Author

F. S. Tedesco

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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Bioengineering· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Organism:human· 1

Frequent Co-Authors

A. Imbert· 1 shared A. Serio· 1 shared C. Hagemann· 1 shared C. Moreno-Gonzalez· 1 shared C. Wells· 1 shared E. Carraro· 1 shared E. Giagnorio· 1 shared F. Muntoni· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperBioengineering

A. Imbert

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

SOL3D: Soft-lithography on 3D vat polymerised moulds for fast, versatile, and accessible high-resolution fabrication of customised multiscale cell culture devices with complex designs

C. Hagemann, M. C. D. Bailey, E. Carraro, N. Khokhar, V. M. Lionello, P. Suklai, C. Moreno-Gonzalez, K. O'Toole, G. Konstantinou, S. Joshi, E. Giagnorio, M. Bergholt, A. Imbert, F. S. Tedesco, A. Serio

This paper introduces a low-cost, high-resolution method for fabricating custom cell culture devices using 3D printing and PDMS soft lithography, enabling widespread use in biological labs.

bioRxiv · Feb 22, 2022 · PreprintBioengineering

DLL4 and PDGF-BB regulate migration of human iPSC-derived skeletal myogenic progenitors

G. Ferrari, S. Choi, L. A. Moyle, K. Mackinlay, N. Naouar, C. Wells, F. Muntoni, F. S. Tedesco

This study shows that DLL4 and PDGF-BB enhance migration of hiPSC-derived myogenic progenitors without affecting proliferation, supporting their use in muscle therapies.

bioRxiv · Feb 28, 2021 · PreprintCell Biology