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Jacques P. Guyette

Researcher at Harvard University

Publications -  24
Citations -  1935

Jacques P. Guyette is an academic researcher from Harvard University. The author has contributed to research in topics: Decellularization & Mesenchymal stem cell. The author has an hindex of 12, co-authored 24 publications receiving 1632 citations. Previous affiliations of Jacques P. Guyette include Worcester Polytechnic Institute.

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Regeneration and experimental orthotopic transplantation of a bioengineered kidney

TL;DR: To regenerate functional tissue, rat kidney scaffolds are seeded with epithelial and endothelial cells and perfused these cell-seeded constructs in a whole-organ bioreactor, resulting in grafts that produced rudimentary urine in vitro when perfused through their intrinsic vascular bed.
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Bioengineering Human Myocardium on Native Extracellular Matrix

TL;DR: Native cardiac extracellular matrix scaffolds maintain matrix components and structure to support the seeding and engraftment of human induced pluripotent stem cell-derived cardiomyocytes and enable the bioengineering of functional human myocardial-like tissue of multiple complexities.
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Perfusion decellularization of human and porcine lungs: bringing the matrix to clinical scale.

TL;DR: SDS-based perfusion decellularization can be applied to whole porcine and human lungs to generate biocompatible organ scaffolds with preserved ECM composition and architecture.
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Perfusion decellularization of whole organs

TL;DR: Combining the unique structural and biochemical properties of native acellular scaffolds with subsequent recellularization techniques offers a novel platform for organ engineering and regeneration, for experimentation ex vivo and potential clinical application in vivo.
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Enhanced lung epithelial specification of human induced pluripotent stem cells on decellularized lung matrix.

TL;DR: Decellularized lung matrix supports the culture and lineage commitment of human iPSC-derived lung progenitor cells and may enable further in vivo graft maturation and enhance early lung fate.