Author

N. Mody

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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Physiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

D. Thompson· 2 shared P. D. Whitfield· 2 shared S. Mahmood· 2 shared G. D. Mcilroy· 1 shared J. J. Rochford· 1 shared M. Delibegovic· 1 shared M. K. Doherty· 1 shared N. Morrice· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersPhysiology

D. Thompson

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2 papers

Recent·Most cited

Hydroxysteroid 17-beta dehydrogenase 13 (Hsd17b13) knockdown attenuates liver steatosis in high-fat diet obese mice

S. Mahmood, N. Z. Morrice, D. Thompson, S. Milanizadeh, S. Wilson, P. D. Whitfield, G. D. Mcilroy, J. J. Rochford, N. Mody

This study shows that knocking down Hsd17b13 in obese mice reduces liver steatosis and improves liver health markers, suggesting HSD17B13 as a therapeutic target for MASLD.

bioRxiv · Feb 27, 2024 · PreprintPhysiology

Fenretinide inhibits obesity and fatty liver disease but induces Smpd3 to increase serum ceramides and worsen atherosclerosis in LDLR-/- mice.

D. Thompson, S. Mahmood, N. Morrice, S. Kamli-Salino, R. Dekeryte, P. Hoffmann, M. K. Doherty, P. D. Whitfield, M. Delibegovic, N. Mody

This study shows that fenretinide reduces obesity and fatty liver but increases ceramides via Smpd3, worsening atherosclerosis in LDLR-/- mice.

bioRxiv · Jul 22, 2022Physiology