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Showing items 91-109 of 109  (5 Page(s) Totally)
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Institution Date Title Author
中國醫藥大學 2002 Hydrops foetalis caused by anti-Mur in first pregnancy - a case report Wu, KH; Chang, JG; Lin, M; Shih, MC; Lin, HC; Lee, CC; Peng, CT; Tsai, CH
國立臺灣大學 2001-12 Molecular basis of the adult i phenotype and the gene responsible for the expression of the human blood group I antigen. Yu, LC; Twu, YC; Chang, CY; Lin, M
國立臺灣大學 2001-10 Polymorphism and distribution of the Secretor alpha (1,2)-fucosyltransferase gene in various Taiwanese populations. Yu, LC; Chu, CC; Chan, YS; Chang, CY; Twu, YC; Lee, HL; Lin, M
國立臺灣大學 2001-03 Molecular basis of the Kell-null phenotype: a mutation at the splice site of human Kel gene abolishes the expression of Kell blood group antigens. Yu, LC; Twu, YC; Chang, CY; Lin, M
國立臺灣大學 2000-07 Human histo-blood group ABO glycosyltransferase genes: different enhancer structures with different transcriptional activities. Yu, LC; Chang, CY; Twu, YC; Lin, M
臺大學術典藏 2000 Human histo-blond group ABO glycosyltransferase genes: Different enhancer structures with different transcriptional activities Yu L.-C.; Chang C.-Y.; Twu Y.-C.; Lin M.; LUNG-CHIH YU
國立臺灣大學 1999-08 The molecular basis for the B(A) allele: an amino acid alteration in the human histoblood group B alpha-(l,3)-galactosyltransferase increases its intrinsic alpha-(l,3)-N-acetylgalactosaminyltransferase activity. Yu, LC; Lee, HL; Chan, YS; Lin, M
國立臺灣大學 1999-01 A newly identified nonsecretor allele of the human histoblood group alpha(1.2)fucosyltransferase gene (FUT2). Yu, LC; Lee, HL; Chu, CC; Broadberry, RE; Lin, M
中國醫藥大學 1999 Proteinuria in diabetics is a strong predictor of acute organ system failure and long-term mortality following acute coronary syndrome for emergency practice Lin, M; Wang, KL; Kuo, SW; Wu, MH; Chettlin, MD
中國醫藥大學 1997 Effects of exposure to carbon disulfide (CS2) on electrocardiographic features of ischemic heart disease among viscose rayon factory workers Kuo, HW; Lai, JS; Lin, M; Su, ES
國立臺灣大學 1995-12 Correlation of a missense mutation in the human Secretor alpha-1, 2-fucosyl-transferase gene with the Lewis (a+b+) phenotype: a potential molecular-basis for the weak Secretor allele (Se-w). Yu, LC; Yang, YH; Broadberry, RE; Chen, YH; Chen, YS; Lin, M
國立臺灣大學 1995-01 Effects of the benzodiazepine inverse agonist RO19-4603 on the maintenance of tolerance to a single dose of ethanol. June, HL; Duemler, SE; Greene, TL; Williams, JA; Lin, M; Devaraju, SL; Chen, SHA; Lewis, MJ; Murphy, JM.
臺大學術典藏 1995 Correlation of a missense mutation in the human Secretor α1,2-fucosyltransferase gene with the Lewis(a+b+) phenotype: A potential molecular basis for the weak Secretor allele (Se(w)) Yu L.-C.; Yang Y.-H.; Broadberry R.E.; Chen Y.-H.; Chan Y.-S.; Lin M.; LUNG-CHIH YU
國立成功大學 1994-03 Cholangiographic CT in differential diagnosis of Caroli's disease and polycystic liver disease - a preliminary study Hsu, P. I.; Lin, Xi-Zhang; Lin, Ching-Yih; Chang, Ting-Tsung; Shin, Jeng-Shiann; Huang, J. J.; Tsai, H. M.; Chen, K. H.; Chiu, N. T.; Lai, K. H.; Lin, M.; Yang, Y. F.
中國醫藥大學 1994 VASODILATOR THERAPY IN CHRONIC AORTIC REGURGITATION - ENALAPRIL VERSUS HYDRALAZINE LIN, M; CHIANG, HT; LIN, SL; CHIANG, BN; CHEITLIN, MD
中國醫藥大學 1994 VASODILATOR THERAPY IN CHRONIC ASYMPTOMATIC AORTIC REGURGITATION - ENALAPRIL VERSUS HYDRALAZINE THERAPY LIN, M; CHIANG, MT; LIN, SL; CHANG, MS; CHIANG, BN; KUO, HW; CHEITLIN, MD
臺大學術典藏 1992 Nosocomial outbreak of scabies. Lin M.;Liu J.C.;Hsieh B.L.;Hwang C.C.;Lin B.H.;PO-REN HSUEH; PO-REN HSUEH; Lin B.H.; Hwang C.C.; Hsieh B.L.; Liu J.C.; Lin M.
臺大學術典藏 1992 Abscess formation complicated in ovarian mucinous cystadenoma: a case report. Young C.; Lin M.; Yen K.P.; PO-REN HSUEH; Hwang C.C.
國立臺灣大學 1976-11 Conceptual knowledge as related to language comprehension and recall. Chang, C. M.; Lin, M.

Showing items 91-109 of 109  (5 Page(s) Totally)
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