Author

E. Mass

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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Immunology· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

A. Pfeifer· 1 shared A. Schlitzer· 1 shared A.-K. Weier· 1 shared C. K. Glass· 1 shared C. Klausen· 1 shared C. Osei-Sarpong· 1 shared C. Ruiz de Almodovar· 1 shared C. Thiele· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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1 shared paperImmunology

A. Pfeifer

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BBSome-dependent ciliary Hedgehog signaling governs cell fate in the white adipose tissue

K. Sieckmann, N. Winnerling, D. J. Silva Ribeiro, R. Kardinal, L. M. Steinheuer, G. Schermann, C. Klausen, N. Blank-Stein, J. Schulte-Schrepping, C. Osei-Sarpong, M. Becker, L. Bonaguro, M. Beyer, K. Thurley, H. May-Simera, , D. Wachten

This study shows that primary cilia dysfunction in Bbs8-/- mice reduces adipose stem cells and promotes fibrogenic progenitors via disrupted Hedgehog signaling, affecting adipogenesis and lipid uptake.

bioRxiv · Jan 25, 2024 · PreprintCell Biology

GPR183 targets lung-resident CD301b+ conventional dendritic cells type 2 to a subtissular TSLP-TSLP receptor-mediated survival niche within the adventitial cuff

L. Zhang, J. Yu, S. Spath, S. Sheoran, D. Bejarano, M. Vandestienne, A.-K. Weier, T. Quast, M. Ibrahim, S. Reimer, S. Uderhardt, E. Mass, J. Hasenauer, A. Pfeifer, E. Kiermaier, , A. Schlitzer

This study identifies GPR183 as a key receptor guiding CD301b+ cDC2 to a TSLP-dependent survival niche in the lung adventitial cuff.

bioRxiv · Aug 28, 2022 · PreprintImmunology

Diet-regulated production of PDGFcc by macrophages controls energy storage

N. Cox, L. Crozet, I. R. Holtman, P.-L. Loyher, T. Lazarov, E. Mass, R. Stanley, C. K. Glass, F. Geissmann

The paper identifies PDGFcc as a diet-regulated macrophage factor that controls energy storage in mammals by acting on adipocytes, independent of inflammation and insulin resistance.

bioRxiv · Jun 15, 2020Immunology