Showing 1 - 7 results of 7 for search 'Dan-Dan Ruan', query time: 0.04s Refine Results
  1. 1
    Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription

    Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription by Yu-mian Gan, Yan-ping Zhang, Dan-dan Ruan, Jian-bin Huang, Yao-bin Zhu, Xin-fu Lin, Xiao-ping Xiao, Qiong Cheng, Zhen-bo Geng, Li-sheng Liao, Fa-qiang Tang, Jie-wei Luo

    Published 2022-06-01
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  2. 2
    A Primary Extraskeletal Osteosarcoma of the Spleen: Rare Case Report

    A Primary Extraskeletal Osteosarcoma of the Spleen: Rare Case Report by Xian Pan, Xian Pan, Han-Lu Wang, Shi-Ming Lin, Jia-Li Lin, Dan-Dan Ruan, Jian-Hui Zhang, Ting Chen, Ting Chen, Jie-Wei Luo, Jie-Wei Luo, Zhu-Ting Fang, Zhu-Ting Fang

    Published 2022-05-01
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  3. 3
    Pharmarcomechanical thrombectomy combined with transluminal balloon angioplasty for treating transplant renal vein thrombosis

    Pharmarcomechanical thrombectomy combined with transluminal balloon angioplasty for treating transplant renal vein thrombosis by Shao-Jie Wu, Chi Zhang, Min Wu, Dan-dan Ruan, Yan-ping Zhang, Bin Lin, Yi Tang, Xin Chen, Chen Wang, Hong-hong Pan, Qing-guo Zhu, Jie-wei Luo, Lie-fu Ye, Zhu-ting Fang

    Published 2023-10-01
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  4. 4
    Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis

    Potential regulatory role of the Nrf2/HMGB1/TLR4/NF-κB signaling pathway in lupus nephritis by Shi-jie Li, Dan-dan Ruan, Wei-zhen Wu, Min Wu, Qiu-yan Wu, Han-lu Wang, Yuan-yuan Ji, Yan-ping Zhang, Xin-fu Lin, Zhu-ting Fang, Li-sheng Liao, Jie-wei Luo, Mei-zhu Gao, Jia-bin Wu

    Published 2023-10-01
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  5. 5
    Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency

    Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency by Han-lu Wang, Dan-dan Ruan, Min Wu, Yuan-yuan Ji, Xing-xing Hu, Qiu-yan Wu, Yan-ping Zhang, Bin Lin, Ya-nan Hu, Hang Wang, Yi Tang, Zhu-ting Fang, Jie-wei Luo, Li-sheng Liao, Mei-zhu Gao

    Published 2023-01-01
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  6. 6
    Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation

    Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation by Dan-dan Ruan, Xing-lin Ruan, Ruo‑li Wang, Xin-fu Lin, Yan-ping Zhang, Bin Lin, Shi-jie Li, Min Wu, Qian Chen, Jian-hui Zhang, Qiong Cheng, Yi-wu Zhang, Fan Lin, Jie-wei Luo, Zheng Zheng, Yun-fei Li

    Published 2024-04-01
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  7. 7
    Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant

    Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant by Ruo-li Wang, Ruo-li Wang, Ruo-li Wang, Dan-dan Ruan, Ya-nan Hu, Yu-mian Gan, Xin-fu Lin, Xin-fu Lin, Zhu-ting Fang, Zhu-ting Fang, Li-sheng Liao, Li-sheng Liao, Fa-qiang Tang, Fa-qiang Tang, Wu-bing He, Wu-bing He, Wu-bing He, Jie-wei Luo, Jie-wei Luo

    Published 2022-05-01
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