Výsledky vyhledávání - Tze-Tze Liu

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  1. 1
    Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria

    Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria Autor Mei‐Ying Liu, Yan-Ling Yang, Ying-Chen Chang, Szu-Hui Chiang, Shuan-Pei Lin, Lian-Shu Han, Yu Qi, Kwang-Jen Hsiao, Tze-Tze Liu

    Vydáno 2010
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  2. 2
    Genetic diversity of capsular polysaccharide biosynthesis in Klebsiella pneumoniae clinical isolates

    Genetic diversity of capsular polysaccharide biosynthesis in Klebsiella pneumoniae clinical isolates Autor Hung‐Yu Shu, Chang-Phone Fung, Yen-Ming Liu, Keh-Ming Wu, Ying-Tsong Chen, Ling-Hui Li, Tze-Tze Liu, Ralph Kirby, Shih-Feng Tsai

    Vydáno 2009
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  3. 3
    Haploinsufficiency of<i>RCBTB1</i>is associated with Coats disease and familial exudative vitreoretinopathy

    Haploinsufficiency of<i>RCBTB1</i>is associated with Coats disease and familial exudative vitreoretinopathy Autor Jeng-Hung Wu, Jorn-Hon Liu, Yu‐Chieh Ko, C Wang, Yu-Chien Chung, Kuo-Chang Chu, Tze-Tze Liu, Hsiao-Ming Chao, Yun‐Jin Jiang, Shih‐Jen Chen, Ming‐Yi Chung

    Vydáno 2016
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  4. 4
    Exome Sequencing Identifies GNB4 Mutations as a Cause of Dominant Intermediate Charcot-Marie-Tooth Disease

    Exome Sequencing Identifies GNB4 Mutations as a Cause of Dominant Intermediate Charcot-Marie-Tooth Disease Autor Bing‐Wen Soong, Yen‐Hua Huang, Pei‐Chien Tsai, Chien‐Chang Huang, Hung-Chuan Pan, Yi-Chun Lu, Hsin-Ju Chien, Tze-Tze Liu, Ming-Hong Chang, Kon-Ping Lin, Pang‐Hsien Tu, Lung‐Sen Kao, Yi‐Chung Lee

    Vydáno 2013
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  5. 5
    Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency

    Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency Autor Yao Lu, Keiko Kobayashi, Miharu Ushikai, Ayako Tabata, Mikio Iijima, Meng Xian Li, Lei Lei, Kotaro Kawabe, Satoru Taura, Yanling Yang, Tze-Tze Liu, Szu-Hui Chiang, Kwang-Jen Hsiao, YL Lau, Lap-Chee Tsui, Dong Hwan Lee, Takeyori Saheki

    Vydáno 2005
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  6. 6
    Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis

    Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis Autor Ming‐Wei Lin, Ding-Dar Lee, Tze Tze Liu, Yong Lin, Shang-Yi Chen, Chih-Cheng Huang, Hui-Ying Weng, Yu Fen Liu, Akio Tanaka, Ken Arita, Joey E. Lai‐Cheong, Francis Palisson, Yun-Ting Chang, Chu-Kwan Wong, Isao Matsuura, John A. McGrath, Shih-Feng Tsai

    Vydáno 2009
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  7. 7
    Mutations in <i>KCND3</i> cause spinocerebellar ataxia type 22

    Mutations in <i>KCND3</i> cause spinocerebellar ataxia type 22 Autor Yi‐Chung Lee, Alexandra Dürr, Karen Majczenko, Yen‐Hua Huang, Yu‐Chao Liu, Cheng‐Chang Lien, Pei‐Chien Tsai, Yaeko Ichikawa, Jun Goto, Marie‐Lorraine Monin, Jun Z. Li, Ming‐Yi Chung, Emeline Mundwiller, Vikram G. Shakkottai, Tze‐Tze Liu, Christelle Tesson, Yi‐Chun Lu, Alexis Brice, Shoji Tsuji, Margit Burmeister, Giovanni Stévanin, Bing‐Wen Soong

    Vydáno 2012
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  8. 8
    Genome Sequencing and Comparative Analysis of<i>Klebsiella pneumoniae</i>NTUH-K2044, a Strain Causing Liver Abscess and Meningitis

    Genome Sequencing and Comparative Analysis of<i>Klebsiella pneumoniae</i>NTUH-K2044, a Strain Causing Liver Abscess and Meningitis Autor Keh-Ming Wu, Ling-Hui Li, Jing-Jou Yan, Nina Tsao, Tsai-Lien Liao, Hui-Chi Tsai, Chang‐Phone Fung, Hsiang-Ju Chen, Yen-Ming Liu, Jin-Tung Wang, Chi‐Tai Fang, Shan‐Chwen Chang, Hung‐Yu Shu, Tze-Tze Liu, Ying-Tsong Chen, Yih‐Ru Shiau, Tsai‐Ling Lauderdale, Ih‐Jen Su, Ralph Kirby, Shih‐Feng Tsai

    Vydáno 2009
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  9. 9
    Description of the Transcriptomes of Immune Response-Activated Hemocytes from the Mosquito Vectors <i>Aedes aegypti</i> and <i>Armigeres subalbatus</i>

    Description of the Transcriptomes of Immune Response-Activated Hemocytes from the Mosquito Vectors <i>Aedes aegypti</i> and <i>Armigeres subalbatus</i> Autor Lyric C. Bartholomay, Wen-Long Cho, Thomas A. Rocheleau, Jon P. Boyle, Eric T. Beck, Jeremy F. Fuchs, Paul Liss, Michael Rusch, Katherine M. Butler, Roy Chen-Chih Wu, Shih‐Pei Lin, Hang-Yen Kuo, I‐Yu Tsao, Chiung-Yin Huang, Tze-Tze Liu, Kwang‐Jen Hsiao, Shih‐Feng Tsai, Ueng‐Cheng Yang, Anthony J. Nappi, Nicole T. Perna, Chen-Cheng Chen, Bruce M. Christensen

    Vydáno 2004
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  10. 10
    A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy

    A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy Autor Pei‐Chien Tsai, Bing‐Wen Soong, Inès Mademan, Yen‐Hua Huang, Chia-Rung Liu, Cheng‐Tsung Hsiao, Hung-Ta Wu, Tze-Tze Liu, Yo-Tsen Liu, Yen-Ting Tseng, Kon-Ping Lin, Ueng‐Cheng Yang, Ki Wha Chung, Byung‐Ok Choi, Garth A. Nicholson, Marina Kennerson, Chih‐Chiang Chan, Peter De Jonghe, Tzu-Hao Cheng, Yi‐Chu Liao, Stephan Züchner, Jonathan Baets, Yi‐Chung Lee

    Vydáno 2017
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