Author

J. Suarez-Ramirez

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

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 2 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:flow cytometry· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

K. Chandiran· 2 shared B. McDonald· 1 shared E. R. Jellison· 1 shared J.-S. low· 1 shared L. Cauley· 1 shared L. S. Cauley· 1 shared S. M. Kaech· 1 shared Y. Hu· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 29 mutual co-author links

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2 shared papersImmunology

K. Chandiran

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2 papers

Recent·Most cited

SMAD4 promotes formation of terminally differentiated CTLs that localize in the microvasculature of the lungs but are excluded from the lumen of the airways

J. Suarez-Ramirez, K. Chandiran, L. Cauley

This study shows SMAD4 promotes the formation of terminally differentiated CTLs that localize in lung microvasculature but are excluded from airway lumens.

bioRxiv · Nov 16, 2023 · PreprintImmunology

SMAD4 and TGFβ are architects of inverse genetic programs during fate-determination of antiviral memory CD8 T cells

K. Chandiran, J. Suarez-Ramirez, Y. Hu, Z. Ugur, E. R. Jellison, J.-S. low, B. McDonald, S. M. Kaech, L. S. Cauley

This study shows SMAD4 and TGFβ regulate gene expression in opposite ways to determine whether antiviral CD8 T cells become circulating or tissue-resident memory cells.

bioRxiv · Dec 16, 2021Immunology