Author

M. Stirm

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· 1 Pathology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:plant (other)· 3 Research Focus:cell type annotation· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell-cell communication· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1

Frequent Co-Authors

A. Baehr· 3 shared B. Shashikadze· 3 shared C. Kupatt· 3 shared E. Wolf· 3 shared N. Klymiuk· 3 shared A. Moretti· 2 shared H. Blum· 2 shared S. Krebs· 2 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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3 shared papersPhysiology

A. Baehr

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Gene Therapy for Cardiomyopathy associated with Duchenne Muscular Dystrophy in a Pig Model

A. Baehr, P. Hoppmann, T. Bozoglu, M. Stirm, I. Luksch, T. Ziegler, N. Hornaschewitz, S. Shresta, B. Shashikadze, J. B. Stöckl, N. Raad, H. Blum, S. Krebs, T. Fröhlich, C. Baumgartner, , C. Kupatt

This study shows that AAV1.SERCA2a gene therapy improves heart function and reduces arrhythmia in a pig model of Duchenne muscular dystrophy.

bioRxiv · Oct 2, 2023 · PreprintPhysiology

Increased pulmonary monocyte infiltration and attenuated phagocytosis defines perinatal dysfunction of innate immunity in Cystic Fibrosis

F. Jaudas, F. Bartenschlager, B. Shashikadze, G. Santamaria, A. Schnell, N. Naumann-Barsch, H. Bruns, S. Y. Graeber, A. Baehr, M. Cambra-Bort, M. Stirm, J. B. Stoeckl, S. Krebs, H. Blum, C. Schulz, , N. Klymiuk

The paper identifies increased monocyte infiltration and reduced phagocytosis in CF lungs at birth, suggesting innate immune dysfunction and the need for early treatment.

bioRxiv · Sep 11, 2023 · PreprintImmunology

A scalable, clinically severe pig model for Duchenne muscular dystrophy

M. Stirm, L. M. Fonteyne, B. Shashikadze, M. Lindner, M. Chirivi, A. Lange, C. Kaufhold, C. Mayer, I. Medugorac, B. Kessler, M. Kurome, V. Zakhartchenko, A. Hinrichs, E. Kemter, S. Krause, , E. Wolf

This paper develops a scalable pig model for Duchenne muscular dystrophy by breeding DMD carriers, enabling large cohorts for disease mechanism studies and therapeutic testing.

Disease Models & Mechanisms · Dec 1, 2021Peer-reviewedPathology