Data belonging to the publication "Predicted effects of patient variability and Notch signaling on in situ vascular tissue engineering"
DOI: 10.4121/f1ca41cd-df90-4aac-9712-8fe4b1c25f80
Datacite citation style
Dataset
This study adopts a previously published multiscale computational framework for arterial growth and remodeling and adapts it for applications in in situ vascular tissue engineering. The framework consists of a constrained mixture model, capturing the mechanics and turnover of arterial constituents, and a cell-cell signaling model, describing Notch signaling dynamics among vascular smooth muscle cells. With the model, we computationally explored potential sources of tissue engineered vascular graft (TEVG) variability and effects of manipulating Notch, a key vascular signaling pathway. We simulated the evolution of a TEVG from a degradable scaffold under varying patient-specific conditions.
This dataset contains the computational codes for the multiscale framework and the raw data from the simulations.
History
- 2025-11-07 first online, published, posted
Publisher
4TU.ResearchDataFormat
.m, .mat, .txtFunding
- Predicting cardiovascular regeneration: integrating mechanical cues and signaling pathways (grant code 802967) [more info...] European Research Council
- The integration of cell signalling and mechanical forces in vascular morphology (grant code 771168) [more info...] European Research Council
- Investigating the crosstalk between Notch and YAP/TAZ in sprouting angiogenesis (grant code 846617) [more info...] European Commission
Organizations
Eindhoven University of Technology, Department of Biomedical Engineering, the NetherlandsÅbo Akademi, Faculty of Science and Engineering, Biosciences, Turku, Finland
Yale University, Department of Biomedical Engineering, New Haven, USA
DATA
Files (1)
- 186,371,767 bytesMD5:
7aa38865d4ae80d2f00afdaea721bdd5Dataset.zip





