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

About TAIR
	About TAIR

Browse By
	Institution
	Author
	Title
	Date
	Statistics Chart
	Institution Facts
	Trend

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

Copyright
	Publisher & Journal Policy
	TAIR Copyright Conference Minutes

Related Links
	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"

Return to Browse by Author
Sorting by Title	Sort by Date

Showing items 201-250 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	2003	Growth hormone (GH) deficiency in patients with beta-thalassemia major and the efficacy of recombinant GH treatment	Wu, KH; Tsai, FJ; Peng, CT
中國醫藥大學	2003	The lack of association between febrile convulsions and polymorphisms in SCN1A	Chou, IC; Peng, CT; Tsai, FJ; Huang, CC; Shi, YR; Tsai, CH
中國醫藥大學	2003	Association of interleukin 10 and receptor antagonist gene polymorphisms with primary open-angle glaucoma	Lin, HJ; Tsai, SC; Tsai, FJ; Chen, WC; Tsai, JJP; Hsu, CD
中國醫藥大學	2003	TAP1 gene Accl polymorphism is associated with atopic bronchial asthma	Hang, LW; Hsia, TC; Chen, WC; Chen, HY; Tsai, FJ
中國醫藥大學	2003	Androgen receptor (AR) gene microsatellite polymorphism in postmenopausal women: correlation to bone mineral density and susceptibility to osteoporosis	Chen, HY; Chen, WC; Wu, MC; Tsai, FJ; Tsai, CH
中國醫藥大學	2003	Mutation of IVS2-12A/C > G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency	Lee, HH; Chang, SF; Tsai, FJ; Tsai, LP; Lin, CY
中國醫藥大學	2003	Insulin-like growth factor-II gene polymorphism is associated with primary open angle glaucoma	Tsai, FJ; Lin, HJ; Chen, WC; Chen, HY; Fan, SS
中國醫藥大學	2002	Characterization of four novel b-galactosidase gene mutations and a polymorphism in Taiwanese patients with GMI-gangliosidosis.	Wu, JY; Yang, CF; Tsai, FJ
中國醫藥大學	2002	Association between angiotensinogen gene M235T polymorphism and mitral valve prolapse syndrome in Taiwan Chinese	Chou, HT; Hung, JS; Chen, YT; Shi, YR; Tsai, FJ
中國醫藥大學	2002	Lack of association between transforming growth factor-beta 1 gene polymorphisms and mitral valve prolapse in Taiwan Chinese	Chou, HT; Shi, YR; Hsu, Y; Tsai, FJ
中國醫藥大學	2002	Correlation of p21 gene codon 31 polymorphism and TNF-alpha gene polymorphism with nasopharyngeal carcinoma	Tsai, MH; Chen, WC; Tsai, FJ
中國醫藥大學	2002	Cytochrome P450c17 alpha (CYP17) gene polymorphism is not associated with leiomyoma susceptibility	Hsieh, YY; Tsai, FJ; Chang, CC; Tsai, CH; Lin, CC; Yeh, LS
中國醫藥大學	2002	The polymorphisms of codon 727 and 52 of thyroid-stimulating hormone receptor gene are not associated with mitral valve prolapse syndrome in Taiwan Chinese	Chou, HT; Shi, YR; Chang, CT; Tsai, FJ
中國醫藥大學	2002	Smith-Magenis syndrome with bilateral vesicoureteral reflux: A case report	Chou, IC; Tsai, FJ; Yu, MT; Tsai, CH
中國醫藥大學	2002	Interleukin-4 intron 3 polymorphism is not related to susceptibility to febrile seizures	Tsai, FJ; Chou, IC; Hsieh, YY; Lee, CC; Lin, CC; Tsai, CH
中國醫藥大學	2002	Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions	Tsai, FJ; Hsieh, YY; Chang, CC; Lin, CC; Tsai, CH
中國醫藥大學	2002	Polymorphisms for interleukin-4 (IL-4)-590 promoter, IL-4 intron3, and tumor necrosis factor alpha-308 promoter: Non-association with endometriosis	Hsieh, YY; Chang, CC; Tsai, FJ; Hsu, Y; Tsai, HD; Tsai, CH
中國醫藥大學	2002	Angiotensin h type 1 receptor gene adenine/cytosine(1166) polymorphism is not associated with mitral valve prolapse syndrome in Taiwan Chinese	Chou, HT; Shi, YR; Wu, JY; Tsai, FJ
中國醫藥大學	2002	The proline form of p53 codon 72 polymorphism is associated with endometriosis	Chang, CC; Hsieh, YY; Tsai, FJ; Tsai, CH; Tsai, HD; Lin, CC
