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機構 日期 題名 作者
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 p21 gene codon 31 arginine/serine polymorphism: Non-association with endometriosis Hsieh, YY; Tsai, FJ; Chang, CC; Chen, WC; Tsai, CH; Tsai, HD; Lin, CC
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 Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD
中國醫藥大學 2001 Rapid monitoring assay of congenital adrenal hyperplasia with microbore high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots Lai, CC; Tsai, CH; Tsai, FJ; Lee, CC; Lin, WD
中國醫藥大學 2001 Leukemia inhibitory factor decreases the arylamine N-acetyltransferase activity in human cumulus granulosa cells Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH
中國醫藥大學 2001 Kinetics of acetyl coenzyme A: Arylamine N-acetyltransferase from human cumulus cells Chang, CC; Hsieh, YY; Chung, JG; Tsai, HD; Tsai, CH
中國醫藥大學 2001 Kinetics of acetyl coenzyme A: Arylamine N-acetyltransferase from human cumulus cells Chang, CC; Hsieh, YY; Chung, JG; 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 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 Longitudinal survey of blood flow at three different locations in the middle cerebral artery in normal fetuses Hsieh, YY; Chang, CC; Tsai, HD; Tsai, CH
中國醫藥大學 2001 Relation of BsmI vitamin D receptor gene polymorphism to bone mineral density and occurrence of osteoporosis in postmenopausal Chinese women in Taiwan Chen, HY; Chen, WC; Hsu, CD; Tsai, FJ; Tsai, CH; Li, CW
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 Molecular analysis of SMN, NAIP and P44 genes of SMA patients and their families Tsai, CH; Jong, YJ; Hu, CJ; Chen, CM; Shih, MC; Chang, CP; Chang, JG
中國醫藥大學 2001 Molecular analysis of SMN, NAIP and P44 genes of SMA patients and their families Tsai, CH; Jong, YJ; Hu, CJ; Chen, CM; Shih, MC; Chang, CP; Chang, JG
中國醫藥大學 2001 Treatment of spinal muscular atrophy by sodium butyrate Chang, JG; Hsieh-Li, HM; Jong, YJ; Wang, NM; Tsai, CH; Li, H
中國醫藥大學 2001 Treatment of spinal muscular atrophy by sodium butyrate Chang, JG; Hsieh-Li, HM; Jong, YJ; Wang, NM; Tsai, CH; Li, H
中國醫藥大學 2001 Reversal caused by n-butylidenephthalide from the deficits of inhibitory avoidance performance in rats Hsieh, MT; Wu, CR; Lin, LW; Hsieh, CC; Tsai, CH
中國醫藥大學 2001 Relation of the estrogen receptor alpha gene microsatellite polymorphism to bone mineral density and the susceptibility to osteoporosis in postmenopausal Chinese women in Taiwan Chen, HY; Chen, WC; Tsai, HD; Hsu, CD; Tsai, FJ; Tsai, CH
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 Longitudinal survey of blood flow at three different locations in the middle cerebral artery in normal fetuses Hsieh, YY; Chang, CC; Tsai, HD; Tsai, CH
中國醫藥大學 2001 Effects of paeoniflorin on the formalin-induced nociceptive behaviour in mice Tsai, HY; Lin, YT; Tsai, CH; Chen, YF
國家衛生研究院 2000-09-30 Identification and characterization of a structural protein of hepatitis B virus: A polymerase and surface fusion protein encoded by a spliced RNA Huang, HL; Jeng, KS; Hu, CP; Tsai, CH; Lo, SJ; Chang, CM
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

顯示項目 451-475 / 594 (共24頁)
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