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Jason A. Burdick

Researcher at University of Pennsylvania

Publications -  363
Citations -  42498

Jason A. Burdick is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Self-healing hydrogels & Tissue engineering. The author has an hindex of 103, co-authored 335 publications receiving 34137 citations. Previous affiliations of Jason A. Burdick include Duke University & University of Kentucky.

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Controlled activation of morphogenesis to generate a functional human microvasculature in a synthetic matrix.

TL;DR: It is shown that the signaling pathways of vascular morphogenesis of ECFCs can be precisely regulated in a synthetic matrix, resulting in a functional microvasculature useful for the study of 3-dimensional vascular biology and toward a range of vascular disorders and approaches in tissue regeneration.
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Matching material and cellular timescales maximizes cell spreading on viscoelastic substrates.

TL;DR: This study systematically examined the dynamics of motor clutches formed between the cell and a viscoelastic substrate using analytical methods and direct Monte Carlo simulation and found that intermediate viscosity maximizes cell spreading on soft substrates, while cell spreading is independent of Viscosity on stiff substrates.
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A Combinatorial Library of Photocrosslinkable and Degradable Materials

TL;DR: This work develops the first combinatorial library of degradable photocrosslinked materials, a library of Krylate-terminated polymers with diverse properties such as cadmium, cadmiferous material, and polymethine.
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Complex 3D-Printed Microchannels within Cell-Degradable Hydrogels

TL;DR: 3D‐printing is emerging as a technology to introduce microchannels into hydrogels, for the perfusion of engineered constructs and can be used for a range of biomedical applications, from engineering vascularized tissue constructs to modeling in vitro cultures.
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Local and sustained miRNA delivery from an injectable hydrogel promotes cardiomyocyte proliferation and functional regeneration after ischemic injury.

TL;DR: The development and application of an injectable hyaluronic acid hydrogel for the local and sustained delivery of miR-302 mimics to the heart promotes cardiomyocyte proliferation and improves cardiac function in mice after myocardial infarction suggests that biomaterial-based miRNA delivery systems can lead to improved outcomes via cardiac regeneration after myocardIAL infarctions.