中國醫藥大學	2002	Urokinase gene 3 '-UTR T/C polymorphism is associated with urolithiasis	Tsai, FJ; Lin, CC; Lu, HF; Chen, HY; Chen, WC
中國醫藥大學	2002	Urokinase gene 3 '-UTR T/C polymorphism is associated with urolithiasis	Tsai, FJ; Lin, CC; Lu, HF; Chen, HY; Chen, WC
中國醫藥大學	2002	A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda	Shi, YR; Lee, CC; Hsu, YA; Wang, CH; Tsai, FJ
中國醫藥大學	2002	A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda	Shi, YR; Lee, CC; Hsu, YA; Wang, CH; Tsai, FJ
中國醫藥大學	2002	Interleukin-1 receptor antagonist gene polymorphism in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2002	Interleukin-1 receptor antagonist gene polymorphism 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	Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method	Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2002	No association of vitamin D receptor gene start codon Fok I Polymorphisms in Chinese patients with systemic lupus erythematosus	Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
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	2002	Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: Identification of five novel mutations	Wu, JY; Shu, SG; Yang, CF; Lee, CC; Tsai, FJ
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	Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma	Tsai, MH; Lin, CD; Hsieh, YY; Chang, FCC; Tsai, FJ; Chen, WC; Tsai, CH
中國醫藥大學	2002	Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots	Lai, CC; Tsai, CH; Tsai, FJ; Wu, JY; Lin, WD; Lee, CC
中國醫藥大學	2002	Turner syndrome with pseudodicentric Y chromosome mosaicism	Hsieh, YY; Lin, WC; Chang, CC; Tsai, FJ; Yu, MT; Tsai, HD; Tsai, CH
中國醫藥大學	2002	Turner syndrome with pseudodicentric Y chromosome mosaicism	Hsieh, YY; Lin, WC; Chang, CC; Tsai, FJ; Yu, MT; Tsai, HD; Tsai, CH
中國醫藥大學	2002	p21 gene codon 31 polymorphism is associated with bladder cancer	Chen, WC; Wu, HC; Hsu, CD; Chen, HY; Tsai, FJ
中國醫藥大學	2002	Relation of vitamin D receptor FokI start codon polymorphism. to bone mineral density and occurrence of osteoporosis in postmenopausal women in Taiwan	Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH
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	Unstable Hb Perth in a Taiwanese subject: A T -> C substitution at codon 32 of the beta-globin gene creates an MspI site	Chang, JG; Liu, HC; Shih, MC; Liu, SC; Chan, WL; Tsai, FJ
中國醫藥大學	2002	Unstable Hb Perth in a Taiwanese subject: A T -> C substitution at codon 32 of the beta-globin gene creates an MspI site	Chang, JG; Liu, HC; Shih, MC; Liu, SC; Chan, WL; Tsai, FJ
中國醫藥大學	2002	Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan	Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2002	Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan	Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2002	Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers	Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC
中國醫藥大學	2002	Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers	Lin, WD; Wu, JY; Tsai, FJ; Gau, MT; Lee, CC
中國醫藥大學	2002	The voltage-gated potassium channel KCNQ2 in Taiwanese children with febrile convulsions	Chou, IC; Tsai, FJ; Huang, CC; Lin, CC; Tsai, CH
中國醫藥大學	2002	Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method	Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學	2002	Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma	Tsai, MH; Lin, CD; Hsieh, YY; Chang, FCC; Tsai, FJ; Chen, WC; Tsai, CH

Showing items 201-250 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 \| Total items :0
	Visitors : 51106537 Online Users : 977 Project Commissioned by the Ministry of Education Project Executed by National Taiwan University Library