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1                 Fourteen patients received a cancellous allograft (CAN group) and the other 14 receiv
2 controls received an intrasocket mineralized cancellous allograft (socket group), and 12 patients rec
3 raft (CAN group) and the other 14 received a cancellous allograft mixed with PRP (PRP group).
4 ine if PRP combined with a rapidly resorbing cancellous allograft would enhance the regenerative resu
5 s treated with BG, such as mineralized human cancellous allograft, were more likely to have greater v
6 te that solvent-preserved, mineralized human cancellous allograft, with or without collagen membrane,
7 nsumption on biomarkers of bone turnover and cancellous and cortical bone architecture in tibia.
8         Lrp4 deficiency promoted progressive cancellous and cortical bone gain in both mutants, altho
9 DBM formulated with hyaluronic acid (HY) and cancellous and cortical bone granules from the same dono
10 antibodies increased bone formation and thus cancellous and cortical bone mass in skeletally mature r
11 Notch2(tm1.1Ecan) mutant mice exhibit severe cancellous and cortical bone osteopenia due to increased
12   In conclusion, Notch2(Q2319X) mice exhibit cancellous and cortical bone osteopenia, enhanced osteoc
13 ntrols; and at 1 month of age they exhibited cancellous and cortical bone osteopenia.
14 eases the density, area and strength of both cancellous and cortical bone.
15       A solvent-preserved, mineralized human cancellous bone allograft (MBA) was recently developed.
16        Sinuses were grafted with mineralized cancellous bone allograft, anorganic bovine bone matrix,
17 orphometric analysis of tetracycline-labeled cancellous bone and dual-energy x-ray absorptiometry, re
18 effects of microstructure on fatigue life in cancellous bone and lattice structures are described emp
19                The mechanical performance of cancellous bone and microarchitectured materials is enha
20                                              Cancellous bone and other natural cellular solids have a
21 ne is rooted in the trajectory hypothesis of cancellous bone architecture.
22    We show that the more ductile surfaces of cancellous bone are a result of reduced accumulation of
23 creased bone density, serum osteocalcin, and cancellous bone area along with trabecular narrowing.
24                                              Cancellous bone area was lower in the patients with CF (
25 ts osteoclastogenesis and bone resorption in cancellous bone but increases intracortical remodeling a
26 Y, 32:68, wt/wt; DBM mixed with cortical and cancellous bone chips 1:4 (DBMC) (11 mg total, of which
27 ociated with enhanced bone resorption in the cancellous bone compartment and with suppressed endocort
28  and there was a trend towards a decrease in cancellous bone connectivity.
29                                   Thirty-six cancellous bone cores were harvested from bovine metatar
30                                              Cancellous bone demonstrated deterioration of bone quali
31 nversely, load-induced improvements of adult cancellous bone depended on glycolysis.
32         The MAT- WT --> Kit(W/W-v) mice lost cancellous bone following 2 weeks of HU.
33                    HU MAT- mice had elevated cancellous bone formation and resorption compared to oth
34 ls in postnatal mice dramatically stimulated cancellous bone formation via marked expansion of the os
35 hymal progenitors" (MMPs), are essential for cancellous bone formation.
36 is study, data suggests GTR using allogeneic cancellous bone graft and absorbable collagen membrane t
37 defects treated with GTR using an allogeneic cancellous bone graft and covered by an absorbable membr
38                                              Cancellous bone histomorphometry revealed an increased n
39                                              Cancellous bone histomorphometry revealed that the incre
40 ne marrow stromal cells (BMSCs) form cortico-cancellous bone in rodent models.
41  Histomorphometric parameters characterizing cancellous bone in the distal radius can be derived from
42                       Furthermore, increased cancellous bone is abolished by Wnt inhibition but furth
43  by PTH or alendronate generated substantial cancellous bone locally in the diaphyseal medulla.
44 ponent of the cascade of events that lead to cancellous bone loss during estrogen deficiency.
45                                              Cancellous bone loss in femur in both genotypes was asso
46 ontribute to the increase in osteoclasts and cancellous bone loss that occurs after loss of estrogen.
47 ion in mediating estrogen deficiency-induced cancellous bone loss was investigated in ovariectomized
48 s associated with exaggerated disuse-induced cancellous bone loss.
49 with Debio0719 prevented ovariectomy-induced cancellous bone loss.
50                                              Cancellous bone marrow R2' measured in the proximal femu
51 s suggest that CMA plays a role in vertebral cancellous bone mass accrual in young adult mice and tha
52  age female L2ACgKO mice had lower vertebral cancellous bone mass compared to wild-type (WT) controls
53  and female L2ACgKO mice had lower vertebral cancellous bone mass compared to WT controls.
54 e, but not in adult mice, whereas epiphyseal cancellous bone mass decreased with loading in both youn
55 likely to accumulate in strut centers making cancellous bone more tolerant of stress concentrations a
56 , bone formation rate, and wall width in the cancellous bone of conditional knock-out mice.
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                                          The cancellous bone showed a similar trend.
63                    Advanced visualization of cancellous bone significantly increased the detection of
64 evised a method for obtaining information on cancellous bone structure from iliac bone histomorphomet
65                                              Cancellous bone structure was treated as a quasi-regular
66 ant decrease in bone mass and alterations in cancellous bone structure.
67 rfaces of the humerus and the periosteal and cancellous bone surfaces of the mandible.
68 tes is essential for osteoclast formation in cancellous bone under physiological conditions, and RANK
69                                              Cancellous bone volume and cortical thickness were decre
70  Notch in the skeleton causes an increase in cancellous bone volume and enhanced osteoblastic differe
71 reatment was associated with preservation of cancellous bone volume and inhibition of osteoclast form
72                                              Cancellous bone volume and osteoid markers correlated wi
73  microstructural abnormalities such as lower cancellous bone volume and reduced trabecular thickness.
