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Results: 1-25/36
Authors:
Chen, WC
Wu, HC
Lin, WC
Wu, MC
Hsu, CD
Tsai, FJ
Citation: Wc. Chen et al., The association of androgen- and oestrogen-receptor gene polymorphisms with urolithiasis in men, BJU INT, 88(4), 2001, pp. 432-436
Authors:
Chen, WC
Chen, HY
Lu, HF
Hsu, CD
Tsai, FJ
Citation: Wc. Chen et al., Association of the vitamin D receptor gene start codon Fok I polymorphism with calcium oxalate stone disease, BJU INT, 87(3), 2001, pp. 168-171
Authors:
Chen, WC
Chen, HY
Hsu, CD
Wu, JY
Tsai, FJ
Citation: Wc. Chen et al., No association of vitamin D receptor gene BsmI polymorphisms with calcium oxalate stone formation, MOL UROL, 5(1), 2001, pp. 7-10
Authors:
Hsieh, YY
Chang, CC
Tsai, FJ
Wu, JY
Shi, YR
Tsai, HD
Tsai, CH
Citation: Yy. Hsieh et al., Polymorphisms for interleukin-1 beta (IL-1 beta)-511 promoter, IL-1 beta exon 5, and IL-1 receptor antagonist: Nonassociation with endometriosis, J AS REPROD, 18(9), 2001, pp. 506-511
Authors:
Tsai, FJ
Walcek, CJ
Citation: Fj. Tsai et Cj. Walcek, Estimating chemical errors in large-scale simulations of aircraft emissions, TERR ATM OC, 12(1), 2001, pp. 79-108
Authors:
Tsai, FJ
Sun, WS
Chen, JP
Citation: Fj. Tsai et al., A composite modeling study of civil aircraft impacts on ozone and sulfate over the Taiwan area, TERR ATM OC, 12(1), 2001, pp. 109-135
Authors:
Lee, HJ
Cho, DY
Tsai, FJ
Shen, WC
Citation: Hj. Lee et al., Antley-Bixler syndrome, description of two new cases and review of the literature, PED NEUROS, 34(1), 2001, pp. 33-39
Authors:
Lai, CC
Tsai, CH
Tsai, FJ
Lee, CC
Lin, WD
Citation: Cc. Lai et al., Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots, RAP C MASS, 15(22), 2001, pp. 2145-2151
Authors:
Chen, HY
Tsai, HD
Chen, WC
Wu, JY
Tsai, FJ
Tsai, CH
Citation: Hy. Chen et al., 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, J CL LAB AN, 15(5), 2001, pp. 251-255
Authors:
Hsieh, YY
Tsai, FJ
Chang, CC
Chen, WC
Tsai, CH
Tsai, HD
Lin, CC
Citation: Yy. Hsieh et al., p21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis, J CL LAB AN, 15(4), 2001, pp. 184-187
Authors:
Tsai, FJ
Wu, JY
Yang, CF
Tsai, CH
Citation: Fj. Tsai et al., Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome, ACT PAEDIAT, 90(5), 2001, pp. 595-597
Authors:
Chen, HY
Chen, WC
Tsai, HD
Hsu, CD
Tsai, FJ
Tsai, CH
Citation: Hy. Chen et al., Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan, MATURITAS, 40(2), 2001, pp. 143-150
Authors:
Chen, WC
Wu, HC
Lu, HF
Chen, HY
Tsai, FJ
Citation: Wc. Chen et al., Calcitonin receptor gene polymorphism: A possible genetic marker for patients with calcium oxalate stones, EUR UROL, 39(6), 2001, pp. 716-719
Authors:
Huang, CM
Tsai, FJ
Wu, JY
Wu, MC
Citation: Cm. Huang et al., Interleukin-1 beta and interleukin-1 receptor antagonist gene polymorphisms in rheumatoid arthritis, SC J RHEUM, 30(4), 2001, pp. 225-228
Authors:
Chen, WC
Wu, HC
Chen, HY
Wu, MC
Hsu, CD
Tsai, FJ
Citation: Wc. Chen et al., Interleukin-1 beta gene and receptor antagonist gene polymorphisms in patients with calcium oxalate stones, UROL RES, 29(5), 2001, pp. 321-324
Authors:
Chen, WC
Lu, HF
Chen, HY
Hsu, CD
Tsai, FJ
Citation: Wc. Chen et al., Arginine form of p21 gene codon 31 is less prominent in patients with calcium oxalate stone, UROL RES, 29(2), 2001, pp. 94-97
Authors:
Chen, WC
Chen, HY
Wu, JY
Chen, YT
Tsai, FJ
Citation: Wc. Chen et al., Osteocalcin gene Hind III polymorphism is not correlated with calcium oxalate stone disease, UROL RES, 29(2), 2001, pp. 98-101
Authors:
Hsieh, YY
Wu, JY
Chang, CC
Tsai, FJ
Lee, CC
Tsai, HD
Tsai, CH
Citation: Yy. Hsieh et al., Prenatal diagnosis of oculocutaneous albinism two mutations located at thesame allele, PRENAT DIAG, 21(3), 2001, pp. 200-201
Authors:
Hsieh, YY
Chang, CC
Tsai, FJ
Wu, JY
Tsai, CH
Tsai, HD
Citation: Yy. Hsieh et al., Androgen receptor trinucleotide polymorphism in endometriosis, FERT STERIL, 76(2), 2001, pp. 412-413
Authors:
Lee, CC
Wu, JY
Tsai, FJ
Kodama, H
Abe, T
Yang, CF
Tsai, CH
Citation: Cc. Lee et al., Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association, J HUM GENET, 45(5), 2000, pp. 275-279
Authors:
Wu, FY
Tsai, FJ
Kuo, HW
Tsai, CH
Wu, WY
Wang, RY
Lai, JS
Citation: Fy. Wu et al., Cytogenetic study of workers exposed to chromium compounds, MUT RES-GTE, 464(2), 2000, pp. 289-296
Authors:
Wang, NM
Chang, JG
Liu, TC
Lin, SF
Peng, CT
Tsai, FJ
Tsai, CH
Citation: Nm. Wang et al., Aberrant transcripts of FHIT, TSG101 and PTEN/MMAC1 genes in normal peripheral mononuclear cells, INT J ONCOL, 16(1), 2000, pp. 75-80
Authors:
Lin, HC
Tsai, FJ
Shen, WC
Tsai, CH
Peng, CT
Citation: Hc. Lin et al., Infantile form G(M1) gangliosidosis with dilated cardiomyopathy: a case report, ACT PAEDIAT, 89(7), 2000, pp. 880-883
Authors:
Tsai, FJ
Wu, JY
Lee, CC
Tsai, CH
Citation: Fj. Tsai et al., A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) causes non-syndromic craniosynostosis, ACT PAEDIAT, 89(6), 2000, pp. 672-674
Authors:
Chang, YT
Tsai, FJ
Shen, WC
Lin, HC
Peng, CT
Tsai, CH
Citation: Yt. Chang et al., Antley-Bixler syndrome associated with Arnold-Chiari malformation, ACT PAEDIAT, 89(6), 2000, pp. 737-739