Jingyan Xia
Zhejiang University
14 Papers
53 Citations
Jingyan Xia is an academic researcher from Zhejiang University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 5, co-authored 5 publications.
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Papers
MiR-127 Modulates Macrophage Polarization and Promotes Lung Inflammation and Injury by Activating the JNK Pathway
Hangjie Ying,Yanhua Kang,Hang Zhang,Dongjiu Zhao,Jingyan Xia,Zhe Lu,Huanhuan Wang,Feng Xu,Liyun Shi +8 more
TL;DR: Mechanistically, miR-127 demonstrated to target B cell lymphoma 6 and remarkably downregulated its expression and subsequently dual specificity phosphatase 1 (Dusp1) and enhanced the activation of JNK kinase and hence the development of proinflammatory macrophages.
•Journal Article
Impact of vitamin D supplementation on the outcome of tuberculosis treatment: a systematic review and meta-analysis of randomized controlled trials.
TL;DR: The meta analysis results indicate that vitamin D supplementation does not seem to have any beneficial effect in the treatment of TB, and future rigorous randomized controlled trials are needed to explore whether the supplementation of vitamin D could shorten treatment duration.
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Hybrid Biomimetic Membrane Coated Particles-Mediated Bacterial Ferroptosis for Acute MRSA Pneumonia.
Huiqun Hu,Shi Yuan Hua,Xiuhui Lin,Lihui Zhou,Jiarong Cui,Ruoxi Wang,Jingyan Xia,Feng Xu,Xiaoyuan Chen,Min Zhou +9 more
TL;DR: In this article , the authors used a hybrid biomimetic membrane composed of an erythrocyte membrane and platelet membrane to obtain lung targeted antibacterial particles (mFe-CA) to induce ferroptosis in acute methicillin resistant Staphylococcus aureus (MRSA) pneumonia.
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Histone deacetylase 3 contributes to the antiviral innate immunity of macrophages by interacting with FOXK1 to regulate STAT1/2 transcription.
Liping Yang,Shengchuan Chen,Qun Zhao,Chaohu Pan,Lin-Tao Peng,Yu Han,Lili Li,Jiayin Ruan,Jingyan Xia,Heng Yang,Feng Xu,Genhong Cheng +11 more
TL;DR: In this paper , the authors showed that HDAC3 interacts with a conserved transcription factor Forkhead Box K1 (FOXK1), co-localizing with FOXK1 at the promoter of STAT1 and STAT2, and is required for protecting FOXK 1 from lysosomal system-mediated degradation.
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