Search Results - "Tu, Zhuchi"

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    Functional disruption of the dystrophin gene in rhesus monkey using CRISPR/Cas9 by Chen, Yongchang, Zheng, Yinghui, Kang, Yu, Yang, Weili, Niu, Yuyu, Guo, Xiangyu, Tu, Zhuchi, Si, Chenyang, Wang, Hong, Xing, Ruxiao, Pu, Xiuqiong, Yang, Shang-Hsun, Li, Shihua, Ji, Weizhi, Li, Xiao-Jiang

    Published in Human molecular genetics (01-07-2015)
    “…CRISPR/Cas9 has been used to genetically modify genomes in a variety of species, including non-human primates. Unfortunately, this new technology does cause…”
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    Promoting Cas9 degradation reduces mosaic mutations in non-human primate embryos by Tu, Zhuchi, Yang, Weili, Yan, Sen, Yin, An, Gao, Jinquan, Liu, Xudong, Zheng, Yinghui, Zheng, Jiezhao, Li, Zhujun, Yang, Su, Li, Shihua, Guo, Xiangyu, Li, Xiao-Jiang

    Published in Scientific reports (03-02-2017)
    “…CRISPR-Cas9 is a powerful new tool for genome editing, but this technique creates mosaic mutations that affect the efficiency and precision of its ability to…”
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    CRISPR/Cas9-mediated disruption of SHANK3 in monkey leads to drug-treatable autism-like symptoms by Tu, Zhuchi, Zhao, Hui, Li, Bang, Yan, Sen, Wang, Lu, Tang, Yongjin, Li, Zhujun, Bai, Dazhang, Li, Caijuan, Lin, Yingqi, Li, Yuefeng, Liu, Jianrong, Xu, Hao, Guo, Xiangyu, Jiang, Yong-hui, Zhang, Yong Q, Li, Xiao-Jiang

    Published in Human molecular genetics (15-02-2019)
    “…Abstract Monogenic mutations in the SHANK3 gene, which encodes a postsynaptic scaffold protein, play a causative role in autism spectrum disorder (ASD)…”
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    CRISPR/Cas9: a powerful genetic engineering tool for establishing large animal models of neurodegenerative diseases by Tu, Zhuchi, Yang, Weili, Yan, Sen, Guo, Xiangyu, Li, Xiao-Jiang

    Published in Molecular neurodegeneration (04-08-2015)
    “…Animal models are extremely valuable to help us understand the pathogenesis of neurodegenerative disorders and to find treatments for them. Since large animals…”
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    Maternal valproic acid exposure leads to neurogenesis defects and autism-like behaviors in non-human primates by Zhao, Hui, Wang, Qiqi, Yan, Ting, Zhang, Yu, Xu, Hui-juan, Yu, Hao-peng, Tu, Zhuchi, Guo, Xiangyu, Jiang, Yong-hui, Li, Xiao-jiang, Zhou, Huihui, Zhang, Yong Q.

    Published in Translational psychiatry (21-10-2019)
    “…Despite the substantial progress made in identifying genetic defects in autism spectrum disorder (ASD), the etiology for majority of ASD individuals remains…”
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    Application of CRISPR/Cas9 System in Establishing Large Animal Models by Lin, Yingqi, Li, Jun, Li, Caijuan, Tu, Zhuchi, Li, Shihua, Li, Xiao-Jiang, Yan, Sen

    “…The foundation for investigating the mechanisms of human diseases is the establishment of animal models, which are also widely used in agricultural industry,…”
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    A Specific Mini‐Intrabody Mediates Lysosome Degradation of Mutant Huntingtin by Li, Caijuan, Lin, Yingqi, Chen, Yizhi, Song, Xichen, Zheng, Xiao, Li, Jiawei, He, Jun, Chen, Xiusheng, Huang, Chunhui, Wang, Wei, Wu, Jianhao, Wu, Jiaxi, Gao, Jiale, Tu, Zhuchi, Li, Xiao‐Jiang, Yan, Sen, Li, Shihua

    Published in Advanced science (01-11-2023)
    “…Abstract Accumulation of misfolded proteins leads to many neurodegenerative diseases that can be treated by lowering or removing mutant proteins. Huntington's…”
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    Tauopathy promotes spinal cord-dependent production of toxic amyloid-beta in transgenic monkeys by Tu, Zhuchi, Yan, Sen, Han, Bofeng, Li, Caijuan, Liang, Weien, Lin, Yingqi, Ding, Yongyan, Wei, Huiyi, Wang, Lu, Xu, Hao, Ye, Jianmeng, Li, Bang, Li, Shihua, Li, Xiao-Jiang

