Items for Author "Chang-Hai Tsai" 

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Showing 9 items.

Collection	Date	Title	Authors	Bitstream
[生物醫學研究所] 期刊論文	2009-06-01	Association of interleukin-10 A-592C polymorphism in Taiwanese children with Kawasaki disease.	Kai-Chung Hsueh; Ying-Ju Lin; Jeng-Sheng Chang; Lei Wan; Yu-Hsin Tsai; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai
[生物醫學研究所] 期刊論文	2009-03-01	The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma	Yao-Yuan Hsieh; Chi-Chen Chang; Da-Tian Bau; Fuu-Jen Tsai; Chang-Hai Tsai; Chih-Ping Chen
[生物醫學研究所] 期刊論文	2008-05-01	XRCC4 codon 247*A and XRCC4 promoter -1394*T related genotypes but not XRCC4 intron 3 gene polymorphism are associated with higher susceptibility for endometriosis	Yao-Yuan Hsieh; Da-Tian Bau; Chi-Chen Chang; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai
[生物醫學研究所] 期刊論文	2008-03-01	Association of vascular endothelial growth factor C-634 G polymorphism in Taiwanese children with Kawasaki disease	Kai-Chung Hsueh; Ying-Ju Lin; Jeng-Sheng Chang; Lei Wan; Yuhsin Tsai; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai
[生物醫學研究所] 期刊論文	2008-02-01	A/C polymorphism in the interleukin-18 coding region among Taiwanese systemic lupus erythematosus patients	Ying-Ju Lin; Lei Wan; Jim Jinn-Chyuan Sheu; Chung-Ming Huang; Cheng-Wen Lin; Yu-Ching Lan; Chih-Ho Lai; Chien-Hui Hung; Yuhsin Tsai,; Chang-Hai Tsai; T-H Lin; Chih-Ping Chen; Fuu-Jen Tsai
[生物醫學研究所] 期刊論文	2008-01-01	Association of interleukin-18 gene polymorphism with asthma in Chinese patients	Cheng-Chun Lee; Wei-Yong Lin; Lei Wan; Yuhsin Tsai; Chang-Hai Tsai; Chung-Ming Huang; Chih-Ping Chen; Fuu-Jen Tsai
[生物醫學研究所] 期刊論文	2007-12-01	Growth hormone (GH) receptor C.1319 G>T polymorphism, but not exon 3 retention or deletion is associated with better first-year growth response to GH therapy in patients with GH deficiency	Lei Wan; Wei-Cheng Chen; Yuhsin Tsai; Yu-Tsun Kao; Yao-Yuan Hsieh; Cheng-Chun Lee; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai
[生物醫學研究所] 期刊論文	2007-09-01	Human gene mutations. Gene symbol: EXT2. Disease: exostoses (multiple) 2	Wei-De Lin; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai
[生物醫學研究所] 期刊論文	2000-02-01	Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese	Hsien-Hsiung Lee; Jing-Mei Kuo; Hsiang-Tai Chao; Yann-Jinn Lee; Jan-Gowth Chang; Chang-Hai Tsai; Bon-chu Chung