Hasil Pencarian - Limeng Dai

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  1. 1
    Monocarboxylate Transporter 1 May Benefit Cerebral Ischemia via Facilitating Lactate Transport From Glial Cells to Neurons

    Monocarboxylate Transporter 1 May Benefit Cerebral Ischemia via Facilitating Lactate Transport From Glial Cells to Neurons oleh Mao Zhang, Yanyan Wang, Yun Bai, Limeng Dai, Hong Guo

    Diterbitkan 2022-04-01
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  2. 2
    A large novel deletion downstream of PAX6 gene in a Chinese family with ocular coloboma.

    A large novel deletion downstream of PAX6 gene in a Chinese family with ocular coloboma. oleh Hong Guo, Limeng Dai, Yanming Huang, Qiong Liao, Yun Bai

    Diterbitkan 2013-01-01
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  3. 3
    A case report of NPHP1 deletion in Chinese twins with nephronophthisis

    A case report of NPHP1 deletion in Chinese twins with nephronophthisis oleh Feng Chen, Limeng Dai, Jun Zhang, Furong Li, Jinbo Cheng, Jinghong Zhao, Bo Zhang

    Diterbitkan 2020-04-01
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  4. 4
    Deubiquitinating enzyme USP30 negatively regulates mitophagy and accelerates myocardial cell senescence through antagonism of Parkin

    Deubiquitinating enzyme USP30 negatively regulates mitophagy and accelerates myocardial cell senescence through antagonism of Parkin oleh Wei Pan, Yaowen Wang, Xinyu Bai, Yuehui Yin, Limeng Dai, Hong Zhou, Qin Wu, Yan Wang

    Diterbitkan 2021-07-01
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  5. 5
    X Chromosome Inactivation Pattern and Pregnancy Outcome of Female Carriers of Pathogenic Heterozygous X-Linked Deletions

    X Chromosome Inactivation Pattern and Pregnancy Outcome of Female Carriers of Pathogenic Heterozygous X-Linked Deletions oleh Yuanyin Zhao, Yuanyin Zhao, Jia Li, Limeng Dai, Yongyi Ma, Yun Bai, Hong Guo, Hong Guo

    Diterbitkan 2021-12-01
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  6. 6
    Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth

    Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth oleh Yuanyuan Wu, Xuedan Chen, Yan Liang, Juan Li, Kun Zhang, Limeng Dai, Xingying Guan, Kai Wang, Yun Bai

    Diterbitkan 2018-05-01
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  7. 7
    A Tiered Genetic Screening Strategy for the Molecular Diagnosis of Intellectual Disability in Chinese Patients

    A Tiered Genetic Screening Strategy for the Molecular Diagnosis of Intellectual Disability in Chinese Patients oleh Limeng Dai, Danyan Zhang, Danyan Zhang, Zhifeng Wu, Xingying Guan, Mingfu Ma, Lianbing Li, Yuping Zhang, Yun Bai, Hong Guo

    Diterbitkan 2021-09-01
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  8. 8
    Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.

    Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families. oleh Limeng Dai, Dan Liu, Min Song, Xueqing Xu, Gang Xiong, Kang Yang, Kun Zhang, Hui Meng, Hong Guo, Yun Bai

    Diterbitkan 2014-01-01
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  9. 9
    <i>Supt16</i> Haploinsufficiency Impairs PI3K/AKT/mTOR/Autophagy Pathway in Human Pluripotent Stem Cells Derived Neural Stem Cells

    <i>Supt16</i> Haploinsufficiency Impairs PI3K/AKT/mTOR/Autophagy Pathway in Human Pluripotent Stem Cells Derived Neural Stem Cells oleh Junwen Wang, Ziyi Wang, Limeng Dai, Xintong Zhu, Xingying Guan, Junyi Wang, Jia Li, Mao Zhang, Yun Bai, Hong Guo

    Diterbitkan 2023-02-01
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  10. 10
    PPARA genetic variants increase the risk for cardiac pumping function reductions following acute high‐altitude exposure: A self‐controlled study

    PPARA genetic variants increase the risk for cardiac pumping function reductions following acute high‐altitude exposure: A self‐controlled study oleh Jie Yang, Chuan Liu, Zhang Jihang, Jie Yu, Limeng Dai, Xiaohan Ding, Youzhu Qiu, Sanjiu Yu, Yuanqi Yang, Yuzhang Wu, Lan Huang

    Diterbitkan 2019-10-01
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  11. 11
    Network Reconfiguration Among Cerebellar Visual, and Motor Regions Affects Movement Function in Spinocerebellar Ataxia Type 3

    Network Reconfiguration Among Cerebellar Visual, and Motor Regions Affects Movement Function in Spinocerebellar Ataxia Type 3 oleh Hui Chen, Limeng Dai, Yuhan Zhang, Liu Feng, Zhenzhen Jiang, Xingang Wang, Dongjing Xie, Jing Guo, Huafu Chen, Jian Wang, Chen Liu

    Diterbitkan 2022-04-01
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  12. 12
    A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review

    A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review oleh Chengning Tan, Limeng Dai, Zhengqiong Chen, Wuchen Yang, Yali Wang, Cheng Zeng, Zheng Xiang, Xiaojie Wang, Xiaomei Zhang, Qian Ran, Hong Guo, Zhongjun Li, Li Chen

    Diterbitkan 2020-04-01
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  13. 13
    Potential biomarkers for inherited thrombocytopenia 2 identified by plasma proteomics

    Potential biomarkers for inherited thrombocytopenia 2 identified by plasma proteomics oleh Xiaojie Wang, Maoshan Chen, Limeng Dai, Chengning Tan, Lanyue Hu, Yichi Zhang, Yanni Xiao, Fengjie Li, Cheng Zeng, Zheng Xiang, Yali Wang, Weiwei Zhang, Xiaomei Zhang, Qian Ran, Zhongjun Li, Li Chen

    Diterbitkan 2022-04-01
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  14. 14
    Generation of the human induced pluripotent stem cell line (SHAMUi001-A) carrying the heterozygous c.-128G>T mutation in the 5′-UTR of the ANKRD26 gene

    Generation of the human induced pluripotent stem cell line (SHAMUi001-A) carrying the heterozygous c.-128G>T mutation in the 5′-UTR of the ANKRD26 gene oleh Chengning Tan, Limeng Dai, Wuchen Yang, Fengjie Li, Li Wang, Yanni Xiao, Xiaojie Wang, Yichi Zhang, Yali Wang, Cheng Zeng, Zheng Xiang, Xiaomei Zhang, Weiwei Zhang, Qian Ran, Maoshan Chen, Zhongjun Li, Li Chen

    Diterbitkan 2020-10-01
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