Hasil Pencarian - Yuchen Niu

  • Menampilkan 1 - 17 hasil dari 17
Perbaiki Hasil
  1. 1
    A Hybrid Rule-Based and Data-Driven Approach to Illegal Transshipment Identification with Interpretable Behavior Features

    A Hybrid Rule-Based and Data-Driven Approach to Illegal Transshipment Identification with Interpretable Behavior Features oleh Lei Deng, Yuchen Niu, Limin Jia, Wen Liu, Yu Zang

    Diterbitkan 2022-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    YOLO-Fall: A Novel Convolutional Neural Network Model for Fall Detection in Open Spaces

    YOLO-Fall: A Novel Convolutional Neural Network Model for Fall Detection in Open Spaces oleh Deao Zhao, Tao Song, Jie Gao, Dong Li, Yuchen Niu

    Diterbitkan 2024-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Data Mining Suggests That CXCL14 Gene Silencing in Colon Cancer Is Due to Promoter Methylation

    Data Mining Suggests That CXCL14 Gene Silencing in Colon Cancer Is Due to Promoter Methylation oleh Yanjing Wang, Siyi Wang, Yuchen Niu, Buyong Ma, Jingjing Li

    Diterbitkan 2023-11-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Insights of Expression Profile of Chemokine Family in Inflammatory Bowel Diseases and Carcinogenesis

    Insights of Expression Profile of Chemokine Family in Inflammatory Bowel Diseases and Carcinogenesis oleh Yinjie Zhang, Yue Jin, Yanjing Wang, Siyi Wang, Yuchen Niu, Buyong Ma, Jingjing Li

    Diterbitkan 2024-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly

    Identification of Novel FBN2 Variants in a Cohort of Congenital Contractural Arachnodactyly oleh Liying Sun, Yingzhao Huang, Yingzhao Huang, Yingzhao Huang, Sen Zhao, Sen Zhao, Sen Zhao, Wenyao Zhong, Jile Shi, Jile Shi, Jile Shi, Yang Guo, Junhui Zhao, Ge Xiong, Yuehan Yin, Zefu Chen, Zefu Chen, Zefu Chen, Nan Zhang, Zongxuan Zhao, Qingyang Li, Dan Chen, Yuchen Niu, Yuchen Niu, Xiaoxin Li, Xiaoxin Li, Guixing Qiu, Guixing Qiu, Guixing Qiu, Zhihong Wu, Zhihong Wu, Zhihong Wu, Terry Jianguo Zhang, Terry Jianguo Zhang, Terry Jianguo Zhang, Wen Tian, Nan Wu, Nan Wu, Nan Wu

    Diterbitkan 2022-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    The mutational burden and oligogenic inheritance in Klippel-Feil syndrome

    The mutational burden and oligogenic inheritance in Klippel-Feil syndrome oleh Ziquan Li, Sen Zhao, Siyi Cai, Yuanqiang Zhang, Lianlei Wang, Yuchen Niu, Xiaoxin Li, Jianhua Hu, Jingdan Chen, Shengru Wang, Huizi Wang, Gang Liu, Ye Tian, Zhihong Wu, Terry Jianguo Zhang, DISCO (Deciphering Disorders Involving Scoliosis and COmorbidities) study, Yipeng Wang, Nan Wu

    Diterbitkan 2020-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  12. 12
    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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  13. 13
    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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  14. 14
    Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine

    Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine oleh Sen Zhao, Hengqiang Zhao, Lina Zhao, Xi Cheng, Zhifa Zheng, Mengfan Wu, Wen Wen, Shengru Wang, Zixiang Zhou, Haibo Xie, Dengfeng Ruan, Qing Li, Xinquan Liu, Chengzhu Ou, Guozhuang Li, Zhengye Zhao, Guilin Chen, Yuchen Niu, Xiangjie Yin, Yuhong Hu, Xiaochen Zhang, Deciphering disorders Involving Scoliosis and COmorbidities (DISCO) study, Pengfei Liu, Guixing Qiu, Wanlu Liu, Chengtian Zhao, Zhihong Wu, Jianguo Zhang, Nan Wu

    Diterbitkan 2024-02-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  15. 15
    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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  16. 16
    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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  17. 17
    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
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: