Hasil Pencarian - Dan-dan Ruan

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  1. 1
    Analyzing three pedigrees in X-linked Alport syndrome with the presentation of nephrotic syndrome

    Analyzing three pedigrees in X-linked Alport syndrome with the presentation of nephrotic syndrome oleh Jian-Hui Zhang, Jian-Hui Zhang, Jie Liu, Jie Liu, Dan-Dan Ruan, Dan-Dan Ruan, Qian Chen, Qian Chen, Jie Yang, Jie Yang, Min Wu, Min Wu, Hong-Ping Yu, Hong-Ping Yu, Li-Sheng Liao, Li-Sheng Liao, Xiao-Ling Zheng, Xiao-Ling Zheng, Jie-Wei Luo, Li Zhang, Li Zhang

    Diterbitkan 2024-08-01
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  2. 2
    Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype

    Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype oleh Li-jun Xie, Dan-dan Ruan, Jian-hui Zhang, Yi Li, Li Chen, Mao-lin Yan, Ming-dian Yu, Jie-wei Luo, Hui-zhen Zhang

    Diterbitkan 2021-01-01
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  3. 3
    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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  4. 4
    Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A

    Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A oleh Yao-Bin Zhu, Jian-Hui Zhang, Yuan-Yuan Ji, Ya-Nan Hu, Han-Lu Wang, Dan-Dan Ruan, Xiao-Rong Meng, Xin-Fu Lin, Jie-Wei Luo, Wei Chen

    Diterbitkan 2022-01-01
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  5. 5
    A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification

    A novel splicing mutation DNAH5 c.13,338 + 5G > C is involved in the pathogenesis of primary ciliary dyskinesia in a family with primary familial brain calcification oleh Xiu-juan Yao, Qian Chen, Hong-ping Yu, Dan-dan Ruan, Shi-jie Li, Min Wu, Li-sheng Liao, Xin-fu Lin, Zhu-ting Fang, Jie-wei Luo, Bao-song Xie

    Diterbitkan 2024-07-01
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  6. 6
    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 oleh 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

    Diterbitkan 2022-06-01
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  7. 7
    A Primary Extraskeletal Osteosarcoma of the Spleen: Rare Case Report

    A Primary Extraskeletal Osteosarcoma of the Spleen: Rare Case Report oleh 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

    Diterbitkan 2022-05-01
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  8. 8
    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 oleh 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

    Diterbitkan 2023-10-01
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  9. 9
    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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  10. 10
    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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  11. 11
    Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation

    Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation oleh 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

    Diterbitkan 2024-09-01
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  12. 12
    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 oleh 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

    Diterbitkan 2024-04-01
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  13. 13
    Rare Cases of Bronchial Aneurysm and Comparison of Interventional Embolization in the Treatment of True Bronchial Aneurysm and Pseudobronchial Aneurysm

    Rare Cases of Bronchial Aneurysm and Comparison of Interventional Embolization in the Treatment of True Bronchial Aneurysm and Pseudobronchial Aneurysm oleh Jia-Li Lin, Yuan-Yuan Ji, Ming-Zhe Zhang, Yi Tang, Yi Tang, Ruo-Li Wang, Dan-Dan Ruan, Yan-Feng Zhou, Yan-Feng Zhou, Shao-Jie Wu, Shao-Jie Wu, Sen-Lin Cai, Sen-Lin Cai, Jian-Hui Zhang, Xiao-Rong Meng, Jie-Wei Luo, Zhu-Ting Fang, Zhu-Ting Fang

    Diterbitkan 2022-03-01
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  14. 14
    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 oleh 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

    Diterbitkan 2022-05-01
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  15. 15
    In vitro study of ATP1A3 p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism

    In vitro study of ATP1A3 p.Ala275Pro mutant causing alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism oleh Dan-dan Ruan, Jing Zou, Li-sheng Liao, Li-sheng Liao, Ming-dong Ji, Ruo-li Wang, Ruo-li Wang, Jian-hui Zhang, Li Zhang, Li Zhang, Mei-zhu Gao, Mei-zhu Gao, Qian Chen, Hong-ping Yu, Wen Wei, Yun-fei Li, Yun-fei Li, Hong Li, Fan Lin, Fan Lin, Jie-wei Luo, Xin-fu Lin, Xin-fu Lin

    Diterbitkan 2024-07-01
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