Author

Z. Ugur

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 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 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. Chenchik· 1 shared B. McDonald· 1 shared D. A. Petrov· 1 shared D. Amar· 1 shared D. Deng· 1 shared E. A. Apilado· 1 shared E. R. Jellison· 1 shared G. D. Wall· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperCancer Biology

A. Chenchik

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Oncogenic context shapes the fitness landscape of tumor suppression

L. M. Blair, J. M. Juan, L. Sebastian, V. B. Tran, W. Nie, G. D. Wall, M. Gerceker, I. K. Lai, E. A. Apilado, G. Grenot, D. Amar, G. Foggetti, M. Do Carmo, Z. Ugur, D. Deng, , I. P. Winters

The paper models tumor suppression fitness landscapes across four oncogenic contexts and finds context-specific tumor suppressor effects.

Nature Communications · Oct 12, 2023Peer-reviewedCancer Biology

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