Author

N. J. Palpant

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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Cell Biology· 2 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Assay:fluorescence / live-cell microscopy· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

A. Hing· 1 shared A. M. Martinson· 1 shared A. Prowse· 1 shared B. G. Fry· 1 shared C. E. Murry· 1 shared C. Kotapati· 1 shared D. Selvakumar· 1 shared D. Sorensen· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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1 shared paperCell Biology

A. Hing

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3 papers

Recent·Most cited

High-content fluorescence bioassay to investigate pore formation, ion channel modulation and cell membrane lysis induced by venoms

S. Kramer, C. Kotapati, Y. Cao, B. G. Fry, N. J. Palpant, G. F. King, F. C. Cardoso

This paper develops a fluorescence-based high-content assay to identify venom-induced cellular activities like membrane lysis, pore formation, and ion channel modulation across different cell types.

bioRxiv · Oct 25, 2023Pharmacology & Toxicology

Cellular Heterogeneity of Pluripotent Stem Cell Derived Cardiomyocyte Grafts is Mechanistically Linked to Treatable Arrhythmias

D. Selvakumar, Z. E. Clayton, A. Prowse, S. Dingwall, J. George, H. Shah, S. Chen, R. D. Hume, L. Tjahjadi, S. Igoor, R. J. P. Skelton, A. Hing, H. Paterson, S. L. Foster, L. Pearson, , J. J. H. Chong

This study identifies arrhythmogenic subpopulations in pluripotent stem cell-derived cardiomyocytes and shows that combination therapy and catheter ablation can reduce engraftment arrhythmias.

bioRxiv · Sep 15, 2022 · PreprintCell Biology

Evidence for minimal cardiogenic potential of Sca-1 positive cells in the adult mouse heart

L. E. Neidig, F. Weinberger, N. J. Palpant, J. Mignone, A. M. Martinson, D. Sorensen, I. Bender, N. Nemoto, H. Reinecke, L. Pabon, J. D. Molkentin, C. E. Murry, J. van Berlo

This study investigates the cardiogenic potential of Sca-1+ cells in adult mouse hearts and finds minimal contribution to cardiomyocyte regeneration under homeostasis or after myocardial infarction.

bioRxiv · Aug 29, 2018Cell Biology