Hasil Pencarian - Jer‐Yuarn Wu

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  1. 1
    Identification of functional single nucleotide polymorphisms in the branchpoint site

    Identification of functional single nucleotide polymorphisms in the branchpoint site oleh Hung-Lun Chiang, Jer-Yuarn Wu, Yuan-Tsong Chen

    Diterbitkan 2017-11-01
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  2. 2
    Overcoming EGFR T790M-based Tyrosine Kinase Inhibitor Resistance with an Allele-specific DNAzyme

    Overcoming EGFR T790M-based Tyrosine Kinase Inhibitor Resistance with an Allele-specific DNAzyme oleh Wei-Yun Lai, Chi-Yuan Chen, Shuenn-Chen Yang, Jer-Yuarn Wu, Cheng-Ju Chang, Pan-Chyr Yang, Konan Peck

    Diterbitkan 2014-01-01
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  3. 3
    Runs of homozygosity associated with speech delay in autism in a taiwanese han population: evidence for the recessive model.

    Runs of homozygosity associated with speech delay in autism in a taiwanese han population: evidence for the recessive model. oleh Ping-I Lin, Po-Hsiu Kuo, Chia-Hsiang Chen, Jer-Yuarn Wu, Susan S-F Gau, Yu-Yu Wu, Shih-Kai Liu

    Diterbitkan 2013-01-01
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  4. 4
    Cell-based screen identifies porphyrins as FGFR3 activity inhibitors with therapeutic potential for achondroplasia and cancer

    Cell-based screen identifies porphyrins as FGFR3 activity inhibitors with therapeutic potential for achondroplasia and cancer oleh Yun-Wen Lin, Hsiao-Jung Kao, Wei-Ting Chen, Cheng-Fu Kao, Jer-Yuarn Wu, Yuan-Tsong Chen, Yi-Ching Lee

    Diterbitkan 2023-11-01
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  5. 5
    Genomic interrogation of familial short stature contributes to the discovery of the pathophysiological mechanisms and pharmaceutical drug repositioning

    Genomic interrogation of familial short stature contributes to the discovery of the pathophysiological mechanisms and pharmaceutical drug repositioning oleh Henry Sung-Ching Wong, Ying-Ju Lin, Hsing-Fang Lu, Wen-Ling Liao, Chien-Hsiun Chen, Jer-Yuarn Wu, Wei-Chiao Chang, Fuu-Jen Tsai

    Diterbitkan 2019-11-01
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  6. 6
    Modifiable factors affecting renal preservation in type I glycogen storage disease after liver transplantation: a single-center propensity-match cohort study

    Modifiable factors affecting renal preservation in type I glycogen storage disease after liver transplantation: a single-center propensity-match cohort study oleh Yi-Chia Chan, Kai-Min Liu, Chao-Long Chen, Aldwin D. Ong, Chih-Che Lin, Chee-Chien Yong, Pei-Chun Tsai, Liang-Suei Lu, Jer-Yuarn Wu

    Diterbitkan 2021-10-01
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  7. 7
    Investigation of associations between NR1D1, RORA and RORB genes and bipolar disorder.

    Investigation of associations between NR1D1, RORA and RORB genes and bipolar disorder. oleh Yin-Chieh Lai, Chung-Feng Kao, Mong-Liang Lu, Hsi-Chung Chen, Po-Yu Chen, Chien-Hsiun Chen, Winston W Shen, Jer-Yuarn Wu, Ru-Band Lu, Po-Hsiu Kuo

    Diterbitkan 2015-01-01
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  8. 8
    A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol

    A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol oleh Chia-Jung Chang, Chien-Hsiun Chen, Bing-Mae Chen, Yu-Cheng Su, Ying-Ting Chen, Michael S. Hershfield, Ming-Ta Michael Lee, Tian-Lu Cheng, Yuan-Tsong Chen, Steve R. Roffler, Jer-Yuarn Wu

