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Showing items 11-19 of 19  (2 Page(s) Totally)
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Institution Date Title Author
國立成功大學 2022-02 Novel potential functions of amoeboid cells in thraustochytrids revealed by Aurantiochytrium limacinum BL10 Chou;Szu-Cheng;Su;Yu-Ming;Liu;Tsunglin;Li;Zhen-Wei;Liao;Hung-En;Renta;Pesona, Person;Chen;Yi-Min
國立成功大學 2022 Microbiome dysbiosis inhibits carcinogen-induced murine oral tumorigenesis Chen;Yuh-Ling;Wu;Jer-Horng;Liu;Tsunglin;Chen;Jiung-Wen;Xie;Jia-Yan;Chen;Meng-Yen;Wu;Li-Wha;Tung;Chun-Liang
國立成功大學 2020-07-23 Dissecting efficiency of a 5 ' rapid amplification of cDNA ends (5 '-RACE) approach for profiling T-cell receptor beta repertoire Lin;Yu-Hung;Hung;Sheng-Jou;Chen;Yi-Lin;Lin;Cheng-Han;Kung;Te-Fang;Yeh;Yi-Chun;Tseng;Joseph, T.;Liu;Tsunglin
國立成功大學 2020-03-14 Joining Illumina paired-end reads for classifying phylogenetic marker sequences Liu;Tsunglin;Chen;Chen-Yu;Chen-Deng;An;Chen;Yi-Lin;Wang;Jiu-Yao;Hou;Yung-;I;Lin;Min-Ching
國立成功大學 2019-09-2 A novel zebrafish model to emulate lung injury by folate deficiency-induced swim bladder defectiveness and protease/antiprotease expression imbalance Lee;Gang-Hui;Cheng;Nai-Wei;Yu;Hsin-Hsuan;Tsai;Jen-Ning;Liu;Tsunglin;Wen;Zhi-Hong;Chen;Bing-Hung;Fu;Tzu-Fun
國立成功大學 2019-07 Expanding the mesodermal transcriptional network by genome-wide identification of Zinc finger homeodomain 1 (Zfh1) targets Wu;Wei-Hang;Kuo;Tai-Hong;Kao;Chia-Wei;Girardot;Charles;Hung;Sheng-Jou;Liu;Tsunglin;Furlong;Eileen, Eileen E. M.;Liu;Ya-Hsin
國立成功大學 2019-03-29 Expressional Profiling of Carpet Glia in the Developing Drosophila Eye Reveals Its Molecular Signature of Morphology Regulators Ho;Tsung-Ying;Wu;Wei-Hang;Hung;Sheng-Jou;Liu;Tsunglin;Lee;Yuan-Ming;Liu;Ya-Hsin
國立成功大學 2018-09 Hepatitis B virus surface gene pre-S-2 mutant as a high-risk serum marker for hepatoma recurrence after curative hepatic resection Yen;Chia-Jui;Ai;Yu-Lin;Tsai;Hung-Wen;Chan;Shih-Huang;Yen;Chia-Sheng;Cheng;Kuang-Hsiung;Lee;Yun-Ping;Kao;Chia-Wei;Wang;Yu-Chun;Chen;Yi-Lin;Lin;Cheng-Han;Liu;Tsunglin;Tsai;Huey-Pin;Wang;Jen-Ren;Su;Ih-Jen;Huang;Wenya
國立成功大學 2018-04-18 Rare Compound Heterozygous Frameshift Mutations in &ITALMS1&IT Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alstrom Syndrome Tsai;Meng-Che;Yu;Hui-Wen;Liu;Tsunglin;Chou;Yen-Yin;Chiou;Yuan-Yow;Chen;Peng-Chieh

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