Author

Y. Chekli

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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Microbiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:bacteria (other)· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:E. coli· 1 Assay:fluorescence / live-cell microscopy· 1 Research Focus:spatial domain detection· 1

Frequent Co-Authors

C. BELOIN· 2 shared J.-M. Ghigo· 2 shared A. Gautier· 1 shared A. Lebreton· 1 shared C. Li· 1 shared C. Peron-Cane· 1 shared D. Dell'Arciprete· 1 shared E. Kornobis· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersMicrobiology

C. BELOIN

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2 papers

Recent·Most cited

Escherichia coli aggregates mediated by native or synthetic adhesins exhibit both core and adhesin-specific transcriptional responses

Y. Chekli, R. J. Stevick, E. Kornobis, V. Briolat, J.-M. Ghigo, C. BELOIN

This study examines transcriptomic responses of E. coli aggregates formed by native or synthetic adhesins, revealing core and adhesin-specific gene expression changes.

bioRxiv · Feb 14, 2023 · PreprintMicrobiology

Visualizing the dynamics of exported bacterial proteins with the chemogenetic fluorescent reporter FAST

Y. Chekli, C. Peron-Cane, D. Dell'Arciprete, J.-F. Allemand, C. Li, J.-M. GHIGO, A. Gautier, A. Lebreton, N. Desprat, C. BELOIN

This study uses FAST, a chemogenetic fluorescent reporter, to visualize exported bacterial proteins in live imaging, demonstrating its functionality on both diderm and monoderm bacteria.

bioRxiv · May 12, 2020Microbiology