Author

M. L. Richter

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· 1 Immunology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

M. Colome-Tatche· 2 shared A. U. Antonova· 1 shared B. U. Schraml· 1 shared C. P. Martinez-Jimenez· 1 shared C. Romagnani· 1 shared C. Stehle· 1 shared D. Dudziak· 1 shared E. Sanchez-Quant· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 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 papersImmunology

M. Colome-Tatche

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Cross-species analyses reveal RORγt-expressing dendritic cells are a lineage of antigen presenting cells conserved across tissues

H. Narasimhan, M. L. Richter, R. Shakiba, N. E. Papaioannou, C. Stehle, K. Ravi Rengarajan, I. Ulmert, V. Küntzel, E.-L. Stange, A. U. Antonova, L. Klein, D. Dudziak, M. Colonna, N. Torow, M. W. Hornef, , B. U. Schraml

The paper identifies RORγt-expressing dendritic cells as a distinct APC lineage conserved across tissues and species, with functions beyond promoting tolerance.

bioRxiv · May 6, 2024Immunology

Single-cell metabolic profiling reveals subgroups of primary human hepatocytes showing heterogeneous responses to drug challenge.

E. Sanchez-Quant, M. L. Richter, M. Colome-Tatche, C. P. Martinez-Jimenez

The paper profiles metabolic responses of primary human hepatocytes to drug challenge and fatty acid accumulation, revealing four subgroups with distinct transcriptional responses.

bioRxiv · Jun 8, 2022 · PreprintCell Biology