臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

???ui.leftmenu.abouttair???
	???ui.leftmenu.explanation???

???ui.leftmenu.bartitle???
	Repositories
	Author
	Title
	Date
	???ui.leftmenu.statisticschart???
	???ui.leftmenu.realtimefacts???
	???ui.leftmenu.trend???

???index.news???
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

???ui.leftmenu.copyrighttitle???
	???ui.leftmenu.copyrightpublisher???
	???ui.leftmenu.copyrightconference???

???ui.leftmenu.link???
	機構典藏計畫網站
	ROAR
	OpenDOAR
	SHERPA
	OAIster
	JAIRO
	Ira
	DSPACE
	RWWR
	臺大學術典藏NTU Scholars

"tsai fj"???jsp.browse.items-by-author.description???

???jsp.browse.items-by-author.back???
???jsp.browse.items-by-author.order1???	???jsp.browse.items-by-author.order2???

Showing items 251-300 of 327 (7 Page(s) Totally)
<< < 1 2 3 4 5 6 7 > >>
View [10|25|50] records per page

Institution	Date	Title	Author
中國醫藥大學	2002	Molecular analysis of thiopurine S-methyltransferase alleles in South-east Asian populations	Chang, JG; Lee, LS; Chen, CM; Shih, MC; Wu, MC; Tsai, FJ; Liang, DC
中國醫藥大學	2002	Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome	Wang, TJ; Huang, CB; Tsai, FJ; Wu, JY; Lai, RB; Hsiao, M
中國醫藥大學	2002	Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome	Wang, TJ; Huang, CB; Tsai, FJ; Wu, JY; Lai, RB; Hsiao, M
中國醫藥大學	2002	Association of vitamin D receptor gene BsmI polymorphisms in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2002	Distributions of p53 codon 72 polymorphism in primary open angle glaucoma	Lin, HJ; Chen, WC; Tsai, FJ; Tsai, SW
中國醫藥大學	2002	Lack of association of interleukin-1 beta gene polymorphisms in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2001	Androgen receptor trinucleotide polymorphism in endometriosis	Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Tsai, CH; Tsai, HD
中國醫藥大學	2001	Molecular analysis of GM1-gangliosidosis: identification and characterization of four novel mutations in two Taiwan Chinese patients.	Tsai, FJ; Yang, CF; Wu, JY
中國醫藥大學	2001	Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome	Tsai, FJ; Wu, JY; Yang, CF; Tsai, CH
中國醫藥大學	2001	Molecular analysis of two patients with 3-hydroxy-methyl-glutaric aciduria: identification of three novel mutations including one de novo mutation.	Wu, JY; Yang, CF; Tsai, FJ
中國醫藥大學	2001	Relation of polymorphism in the promotor region for the human osteocalcin gene to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan	Chen, HY; Tsai, HD; Chen, WC; Wu, JY; Tsai, FJ; Tsai, CH
中國醫藥大學	2001	Calcitonin receptor gene polymorphism: A possible genetic marker for patients with calcium oxalate stones	Chen, WC; Wu, HC; Lu, HF; Chen, HY; Tsai, FJ
中國醫藥大學	2001	Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: Nonassociation with endometriosis	Hsieh, YY; Chang, CC; Tsai, FJ; Wu, JY; Shi, YR; Tsai, HD; Tsai, CH
中國醫藥大學	2001	p21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis	Hsieh, YY; Tsai, FJ; Chang, CC; Chen, WC; Tsai, CH; Tsai, HD; Lin, CC
中國醫藥大學	2001	Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease	Chen, WC; Chen, HY; Wu, JY; Chen, YT; Tsai, FJ
中國醫藥大學	2001	Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease	Chen, WC; Chen, HY; Wu, JY; Chen, YT; Tsai, FJ
中國醫藥大學	2001	Antley-Bixler syndrome, description of two new cases and review of the literature	Lee, HJ; Cho, DY; Tsai, FJ; Shen, WC
中國醫藥大學	2001	Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients	Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC
中國醫藥大學	2001	Lack of evidence for the association of tumor necrosis factor-alpha gene promoter polymorphism with calcium oxalate stone and bladder cancer patients	Tsai, FJ; Lu, HF; Yeh, LS; Hsu, CD; Chen, WC
中國醫藥大學	2001	Interleukin-1 beta gene and receptor antagonist gene polymorphisms in patients with calcium oxalate stones	Chen, WC; Wu, HC; Chen, HY; Wu, MC; Hsu, CD; Tsai, FJ
中國醫藥大學	2001	Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD
中國醫藥大學	2001	Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD
中國醫藥大學	2001	Interleukin-1 beta and interleukin-1 receptor antagonist gene polymorphisms in rheumatoid arthritis	Huang, CM; Tsai, FJ; Wu, JY; Wu, MC
