Author

C.-M. Chiang

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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Cancer Biology· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:differential expression· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

A. Dubey· 1 shared A. H. P. Loh· 1 shared A. T. Prabhakar· 1 shared C. D. James· 1 shared C. Fontan· 1 shared D. Das· 1 shared I. M. Morgan· 1 shared J. Y. Leung· 1 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperCancer Biology

A. Dubey

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Author profile →

2 papers

Recent·Most cited

BRD4 isoforms have distinct roles in tumor progression and metastasis in embryonal rhabdomyosarcoma

R. Taneja, D. Das, J. Y. Leung, V. Tergaonkar, A. H. P. Loh, C.-M. Chiang

This study shows BRD4-L and BRD4-S isoforms have distinct roles in embryonal rhabdomyosarcoma, with BRD4-L promoting tumor growth and BRD4-S preventing metastasis.

bioRxiv · Jul 26, 2023 · PreprintCancer Biology

Direct interaction with the BRD4 carboxyl-terminal motif (CTM) and TopBP1 is required for human papillomavirus 16 E2 association with mitotic chromatin and plasmid segregation function

A. T. Prabhakar, C. D. James, C. Fontan, R. Otoa, X. Wang, M. L. Bristol, R. D. Hill, A. Dubey, S.-Y. Wu, C.-M. Chiang, I. M. Morgan

This study shows that E2 protein interaction with BRD4's CTM and TopBP1 is essential for HPV16's mitotic chromatin association and plasmid segregation, offering therapeutic targets for viral genome targeting.

bioRxiv · May 25, 2023Cancer Biology