Zobrazuji výsledky 1 - 15 z 15 pro vyhledávání 'Xiao-Zhou Liu', doba hledání: 0,09 s. Upřesnit hledání
  1. 1
    Wayside Detection of Wheel Minor Defects in High-Speed Trains by a Bayesian Blind Source Separation Method

    Wayside Detection of Wheel Minor Defects in High-Speed Trains by a Bayesian Blind Source Separation Method Autor Xiao-Zhou Liu, Chi Xu, Yi-Qing Ni

    Vydáno 2019-09-01
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  2. 2
    Automatic Detection and Association Analysis of Multiple Surface Defects on Shield Subway Tunnels

    Automatic Detection and Association Analysis of Multiple Surface Defects on Shield Subway Tunnels Autor Ziren Yin, Zhanzhan Lei, Ao Zheng, Jiasong Zhu, Xiao-Zhou Liu

    Vydáno 2023-08-01
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  3. 3
    Long-Term Monitoring for Track Slab in High-Speed Rail via Vision Sensing

    Long-Term Monitoring for Track Slab in High-Speed Rail via Vision Sensing Autor Zai-Wei Li, Yue-Lei He, Xiao-Zhou Liu, Yun-Lai Zhou

    Vydáno 2020-01-01
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  4. 4
    A Quantitative Detection Method for Surface Cracks on Slab Track Based on Infrared Thermography

    A Quantitative Detection Method for Surface Cracks on Slab Track Based on Infrared Thermography Autor Xuan-Yu Ye, Yan-Yun Luo, Zai-Wei Li, Xiao-Zhou Liu

    Vydáno 2023-05-01
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  5. 5
    Fat-Soluble Vitamin Deficiency in Pediatric Patients with Biliary Atresia

    Fat-Soluble Vitamin Deficiency in Pediatric Patients with Biliary Atresia Autor Rui Dong, Song Sun, Xiao-Zhou Liu, Zhen Shen, Gong Chen, Shan Zheng

    Vydáno 2017-01-01
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  6. 6
    Correlation Analysis between Rail Track Geometry and Car-Body Vibration Based on Fractal Theory

    Correlation Analysis between Rail Track Geometry and Car-Body Vibration Based on Fractal Theory Autor Xiao-Zhou Liu, Zai-Wei Li, Jun Wu, Cheng-Jie Song, Jun-Hua Xiao

    Vydáno 2022-12-01
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  7. 7
    Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the PTPRQ Gene Causing Autosomal Recessive Hearing Loss in a Chinese Family

    Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the PTPRQ Gene Causing Autosomal Recessive Hearing Loss in a Chinese Family Autor Yuan Jin, Xiao-Zhou Liu, Le Xie, Wen Xie, Sen Chen, Yu Sun, Yu Sun

    Vydáno 2022-07-01
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  8. 8
    N-Acetylcysteine Combined With Dexamethasone Treatment Improves Sudden Sensorineural Hearing Loss and Attenuates Hair Cell Death Caused by ROS Stress

    N-Acetylcysteine Combined With Dexamethasone Treatment Improves Sudden Sensorineural Hearing Loss and Attenuates Hair Cell Death Caused by ROS Stress Autor Xue Bai, Sen Chen, Kai Xu, Yuan Jin, Xun Niu, Le Xie, Yue Qiu, Xiao-Zhou Liu, Yu Sun

    Vydáno 2021-03-01
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  9. 9
    The protective effects of systemic dexamethasone on sensory epithelial damage and hearing loss in targeted Cx26-null mice

    The protective effects of systemic dexamethasone on sensory epithelial damage and hearing loss in targeted Cx26-null mice Autor Kai Xu, Sen Chen, Le Xie, Yue Qiu, Xiao-zhou Liu, Xue Bai, Yuan Jin, Xiao-hui Wang, Yu Sun

    Vydáno 2022-06-01
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  10. 10
    Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children

    Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children Autor Le Xie, Yue Qiu, Yuan Jin, Kai Xu, Xue Bai, Xiao-Zhou Liu, Xiao-Hui Wang, Sen Chen, Yu Sun

    Vydáno 2021-01-01
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  11. 11
    Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss

    Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss Autor Xiao-Hui Wang, Le Xie, Sen Chen, Kai Xu, Xue Bai, Yuan Jin, Yue Qiu, Xiao-Zhou Liu, Yu Sun, Wei-Jia Kong

    Vydáno 2021-01-01
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  12. 12
    Auditory Neuropathy Spectrum Disorder due to Two Novel Compound Heterozygous OTOF Mutations in Two Chinese Families

    Auditory Neuropathy Spectrum Disorder due to Two Novel Compound Heterozygous OTOF Mutations in Two Chinese Families Autor Yue Qiu, Sen Chen, Le Xie, Kai Xu, Yi Lin, Xue Bai, Hui-Min Zhang, Xiao-Zhou Liu, Yuan Jin, Yu Sun, Wei-Jia Kong

    Vydáno 2019-01-01
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  13. 13
    A Novel Spontaneous Mutation of the SOX10 Gene Associated with Waardenburg Syndrome Type II

    A Novel Spontaneous Mutation of the SOX10 Gene Associated with Waardenburg Syndrome Type II Autor Sen Chen, Yuan Jin, Le Xie, Wen Xie, Kai Xu, Yue Qiu, Xue Bai, Hui-Min Zhang, Xiao-Zhou Liu, Xiao-Hui Wang, Wei-Jia Kong, Yu Sun

    Vydáno 2020-01-01
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  14. 14
    Local Macrophage-Related Immune Response Is Involved in Cochlear Epithelial Damage in Distinct Gjb2-Related Hereditary Deafness Models

    Local Macrophage-Related Immune Response Is Involved in Cochlear Epithelial Damage in Distinct Gjb2-Related Hereditary Deafness Models Autor Kai Xu, Sen Chen, Le Xie, Yue Qiu, Xue Bai, Xiao-Zhou Liu, Hui-Min Zhang, Xiao-Hui Wang, Yuan Jin, Yu Sun, Wei-Jia Kong, Wei-Jia Kong

    Vydáno 2021-01-01
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  15. 15
    Jervell and Lange-Nielsen Syndrome due to a Novel Compound Heterozygous KCNQ1 Mutation in a Chinese Family

    Jervell and Lange-Nielsen Syndrome due to a Novel Compound Heterozygous KCNQ1 Mutation in a Chinese Family Autor Yue Qiu, Sen Chen, Xia Wu, Wen-Juan Zhang, Wen Xie, Yuan Jin, Le Xie, Kai Xu, Xue Bai, Hui-Min Zhang, Xiao-Zhou Liu, Xiao-Hui Wang, Yu Sun, Wei-Jia Kong

    Vydáno 2020-01-01
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