Hasil Pencarian - Yuzhi Zuo

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  1. 1
    Melanocyte stem cells in the skin: Origin, biological characteristics, homeostatic maintenance and therapeutic potential

    Melanocyte stem cells in the skin: Origin, biological characteristics, homeostatic maintenance and therapeutic potential oleh Luling Huang, Yuzhi Zuo, Shuli Li, Chunying Li

    Diterbitkan 2024-05-01
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  2. 2
    Multiple inferior vena cava aneurysms mimic a retroperitoneal tumor: a case report

    Multiple inferior vena cava aneurysms mimic a retroperitoneal tumor: a case report oleh Yuzhi Zuo, Zhenyu Zhang, Bingbing Shi, Zhigang Ji, Zhongming Huang

    Diterbitkan 2020-09-01
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  3. 3
    Change in the cause of inpatient mortality after arthroplasty: a retrospective study

    Change in the cause of inpatient mortality after arthroplasty: a retrospective study oleh Yuzhi Zuo, Jin Lin, Jin Jin, Wenwei Qian, Guixing Qiu, Xisheng Weng

    Diterbitkan 2019-06-01
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  4. 4
    Comprehensive prediction of immune microenvironment and hot and cold tumor differentiation in cutaneous melanoma based on necroptosis-related lncRNA

    Comprehensive prediction of immune microenvironment and hot and cold tumor differentiation in cutaneous melanoma based on necroptosis-related lncRNA oleh Miao Zhang, Lushan Yang, Yizhi Wang, Yuzhi Zuo, Dengdeng Chen, Xing Guo

    Diterbitkan 2023-05-01
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  5. 5
    A novel signature for predicting prognosis and immune landscape in cutaneous melanoma based on anoikis-related long non-coding RNAs

    A novel signature for predicting prognosis and immune landscape in cutaneous melanoma based on anoikis-related long non-coding RNAs oleh Miao Zhang, Yuzhi Zuo, Jian Guo, Lushan Yang, Yizhi Wang, Meiyun Tan, Xing Guo

    Diterbitkan 2023-09-01
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  6. 6
    Phenotypic heterogeneity of intellectual disability in patients with congenital insensitivity to pain with anhidrosis: A case report and literature review

    Phenotypic heterogeneity of intellectual disability in patients with congenital insensitivity to pain with anhidrosis: A case report and literature review oleh Zhenlei Liu, Jiaqi Liu, Gang Liu, Wenjian Cao, Sen Liu, Yixin Chen, Yuzhi Zuo, Weisheng Chen, Jun Chen, Yu Zhang, Shishu Huang, Guixing Qiu, Philip F. Giampietro, Feng Zhang, Zhihong Wu, Nan Wu

    Diterbitkan 2018-06-01
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  7. 7
    Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis

    Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosi... oleh Gang Liu, Gang Liu, Lianlei Wang, Lianlei Wang, Xinyu Wang, Zihui Yan, Zihui Yan, Xinzhuang Yang, Xinzhuang Yang, Mao Lin, Mao Lin, Sen Liu, Sen Liu, Yuzhi Zuo, Yuzhi Zuo, Yuchen Niu, Yuchen Niu, Sen Zhao, Sen Zhao, Yanxue Zhao, Yanxue Zhao, Jianguo Zhang, Jianguo Zhang, Jianguo Zhang, Jianxiong Shen, Jianxiong Shen, Jianxiong Shen, Yipeng Wang, Yipeng Wang, Yipeng Wang, Guixing Qiu, Guixing Qiu, Guixing Qiu, Zhihong Wu, Zhihong Wu, Zhihong Wu, Nan Wu, Nan Wu, Nan Wu

    Diterbitkan 2019-12-01
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  8. 8
    Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders

    Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders oleh Sen Zhao, Yuanqiang Zhang, Sigrun Hallgrimsdottir, Yuzhi Zuo, Xiaoxin Li, Dominyka Batkovskyte, Sen Liu, Hillevi Lindelöf, Shengru Wang, Anna Hammarsjö, Yang Yang, Yongyu Ye, Lianlei Wang, Zihui Yan, Jiachen Lin, Chenxi Yu, Zefu Chen, Yuchen Niu, Huizi Wang, Zhi Zhao, Pengfei Liu, Guixing Qiu, Jennifer E. Posey, Zhihong Wu, James R. Lupski, Ieva Micule, Britt-Marie Anderlid, Ulrika Voss, Dennis Sulander, Ekaterina Kuchinskaya, Ann Nordgren, Ola Nilsson, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Terry Jianguo Zhang, Giedre Grigelioniene, Nan Wu

    Diterbitkan 2022-02-01
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  9. 9
    Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

    Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1 oleh Mao Lin, Zhenlei Liu, Gang Liu, Sen Zhao, Chao Li, Weisheng Chen, Zeynep Coban Akdemir, Jiachen Lin, Xiaofei Song, Shengru Wang, Qiming Xu, Yanxue Zhao, Lianlei Wang, Yuanqiang Zhang, Zihui Yan, Sen Liu, Jiaqi Liu, Yixin Chen, Yuzhi Zuo, Xu Yang, Tianshu Sun, Xin‐Zhuang Yang, Yuchen Niu, Xiaoxin Li, Wesley You, Bintao Qiu, Chen Ding, Pengfei Liu, Shuyang Zhang, Claudia M. B. Carvalho, Jennifer E. Posey, Guixing Qiu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, James R. Lupski, Zhihong Wu, Jianguo Zhang, Nan Wu

    Diterbitkan 2020-01-01
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