Author

D. M. Gendoo

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

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1

Frequent Co-Authors

A. H. Baker· 1 shared A. Molinolo· 1 shared A. Zougman· 1 shared B. A. Scheven· 1 shared B. K. Irving· 1 shared E. Polson· 1 shared F. Khanim· 1 shared H. Briggs· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCancer Biology

A. H. Baker

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2 papers

Recent·Most cited

The cell cycle state defines TACC3 as a regulator gene in glioblastoma

H. Briggs, E. Polson, B. K. Irving, A. Zougman, R. K. Mathew, D. M. Gendoo, H. Wurdak

The paper identifies TACC3-dependent genes that correlate with poor survival in glioblastoma patients, revealing its role in cell cycle-regulated gene networks.

bioRxiv · Oct 20, 2020 · PreprintCancer Biology

The common analgesic paracetamol enhances the anti-tumour activity of decitabine through exacerbation of oxidative stress

H. J. Gleneadie, A. H. Baker, N. Batis, J. Bryant, Y. Jiang, S. J. Clokie, H. Mehanna, P. Garcia, D. M. Gendoo, S. Roberts, A. Molinolo, S. Gutkind, B. A. Scheven, P. R. Cooper, F. Khanim, M. Wiench

This study shows that paracetamol enhances decitabine's anti-tumour effects by increasing oxidative stress without worsening DNA damage.

bioRxiv · Mar 31, 2020 · PreprintCancer Biology