ライフサイエンスコーパス: bone substitute

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1 pressed alkaline phosphatase activity in the bone substitute.

2 a popular source for several of the natural bone substitutes.

3 nation with a mixture of autogenous bone and bone substitutes, 14 in association with bone substitute

4 mplants placed in such situations, even with bone substitutes alone, prompted the authors of this stu

5 ate-based materials have been widely used as bone substitutes and more recently are being exploited t

6 al regeneration has focused predominantly on bone substitutes and/or barrier membrane application to

7 Osseous wound healing may be enhanced if bone substitutes are combined with autologous bone marro

8 Synthetic bone substitutes are effective, but healing is slow and

9 improved bone fill as compared to a beta-TCP bone substitute at 6 months.

10 We then engineered functional bone substitutes by culturing hiPSC-derived mesenchymal

11 Bone substitutes can be designed to replicate physiologi

12 (PA) (PPCH-PA) composite graft material as a bone substitute compared to positive and negative contro

13 or 24 hr, whereas this percentage doubled on bone substitute containing NAC.

14 ytokine levels from human osteoblasts on the bone substitute decreased by one-third or more with addi

15 flap elevation, membrane usage, and type of bone substitute employed) on the outcomes of ridge prese

16 and bone substitutes, 14 in association with bone substitutes, five using only titanium grids.

17 ts pave the way for growing patient-specific bone substitutes for reconstructive treatments of the sk

18 Because alloplastic bone substitutes generally have relatively poor osteogen

19 radiographs of thirty children with ceramic bone substitute grafting were analyzed using the softwar

20 defect randomly distributed to: 1) group 1: bone-substitute grafting control (n = 10); 2) group 2: e

21 The availability of bovine derived xenogenic bone substitutes has made it possible to avoid traumatic

22 Lack of cytocompatibility in bone substitutes impairs healing in surrounding bone.

23 ar analysis confirmed that the maturation of bone substitutes in perfusion bioreactors results in glo

24 ypothesized that a clinically used inorganic bone substitute is cytotoxic to osteoblasts due to oxida

25 f bone formation than that produced with the bone substitute materials alone or rhBMP-2/(ACS) and CL

26 ogenetic protein 2 (rhBMP-2) associated with bone substitute materials beta-tricalcium phosphate (bet

27 llagen sponge (ACS) combined with all of the bone substitute materials tested resulted in a greater a

28 a greater level of biodegradation of all the bone substitute materials tested.

29 %), and regenerative surgery procedures with bone substitute materials were chosen in 20% of the case

30 le in the tests a deantigenated collagenated bone substitute of porcine origin was used to fill the g

31 ts of GTR therapy without the use of bone or bone substitutes on Class II furcation defects.

32 aluation of resorbable membranes, and use of bone substitutes or growth factors to enhance bone regen

33 e purpose of this study was to compare three bone substitute pastes of different HA content and parti

34 Engineering of viable bone substitutes that can be personalized to meet specif

35 NAC alleviated cytotoxicity of the bone substitute to osteoblastic viability and function,

36 remain to be clarified as to the efficacy of bone substitutes used in GTR procedures.

37 r ROS levels markedly increased on and under bone substitutes, which were reduced by prior addition o

38 ely; P < 0.001) than the sites receiving the bone substitute with buffer at 6 months.

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