ライフサイエンスコーパス: cancellous bone

1 matory process that demineralizes trabecular cancellous bone.

2 m in cortical bone, but tempers bone gain in cancellous bone.

3 c stem and progenitor cells (HSPCs) in human cancellous bone.

4 localized throughout the marrow cavities of cancellous bone.

5 in mouse femur is also present within human cancellous bone.

6 tion of a threaded titanium cage packed with cancellous bone.

7 A solvent-preserved, mineralized human cancellous bone allograft (MBA) was recently developed.

8 Sinuses were grafted with mineralized cancellous bone allograft, anorganic bovine bone matrix,

9 orphometric analysis of tetracycline-labeled cancellous bone and dual-energy x-ray absorptiometry, re

10 Cancellous bone and other natural cellular solids have a

11 ne is rooted in the trajectory hypothesis of cancellous bone architecture.

12 We show that the more ductile surfaces of cancellous bone are a result of reduced accumulation of

13 creased bone density, serum osteocalcin, and cancellous bone area along with trabecular narrowing.

14 Cancellous bone area was lower in the patients with CF (

15 Y, 32:68, wt/wt; DBM mixed with cortical and cancellous bone chips 1:4 (DBMC) (11 mg total, of which

16 ociated with enhanced bone resorption in the cancellous bone compartment and with suppressed endocort

17 and there was a trend towards a decrease in cancellous bone connectivity.

18 The MAT- WT --> Kit(W/W-v) mice lost cancellous bone following 2 weeks of HU.

19 HU MAT- mice had elevated cancellous bone formation and resorption compared to oth

20 ls in postnatal mice dramatically stimulated cancellous bone formation via marked expansion of the os

21 hymal progenitors" (MMPs), are essential for cancellous bone formation.

22 Cancellous bone histomorphometry revealed an increased n

23 Cancellous bone histomorphometry revealed that the incre

24 ne marrow stromal cells (BMSCs) form cortico-cancellous bone in rodent models.

25 Histomorphometric parameters characterizing cancellous bone in the distal radius can be derived from

26 Furthermore, increased cancellous bone is abolished by Wnt inhibition but furth

27 ponent of the cascade of events that lead to cancellous bone loss during estrogen deficiency.

28 ontribute to the increase in osteoclasts and cancellous bone loss that occurs after loss of estrogen.

29 ion in mediating estrogen deficiency-induced cancellous bone loss was investigated in ovariectomized

30 s associated with exaggerated disuse-induced cancellous bone loss.

31 with Debio0719 prevented ovariectomy-induced cancellous bone loss.

32 Cancellous bone marrow R2' measured in the proximal femu

33 e, but not in adult mice, whereas epiphyseal cancellous bone mass decreased with loading in both youn

34 likely to accumulate in strut centers making cancellous bone more tolerant of stress concentrations a

35 , bone formation rate, and wall width in the cancellous bone of conditional knock-out mice.

36 These differences appeared whether light, cancellous bone or heavier endosteal bone was removed.

37 creased prevalence of apoptosis in vertebral cancellous bone osteocytes and osteoblasts that follows

38 lysis revealed thin cortical bone and sparse cancellous bone patterns.

39 of osteoblast recruitment during adult human cancellous bone remodeling is lacking.

40 t of estrogens against endocortical, but not cancellous, bone resorption.

41 Advanced visualization of cancellous bone significantly increased the detection of

42 evised a method for obtaining information on cancellous bone structure from iliac bone histomorphomet

43 Cancellous bone structure was treated as a quasi-regular

44 ant decrease in bone mass and alterations in cancellous bone structure.

45 rfaces of the humerus and the periosteal and cancellous bone surfaces of the mandible.

46 We demonstrate that in cancellous bone, the foam-like component of whole bones,

47 tes is essential for osteoclast formation in cancellous bone under physiological conditions, and RANK

48 Cancellous bone volume and cortical thickness were decre

49 Notch in the skeleton causes an increase in cancellous bone volume and enhanced osteoblastic differe

50 reatment was associated with preservation of cancellous bone volume and inhibition of osteoclast form

51 Cancellous bone volume and osteoid markers correlated wi

52 microstructural abnormalities such as lower cancellous bone volume and reduced trabecular thickness.

53 mined by dual-energy densitometry; decreased cancellous bone volume and trabecular width and increase

54 Cancellous bone volume fraction was lower in flight anim

55 e- and bone compartment-specific deficits in cancellous bone volume fraction.

56 Our results demonstrate low cancellous bone volume in adult patients with CF with lo

57 e characterized by a significant decrease in cancellous bone volume in the tibial and femoral metaphy

58 As the mice matured, cancellous bone volume was restored partially in male bu

59 usly over the calvaria of mice and increased cancellous bone volume when orally administered to rats.

60 7(-/-)) exhibit higher bone mineral density, cancellous bone volume, and mechanical strength compared

61 iblings, demonstrated a striking decrease in cancellous bone volume, connectivity, and trabecular num

62 m, and normalization of bone markers such as cancellous bone volume, trabecular number, osteoblast su

63 Cancellous bone volume/tissue volume was below normal co

64 Cancellous bone volumes of ARKO male mice are reduced co

65 ature osteocytes in mineralized cortical and cancellous bone was positive for sclerostin with diffuse

66 However, cancellous bone was preferentially lost in the metaphysi

67 ate loading, especially in those areas where cancellous bone was present.

68 Metal distribution within the part of cancellous bone was revealed for silver as well as for t

69 fiber reinforcement reached the strength of cancellous bone, which was much stronger than previous i