Author

T. A. Perry

University of Connecticut

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 Developmental Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:metabolomics· 1 Organism:mouse· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1

Frequent Co-Authors

C. Ludwig· 1 shared G. E. Pratt· 1 shared J. Roberts· 1 shared James Y. H. LiiD· 1 shared M. A. C. Reed· 1 shared M. Hoogenkamp· 1 shared Nagham Khouri‐FarahiD· 1 shared Qiuxia GuoiD· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCancer Biology

C. Ludwig

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2 papers

Recent·Most cited

FOXP Genes Regulate Purkinje Cell Diversity in Cerebellar Development and Evolution

Nagham Khouri‐Farah, Qiuxia Guo, T. A. Perry, Ryan Dussault, James Y. H. Li

The paper identifies Foxp genes as regulators of Purkinje cell diversity in cerebellar development and evolution, showing their role in subtype specification and species-specific cerebellar organization.

Nature Neuroscience · Aug 18, 2025Peer-reviewedDevelopmental Biology

T-ALL Proliferation Relies on Glutamine Uptake and EAAT1-dependent Conversion of Glutamine to Aspartate and Nucleotides

V. S. Stanulovic, S. Al Omair, M. A. C. Reed, S. Potluri, J. Roberts, T. A. Perry, S. Sarkar, G. E. Pratt, U. L. Gunther, C. Ludwig, M. Hoogenkamp

This study identifies EAAT1 as a critical target for T-ALL treatment by showing its role in glutamine conversion to nucleotides and aspartate essential for cell proliferation.

bioRxiv · Feb 8, 2020 · PreprintCancer Biology