Author

S. Friis

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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Biophysics· 2 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:drug response / drug discovery· 2 Assay:electrophysiology· 2 Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:differential expression· 1

Frequent Co-Authors

S. A. Pless· 2 shared A. Sinz· 1 shared A. W. Purcell· 1 shared B. Rono· 1 shared C. Garde· 1 shared C. Ihling· 1 shared D. Kleine-Kohlbrecher· 1 shared E. J. Lange· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersBiophysics

S. A. Pless

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Endogenous viral elements constitute a complementary source of antigens for personalized cancer vaccines

C. Garde, M. A. Pavlidis, P. Garces, E. J. Lange, S. H. Ramarathinam, M. Sokac, K. Pandey, P. Faridi, J. Ahrenfeldt, S. Chung, S. Friis, D. Kleine-Kohlbrecher, N. J. Birkbak, J. V. Kringelum, B. Rono, , T. Trolle

This paper identifies endogenous viral elements as a new source of antigens for personalized cancer vaccines and introduces a computational pipeline to predict and test their therapeutic potential.

bioRxiv · Mar 23, 2023Cancer Biology

The M1 and pre-M1 segments contribute differently to ion selectivity in ASICs and ENaCs

Z. P. Sheikh, M. Wulf, S. Friis, M. Althaus, T. Lynagh, S. A. Pless

This study shows that the pre-M1 and M1 regions of ASICs and ENaCs differentially contribute to ion selectivity through structural and functional analyses.

bioRxiv · Feb 16, 2021Biophysics

High-throughput characterization of photocrosslinker-bearing ion channel variants to map residues critical for function and pharmacology

N. Braun, S. Friis, C. Ihling, A. Sinz, J. Andersen, S. A. Pless

The paper develops a high-throughput method to study functional and pharmacological properties of ncAA-containing hASIC1a variants using automated patch-clamp.

bioRxiv · Nov 24, 2020Biophysics