Showing 1 - 18 results of 18 for search 'Wen-Lang Fan', query time: 0.07s Refine Results
  1. 1
    Universal global imprints of genome growth and evolution--equivalent length and cumulative mutation density.

    Universal global imprints of genome growth and evolution--equivalent length and cumulative mutation density. by Hong-Da Chen, Wen-Lang Fan, Sing-Guan Kong, Hoong-Chien Lee

    Published 2010-01-01
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  2. 2
    Long-Term Outcome of Neonatal Seizure with <i>PACS2</i> Mutation: Case Series and Literature Review

    Long-Term Outcome of Neonatal Seizure with <i>PACS2</i> Mutation: Case Series and Literature Review by I-Jun Chou, Ju-Yin Hou, Wen-Lang Fan, Meng-Han Tsai, Kuang-Lin Lin

    Published 2023-03-01
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  3. 3
    Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome

    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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  4. 4
    Characteristics and genetic analysis of patients suspected with early-onset systemic lupus erythematosus

    Characteristics and genetic analysis of patients suspected with early-onset systemic lupus erythematosus by Wan-Fang Lee, Wen-Lang Fan, Min-Hua Tseng, Huang-Yu Yang, Jing-Long Huang, Chao-Yi Wu

    Published 2022-08-01
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  5. 5
    Lipopolysaccharide stimulation test on cultured PBMCs assists the discrimination of cryopyrin-associated periodic syndrome from systemic juvenile idiopathic arthritis

    Lipopolysaccharide stimulation test on cultured PBMCs assists the discrimination of cryopyrin-associated periodic syndrome from systemic juvenile idiopathic arthritis by Chao-Yi Wu, Wen-Lang Fan, Ying-Ming Chiu, Huang-Yu Yang, Wen-I. Lee, Jing-Long Huang

    Published 2021-06-01
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  6. 6
    Inverse symmetry in complete genomes and whole-genome inverse duplication.

    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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  7. 7
    Ghrelin Upregulates Oncogenic Aurora A to Promote Renal Cell Carcinoma Invasion

    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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  8. 8
    Prognostic Genetic Biomarkers Based on Oncogenic Signaling Pathways for Outcome Prediction in Patients with Oral Cavity Squamous Cell Carcinoma

    Prognostic Genetic Biomarkers Based on Oncogenic Signaling Pathways for Outcome Prediction in Patients with Oral Cavity Squamous Cell Carcinoma by Wen-Lang Fan, Lan-Yan Yang, Jason Chia-Hsun Hsieh, Tsung-Chieh Lin, Mei-Yeh Jade Lu, Chun-Ta Liao

    Published 2021-05-01
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  9. 9
    Association of AXIN1 With Parkinson’s Disease in a Taiwanese Population

    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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  10. 10
    Leptin Is Associated with Poor Clinical Outcomes and Promotes Clear Cell Renal Cell Carcinoma Progression

    Leptin Is Associated with Poor Clinical Outcomes and Promotes Clear Cell Renal Cell Carcinoma Progression by Wen-Lang Fan, Yuan-Ming Yeh, Tsung-Ta Liu, Wei-Ming Lin, Tse-Yen Yang, Chao-Wei Lee, Tsung-Chieh Lin

    Published 2021-03-01
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  11. 11
    The abundances of LTF and SOD2 in amniotic fluid are potential biomarkers of gestational age and preterm birth

    The abundances of LTF and SOD2 in amniotic fluid are potential biomarkers of gestational age and preterm birth by Te-Yao Hsu, Hsin-Hsin Cheng, Kuo-Chung Lan, Hsuan-Ning Hung, Yun-Ju Lai, Chih-Chang Tsai, Wen-Lang Fan, Sung-Chou Li

    Published 2023-03-01
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  12. 12
    Genome-wide prediction of CRISPR/Cas9 targets in Kluyveromyces marxianus and its application to obtain a stable haploid strain

    Genome-wide prediction of CRISPR/Cas9 targets in Kluyveromyces marxianus and its application to obtain a stable haploid strain by Ming-Hsuan Lee, Jinn-Jy Lin, Yu-Ju Lin, Jui-Jen Chang, Huei-Mien Ke, Wen-Lang Fan, Tzi-Yuan Wang, Wen-Hsiung Li

    Published 2018-05-01
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  13. 13
    Author Correction: The abundances of LTF and SOD2 in amniotic fluid are potential biomarkers of gestational age and preterm birth

    Author Correction: The abundances of LTF and SOD2 in amniotic fluid are potential biomarkers of gestational age and preterm birth by Te-Yao Hsu, Hsin-Hsin Cheng, Kuo-Chung Lan, Hsuan-Ning Hung, Yun-Ju Lai, Chih-Chang Tsai, Wen-Lang Fan, Sung-Chou Li

    Published 2023-03-01
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  14. 14
    Effect of Hydrocortisone on Angiotensinogen (<i>AGT</i>) Mutation–Causing Autosomal Recessive Renal Tubular Dysgenesis

    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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  15. 15
    Rare Occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers

    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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  16. 16
    Complement Factor I Mutation May Contribute to Development of Thrombotic Microangiopathy in Lupus Nephritis

    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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  17. 17
    Whole-Exome Sequencing Identified Novel CLMP Mutations in a Family With Congenital Short Bowel Syndrome Presenting Differently in Two Probands

    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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  18. 18
    A Novel CD3G Mutation in a Taiwanese Patient With Normal T Regulatory Function Presenting With the CVID Phenotype Free of Autoimmunity—Analysis of all Genotypes and Phenotypes

    A Novel CD3G Mutation in a Taiwanese Patient With Normal T Regulatory Function Presenting With the CVID Phenotype Free of Autoimmunity—Analysis of all Genotypes and Phenotypes by Wen-I Lee, Wen-I Lee, Wen-Lang Fan, Chun-Hao Lu, Shih-Hsiang Chen, Shih-Hsiang Chen, Ming-Ling Kuo, Syh-Jae Lin, Weng-Sheng Tsai, Tang-Her Jaing, Tang-Her Jaing, Li-Chen Chen, Kuo-Wei Yeh, Tsung-Chieh Yao, Jing-Long Huang, Jing-Long Huang

    Published 2019-12-01
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