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機構 日期 題名 作者
國立臺灣大學 2007-01 Mutation of keratin 9 (R163W) in a family with epidermolytic palmoplantar keratoderma and knuckle pads. Sheen, YS; Chu, CY; Lin, PJ; Liaw, SH; Chiu, HC; Jee, SH
慈濟大學 1996 Mutation of Lysines in a Plasminogen Binding Region of Streptokinase Identifies Residues Important for Generating a Functional Activator Complex Lin, Lee-Fong;Oeun, Saravuth;Houng, Aiilyan;Reed, Guy L.
國立臺灣大學 2008 Mutation of Mitochondrial DNA G13513a Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy 王緖斌; 翁妏謹; 李妮鍾; 胡務亮; 范碧娟; 李旺祚; WANG, SHI-BING; WENG, WEN-CHIN; LEE, NI-CHUNG; HWU, WUH-LIANG; FAN, PI-CHUAN; LEE, WANG-TSO
臺大學術典藏 2020-12-09T01:38:40Z Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.;Weng W.-C.;Ni-Chung Lee;Hwu W.-L.;Fan P.-C.;Lee W.-T.; Wang S.-B.; Weng W.-C.; NI-CHUNG LEE; Hwu W.-L.; Fan P.-C.; Lee W.-T.
臺大學術典藏 2020-12-16T02:25:55Z Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.;Weng W.-C.;Lee N.-C.;Wuh-Liang Hwu;Fan P.-C.;Lee W.-T.; Wang S.-B.; Weng W.-C.; Lee N.-C.; WUH-LIANG HWU; Fan P.-C.; Lee W.-T.
臺大學術典藏 2020-12-18T02:21:52Z Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.;Weng W.-C.;Lee N.-C.;Hwu W.-L.;Fan P.-C.;Wang-Tso Lee; Wang S.-B.; Weng W.-C.; Lee N.-C.; Hwu W.-L.; Fan P.-C.; WANG-TSO LEE
臺大學術典藏 2008 Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.; Weng W.-C.; Lee N.-C.; Hwu W.-L.; PI-CHUAN FAN; Lee W.-T.
臺大學術典藏 2021-01-05T06:41:17Z Mutation of Mitochondrial DNA G13513A Presenting with Leigh Syndrome, Wolff-Parkinson-White Syndrome and Cardiomyopathy Wang S.-B.;Wen-Chin Weng;Lee N.-C.;Hwu W.-L.;Fan P.-C.;Lee W.-T.; Wang S.-B.; WEN-CHIN WENG; Lee N.-C.; Hwu W.-L.; Fan P.-C.; Lee W.-T.
中山醫學大學 2000 Mutation of p53 gene codon 63 in saliva as a molecular marker for oral squamous cell carcinomas. Liao, PH; Chang, YC; Huang, MF; Tai, KW; Chou, MY
臺大學術典藏 2018-09-10T04:05:49Z Mutation of p53 gene in hepatocellular carcinoma in Taiwan Sheu, J.-C.; Sheu, J.-C.; HSUAN-SHU LEE et al.
臺大學術典藏 2018-09-10T04:04:36Z Mutation of p53 gene in hepatocellular carcinoma in Taiwan Sheu, J.-C. and Huang, G.-T. and Lee, P.-H. and Chung, J.-C. and Chou, H.-C. and Lai, M.-Y. and Wang, J.-T. and Lee, H.-S. and Shih, L.-N. and Yang, P.-M. and Wang, T.-H. and Chen, D.-S.; PO-HUANG LEE
國立臺灣大學 1992 Mutation of P53 Gene in Hepatocellular Carcinoma in Taiwan 許金川; Lee, P. H.; Chung, J. C.; Chou, H. C.; Lai, M. Y.; Wang, J. T.; Lee, H. S.; Shih, L. N.; Yang, P. M.; Wang, T. H.; Chen, D. S.; Sheu, Jin-Chuan; Lee, P. H.; Chung, J. C.; Chou, H. C.; Lai, M. Y.; Wang, J. T.; Lee, H. S.; Shih, L. N.; Yang, P. M.; Wang, T. H.; Chen, D. S.
