Showing 1 - 20 results of 21 for search 'Lang Fan', query time: 0.07s
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Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome by Shao-Yu Chang, Naotomo Kambe, Wen-Lang Fan, Jing-Long Huang, Wen-I Lee, Chao-Yi Wu
Published 2022-10-01
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Inverse symmetry in complete genomes and whole-genome inverse duplication. by Sing-Guan Kong, Wen-Lang Fan, Hong-Da Chen, Zi-Ting Hsu, Nengji Zhou, Bo Zheng, Hoong-Chien Lee
Published 2009-11-01
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Ghrelin Upregulates Oncogenic Aurora A to Promote Renal Cell Carcinoma Invasion by Tsung-Chieh Lin, Yuan-Ming Yeh, Wen-Lang Fan, Yu-Chan Chang, Wei-Ming Lin, Tse-Yen Yang, Michael Hsiao
Published 2019-03-01
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Association of AXIN1 With Parkinson’s Disease in a Taiwanese Population by Hwa-Shin Fang, Chih-Ying Chao, Chun-Chieh Wang, Wen-Lang Fan, Po-Jung Huang, Hon-Chung Fung, Yih-Ru Wu
Published 2022-01-01
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Effect of Hydrocortisone on Angiotensinogen (<i>AGT</i>) Mutation–Causing Autosomal Recessive Renal Tubular Dysgenesis by Min-Hua Tseng, Shih-Ming Huang, Martin Konrad, Jing-Long Huang, Steven W. Shaw, Ya-Chung Tian, Ho-Yen Chueh, Wen-Lang Fan, Tai-Wei Wu, Jhao-Jhuang Ding, Ming-Chou Chiang, Shih-Hua Lin
Published 2021-04-01
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Targeting EGFR-dependent tumors by disrupting an ARF6-mediated sorting system by Huiling Guo, Juan Wang, Su Ren, Lang-Fan Zheng, Yi-Xuan Zhuang, Dong-Lin Li, Hui-Hui Sun, Li-Ying Liu, Changchuan Xie, Ya-Ying Wu, Hong-Rui Wang, Xianming Deng, Peng Li, Tong-Jin Zhao
Published 2022-10-01
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Rare Occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers by Abner Herbert Lim, Jason Yongsheng Chan, Ming-Chin Yu, Tsung-Han Wu, Jing Han Hong, Cedric Chuan Young Ng, Zhen Jie Low, Wei Liu, Rajasegaran Vikneswari, Pin-Cheng Sung, Wen-Lang Fan, Bin Tean Teh, Sen-Yung Hsieh
Published 2022-01-01
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Complement Factor I Mutation May Contribute to Development of Thrombotic Microangiopathy in Lupus Nephritis by Min-Hua Tseng, Min-Hua Tseng, Wen-Lang Fan, Hsuan Liu, Hsuan Liu, Hsuan Liu, Chia-Yu Yang, Chia-Yu Yang, Chia-Yu Yang, Chia-Yu Yang, Jhao-Jhuang Ding, Hwei-Jen Lee, Shih-Ming Huang, Shih-Hua Lin, Jing-Long Huang
Published 2021-02-01
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Whole-Exome Sequencing Identified Novel CLMP Mutations in a Family With Congenital Short Bowel Syndrome Presenting Differently in Two Probands by Yao-Hung Chuang, Wen-Lang Fan, Yu-De Chu, Kung-Hao Liang, Kung-Hao Liang, Kung-Hao Liang, Yuan-Ming Yeh, Chien-Chang Chen, Chien-Chang Chen, Cheng-Hsun Chiu, Cheng-Hsun Chiu, Cheng-Hsun Chiu, Ming-Wei Lai, Ming-Wei Lai, Ming-Wei Lai
Published 2020-12-01
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