Author

D. Kirrmaier

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· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Assay:CRISPR screen· 1 Approach:genetic perturbation / CRISPR· 1 Organism:mouse· 1

Frequent Co-Authors

M. Knop· 2 shared A. Jäschke· 1 shared B. Buchmuller· 1 shared B. Kurtulmus· 1 shared D. Ibberson· 1 shared D. Kuster· 1 shared G. Nübel· 1 shared G. Pereira· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCell Biology

M. Knop

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2 papers

Recent·Most cited

CRISPR-Cas12a-assisted PCR tagging of mammalian genes

J. Fueller, K. Herbst, M. Meurer, K. Gubicza, B. Kurtulmus, J. D. Knopf, D. Kirrmaier, B. Buchmuller, G. Pereira, M. K. Lemberg, M. Knop

This paper describes a method for efficient endogenous gene tagging in mammalian cells using CRISPR-Cas12a and PCR cassettes, achieving up to 60% tagging efficiency with selection.

Journal of Cell Biology · May 13, 2020Peer-reviewedCell Biology

Extensive 5'-Surveillance Guards Against Non-Canonical NAD-Caps of Nuclear mRNAs in Yeast

Y. Zhang, D. Kuster, T. Schmidt, D. Kirrmaier, G. Nübel, D. Ibberson, V. Benes, H. Hombauer, M. Knop, A. Jäschke

The paper identifies NAD-RNAs in yeast, showing they are abundant, short, and guarded by decapping enzymes, with in vitro evidence of translational rejection.

bioRxiv · Apr 28, 2020Cell Biology