Author

A. C. Grammer

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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Immunology· 3

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:cancer & tumor microenvironment· 1 Approach:experimental assay· 1

Frequent Co-Authors

P. E. Lipsky· 3 shared A. R. Daamen· 2 shared E. L. Hubbard· 2 shared P. Bachali· 2 shared A. C. Labonte· 1 shared C. L. Mayberry· 1 shared C.-H. Chang· 1 shared D. C. Roopenian· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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3 shared papersImmunology

P. E. Lipsky

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3 papers

Recent·Most cited

ImmunologybioRxivFeb 1, 2022

Augmented glucose dependency of autoreactive B cells provides a treatment target forlupus

J. J. Wilson, J. Wei, A. R. Daamen…·C.-H. Chang

This study identifies glycolysis-dependent autoreactive B cells as key mediators of lupus and shows that targeting them with 2DG or BCMA-specific CAR T-cells improves disease outcomes.

DOI 10.1016/j.isci.2023.107487

mouseexperimental assay

𝕏 PostBluesky

ImmunologybioRxivPreprintJun 19, 2020

Analysis of Gene Expression from Systemic Lupus Erythematosus Synovium Reveals a Profile of Activated Immune Cells and Inflammatory Pathways

E. L. Hubbard, M. D. Catalina, S. Heuer…·P. E. Lipsky

This study analyzes gene expression in SLE synovium to identify immune cell activation and inflammatory pathways, revealing potential therapeutic targets for lupus arthritis.

DOI 10.1101/2020.06.19.123307

humanbulk RNA-seq

𝕏 PostBluesky

ImmunologybioRxivMay 28, 2020

Comprehensive Transcriptomic Analysis of COVID-19 Blood, Lung, and Airway

A. R. Daamen, P. Bachali, K. A. Owen…·P. E. Lipsky

This study analyzes gene expression in blood, lung, and airway tissues of COVID-19 patients to identify myeloid cell-driven inflammation and potential therapeutic targets.

DOI 10.1038/s41598-021-86002-x

humanbulk RNA-seq

𝕏 PostBluesky