By Minoru Ueda (Ed.)
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References 1. Rheinwald JG, Green H. Serial cultivation of strains of human epidermal keratinocytes: the formation of keratinizing colonies from single cells. Cell. 6: 331,1975 2. Pellegrini G, Traverso CE, Franzi AT. Long-term restoration of damaged corneal surfaces with autologous cultivated corneal epithelium. Lancet. 349: 990,1997 3. Dua HS, Azuara-Blanco A. Limbal stem cell of the corneal epithelium. Surv Ophthalmol. 44: 415,2000 4. Green H, Kehinde O, Thomas J. Growth of cultured human epidermal cells into multiple epithelia suitable for grafting.
Thus bone regeneration may indicate early bone formation and enhanced bone quality as the main advantages of BMDSCs, since our results were consistent with the report of our previous animal experiments [8, 23, 44]. This technique might be effective for maxillary sinus augmentation. This result also might be the effect of this grafted material, tissue-engineered bone by BMDSCs and PRP, and not the effect of sinus membrane elevation alone. The BMDSCs in the bone marrow are induced in cells with osteogenic capacity, and the MSCs in BMDSCs are considered more feasible for tissue engineering because the former proliferates faster due to a lower degree of differentiation.
24: 346,1996 7. Taylar MJ, Hunt CJ. Tolerance of corneas to multimolar dimethyl sulfoxide at 0°C; implications for cryopreservation. Invest Ophthalmol Vis Sci. 30: 400,1989 Chapter 2: Cornea 19 8. Bravo D, Rigley TH, Gibran N. Effect of storage and preservation methods on viability in transplantable human skin allografts. Burns. 26: 367,2000 9. Bank HL, Brokbank KGM. Basic Principles of Cryobiology, J Card Surg. 1: 137,1987 10. Schachar NS, McGann LE. Investigations of low-temperature storage of articular cartilage for transplantation.