Author

V. Hilsenstein

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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Biochemistry· 1 Cell Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Assay:fluorescence / live-cell microscopy· 1 Assay:imaging· 1

Frequent Co-Authors

A. Eisenbarth· 1 shared A. M. Steyer· 1 shared A. Neild· 1 shared A. Oddo· 1 shared A. Schulze· 1 shared B. Neumann· 1 shared C. A. Hernandez· 1 shared C. Tischer· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperBiochemistry

A. Eisenbarth

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Spatial single-cell isotope tracing reveals heterogeneity of de novo fatty acid synthesis in cancer cells

E. Buglakova, M. Ekelöf, M. Schwaiger-Haber, L. Schlicker, M. R. Molenaar, S. Mohammed, L. Stuart, A. Eisenbarth, V. Hilsenstein, G. Patti, A. Schulze, M. Snaebjornsson, T. Alexandrov

This paper introduces 13C-SpaceM, a method for spatial single-cell isotope tracing of de novo fatty acid synthesis in cancer cells, revealing metabolic heterogeneity in liver and glioma tissues.

bioRxiv · Aug 18, 2023 · PreprintBiochemistry

CLEMSite, a software for automated phenotypic screens using light microscopy and FIB-SEM

J. M. Serra Lleti, A. M. Steyer, N. L. Schieber, B. Neumann, C. Tischer, V. Hilsenstein, M. Holtstrom, D. Unrau, R. Kirmse, J. M. Lucocq, R. Pepperkok, Y. Schwab

The paper introduces CLEMSite, a software tool for automated phenotypic screens using light microscopy and FIB-SEM, enabling high-throughput volume acquisition with reduced operator supervision.

bioRxiv · Mar 19, 2021Cell Biology

Bacteriophage uptake by Eukaryotic cell layers represents a major sink for phages during therapy

M. C. Bichet, W. H. Chin, W. Richards, Y.-W. Lin, L. Avellaneda-Franco, C. A. Hernandez, A. Oddo, O. Chernyavskiy, V. Hilsenstein, A. Neild, J. C. Li, N. H. Voelcker, R. Patwa, J. J. Barr

The paper shows that eukaryotic cells internalize phages, with smaller phages being taken up more efficiently, and demonstrates this impacts phage distribution and therapy efficacy.

bioRxiv · Sep 7, 2020Microbiology