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1 nd physical properties of human cortical and cancellous bone.
2 matory process that demineralizes trabecular cancellous bone.
3 m in cortical bone, but tempers bone gain in cancellous bone.
4 c stem and progenitor cells (HSPCs) in human cancellous bone.
5  localized throughout the marrow cavities of cancellous bone.
6  in mouse femur is also present within human cancellous bone.
7 tion of a threaded titanium cage packed with cancellous bone.
8 d unique metabolic programs for cortical and cancellous bone.
9 osteum but not in cells from endocortical or cancellous bone.
10                        Here, we show that in cancellous bone, a naturally occurring lightweight micro
11       A solvent-preserved, mineralized human cancellous bone allograft (MBA) was recently developed.
12        Sinuses were grafted with mineralized cancellous bone allograft, anorganic bovine bone matrix,
13 orphometric analysis of tetracycline-labeled cancellous bone and dual-energy x-ray absorptiometry, re
14 effects of microstructure on fatigue life in cancellous bone and lattice structures are described emp
15                The mechanical performance of cancellous bone and microarchitectured materials is enha
16                                              Cancellous bone and other natural cellular solids have a
17 ne is rooted in the trajectory hypothesis of cancellous bone architecture.
18    We show that the more ductile surfaces of cancellous bone are a result of reduced accumulation of
19 creased bone density, serum osteocalcin, and cancellous bone area along with trabecular narrowing.
20                                              Cancellous bone area was lower in the patients with CF (
21 palpable difference between the cortical and cancellous bone, both of which have different material p
22 ts osteoclastogenesis and bone resorption in cancellous bone but increases intracortical remodeling a
23 Y, 32:68, wt/wt; DBM mixed with cortical and cancellous bone chips 1:4 (DBMC) (11 mg total, of which
24 ociated with enhanced bone resorption in the cancellous bone compartment and with suppressed endocort
25  and there was a trend towards a decrease in cancellous bone connectivity.
26                                   Thirty-six cancellous bone cores were harvested from bovine metatar
27                                              Cancellous bone demonstrated deterioration of bone quali
28 nversely, load-induced improvements of adult cancellous bone depended on glycolysis.
29         The MAT- WT --> Kit(W/W-v) mice lost cancellous bone following 2 weeks of HU.
30                    HU MAT- mice had elevated cancellous bone formation and resorption compared to oth
31 ls in postnatal mice dramatically stimulated cancellous bone formation via marked expansion of the os
32 hymal progenitors" (MMPs), are essential for cancellous bone formation.
33 is study, data suggests GTR using allogeneic cancellous bone graft and absorbable collagen membrane t
34 defects treated with GTR using an allogeneic cancellous bone graft and covered by an absorbable membr
35                                              Cancellous bone histomorphometry revealed an increased n
36                                              Cancellous bone histomorphometry revealed that the incre
37 ne marrow stromal cells (BMSCs) form cortico-cancellous bone in rodent models.
38  Histomorphometric parameters characterizing cancellous bone in the distal radius can be derived from
39 anatomical structures including cortical and cancellous bone, intervertebral discs, ligaments, and ca
40                       Furthermore, increased cancellous bone is abolished by Wnt inhibition but furth
41   The ability to create mechanically strong 'cancellous bone-like' printable implants for tissue repa
42  by PTH or alendronate generated substantial cancellous bone locally in the diaphyseal medulla.
43 ponent of the cascade of events that lead to cancellous bone loss during estrogen deficiency.
44                                              Cancellous bone loss in femur in both genotypes was asso
45 ontribute to the increase in osteoclasts and cancellous bone loss that occurs after loss of estrogen.
46 ion in mediating estrogen deficiency-induced cancellous bone loss was investigated in ovariectomized
47 s associated with exaggerated disuse-induced cancellous bone loss.
48 with Debio0719 prevented ovariectomy-induced cancellous bone loss.
