Author

R. Ferrero

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

Cell Biology· 3 Physiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Assay:bulk RNA-seq· 2 Research Focus:cell-cell communication· 2 Research Focus:differential expression· 2 Organism:mouse· 2 Assay:behavioral assay· 1 Research Focus:cell signaling & trafficking· 1

Frequent Co-Authors

B. Deplancke· 2 shared D. Alpern· 2 shared J. Russeil· 2 shared M. Zachara· 2 shared A. J. Baumler· 1 shared C. Canto· 1 shared C. Lebrilla· 1 shared C. Maisonneuve· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 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

B. Deplancke

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

A human omentum-specific mesothelial-like stromal population inhibits adipogenesis through IGFBP2 secretion

R. Ferrero, P. Rainer, J. Russeil, M. Zachara, J. Pezoldt, G. van Mierlo, V. Gardeux, W. Saelens, D. Alpern, L. Favre, S. Mantziari, T. Zingg, N. Pitteloud, M. Suter, M. Matter, , B. Deplancke

The paper identifies an omental-specific stromal population that inhibits adipogenesis via IGFBP2 secretion in human adipose tissue.

bioRxiv · May 1, 2023Cell Biology

Live imaging of the co-translational recruitment of XBP1 mRNA to the ER and its processing by diffuse, non-polarized IRE1a.

S. Gomez-Puerta, R. Ferrero, T. Hochstoeger, I. Zubiri, J. A. Chao, T. Aragon, F. Voigt

The paper uses live imaging to show XBP1 mRNA is recruited to the ER and processed by IRE1a, without forming large IRE1 clusters.

bioRxiv · Nov 15, 2021Cell Biology

Mammalian adipogenesis regulators (Aregs) exhibit robust non- and anti-adipogenic properties that arise with age and involve retinoic acid signalling

M. Zachara, P. Y. Rainer, J. Russeil, H. Hashimi, D. Alpern, R. Ferrero, M. Litovchenko, B. Deplancke

The paper characterizes CD142+ adipose stem and precursor cells (ASPCs) and shows their non- and anti-adipogenic properties emerge with age via retinoic acid signaling.

bioRxiv · Feb 24, 2021 · PreprintCell Biology

Nod-like receptors are critical for gut-brain axis signaling

M. Pusceddu, M. Barboza, M. Schneider, P. Stokes, J. Sladek, C. Torres Fuentes, L. Goldfild, S. Gillis, I. Brust-Mascher, G. Rabasa, K. Wong, C. Lebrilla, M. Byndloss, C. Maisonneuve, A. J. Baumler, , M. Gareau

This study identifies Nod1 and Nod2 as critical regulators of gut-brain axis signaling, showing their role in stress-induced behavioral and physiological changes.

bioRxiv · May 24, 2019 · PreprintPhysiology