臺大學術典藏 2019-09-02T08:58:49Z Mutation of p53 gene in Hepatocellular Carcinoma in Taiwan Sheu J.-C.;Huang G.-T.;Chung J.-C.;Chou H.-C.;Lai M.-Y.;Wang, Jin-Town;Lee H.-S.;Shih L.-N.;Yang P.-M.;Wang T.-H.;Chen D.-S.; Sheu J.-C.; Huang G.-T.; Chung J.-C.; Chou H.-C.; Lai M.-Y.; Wang, Jin-Town; Lee H.-S.; Shih L.-N.; Yang P.-M.; Wang T.-H.; Chen D.-S.
臺大學術典藏 2021-02-02T06:41:28Z Mutation of p53 gene in Hepatocellular Carcinoma in Taiwan Sheu J.-C.; Huang G.-T.; Chung J.-C.; Chou H.-C.; Lai M.-Y.; Wang J.-T.; Lee, Hsuan-Shu; Shih L.-N.; Yang P.-M.; Wang T.-H.; Chen D.-S.
臺大學術典藏 2021-04-22T06:57:09Z Mutation of p53 gene in Hepatocellular Carcinoma in Taiwan Sheu J.-C.; Huang G.-T.; Chung J.-C.; Chou H.-C.; Lai M.-Y.; Wang J.-T.; Lee H.-S.; Shih L.-N.; PEI-MING YANG; Wang T.-H.; Chen D.-S.
中山醫學大學 1995 Mutation of p53 gene on transformed C3H10T1 / 2 cells by N - nitroso Maillard reaction products 蘇文男; Su, Wen-Nan
慈濟大學 2021 Mutation of the Carboxy-Terminal Processing Protease Gene in Acinetobacter baumannii and its Impact on Membrane Integrity and Virulence Properties RakeshRoy
臺大學術典藏 2018-09-10T04:13:04Z Mutation of the DR5/TRAIL receptor 2 gene is infrequent in hepatocellular carcinoma Jeng, Y.-M. and Hsu, H.-C.; YUNG-MING JENG
國立臺灣大學 2002 Mutation of the Dr5/Trail Receptor 2 Gene Is Infrequent in Hepatocellular Carcinoma 鄭永銘; 許輝吉; JENG, YUNG-MING; HSU, HEY-CHI
臺大學術典藏 2020-03-06T08:25:41Z Mutation of the DR5/TRAIL receptor 2 gene is infrequent in hepatocellular carcinoma Yung-Ming Jeng;Hsu H.-C.; YUNG-MING JENG; Hsu H.-C.
國立成功大學 2016-08-12 Mutation of the Enterohemorrhagic Escherichia coli Core LPS Biosynthesis Enzyme RfaD Confers Hypersusceptibility to Host Intestinal Innate Immunity In vivo Kuo, Cheng-Ju; Chen, Jenn-Wei; Chiu, Hao-Chieh; Teng, Ching-Hao; Hsu, Tai-I; Lu, Pei-Jung; Syu, Wan-Jr; Wang, Sin-Tian; Chou, Ting-Chen; Chen, Chang-Shi
國立臺灣大學 2016 Mutation of the Enterohemorrhagic Escherichia coli Core LPS Biosynthesis Enzyme RfaD Confers Hypersusceptibility to Host Intestinal Innate Immunity In vivo Kuo, Cheng-Ju; Chen, Jenn-Wei; Chiu, Hao-Chieh; Teng, Ching-Hao; Hsu, Tai-I; Lu, Pei-Jung; Syu, Wan-Jr; Wang, Sin-Tian; Chou, Ting-Chen; Chen, Chang-Shi; 邱浩傑
臺大學術典藏 2021-06-24T01:53:52Z Mutation of the enterohemorrhagic escherichia coli core LPS biosynthesis enzyme RfaD confers hypersusceptibility to host intestinal innate immunity in vivo Kuo C.-J.; Chen J.-W.; HAO-CHIEH CHIU; Teng C.-H.; Hsu T.-I.; Lu P.-J.; Syu W.-J.; Wang S.T.; Chou T.-C.; Chen C.-S.
