Author

K. Apelt

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:chromatin & epigenetic regulation· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1

Frequent Co-Authors

D. van den Heuvel· 2 shared M. S. Luijsterburg· 2 shared A. C. O. Vertegaal· 1 shared A. Kragten· 1 shared C. G. Spruijt· 1 shared D. Y. Gout· 1 shared D. Zhou· 1 shared H. Wu· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersCell Biology

D. van den Heuvel

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

A CSB-PAF1C axis restores processive transcription elongation after DNA damage repair

D. van den Heuvel, C. G. Spruijt, R. Gonzalez-Prieto, A. Kragten, M. T. Paulsen, D. Zhou, H. Wu, K. Apelt, Y. van der Weegen, K. Yang, M. Dijk, L. Daxinger, J. A. Marteijn, A. C. O. Vertegaal, M. Ljungman, , M. S. Luijsterburg

This study identifies a PAF1C-dependent pathway that restores transcription elongation after DNA damage repair in human cells.

bioRxiv · Jan 4, 2020Cell Biology

Human HMGN1 and HMGN2 are not required for transcription-coupled DNA repair

K. Apelt, I. Zoutendijk, D. Y. Gout, D. van den Heuvel, M. S. Luijsterburg

This study shows that HMGN1 and HMGN2 are not required for human transcription-coupled DNA repair, as their knockout or knockdown does not impair UV or Illudin S-induced lesion repair.

bioRxiv · Nov 9, 2019Cell Biology