Author

P. Gennemark

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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Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Approach:biophysical modeling· 1 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:simulation· 1

Frequent Co-Authors

K. P. Kanebratt· 2 shared A. Noel· 1 shared B. Casas· 1 shared C. Ammala· 1 shared C. Wennberg Huldt· 1 shared E. Mullers· 1 shared F. Kalrsson· 1 shared G. Cedersund· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersBiophysics

K. P. Kanebratt

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2 papers

Recent·Most cited

3D Cell Cultures Amplify Diffusion Signals

H. Arjmandi, K. P. Kanebratt, L. Vilen, P. Gennemark, A. Noel

This paper develops a biophysical model to predict diffusion in 3D cell aggregates by addressing boundary conditions, validated through simulations and experiments with liver spheroids and glucose.

PLOS ONE · Sep 12, 2024Peer-reviewedBiophysics

Diseased human pancreas and liver microphysiological system for preclinical diabetes research

S. Rigal, B. Casas, K. P. Kanebratt, C. Wennberg Huldt, L. U. Magnusson, E. Mullers, F. Kalrsson, M. Clausen, S. F. Hansson, R. Jansson Lofmark, C. Ammala, U. Marx, P. Gennemark, G. Cedersund, T. B. Andersson, L. K. Vilen

This paper develops a microphysiological system combining pancreas and liver to study diabetes, showing disease phenotypes and therapeutic potential.

bioRxiv · Jul 3, 2023 · PreprintCell Biology