Hasil Pencarian - Lu-Si Zhang

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  1. 1
    Knobloch syndrome caused by homozygous frameshift mutation of the COL18A1 gene in a Chinese pedigree

    Knobloch syndrome caused by homozygous frameshift mutation of the COL18A1 gene in a Chinese pedigree oleh Lu-Si Zhang, Hai-Bo Li, Jun Zeng, Yan Yang, Chun Ding

    Diterbitkan 2018-06-01
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  2. 2
    A novel mutation in FBN1 gene in autosomal dominant Marfan syndrome and macular degeneration in a Chinese consanguineous family

    A novel mutation in FBN1 gene in autosomal dominant Marfan syndrome and macular degeneration in a Chinese consanguineous family oleh Ping-Bo Ouyang, Yuan Zhao, Ying-Qian Peng, Lu-Si Zhang, Jian Cao, Yun Li

    Diterbitkan 2019-05-01
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  3. 3
    Diverse roles of macrophages in intraocular neovascular diseases: a review

    Diverse roles of macrophages in intraocular neovascular diseases: a review oleh Ye-Di Zhou, Shigeo Yoshida, Ying-Qian Peng, Yoshiyuki Kobayashi, Lu-Si Zhang, Luo-Sheng Tang

    Diterbitkan 2017-12-01
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  4. 4
    Identification of altered microRNAs in retinas of mice with oxygen-induced retinopathy

    Identification of altered microRNAs in retinas of mice with oxygen-induced retinopathy oleh Lu-Si Zhang, Ye-Di Zhou, Ying-Qian Peng, Hui-Lan Zeng, Shigeo Yoshida, Tan-Tai Zhao

    Diterbitkan 2019-05-01
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  5. 5
    Attenuation of periostin in retinal Müller glia by TNF-α and IFN-γ

    Attenuation of periostin in retinal Müller glia by TNF-α and IFN-γ oleh Ying-Qian Peng, Man-Jing Cao, Shigeo Yoshida, Lu-Si Zhang, Hui-Lan Zeng, Jing-Ling Zou, Yoshiyuki Kobayashi, Takahito Nakama, Jing-Ming Shi, Song-Bai Jia, Ye-Di Zhou

    Diterbitkan 2019-02-01
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