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- W2014813902 abstract "Purpose The main aim of the present study was to evaluate the capacity of stem cells from human exfoliated deciduous teeth (SHED) to enhance mandibular distraction osteogenesis (DO) in rabbits. Materials and Methods A randomized controlled trial was conducted. Eighteen skeletally immature New Zealand white rabbits were divided into 2 groups, with 9 in the control group and 9 in the SHED group. The SHED were isolated, expanded, and characterized. Six million cells were transplanted into the distracted area during the osteotomy period. After a 4-day latency period, a total of 6 mm was distracted for 6 days. The newly formed bone was analyzed radiologically, histologically, and histomorphometrically at 2, 4, and 6 weeks postoperatively. Nonparametric analysis of variance (Kruskal-Wallis test) was used for data analysis, and P < .05 was considered statistically significant. Results The cell lineage was positive for the 2 mesenchymal stem cell markers tested (CD105 and CD166). More mature bone in the SHED transplanted group was observed radiographically and histologically. Histomorphologically, the percentage of newly formed bone after 2, 4, and 6 weeks was 18.41% and 41.53%, 31.68% and 59.78%, and 52.34% and 65.24% in the control and SHED groups, respectively. The difference between the groups was statistically significant (P = .012). The bone union and stage of bone maturity scores were significantly different between the control and SHED groups (P = .006 and P = .011, respectively). Conclusions Our findings suggest that SHED can serve as an additional cell resource for DO enhancement in rabbits and might be a promising model for the reconstruction of large mandibular defects in human oral maxillofacial surgery. The main aim of the present study was to evaluate the capacity of stem cells from human exfoliated deciduous teeth (SHED) to enhance mandibular distraction osteogenesis (DO) in rabbits. A randomized controlled trial was conducted. Eighteen skeletally immature New Zealand white rabbits were divided into 2 groups, with 9 in the control group and 9 in the SHED group. The SHED were isolated, expanded, and characterized. Six million cells were transplanted into the distracted area during the osteotomy period. After a 4-day latency period, a total of 6 mm was distracted for 6 days. The newly formed bone was analyzed radiologically, histologically, and histomorphometrically at 2, 4, and 6 weeks postoperatively. Nonparametric analysis of variance (Kruskal-Wallis test) was used for data analysis, and P < .05 was considered statistically significant. The cell lineage was positive for the 2 mesenchymal stem cell markers tested (CD105 and CD166). More mature bone in the SHED transplanted group was observed radiographically and histologically. Histomorphologically, the percentage of newly formed bone after 2, 4, and 6 weeks was 18.41% and 41.53%, 31.68% and 59.78%, and 52.34% and 65.24% in the control and SHED groups, respectively. The difference between the groups was statistically significant (P = .012). The bone union and stage of bone maturity scores were significantly different between the control and SHED groups (P = .006 and P = .011, respectively). Our findings suggest that SHED can serve as an additional cell resource for DO enhancement in rabbits and might be a promising model for the reconstruction of large mandibular defects in human oral maxillofacial surgery." @default.
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- W2014813902 date "2013-10-01" @default.
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- W2014813902 title "Transplantation of Human Dental Pulp Stem Cells: Enhance Bone Consolidation in Mandibular Distraction Osteogenesis" @default.
- W2014813902 cites W1718946616 @default.
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- W2014813902 cites W1918057567 @default.
- W2014813902 cites W1964759217 @default.
- W2014813902 cites W1969696192 @default.
- W2014813902 cites W1971245271 @default.
- W2014813902 cites W1979089029 @default.
- W2014813902 cites W1979834092 @default.
- W2014813902 cites W1982989235 @default.
- W2014813902 cites W1983543109 @default.
- W2014813902 cites W1983582703 @default.
- W2014813902 cites W1983919104 @default.
- W2014813902 cites W1984875989 @default.
- W2014813902 cites W1988147562 @default.
- W2014813902 cites W1989078866 @default.
- W2014813902 cites W1993326869 @default.
- W2014813902 cites W1998669825 @default.
- W2014813902 cites W2002154287 @default.
- W2014813902 cites W2006735539 @default.
- W2014813902 cites W2007623810 @default.
- W2014813902 cites W2008792188 @default.
- W2014813902 cites W2014336192 @default.
- W2014813902 cites W2016931709 @default.
- W2014813902 cites W2023001629 @default.
- W2014813902 cites W2035976926 @default.
- W2014813902 cites W2038790375 @default.
- W2014813902 cites W2046393728 @default.
- W2014813902 cites W2061522812 @default.
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- W2014813902 cites W2070556700 @default.
- W2014813902 cites W2079487768 @default.
- W2014813902 cites W2080137511 @default.
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- W2014813902 cites W2090103863 @default.
- W2014813902 cites W2090831878 @default.
- W2014813902 cites W2091641760 @default.
- W2014813902 cites W2093571518 @default.
- W2014813902 cites W2098968833 @default.
- W2014813902 cites W2106370377 @default.
- W2014813902 cites W2116864112 @default.
- W2014813902 cites W2119610794 @default.
- W2014813902 cites W2132146530 @default.
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- W2014813902 cites W2158048826 @default.
- W2014813902 cites W2168424538 @default.
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- W2014813902 doi "https://doi.org/10.1016/j.joms.2013.05.016" @default.
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