Author

K. Lund

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 Cancer Biology· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:drug response / drug discovery· 1 Approach:genetic perturbation / CRISPR· 1

Frequent Co-Authors

A. Corthay· 1 shared A. Tveita· 1 shared B. Nystrom· 1 shared B. Thiede· 1 shared C. H. Stuelten· 1 shared C. Hammarstrom· 1 shared E. Dybing· 1 shared E. Hovig· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperCancer Biology

A. Corthay

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

A GPCR screening in human keratinocytes identifies that the metabolite receptor HCAR3 controls epithelial proliferation, migration, and cellular respiration.

M. P. Pedro, K. Lund, S. W. S. Kang, T. Chen, C. H. Stuelten, N. Porat-Shliom, R. Iglesias-Bartolome

This study identifies HCAR3 as a GPCR that regulates epithelial cell proliferation, migration, and respiration in human keratinocytes through altered metabolism and mitochondrial function.

bioRxiv · May 30, 2023Cell Biology

Tankyrase inhibition sensitizes melanoma to PD-1 immune checkpoint blockade in syngeneic mouse models

J. Waaler, L. Mygland, A. Tveita, M. F. Strand, N. T. Solberg, P. Angell Olsen, K. Lund, S. Alam Brinch, M. Lycke, E. Dybing, V. Nygaard, S. L. Boe, K.-M. Heintz, E. Hovig, C. Hammarstrom, , S. Krauss

This study shows that tankyrase inhibition makes melanoma more responsive to PD-1 checkpoint blockade in mouse models by reducing WNT/β-catenin and YAP signaling.

bioRxiv · Jan 22, 2019Cancer Biology

Comparison of ultracentrifugation and a commercial kit for isolation of exosomes derived from glioblastoma and breast cancer cell lines

F. S. Skottvoll, H. E. Berg, K. Bjorseth, K. Lund, N. Roos, S. Bekhradnia, B. Thiede, H. Roberg-Larsen, B. Nystrom, E. Lundanes, S. R. Wilson

This study compares ultracentrifugation and a commercial kit for isolating exosomes from glioblastoma and breast cancer cell lines, finding similar performance with minor differences based on cell origin.

bioRxiv · Aug 1, 2018 · PreprintBiochemistry