Hasil Pencarian - Yuanlin Zhou

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  1. 1
    Case Report: Charcot-marie-tooth disease caused by a de novo MORC2 gene mutation - novel insights into pathogenicity and treatment

    Case Report: Charcot-marie-tooth disease caused by a de novo MORC2 gene mutation - novel insights into pathogenicity and treatment oleh Feng Zhu, Chengcheng Gao, Xiangxiang Zhu, Huihua Jiang, Mingchun Huang, Yuanlin Zhou

    Diterbitkan 2024-10-01
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  2. 2
    Synthesis and Preparation of (Acrylic Copolymer) Ternary System Peelable Sealing Decontamination Material

    Synthesis and Preparation of (Acrylic Copolymer) Ternary System Peelable Sealing Decontamination Material oleh Zhiyu He, Yintao Li, Zhiqiang Xiao, Huan Jiang, Yuanlin Zhou, Deli Luo

    Diterbitkan 2020-07-01
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  3. 3
    An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway

    An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway oleh Yuanlin Zhou, Na Ouyang, Lingjuan Liu, Jie Tian, Xupei Huang, Tiewei Lu

    Diterbitkan 2019-03-01
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  4. 4
    The expression of RBPJ and its potential role in rheumatoid arthritis

    The expression of RBPJ and its potential role in rheumatoid arthritis oleh Shuaishuai Chen, Weibo Zhao, Juping Du, Suyun Chen, Jun Li, Bo Shen, Yuanlin Zhou, Shiyong Chen

    Diterbitkan 2024-09-01
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  5. 5
    Ataxia with oculomotor apraxia type 2 caused by a novel homozygous mutation in SETX gene, and literature review

    Ataxia with oculomotor apraxia type 2 caused by a novel homozygous mutation in SETX gene, and literature review oleh Shuaishuai Chen, Juping Du, Huihua Jiang, Weibo Zhao, Na Wang, Anna Ying, Jun Li, Shiyong Chen, Bo Shen, Yuanlin Zhou

    Diterbitkan 2022-11-01
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  6. 6
    The FGG c.952G>A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral infarction: a case report

    The FGG c.952G>A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral infarction: a case report oleh Anna Ying, Yuanlin Zhou, Chunyue Wang, Tao Wang, Xuan Zhang, Shanshan Wang, Shaofa Ke, Yuyan Bao, Yang Liu, Yang Liu, Feng Wang

    Diterbitkan 2024-01-01
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  7. 7
    A de novo Mutation in the MTUS1 Gene Decreases the Risk of Non-compaction of Ventricular Myocardium via the Rac1/Cdc42 Pathway

    A de novo Mutation in the MTUS1 Gene Decreases the Risk of Non-compaction of Ventricular Myocardium via the Rac1/Cdc42 Pathway oleh Xuehan Bai, Xuehan Bai, Yuanlin Zhou, Na Ouyang, Na Ouyang, Lingjuan Liu, Lingjuan Liu, Xupei Huang, Jie Tian, Jie Tian, Tiewei Lv, Tiewei Lv

    Diterbitkan 2019-07-01
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