Search Results - "WENXUE TANG"

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  1. 1

    Myeloid-derived suppressor cells-new and exciting players in lung cancer by Yang, Zhenzhen, Guo, Jiacheng, Weng, Lanling, Tang, Wenxue, Jin, Shuiling, Ma, Wang

    Published in Journal of hematology and oncology (31-01-2020)
    “…Lung cancer (LC) is the leading cause of cancer-related death worldwide due to its late diagnosis and poor outcomes. As has been found for other types of…”
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    Assessing Community-Level Livability Using Combined Remote Sensing and Internet-Based Big Geospatial Data by Zhu, Likai, Guo, Yuanyuan, Zhang, Chi, Meng, Jijun, Ju, Lei, Zhang, Yuansuo, Tang, Wenxue

    Published in Remote sensing (Basel, Switzerland) (01-12-2020)
    “…With rapid urbanization, retrieving livability information of human settlements in time is essential for urban planning and governance. However, livability…”
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  4. 4

    Timed conditional null of connexin26 in mice reveals temporary requirements of connexin26 in key cochlear developmental events before the onset of hearing by Chang, Qing, Tang, Wenxue, Kim, Yeunjung, Lin, Xi

    Published in Neurobiology of disease (2015)
    “…Abstract Mutations in the Gjb2 gene, which encodes a gap junction protein connexin26 (Cx26), are the most prevalent form of hereditary deafness in humans and…”
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    Superoxide dismutase@zeolite Imidazolate Framework-8 Attenuates Noise-Induced Hearing Loss in Rats by Zhang, Yan, Li, Qing, Han, Chengzhou, Geng, Fang, Zhang, Sen, Qu, Yan, Tang, Wenxue

    Published in Frontiers in pharmacology (16-05-2022)
    “…Reactive oxygen species (ROS) and inflammation have been considered major contributors to noise-induced hearing loss (NIHL) that constituted a public health…”
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  7. 7

    A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family by Zeng, Beiping, Xu, Hongen, Tian, Yongan, Lin, Qianyu, Feng, Haifeng, Zhang, Zhifeng, Li, Siqi, Tang, Wenxue

    Published in Chinese medical journal (05-11-2022)
    “…The parents were non-consanguineous and the proband had no history of noise exposure, ototoxic drug usage, external ear trauma, birth injury, hypoxia or…”
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  8. 8

    Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through TLR4/NF-κB pathway by Yao, Yanmei, Lin, Leqing, Tang, Wenxue, Shen, Yueliang, Chen, Fayu, Li, Ning, Wang, Baiyong

    Published in European journal of histochemistry (08-09-2023)
    “…Geniposide (GEN), a medical herb, is known for its therapeutic applications in cardiovascular diseases, though its efficacy in treating myocardial…”
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  9. 9

    Near‐infrared laser‐activated aggregation‐induced emission nanoparticles boost tumor carbonyl stress and immunotherapy of breast cancer by Pan, You, Suo, Meng, Huang, Qinqin, Lyu, Meng, Jiang, Yi, Wang, Shile, Tang, Wenxue, Ning, Shipeng, Zhang, Tianfu

    Published in Aggregate (Hoboken) (01-04-2024)
    “…The induction of tumor carbonyl stress is reported to efficiently revert immune suppression in the tumor microenvironment and enhance cancer immunotherapy…”
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  10. 10

    Novel likely pathogenic variant in the EYA1 gene causing Branchio oto renal syndrome and the exploration of pathogenic mechanisms by Zhang, Hui, Gao, Jian, Wang, Hanjun, Liu, Mengli, Lu, Shuangshuang, Xu, Hongen, Tang, Wenxue, Zheng, Guoxi

    Published in BMC medical genomics (16-04-2024)
    “…Branchio-oto-renal syndrome (BOR, OMIM#113,650) is a rare autosomal dominant disorder that presents with a variety of symptoms, including hearing loss…”
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    Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities by Lin, Xi, Tang, Wenxue, Ahmad, Shoeb, Lu, Jingqiao, Colby, Candice C., Zhu, Jason, Yu, Qing

    Published in Hearing research (01-06-2012)
    “…The goal of sequencing the entire human genome for $1000 is almost in sight. However, the total costs including DNA sequencing, data management, and analysis…”
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  12. 12

