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教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
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機構 日期 題名 作者
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
義守大學 1999-06 Enhancement of enantioselectivity by altering alcohol concentration for esterification in supercritical CO2 Wu JY; Liang MT
臺北醫學大學 1999 Investigation of guanidinium group involved in RNA recognition by paralleled in vitro selection of streptomycin- and arginine-binding RNAs 吳瑞裕; Wu JY; Taila RR; Lamsem L; Chow CS; ;
中國醫藥大學 1999 Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data Tsai, FJ; Tsai, CH; Chang, JG; Wu, JY
中國醫藥大學 1999 Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity Tsai, FJ; Wu, JY; Tsai, CH; Chang, JG
中國醫藥大學 1999 Further characterization of Wilson disease in Taiwan: identification of two novel mutations and high correlation between haplotype and mutation. Wu, JY; Tsai, FJ; Lee, CC; Chang, JG; Tsai, CH
中國醫藥大學 1999 Different race, different face: minor anomalies in Chinese newborn infants Tsai, FJ; Tsai, CH; Peng, CT; Wu, JY; Lien, CH; Wang, TR
義守大學 1998-12 Effect of axial dispersion on the evaluation of enantiomeric ratio by a fixed-bed reactor Wu JY
臺北醫學大學 1998 Identification of inosine as an endogenous modulator for the benzodiazepine binding site of the GABAA receptors 李怡萱; Yarom M; Tang XW; Wu E; Carlson RG; Vander Velde D; Lee YH; Wu JY
臺北醫學大學 1998 Kainic acid induces calcium-dependent neurotropic responses in developing cortical neurons 李怡萱; Lee YH; Fang KM; Yang CM; Chiu CT; Yang CP; Wu JY
中國醫藥大學 1998 Mutation analysis in fibroblast growth factor receptor genes: Chinese data Lin, SP; Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH
中國醫藥大學 1998 Mutation analysis of Chinese patients with Wilson disease Tsai, FJ; Wu, JY; Chang, JG; Lin, SP; Peng, CT; Tsai, CH
中國醫藥大學 1998 Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis Peng, CT; Wu, JY; Tsai, CH; Tsai, FJ; Chang, JG
中國醫藥大學 1998 Prenatal diagnosis of Apert syndrome Chang, CC; Tsai, FJ; Tsai, HD; Tsai, CH; Hsieh, YY; Lee, CC; Yang, TC; Wu, JY
中國醫藥大學 1998 Molecular analysis of type I oculocutaneous albinism in Chinese Wu, JY; Lin, SP; Tsai, LP; Tsai, FJ; Peng, CT; Tsai, CH
中國醫藥大學 1997 Mutations in fibroblast growth factor receptor genes: Chinese data. Tsai, FJ; Wu, JY; Peng, CT; Tsai, CH
臺北醫學大學 1993 Action of myenteric GABAergic neurons in guinea pig stomach 蔡麗雪; Tsai LH; Tsai WH; Wu JY; ; ;
國立臺灣大學 1980-01 Dietary survey on the juvenile group of Taipei city area.(in Chinese). Tsai, YC; Chen, HH; Wu, JY; Hsu, CP; Huang, CJ

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