    Diterbitkan 2017-09-01
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  9. 9
    Role of S-Palmitoylation by ZDHHC13 in Mitochondrial function and Metabolism in Liver

    Role of S-Palmitoylation by ZDHHC13 in Mitochondrial function and Metabolism in Liver oleh Li-Fen Shen, Yi-Ju Chen, Kai-Ming Liu, Amir N. Saleem Haddad, I-Wen Song, Hsiao-Yuh Roan, Li-Ying Chen, Jeffrey J. Y. Yen, Yu-Ju Chen, Jer-Yuarn Wu, Yuan-Tsong Chen

    Diterbitkan 2017-05-01
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  10. 10
    Palmitoyl acyltransferase, Zdhhc13, facilitates bone mass acquisition by regulating postnatal epiphyseal development and endochondral ossification: a mouse model.

    Palmitoyl acyltransferase, Zdhhc13, facilitates bone mass acquisition by regulating postnatal epiphyseal development and endochondral ossification: a mouse model. oleh I-Wen Song, Wei-Ru Li, Li-Ying Chen, Li-Fen Shen, Kai-Ming Liu, Jeffrey J Y Yen, Yi-Ju Chen, Yu-Ju Chen, Virginia Byers Kraus, Jer-Yuarn Wu, M T Michael Lee, Yuan-Tsong Chen

    Diterbitkan 2014-01-01
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  11. 11
    Genetic loci associated with an earlier age at onset in multiplex schizophrenia

    Genetic loci associated with an earlier age at onset in multiplex schizophrenia oleh Annemarie L. Woolston, Po-Chang Hsiao, Po-Hsiu Kuo, Shi-Heng Wang, Yin-Ju Lien, Chih-Min Liu, Hai-Gwo Hwu, Tzu-Pin Lu, Eric Y. Chuang, Li-Ching Chang, Chien-Hsiun Chen, Jer-Yuarn Wu, Ming T. Tsuang, Wei J. Chen

    Diterbitkan 2017-07-01
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  12. 12
    Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus.

    Longitudinal evaluation of an N-ethyl-N-nitrosourea-created murine model with normal pressure hydrocephalus. oleh Ming-Jen Lee, Ching-Pang Chang, Yi-Hsin Lee, Yi-Chih Wu, Hsu-Wen Tseng, Yu-Ying Tung, Min-Tzu Wu, Yen-Hui Chen, Lu-Ting Kuo, Dennis Stephenson, Shuen-Iu Hung, Jer-Yuarn Wu, Chen Chang, Yuan-Tsong Chen, Yijuang Chern

    Diterbitkan 2009-11-01
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  13. 13
    Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.

    Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population. oleh Po-Hsiu Kuo, Li-Chung Chuang, Mei-Hsin Su, Chia-Hsiang Chen, Chien-Hsiun Chen, Jer-Yuarn Wu, Chung-Jen Yen, Yu-Yu Wu, Shih-Kai Liu, Miao-Chun Chou, Wen-Jiun Chou, Yen-Nan Chiu, Wen-Che Tsai, Susan Shur-Fen Gau

    Diterbitkan 2015-01-01
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  14. 14
    Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study.

    Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study. oleh Fuu-Jen Tsai, Yi-Ching Lee, Jeng-Sheng Chang, Li-Min Huang, Fu-Yuan Huang, Nan-Chang Chiu, Ming-Ren Chen, Hsin Chi, Yann-Jinn Lee, Li-Ching Chang, Yi-Min Liu, Hsiang-Hua Wang, Chien-Hsiun Chen, Yuan-Tsong Chen, Jer-Yuarn Wu

    Diterbitkan 2011-01-01
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  15. 15
    A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.