    Novel compound heterozygous pathogenic variants in the SLC3A1 gene in a Chinese family with cystinuria by Liu, Danhua, Zhao, Yongli, Xue, Xia, Hou, Xinyue, Xu, Hongen, Zhao, Xinghua, Tian, Yongan, Tang, Wenxue, Guo, Jiancheng, Xu, Changbao

    Published in BMC medical genomics (19-12-2023)
    “…Cystinuria is an autosomal recessive disorder characterized by a cystine transport deficiency in the renal tubules due to mutations in two genes: SLC3A1 and…”
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  13. 13

    Genetic and Phenotypic Variability in Chinese Patients With Branchio-Oto-Renal or Branchio-Oto Syndrome by Feng, Haifeng, Xu, Hongen, Chen, Bei, Sun, Shuping, Zhai, Rongqun, Zeng, Beiping, Tang, Wenxue, Lu, Wei

    Published in Frontiers in genetics (15-11-2021)
    “…Background: Branchio-oto-renal syndrome (BOR) and branchio-oto syndrome (BOS) are rare autosomal dominant disorders defined by varying combinations of…”
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    Roles of HMGB1 in regulating myeloid-derived suppressor cells in the tumor microenvironment by Jin, Shuiling, Yang, Zhenzhen, Hao, Xin, Tang, Wenxue, Ma, Wang, Zong, Hong

    Published in Biomarker research (16-06-2020)
    “…Myeloid-derived suppressor cells (MDSCs) are notable contributors to the immunosuppressive tumor microenvironment (TME) and are closely associated with tumor…”
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    Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant by Dou, Qian, Xu, HongEn, Ma, LiYing, Tan, Li, Tang, WenXue

    Published in BMC medical genomics (30-10-2023)
    “…Tubulin beta-8 ( TUBB8 ) is expressed exclusively in the oocyte and early embryo, encoding a beta-tubulin polypeptide that participates in the assembly of…”
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  16. 16

    Detection and clinical significance of circulating tumor cells in colorectal cancer by Jiang, Miao, Jin, Shuiling, Han, Jinming, Li, Tong, Shi, Jianxiang, Zhong, Qian, Li, Wen, Tang, Wenxue, Huang, Qinqin, Zong, Hong

    Published in Biomarker research (19-11-2021)
    “…Histopathological examination (biopsy) is the “gold standard” for the diagnosis of colorectal cancer (CRC). However, biopsy is an invasive method, and due to…”
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  17. 17

    Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea by Sun, Yu, Tang, Wenxue, Chang, Qing, Wang, Yunfeng, Kong, Weijia, Lin, Xi

    Published in Journal of comparative neurology (1911) (20-10-2009)
    “…Mutations in connexin26 (Cx26) and Cx30 are the most common cause of nonsyndromic inherited deafness in humans. To understand the underlying molecular…”
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    Hydrogel co-loading SO2 prodrug and FeGA nanoparticles for enhancing chemodynamic therapy by photothermal-triggered SO2 gas therapy by Huang, Qinqin, Lyu, Meng, Tang, Wenxue, Qi, Pengyuan, Hu, Hongzhi

    “…Chemodynamic therapy (CDT) is an effective anti-tumor method, while CDT alone cannot achieve a good therapeutic effect. Moreover, the overexpression of…”
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    Involvement of Glutathione Depletion in Selective Cytotoxicity of Oridonin to p53-Mutant Esophageal Squamous Carcinoma Cells by Li, Yinchao, Li, Nana, Shi, Jianxiang, Ahmed, Tanzeel, Liu, Hongmin, Guo, Jiancheng, Tang, Wenxue, Guo, Yongjun, Zhang, Qi

    Published in Frontiers in oncology (15-01-2020)
    “…Oridonin, a diterpenoid compound isolated from traditional Chinese medicine Rabdosia rubescens, has shown antitumor effects to esophageal cancer. However, its…”
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    Establishment of an induced pluripotent stem cell line (ZZUPMCi001-A) derived from peripheral blood mononuclear cells in a patient with type 1 Waardenburg syndrome by Wang, Xiaoxuan, Zhang, Sen, Hu, Sang, Xu, Hongen, Zhang, Qi, Tang, Wenxue

    Published in Stem cell research (01-12-2021)
    “…Waardenburg syndrome type I (WS1) is a human autosomal dominant genetic disease characterized by sensorineural hearing loss, pigmentary abnormalities, and…”
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