| 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 |
| 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 |
