Author

S. Balu

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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Pharmacology & Toxicology· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 3 Research Focus:differential expression· 3 Organism:human· 3 Approach:experimental assay· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

R. Mesnage· 2 shared A. Levescot· 1 shared A. Morris· 1 shared A. Phedonos· 1 shared A. Wactor· 1 shared C. A. Mein· 1 shared C. Frainay· 1 shared D. A. Rao· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersPharmacology & Toxicology

R. Mesnage

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Arthritis Flares Mediated by Tissue Resident Memory T Cells in the Joint

M. H. Chang, A. Levescot, N. Nelson-Maney, R. B. Blaustein, K. D. Winden, A. Morris, A. Wactor, S. Balu, R. Grieshaber-Bouyer, K. Wei, L. A. Henderson, Y. Iwakura, R. A. Clark, D. A. Rao, R. C. Fuhlbrigge, P. A. Nigrovic

This study identifies synovial tissue-resident memory T cells as mediators of arthritis flares in murine models and finds a comparable population in human rheumatoid arthritis tissues.

bioRxiv · Jun 4, 2021Immunology

Integrated transcriptomics and metabolomics reveal signatures of lipid metabolism dysregulation in HepaRG liver cells exposed to PCB 126

R. Mesnage, M. Biserni, S. Balu, C. Frainay, N. Poupin, F. Jourdan, E. Wozniak, T. Xenakis, C. A. Mein, M. A. Antoniou

This study uses transcriptomics and metabolomics to show PCB 126 exposure disrupts lipid metabolism in HepaRG cells, causing oxidative stress and altered metabolite levels.

bioRxiv · Feb 3, 2018Pharmacology & Toxicology

Transcriptome profiling reveals bisphenol A alternatives activate estrogen receptor alpha in human breast cancer cells

R. Mesnage, A. Phedonos, M. Arno, S. Balu, J. C. Corton, M. N. Antoniou

This study compares the estrogenic activity of bisphenol alternatives to BPA in breast cancer cells, finding some are more potent ER agonists.

bioRxiv · Mar 2, 2017Pharmacology & Toxicology