Author

S. Herzog

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 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Approach:genetic perturbation / CRISPR· 1 Organism:mouse· 1

Frequent Co-Authors

A. Villunger· 2 shared A. Mattivi· 1 shared B. C. Bornhauser· 1 shared C. Soratroi· 1 shared D. Rizzotto· 1 shared E. D. Jacotot· 1 shared F. Bellutti· 1 shared F. Gallob· 1 shared

Activity by Year

2022-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersCell Biology

A. Villunger

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Caspase-2 kills cells with extra centrosomes

D. Rizzotto, V. Vigorito, P. Rieder, F. Gallob, G. M. Moretta, C. Soratroi, J. Riley, F. Bellutti, S. Li Veli, A. Mattivi, M. Lohmueller, S. Herzog, B. C. Bornhauser, E. D. Jacotot, A. Villunger, L. L. Fava

The paper shows that caspase-2 triggers apoptosis in cells with extra centrosomes, preventing polyploidization through mitochondrial pathways.

bioRxiv · Feb 13, 2024Cell Biology

A CRISPR-screen in intestinal epithelial cells identifies novel factors for polarity and apical transport

K. M. Klee, M. W. Hess, M. Lohmüller, S. Herzog, K. Pfaller, T. Müller, G. F. Vogel, L. A. Huber

The paper identifies novel factors for epithelial polarization and apical transport using a CRISPR screen in human intestinal epithelial cells.

bioRxiv · May 16, 2022Cell Biology

The miR-15a/16-1 and miR-15b/16-2 clusters regulate early B cell development by limiting IL-7 receptor expression

K. Hutter, S. Herzog, A. Villunger, T. Rülicke, L. Andersen, T. Szabo

This study shows that miR-15a/16-1 and miR-15b/16-2 clusters regulate early B cell development by limiting IL-7 receptor expression, leading to increased pro-B cell proliferation.

bioRxiv · Mar 18, 2022Immunology