Hasil Pencarian - Yu‐Shuen Tsai

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  1. 1
    Identification of single- and multiple-class specific signature genes from gene expression profiles by group marker index.

    Identification of single- and multiple-class specific signature genes from gene expression profiles by group marker index. oleh Yu-Shuen Tsai, Kripamoy Aguan, Nikhil R Pal, I-Fang Chung

    Diterbitkan 2011-01-01
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  2. 2
    Generating transcriptional regulatory networks from time-ordered stem cell differentiation RNA sequencing data

    Generating transcriptional regulatory networks from time-ordered stem cell differentiation RNA sequencing data oleh Yu-Shuen Tsai, Yao-Ming Chang, Yang-Mooi Lim, Soon-Keng Cheong, I-Fang Chung, Chee-Yin Wong

    Diterbitkan 2022-09-01
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  3. 3
    Mutation spectrum of Charcot‐Marie‐Tooth disease among the Han Chinese in Taiwan

    Mutation spectrum of Charcot‐Marie‐Tooth disease among the Han Chinese in Taiwan oleh Yun‐Hsin Hsu, Kon‐Ping Lin, Yuh‐Cherng Guo, Yu‐Shuen Tsai, Yi‐Chu Liao, Yi‐Chung Lee

    Diterbitkan 2019-06-01
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  4. 4
    Hand‐onset weakness is a common feature of ALS patients with a NEK1 loss‐of‐function variant

    Hand‐onset weakness is a common feature of ALS patients with a NEK1 loss‐of‐function variant oleh Yu‐Shuen Tsai, Kon‐Ping Lin, Kang‐Yang Jih, Pei‐Chien Tsai, Yi‐Chu Liao, Yi‐Chung Lee

    Diterbitkan 2020-06-01
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  5. 5
    Airway Microbial Diversity is Inversely Associated with Mite-Sensitized Rhinitis and Asthma in Early Childhood

    Airway Microbial Diversity is Inversely Associated with Mite-Sensitized Rhinitis and Asthma in Early Childhood oleh Chih-Yung Chiu, Yi-Ling Chan, Yu-Shuen Tsai, Ssu-An Chen, Chia-Jung Wang, Kuan-Fu Chen, I.-Fang Chung

    Diterbitkan 2017-05-01
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  6. 6
    Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia

    Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia oleh Cheng‐Tsung Hsiao, Tzu‐Yun Tsai, Ting‐Yi Shen, Yu‐Shuen Tsai, Yi‐Chu Liao, Yi‐Chung Lee, Pei‐Chien Tsai

    Diterbitkan 2024-07-01
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  7. 7
    Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia

    Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia oleh Shao-Lun Hsu, Yi-Jiun Lu, Yu-Shuen Tsai, Hua-Chuan Chao, Jong-Ling Fuh, Yi-Chu Liao, Yi-Chung Lee

    Diterbitkan 2022-01-01
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  8. 8
    Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

    Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5 oleh Cheng‐Ta Chou, Bing‐Wen Soong, Kon‐Ping Lin, Yu‐Shuen Tsai, Kang‐Yang Jih, Yi‐Chu Liao, Yi‐Chung Lee

    Diterbitkan 2020-04-01
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  9. 9
    Biallelic DDHD2 mutations in patients with adult‐onset complex hereditary spastic paraplegia

    Biallelic DDHD2 mutations in patients with adult‐onset complex hereditary spastic paraplegia oleh Ying‐Tsen Chou, Shao‐Lun Hsu, Yu‐Shuen Tsai, Yi‐Jiun Lu, Kai‐Wei Yu, Hsiu‐Mei Wu, Yi‐Chu Liao, Yi‐Chung Lee

    Diterbitkan 2023-09-01
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  10. 10
    Decoding the differentiation of mesenchymal stem cells into mesangial cells at the transcriptomic level

    Decoding the differentiation of mesenchymal stem cells into mesangial cells at the transcriptomic level oleh Chee-Yin Wong, Yao-Ming Chang, Yu-Shuen Tsai, Wailap Victor Ng, Soon-Keng Cheong, Ting-Yu Chang, I-Fang Chung, Yang-Mooi Lim

    Diterbitkan 2020-07-01
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  11. 11
    Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia.

    Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia. oleh Ying-Hao Chen, Yi-Chung Lee, Yu-Shuen Tsai, Yuh-Cherng Guo, Cheng-Tsung Hsiao, Pei-Chien Tsai, Jin-An Huang, Yi-Chu Liao, Bing-Wen Soong

    Diterbitkan 2017-01-01
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  12. 12
    Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia

    Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia oleh Shih‐Yu Fang, Ying‐Tsen Chou, Kuo‐Chou Hsu, Shao‐Lun Hsu, Kai‐Wei Yu, Yu‐Shuen Tsai, Yi‐Chu Liao, Pei‐Chien Tsai, Yi‐Chung Lee

    Diterbitkan 2023-03-01
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  13. 13
    Clinical and genetic characterization of adult‐onset leukoencephalopathy caused by CSF1R mutations

    Clinical and genetic characterization of adult‐onset leukoencephalopathy caused by CSF1R mutations oleh Pei‐Chien Tsai, Jong‐Ling Fuh, Chih‐Chao Yang, Anna Chang, Li‐Ming Lien, Pei‐Ning Wang, Kuan‐Lin Lai, Yu‐Shuen Tsai, Yi‐Chung Lee, Yi‐Chu Liao

    Diterbitkan 2021-11-01
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  14. 14
    Lymphoid Enhancer Factor 1 Contributes to Hepatocellular Carcinoma Progression Through Transcriptional Regulation of Epithelial‐Mesenchymal Transition Regulators and Stemness Genes

    Lymphoid Enhancer Factor 1 Contributes to Hepatocellular Carcinoma Progression Through Transcriptional Regulation of Epithelial‐Mesenchymal Transition Regulators and Stemness Genes... oleh Chih‐Li Chen, Yu‐Shuen Tsai, Yen‐Hua Huang, Yuh‐Jin Liang, Ya‐Yun Sun, Chien‐Wei Su, Gar‐Yang Chau, Yi‐Chen Yeh, Yung‐Sheng Chang, Jui‐Ting Hu, Jaw‐Ching Wu

    Diterbitkan 2018-11-01
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  15. 15
    A missense mutation in human INSC causes peripheral neuropathy

    A missense mutation in human INSC causes peripheral neuropathy oleh Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan

    Diterbitkan 2024-04-01
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