Author

J. J. Sandow

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Cell Biology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Assay:proteomics· 3 Research Focus:cell signaling & trafficking· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

A. I. Webb· 3 shared A. J. M. Kueh· 1 shared D. Chau· 1 shared D. De Bellis· 1 shared D. M. Leslie Pedrioli· 1 shared E. Morrish· 1 shared G. Infusini· 1 shared J. M. Murphy· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersCell Biology

A. I. Webb

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Simplified high-throughput methods for deep proteome analysis on the timsTOF Pro

J. J. Sandow, G. Infusini, L. Dagley, R. Larsen, A. I. Webb

The paper describes simplified high-throughput methods for deep proteome analysis using the timsTOF Pro instrument, achieving high protein identifications with short separation gradients.

bioRxiv · Apr 7, 2021 · PreprintBiochemistry

Tankyrase-mediated ADP-ribosylation is a novel regulator of TNF-induced death

L. Liu, J. J. Sandow, D. M. Leslie Pedrioli, N. Silke, Z. Hu, E. Morrish, D. Chau, T. Kratina, A. J. M. Kueh, M. O. Hottiger, A. I. Webb, N. Lalaoui, J. Silke

This study identifies tankyrase-mediated ADP-ribosylation as a regulator of TNF-induced cell death by promoting complex 2 assembly and interacting with RNF146.

bioRxiv · Feb 9, 2021Cell Biology

Phosphorylation by Aurora B kinase regulates caspase-2 activity and function

S. Kumar, Y. Lim, D. De Bellis, J. J. Sandow, L. Capalbo, P. P. D'Avino, J. M. Murphy, A. I. Webb, L. Dorstyn

This study identifies Aurora B kinase-mediated phosphorylation of caspase-2 at S384, which inhibits its catalytic activity and apoptosis function during mitotic catastrophe.

bioRxiv · Mar 5, 2020Cell Biology