Author

E. Cheung

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· 1 Cell Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

A. Clear· 1 shared A. D'Avola· 1 shared A. Gunawan· 1 shared A. P. Hutchins· 1 shared C. Chang· 1 shared D. Calado· 1 shared G. Ma· 1 shared H. King· 1 shared

Activity by Year

2018-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperImmunology

A. Clear

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

PHGDH is required for germinal center formation and is a therapeutic target in MYC-driven lymphoma

A. D'Avola, N. Legrave, M. Tajan, P. Chakravarty, R. Shearer, H. King, E. Cheung, A. Clear, A. Gunawan, L. Zhang, L. James, J. MacRae, J. Gribben, D. Calado, K. Vousden, J. Riches

This study identifies PHGDH as essential for germinal center formation and shows its inhibition reduces lymphoma progression and improves survival.

bioRxiv · Nov 11, 2021Immunology

A programmable system to methylate and demethylate m6A on specific mRNAs

C. Chang, G. Ma, E. Cheung, A. P. Hutchins

This paper introduces a CRISPR/dCas13a-based system to methylate and demethylate m6A on specific mRNAs, enabling targeted exploration of m6A's role in biological processes.

bioRxiv · Apr 16, 2021 · PreprintCell Biology

A novel long noncoding RNA LINC00844 regulates prostate cancer cell migration and invasion through androgen receptor signaling

S. Lingadahalli, S. Jadhao, Y. Y. Sung, M. Chen, L. Hu, X. Chen, E. Cheung

This study identifies LINC00844 as an androgen-regulated lncRNA that suppresses prostate cancer migration and invasion by modulating AR chromatin binding and NDRG1 expression.

bioRxiv · Jan 7, 2018Cancer Biology