Hasil Pencarian - Yu-Xing Liu

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  1. 1
    Case report: Whole-exome sequencing identifies a novel DES mutation (p. E434K) in a Chinese family with cardiomyopathy and sudden cardiac death

    Case report: Whole-exome sequencing identifies a novel DES mutation (p. E434K) in a Chinese family with cardiomyopathy and sudden cardiac death oleh Yu-Xing Liu, Yu-Xing Liu, Yu-Xing Liu, Rong Yu, Yue Sheng, Yue Sheng, Liang-Liang Fan, Liang-Liang Fan, Liang-Liang Fan, Yao Deng

    Diterbitkan 2022-10-01
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  2. 2
    Doubly bi-allelic variants of MTHFR and MTHFD1 in a Chinese patient with hyperhomocysteinemia and failure of folic acid therapy

    Doubly bi-allelic variants of MTHFR and MTHFD1 in a Chinese patient with hyperhomocysteinemia and failure of folic acid therapy oleh Yu-Xing Liu, Yu-Xing Liu, Man-Hua Ding, Yue Sheng, Meng-Fei Sun, Lv Liu, Yang Zhang

    Diterbitkan 2023-01-01
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  3. 3
    Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis

    Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis oleh Yu-Xing Liu, Yu-Xing Liu, Yu-Xing Liu, Yu-Xing Liu, Ai-Qian Zhang, Fang-Mei Luo, Fang-Mei Luo, Yue Sheng, Yue Sheng, Chen-Yu Wang, Chen-Yu Wang, Yi Dong, Yi Dong, Liangliang Fan, Liangliang Fan, Liangliang Fan, Liangliang Fan, Lv Liu

    Diterbitkan 2021-08-01
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  4. 4
    Case report: A novel WASHC5 variant altering mRNA splicing causes spastic paraplegia in a patient

    Case report: A novel WASHC5 variant altering mRNA splicing causes spastic paraplegia in a patient oleh Shan-Yu Gao, Shan-Yu Gao, Shan-Yu Gao, Yu-Xing Liu, Yu-Xing Liu, Yi Dong, Liang-Liang Fan, Qi Ding, Lv Liu

    Diterbitkan 2023-10-01
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  5. 5
    Novel heterozygous mutation of CACNA2D1 gene in a Chinese family with arrhythmia

    Novel heterozygous mutation of CACNA2D1 gene in a Chinese family with arrhythmia oleh Qian Wang, Yong Deng, Liang-Liang Fan, Yi Dong, Ai-Qian Zhang, Yu-Xing Liu

    Diterbitkan 2024-10-01
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  6. 6
    The first case report of CODAS syndrome in Chinese population caused by two LONP1 pathogenic mutations

    The first case report of CODAS syndrome in Chinese population caused by two LONP1 pathogenic mutations oleh Yi Tang, Yu-Xing Liu, Yue Sheng, Liang-Liang Fan, Ai-Qian Zhang, Zhao-Fen Zheng

    Diterbitkan 2023-01-01
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  7. 7
    Correction to: Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK‐IDH2 pathway

    Correction to: Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK‐IDH2 pathway oleh Hao Huang, Shuai Guo, Ya‐Qin Chen, Yu‐Xing Liu, Jie‐Yuan Jin, Yun Liang, Liang‐Liang Fan, Rong Xiang

    Diterbitkan 2024-02-01
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  8. 8
    Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK–IDH2 pathway

    Increased RTN3 phenocopies nonalcoholic fatty liver disease by inhibiting the AMPK–IDH2 pathway oleh Hao Huang, Shuai Guo, Ya‐Qin Chen, Yu‐Xing Liu, Jie‐Yuan Jin, Yun Liang, Liang‐Liang Fan, Rong Xiang

    Diterbitkan 2023-04-01
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  9. 9
    Case report: A novel mutation of RecQ-like helicase 5 in a Chinese family with early myocardial infarction, coronary artery disease, and stroke hemiplegia

    Case report: A novel mutation of RecQ-like helicase 5 in a Chinese family with early myocardial infarction, coronary artery disease, and stroke hemiplegia oleh Yi Tang, Qian Wang, Wei-Kai Zhang, Yu-Xing Liu, Zhao-Fen Zheng, Liang-Liang Fan, Lv Liu, Jin He

    Diterbitkan 2023-04-01
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  10. 10
    A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly

    A Novel Homozygous Variant of TMEM231 in a Case With Hypoplasia of the Cerebellar Vermis and Polydactyly oleh Tao Wang, Yu-Xing Liu, Fang-Mei Luo, Yi Dong, Ya-Li Li, Liang-Liang Fan, Liang-Liang Fan, Liang-Liang Fan

    Diterbitkan 2021-11-01
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  11. 11
    Single-cell transcriptomic profiling reveals decreased ER protein Reticulon3 drives the progression of renal fibrosis

    Single-cell transcriptomic profiling reveals decreased ER protein Reticulon3 drives the progression of renal fibrosis oleh Shuai Guo, Yi Dong, Ran Du, Yu-Xing Liu, Shu Liu, Qin Wang, Ji-Shi Liu, Hui Xu, Yu-Jie Jiang, Huang Hao, Liang-Liang Fan, Rong Xiang

    Diterbitkan 2024-06-01
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  12. 12
    Postoperative clinical outcomes of patients with thymic epithelial tumors after over-3-year follow-up at a single-center

    Postoperative clinical outcomes of patients with thymic epithelial tumors after over-3-year follow-up at a single-center oleh Peng Jiao, Wen-Xin Tian, Fan-Juan Wu, Yu-Xing Liu, Jiang-Yu Wu, Yao-Guang Sun, Han-Bo Yu, Chuan Huang, Qing-Jun Wu, Chao Ma, Dong-Hang Li, Hong-Feng Tong, Jun Li

    Diterbitkan 2023-02-01
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