Author

A. Warman

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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Biochemistry· 3 Pathology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Approach:experimental assay· 3 Organism:human· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

I. Choi· 4 shared S. Rajagopal· 4 shared A. Inoue· 2 shared D. S. Eiger· 2 shared J. Gardner· 2 shared J. S. Smith· 2 shared K. Zheng· 2 shared A. Ganapathi· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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4 shared papersBiochemistry

I. Choi

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Phosphorylation barcodes direct biased chemokine signaling at CXCR3

D. S. Eiger, J. S. Smith, T. Shi, T. M. Stepniewski, C.-F. Tsai, C. Honeycutt, N. Boldiszar, J. Gardner, C. D. Nicora, A. M. Moghieb, K. Kawakami, I. Choi, K. Zheng, A. Warman, P. Alagesan, , S. Rajagopal

The paper shows that CXCR3 chemokines use different phosphorylation barcodes to activate distinct signaling pathways, leading to varied physiological outcomes.

bioRxiv · Mar 14, 2023Biochemistry

Single-Cell Analysis Identifies Distinct Immune and Smooth Muscle Cell Populations that Contribute to Chronic Thromboembolic Pulmonary Hypertension

G. Viswanathan, H. F. Kirshner, N. Nazo, A. Ganapathi, I. Cumming, I. Choi, A. Warman, S. Almeida-Peters, J. Haney, D. Corcoran, Y.-R. A. Yu, S. Rajagopal

This study uses single-cell RNA sequencing to identify immune and smooth muscle cell populations in CTEPH thrombus, revealing inflammatory mechanisms and a potential therapeutic target.

bioRxiv · Jan 26, 2022Pathology

Location bias contributes to functionally selective responses of biased CXCR3 agonists

D. S. Eiger, N. Boldizsar, C. C. Honeycutt, J. Gardner, S. Kirchner, C. Hicks, I. Choi, U. Pham, K. Zheng, A. Warman, J. Smith, J. Zhang, S. Rajagopal

The paper shows that biased CXCR3 agonists produce different signaling outcomes based on subcellular location, with endosomal signaling playing a key role in biased activation.

bioRxiv · Jan 13, 2022Biochemistry

Biased agonists of the chemokine receptor CXCR3 differentially drive formation of Gαi:β-arrestin complexes

K. Z. Zheng, J. S. Smith, A. Warman, I. Choi, J. Gundry, T. F. Pack, A. Inoue, M. Caron, S. Rajagopal

The paper shows that biased agonists of CXCR3 differentially drive the formation of Gi:β-arrestin complexes, independent of G protein signaling or β-arrestin recruitment.

bioRxiv · Jun 11, 2020 · PreprintBiochemistry