Hasil Pencarian - Zihui Yan

  • Menampilkan 1 - 18 hasil dari 18
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  1. 1
    Jianpi Qinghua Fomula alleviates insulin resistance via restraining of MAPK pathway to suppress inflammation of the small intestine in DIO mice

    Jianpi Qinghua Fomula alleviates insulin resistance via restraining of MAPK pathway to suppress inflammation of the small intestine in DIO mice oleh Yahua Liu, Xu Han, Mengjie Cai, Shenyi Jin, Zihui Yan, Hao Lu, Qingguang Chen

    Diterbitkan 2022-05-01
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  2. 2
    Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function Mechanism

    Variants Affecting the C-Terminal of CSF1R Cause Congenital Vertebral Malformation Through a Gain-of-Function Mechanism oleh Bowen Liu, Bowen Liu, Sen Zhao, Sen Zhao, Zihui Yan, Zihui Yan, Zihui Yan, Lina Zhao, Lina Zhao, Jiachen Lin, Jiachen Lin, Jiachen Lin, Shengru Wang, Shengru Wang, Yuchen Niu, Yuchen Niu, Xiaoxin Li, Xiaoxin Li, Guixing Qiu, Guixing Qiu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Terry Jianguo Zhang, Terry Jianguo Zhang, Zhihong Wu, Zhihong Wu, Nan Wu, Nan Wu

    Diterbitkan 2021-03-01
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  3. 3
    JianPi-QingHua formula attenuates nonalcoholic fatty liver disease by regulating the AMPK/SIRT1/NF-κB pathway in high-fat-diet-fed C57BL/6 mice

    JianPi-QingHua formula attenuates nonalcoholic fatty liver disease by regulating the AMPK/SIRT1/NF-κB pathway in high-fat-diet-fed C57BL/6 mice oleh Jing Tian, Mengjie Cai, Shenyi Jin, Qingguang Chen, Jiahui Xu, Qiuyue Guo, Zihui Yan, Xu Han, Hao Lu

    Diterbitkan 2023-12-01
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  4. 4
    Factors associated with oral health service utilization among young people in southern China

    Factors associated with oral health service utilization among young people in southern China oleh Yunquan Cai, Shaobo Zeng, Yimei Hu, Lingfeng Xiao, Yanqing Liao, Zihui Yan, Wenxiang Zha, Junwang Gu, Qi Wang, Ming Hao, Chunmei Wu

    Diterbitkan 2024-02-01
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  5. 5
    Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis

    Whole-genome methylation analysis reveals novel epigenetic perturbations of congenital scoliosis oleh Gang Liu, Hengqiang Zhao, Zihui Yan, Sen Zhao, Yuchen Niu, Xiaoxin Li, Shengru Wang, Yang Yang, Sen Liu, Terry Jianguo Zhang, Zhihong Wu, Nan Wu

    Diterbitkan 2021-03-01
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  6. 6
    Genetic Regulation of N6-Methyladenosine-RNA in Mammalian Gametogenesis and Embryonic Development

    Genetic Regulation of N6-Methyladenosine-RNA in Mammalian Gametogenesis and Embryonic Development oleh Yuguang Chang, Mingliang Yi, Jing Wang, Zhikun Cao, Tingting Zhou, Wei Ge, Zafir Muhammad, Zijun Zhang, Yanqin Feng, Zihui Yan, Massimo De Felici, Wei Shen, Hongguo Cao

    Diterbitkan 2022-03-01
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  7. 7
    A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia

    A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia oleh Jiashen Shao, Sen Zhao, Zihui Yan, Lianlei Wang, Yuanqiang Zhang, Mao Lin, Chenxi Yu, Shengru Wang, Yuchen Niu, Xiaoxin Li, Guixing Qiu, Jianguo Zhang, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Zhihong Wu, Nan Wu

    Diterbitkan 2020-05-01
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  8. 8
    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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  9. 9
    Mutational burden and potential oligogenic model of TBX6‐mediated genes in congenital scoliosis

    Mutational burden and potential oligogenic model of TBX6‐mediated genes in congenital scoliosis oleh Yang Yang, Sen Zhao, Yuanqiang Zhang, Shengru Wang, Jiashen Shao, Bowen Liu, Yaqi Li, Zihui Yan, Yuchen Niu, Xiaoxin Li, Lianlei Wang, Yongyu Ye, Xisheng Weng, Zhihong Wu, Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study, Jianguo Zhang, Nan Wu

    Diterbitkan 2020-10-01
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  10. 10
    Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis

    Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis oleh Zefu Chen, Zihui Yan, Chenxi Yu, Jiaqi Liu, Yanbin Zhang, Sen Zhao, Jiachen Lin, Yuanqiang Zhang, Lianlei Wang, Mao Lin, Yingzhao Huang, Xiaoxin Li, Yuchen Niu, Shengru Wang, Zhihong Wu, DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) study group, Guixing Qiu, Terry Jianguo Zhang, Nan Wu

    Diterbitkan 2020-09-01
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  11. 11
    Deciphering the mutational signature of congenital limb malformations

