Author

A. Tseng

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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Microbiology· 2 Pathology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Organism:mouse· 2 Assay:proteomics· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

A. Cupic· 1 shared A. Garcia-Sastre· 1 shared A. Goodspeed· 1 shared A. M. Bujor· 1 shared A. Marin· 1 shared A. S. Gonzalez-Reiche· 1 shared A. Saqi· 1 shared B. D. Gomez· 1 shared

Activity by Year

2022-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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1 shared paperMicrobiology

A. Cupic

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Divergent Outcomes Of Myeloid Cell Infection By Gammaherpesvirus 68 Reveal Stepwise Regulation By Host And Viral Factors

G. Vragel, K. S. Noell, A. Tseng, R. E. Kostelecky, E. A. Alexander, S. Cohen, C. Galvan, M. Dalwadi, B. D. Gomez, E. M. Medina, D. Oldenburg, A. Goodspeed, E. T. Clambey, L. F. van Dyk

This study shows that myeloid cells infected by gammaherpesvirus 68 exhibit divergent outcomes regulated by viral and host factors, with IL-4 converting restricted infection to productive replication.

bioRxiv · Jun 21, 2023 · PreprintMicrobiology

Extensive and Persistent Extravascular Dermal Fibrin Deposition Characterizes Systemic Sclerosis

J. L. Browning, J. Bhawan, A. Tseng, N. Crossland, A. M. Bujor, K. Akassoglou, S. Assassi, B. Skaug, J. Ho

This study identifies extensive and persistent dermal fibrin deposition in systemic sclerosis, suggesting ongoing vascular leakage and impaired fibrin clearance contribute to fibrosis.

bioRxiv · Jan 16, 2023 · PreprintPathology

Impact of SARS-CoV-2 ORF6 and its variant polymorphisms on host responses and viral pathogenesis.

T. Kehrer, A. Cupic, C. Ye, S. Yildiz, M. Bouhhadou, N. A. Crossland, E. Barrall, P. Cohen, A. Tseng, T. Cagatay, R. Rathnasinghe, D. Flores, S. Jangra, F. Alam, N. Mena, , L. Miorin

This study shows SARS-CoV-2 ORF6 disrupts nucleo-cytoplasmic trafficking, inhibits IFN signaling, and modulates viral protein expression, with variant polymorphisms affecting its function.

bioRxiv · Oct 18, 2022Microbiology