Author

E. Ambrosetti

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· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:imaging· 1 Organism:mouse· 1 Research Focus:spatial domain detection· 1

Frequent Co-Authors

A. I. Teixeira· 2 shared B. Hogberg· 1 shared B. M. Hällberg· 1 shared E. Petrova· 1 shared G. Bernardinelli· 1 shared G. Kiriako· 1 shared I. Andre· 1 shared I. T. Hoffecker· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersBioengineering

A. I. Teixeira

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Engineering multivalent Fc display for FcγR blockade

E. Petrova, G. Kiriako, J. Rebetz, K. Johansson, S. Wennmalm, N. E. J. Meijer, B. M. Hällberg, I. Andre, E. Ambrosetti, J. W. Semple, A. I. Teixeira

This study engineers multivalent Fc-displaying virus-like particles to block FcγR activation, showing that higher valency reduces receptor activation and enhances inhibition of immune complex-mediated phagocytosis.

bioRxiv · Jan 20, 2024 · PreprintBioengineering

A DNA nanoassembly-based approach to map membrane protein nanoenvironments

E. Ambrosetti, G. Bernardinelli, I. T. Hoffecker, L. Hartmanis, R. Sandberg, B. Hogberg, A. I. Teixeira

The paper introduces NanoDeep, a DNA nanoassembly-based method to map membrane protein nanoenvironments, revealing similar occupancy patterns of Her2, Her3, and EGFR in different cell lines and changes upon Heregulin-{beta}1 treatment.

bioRxiv · Nov 8, 2019Bioengineering