Author

M. Lindberg

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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Cancer Biology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Assay:imaging· 1 Organism:mouse· 1

Frequent Co-Authors

A. F. Pinto· 1 shared A. Nordstrom· 1 shared A. R. Clausen· 1 shared A. Stahlberg· 1 shared A.-G. Thorsell· 1 shared C. Bjorkegren· 1 shared E. Larsson· 1 shared E. Loverli· 1 shared

Activity by Year

2018-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperBiochemistry

A. F. Pinto

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Epigenetic therapy to enhance therapeutic effects of PD-1 inhibition in uveal melanoma

V. R. Sah, H. Jespersen, J. Karlsson, M. Lindberg, L. M. Nilsson, L. Ny, J. A. Nilsson

This study investigates enhancing PD-1 inhibitor efficacy in uveal melanoma through epigenetic modulation with HDAC or BET inhibitors, finding that HDAC inhibition synergizes with immunotherapy.

bioRxiv · Feb 4, 2021Cancer Biology

Elevated pyrimidine dimer formation at distinct genomic bases underlie promoter mutation hotspots in UV-exposed cancers

K. Elliott, M. Bostrom, S. Filges, M. Lindberg, J. Van den Eynden, A. Stahlberg, A. R. Clausen, E. Larsson

The paper shows that UV-induced mutations in cancer promoters are due to base-specific increases in pyrimidine dimer formation, not inhibited repair.

bioRxiv · Aug 31, 2018Cancer Biology

14-3-3 proteins activate Pseudomonas exotoxins-S and -T by chaperoning a hydrophobic surface

T. Karlberg, P. Hornyak, A. F. Pinto, S. Milanova, M. Ebrahimi, M. Lindberg, N. Pullen, A. Nordstrom, E. Loverli, R. Caraballo, E. V. Wong, K. Nareoja, A.-G. Thorsell, M. Elofsson, E. M. De La Cruz, , H. Schuler

This study identifies a novel hydrophobic interface between 14-3-3 proteins and Pseudomonas exotoxins-S and -T, showing 14-3-3 activates these toxins by preventing aggregation, independent of their C-terminal phosphopeptide binding motifs.

bioRxiv · Jun 8, 2018Biochemistry