Hasil Pencarian - Qiu-yan Wu

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  1. 1
    Selenomethionine Ameliorates Neuropathology in the Olfactory Bulb of a Triple Transgenic Mouse Model of Alzheimer’s Disease

    Selenomethionine Ameliorates Neuropathology in the Olfactory Bulb of a Triple Transgenic Mouse Model of Alzheimer’s Disease oleh Zhong-Hao Zhang, Chen Chen, Qiu-Yan Wu, Rui Zheng, Yao Chen, Qiong Liu, Jia-Zuan Ni, Guo-Li Song

    Diterbitkan 2016-09-01
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  2. 2
    A rare concurrence of acute tubular necrosis and chronic glomerular sclerosis in a patient with wasp stings

    A rare concurrence of acute tubular necrosis and chronic glomerular sclerosis in a patient with wasp stings oleh Jian-hui Zhang, Jing Zou, Dan-dan Ruan, Qian Chen, Min Wu, Hong-ping Yu, Qiu-yan Wu, Fan Lin, Jie-wei Luo, Li Zhang

    Diterbitkan 2024-07-01
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  3. 3
    The value of computed tomography angiography for evaluation of left atrial enlargement in patients with persistent atrial fibrillation

    The value of computed tomography angiography for evaluation of left atrial enlargement in patients with persistent atrial fibrillation oleh Fang-fang Lin, Qian Chen, Qiu-yan Wu, Shi-jie Li, Yao-bin Zhu, Yi Tang, Yun-jing Xue, Jie-wei Luo, Zuo-an Li, Hong-yi Chen

    Diterbitkan 2024-09-01
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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 oleh 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

    Diterbitkan 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 oleh 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

    Diterbitkan 2023-01-01
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  6. 6
    Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation

    Clinical and Genetic Analysis of a Family With Sitosterolemia Caused by a Novel ATP-Binding Cassette Subfamily G Member 5 Compound Heterozygous Mutation oleh Ming-fang Shen, Ming-fang Shen, Ya-nan Hu, Wei-xiang Chen, Wei-xiang Chen, Li-sheng Liao, Li-sheng Liao, Min Wu, Qiu-yan Wu, Jian-hui Zhang, Yan-ping Zhang, Jie-wei Luo, Jie-wei Luo, Xin-fu Lin, Xin-fu Lin

    Diterbitkan 2022-04-01
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