Search Results - CHIOU, Yi-Ning

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  1. 1
    Phenolic Glycosides from Viscum angulatum

    Phenolic Glycosides from Viscum angulatum by LIN, Jer-Huei, CHIOU, Yi-Ning, LIN, Yun-Lian

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  2. 2
    Phenolic Glycosides from Viscum a ngulatum

    Phenolic Glycosides from Viscum a ngulatum by Lin, Jer-Huei, Chiou, Yi-Ning, Lin, Yun-Lian

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  3. 3
    In Vitro and In Vivo Antifibrotic Effects of Fraxetin on Renal Interstitial Fibrosis via the ERK Signaling Pathway

    In Vitro and In Vivo Antifibrotic Effects of Fraxetin on Renal Interstitial Fibrosis via the ERK Signaling Pathway by Hsieh, Yi-Hsien, Hung, Tung-Wei, Chen, Yong-Syuan, Huang, Yi-Ning, Chiou, Hui-Ling, Lee, Chu-Che, Tsai, Jen-Pi

    Published in Toxins
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  4. 4
    Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene

    Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene by Hung, Chia-Cheng, Lin, Shin-Yu, Lee, Chien-Nan, Chen, Chih-Ping, Lin, Shuan-Pei, Chao, Mei-Chyn, Chiou, Shyh-Shin, Su, Yi-Ning

    Published in BMC medical genetics
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  5. 5
    Efficient detection of factor IX mutations by denaturing high-performance liquid chromatography in Taiwanese hemophilia B patients, and the identification of two novel mutations

    Efficient detection of factor IX mutations by denaturing high-performance liquid chromatography in Taiwanese hemophilia B patients, and the identification of two novel mutations by Lin, Pei-Chin, Su, Yi-Ning, Liao, Yu-Mei, Chang, Tai-Tsung, Tsai, Shih-Pien, Shu, Hsiu-Lan, Chiou, Shyh-Shin

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  6. 6
    Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1

    Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1 by Lee, Ming-Jen, Su, Yi-Ning, You, Huey-Ling, Chiou, Shinn-Chong, Lin, Li-Chu, Yang, Chih-Chao, Lee, Wang-Chao, Hwu, Wu-Liang, Hsieh, Fon-Jou, Stephenson, Dennis A., Yu, Chia-Li

    Published in Human mutation
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  7. 7
    Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM

    Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM by Lin, Shin-Yu, Su, Yi-Ning, Hung, Chia-Cheng, Tsay, Woei, Chiou, Shyh-Shin, Chang, Chieh-Ting, Ho, Hong-Nerng, Lee, Chien-Nan

    Published in BMC medical genetics
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  8. 8
    Mutation spectrum of the fibrillin‐1 (FBN1) gene in Taiwanese patients with Marfan syndrome

    Mutation spectrum of the fibrillin‐1 (FBN1) gene in Taiwanese patients with Marfan syndrome by Hung, Chia‐Cheng, Lin, Shin‐Yu, Lee, Chien‐Nan, Cheng, Hui‐Yu, Lin, Shuan‐Pei, Chen, Ming‐Ren, Chen, Chih‐Ping, Chang, Chien‐Hui, Lin, Chiou‐Ya, Yu, Chih‐Chieh, Chiu, Hsin‐Hui, Cheng, Wen‐Fang, Ho, Hong‐Nerng, Niu, Dau‐Ming, Su, Yi‐Ning

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  9. 9
    Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome

    Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome by Lin, Shin-Yu, Lee, Chien-Nan, Hung, Chia-Cheng, Tsai, Wen-Yu, Lin, Shuan-Pei, Li, Ni-Chung, Hsieh, Wu-Shiun, Tung, Yi-Ching, Niu, Dau-Ming, Hsu, Wen-Ming, Chen, Lang-Yao, Fang, Mei-Ya, Tu, Mei-Pin, Kuo, Pei-Wen, Lin, Chiou-Ya, Su, Yi-Ning, Ho, Hong-Nerng

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  10. 10
    Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis

    Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis by Hung, Chia-Cheng, Lin, Shin-Yu, Lee, Chien-Nan, Cheng, Hui-Yu, Lin, Chiou-Ya, Chang, Chien-Hui, Chiu, Hsin-Hui, Yu, Chih-Chieh, Lin, Shuan-Pei, Cheng, Wen-Fang, Ho, Hong-Nerng, Niu, Dau-Ming, Su, Yi-Ning

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  11. 11
    Identification of forty-five novel and twenty-three knownNF1 mutations in Chinese patients with neurofibromatosis type 1

    Identification of forty-five novel and twenty-three knownNF1 mutations in Chinese patients with neurofibromatosis type 1 by Lee, Ming-Jen, Su, Yi-Ning, You, Huey-Ling, Chiou, Shinn-Chong, Lin, Li-Chu, Yang, Chih-Chao, Lee, Wang-Chao, Hwu, Wu-Liang, Hsieh, Fon-Jou, Stephenson, Dennis A., Yu, Chia-Li

    Published in Human mutation
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