Author

J. P. Burton

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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Microbiology· 2 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Organism:human· 2 Research Focus:host-pathogen & immune response· 1 Assay:imaging· 1 Research Focus:metabolism & bioenergetics· 1 Assay:metabolomics· 1 Assay:proteomics· 1

Frequent Co-Authors

G. Reid· 2 shared A. M. Pena-Diaz· 1 shared A. S. Kucey· 1 shared A. Shair· 1 shared B. Abbasian· 1 shared B. L. Urquhart· 1 shared D. B. O'Gorman· 1 shared D. E. Goldhawk· 1 shared

Activity by Year

2019-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersMicrobiology

G. Reid

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3 papers

Recent·Most cited

Bacterial association with metals enables in vivo tracking of microbiota using magnetic resonance imaging

S. C. Donnelly, N. Gelman, R. T. Thompson, F. S. Prato, J. P. Burton, D. E. Goldhawk

This paper shows that certain bacteria have distinct MRI relaxation rates that could be used to track them in the body, with lactobacilli showing particularly high signal due to manganese content.

bioRxiv · May 5, 2022Microbiology

Potential role of extracellular ATP released by bacteria in bladder infection and contractility

J. P. Burton, B. Abbasian, A. Shair, D. B. O'Gorman, A. M. Pena-Diaz, K. C. Engelbrecht, D. W. Koenig, G. Reid

The paper investigates how extracellular ATP from bacteria affects bladder contraction and urgency urinary incontinence, finding that some bacteria induce contraction while others inhibit it.

bioRxiv · Feb 2, 2019Microbiology

The Impact of Uremia and Intestinal Dysbiosis on Hepatic Drug Metabolism in a Rat Model of Progressive Chronic Kidney Disease

E. D. Hartjes, Y. J. Lim, T. J. Velenosi, K. F. Al, J. M. Macklaim, A. S. Kucey, G. Reid, J. P. Burton, G. B. Gloor, B. L. Urquhart

This study investigates how uremia and intestinal dysbiosis affect hepatic drug metabolism in a rat CKD model, finding that CYP3A2 and CYP2C11 are downregulated before dysbiosis and correlate with uremic toxins.

bioRxiv · Jan 29, 2019 · PreprintPharmacology & Toxicology