Author

J. Kayser

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· 2 Cell Biology· 1 Evolutionary Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Assay:proteomics· 3 Organism:yeast· 3 Research Focus:cell signaling & trafficking· 2 Research Focus:development & morphogenesis· 2 Approach:statistical model· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

O. Hallatschek· 4 shared D. Fusco· 2 shared C. F. Schreck· 1 shared C. Schreck· 1 shared G. Poterewicz· 1 shared J. Choi· 1 shared L. Holt· 1 shared L. Kampman· 1 shared

Activity by Year

2017-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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4 shared papersBiophysics

O. Hallatschek

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Impact of crowding on the diversity of expanding populations

C. F. Schreck, D. Fusco, Y. Karita, S. Martis, J. Kayser, M.-C. Duvernoy, O. Hallatschek

The paper quantifies how crowding affects genetic diversity in expanding microbial populations by showing a power-law distribution of low-frequency clones due to volume-exclusion interactions.

bioRxiv · Jun 2, 2022Evolutionary Biology

Evolutionary rescue is promoted in compact cellular populations

S. Aif, N. Appold, L. Kampman, O. Hallatschek, J. Kayser

The paper shows that dense microbial populations increase the likelihood of evolutionary rescue by stabilizing less-fit resistant subclones through population dynamics.

bioRxiv · May 27, 2022Biophysics

Collective motion conceals fitness differences in crowded cellular populations

J. Kayser, C. Schreck, M. Gralka, D. Fusco, O. Hallatschek

The paper shows that collective motion in crowded yeast populations masks fitness differences, allowing deleterious mutations to persist and increase their chance of evolutionary rescue.

bioRxiv · Feb 18, 2018Biophysics

The SCWISh network is essential for survival under mechanical pressure.

M. Delarue, G. Poterewicz, O. Hoxha, J. Choi, W. Yoo, J. Kayser, L. Holt, O. Hallatschek

The paper identifies a mechanosensitive pathway, SCWISh, essential for yeast survival under mechanical pressure by integrating signals from the SMuSh and CWI pathways.

bioRxiv · Nov 15, 2017Cell Biology