Showing 1 - 2 results of 2 for search 'Caixia Xian', query time: 0.02s Refine Results
  1. 1
    Novel de novo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation

    Novel de novo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation by Ping Wei, Weizhe Shi, Tianying Nong, Caixia Xian, Xia Li, Zhaohui Li, Xin Li, Jianping Wu, Liyuan Shang, Fulong Xu, Yibo Xu, Hongwen Xu, Mingwei Zhu

    Published 2024-05-01
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    Article
  2. 2
    A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate

    A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate by Caixia Xian, Mingwei Zhu, Tianying Nong, Yiqiang Li, Xingmei Xie, Xia Li, Jiangui Li, Jingchun Li, Jianping Wu, Weizhe Shi, Ping Wei, Hongwen Xu, Ya-ping Tang

    Published 2021-05-01
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    Article

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