    Published in Signal transduction and targeted therapy (22-09-2023)
    “…Tauopathy, characterized by the hyperphosphorylation and accumulation of the microtubule-associated protein tau, and the accumulation of Aβ oligomers,…”
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    Generation of inactivated IL2RG and RAG1 monkeys with severe combined immunodeficiency using base editing by Zheng, Xiao, Huang, Chunhui, Lin, Yingqi, Han, Bofeng, Chen, Yizhi, Li, Caijuan, Li, Jiawei, Ding, Yongyan, Song, Xichen, Wang, Wei, Liang, Weien, Wu, Jianhao, Wu, Jiaxi, Gao, Jiale, Wei, Chengxi, Zhang, Xudong, Tu, Zhuchi, Yan, Sen

    Published in Signal transduction and targeted therapy (04-09-2023)
    “…Severe combined immunodeficiency (SCID) encompasses a range of inherited disorders that lead to a profound deterioration of the immune system. Among the…”
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    Intravenous AAV9 administration results in safe and widespread distribution of transgene in the brain of mini-pig by Lin, Yingqi, Li, Caijuan, Wang, Wei, Li, Jiawei, Huang, Chunhui, Zheng, Xiao, Liu, Zhaoming, Song, Xichen, Chen, Yizhi, Gao, Jiale, Wu, Jianhao, Wu, Jiaxi, Tu, Zhuchi, Lai, Liangxue, Li, Xiao-Jiang, Li, Shihua, Yan, Sen

    “…Animal models are important for understanding the pathogenesis of human diseases and for developing and testing new drugs. Pigs have been widely used in the…”
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    A Huntingtin Knockin Pig Model Recapitulates Features of Selective Neurodegeneration in Huntington’s Disease by Yan, Sen, Tu, Zhuchi, Liu, Zhaoming, Fan, Nana, Yang, Huiming, Yang, Su, Yang, Weili, Zhao, Yu, Ouyang, Zhen, Lai, Chengdan, Yang, Huaqiang, Li, Li, Liu, Qishuai, Shi, Hui, Xu, Guangqing, Zhao, Heng, Wei, Hongjiang, Pei, Zhong, Li, Shihua, Lai, Liangxue, Li, Xiao-Jiang

    Published in Cell (03-05-2018)
    “…Huntington’s disease (HD) is characterized by preferential loss of the medium spiny neurons in the striatum. Using CRISPR/Cas9 and somatic nuclear transfer…”
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    Use of CRISPR/Cas9 to model brain diseases by Yan, Sen, Tu, Zhuchi, Li, Shihua, Li, Xiao-Jiang

    “…•Genomic editing has been used to generate animal models of human diseases to mimic neurological symptoms and to study disease pathogenesis and treatments.•Of…”
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    Altered neurogenesis and disrupted expression of synaptic proteins in prefrontal cortex of SHANK3-deficient non-human primate by Zhao, Hui, Tu, Zhuchi, Xu, Huijuan, Yan, Sen, Yan, Huanhuan, Zheng, Yinghui, Yang, Weili, Zheng, Jiezhao, Li, Zhujun, Tian, Rui, Lu, Youming, Guo, Xiangyu, Jiang, Yong-hui, Li, Xiao-Jiang, Zhang, Yong Q

    Published in Cell research (01-10-2017)
    “…Dear Editor, Despite substantial progress made toward under- standing the molecular changes contributing to autism spectrum disorders (ASD), the…”
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    TBN improves motor function and prolongs survival in a TDP-43M337V mouse model of ALS by Huang, Chunhui, Li, Jun, Zhang, Guiliang, Lin, Yingqi, Li, Caijuan, Zheng, Xiao, Song, Xichen, Han, Bofeng, Guo, Baojian, Tu, Zhuchi, Zhang, Jun, Sun, Yewei, Wang, Yuqiang, Zhang, Zaijun, Yan, Sen

    Published in Human molecular genetics (28-07-2021)
    “…Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are serious neurodegenerative diseases. Although their pathogenesis is…”
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    Large animal models for Huntington's disease research by Han, Bofeng, Liang, Weien, Li, Xiao-Jiang, Li, Shihua, Yan, Sen, Tu, Zhuchi

    Published in Dōngwùxué yánjiū (18-03-2024)
    “…Huntington's disease (HD) is a hereditary neurodegenerative disorder for which there is currently no effective treatment available. Consequently, the…”
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