Author

J. M. Taube

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Immunology· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 2 Research Focus:clustering· 2 Approach:deep learning· 2 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Organism:mouse· 2 Assay:scRNA-seq· 2

Frequent Co-Authors

A. Tam· 2 shared D. M. Pardoll· 2 shared A. G. Dykema· 1 shared A. J. Munoz· 1 shared B. Zhang· 1 shared C. A. Sawosik· 1 shared C. Cherry· 1 shared C. M. Cherry· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersImmunology

A. Tam

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Lung tumor-infiltrating Treg have divergent transcriptional profiles and function linked to checkpoint blockade response

A. G. Dykema, J. Zhang, B. Zhang, L. S. Cheung, Z. Zeng, C. M. Cherry, T. Li, J. X. Caushi, M. Nishimoto, S. Connor, Z. Ji, A. J. Munoz, W. Hou, W. Zhan, D. Singh, , K. N. Smith

The paper identifies 10 subsets of lung cancer-infiltrating Tregs, showing one subset is suppressive and linked to anti-PD-1 resistance while another is Th1-like and associated with PD-1 response.

bioRxiv · Dec 13, 2022 · PreprintImmunology

Single cell RNA-seq in regenerative and fibrotic biomaterial environments defines new macrophage subsets

S. D. Sommerfeld, C. Cherry, R. M. Schwab, L. Chung, D. R. Maestas, P. Laffont, J. E. Stein, A. Tam, F. Housseau, J. M. Taube, D. M. Pardoll, P. Cahan, J. H. Elisseeff

The paper uses single-cell RNA sequencing to identify distinct macrophage subsets in regenerative and fibrotic environments, revealing new phenotypes and potential therapeutic targets.

bioRxiv · May 20, 2019Immunology