Search Results - "Yingjun, Xie"

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  1. 1

    Circulating MicroRNAs in Cancer: Potential and Challenge by Cui, Mengying, Wang, Hongdan, Yao, Xiaoxiao, Zhang, Dan, Xie, Yingjun, Cui, Ranji, Zhang, Xuewen

    Published in Frontiers in genetics (18-07-2019)
    “…MicroRNAs (miRNAs) are endogenous non-coding small RNA molecules that can be secreted into the circulation and exist in remarkably stable forms. Like…”
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  2. 2

    Multi-omics study unravels gut microbiota and metabolites alteration in patients with Wilson's disease by Cai, Xiangsheng, Dai, Jincheng, Xie, Yingjun, Xu, Shu, Liu, Minqi

    Published in Scientific reports (09-09-2024)
    “…Hepatolenticular degeneration (HLD), also known as Wilson's disease (WD), is a rare autosomal recessive disorder regarding copper metabolism. Whether gut…”
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  3. 3

    Saracatinib prompts hemin-induced K562 erythroid differentiation but suppresses erythropoiesis of hematopoietic stem cells by Ding, Lina, Chen, Diyu, Li, Yuanshuai, Xie, Yingjun, Sun, Xiaofang, Wang, Ding

    “…Human myeloid leukemia cells (such as K562) could be used for the study of erythropoiesis, and mature erythroid markers and globins could be induced during…”
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  4. 4

    MiR-6875-3p promotes the proliferation, invasion and metastasis of hepatocellular carcinoma via BTG2/FAK/Akt pathway by Xie, Yingjun, Du, Jian, Liu, Zefeng, Zhang, Dan, Yao, Xiaoxiao, Yang, Yongsheng

    “…Increasing evidence supports the association of microRNA with tumor occurrence and development. However, the expression of miR-6875-3p and its role in cell…”
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  5. 5

    The connection between innervation and metabolic rearrangements in pancreatic cancer through serine by Dong, Mengmeng, Cao, Lidong, Cui, Ranji, Xie, Yingjun

    Published in Frontiers in oncology (13-12-2022)
    “…Pancreatic cancer is a kind of aggressive tumor famous for its lethality and intractability, and pancreatic ductal adenocarcinoma is the most common type…”
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  6. 6

    Immunotherapy for Hepatocellular Carcinoma: Current Advances and Future Expectations by Zhang, Xuewen, Yao, Xiaoxiao, Zhang, Dan, Sheng, Jiyao, Xiang, Yien, Xie, Yingjun, Yang, Yongsheng

    Published in Journal of immunology research (01-01-2018)
    “…Primary liver cancer is a common kind of digestive cancers with high malignancy, causing 745,500 deaths each year. Hepatocellular carcinoma is the major…”
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  7. 7

    Different culture method changing CD105 expression in amniotic fluid MSCs without affecting differentiation ability or immune function by Wang, Ding, Liu, Nengqing, Xie, Yingjun, Song, Bing, Kong, Shu, Sun, Xiaofang

    Published in Journal of cellular and molecular medicine (01-04-2020)
    “…MSCs are kind of cultured cells that reside in different tissues as inducers or regulators of physiological and pathological processes. Here, we derived MSCs…”
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  8. 8

    RS12574989 and haplotype associated with α/β-chain imbalance and population HbA2 reduction by Lin, Qiyin, Xie, Yingjun, Zhong, Xuan, Sun, Xiaofang, Wang, Ding

    Published in BMC medical genomics (15-08-2022)
    “…Abstract Determining the associated relationship of genotype and phenomenon would benefit the understanding of disease and renew disease intervention means…”
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  9. 9

    Application of MFI-5 in severe complications and unfavorable outcomes after radical resection of colorectal cancer by Huang, Lihong, Li, Zhifa, Jian, Mengru, Wu, Xiaobing, Chen, Huixian, Qin, Haifeng, Li, Ziqiao, Song, Shixi, Xie, Yingjun, Chen, Rong

    Published in World journal of surgical oncology (26-09-2023)
    “…Abstract Background Frailty is considered a characteristic manifestation of physiological decline in multiple organ systems, which significantly increases the…”
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  10. 10

    The use of high-resolution SNP arrays to detect congenital cardiac defects by Linhuan, Huang, Danlei, Cai, Zhiming, He, Shu, Kong, Jiayi, Chen, Jiayi, Peng, Chuqi, Su, Yinghong, Yang, Ding, Wang, Yingjun, Xie, Yanmin, Luo

    “…Copy number variations (CNVs) detected by high-resolution single nucleotide polymorphism microarrays (SNP arrays) have been associated with congenital heart…”
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  11. 11

    MSCs derived from amniotic fluid and umbilical cord require different administration schemes and exert different curative effects on different tissues in rats with CLP-induced sepsis by Chen, Rui, Xie, Yingjun, Zhong, Xuan, Chen, Fei, Gong, Yu, Wang, Na, Wang, Ding

