ライフサイエンスコーパス: femora

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1 stantial functional role than tibiotarsi and femora.

2 ads, and showed reduced BMD compared with WT femora.

3 mes were not affected in proximal and distal femora.

4 ated distal femora or nonirradiated proximal femora.

5 survival of MSCs in both distal and proximal femora.

6 but no changes were observed in the proximal femora.

7 angiographic images, but not in the proximal femora.

8 tinct from contemporaneous near-modern human femora.

9 c abnormalities, and proximal defects of the femora.

10 h a completely or partially open physis (110 femora, 102 tibiae) and in 56 femora and 60 tibiae in th

11 reased bone ossification in developing chick femora (6%) and tibiae (11%).

12 and osteoblasts were decreased in the distal femora after irradiation, but no changes were observed i

13 Thirty-five femora and 35 tibiae showed no stripe; all patients were

14 en physis (110 femora, 102 tibiae) and in 56 femora and 60 tibiae in the patients with fused physes.

15 Tumor burden in femora and tibiae was also reduced after TbetaRI-I treat

16 results might explain why 4T mice have wider femora and ulnae than do B6 control mice and suggest tha

17 taOsx1) mice had lower cortical thickness in femora and vertebrae because of reduced bone formation a

18 Neandertal femora are distinct from contemporaneous near-modern hum

19 In brief, the tibia and femora are isolated and crushed using a pestle and morta

20 mice had longer and thinner faces and longer femora as revealed by micro-computed tomography analysis

21 Fossil femora discovered in Kenya and attributed to Orrorin tug

22 icate that both hominin and modern great ape femora evolved in different directions from a primitive

23 In the metaphysis of distal femora from ovariectomized rats, analysis showed a signi

24 ular bone volume and bone mineral density in femora from TG mice.

25 ebrae are the most common sites in adults vs femora in children.

26 fragility, as reflected in brittle and weak femora, is an inherent feature of PKU.

27 0.028), whilst a weak relationship exists in femora (mass(0.004)) and tibiotarsi (mass(0.004)).

28 metrical trabecular patterns in the proximal femora may also reflect the different developmental 'fie

29 ion rates were also greater in the ulnae and femora of 6-wk-old 4T mice engaged in normal cage activi

30 Bone fracture repair was analyzed in femora of adult mice on days 7 and 14 postfracture.

31 These predictions were analysed in proximal femora of chimpanzees and modern humans, and in calcanei

32 ma-sprayed (TPS) implants were placed in the femora of each animal 2 weeks following diabetic inducti

33 ma-sprayed (TPS) implants were placed in the femora of each animal, and allowed to osseointegrate for

34 Femora of male Col1a2(oim/+) offspring from natural mati

35 riation, most contrasts in shape between the femora of Neandertals and near-modern humans seem to be

36 nd dramatically stimulated MCP-1 mRNA in the femora of rats receiving daily injections of PTH or in p

37 ls (MSCs) were detected in irradiated distal femora or nonirradiated proximal femora.

38 (<1 mmx1 mmxLength) prepared from four human femora tested in three-point bending.

39 alysis (FEA) of abstract and realistic human femora to address this issue.

40 Vascularity in whole knees and distal femora was significantly increased at 21 days after MIA

41 The blood vessels in the distal femora were destroyed in angiographic images, but not in

42 FINDINGS: Regardless of diet and sex, PKU femora were more brittle, as manifested by lower post-yi

43 mained at this high level for 4 wk in distal femora, whereas the levels were increased at 1 wk and re

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