Author

T. V. Le

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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Bioengineering· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:drug response / drug discovery· 1 Assay:proteomics· 1

Frequent Co-Authors

C. Perrone· 1 shared D. Bolidong· 1 shared D. Nicastro· 1 shared D. Tritschler· 1 shared E. Dymek· 1 shared E. F. Smith· 1 shared E. O'Toole· 1 shared G. Fu· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperCell Biology

C. Perrone

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2 papers

Recent·Most cited

Surface-engineered extracellular vesicles to modulate antigen-specific T cell expansion for cancer immunotherapy

X. Lyu, T. Yamano, S. Imai, T. V. Le, D. Bolidong, M. Ueda, S. Warashina, H. Mukai, S. Hayashi, K. Matoba, T. Nishino, R. Hanayama

The paper develops antigen-presenting extracellular vesicles (AP-EVs) engineered to enhance T cell expansion and anticancer immunity through combined immunotherapy.

bioRxiv · Sep 25, 2023 · PreprintBioengineering

FAP57/WDR65 targets assembly of a subset of inner arm dyneins and connects to regulatory hubs in cilia

J. Lin, T. V. Le, K. Augspurger, D. Tritschler, R. Bower, G. Fu, C. Perrone, E. O'Toole, K. V. Mills, E. Dymek, E. F. Smith, D. Nicastro, M. E. Porter

This study identifies FAP57/WDR65 as a docking factor that targets specific inner dynein arms to the 96 nm axonemal repeat and connects to regulatory hubs in cilia.

bioRxiv · Jul 1, 2019Cell Biology