Author

H. Redl

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· 2 Cell Biology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell type annotation· 2 Research Focus:development & morphogenesis· 2 Organism:human· 2 Assay:organoid / primary culture· 2 Research Focus:cell-cell communication· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

P. Ertl· 3 shared B. Bachmann· 2 shared S. Spitz· 2 shared W. Holnthoner· 2 shared A. Fischer· 1 shared A. R. Perestrelo· 1 shared B. E. M. Bachmann· 1 shared B. Haddadi Sisakht· 1 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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3 shared papersBioengineering

P. Ertl

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

The p-rpS6-zone delineates wounding response and the healing process

N. A. R. Ring, H. Dworak, B. Bachmann, B. Schaedl, K. Valdivieso, T. Rozmaric, P. Heimel, K. Schuetzenberger, G. Leinfellner, J. Ferguson, S. Drechsler, M. Mildner, M. Schosserer, P. Slezak, O. Meyuhas, , M. Ogrodnik

The paper identifies a p-rpS6-zone around wounds that marks the healing process and shows its role in tissue repair.

bioRxiv · Sep 27, 2022 · PreprintPhysiology

Generation and Maturation of Human iPSC-derived Cardiac Organoids in Long Term Culture

E. Ergir, J. Oliver-de la Cruz, S. Fernandes, M. Cassani, F. Niro, D. Sousa, J. Vrbsky, V. Vinarsky, A. R. Perestrelo, D. Debellis, F. Cavalieri, S. Pagliari, H. Redl, P. Ertl, G. Forte

This study develops a scaffold-free protocol to generate long-term beating human cardiac organoids from hiPSCs, showing improved maturation and functionality for drug testing and cardiotoxicity studies.

bioRxiv · Mar 7, 2022 · PreprintCell Biology

Microvasculature-on-a-Chip: Bridging the interstitial blood-lymph interface via mechanobiological stimuli

B. Bachmann, S. Spitz, C. Jordan, P. Schuller, H. D. Wanzenboeck, B. Haddadi Sisakht, M. Harasek, H. Redl, W. Holnthoner, P. Ertl

This paper introduces a microvascular-on-a-chip model that mimics the interstitial blood-lymph interface, showing increased vessel sprouting under dynamic mechanobiological stimulation.

bioRxiv · Apr 8, 2021 · PreprintBioengineering

Establishment of a human three-dimensional chip-based chondro-synovial co-culture joint model for reciprocal cross-talk studies in arthritis research

M. Rothbauer, R. A. Byrne, S. Schobesberger, I. Olmos Calvo, A. Fischer, E. Reihs, S. Spitz, B. E. M. Bachmann, F. Sevelda, J. Holinka, W. Holnthoner, H. Redl, S. Toegel, R. Windhager, H. P. Kiener, P. Ertl

This study establishes a 3D microfluidic co-culture model of synovial and chondral organoids to study reciprocal cross-talk in arthritis, showing enhanced cartilage physiology and cytokine responses in co-cultures.

bioRxiv · Feb 19, 2021Bioengineering