Author

J. D. F. Licchesi

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

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Research Focus:cell signaling & trafficking· 2 Approach:experimental assay· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

N. Scholz· 2 shared C. Lindon· 1 shared F. A. Siebzehnrubl· 1 shared N. Vaughan· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

4 top collaborators · 4 mutual co-author links

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2 shared papersCell Biology

N. Scholz

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintFeb 17, 2023

HECTD1 is both a positive regulator and substrate of caspase-3 activity during apoptotic cell death

N. Scholz, F. A. Siebzehnrubl, J. D. F. Licchesi

This study identifies HECTD1 as a caspase-3 substrate during apoptosis, showing cleavage does not affect its HECT domain function and suggests a feedback loop between caspase-3 and HECTD1.

DOI 10.1101/2023.02.17.528998

experimental assaycell signaling & trafficking

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Cell BiologybioRxivPreprintDec 17, 2021

The E3 ubiquitin ligase HECTD1 contributes to cell cycle progression through an effect on mitosis

N. Vaughan, N. Scholz, C. Lindon, J. D. F. Licchesi

This study shows that HECTD1 ubiquitin ligase activity promotes cell cycle progression through its role in mitosis by affecting chromosome alignment and spindle assembly checkpoint activity.

DOI 10.1101/2021.12.17.473173

humanproteomics

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