Author

A. C. Arnold

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 Animal Behavior & Cognition· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Research Focus:development & morphogenesis· 1 Research Focus:metabolism & bioenergetics· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

A. E. Snyder· 1 shared A. M. Snyder· 1 shared C. R. Coker· 1 shared D. C. Chan· 1 shared E. A. Aguilar· 1 shared E. A. Proctor· 1 shared E. S. Halstead· 1 shared E. Yau· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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1 shared paperAnimal Behavior & Cognition

A. E. Snyder

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3 papers

Recent·Most cited

Predictive link between systemic metabolism and cytokine signatures in the brain of apolipoprotein E ϵ4 mice

R. M. Fleeman, A. M. Snyder, M. K. Kuhn, D. C. Chan, G. C. Smith, N. A. Crowley, A. C. Arnold, E. A. Proctor

This study identifies a predictive link between systemic metabolism and cytokine signatures in the brain of APOE4 mice, showing APOE genotype-dependent differences in aging mice.

bioRxiv · Feb 11, 2022Physiology

Disruption of the surfactant protein A receptor SP-R210L (CD245α/MYO18Aα) alters respiratory function and iron sequestration in alveolar macrophages of aged mice

E. Yau, T. M. Umstead, R. Abdulqadir, K. Fino, Z. Guan, S. Hu, S. Diangelo, K. Hassan, S. Bingaman, H. M. Atkins, T. K. Cooper, A. C. Arnold, E. S. Halstead, Z. C. Chroneos

This study shows that disrupting the SP-R210L isoform in aged mice impairs respiratory function and iron sequestration in alveolar macrophages, leading to chronic dysregulation and increased interstitial lung disease risk.

bioRxiv · Apr 14, 2021 · PreprintPhysiology

Access schedules mediate the impact of high fat diet on ethanol intake and insulin and glucose function in mice.

C. R. Coker, E. A. Aguilar, A. E. Snyder, S. S. Bingaman, N. M. Graziane, K. N. Browning, A. C. Arnold, Y. Silberman

This study shows that high fat diet (HFD) affects ethanol intake and metabolic function differently depending on ethanol access schedules in mice.

bioRxiv · Jun 20, 2019Animal Behavior & Cognition