Author

C. Savage

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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Cancer Biology· 1 Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Organism:bacteria (other)· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:clustering· 1 Approach:deep learning· 1

Frequent Co-Authors

A. A. R. Thompson· 1 shared A. C. Krusenstjerna· 1 shared A. G. Patel· 1 shared A. Meijer· 1 shared A. Rahman· 1 shared A. Reese· 1 shared B. Stevenson· 1 shared C. A. Brissette· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperImmunology

A. A. R. Thompson

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

An integrated single-cell RNA-seq map of human neuroblastoma tumors and preclinical models uncovers divergent mesenchymal-like gene expression programs.

R. H. Chapple, X. Liu, S. Natarajan, M. I. M. Alexander, Y. Kim, A. G. Patel, C. W. LaFlamme, M. Pan, W. C. Wright, H.-M. Lee, Y. Zhang, M. Lu, S. C. Koo, C. Long, J. Harper, , P. Geeleher

The paper compares mesenchymal-like gene expression programs in neuroblastoma preclinical models and patient tumors using single-cell RNA-seq and identifies chemotherapy-induced changes in PDX and GEMM.

bioRxiv · Apr 13, 2023Cancer Biology

Borrelia burgdorferi PlzA is a cyclic-di-GMP dependent DNA- and RNA-binding protein

N. Jusufovic, A. C. Krusenstjerna, C. Savage, T. C. Saylor, C. A. Brissette, W. R. Zueckert, P. Schlax, M. A. R. MOTALEB, B. Stevenson

This study identifies PlzA as a cyclic-di-GMP-dependent DNA and RNA-binding protein in Borrelia burgdorferi, showing that nucleic acid binding requires c-di-GMP and involves specific domain interactions.

bioRxiv · Jan 30, 2023Microbiology

Inhibition of ErbB kinase signalling promotes resolution of neutrophilic inflammation

L. Prince, S. Renshaw, A. Rahman, K. M. Henry, K. Herman, A. A. R. Thompson, H. Isles, C. Tulotta, D. Sammut, J. Rougeot, N. Khoshaein, A. Reese, K. Higgins, C. Tabor, I. Sabroe, , D. Dockrell

The paper identifies ErbB kinase inhibitors as potential therapies for neutrophilic inflammation by showing they accelerate neutrophil apoptosis in multiple models.

bioRxiv · Aug 19, 2019Immunology