Author

M. R. Baumgartner

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· 2 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:host-pathogen & immune response· 1 Research Focus:metabolism & bioenergetics· 1 Organism:mouse· 1 Assay:protein structure· 1

Frequent Co-Authors

D. S. Froese· 3 shared W. W. Yue· 2 shared A. Chaikuad· 1 shared A. Kaech· 1 shared B. Fowler· 1 shared B. Rathkolb· 1 shared C. Buerer· 1 shared C. Bürer· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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3 shared papersBiochemistry

D. S. Froese

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Author profile →

3 papers

Recent·Most cited

Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria

M. Lucienne, R. Gerlini, B. Rathkolb, J. Calzada-Wack, P. Forny, S. Wüest, A. Kaech, F. Traversi, M. Forny, C. Bürer, J. A. Aguilar-Pimentel, M. Irmler, J. Beckers, S. Sauer, S. Kölker, , M. Hrabe de Angelis

This study examines a mouse model of methylmalonic aciduria, finding reduced energy expenditure, altered metabolism, and metabolic inflexibility.

bioRxiv · Nov 30, 2021Physiology

Naturally occurring cobalamin (B12) analogs can function as cofactors for human methylmalonyl-CoA mutase

O. M. Sokolovskaya, T. Plessl, H. Bailey, S. Mackinnon, M. R. Baumgartner, W. W. Yue, D. S. Froese, M. E. Taga

The paper investigates how different cobamides affect the function of methylmalonyl-CoA mutase and shows that non-cobalamin cobamides can also support its activity.

bioRxiv · Mar 20, 2020Biochemistry

Genetic, structural, and functional analysis of mutations causing methylmalonyl-CoA epimerase deficiency

K. Heuberger, H. J. Bailey, P. Burda, A. Chaikuad, E. Krysztofinska, T. Suormala, C. Buerer, S. Lutz, B. Fowler, D. S. Froese, W. W. Yue, M. R. Baumgartner

The paper identifies ten new patients with MCEE deficiency, analyzes mutations in the MCEE gene, and reveals structural and functional defects in the enzyme caused by these mutations.

bioRxiv · Nov 30, 2018Biochemistry