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Showing items 451-500 of 596 (12 Page(s) Totally)
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Institution	Date	Title	Author
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	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	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
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	Treatment of spinal muscular atrophy by compound S.	Chang, J; Lee, H; HsiehLi, HM; Jong, YJ; Wang, NM; Tsai, CH
中國醫藥大學	2000	Cytogenetic study of workers exposed to chromium compounds	Wu, FY; Tsai, FJ; Kuo, HW; Tsai, CH; Wu, WY; Wang, RY; Lai, JS
中國醫藥大學	2000	Outbreak investigation of nosocomial Enterobacter cloacae bacteraemia in a neonatal intensive care unit	Yu, WL; Cheng, HS; Lin, HC; Peng, CT; Tsai, CH
中國醫藥大學	2000	Longitudinal survey of fetal ventricular ejection and shortening fraction throughout pregnancy	Hsieh, YY; Chang, FCC; Tsai, HD; Tsai, CH
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	Infantile form G(M1) gangliosidosis with dilated cardiomyopathy: a case report	Lin, HC; Tsai, FJ; Shen, WC; Tsai, CH; Peng, CT
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
中國醫藥大學	2000	Antley-Bixler syndrome associated with Arnold-Chiari malformation	Chang, YT; Tsai, FJ; Shen, WC; Lin, HC; Peng, CT; Tsai, CH
中國醫藥大學	2000	MRI of Enterovirus 71 myelitis with monoplegia	Shen, WC; Tsai, CH; Chiu, HH; Chow, KC
中國醫藥大學	2000	Breech deformation complex in neonates	Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH
中國醫藥大學	2000	Breech deformation complex in neonates	Hsieh, YY; Tsai, FJ; Lin, CC; Chang, FCC; Tsai, CH
中國醫藥大學	2000	Successful application of extracorporeal membrane oxygenation and intra-aortic balloon counterpulsation as lifesaving therapy for a patient with amniotic fluid embolism	Hsieh, YY; Chang, CC; Li, PC; Tsai, HD; Tsai, CH
中國醫藥大學	2000	Longitudinal Doppler sonographic measurements of vascular impedance in the central and peripheral spiral arteries throughout pregnancy	Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, CH
中國醫藥大學	2000	Longitudinal Doppler sonographic measurements of vascular impedance in the central and peripheral spiral arteries throughout pregnancy	Hsieh, YY; Chang, CC; Tsai, HD; Lee, CC; Tsai, CH
中國醫藥大學	2000	Lewis (FUT3) genotypes in Taiwanese, Thai, and Filipino populations	Liu, TC; Chang, JG; Lin, SF; Chang, WC; Yang, TY; Lin, CL; Wang, NM; Tsai, CH
中國醫藥大學	2000	Lewis (FUT3) genotypes in Taiwanese, Thai, and Filipino populations	Liu, TC; Chang, JG; Lin, SF; Chang, WC; Yang, TY; Lin, CL; Wang, NM; Tsai, CH
中國醫藥大學	2000	G protein beta 3 subunit variant and essential hypertension in Taiwan - a case-control study	Tsai, CH; Yeh, HI; Chou, YS; Liu, HF; Yang, TY; Wang, JC; Wang, NM; Chang, JG
中國醫藥大學	2000	Genetic risk factors of sporadic Alzheimer's disease among Chinese in Taiwan	Hu, CJ; Sung, SM; Liu, HC; Hsu, WC; Lee, LS; Lee, CC; Tsai, CH; Chang, JG
中國醫藥大學	2000	Genetic risk factors of sporadic Alzheimer's disease among Chinese in Taiwan	Hu, CJ; Sung, SM; Liu, HC; Hsu, WC; Lee, LS; Lee, CC; Tsai, CH; Chang, JG
中國醫藥大學	2000	Polymorphisms of the parkin gene in sporadic Parkinson's disease among Chinese in Taiwan	Hu, CJ; Sung, SM; Liu, HC; Lee, CC; Tsai, CH; Chang, JG
中國醫藥大學	2000	Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency	Lee, HH; Chang, JG; Tsai, CH; Tsai, FJ; Chao, HT; Chung, BC
中國醫藥大學	2000	No evidence of correlation between mutation at codon 531 of src and the risk of colon cancer in Chinese	Wang, NM; Yeh, KT; Tsai, CH; Chen, SJ; Chang, JG

Showing items 451-500 of 596 (12 Page(s) Totally)
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