Author

M. J. Munson

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 Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell signaling & trafficking· 2 Organism:human· 2 Organism:C. elegans· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell-cell communication· 1 Assay:proteomics· 1 Organism:zebrafish· 1

Frequent Co-Authors

A. Simonsen· 2 shared S. Singh· 2 shared A. Collen· 1 shared A. Gallud· 1 shared A. H. Lystad· 1 shared A. Idstrom· 1 shared A. S. D. S. Lapao· 1 shared A. Sabirsh· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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Curved chords = mutual co-authorship

2 shared papersBiochemistry

A. Simonsen

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Time evolution of PEG-shedding and serum protein coronation determines the cell uptake kinetics and delivery of lipid nanoparticle formulated mRNA

A. Gallud, M. J. Munson, K. Liu, A. Idstrom, H. M. Barriga, S. Tabaei, N. Aliakbarinodehi, M. Ojansivu, Q. Lubart, J. J. Doutch, M. N. Holme, L. Evenas, L. Lindfors, M. M. Stevens, A. Collen, , E. K. Esbjorner

This study models protein corona formation on LNPs and identifies time-dependent steps that affect their uptake and mRNA delivery, showing that pre-incubation in serum can eliminate a lag-time.

bioRxiv · Aug 20, 2021 · PreprintBiophysics

GRAMD1C promotes autophagy initiation and mitochondrial bioenergetics through regulation of ER-mitochondria cholesterol transport

M. Y. W. Ng, C. Charsou, A. S. D. S. Lapao, S. Singh, L. Trachsel-Moncho, S. Nakken, M. J. Munson, A. Simonsen

This study identifies GRAMD1C as a negative regulator of starvation-induced autophagy and mitochondrial function through cholesterol transport between the ER and mitochondria.

bioRxiv · Aug 4, 2021 · PreprintBiochemistry

GAK and PRKCD are positive regulators of PRKN-independent mitophagy

M. J. Munson, B. J. Mathai, L. Trachsel, M. Yoke Wui Ng, L. Rodriguez de la Ballina, S. Schultz, Y. Aman, A. H. Lystad, S. Singh, S. Singh, J. Wesche, E. F. Fang, A. Simonsen

This study identifies GAK and PRKCD as positive regulators of PRKN-independent mitophagy through genetic screening and functional analysis in vitro and in vivo.

bioRxiv · Nov 5, 2020Cell Biology