國立成功大學 2019-11-8 Mutation of the PTCH1 gene predicts recurrence of breast cancer Wang;Chih-Yang;Chang;Yung-Chieh;Kuo;Yao-Lung;Lee;Kuo-Ting;Chen;Pai-Sheng;Cheung;Antonio, Chun Hei;Chang;Chih-Peng;Phan, Nam Nhut;Shen;Meng-Ru;Hsu;Hui-Ping
國立成功大學 2019-12-1 Mutation of the PTCH1 gene predicts recurrence of breast cancer 徐慧萍; HSU, HUI-PING; Wang, Chih-Yang;Chang, Yung-Chieh;Kuo, Yao-Lung;Lee, Kuo-Ting;Chen, Pai-Sheng;Cheung, Chun Hei Antonio;Chang, Chih-Peng;Phan, Nam Nhut;Shen, Meng-Ru;Hsu, Hui-Ping
國立臺灣大學 1989-06 Mutation of the Retinoblastoma Gene in a Human Prostate Carcinoma Cell Line Bookstein, R.; 許金玉; Scully, P.; Lee, W. H.; Bookstein, R.; Shew, Jin-Yuh; Scully, P.; Lee, W. H.
國立臺灣大學 2002 Mutation of the Sterol 27-Hydroxylase Gene (Cyp27a1) in a Taiwanese Family with Cerebrotendinous Xanthomatosis 葉炳強; YIP, PING-KEUNG
臺大學術典藏 2018-09-10T04:05:42Z Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4] Lee, M.-J. and Huang, Y.-C. and Sweeney, M.G. and Wood, N.W. and Reilly, M.M. and Yip, P.-K.; MING-JEN LEE
臺大學術典藏 2020-03-03T02:33:36Z Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4] MING-JEN LEE; Huang Y.-C.; Sweeney M.G.; Wood N.W.; Reilly M.M.; Yip P.-K.
臺大學術典藏 2002 Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4] Yip P.-K.; Reilly M.M.; Wood N.W.; Sweeney M.G.; Huang Y.-C.; MING-JEN LEE
國家衛生研究院 2020-08 Mutation of the STK11 gene predicts recurrence of breast cancer Wang, CY;Chang, YC;Kuo, YL;Lee, KT;Chen, PS;Cheung, CHA;Shen, CH;Chang, CP;Lai, MD;Shen, MR;Hsu, HP
中山醫學大學 2009 Mutation ofgyrA andparC in clinical isolates ofAcinetobacter baumannii and its relationship with antimicrobial drugs resistance in Taiwan Chien, Shang-Tao; Lin, Chun-Hsiu; Hsueh, Jui-Chen; Li, Pei-Ling; Hsu, Chao-Hsun; Chang, Shu-Hui; Chien, Hsin-I; Ben, Ren-Jy; Chang, Fu-Hsin; Hsu, Li-Sung
中山醫學大學 2010 Mutation R184Q of connexin 26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30 Su CC; Li SY; Su MC; Chen WC;Yang JJ
中山醫學大學 2010 Mutation R184Q of connexin 26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30 Ching-Chyuan Su;Shuan-Yow Li;Mao-Chang Su;Wei-Chi Chen;Jiann-Jou Yang
嘉南藥理大學 2009 Mutation Research Letters Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/DNA Repair Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/DNAging Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/Environmental Mutagenesis and Related Subjects Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/Genetic Toxicology Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/Genetic Toxicology and Environmental Mutagenesis Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/Mutation Research Genomics Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/Reviews in Genetic Toxicology Elsevier SDOL
嘉南藥理大學 2009 Mutation Research/Reviews in Mutation Research Elsevier SDOL
亞洲大學 2002 Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan Shi YR;Wu,Jer-Yuarn;Hsu YA;Cheng-Chun Lee;Chang-Hai Tsai;Fuu-Jen Tsai
中國醫藥大學 2002 Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學 2002 Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan Shi, YR; Wu, JY; Hsu, YA; Lee, CC; Tsai, CH; Tsai, FJ
中國醫藥大學 2002 Mutation screening of the EXT genes in patients with hereditary multiple exostoses in Taiwan 施怡如(Shi YR); 鄔哲源; (Hsu YA); 李正淳(Cheng-Chun Lee); 蔡長海(Chang-Hai Tsai); 蔡輔仁(Fuu-Jen Tsai)*
臺大學術典藏 2020-04-24T01:34:23Z Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome Wang S.-H.; Chen-Chi Wu; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; Hwu W.-L.; Yu I.-S.; Hsu C.-J.
臺大學術典藏 2020-12-16T02:25:37Z Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome Wang S.-H.; Wu C.-C.; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; WUH-LIANG HWU; Yu I.-S.; Hsu C.-J.

顯示項目 597551-597600 / 2314743 (共46295頁)
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