Author

N. Dong

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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Cell Biology· 1 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1

Frequent Co-Authors

D. Wu· 1 shared E. Chan· 1 shared F. Shao· 1 shared H. Xu· 1 shared J. Shi· 1 shared K. Chen· 1 shared K. Yin· 1 shared M. Yang· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperCell Biology

D. Wu

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Small-molecule cocktails induce the differentiation of human adipose-derived mesenchymal stem cells into hepatocyte-like cells

K. Yin, Y. Xu, D. Wu, W. Yang, N. Dong, N. Li, R. C. Zhao

This study induces human adipose-derived mesenchymal stem cells into hepatocyte-like cells using small-molecule cocktails and growth factors, producing cells with mature phenotype and function.

bioRxiv · Jul 19, 2021 · PreprintCell Biology

Genomic and protein structure modelling analysis depicts the origin and infectivity of 2019-nCoV, a new coronavirus which caused a pneumonia outbreak in Wuhan, China

N. Dong, X. Yang, K. Chen, E. Chan, M. Yang, S. Chen

The paper analyzes the genomic and protein structure of 2019-nCoV to determine its origin and infectivity, finding it is a bat coronavirus with weak human ACE2 receptor binding.

bioRxiv · Jan 20, 2020Microbiology

The N-end rule E3 ligase UBR2 activates Nlrp1b inflammasomes

H. Xu, J. Shi, Z. Yang, F. Shao, N. Dong

This study identifies UBR2 as an essential E3 ligase for LF-induced Nlrp1b inflammasome activation through degradation of Nlrp1b's N-terminal fragment.

bioRxiv · Sep 27, 2018 · PreprintImmunology