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Results: 1-13 |
Results: 13
A silent mutation induces exon skipping in the phenylalanine hydroxylase gene in phenylketonuria
Authors: Chao, HK Hsiao, KJ Su, TS
Citation: Hk. Chao et al., A silent mutation induces exon skipping in the phenylalanine hydroxylase gene in phenylketonuria, HUM GENET, 108(1), 2001, pp. 14-19
Tetrahydrobiopterin-deficient hyperphenylalaninemia in the Chinese
Authors: Liu, TT Chiang, SH Wu, SJ Hsiao, KJ
Citation: Tt. Liu et al., Tetrahydrobiopterin-deficient hyperphenylalaninemia in the Chinese, CLIN CHIM A, 313(1-2), 2001, pp. 157-169
Detection of kaposi sarcoma-associated herpesvirus in bone marrow biopsy samples from patients with multiple myeloma
Authors: Hsu, HC Lee, YM Yang, CF Hsiao, KJ Liu, TT Ho, CK Ho, CH Wang, SY Liu, WT
Citation: Hc. Hsu et al., Detection of kaposi sarcoma-associated herpesvirus in bone marrow biopsy samples from patients with multiple myeloma, CANCER, 91(8), 2001, pp. 1409-1413
A genetic factor for age-related cataract: Identification and characterization of a novel galactokinase variant, "Osaka," in Asians
Authors: Okano, Y Asada, M Fujimoto, A Ohtake, A Murayama, K Hsiao, KJ Choeh, K Yang, YL Cao, QX Reichardt, JKV Niihira, S Imamura, T Yamano, T
Citation: Y. Okano et al., A genetic factor for age-related cataract: Identification and characterization of a novel galactokinase variant, "Osaka," in Asians, AM J HU GEN, 68(4), 2001, pp. 1036-1042
Detection of Borna disease virus RNA from peripheral blood cells in schizophrenic patients and mental health workers
Authors: Chen, CH Chiu, YL Shaw, CK Tsai, MT Hwang, AL Hsiao, KJ
Citation: Ch. Chen et al., Detection of Borna disease virus RNA from peripheral blood cells in schizophrenic patients and mental health workers, MOL PSYCHI, 4(6), 1999, pp. 566-571
Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from Taiwan
Authors: Tsai, MT Shaw, CK Hsiao, KJ Chen, CH
Citation: Mt. Tsai et al., Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from Taiwan, MOL PSYCHI, 4(3), 1999, pp. 271-273
High seroprevalence of Borna virus infection in schizophrenic patients, family members and mental health workers in Taiwan
Authors: Chen, CH Chiu, YL Wei, FC Koong, FJ Liu, HC Shaw, CK Hwu, HG Hsiao, KJ
Citation: Ch. Chen et al., High seroprevalence of Borna virus infection in schizophrenic patients, family members and mental health workers in Taiwan, MOL PSYCHI, 4(1), 1999, pp. 33-38
Classical galactosaemia in Chinese: A case report and review of disease incidence
Authors: Cheung, KL Tang, NLS Hsiao, KJ Law, LK Wong, W Ng, PC Pang, CP Applegarth, DA Fok, TF Hjelm, NM
Citation: Kl. Cheung et al., Classical galactosaemia in Chinese: A case report and review of disease incidence, J PAEDIAT C, 35(4), 1999, pp. 399-400
Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutation
Authors: Hwu, WL Wang, PJ Hsiao, KJ Wang, TR Chiou, YW Lee, YM
Citation: Wl. Hwu et al., Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutation, HUM GENET, 105(3), 1999, pp. 226-230
Towards metabolic sink therapy for mut methylmalonic acidaemia: Retrovirus-mediated transfer of the human methylmalonyl-CoA mutase cDNA into peripheral blood progenitor cells of a child with mut methylmalonic acidaemia
Authors: Chang, CC Hsiao, KJ Chen, ML Lin, CM
Citation: Cc. Chang et al., Towards metabolic sink therapy for mut methylmalonic acidaemia: Retrovirus-mediated transfer of the human methylmalonyl-CoA mutase cDNA into peripheral blood progenitor cells of a child with mut methylmalonic acidaemia, J INH MET D, 22(8), 1999, pp. 951-952
Towards metabolic sink therapy for mut methylmalonic acidaemia: Correctionof methylmalonyl-CoA mutase deficiency in T lymphocytes from a mut methylmalonic acidaemia child by retroviral-mediated gene transfer
Authors: Chang, CC Hsiao, KJ Lee, YM Lin, CM
Citation: Cc. Chang et al., Towards metabolic sink therapy for mut methylmalonic acidaemia: Correctionof methylmalonyl-CoA mutase deficiency in T lymphocytes from a mut methylmalonic acidaemia child by retroviral-mediated gene transfer, J INH MET D, 22(7), 1999, pp. 773-787
Methanol/acetone treatment helps the amplification of FMR1 CGG repeat fragment in dried blood spots from Guthrie cards
Authors: Hong, CJ Song, HL Lai, HC Tsai, SJ Hsiao, KJ
Citation: Cj. Hong et al., Methanol/acetone treatment helps the amplification of FMR1 CGG repeat fragment in dried blood spots from Guthrie cards, LANCET, 353(9159), 1999, pp. 1153-1154
Systematic mutation analysis of the catechol O-methyltransferase gene as acandidate gene for schizophrenia
Authors: Chen, CH Lee, YR Chung, MY Wei, FC Koong, FJ Shaw, CK Yeh, JI Hsiao, KJ
Citation: Ch. Chen et al., Systematic mutation analysis of the catechol O-methyltransferase gene as acandidate gene for schizophrenia, AM J PSYCHI, 156(8), 1999, pp. 1273-1275
Risultati: 1-13 |