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Andrew Lee

Researcher at Carnegie Mellon University

Publications -  16
Citations -  2169

Andrew Lee is an academic researcher from Carnegie Mellon University. The author has contributed to research in topics: Self-healing hydrogels & Myocyte. The author has an hindex of 11, co-authored 16 publications receiving 1435 citations. Previous affiliations of Andrew Lee include Sandia National Laboratories & University of California, San Diego.

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3D bioprinting of collagen to rebuild components of the human heart

TL;DR: 3D-bioprinted hearts accurately reproduce patient-specific anatomical structure as determined by micro–computed tomography and showed synchronized contractions, directional action potential propagation, and wall thickening up to 14% during peak systole.
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Stem cell migration and mechanotransduction on linear stiffness gradient hydrogels

TL;DR: A method of polymerization control in which the differential diffusion distance of unreacted cross-linker and monomer into a prepolymerized hydrogel sink results in a tunable stiffness gradient at the cell–matrix interface is developed, making it possible to pinpoint optimal stiffness values for a wide range of biological phenomena without the confounding effects of durotaxis.
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3D Printing PDMS Elastomer in a Hydrophilic Support Bath via Freeform Reversible Embedding

TL;DR: The results demonstrate that hydrophobic polymers with low viscosity and long cure times can be 3D printed using a hydrophilic support, expanding the range of biomaterials that can be used in additive manufacturing.
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The alignment and fusion assembly of adipose-derived stem cells on mechanically patterned matrices.

TL;DR: It is suggested that mechanically-patterned hydrogels could provide a platform to create tissue engineered, innervated micro-muscles of neural and muscle phenotypes juxtaposed next to each other in order better recreate a muscle niche.
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Mechanical derivation of functional myotubes from adipose-derived stem cells.

TL;DR: Together these data imply enhanced mechanosensitivity for ASCs, making them a better therapeutic cell source for fibrotic muscle, and to exceed BMSC myogenic capacity.