Rezultati - Huizhi Zhao

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  1. 1
    Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B

    Lysosomal accumulation of SCMAS (subunit c of mitochondrial ATP synthase) in neurons of the mouse model of mucopolysaccharidosis III B od Sergey Ryazantsev, Wei-Hong Yu, Huizhi Zhao, Elizabeth F. Neufeld, Kazuhiro Ohmi

    Izdano 2006
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  2. 2
    Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy

    Sanfilippo syndrome type B, a lysosomal storage disease, is also a tauopathy od Kazuhiro Ohmi, Lili C. Kudo, Sergey Ryazantsev, Huizhi Zhao, Stanislav L. Karsten, Elizabeth F. Neufeld

    Izdano 2009
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  3. 3
    Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects

    Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects od Li Wang, Fang Wang, Jing Guan, Jing Le, Lihua Wu, Jizhen Zou, Huizhi Zhao, Lijun Pei, Xiaoying Zheng, Ting Zhang

    Izdano 2010
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  4. 4
    DNMT1 regulates human erythropoiesis by modulating cell cycle and endoplasmic reticulum stress in a stage-specific manner

    DNMT1 regulates human erythropoiesis by modulating cell cycle and endoplasmic reticulum stress in a stage-specific manner od Qianqian Yang, Lixiang Chen, Hengchao Zhang, Mengjia Li, Lei Sun, Xiuyun Wu, Huizhi Zhao, Xiaoli Qu, Xiuli An, Ting Ting Wang

    Izdano 2024
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  5. 5
    Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding α- <i>N</i> -acetylglucosaminidase

    Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding α- <i>N</i> -acetylglucosaminidase od Hong Hua Li, Wei-Hong Yu, Nora Rozengurt, Huizhi Zhao, Karen M. Lyons, Stephan Anagnostaras, Michael S. Fanselow, Kunihiko Suzuki, Marie T. Vanier, Elizabeth F. Neufeld

    Izdano 1999
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  6. 6
    Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency

    Impairment of human terminal erythroid differentiation by histone deacetylase 5 deficiency od Yaomei Wang, Wei Li, Vincent Schulz, Huizhi Zhao, Xiaoli Qu, Qi Qian, Yong Cheng, Xinhua Guo, Shijie Zhang, Xin Wei, Donghao Liu, Karina Yazdanbakhsh, Christopher D. Hillyer, Narla Mohandas, Lixiang Chen, Patrick G. Gallagher, Xiuli An

    Izdano 2021
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  7. 7
    TET2 deficiency leads to stem cell factor–dependent clonal expansion of dysfunctional erythroid progenitors

    TET2 deficiency leads to stem cell factor–dependent clonal expansion of dysfunctional erythroid progenitors od Xiaoli Qu, Shijie Zhang, Shihui Wang, Yaomei Wang, Wei Li, Yu-Min Huang, Huizhi Zhao, Xiuyun Wu, Chao An, Xinhua Guo, John Hale, Jie Li, Christopher D. Hillyer, Narla Mohandas, Jing Liu, Karina Yazdanbakhsh, Francesca Vinchi, Lixiang Chen, Qiaozhen Kang, Xiuli An

    Izdano 2018
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  8. 8
    Identification and transcriptome analysis of erythroblastic island macrophages

    Identification and transcriptome analysis of erythroblastic island macrophages od Wei Li, Yaomei Wang, Huizhi Zhao, Huan Zhang, Yuanlin Xu, Shihui Wang, Xinhua Guo, Yu-Min Huang, Shijie Zhang, Yongshuai Han, Xianfang Wu, Charles M. Rice, Gang Huang, Patrick G. Gallagher, Avital Mendelson, Karina Yazdanbakhsh, Jing Liu, Lixiang Chen, Xiuli An

    Izdano 2019
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