Author

R. Kageyama

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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Immunology· 2 Evolutionary Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Approach:statistical model· 2 Approach:biophysical modeling· 1 Assay:bulk RNA-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:CITE-seq· 1

Frequent Co-Authors

A. L. S. Chang· 1 shared A. T. Satpathy· 1 shared C. Curtis· 1 shared C. H. Johnson· 1 shared C. Hess· 1 shared C. Rakers· 1 shared C. Wang· 1 shared D. A. Golombek· 1 shared

Activity by Year

2019-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperImmunology

A. L. S. Chang

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Author profile →

3 papers

Recent·Most cited

The non-coding RNA miR-17~92 is a central mediator of T cell activation

M. Doelz, J. D. Gagnon, M. Kornete, R. Marone, G. Bantug, R. Kageyama, C. Hess, K. M. Ansel, D. Seyres, J. Roux, L. T. Jeker

This study identifies miR-17~92 as a central mediator of T cell activation by enhancing the calcineurin/NFAT pathway and repressing negative regulators of activation.

bioRxiv · Oct 13, 2020Immunology

The methyl cycle is a conserved regulator of biological clocks.

J.-M. Fustin, S. Ye, C. Rakers, M. Versteven, S. J. Cargill, K. T. Tamai, Y. Xu, M. L. Jabbur, R. Kojima, M. L. Lamberti, D. Whitmore, R. Stanewsky, R. Kageyama, T. Matsuo, K. Yoshioka-Kobayashi, , H. Okamura

This study shows the methyl cycle regulates circadian and somite segmentation clocks across species, highlighting its role as a conserved metabolic regulator of biological clocks.

bioRxiv · May 29, 2019 · PreprintEvolutionary Biology

Clonal replacement of tumor-specific T cells following PD-1 blockade

K. E. Yost, A. T. Satpathy, D. K. Wells, Y. Qi, C. Wang, R. Kageyama, K. McNamara, J. M. Granja, K. Y. Sarin, R. A. Brown, R. K. Gupta, C. Curtis, S. L. Bucktrout, M. M. Davis, A. L. S. Chang, H. Y. Chang

This study tracks T cell clonal dynamics before and after PD-1 blockade in cancer patients, finding that new T cell clones, not pre-existing ones, expand in response to treatment.

bioRxiv · May 24, 2019Immunology