Search Results - "Yexing, Xian"

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  1. 1

    Oxidative stress and inflammatory markers in ovarian follicular fluid of women with diminished ovarian reserve during in vitro fertilization by Huang, Yan, Cheng, Yi, Zhang, Min, Xia, Yan, Chen, Xiaoyan, Xian, Yexing, Lin, Dewei, Xie, Suyan, Guo, Xinyu

    Published in Journal of ovarian research (23-10-2023)
    “…Background Follicular microenvironment has been proposed as an important factor for oocyte grown and maturation. We sought to evaluate the oxidative stress and…”
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    Journal Article
  2. 2

    The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice by Xian, Yexing, Xie, Yingjun, Song, Bing, Ou, Zhanhui, Ouyang, Shuming, Xie, Yuhuan, Yang, Yi, Xiong, Zeyu, Li, Haoxian, Sun, Xiaofang

    Published in Stem cell research & therapy (16-07-2020)
    “…Background β-Thalassaemia is a clinically common cause of hereditary haemolytic anaemia stemming from mutations in important functional regions of the β-globin…”
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    Journal Article
  3. 3

    Autophagy Promoted the Degradation of Mutant ATXN3 in Neurally Differentiated Spinocerebellar Ataxia-3 Human Induced Pluripotent Stem Cells by OuYang, Shuming, Sun, Xiaofang, Fan, Di, Song, Bing, He, Wenyin, Xie, Yingjun, Chen, Yuchang, Niu, Xiaohua, Luo, Min, Ou, Zhanhui, Xian, Yexing

    Published in BioMed research international (01-01-2016)
    “…Spinocerebellar ataxia-3 (SCA3) is the most common dominant inherited ataxia worldwide and is caused by an unstable CAG trinucleotide expansion mutation within…”
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    Journal Article
  4. 4

    Noninvasive prenatal diagnosis of β‐thalassemia by relative haplotype dosage without analyzing proband by Li, Haoxian, Du, Bole, Jiang, Fuman, Guo, Yulai, Wang, Yang, Zhang, Chunsheng, Zeng, Xiaojing, Xie, Yuhuan, Ouyang, Shuming, Xian, Yexing, Chen, Min, Liu, Weiqiang, Sun, Xiaofang

    Published in Molecular genetics & genomic medicine (01-11-2019)
    “…Background β‐thalassemia is one of the most common monogenic diseases in the world. Southeast China is a highly infected area affected by four β‐thalassemia…”
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    Journal Article
  5. 5

    Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient by Chen, Yuchang, Ou, Zhanhui, Song, Bing, Xian, Yexing, Ouyang, Shuming, Xie, Yuhuan, Xue, Yanting, Sun, Xiaofang

    Published in Stem cell research (01-08-2017)
    “…47, XXX syndrome is one of several sex-chromosomal aneuploidies, and it has an incidence of approximately 1/1000 in newborn females. Because of heterogeneity…”
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  6. 6

    Generation of GZKHQi001-A and GZWWTi001-A, two induced pluripotent stem cell lines derived from peripheral blood mononuclear cells of Duchenne muscular dystrophy patients by Yuhuan, Xie, Yingjun, Xie, Yanting, Xue, Yuchang, Chen, Bing, Song, Shaoying, Li, Haoxian, Li, Yexing, Xian, Shuming, Ouyang, Zeyu, Xiong, Xiaofang, Sun

    Published in Stem cell research (01-04-2018)
    “…Duchenne muscular dystrophy (DMD) is an X-linked disease caused by mutations in the DMD gene, which spans ~2.4Mb of genomic sequence at locus Xp21. This…”
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    Journal Article
  7. 7

    The Combination of CRISPR/Cas9 and iPSC Technologies in the Gene Therapy of Human β-thalassemia in Mice by Ou, Zhanhui, Niu, Xiaohua, He, Wenyin, Chen, Yuchang, Song, Bing, Xian, Yexing, Fan, Di, Tang, Daolin, Sun, Xiaofang

    Published in Scientific reports (01-09-2016)
    “…β-thalassemia results from point mutations or small deletions in the β-globin ( HBB ) gene that ultimately cause anemia. The generation of induced pluripotent…”
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    Journal Article
  8. 8

    CRISPR/Cas9-mediated β-globin gene knockout in rabbits recapitulates human β-thalassemia by Yang, Yi, Kang, Xiangjin, Hu, Shiqi, Chen, Bangzhu, Xie, Yingjun, Song, Bing, Zhang, Quanjun, Wu, Han, Ou, Zhanhui, Xian, Yexing, Fan, Yong, Li, Xiaoping, Lai, Liangxue, Sun, Xiaofang

    Published in The Journal of biological chemistry (01-01-2021)
    “…β-thalassemia, an autosomal recessive blood disorder that reduces the production of hemoglobin, is majorly caused by the point mutation of the HBB gene…”
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  9. 9

    The safety and effectiveness of genetically corrected iPSCs derived from [beta]-thalassaemia patients in nonmyeloablative [beta]-thalassaemic mice by Xian, Yexing, Xie, Yingjun, Song, Bing, Ou, Zhanhui, Ouyang, Shuming, Xie, Yuhuan, Yang, Yi, Xiong, Zeyu, Li, Haoxian, Sun, Xiaofang

    Published in Stem cell research & therapy (16-07-2020)
    “…Background [beta]-Thalassaemia is a clinically common cause of hereditary haemolytic anaemia stemming from mutations in important functional regions of the…”
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    Journal Article
  10. 10

    Antioxidants retard the ageing of mouse oocytes by Xian, Yexing, Liang, Lifeng, Qi, Shutao, Xie, Yingjun, Song, Bing, Ouyang, Shuming, Xie, Yuhuan, Sun, Xiaofang, Wang, Weihua

    Published in Molecular medicine reports (01-08-2018)
    “…The aim of the present study was to verify the effects of heavy metal coupling agents (sodium citrate and EDTA) and antioxidants (acetyl carnitine and lipoic…”
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    Journal Article
  11. 11

    The Combination of CRISPR/Cas9 and iPSC Technologies in the Gene Therapy of Human [beta]-thalassemia in Mice by Ou, Zhanhui, Niu, Xiaohua, He, Wenyin, Chen, Yuchang, Song, Bing, Xian, Yexing, Fan, Di, Tang, Daolin, Sun, Xiaofang

    Published in Scientific reports (01-09-2016)
    “…β-thalassemia results from point mutations or small deletions in the β-globin (HBB) gene that ultimately cause anemia. The generation of induced pluripotent…”
    Get full text
    Journal Article