Author

A. Meng

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Developmental Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

C. Ma· 1 shared j. c. wang· 1 shared J. Li· 1 shared J. Ning· 1 shared J. Qiao· 1 shared J. Zhang· 1 shared L. Meng· 1 shared L. Wei· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperMicrobiology

C. Ma

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Activation of the chemokine receptor CCR1 and preferential recruitment of Gαi suppress RSV replication: implications for developing novel RSV treatment strategies

J. Li, L. Xue, j. c. wang, A. Meng, J. Qiao, M. Li, X. Wang, L. Meng, J. Ning, X. Gao, W. Li, C. Ma, L. Wei

This study shows that CCR1 activation on respiratory epithelial cells suppresses RSV replication via Gi-mediated inhibition of STAT3 phosphorylation and HSP90 activity, independent of IFN-I.

bioRxiv · Mar 18, 2022 · PreprintMicrobiology

Repression of MAPK/Erk signaling by Efnb2-Ephb4-Rasa1 is required for lymphatic valve formation

S. Jia, Y. Meng, T. Lv, J. Zhang, A. Meng

This study identifies the role of Efnb2-Ephb4-Rasa1 in repressing MAPK/Erk signaling to regulate lymphatic valve formation and suggests potential therapeutic targets.

bioRxiv · Oct 17, 2021 · PreprintDevelopmental Biology