipatros A., Verma, Somya, Robinson-White, Audrey J., Nesterova, Maria, Lacroix, André, Stratakis, Constantine A.

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Maternal diabetes or hypertension and lifestyle factors may be associated with metabolic syndrome: A population-based study in Taiwan von Chen, Tzu-Hua, Hsiao, Hui-Pin, Chiu, Yu-Wen, Shih, Nai-Hua, Chuang, Hung-Yi, Huang, Chia-Tsuan

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A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 ( PDE11A ) in individuals with adrenocortical hyperplasia von Bertherat, Jérôme, Bertagna, Xavier, Keil, Meg, Delimpasi, Georgia, Levine, Elizabeth, Fratticci, Amato, Libè, Rossella, Carney, J Aidan, Matyakhina, Ludmila, Groussin, Lionel, Hsiao, Hui Pin, Heyerdahl, Sarah, Kirschner, Lawrence S, Giatzakis, Christoforos, Gaillard, Rolf C, Stein, Erica, Robinson-White, Audrey, Horvath, Anelia, Stratakis, Constantine A, Boikos, Sosipatros, Griffin, Kurt J, Bossis, Ioannis, Cramer, Kevin

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Role of thyrotropin-releasing hormone test in re-evaluation of congenital hypothyroidism von Chen, Li-Min, Chen, Yen-Chun, Hsiao, Hui-Pin, Chen, Bai-Hsiun, Chao, Mei-Chyn

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Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 Patients von Su, Pen-Hua, Yu, Ju-Shan, Wu, Yu-Zhen, Tsai, Yu-Shen, Lo, Fu-Sung, Lin, Ju-Li, Chao, Mei-Chyn, Hsu, Chia-Chi, Ke, Yu-Yuan, Chiu, Pao-Chin, Chen, Jo-Ching, Huang, Ying-Hua, Lin, Shuan-Pei, Chou, Yen-Yin, Ting, Wei-Hsin, Wang, Shuo-Yu, Chiu, Chiao-Fan, Huang, Yen-Chun, Hsiao, Hui-Pin, Lin, Chao-Hsu, Wang, Chung-Hsing, Bau, DA-Tian, Lin, Ching-Yuang

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Integrated Genomic Analysis of Nodular Tissue in Macronodular Adrenocortical Hyperplasia: Progression of Tumorigenesis in a Disorder Associated with Multiple Benign Lesions von Almeida, Madson Q, Harran, Michelle, Bimpaki, Eirini I, Hsiao, Hui-Pin, Horvath, Anelia, Cheadle, Chris, Watkins, Tonya, Nesterova, Maria, Stratakis, Constantine A

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A Taiwanese Boy With Congenital Generalized Lipodystrophy Caused by Homozygous Ile262fs Mutation in the BSCL2 Gene von Huang, Hsiu-Hui, Chen, Tai-Heng, Hsiao, Hui-Pin, Huang, Chia-Tsuan, Wang, Cheng-Chu, Shiau, Ya-Huei, Chao, Mei-Chyn

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The effects of acarbose on chemokine and cytokine production in human monocytic THP-1 cells von Lin, Yi-Ching, Chen, Yen-Chun, Hsiao, Hui-Pin, Kuo, Chang-Hung, Chen, Bai-Hsiun, Chen, Yi-Ting, Wang, Shih-Ling, Tsai, Mei-Lan, Hung, Chih-Hsing

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Respiratory Adenoviral Infections in Children: A Study of Hospitalized Cases in Southern Taiwan in 2001–2002 von Chen, Hsiu-Lin, Chiou, Shyh-Shin, Hsiao, Hui-Pin, Ke, Guan-Ming, Lin, Yung-Cheng, Lin, Kuei-Hsiang, Jong, Yuh-Jyh

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Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell Syndrome von Lin, Hsiang-Yu, Lee, Chung-Lin, Tu, Yuan-Rong, Chang, Ya-Hui, Niu, Dau-Ming, Chang, Chia-Ying, Chiu, Pao Chin, Chou, Yen-Yin, Hsiao, Hui-Pin, Tsai, Meng-Che, Chao, Mei-Chyn, Tsai, Li-Ping, Yang, Chia-Feng, Su, Pen-Hua, Pan, Yu-Wen, Lee, Chen-Hao, Chu, Tzu-Hung, Chuang, Chih-Kuang, Lin, Shuan-Pei

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The AGG interruption pattern within the CGG repeat of the FMR1 gene among Taiwanese population von Chiu, Hua-Hsien, Tseng, Yi-Ting, Hsiao, Hui-Pin, Hsiao, Hui-Hua

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