Author

M. Lisby

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 Biochemistry· 1 Biophysics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 6 Research Focus:cell signaling & trafficking· 5 Research Focus:chromatin & epigenetic regulation· 4 Research Focus:cancer & tumor microenvironment· 3 Research Focus:development & morphogenesis· 2 Approach:genetic perturbation / CRISPR· 2 Organism:human· 2 Assay:proteomics· 2

Frequent Co-Authors

J. Nilsson· 2 shared V. H. Oestergaard· 2 shared A. Chen· 1 shared A. Kettenbach· 1 shared B. Ferlez· 1 shared B. Lopez Mendez· 1 shared B. Pfander· 1 shared B. Qin· 1 shared

Activity by Year

2020-2022 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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2 shared papersCell Biology

J. Nilsson

Mutual co-authors in cluster

Author profile →

6 papers

Recent·Most cited

Rdh54 stabilizes Rad51 at displacement loop intermediates to regulate genetic exchange between chromosomes

M. Keymakh, J. Dau, B. Ferlez, M. Lisby, J. B. Crickard

This study identifies Rdh54's role in stabilizing Rad51 at displacement loops to regulate genetic exchange during homologous recombination.

bioRxiv · May 19, 2022Biochemistry

Spatiotemporal transcriptomic atlas of mouse organogenesis using DNA nanoball patterned arrays

A. Chen, S. Liao, M. Cheng, K. Ma, L. Wu, Y. Lai, X. Qiu, J. Yang, W. Li, J. Xu, S. Hao, X. Wang, H. Lu, X. Chen, X. Liu, , J. Wang

This study develops Stereo-seq, a high-resolution spatial transcriptomic method, to analyze mouse organogenesis and map developmental disease loci.

Cell · May 1, 2022Peer-reviewedCell Biology

A conserved PLK1 docking site in TopBP1 maintains genome integrity during mitosis

J. Li, J. V. Bagge, M. Lisby, J. Nilsson, V. H. Oestergaard

This study identifies a conserved PLK1 docking site in TopBP1 that is essential for maintaining genome integrity during mitosis, as its deletion increases DNA damage and mitotic errors.

bioRxiv · Mar 30, 2022 · PreprintCell Biology

Cdc48 targets INQ-localized Mrc1 to facilitate recovery from replication stress

C. Colding, J. Autzen, B. Pfander, M. Lisby

The paper shows that Cdc48 helps release Mrc1 from the INQ compartment during recovery from replication stress, facilitating replication restart.

bioRxiv · Sep 16, 2021 · PreprintCell Biology

A complex of BRCA2 and PP2A-B56 is required for DNA repair by homologous recombination

S. M. Ambjoern, J. P. Duxin, E. P. Hertz, I. Nasa, J. Duro, T. Kruse, B. Lopez Mendez, B. Rymarczyk, L. E. Cressey, T. Hansen, A. Kettenbach, V. H. Oestergaard, M. Lisby, J. Nilsson

This study identifies the BRCA2-PP2A-B56 complex as essential for efficient DNA repair by homologous recombination and shows that cancer mutations disrupt this interaction, increasing sensitivity to PARP inhibition.

bioRxiv · Apr 10, 2021Cell Biology

Rad51 paralog complex Rad55-Rad57 acts as a molecular chaperone during homologous recombination

U. Roy, Y. Kwon, L. Marie, L. Symington, P. Sung, M. Lisby, E. C. Greene

This study shows Rad55-Rad57 acts as a molecular chaperone in HR by facilitating Rad51 filament reassembly after Srs2 disruption.

bioRxiv · Nov 4, 2020Biophysics