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Dustin J. Hadley

Researcher at University of California, Davis

Publications -  7
Citations -  85

Dustin J. Hadley is an academic researcher from University of California, Davis. The author has contributed to research in topics: Self-healing hydrogels & Lymphangiogenesis. The author has an hindex of 3, co-authored 6 publications receiving 54 citations.

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Alginate hydrogels allow for bioactive and sustained release of VEGF-C and VEGF-D for lymphangiogenic therapeutic applications

TL;DR: It is demonstrated that alginate hydrogels can provide sustained and bioactive release of VEGF-C and V EGF-D which could have applications for therapeutic lymphangiogenesis.
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An electrochemical aptasensor for detection of bovine interferon gamma

TL;DR: An electrochemical aptasensor for sensitive and specific determination of bovine interferon gamma (BoIFN-γ) is developed for the first time and may, in the future, be used for on-site testing ofbovine blood to help better identify and contain outbreaks of Bovine TB.
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Computational-Based Design of Hydrogels with Predictable Mesh Properties.

TL;DR: This work postulated and confirmed that the computational model could incorporate properties of alginate polymers, including polymer content, monomer composition and polymer chain radius, to accurately predict cross-link density and mesh size for a wide range ofAlginate hydrogels.
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Thaw-Induced Gelation of Alginate Hydrogels for Versatile Delivery of Therapeutics

TL;DR: The utility of TIG strategies are particularly promising for the delivery of therapeutic cargos smaller than the mesh size of the alginate hydrogel, as it enables controlled release of these cargo without any further chemical modifications of the hydrogels.
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Isolating and characterizing lymphatic endothelial progenitor cells for potential therapeutic lymphangiogenic applications

TL;DR: In this article, the authors investigated the role of isolated blood and lymphatic EPC subpopulations in promoting the early stages of vascularization and the utility of alginate hydrogels to deliver lymphatic endothelial progenitor cells (EPCs).