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1 ors, we prepared conditioned media (CM) from calvariae.
2 eavage ends in wild-type but not Col1a1(r/r) calvariae.
3 nto the subcutaneous tissues overlying mouse calvariae.
4 lonal cell line, 2T3, derived from the mouse calvariae.
5 ae vs. an increase in Alx4 in Ambn-deficient calvariae.
6  months in long bones and vertebrae, but not calvariae.
7         Analysis of Amel- and Ambn-deficient calvariae and calvarial osteoblast cultures revealed a d
8 n-deficient osteoblasts from neonatal murine calvariae and found that the absence of bgn caused less
9  maximally induced mkp1 mRNA levels in mouse calvariae and long bones in vivo at 0.5 hours.
10 d to determine PTH's effect on mkp1 in mouse calvariae and long bones.
11                                     In mouse calvariae and MC3T3 cells, expression profiles of enamel
12 ormation in organ cultures of neonatal mouse calvariae, and a neutralizing antibody to hPDGF-BB block
13 ed by sequential digestion of neonatal mouse calvariae, and cultured with fetal calf serum (10% for o
14   Critical-sized defects were created in rat calvariae, and GBR procedures were performed with a coll
15 of osteopetrosis in tibiae and osteolysis in calvariae as a result of cathepsin K mutation.
16 brae in one strain) and cortical bone in the calvariae (bone mineral density was decreased on average
17 extreme ends of the osteogenic fronts of the calvariae, facilitating expansion of the skull and closu
18 ns, we detect empty lacunae in osteocytes in calvariae from Col1a1(r/r) mice at age 2 weeks, increasi
19 d periosteal proliferation were increased in calvariae from PTH-treated +/+ mice, whereas in r/r mice
20 at BIG-3 was expressed in the osteoblasts of calvariae isolated from mouse embryos.
21 on in cultures of osteoblasts from fetal rat calvariae (Ob cells).
22 blast-enriched cells from 22-d-old fetal rat calvariae (Ob cells).
23  in osteoblast-enriched cells from fetal rat calvariae (Ob cells).
24  of osteoblast-enriched cells from fetal rat calvariae (Ob cells).
25     Injection of recombinant MIP-1alpha over calvariae of normal mice evoked a striking increase in o
26                               Long bones and calvariae of TG mice showed reduced COL1A1 and osteocalc
27 e osteoprogenitor cell line derived from the calvariae of transgenic mice containing the SV40 T-antig
28 emthyl-methacrylate particle implantation on calvariae of wild-type animals.
29 sts cultured on dentine or explants of mouse calvariae prelabeled with (45)Ca, we could not detect si
30   Critical-sized defects were created in rat calvariae previously treated with radiation.
31 were harvested from fetal Swiss Webster mice calvariae prior to osteoblast differentiation and calcif
32                    qRT-PCR analysis of total calvariae versus isolated osteoblasts showed that DKK3,
33 n, and a reduction in Alx4 in Amel-deficient calvariae vs. an increase in Alx4 in Ambn-deficient calv
34                               Neonatal mouse calvariae were cultured in acid (Acid; pH = 7.06 +/- 0.0
35                                              Calvariae were harvested at 10 weeks post-surgery and ev
36                                          The calvariae were harvested at 30 and 60 postoperative days
37                Treatment of Bmpr1a-deficient calvariae with sclerostin repressed the Wnt signaling an