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Showing items 176-225 of 257 (6 Page(s) Totally)
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Institution	Date	Title	Author
臺北醫學大學	2004	Maxillary Ameloblastoma: A Case Report	羅金文; Wu JY; Luo CW; Pemg BY;
臺北醫學大學	2004	ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease	李信昌; Wu. JY;Kao. HJ;Li. SC;Stevens R;Hillman. S;Millington D; Chen. Y.T.
中國醫藥大學	2004	A marker for Stevens-Johnson syndrome	Chung, WH; Hung, SI; Hong, HS; Hsih, MS; Yang, LC; Ho, HC; Wu, JY; Chen, YT
中國醫藥大學	2004	EFFECTS OF ASPIRIN ON THE IN VITRO AND IN VIVO ACETYLATION OF 2-AMINOFLUORENE IN SPRAGUE-DAWLEYS RATS	Lin, SS; Yu, CS; Wu, JY; Tyan, YS; Lin, WC; Chung, JG
中國醫藥大學	2004	Lack of association between perlecan gene intron 6 BamHI polymorphism and risk of mitral valve prolapse in Taiwan Chinese	Chou, HT; Chen, YT; Wu, JY; Tsai, FJ
中國醫藥大學	2004	Polymorphisms of TAP1 transporter genes in Chinese patients with systemic lupus erythematosus in Taiwan	Huang, CM; Hang, LW; Chen, CL; Wu, JY; Tsai, FJ
中國醫藥大學	2004	Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13	Chen, WM; Liu, YF; Lin, MW; Chen, IC; Lin, PY; Lin, GL; Jou, YS; Lin, YT; Fann, CSJ; Wu, JY; Hsiao, KJ; Tsai, SF
中國醫藥大學	2004	Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13	Chen, WM; Liu, YF; Lin, MW; Chen, IC; Lin, PY; Lin, GL; Jou, YS; Lin, YT; Fann, CSJ; Wu, JY; Hsiao, KJ; Tsai, SF
中國醫藥大學	2004	Association between COL3A1 collagen gene exon 31 polymorphism and risk of floppy mitral valve/mitral valve prolapse	Chou, HT; Hung, JS; Chen, YT; Wu, JY; Tsai, FJ
中國醫藥大學	2004	Association of TAP2 gene polymorphisms in Chinese patients with rheumatoid arthritis	Yu, MC; Huang, CM; Wu, MC; Wu, JY; Tsai, FJ
中國醫藥大學	2004	ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease	Wu, JY; Kao, HJ; Li, SC; Stevens, R; Hillman, S; Millington, D; Chen, YT
中國醫藥大學	2004	ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease	Wu, JY; Kao, HJ; Li, SC; Stevens, R; Hillman, S; Millington, D; Chen, YT
中國醫藥大學	2003	No association between the dopamine transporter gene polymorphism and sporadic Parkinson's disease among Chinese in Taiwan.	蔡宗璋(Tzung-Chang Tsai); (Wu JY); 李正淳(Cheng-Chun Lee); 蔡崇豪(Chon-Haw Tsai); 蔡輔仁(Fuu-Jen Tsai); (Chang FC); (Kuo CC)
中國醫藥大學	2003	Association of the neuronal nicotinic acetylcholine receptor subunit alpha 4 polymorphisms with febrile convulsions	Chou, IC; Lee, CC; Huang, CC; Wu, JY; Tsai, JP; Tsai, CH; Tsai, FJ
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	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

Showing items 176-225 of 257 (6 Page(s) Totally)
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