    Deciphering the mutational signature of congenital limb malformations oleh Liying Sun, Yingzhao Huang, Sen Zhao, Junhui Zhao, Zihui Yan, Yang Guo, Mao Lin, Wenyao Zhong, Yuehan Yin, Zefu Chen, Nan Zhang, Yuanqiang Zhang, Zongxuan Zhao, Qingyang Li, Lianlei Wang, Xiying Dong, Yaqi Li, Xiaoxin Li, Guixing Qiu, Terry Jianguo Zhang, Zhihong Wu, Wen Tian, Nan Wu

    Diterbitkan 2021-06-01
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  12. 12
    Changes in seminal plasma microecological dynamics and the mechanistic impact of core metabolite hexadecanamide in asthenozoospermia patients

    Changes in seminal plasma microecological dynamics and the mechanistic impact of core metabolite hexadecanamide in asthenozoospermia patients oleh Baoquan Han, Yongyong Wang, Wei Ge, Junjie Wang, Shuai Yu, Jiamao Yan, Lei Hua, Xiaoyuan Zhang, Zihui Yan, Lu Wang, Jinxin Zhao, Cong Huang, Bo Yang, Yan Wang, Qian Ma, Yong Zhao, Hui Jiang, Yunqi Zhang, Shaolin Liang, Jianjuan Zhao, Zhongyi Sun, Wei Shen, Yaoting Gui

    Diterbitkan 2024-04-01
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  13. 13
    Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature

    Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature oleh Baoheng Gui, Baoheng Gui, Baoheng Gui, Chenxi Yu, Chenxi Yu, Xiaoxin Li, Sen Zhao, Sen Zhao, Hengqiang Zhao, Hengqiang Zhao, Zihui Yan, Zihui Yan, Xi Cheng, Xi Cheng, Jiachen Lin, Jiachen Lin, Haiyang Zheng, Haiyang Zheng, Haiyang Zheng, Jiashen Shao, Jiashen Shao, Zhengye Zhao, Zhengye Zhao, Lina Zhao, Yuchen Niu, Zhi Zhao, Huizi Wang, Bobo Xie, Bobo Xie, Bobo Xie, Xianda Wei, Xianda Wei, Chunrong Gui, Chunrong Gui, Chuan Li, Chuan Li, Chuan Li, Shaoke Chen, Shaoke Chen, Shaoke Chen, Yi Wang, Yanning Song, Chunxiu Gong, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang

    Diterbitkan 2021-04-01
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  14. 14
    Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants

    Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants oleh Wen Tian, Yingzhao Huang, Liying Sun, Yang Guo, Sen Zhao, Mao Lin, Xiying Dong, Wenyao Zhong, Yuehan Yin, Zefu Chen, Nan Zhang, Yuanqiang Zhang, Lianlei Wang, Jiachen Lin, Zihui Yan, Xinzhuang Yang, Junhui Zhao, Guixing Qiu, Jianguo Zhang, Zhihong Wu, Nan Wu, (Deciphering Disorders Involving Scoliosis, COmorbidities) study group

    Diterbitkan 2020-10-01
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  15. 15
    Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients

    Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients oleh Chenxi Yu, Chenxi Yu, Chenxi Yu, Bobo Xie, Bobo Xie, Bobo Xie, Zhengye Zhao, Zhengye Zhao, Sen Zhao, Sen Zhao, Lian Liu, Lian Liu, Xi Cheng, Xi Cheng, Xiaoxin Li, Xiaoxin Li, Bingyan Cao, Jiashen Shao, Jiashen Shao, Jiajia Chen, Hengqiang Zhao, Hengqiang Zhao, Zihui Yan, Zihui Yan, Chang Su, Yuchen Niu, Yuchen Niu, Yanning Song, Liya Wei, Yi Wang, Xiaoya Ren, Lijun Fan, Beibei Zhang, Chuan Li, Chuan Li, Chuan Li, Baoheng Gui, Baoheng Gui, Baoheng Gui, Yuanqiang Zhang, Lianlei Wang, Shaoke Chen, Shaoke Chen, Shaoke Chen, Jianguo Zhang, Jianguo Zhang, Jianguo Zhang, Zhihong Wu, Zhihong Wu, Zhihong Wu, Zhihong Wu, Chunxiu Gong, Xin Fan, Xin Fan, Xin Fan, Nan Wu, Nan Wu, Nan Wu, Nan Wu

    Diterbitkan 2021-09-01
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  16. 16
    DrABC: deep learning accurately predicts germline pathogenic mutation status in breast cancer patients based on phenotype data

    DrABC: deep learning accurately predicts germline pathogenic mutation status in breast cancer patients based on phenotype data oleh Jiaqi Liu, Hengqiang Zhao, Yu Zheng, Lin Dong, Sen Zhao, Yukuan Huang, Shengkai Huang, Tianyi Qian, Jiali Zou, Shu Liu, Jun Li, Zihui Yan, Yalun Li, Shuo Zhang, Xin Huang, Wenyan Wang, Yiqun Li, Jie Wang, Yue Ming, Xiaoxin Li, Zeyu Xing, Ling Qin, Zhengye Zhao, Ziqi Jia, Jiaxin Li, Gang Liu, Menglu Zhang, Kexin Feng, Jiang Wu, Jianguo Zhang, Yongxin Yang, Zhihong Wu, Zhihua Liu, Jianming Ying, Xin Wang, Jianzhong Su, Xiang Wang, Nan Wu

    Diterbitkan 2022-02-01
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  17. 17
    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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  18. 18
    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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