Author

J. J. Skalicky

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· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Research Focus:cell signaling & trafficking· 2 Research Focus:cell type annotation· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

D. R. Mackay· 2 shared E. L. Paine· 2 shared K. S. Ullman· 2 shared W. I. Sundquist· 2 shared B. J. Graves· 1 shared B. J. Madison· 1 shared C. P. Hill· 1 shared D. K. W. Lau· 1 shared

Activity by Year

2017-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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2 shared papersBiochemistry

D. R. Mackay

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3 papers

Recent·Most cited

The Calpain-7 protease functions together with the ESCRT-III protein IST1 within the midbody to regulate the timing and completion of abscission

E. L. Paine, J. J. Skalicky, F. G. Whitby, D. R. Mackay, K. S. Ullman, C. P. Hill, W. I. Sundquist

This study shows that CAPN7 interacts with IST1 at midbodies to regulate abscission and the NoCut checkpoint through proteolytic activity.

bioRxiv · Oct 18, 2022Biochemistry

Comprehensive analysis of the human ESCRT-III-MIT domain interactome reveals new cofactors for cytokinetic abscission

D. M. Wenzel, D. R. Mackay, J. J. Skalicky, E. L. Paine, M. S. Miller, K. S. Ullman, W. I. Sundquist

This study maps the human MIT-ESCRT-III interactome, identifies new cofactors for cytokinetic abscission, and reveals their functional roles in abscission and regulation.

bioRxiv · Feb 9, 2022Biochemistry

ETV4 And AP1 Transcription Factors Form Multivalent Interactions With Three Sites On The MED25 Activator-Interacting Domain

S. L. Currie, J. J. Doane, K. S. Evans, N. Bhachech, B. J. Madison, D. K. W. Lau, L. P. McIntosh, J. J. Skalicky, K. A. Clark, B. J. Graves

This study identifies multivalent interactions between ETV4, AP1 factors, and MED25, showing how these interactions enhance transcriptional regulation and are relevant in prostate cancer.

bioRxiv · Apr 11, 2017Biochemistry