Author

F. Hager

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· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Organism:bacteria (other)· 1 Research Focus:cell signaling & trafficking· 1 Approach:experimental assay· 1 Assay:fluorescence / live-cell microscopy· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Approach:microscopy & imaging analysis· 1

Frequent Co-Authors

A. Kemmler· 1 shared B. Rieger· 1 shared C. P. Richter· 1 shared D. Fischer· 1 shared I. I. Oberheim· 1 shared K. B. Busch· 1 shared K. M. Thormann· 1 shared K. Psathaki· 1 shared

Activity by Year

2018-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperMicrobiology

A. Kemmler

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Author profile →

2 papers

Recent·Most cited

Identifying the components of the Shewanella phage LambdaSo lysis system

S. W. Thöneböhn, D. Fischer, V. Kreiling, A. Kemmler, I. I. Oberheim, F. Hager, N. E. Schmid, K. M. Thormann

The paper identifies four protein factors required for LambdaSo phage-induced lysis in Shewanella oneidensis, including a pinholin/SAR-endolysin system and a previously unknown transmembrane protein Lcc6.

bioRxiv · Jan 23, 2024 · PreprintMicrobiology

F1FO ATP synthase responds to glycolysis inhibition by localization into the inner boundary membrane

K. Zalyevskiy, B. Rieger, F. Hager, C. P. Richter, K. Psathaki, T. Appelhans, K. B. Busch

This study shows that mitochondrial F1F0 ATP synthase relocates from cristae to the inner boundary membrane when glycolysis is inhibited, indicating dynamic spatial organization.

bioRxiv · Jul 23, 2018 · PreprintCell Biology