Author

L. S. Kremer

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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Biochemistry· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1 Research Focus:metabolism & bioenergetics· 1 Assay:metabolomics· 1

Frequent Co-Authors

F. M. Hansen· 2 shared M. Mann· 2 shared N.-G. Larsson· 2 shared A. Krook· 1 shared A. Unger· 1 shared C. Koolmeister· 1 shared D. Alsina· 1 shared D. Rubalcava-Gracia· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersPhysiology

F. M. Hansen

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Author profile →

2 papers

Recent·Most cited

PhysiologybioRxivPreprintSep 22, 2023

Inhibition of mammalian mtDNA transcription paradoxically activates liver fatty acid oxidation to reverse diet-induced hepatosteatosis and obesity

S. Jiang, T. Yuan, L. S. Kremer…·N.-G. Larsson

The paper shows that inhibiting mitochondrial DNA transcription in mice increases fatty acid oxidation, reducing obesity and liver fat while decreasing oxidative phosphorylation capacity.

DOI 10.1101/2023.09.22.558955

mouseproteomics

𝕏 PostBluesky

BiochemistrybioRxivMar 23, 2022

Mitochondrial phosphoproteomes are functionally specialized across tissues

M. Mann, F. M. Hansen, L. S. Kremer…·N.-G. Larsson

The paper quantitatively profiles mitochondrial proteomes and phosphoproteomes across multiple tissues in mice, revealing tissue-specific kinase and phosphatase repertoires and functional phosphorylation events.

DOI 10.26508/lsa.202302147

mouseproteomics

𝕏 PostBluesky