Author

C. K. Damgaard

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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Biochemistry· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:protein folding & dynamics· 1 Assay:proteomics· 1 Assay:Ribo-seq· 1

Frequent Co-Authors

A. K. Hollensen· 2 shared A. J. Berman· 1 shared A. Ruggieri· 1 shared A.-D. Yang· 1 shared B. D. Fonseca· 1 shared C. Dajadian· 1 shared C. Mongis· 1 shared D. Lindner· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersBiochemistry

A. K. Hollensen

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Author profile →

2 papers

Recent·Most cited

CDK1 couples proliferation with protein synthesis

K. Haneke, J. Schott, D. Lindner, A. K. Hollensen, C. K. Damgaard, C. Mongis, M. Knop, W. Palm, A. Ruggieri, G. Stoecklin

This study identifies CDK1 as a regulator of translation that couples cell proliferation with protein synthesis by modulating 5TOP mRNA translation through LARP1.

bioRxiv · Oct 24, 2019Biochemistry

LARP1 is a major phosphorylation substrate of mTORC1

B. D. Fonseca, J.-J. Jia, A. K. Hollensen, R. Pointet, H.-D. Hoang, M. R. Niklaus, I. A. Pena, R. M. Lahr, E. M. Smith, J. Hearnden, X.-D. Wang, A.-D. Yang, G. Celucci, T. E. Graber, C. Dajadian, , T. Alain

This study identifies LARP1 as a major phosphorylation substrate of mTORC1 and elucidates its role in regulating TOP mRNA translation.

bioRxiv · Dec 8, 2018 · PreprintBiochemistry