Author

F. Faber

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

Microbiology· 3 Biochemistry· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Research Focus:host-pathogen & immune response· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Organism:C. elegans· 1 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

L. Barquist· 2 shared L. Spiga· 2 shared M. Fuchs· 2 shared V. Lamm-Schmidt· 2 shared W. Zhu· 2 shared A. J. Westermann· 1 shared A.-S. Ruttiger· 1 shared C. Behlendorf· 1 shared

Activity by Year

2020-2023 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 26 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 papersMicrobiology

L. Barquist

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

The RNA-binding protein RbpB is a central regulator of polysaccharide utilization in gut Bacteroides

A.-S. Ruttiger, D. Ryan, L. Spiga, V. Lamm-Schmidt, G. Prezza, S. Reichardt, L. Barquist, F. Faber, W. Zhu, A. J. Westermann

This study identifies RbpB as a key RNA-binding protein regulating polysaccharide utilization in gut Bacteroides through post-transcriptional control of PULs.

bioRxiv · Dec 22, 2023 · PreprintMicrobiology

Formation of the pyruvoyl-dependent proline reductase Prd from Clostridioides difficile requires the maturation enzyme PrdH

C. Behlendorf, M. G. Diwo, M. Neumann-Schaal, M. Fuchs, F. Faber, W. Blankenfeldt

This paper identifies PrdH as the maturation enzyme required for the formation of the pyruvoyl group in the proline reductase Prd of C. difficile, essential for proline utilization and toxin production.

bioRxiv · Dec 15, 2023 · PreprintBiochemistry

Byproducts of inflammatory radical metabolism provide transient nutrient niches for microbes in the inflamed gut

L. Spiga, M. G. Winter, M. Muramatsu, V. Rojas, R. Chanin, W. Zhu, E. R. Hughes, S. Taylor, F. Faber, S. Porwollik, T. Carvalho, T. Qin, R. Santos, H. L. Andrews-Polymenis, M. McClelland, S. E. Winter

The paper investigates how inflammatory radicals generate tartaric acid isomers, which serve as transient nutrients for gut pathogens in murine models.

bioRxiv · Dec 8, 2023 · PreprintMicrobiology

An RNA-centric global view of Clostridioides difficile reveals broad activity of Hfq in a clinically important Gram-positive bacterium

M. Fuchs, V. Lamm-Schmidt, F. Ponath, L. Jenniches, L. Barquist, J. Vogel, F. Faber

This study maps the transcriptome of C. difficile and reveals Hfq's role in post-transcriptional regulation through RNA-centric techniques and Hfq RIP-seq.

bioRxiv · Aug 10, 2020Microbiology