Author

M. Simic

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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Cell Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

A. Dillin· 1 shared C. Siret· 1 shared D. Hockemeyer· 1 shared D. Jullie· 1 shared E. Moehle· 1 shared F. Lorbeer· 1 shared J. Halloran· 1 shared K. Heydari· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperCell Biology

A. Dillin

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2 papers

Recent·Most cited

Brain endothelial CXCL12 attracts protective Natural Killer cells during ischemic stroke

S. Wang, L. de Fabritus, P. Ashok Kumar, Y. Werner, C. Siret, M. Simic, Y. M. Kerdiles, R. Stumm, S. A. van de Pavert

The paper identifies that CXCL12 at the blood-brain barrier attracts NK cells and ILCs to ischemic brain lesions, improving outcomes after stroke.

bioRxiv · Feb 18, 2021 · PreprintImmunology

Transient activation of the UPRER is an essential step in the acquisition of pluripotency during reprogramming

M. Simic, E. Moehle, R. Schinzel, F. Lorbeer, D. Jullie, J. Halloran, K. Heydari, M. Sanchez, D. Hockemeyer, A. Dillin

This study shows that transient activation of the UPRER is essential for successful reprogramming of somatic cells into pluripotency and can predict reprogramming efficiency.

bioRxiv · Nov 17, 2018Cell Biology