Author

Tracey Davey

Newcastle UniversityORCID 0000-0001-9409-7410Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Assay:electronic health records· 2 Organism:mouse· 2 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

Amy E. VincentiD· 2 shared Julie FaitgiD· 2 shared Ross LawsiD· 2 shared Amy Katherine ReeveiD· 1 shared Caroline ThaungiD· 1 shared Clay LacefieldiD· 1 shared Conor LawlessiD· 1 shared Dinesh C. SoaresiD· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 23 mutual co-author links

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2 shared papersMolecular Biology

Amy E. VincentORCID

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3 papers

Recent·Most cited

Mitochondrial morphology and function in mitochondrial disease

Julie Faitg, Tracey Davey, Ross Laws, Conor Lawless, Helen A. L. Tuppen, Eric Fitton, Douglass M. Turnbull, Amy E. Vincent

This study uses COX-SBFSEM to examine mitochondrial morphology and function in human muscle biopsies with mtDNA deletions, revealing distinct mitochondrial populations and spatial patterns of oxidative phosphorylation.

bioRxiv · Dec 20, 2023 · PreprintMolecular Biology

3D Neuronal Mitochondrial Morphology in Axons, Dendrites, and Somata of the Aging Mouse Hippocampus

Julie Faitg, Clay Lacefield, Tracey Davey, Kathryn White, Ross Laws, Stylianos Kosmidis, Amy Katherine Reeve, Eric R. Kandel, Amy E. Vincent, Martin A. Picard

This study maps mitochondrial morphology in different neuronal compartments of the aging mouse hippocampus using 3D electron microscopy, revealing age-related differences in mitochondrial structure across cell types.

Cell Reports · Aug 1, 2021Peer-reviewedNeuroscience

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

Sally H. Cross, Lisa McKie, Margaret Keighren, Katrine M. West, Caroline Thaung, Tracey Davey, Dinesh C. Soares, Luis Sánchez‐Pulido, Ian J. Jackson

The paper identifies TMEM98 mutations in mice that cause retinal defects similar to human nanophthalmos, showing localized photoreceptor laminar disruption rather than small eyes.

Investigative Ophthalmology & Visual Science · Jul 2, 2019Peer-reviewedMolecular Biology