49                                              Cancellous bone marrow R2' measured in the proximal femu
50 s suggest that CMA plays a role in vertebral cancellous bone mass accrual in young adult mice and tha
51  age female L2ACgKO mice had lower vertebral cancellous bone mass compared to wild-type (WT) controls
52  and female L2ACgKO mice had lower vertebral cancellous bone mass compared to WT controls.
53 e, but not in adult mice, whereas epiphyseal cancellous bone mass decreased with loading in both youn
54 likely to accumulate in strut centers making cancellous bone more tolerant of stress concentrations a
55 , bone formation rate, and wall width in the cancellous bone of conditional knock-out mice.
56 tructed and registered, and the cortical and cancellous bones of the mandible and the maxilla were se
57    These differences appeared whether light, cancellous bone or heavier endosteal bone was removed.
58 creased prevalence of apoptosis in vertebral cancellous bone osteocytes and osteoblasts that follows
59 n conclusion, Notch2(tm1.1Ecan) mice exhibit cancellous bone osteopenia that can be ameliorated by sy
60 lysis revealed thin cortical bone and sparse cancellous bone patterns.
61 of osteoblast recruitment during adult human cancellous bone remodeling is lacking.
62 t of estrogens against endocortical, but not cancellous, bone resorption.
63                                          The cancellous bone showed a similar trend.
64                    Advanced visualization of cancellous bone significantly increased the detection of
65 evised a method for obtaining information on cancellous bone structure from iliac bone histomorphomet
66                                              Cancellous bone structure was treated as a quasi-regular
67 ant decrease in bone mass and alterations in cancellous bone structure.
68 rfaces of the humerus and the periosteal and cancellous bone surfaces of the mandible.
69                       We demonstrate that in cancellous bone, the foam-like component of whole bones,
70 tes is essential for osteoclast formation in cancellous bone under physiological conditions, and RANK
71                                              Cancellous bone volume and cortical thickness were decre
72  Notch in the skeleton causes an increase in cancellous bone volume and enhanced osteoblastic differe
73 reatment was associated with preservation of cancellous bone volume and inhibition of osteoclast form
74                                              Cancellous bone volume and osteoid markers correlated wi
75  microstructural abnormalities such as lower cancellous bone volume and reduced trabecular thickness.
76 mined by dual-energy densitometry; decreased cancellous bone volume and trabecular width and increase
77    ob/ob mice pair-fed to WT mice had normal cancellous bone volume fraction (BV/TV) in distal femur,
78  content (BMC) and density (BMD), and higher cancellous bone volume fraction in lumbar vertebra (LV).
79                                              Cancellous bone volume fraction was lower in flight anim
80 e- and bone compartment-specific deficits in cancellous bone volume fraction.
81                  Our results demonstrate low cancellous bone volume in adult patients with CF with lo
82 e characterized by a significant decrease in cancellous bone volume in the tibial and femoral metaphy
83                         As the mice matured, cancellous bone volume was restored partially in male bu
84 usly over the calvaria of mice and increased cancellous bone volume when orally administered to rats.
85 7(-/-)) exhibit higher bone mineral density, cancellous bone volume, and mechanical strength compared
86 iblings, demonstrated a striking decrease in cancellous bone volume, connectivity, and trabecular num
87 m, and normalization of bone markers such as cancellous bone volume, trabecular number, osteoblast su
88 ed with declines in bone mineral density and cancellous bone volume.
89                                              Cancellous bone volume/tissue volume was below normal co
90                                              Cancellous bone volumes of ARKO male mice are reduced co
91 ature osteocytes in mineralized cortical and cancellous bone was positive for sclerostin with diffuse
92                                     However, cancellous bone was preferentially lost in the metaphysi
93 ate loading, especially in those areas where cancellous bone was present.
94        Metal distribution within the part of cancellous bone was revealed for silver as well as for t
95  fiber reinforcement reached the strength of cancellous bone, which was much stronger than previous i