Author

A. Bartke

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 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:metabolism & bioenergetics· 2 Assay:behavioral assay· 1 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

Y. Fang· 2 shared A. Lee· 1 shared A. Schneider· 1 shared C. Barros· 1 shared C. D. Camell· 1 shared D. Garcia· 1 shared D. Medina· 1 shared E. L. Goldberg· 1 shared

Activity by Year

2019-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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2 shared papersPhysiology

Y. Fang

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Sexual Dimorphic Metabolic and Cognitive Responses of C57BL/6 Mice to Fisetin or Dasatinib and Quercetin Cocktail Oral Treatment

Y. Fang, D. Medina, R. Stockwell, S. McFadden, K. Quinn, M. R. Peck, A. Bartke, K. N. Hascup, E. R. Hascup

This study examines sex-specific effects of senolytic treatments in mice, finding that Fisetin benefits males but not females, while D+Q harms females and has little effect on males.

bioRxiv · Nov 8, 2021Physiology

DNA damage and macrophage infiltration in the ovaries of the long-lived GH deficient Ames Dwarf and the short-lived bGH transgenic mice

T. D. Saccon, M. Rovani, D. Garcia, J. Pradiee, R. Mondadori, L. Cruz, C. Barros, Y. Fang, S. McFaden, A. Bartke, M. masternak, A. Schneider

This study compares DNA damage, macrophage infiltration, and granulosa cell numbers in GH-deficient and GH-overexpressing mice to assess GH's role in ovarian health.

bioRxiv · Jan 19, 2020 · PreprintPhysiology

Aging induces Nlrp3 inflammasome dependent adipose B cell expansion to impair metabolic homeostasis

C. D. Camell, A. Lee, P. Günther, E. L. Goldberg, O. Spadaro, Y.-H. Youm, A. Bartke, G. B. Hubbard, Y. Ikeno, N. H. Ruddle, J. L. Schultz, V. D. Dixit

This study shows aging increases adipose B cells and FALCs via Nlrp3 inflammasome, impairing metabolism, and B cell depletion improves metabolic function in aged mice.

bioRxiv · Apr 13, 2019Immunology