Author

J. T. Vu

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· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:CRISPR screen· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

C. D. Richardson· 2 shared A. S. Wang· 1 shared B. G. Gowen· 1 shared B. M. Gardner· 1 shared C. J. Sheedy· 1 shared J. Bacal· 1 shared J. C. Walter· 1 shared J. Corn· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersCell Biology

C. D. Richardson

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Author profile →

2 papers

Recent·Most cited

A genome-wide screen links peroxisome regulation with Wnt signaling through RNF146 and tankyrase

J. T. Vu, K. U. Tavasoli, L. Mandjikian, C. J. Sheedy, J. Bacal, M. A. Morrissey, C. D. Richardson, B. M. Gardner

The paper identifies RNF146 and tankyrase as regulators of peroxisome function and links them to Wnt signaling through their role in PARsylation and beta-catenin degradation.

bioRxiv · Feb 2, 2024 · PreprintCell Biology

The histone chaperone FACT induces Cas9 multi-turnover behavior and modifies genome manipulation in human cells

A. S. Wang, L. Chen, R. A. Wu, C. D. Richardson, B. G. Gowen, K. R. Kazane, J. T. Vu, S. K. Wyman, J. Shin, J. C. Walter, J. Corn

This study identifies FACT as a factor that influences Cas9 turnover and genome editing efficiency in human cells.

bioRxiv · Jul 23, 2019Cell Biology