Author

N. Divecha

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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Cancer Biology· 2 Cell Biology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Organism:human· 4 Assay:proteomics· 4 Research Focus:cell signaling & trafficking· 3 Research Focus:cancer & tumor microenvironment· 2 Research Focus:cell type annotation· 2 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

B. Sheth· 2 shared P. Skipp· 2 shared R. M. Ewing· 2 shared Y. Wang· 2 shared A. A. Mironov· 1 shared A. Ferrari· 1 shared A. Ghisleni· 1 shared A. Lester· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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Curved chords = mutual co-authorship

2 shared papersMicrobiology

B. Sheth

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Mechanisms of SARS-CoV-2 Inactivation using UVC Laser Radiation

G. Devitt, P. B. Johnson, N. Hanrahan, S. I. R. Lane, M. C. Vidale, B. Sheth, J. D. Allen, M. V. Humbert, C. M. Spalluto, R. C. Herve, K. Staples, J. West, R. Forster, N. Divecha, C. J. McCormick, , S. Mahajan

This study investigates the inactivation of SARS-CoV-2 using UVC laser radiation and identifies mechanisms involving RNA damage and disruption of spike protein function.

bioRxiv · Feb 3, 2023Microbiology

PIP4K2B is a mechanosensor and induces heterochromatin-driven nuclear softening through UHRF1.

A. Poli, F. A. Pennacchio, P. Nastaly, A. Ghisleni, M. Crestani, F. M. Pramotton, F. Iannelli, G. Beznusenko, A. A. Mironov, V. Panzetta, S. Fusco, B. Sheth, N. Paolo, D. Poulikakos, A. Ferrari, , P. Maiuri

The paper identifies PIP4K2B as a mechanosensor that induces nuclear softening via UHRF1, affecting YAP activity and cell motility in cancer.

bioRxiv · Mar 25, 2022 · PreprintCell Biology

Proteomic characterization of GSK3β knockout shows altered cell adhesion and metabolic pathway utilisation in colorectal cancer cells

E. Bowler-Barnett, F. Martinez-Garcia, M. Sherwood, S. Weston, Y. Wang, N. Divecha, P. Skipp, R. M. Ewing

This study uses proteomic analysis of GSK3β knockout colorectal cancer cells to identify altered cell adhesion and metabolic pathways.

bioRxiv · Jan 26, 2021 · PreprintCancer Biology

Deep proteomic analysis of Dnmt1 mutant/hypomorphic colorectal cancer cells reveals dys-regulation of Epithelial-Mesenchymal Transition and subcellular re-localization of Beta-Catenin

E. Bowler, A. Smith-Vidal, A. Lester, J. Bell, Z. Wang, C. Bell, Y. Wang, N. Divecha, P. Skipp, R. M. Ewing

This study performs a proteomic analysis of Dnmt1 hypomorph colorectal cancer cells, revealing dysregulation of EMT and subcellular relocalization of Beta-Catenin.

bioRxiv · Feb 13, 2019Cancer Biology