Author

L. Flachsmann

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Immunology· 1

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Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:metabolism & bioenergetics· 1 Assay:metabolomics· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Castoldi· 1 shared A. M. Kabat· 1 shared A. Patterson· 1 shared D. E. Sanin· 1 shared D. O'Sullivan· 1 shared E. J. Pearce· 1 shared E. L. Pearce· 1 shared F. Haessler· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperImmunology

A. Castoldi

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1 paper

Recent·Most cited

In macrophages fatty acid oxidation spares glutamate for use in diverse metabolic pathways required for alternative activation

N. van Teijlingen Bakker, L. Flachsmann, G. E. Carrizo, D. E. Sanin, S. Lawless, A. Castoldi, L. Monteiro, A. M. Kabat, M. Matsushita, F. Haessler, A. Patterson, R. Klein Geltink, D. O'Sullivan, E. L. Pearce, E. J. Pearce

This study shows that fatty acid oxidation in macrophages supports alternative activation by maintaining glutamate levels, and that glutamine metabolism compensates for FAO disruption.

bioRxiv · Apr 13, 2022 · PreprintImmunology