Author

Sabine Gärtner

German Primate Center

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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Microbiology· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Organism:non-human primate· 1 Assay:proteomics· 1

Frequent Co-Authors

Michael WinkleriD· 3 shared Stefan PöhlmanniD· 3 shared Markus HoffmanniD· 2 shared Pamela Stomberg· 2 shared Amy Madeleine Kempf· 1 shared Anke WerneriD· 1 shared Eva Böttcher‐FriebertshäuseriD· 1 shared Friedemann WeberiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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3 shared papersMicrobiology

Michael WinklerORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Development of immortalized Callithrix jacchus kidney cell lines supporting infection with a panel of viruses

Sabine Gärtner, Pamela Stomberg, Stefan Pöhlmann, Michael Winkler

The paper develops and characterizes three immortalized kidney cell lines from common marmosets that support infection with multiple viruses, including Zika and Herpes simplex virus 1.

PLoS ONE · Mar 2, 2026Peer-reviewedMicrobiology

Proteolytic processing of the Marburg virus glycoprotein depends on Sec616β and is required for cell entry

Katharina E. Decker, Anke Werner, Markus Hoffmann, Heike Hofmann-Winkler, Qi-Yin Chen, Lu Zhang, Pamela Stomberg, Sabine Gärtner, Amy Madeleine Kempf, Inga Nehlmeier, Hendrik Luesch, Torsten Steinmetzer, Eva Böttcher‐Friebertshäuser, Nabil Georges Seidah, Stefan Pöhlmann, Michael Winkler

This paper identifies Sec61β as essential for proteolytic processing and cell entry of Marburg virus glycoprotein, unlike Ebola virus, and suggests Sec61 as a therapeutic target.

bioRxiv · Jun 26, 2025 · PreprintMicrobiology

Interferon induction and not replication interference mainly determines anti-influenza virus activity of defective interfering particles

Prerna Arora, Najat Bdeir, Sabine Gärtner, Stefanie Reiter, Lars Pelz, Ulrike Felgenhauer, Udo Reichl, Stephan Ludwig, Friedemann Weber, Markus Hoffmann, Michael Winkler, Stefan Pöhlmann

This study shows that defective interfering particles (DIPs) primarily exert antiviral activity through interferon (IFN) system activation rather than suppression of viral replication.

bioRxiv · Sep 20, 2021 · PreprintMolecular Biology