Author

M. Gotthardt

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· 4

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 4 Approach:experimental assay· 3 Research Focus:cell-cell communication· 2 Research Focus:development & morphogenesis· 2 Organism:human· 2 Assay:imaging· 2 Organism:mouse· 2 Assay:proteomics· 2

Frequent Co-Authors

C. Fink· 1 shared C. H. Vieira-Vieira· 1 shared C. Matthaeus· 1 shared C. Zhu· 1 shared D. Friedrich· 1 shared E. Wagner· 1 shared F. G. Rathjen· 1 shared F. Rudolph· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperCell Biology

C. Fink

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Author profile →

4 papers

Recent·Most cited

Visualizing sarcomere and cellular dynamics in skeletal muscle to improve cell therapies

J. Hüttemeister, F. Rudolph, M. Radke, C. Fink, D. Friedrich, S. Preibisch, M. Falcke, E. Wagner, S. E. Lehnart, M. Gotthardt

This study uses mCherry-titin mice to visualize sarcomere dynamics during skeletal muscle development and injury repair, revealing titin mobility and localization patterns in myocytes.

bioRxiv · Feb 1, 2024 · PreprintCell Biology

The IgCAM CAR regulates gap junction mediated coupling on embryonic cardiomyocytes and affects their beating frequency

C. Matthaeus, R. Juettner, M. Gotthardt, F. G. Rathjen

The study shows CAR regulates Cx43 clustering in embryonic cardiomyocytes, affecting gap junction coupling and beating frequency.

bioRxiv · Nov 2, 2022Cell Biology

Proteome-wide quantitative RNA interactome capture (qRIC) identifies phosphorylation sites with regulatory potential in RBM20

C. H. Vieira-Vieira, V. Dauksaite, M. Gotthardt, M. Selbach

The paper introduces qRIC to quantify RNA-binding protein-mRNA interactions and identifies phosphorylation sites in RBPs that regulate their function.

bioRxiv · Jul 12, 2021Cell Biology

RBM20 phosphorylation on serine/arginine domain is crucial to regulate pre-mRNA splicing and protein shuttling in the heart

M. Sun, Y. Jin, C. Zhu, Y. Zhang, M. Liss, M. Gotthardt, J. Ren, Y. Ge, W. Guo

This study identifies phosphorylated residues in RBM20, showing their role in splicing control and protein shuttling, and links their mutation to cardiac dysfunction.

bioRxiv · Sep 15, 2020 · PreprintCell Biology