Author

E. M. Payne

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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Bioengineering· 1 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Assay:metabolomics· 1 Assay:proteomics· 1 Organism:zebrafish· 1

Frequent Co-Authors

A. Lubin· 1 shared A. R. Abate· 1 shared C. A. Hockings· 1 shared C. Böiers· 1 shared C. Modavi· 1 shared C. Palmer· 1 shared D. S. Cornett· 1 shared H. S. Alper· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperCancer Biology

A. Lubin

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2 papers

Recent·Most cited

Mapping enzyme catalysis with metabolomic biosensing

L. Xu, K.-C. Chang, E. M. Payne, C. Modavi, L. Liu, C. Palmer, N. Tao, H. S. Alper, R. T. Kennedy, D. S. Cornett, A. R. Abate

The paper introduces a method to sense enzyme product formation using host cell metabolism and mass spectrometry to map enzyme activity and mutagenesis effects.

bioRxiv · Oct 15, 2021 · PreprintBioengineering

TLR7 ligation augments haematopoiesis in Rps14 (uS11) deficiency via paradoxical suppression of inflammatory signalling and enhanced differentiation

O. C. Pena, A. Lubin, J. Rowell, C. A. Hockings, Y. Jung, Y. Hoade, P. Dace, L. E. Valdivia, K. Tuschl, C. Böiers, M. C. Virgilio, S. Richardson, E. M. Payne

This study identifies imiquimod, a TLR7 agonist, as a therapeutic for MDS by enhancing haematopoiesis through paradoxical anti-inflammatory effects and increased differentiation.

bioRxiv · Jul 6, 2020Cancer Biology