Author

C. D. Camell

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

Frequent Co-Authors

E. L. Goldberg· 2 shared V. D. Dixit· 2 shared Y.-H. Youm· 2 shared A. Bartke· 1 shared A. Lee· 1 shared G. B. Hubbard· 1 shared I. Shchukina· 1 shared J. L. Schultz· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersImmunology

E. L. Goldberg

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2 papers

Recent·Most cited

ImmunologybioRxivPreprintSep 8, 2020

Dysregulation of adipose ILC2 underlies thermogenic failure in aging

E. L. Goldberg, I. Shchukina, Y.-H. Youm…·V. D. Dixit

The paper identifies age-related changes in adipose tissue that reprogram ILC2, leading to impaired cold tolerance in aged mice.

DOI 10.1101/2020.09.08.288431

mousebulk RNA-seq

𝕏 PostBluesky

ImmunologybioRxivApr 13, 2019

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

C. D. Camell, A. Lee, P. Günther…·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.

DOI 10.1093/geroni/igz038.397

mousebulk RNA-seq

𝕏 PostBluesky