    Published in Stem cell research & therapy (06-03-2021)
    “…Mesenchymal stem cells (MSCs) are derived from multiple tissues, including amniotic fluid (AF-MSCs) and the umbilical cord (UC-MSCs). Although the therapeutic…”
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  12. 12

    Generation of two induced pluripotent stem cell lines, GZHMCi009-A and GZHMCi010-A, derived from peripheral blood mononuclear cells of two SCA3 patients with 14/74 CAG repeats of the ATXN3 mutation by Yinghong, Yang, Qian, Luo, Bing, Song, Yingjun, Xie, Wenzhi, He, Bangzhu, Chen, Xiaofang, Sun

    Published in Stem cell research (01-05-2022)
    “…•SCA3 is the result of abnormal repeat amplification of CAG of the ATXN3 gene.•Generation of iPSCs from PBMCs donated by SCA3 patients with ATXN3 mutation.•The…”
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  13. 13

    Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective Study by Zhuang, Jianlong, Zhang, Na, Wang, Yuanbai, Zhang, Hegan, Zheng, Yu, Jiang, Yuying, Xie, Yingjun, Chen, Dongmei

    Published in Frontiers in genetics (30-09-2021)
    “…Background: There are limited reports available on investigations into the molecular spectrum of thalassemia and hemoglobinopathy in Fujian province, Southeast…”
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  14. 14

    A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures by Zhuang, Jianlong, Xie, Meihua, Yao, Jianfeng, Fu, Wanyu, Zeng, Shuhong, Jiang, Yuying, Wang, Yuanbai, Xie, Yingjun, Wang, Gaoxiong, Chen, Chunnuan

    Published in BMC medical genomics (09-01-2023)
    “…Pathogenic PAK1 variants were described to be causative of neurodevelopmental disorder with macrocephaly, seizures, and speech delay. Herein, we present a de…”
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  15. 15

    A retrospective analysis of MS/MS screening for IEM in high-risk areas by He, Xiao, Kuang, Juan, Lai, Jiahong, Huang, Jingxiong, Wang, Yijin, Lan, Guofeng, Xie, Yingjun, Shi, Xuekai

    Published in BMC medical genomics (16-03-2023)
    “…Inborn errors of metabolism (IEM) can lead to severe motor and neurological developmental disorders and even disability and death in children due to untimely…”
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  16. 16

    Extracellular Vesicles of Mesenchymal Stem Cells Are More Effectively Accessed through Polyethylene Glycol-Based Precipitation than by Ultracentrifugation by Jia, Lei, Li, Bo, Fang, Cong, Liang, Xiaoyan, Xie, Yingjun, Sun, Xiaofang, Wang, Wen, Zheng, Lei, Wang, Ding

    Published in Stem cells international (06-09-2022)
    “…Extracellular vesicles (EVs) have been identified as cell-cell communication agents, and EVs derived from mesenchymal stem cells (MSCs) exhibit therapeutic…”
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  17. 17

    Complex Chromosomal Rearrangement Causes Male Azoospermia: A Case Report and Literature Review by Liang, Yi, Xie, Yingjun, Kong, Shu, Pan, Qianying, Qiu, Wenjun, Wang, Ding, Li, Mengting, Lin, Sisi, Liu, Zihang, Sun, Xiaofang

    Published in Frontiers in genetics (24-02-2022)
    “…Male carriers of complex chromosomal rearrangements (CCRs) may have decreased fertility and usually present with azoospermia, oligospermia or teratospermia…”
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  18. 18

    A Tumor Microenvironment Responsive Nanotheranostics Agent for Magnetic Resonance Imaging and Synergistic Photodynamic Therapy/Photothermal Therapy of Liver Cancer by Zhu, Yuwan, Deng, Mo, Xu, Nannan, Xie, Yingjun, Zhang, Xuewen

    Published in Frontiers in chemistry (07-04-2021)
    “…Surgery is the main treatment for liver cancer in clinic owing to its low sensitivity to chemotherapy and radiotherapy, but this results in high mortality,…”
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  19. 19

    Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication by Zhuang, Jianlong, Chen, Chunnuan, Wang, Yuanbai, Zeng, Shuhong, Chen, Yu’e, Jiang, Yuying, Xie, Yingjun, Wang, Gaoxiong

    Published in Frontiers in genetics (05-07-2022)
    “…Background: Pathogenic mutations in the KCNH2 gene were associated with long QT syndrome 2 (LQT2), which typically manifest in a prolonged QT interval and may…”
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  20. 20

    Prenatal diagnosis of dent disease type I with a nonsense pathogenic variant in CLCN5: a case study by Zhu, Ruijue, Zhu, Mingming, Wang, Boye, Chen, Enen, Cai, Danlei, Yang, Yinghong, Liang, Yi, Su, Chuqi, Wang, Ding, Sun, Xiaofang, Huang, Linhuan, Xie, Yingjun

    Published in BMC medical genomics (24-01-2024)
    “…Dent disease type I is a rare X-linked recessive renal tubular disease resulting from pathogenic variants in the CLCN5 gene. Due to the rarity of Dent disease…”
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