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Results: 1-25 | 26-50 | 51-52
Results: 26-50/52

Authors: Hu, CJ Sung, SM Liu, HC Hsu, WC Lee, LS Lee, CC Tsai, CH Chang, JG
Citation: Cj. Hu et al., Genetic risk factors of sporadic Alzheimer's disease among Chinese in Taiwan, J NEUR SCI, 181(1-2), 2000, pp. 127-131

Authors: Jong, YJ Chang, JG Lin, SP Yang, TY Wang, JC Chang, CP Lee, CC Li, H Hsieh-Li, HM Tsai, CH
Citation: Yj. Jong et al., Analysis of the mRNA transcripts of the survival motor neuron (SMN) gene in the tissue of an SMA fetus and the peripheral blood mononuclear cells of normals, carriers and SMA patients, J NEUR SCI, 173(2), 2000, pp. 147-153

Authors: Lee, HH Kuo, JM Chao, HT Lee, YJ Chang, JG Tsai, CH Chung, BC
Citation: Hh. Lee et al., Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese, J CLIN END, 85(2), 2000, pp. 597-600

Authors: Wang, JT Weng, CI Chang, JG Hwang, CC
Citation: Jt. Wang et al., The influence of temperature and surface conditions on surface absorptivity in laser surface treatment, J APPL PHYS, 87(7), 2000, pp. 3245-3253

Authors: Hu, CJ Sung, SM Liu, HC Lee, CC Tsai, CH Chang, JG
Citation: Cj. Hu et al., Polymorphisms of the parkin gene in sporadic Parkinson's disease among Chinese in Taiwan, EUR NEUROL, 44(2), 2000, pp. 90-93

Authors: Lee, HH Chang, JG Tsai, CH Tsai, FJ Chao, HT Chung, BC
Citation: Hh. Lee et al., Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency, CLIN CHEM, 46(5), 2000, pp. 606-611

Authors: Liu, TC Lin, PM Chang, JG Lee, JP Chen, TP Sue, YC Lin, SF
Citation: Tc. Liu et al., Mutation analysis of BCL 10 in acute myeloid leukaemia, BR J HAEM, 109(1), 2000, pp. 250-252

Authors: Wang, NM Tsai, CH Yeh, KT Chen, SJ Chang, JG
Citation: Nm. Wang et al., P53 codon 72Arg polymorphism is not a risk factor for carcinogenesis in the Chinese, INT J MOL M, 4(3), 1999, pp. 249-252

Authors: Wang, NM Chang, JG
Citation: Nm. Wang et Jg. Chang, Are aberrant transcripts of FHIT, TSG101, and PTEN/MMAC1 oncogenesis related? (Review), INT J MOL M, 3(5), 1999, pp. 491-495

Authors: Chang, JG Weng, CI
Citation: Jg. Chang et Ci. Weng, Finite element simulation of twin-roll casting process with an implementation of slip/friction boundary condition, J MANUF SCI, 121(4), 1999, pp. 665-673

Authors: Ou, CY Chang, JG Tseng, HH Wei, HJ Su, TH Hsu, TY Chang, CP Lee, HH
Citation: Cy. Ou et al., Analysis of microsatellite instability in cervical cancer, INT J GYN C, 9(1), 1999, pp. 67-71

Authors: Chang, JG Chen, YJ Perng, LI Wang, NM Kao, MC Yang, TY Chang, CP Tsai, CH
Citation: Jg. Chang et al., Mutation analysis of the PTEN/MMAC1 gene in cancers of the digestive tract, EUR J CANC, 35(4), 1999, pp. 647-651

Authors: Chen, YJ Chen, PH Lin, SY Chang, JG
Citation: Yj. Chen et al., Analysis of aberrant transcription of TSG101 in hepatocellular carcinomas, EUR J CANC, 35(2), 1999, pp. 302-308

Authors: Peng, CT Tsai, CH Lin, TP Perng, LI Kao, MC Yang, TY Wang, NM Liu, TC Lin, SF Chang, JG
Citation: Ct. Peng et al., Molecular characterization of secretor type alpha(1,2)-fucosyltransferase gene deficiency in the Philippine population, ANN HEMATOL, 78(10), 1999, pp. 463-467

Authors: Chang, JG Yang, TY Perng, LI Wang, NM Peng, CT Tsai, CH
Citation: Jg. Chang et al., Hb Siriraj: a G -> A substitution at codon 7 of the beta-globin chain creates an MboII cutting site, HEMOGLOBIN, 23(2), 1999, pp. 197-199

Authors: Chang, SJ Chang, JG Chen, CJ Wang, JC Ou, TT Chang, KL Ko, YC
Citation: Sj. Chang et al., Identification of a new single nucleotide substitution on the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTTsou)from a Taiwanese aboriginal family with severe gout, J RHEUMATOL, 26(8), 1999, pp. 1802-1807

Authors: Lin, SP Chang, JG Jong, YJ Yang, TY Tsai, CH Wang, NM Li, H Hsieh-Li, HM Hu, CJ
Citation: Sp. Lin et al., Prenatal prediction of spinal muscular atrophy in Chinese, PRENAT DIAG, 19(7), 1999, pp. 657-661

Authors: Chen, ST Yu, SY Tsai, M Yeh, KT Wang, JC Kao, MC Shih, MC Chang, JG
Citation: St. Chen et al., Mutation analysis of the putative tumor suppression gene PTEN/MMAC1 in sporadic breast cancer, BREAST CANC, 55(1), 1999, pp. 85-89

Authors: Tsai, FJ Tsai, CH Chang, JG Wu, JY
Citation: Fj. Tsai et al., Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data, AM J MED G, 86(3), 1999, pp. 300-301

Authors: Chang, JG Yang, TY Liu, TC Lin, TP Hu, CJ Kao, MC Wang, NM Tsai, FJ Peng, CT Tsai, CH
Citation: Jg. Chang et al., Molecular analysis of secretor type alpha(1,2)-fucosyltransferase gene mutations in the Chinese and Thai populations, TRANSFUSION, 39(9), 1999, pp. 1013-1017

Authors: Hu, CJ Sung, SM Liu, HC Lee, KY Hsu, WC Wong, WK Lee, CC Tsai, CH Chang, JG
Citation: Cj. Hu et al., No association of alpha-2 macroglobulin gene five-nucleotide deletion withAD in Taiwan Chinese, NEUROLOGY, 53(3), 1999, pp. 642-643

Authors: Hu, CJ Sung, SM Liu, HC Chang, JG
Citation: Cj. Hu et al., No mutation of G209A in the alpha-synuclein gene in sporadic Parkinson's disease among Taiwan Chinese, EUR NEUROL, 41(2), 1999, pp. 85-87

Authors: Tsai, FJ Wu, JY Tsai, CH Chang, JG
Citation: Fj. Tsai et al., Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity, CLIN GENET, 55(4), 1999, pp. 279-280

Authors: Chang, JG Su, TH Wei, HJ Wang, JC Cheng, YJ Chang, CP Jeng, CJ
Citation: Jg. Chang et al., Analysis of TSG101 tumour susceptibility gene transcripts in cervical and endometrial cancers, BR J CANC, 79(3-4), 1999, pp. 445-450

Authors: Peng, CT Wu, JY Tsai, CH Tsai, FJ Chang, JG
Citation: Ct. Peng et al., Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis, J HUM GENET, 43(4), 1998, pp. 237-241
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