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Noritaka Isogai

Researcher at Kindai University

Publications -  106
Citations -  2029

Noritaka Isogai is an academic researcher from Kindai University. The author has contributed to research in topics: Cartilage & Tissue engineering. The author has an hindex of 19, co-authored 104 publications receiving 1884 citations. Previous affiliations of Noritaka Isogai include Harvard University & Northeast Ohio Medical University.

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Creation Of Viable Pulmonary Artery Autografts Through Tissue Engineering

TL;DR: Living vascular grafts engineered from autologous cells and biodegradable polymers functioned well in the pulmonary circulation as a pulmonary artery replacement and demonstrated an increase in diameter suggesting growth and development of endothelial lining and extracellular matrix, including collagen and elastic fibers.
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Formation of phalanges and small joints by tissue-engineering.

TL;DR: In this article, the authors describe the formation of small phalanges and whole joints from three types of bovine-cell sources transplanted onto biodegradable polymer matrices.
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Comparison of different chondrocytes for use in tissue engineering of cartilage model structures.

TL;DR: Bovine chondrocytes obtained from different cartilaginous sites in an animal may elicit distinct responses during their respective development of a tissue-engineered neocartilage, and this observation is critical in the design and elaboration of any tissue- engineered cartilage model.
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Tissue engineering a model for the human ear: Assessment of size, shape, morphology, and gene expression following seeding of different chondrocytes

TL;DR: The collective data suggest that nasoseptal, articular, and auricular cartilages represent harvest sites suitable for development of tissue‐engineered human ear models with retention over time of three‐dimensional construct architecture, gene expression, and extracellular matrix composition comparable to normal, nonmineralizing cartilage.
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Experimental use of fibrin glue to induce site-directed osteogenesis from cultured periosteal cells.

TL;DR: The feasibility of initiating site-directed formation of bone structures at heterotopic tissue sites by means of injection of cultured periosteal cells and matrix in a fibrin glue carrier is supported.