中國醫藥大學	2001	The association of androgen- and oestrogen-receptor gene polymorphisms with urolithiasis in men	Chen, WC; Wu, HC; Lin, WC; Wu, MC; Hsu, CD; Tsai, FJ
中國醫藥大學	2001	Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele	Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele	Hsieh, YY; Wu, JY; Chang, CC; Tsai, FJ; Lee, CC; Tsai, HD; Tsai, CH
中國醫藥大學	2001	Relation of BsmI vitamin D receptor gene polymorphism to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan	Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH; Li, CW
中國醫藥大學	2001	No association of vitamin D receptor gene BsmI polymorphisms with calcium oxalate stone formation	Chen, WC; Chen, HY; Hsu, CD; Wu, JY; Tsai, FJ
中國醫藥大學	2001	Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation	Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH
中國醫藥大學	2001	Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation	Lin, WD; Wu, JY; Hsu, HB; Tsai, FJ; Lee, CC; Tsai, CH
中國醫藥大學	2001	Mucopolysaccharidosis type VI: Report of two Taiwanese patients and identification of one novel mutation	Yang, CF; Wu, JY; Lin, SP; Tsai, FJ
中國醫藥大學	2001	Haplotype analysis in patients with velopharyngeal insufficiency (VPI) minimizes one VPI locus in 2.8Mb region of 22q11.	Tsai, LP; Tsou, KS; Shi, YR; Wu, JY; Tsai, FJ
中國醫藥大學	2001	Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan	Chen, HY; Chen, WC; Tsai, HD; Hsu, CD; Tsai, FJ; Tsai, CH
中國醫藥大學	2001	Arginine form of p21 gene codon 31 is less prominent in patients with calcium oxalate stone	Chen, WC; Lu, HF; Chen, HY; Hsu, CD; Tsai, FJ
中國醫藥大學	2001	Lack of evidence for the association of tumor necrosis factor-alpha gene promoter polymorphism with calcium oxalate stone and bladder cancer patients	Tsai, FJ; Lu, HF; Yeh, LS; Hsu, CD; Chen, WC
中國醫藥大學	2001	Association of the vitamin D receptor gene start codon Fok I polymorphism with calcium oxalate stone disease	Chen, WC; Chen, HY; Lu, HF; Hsu, CD; Tsai, FJ
中國醫藥大學	2001	Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients	Tsai, FJ; Yang, CF; Wu, JY; Tsai, CH; Lee, CC
中國醫藥大學	2001	Interleukin-1 beta and interleukin-1 receptor antagonist gene polymorphisms in rheumatoid arthritis	Huang, CM; Tsai, FJ; Wu, JY; Wu, MC
中國醫藥大學	2000	Mutation analysis of type 2 Gaucher disease in Taiwan Chinese and identification of two novel mutations.	Tsai, FJ; Wu, JY; Lin, SP; Chang, JG; Lee, CC; Tsai, CH
中國醫藥大學	2000	Molecular analysis of syndromic congenital heart disease by using short tandem-repeat polymorphic markers.	Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2000	Molecular analysis of the N-acetylgalactosamina-6-sulfate sulfatase gene in Taiwanese patients with Mucopolysaccharidosis IVA.	Yang, CF; Tsai, FJ; Lin, SP; Wu, JY
中國醫藥大學	2000	Cytogenetic study of workers exposed to chromium compounds	Wu, FY; Tsai, FJ; Kuo, HW; Tsai, CH; Wu, WY; Wang, RY; Lai, JS
中國醫藥大學	2000	Distributions of p53 codon 72 polymorphism in bladder cancer - proline form is prominent in invasive tumor	Chen, WC; Tsai, FJ; Wu, JY; Wu, HC; Lu, HF; Li, CW
中國醫藥大學	2000	A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia	Tsai, FJ; Wu, JY; Lin, WD; Tsai, CH
中國醫藥大學	2000	Infantile form G(M1) gangliosidosis with dilated cardiomyopathy: a case report	Lin, HC; Tsai, FJ; Shen, WC; Tsai, CH; Peng, CT
中國醫藥大學	2000	A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) causes non-syndromic craniosynostosis	Tsai, FJ; Wu, JY; Lee, CC; Tsai, CH
中國醫藥大學	2000	Antley-Bixler syndrome associated with Arnold-Chiari malformation	Chang, YT; Tsai, FJ; Shen, WC; Lin, HC; Peng, CT; Tsai, CH
中國醫藥大學	2000	Breech deformation complex in neonates	Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH
中國醫藥大學	2000	Breech deformation complex in neonates	Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH
中國醫藥大學	2000	Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency	Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC

Showing items 251-300 of 327 (7 Page(s) Totally)
<< < 1 2 3 4 5 6 7 > >>
View [10|25|50] records per page

	English \| 正體中文 \| 简体中文 \| 0
	???header.visitor??? : 50911524 ???header.onlineuser??? : 880 ???header.sponsordeclaration???