Author

I. Ulmert

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

Frequent Co-Authors

K. Lahl· 2 shared V. Bekiaris· 2 shared A. Garcias Lopez· 1 shared A. Schlitzer· 1 shared B. Holzmann· 1 shared B. Malissen· 1 shared B. Schraml· 1 shared D. Baumjohann· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersImmunology

K. Lahl

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genomic deletion of Bcl6 differentially affects conventional dendritic cell subsets and compromises Tfh/Tfr/Th17 cell responses

H. Xiao, I. Ulmert, L. Bach, J. Huber, H. Narasimhan, I. Kurochkin, Y. Chang, S. Holst, U. Moerbe, L. Zhang, A. Schlitzer, F. Pereira, B. Schraml, D. Baumjohann, K. Lahl

bioRxiv · Aug 10, 2022Immunology

The cIAP ubiquitin ligases sustain type 3 γδ T and innate lymphoid cells during aging to allow normal cutaneous and mucosal responses

J. Rizk, U. M. Morbe, R. Agerholm, I. Ulmert, E. C. Tardos, D. Kadekar, M. V. Baglioni, M. T. Vinals, V. Bekiaris

This study shows that cIAP1/2 ubiquitin ligases are essential in early life for maintaining IL-17-producing γδT17 and ILC3 cells, which are critical for immune responses during aging.

bioRxiv · May 14, 2020Immunology

Migration of intestinal dendritic cell subsets upon intrinsic and extrinsic TLR3 stimulation

A. Garcias Lopez, V. Bekiaris, K. Müller Luda, J. Hütter, K. Getachew Muleta, J. Nakawesi, I. Ulmert, K. Kotarsky, B. Malissen, M. O'Keeffe, B. Holzmann, W. W. Agace, K. Lahl

This study shows that cDC1 and cDC2 subsets migrate similarly in response to TLR3 stimulation, but cDC1 requires type I interferon signaling, highlighting distinct pathways in DC subset migration.

bioRxiv · Nov 14, 2019Immunology