74 mined by dual-energy densitometry; decreased cancellous bone volume and trabecular width and increase
75    ob/ob mice pair-fed to WT mice had normal cancellous bone volume fraction (BV/TV) in distal femur,
76  content (BMC) and density (BMD), and higher cancellous bone volume fraction in lumbar vertebra (LV).
77                                              Cancellous bone volume fraction was lower in flight anim
78 e- and bone compartment-specific deficits in cancellous bone volume fraction.
79                  Our results demonstrate low cancellous bone volume in adult patients with CF with lo
80 e characterized by a significant decrease in cancellous bone volume in the tibial and femoral metaphy
81                         As the mice matured, cancellous bone volume was restored partially in male bu
82 usly over the calvaria of mice and increased cancellous bone volume when orally administered to rats.
83 7(-/-)) exhibit higher bone mineral density, cancellous bone volume, and mechanical strength compared
84 iblings, demonstrated a striking decrease in cancellous bone volume, connectivity, and trabecular num
85 m, and normalization of bone markers such as cancellous bone volume, trabecular number, osteoblast su
86 ed with declines in bone mineral density and cancellous bone volume.
87                                              Cancellous bone volume/tissue volume was below normal co
88                                              Cancellous bone volumes of ARKO male mice are reduced co
89 ature osteocytes in mineralized cortical and cancellous bone was positive for sclerostin with diffuse
90                                     However, cancellous bone was preferentially lost in the metaphysi
91 ate loading, especially in those areas where cancellous bone was present.
92        Metal distribution within the part of cancellous bone was revealed for silver as well as for t
93                        Here, we show that in cancellous bone, a naturally occurring lightweight micro
94 palpable difference between the cortical and cancellous bone, both of which have different material p
95 anatomical structures including cortical and cancellous bone, intervertebral discs, ligaments, and ca
96                       We demonstrate that in cancellous bone, the foam-like component of whole bones,
97  fiber reinforcement reached the strength of cancellous bone, which was much stronger than previous i
98   The ability to create mechanically strong 'cancellous bone-like' printable implants for tissue repa
99 nd physical properties of human cortical and cancellous bone.
100 tion of a threaded titanium cage packed with cancellous bone.
101 d unique metabolic programs for cortical and cancellous bone.
102 osteum but not in cells from endocortical or cancellous bone.
103 matory process that demineralizes trabecular cancellous bone.
104 m in cortical bone, but tempers bone gain in cancellous bone.
105 c stem and progenitor cells (HSPCs) in human cancellous bone.
106  localized throughout the marrow cavities of cancellous bone.
107  in mouse femur is also present within human cancellous bone.
108 t of estrogens against endocortical, but not cancellous, bone resorption.
109 tructed and registered, and the cortical and cancellous bones of the mandible and the maxilla were se
110 n derivative (EMD) and particulate anorganic cancellous bovine-derived bone xenograft (BDX) have both
111   In summary, both the particulate anorganic cancellous bovine-derived bone xenograft used alone and
112                  This protection occurred in cancellous, but not cortical, bone and was associated wi
113 or the protective effect of estrogens on the cancellous, but not the cortical, bone compartment that
114 sayed demineralized bone matrix and cortical cancellous chips uniformly dispersed in a thermoplastic
115 iaphysis, and metaphyseal cortical shell and cancellous core.
116 garding use of a combination 50%/50% cortico-cancellous FDBA compared with a 100% cortical or 100% ca
117 in the cortical FDBA group compared with the cancellous FDBA group (P = 0.019).
118 neralized CT/other material was found in the cancellous FDBA group compared with the cortical FDBA gr
119  new bone formation between the cortical and cancellous FDBA groups (P = 0.857).
120 s FDBA compared with a 100% cortical or 100% cancellous FDBA in ridge preservation.
121 ion in non-molar sites using 50%/50% cortico-cancellous FDBA versus 100% cortical and 100% cancellous
122 ancellous FDBA, 100% cortical FDBA, and 100% cancellous FDBA when used in ridge preservation of non-m
123 omly assigned to each group (cortical versus cancellous FDBA).
124 or dimensional changes among 50%/50% cortico-cancellous FDBA, 100% cortical FDBA, and 100% cancellous
125 ancellous FDBA versus 100% cortical and 100% cancellous FDBA.
126  100% cancellous FDBA; or 3) 50%/50% cortico-cancellous FDBA.
127 preservation in humans using cortical versus cancellous FDBA.
128 he following: 1) 100% cortical FDBA; 2) 100% cancellous FDBA; or 3) 50%/50% cortico-cancellous FDBA.
129  years would result in measurable changes to cancellous features and the biochemical markers compared
130 d ridge preservation with either cortical or cancellous freeze-dried bone allograft (FDBA) in non-mol
131  greater loss of lingual ridge height in the cancellous group.
132 ative concentration of HSPCs and BVFs within cancellous marrow was observed to diminish with increasi
133 ralized bone matrix (GDBM) by comparing with cancellous mineralized bone matrix (CMBM) and anorganic
134                                 Cortical and cancellous mineralized freeze-dried bone allografts (FDB
135  osteoblasts or osteocytes did not influence cancellous or cortical bone mass.
136   Surprisingly, we found no effect on either cancellous or cortical bone, even following mechanical l
137 orticoid-induced osteoporosis, the number of cancellous osteoclasts increased, even though osteoclast
138 dministration of Notch2 ASOs ameliorates the cancellous osteopenia of Notch2(tm1.1Ecan) mice, and bon
139 nous (type I) bone versus more trabeculated, cancellous (type III) bone.
140 e socket graft procedure plus buccal overlay cancellous xenograft (overlay group).

 
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