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1 hese data, JDP2(-/-) mice were found to have increased bone mass.
2 show decreased lysosomal gene expression and increased bone mass.
3 ion, which results in decreased body fat and increased bone mass.
4 istance to PPARgamma is dominant, leading to increased bone mass.
5 As a consequence, Ciz-deficient mice develop increased bone mass.
6 overexpressing a soluble receptor for leptin increased bone mass.
7 a single allele of OF45 caused significantly increased bone mass.
8 Ablation of OF45 resulted in increased bone mass.
9 tivation of osteoclastogenesis, resulting in increased bone mass.
11 n of cannabinoid type 1 (CB1) receptors have increased bone mass and are protected from ovariectomy-i
12 deletion of Phd2 in chondrocytes resulted in increased bone mass and bone formation rate (normalized
15 formation, improved bone microarchitecture, increased bone mass and enhanced mechanical properties i
16 rostin antibody and zoledronic acid combined increased bone mass and fracture resistance when compare
18 signaling in mature osteoblasts resulted in increased bone mass and protection from bone loss in old
19 eceptor signaling in osteocytes that exhibit increased bone mass and remodeling, recognized skeletal
21 eletal impact, female HeyL null mice display increased bone mass, and Hey2 inactivation is developmen
26 C5aR1(-/-) and C5aR2(-/-) mice displayed an increased bone mass compared to wild-type controls due t
29 tion of central ERalpha signaling results in increased bone mass, demonstrating that the balance betw
30 t low oral dose of 1 (mg/kg)/day body weight increased bone mass density and volume, expression of os
31 However, a second phenotype of significantly increased bone mass developed by 2 months, which continu
32 Shn3 display adult-onset osteosclerosis with increased bone mass due to augmented osteoblast activity
33 tion of Atp6v0d2 in mice results in markedly increased bone mass due to defective osteoclasts and enh
35 lower spacing between trabeculae as well as increased bone mass in both males and females compared t
36 ation of giant, nonresorbing osteoclasts and increased bone mass in male mice and protected female mi
41 inc finger protein Schnurri-3 (Shn3) display increased bone mass, in part, attributable to augmented
42 terized by reduced bone mass (osteoporosis), increased bone mass (osteopetrosis), or abnormalities in
43 he current study, we postulated that IGFBP-2 increased bone mass partly through the activity of its h
44 mice develop osteopetrosis characterized by increased bone mass, reduced medullary cavity space and
47 lous bone histomorphometry revealed that the increased bone mass was the result of increased osteobla
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