Author

B. Kammerer

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Biochemistry· 1 Cancer Biology· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 3 Organism:human· 3 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:metabolism & bioenergetics· 1 Assay:metabolomics· 1 Organism:mouse· 1

Frequent Co-Authors

S. Lagies· 2 shared A. Brandel· 1 shared A. Izzo· 1 shared A. Lehmann· 1 shared A. P. Masilamani· 1 shared A. Saiardi· 1 shared A. V. Melendez· 1 shared A. Wasilenko· 1 shared

Activity by Year

2020-2020 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersCell Biology

S. Lagies

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Analysis of Inositol Phosphate Metabolism by Capillary Electrophoresis Electrospray Ionization Mass Spectrometry (CE-ESI-MS)

D. Qiu, M. S. Wilson, V. B. Eisenbeis, R. Harmel, E. Riemer, T. M. Haas, C. Wittwer, N. Jork, C. Gu, S. B. Shears, G. Schaaf, B. Kammerer, D. Fiedler, A. Saiardi, H. J. Jessen

This paper develops a CE-ESI-MS method to analyze inositol phosphates and pyrophosphates, revealing unknown synthesis pathways in mammals.

bioRxiv · Aug 27, 2020Biochemistry

The Gb3-enriched CD59/flotillin plasma membrane domain regulates host cell invasion by Pseudomonas aeruginosa

A. Brandel, S. Aigal, S. Lagies, M. Schlimpert, A. Lehmann, D. Hummel, D. Fisch, A. V. Melendez, J. Madl, T. Eierhoff, B. Kammerer, W. Roemer

This study identifies CD59 and flotillins as key host proteins interacting with Pseudomonas aeruginosa's LecA, essential for bacterial invasion via a Gb3-enriched plasma membrane domain.

bioRxiv · Jun 26, 2020Cell Biology

ZBTB18 inhibits SREBP-dependent fatty acid synthesis by counteracting CTBPs and KDM1A/LSD1 activity in glioblastoma

R. Ferrarese, A. Izzo, G. Andrieux, S. Lagies, J. P. Bartmuss, A. P. Masilamani, A. Wasilenko, D. Osti, S. Faletti, R. Schulzki, S. Yuan, E. Kling, V. Ribecco, H. D. Heiland, S. G. Tholen, , M. S. Carro

This study identifies ZBTB18 as a regulator of SREBP gene expression in glioblastoma by modulating CTBP and LSD1 activity, leading to epigenetic repression of fatty acid synthesis.

bioRxiv · Apr 17, 2020 · PreprintCancer Biology