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Yan Xie
Researcher at Central South University
Publications - 9
Citations - 536
Yan Xie is an academic researcher from Central South University. The author has contributed to research in topics: Microvesicles & Virus. The author has an hindex of 8, co-authored 9 publications receiving 340 citations. Previous affiliations of Yan Xie include Chinese Ministry of Education.
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Journal ArticleDOI
The MERS-CoV Receptor DPP4 as a Candidate Binding Target of the SARS-CoV-2 Spike.
TL;DR: Bioinformatics approaches combining human-virus protein interaction prediction and protein docking based on crystal structures have revealed the high affinity between human dipeptidyl peptidase 4 (DPP4) and the spike (S) receptor-binding domain of SARS-CoV-2.
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The role of exosomal noncoding RNAs in cancer
TL;DR: The role of exosomal ncRNAs, including miRNAs and long noncoding RNAs, in tumor biological processes is reviewed and may eventually become novel biomarkers and therapeutic targets in cancer progression.
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N6-Methyladenosine and Viral Infection
TL;DR: The positive and negative effects of m6A in distinct viral infection are summarized and, given the increasingly important roles of m 6A in diverse viruses,m6A represents a novel potential target for antiviral therapy.
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Targeting Exosomal EBV-LMP1 Transfer and miR-203 Expression via the NF-κB Pathway: The Therapeutic Role of Aspirin in NPC.
Lielian Zuo,Yan Xie,Jinyong Tang,Shuyu Xin,Shuyu Xin,Lingzhi Liu,Lingzhi Liu,Siwei Zhang,Siwei Zhang,Qijia Yan,Fanxiu Zhu,Jianhong Lu,Jianhong Lu +12 more
TL;DR: The study revealed that aspirin is a promising drug for NPC therapy via its targeting of exo-LMP1 transfer and the regulatory effect of LMP1 on miR-203 expression, opening a new avenue for understanding the pathogenesis of this tumor virus.
Journal ArticleDOI
The MERS-CoV Receptor DPP4 as a Candidate Binding Target of the SARS-CoV-2 Spike
TL;DR: Bioinformatics approaches combining human-virus protein interaction prediction and protein docking based on crystal structures have revealed the high affinity between human dipeptidyl peptidase 4 (DPP4) and the spike (S) receptor-binding domain of SARS-CoV-2.