ライフサイエンスコーパス: spongiosa

1 ese genes in rat femoral metaphyseal primary spongiosa.

2 nd also abolishes development of the primary spongiosa.

3 e zones in growth plates and reduced primary spongiosa.

4 rimary spongiosa, and 0.99 for the secondary spongiosa across all datasets; statistical equivalence w

5 in trabecular bone formation in the primary spongiosa and a delay in vascular invasion of the early

6 r both skeletal sites, regions of trabecular spongiosa and cortical bone were identified and segmente

7 hs was accompanied by a reduction in primary spongiosa and increased osteoclast surfaces on histomorp

8 on is dramatically diminished in the primary spongiosa and is eventually lost.

9 ric analysis was performed to study alveolar spongiosa and periodontal ligament (PDL) modeling dynami

10 mnar structure of the physis and metaphyseal spongiosa and provides measures of tract volume and leng

11 5 for the growth plate, 0.92 for the primary spongiosa, and 0.99 for the secondary spongiosa across a

12 7 for the growth plate, 0.92 for the primary spongiosa, and 1.0 for the secondary spongiosa; statisti

13 lar bone within the epiphyseal bone, primary spongiosa, and secondary spongiosa using a deep learning

14 ents, epiphyseal bone, growth plate, primary spongiosa, and secondary spongiosa, using a 2D slice-wis

15 ation induced increased turnover of alveolar spongiosa, and the activity was localized; dramatic esca

16 p had significantly (P <0.05) less calcified spongiosa bone surface, greater periodontal ligament sur

17 ss density and RSP estimation for 45% HA and spongiosa bone, with MAPE values of 0.23% and 0.09% for

18 adipose tissue, 45% hydroxyapatite (HA), and spongiosa bone.

19 sts in either the bone collar or the primary spongiosa but generate ectopic chondrocytes.

20 ed presence of cartilaginous remnants in the spongiosa, confirming a decrease in resorption of the ca

21 ion rate) were three-fold greater, calcified spongiosa decreased by two-fold, and PDL surface increas

22 ue rather than to an increased volume of the spongiosa element of the leaflet itself.

23 All leaflets had variable increases in the spongiosa element within the leaflet itself with some di

24 asionally complete separation of it from the spongiosa element.

25 Primary bone spongiosa formation was also disturbed and was accompani

26 cells of the perichondrium, and the primary spongiosa in fetal growth plates of mice and chickens.

27 ing collagen synthesis) was increased in the spongiosa layer.

28 4 mm; P<0.0001) at 60 days with an increased spongiosa layer.

29 roscale Monte Carlo code that incorporates a spongiosa microstructure model.

30 Here we show that MSPCs in primary spongiosa of long bone in mice at late puberty undergo n

31 Histomorphometric analyses at secondary spongiosa of the femur and at metaphysis of the L4 verte

32 Hairy attachment structures (fossula spongiosa), present in the ancestor of Reduvioidea, were

33 enchyme and correlated with expansion of the spongiosa (proteoglycan-rich) region in Adamts5(-/-) val

34 However, the primary spongiosa region of adult Col9a1 mutant mice showed an a

35 primary spongiosa, and 1.0 for the secondary spongiosa; statistical equivalence within 0.05 mm, [Form

36 mulations and those estimated under infinite spongiosa transport techniques.

37 yseal bone, primary spongiosa, and secondary spongiosa using a deep learning-based segmentation model

38 owth plate, primary spongiosa, and secondary spongiosa, using a 2D slice-wise classification model co

39 emonstrated, however, that a close surrogate-spongiosa volume (combined tissues of trabecular bone an

40 e obtained given knowledge of the trabecular spongiosa volume (SV) of the bone site.

41 ly, a predictive model of the total skeletal spongiosa volume (TSSV) would be a clinically useful too

42 Although the utility of spongiosa volume in estimating patient-specific active m

43 Physical sections of interior spongiosa were then taken and subjected to nuclear magne

44 had a defect in the formation of the primary spongiosa with reduced immature osteoid (new bone format

45 cked within an infinite extent of trabecular spongiosa, with no allowance for particle escape to cort

46 ligence-driven workflow to segment vertebral spongiosa within the field of view (FOV).