Author

C. J. Clarke

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· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Campbell· 1 shared A. Hilderink· 1 shared A. Kalyuzhnyy· 1 shared A. R. Jones· 1 shared C. E. Eyers· 1 shared C. G. Burd· 1 shared D. Mason· 1 shared D. P. Byrne· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperBiochemistry

A. Campbell

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Author profile →

2 papers

Recent·Most cited

Ca2+-activated sphingomyelin scrambling and turnover mediate ESCRT-independent lysosomal repair

P. Niekamp, T. Sokoya, L. Vittadello, Y. Deng, Y. Kim, A. Hilderink, M. Imlau, C. J. Clarke, C. G. Burd, J. C. M. Holthuis

The paper identifies a Ca2+-activated sphingomyelin scrambling pathway that mediates ESCRT-independent lysosomal repair by converting sphingomyelin into repair intermediates.

bioRxiv · Mar 12, 2021Cell Biology

Use of the Polo-like kinase 4 (PLK4) inhibitor centrinone to investigate intracellular signaling networks using SILAC-based phosphoproteomics

D. P. Byrne, C. J. Clarke, P. Brownridge, A. Kalyuzhnyy, S. Perkins, A. Campbell, D. Mason, A. R. Jones, P. A. Eyers, C. E. Eyers

This study uses centrinone and SILAC-based phosphoproteomics to identify PLK4 substrates and reveal a network of PLK4-regulated phosphorylation motifs in human cells.

bioRxiv · May 22, 2020Biochemistry