戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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  have increased total body weight and longer femora.
10 c abnormalities, and proximal defects of the femora.
11 h a completely or partially open physis (110 femora, 102 tibiae) and in 56 femora and 60 tibiae in th
12 reased bone ossification in developing chick femora (6%) and tibiae (11%).
13 and osteoblasts were decreased in the distal femora after irradiation, but no changes were observed i
14                                  Thirty-five femora and 35 tibiae showed no stripe; all patients were
15 en physis (110 femora, 102 tibiae) and in 56 femora and 60 tibiae in the patients with fused physes.
16 ry of microcomputed tomography data from the femora and humeri of 35 skeletons (17 female and 18 male
17 gth remained unchanged through age in female femora and male diaphyses but declined in female humeri
18 dmark localization, bone segmentation of the femora and pelvis, and a shape model for annotation tran
19                              Tumor burden in femora and tibiae was also reduced after TbetaRI-I treat
20 , as humeri are more sensitive to aging than femora and tibiae.
21 results might explain why 4T mice have wider femora and ulnae than do B6 control mice and suggest tha
22 taOsx1) mice had lower cortical thickness in femora and vertebrae because of reduced bone formation a
23 ropean Holocene sample of 1881 adult humeri, femora, and tibiae.
24                                   Neandertal femora are distinct from contemporaneous near-modern hum
25                      In brief, the tibia and femora are isolated and crushed using a pestle and morta
26 mice had longer and thinner faces and longer femora as revealed by micro-computed tomography analysis
27                                       Fossil femora discovered in Kenya and attributed to Orrorin tug
28 Our results based on complete and fragmented femora evidenced a dimorphism characterized by variation
29 icate that both hominin and modern great ape femora evolved in different directions from a primitive
30                  In the metaphysis of distal femora from ovariectomized rats, analysis showed a signi
31 ular bone volume and bone mineral density in femora from TG mice.
32 ebrae are the most common sites in adults vs femora in children.
33 ze and shape compared to WT controls; distal femora in Prg4(-/-) mice are enlarged, extended (anterop
34  fragility, as reflected in brittle and weak femora, is an inherent feature of PKU.
35 0.028), whilst a weak relationship exists in femora (mass(0.004)) and tibiotarsi (mass(0.004)).
36 metrical trabecular patterns in the proximal femora may also reflect the different developmental 'fie
37 ion rates were also greater in the ulnae and femora of 6-wk-old 4T mice engaged in normal cage activi
38         Bone fracture repair was analyzed in femora of adult mice on days 7 and 14 postfracture.
39  These predictions were analysed in proximal femora of chimpanzees and modern humans, and in calcanei
40 e performed on metacarpal bones and proximal femora of different primate species to confirm prior stu
41 ma-sprayed (TPS) implants were placed in the femora of each animal 2 weeks following diabetic inducti
42 ma-sprayed (TPS) implants were placed in the femora of each animal, and allowed to osseointegrate for
43 , maxillary and labial palps, and unmodified femora of hind legs, providing key information for the e
44                                              Femora of male Col1a2(oim/+) offspring from natural mati
45 riation, most contrasts in shape between the femora of Neandertals and near-modern humans seem to be
46 nd dramatically stimulated MCP-1 mRNA in the femora of rats receiving daily injections of PTH or in p
47 across trabecular sections from the proximal femora of three groups (n = 10 each): ageing non-fractur
48 ls (MSCs) were detected in irradiated distal femora or nonirradiated proximal femora.
49                            Micro-CT scans of femora revealed a reduction in inner and outer surface e
50 eometric morphometrics to characterize mouse femora shape changes, which were correlated to cross-sec
51 orate these findings and murine Emilin1(-/-) femora show abnormal trabecular bone formation and stren
52 (<1 mmx1 mmxLength) prepared from four human femora tested in three-point bending.
53 alysis (FEA) of abstract and realistic human femora to address this issue.
54                       We find that Prg4(-/-) femora vary in size and shape compared to WT controls; d
55        Vascularity in whole knees and distal femora was significantly increased at 21 days after MIA
56              The blood vessels in the distal femora were destroyed in angiographic images, but not in
57    FINDINGS: Regardless of diet and sex, PKU femora were more brittle, as manifested by lower post-yi
58                                              Femora were obtained post-mortem from animals exposed to
59 mained at this high level for 4 wk in distal femora, whereas the levels were increased at 1 wk and re