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Showing items 191-240 of 257 (6 Page(s) Totally)
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Institution	Date	Title	Author
中國醫藥大學	2003	Lack of association of tumor necrosis factor alpha gene polymorphism in patients with rheumatoid arthritis in central Taiwan	Lo, SF; Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2003	Genetic analysis of chromosome 22q11.2 markers in congenital heart disease	Shi, YR; Hsieh, KS; Wu, JY; Lee, CC; Tsai, CH; Yu, MT; Chang, JS; Tsai, FJ
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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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
義守大學	1999-07	Evaluation of intrinsic enantiomeric ratio by transient response method in a packed-bed enzymatic reactor	Wu JY

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