Author

D. Doherty

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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Cell Biology· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Assay:fluorescence / live-cell microscopy· 1

Frequent Co-Authors

A. Mullan· 1 shared B. Huang· 1 shared E. Jokl· 1 shared G. Garcia· 1 shared G. J. Pazour· 1 shared J. C. Van De Weghe· 1 shared J. F. Reiter· 1 shared J. Pritchett· 1 shared

Activity by Year

2017-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperCell Biology

A. Mullan

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Author profile →

2 papers

Recent·Most cited

SOX9 is required for kidney fibrosis and regulates NAV3 to control renal myofibroblast function in mice and humans

S. Raza, E. Jokl, J. Pritchett, K. Martin, K. Su, K. Simpson, A. Mullan, V. Athwal, D. Doherty, L. Zeef, N. Henderson, P. Kalra, N. Hanley, K. Piper Hanley

This study identifies SOX9 as essential for kidney fibrosis and shows it regulates NAV3 to control myofibroblast function in mice and humans.

bioRxiv · Nov 12, 2019 · PreprintCell Biology

Super-Resolution Microscopy Reveals That Disruption Of Ciliary Transition Zone Architecture Is A Cause Of Joubert Syndrome

X. Shi, G. Garcia, J. C. Van De Weghe, R. McGorty, G. J. Pazour, D. Doherty, B. Huang, J. F. Reiter

This study uses super-resolution microscopy to show that mutations in RPGRIP1L and TCTN2 disrupt transition zone architecture in Joubert syndrome, affecting ciliary protein localization and signaling.

bioRxiv · May 25, 2017Cell Biology