Author

Jeremy Meyers

University of Arizona

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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Molecular Biology· 2

Signature Assays, Organisms & Methods

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Organism:C. elegans· 2 Approach:experimental assay· 2 Research Focus:drug response / drug discovery· 1 Assay:metabolomics· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

George L. SutphiniD· 2 shared Hope T. L. Dang· 2 shared Luis S. EspejoiD· 2 shared Raúl Castro-PortugueziD· 2 shared Samuel FreitasiD· 2 shared Alana M. Hendrickson· 1 shared Bradford HulliD· 1 shared Caroline CorbaniD· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersMolecular Biology

George L. SutphinORCID

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Author profile →

2 papers

Recent·Most cited

Inhibition of haao-1 enhances oxidative stress response by activating hormetic redox signaling in C. elegans.

Raúl Castro-Portuguez, Kayla M. Raymond, Emma Thullen, Alana M. Hendrickson, Samuel Freitas, Bradford Hull, Jeremy Meyers, Niall Thorns, Emily A. Gardea, Hope T. L. Dang, Luis S. Espejo, George L. Sutphin

The paper shows that inhibiting haao-1 in C. elegans enhances oxidative stress resistance by activating the Nrf2/SKN-1 pathway through a hormetic redox mechanism.

bioRxiv · Feb 16, 2023 · PreprintMolecular Biology

3-hydroxyanthranilic acid - a new metabolite for healthy lifespan extension

Hope T. L. Dang, Raúl Castro-Portuguez, Luis S. Espejo, Grant Backer, Samuel Freitas, Erica Spence, Jeremy Meyers, Karissa Shuck, Caroline Corban, Teresa Liu, Shannon Bean, Susan Sheehan, Ron Korstanje, George L. Sutphin

This study identifies 3-hydroxyanthranilic acid (3HAA) as a metabolite that extends lifespan and improves health in C. elegans and mice by reducing oxidative stress and activating the Nrf2/SKN-1 pathway.

bioRxiv · Jun 1, 2021 · PreprintMolecular Biology