    A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. oleh Fuu-Jen Tsai, Chi-Fan Yang, Ching-Chu Chen, Lee-Ming Chuang, Chieh-Hsiang Lu, Chwen-Tzuei Chang, Tzu-Yuan Wang, Rong-Hsing Chen, Chiung-Fang Shiu, Yi-Min Liu, Chih-Chun Chang, Pei Chen, Chien-Hsiun Chen, Cathy S J Fann, Yuan-Tsong Chen, Jer-Yuarn Wu

    Diterbitkan 2010-02-01
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  16. 16
    Mice with alopecia, osteoporosis, and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferase.

    Mice with alopecia, osteoporosis, and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferase. oleh Amir N Saleem, Yen-Hui Chen, Hwa Jin Baek, Ya-Wen Hsiao, Hong-Wen Huang, Hsiao-Jung Kao, Kai-Ming Liu, Li-Fen Shen, I-Wen Song, Chen-Pei D Tu, Jer-Yuarn Wu, Tateki Kikuchi, Monica J Justice, Jeffrey J Y Yen, Yuan-Tsong Chen

    Diterbitkan 2010-06-01
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  17. 17
    Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan

    Association of human height-related genetic variants with familial short stature in Han Chinese in Taiwan oleh Ying-Ju Lin, Wen-Ling Liao, Chung-Hsing Wang, Li-Ping Tsai, Chih-Hsin Tang, Chien-Hsiun Chen, Jer-Yuarn Wu, Wen-Miin Liang, Ai-Ru Hsieh, Chi-Fung Cheng, Jin-Hua Chen, Wen-Kuei Chien, Ting-Hsu Lin, Chia-Ming Wu, Chiu-Chu Liao, Shao-Mei Huang, Fuu-Jen Tsai

    Diterbitkan 2017-07-01
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  18. 18
    Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese

    Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese oleh Chun-Yu Wei, Jenn-Hwai Yang, Erh-Chan Yeh, Ming-Fang Tsai, Hsiao-Jung Kao, Chen-Zen Lo, Lung-Pao Chang, Wan-Jia Lin, Feng-Jen Hsieh, Saurabh Belsare, Anand Bhaskar, Ming-Wei Su, Te-Chang Lee, Yi-Ling Lin, Fu-Tong Liu, Chen-Yang Shen, Ling-Hui Li, Chien-Hsiun Chen, Jeffrey D. Wall, Jer-Yuarn Wu, Pui-Yan Kwok

    Diterbitkan 2021-02-01
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  19. 19
    Association between GRIN3A gene polymorphism in Kawasaki disease and coronary artery aneurysms in Taiwanese children.

    Association between GRIN3A gene polymorphism in Kawasaki disease and coronary artery aneurysms in Taiwanese children. oleh Ying-Ju Lin, Jeng-Sheng Chang, Xiang Liu, Chien-Hui Hung, Ting-Hsu Lin, Shao-Mei Huang, Kuan-Teh Jeang, Chia-Yen Chen, Chiu-Chu Liao, Cheng-Wen Lin, Chih-Ho Lai, Ni Tien, Yu-Ching Lan, Mao-Wang Ho, Wen-Kuei Chien, Jin-Hua Chen, Yu-Chuen Huang, Hsinyi Tsang, Jer-Yuarn Wu, Chien-Hsiun Chen, Li-Ching Chang, Fuu-Jen Tsai

    Diterbitkan 2013-01-01
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  20. 20
    Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan.

    Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. oleh Hsin-Chou Yang, Yu-Jen Liang, Yi-Lin Wu, Chia-Min Chung, Kuang-Mao Chiang, Hung-Yun Ho, Chih-Tai Ting, Tsung-Hsien Lin, Sheng-Hsiung Sheu, Wei-Chuan Tsai, Jyh-Hong Chen, Hsin-Bang Leu, Wei-Hsian Yin, Ting-Yu Chiu, Chin-Iuan Chen, Cathy S J Fann, Jer-Yuarn Wu, Teng-Nan Lin, Shing-Jong Lin, Yuan-Tsong Chen, Jaw-Wen Chen, Wen-Harn Pan

    Diterbitkan 2009-01-01
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