Author

M. B. Doshi

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 Cancer Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:drug response / drug discovery· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

A. J. Church· 1 shared A. L. Hong· 1 shared A. Sayeed· 1 shared A. Tracy· 1 shared A. Ward· 1 shared B. D. Crompton· 1 shared B. D. Kynnap· 1 shared B. McSteen· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperCancer Biology

A. J. Church

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2 papers

Recent·Most cited

Selenium reduction of ubiquinone via SQOR suppresses ferroptosis

N. Lee, S. J. Park, M. Lange, T. Tseyang, M. B. Doshi, T. Kim, Y. Song, D. Kim, P. L. Greer, J. A. Olzmann, J. Spinelli, D. Kim

The paper shows selenium reduces ubiquinone to ubiquinol via SQOR, protecting against ferroptosis independently of selenoprotein production.

bioRxiv · Apr 13, 2023Biochemistry

Renal medullary carcinomas depend upon SMARCB1 loss and are sensitive to proteasome inhibition

A. L. Hong, Y.-Y. Tseng, J. A. Wala, W. J. Kim, B. D. Kynnap, M. B. Doshi, G. Kugener, G. J. Sandoval, T. P. Howard, J. Li, X. Yang, M. Tillgren, M. Ghandi, A. Sayeed, R. Deasy, , W. Hahn

This study identifies SMARCB1 loss as critical for RMC survival and shows proteasome inhibition as a potential therapeutic strategy.

bioRxiv · Dec 5, 2018Cancer Biology