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1 ngiogenesis, which was completely blocked by osteoprotegerin.
2 sible using antibodies to RANKL or synthetic osteoprotegerin.
3 ifically blocked by the RANKL decoy receptor osteoprotegerin.
4 decreased expression of RANKL and increased osteoprotegerin.
5 ) that could be blocked by pretreatment with osteoprotegerin.
6 shed expression of the RANKL decoy receptor, osteoprotegerin.
7 P, fibrinogen, sICAM-1, sTNFRI, sTNFRII, and osteoprotegerin.
8 ing factor-1, and decrease the expression of osteoprotegerin.
9 by concurrent treatment with ibandronate or osteoprotegerin.
10 K on osteoclast surfaces by RANKL similar to osteoprotegerin.
11 colony-stimulating factor, RANK ligand, and osteoprotegerin.
12 to that of its physiological decoy receptor osteoprotegerin.
13 asma levels of osteopontin, osteocalcin, and osteoprotegerin (204%, 148%, and 55%, respectively; P <
14 epressed osteoclast progenitor expression of osteoprotegerin, a decoy receptor for RANKL previously t
17 proteins regulates osteoblast expression of Osteoprotegerin, a major inhibitor of osteoclast differe
18 e of the genes identified in this screen was osteoprotegerin, a member of the tumor necrosis factor r
22 king finding was the significant decrease in osteoprotegerin, an osteoclastogenesis inhibitory factor
23 up EP-HN019 presented greater expressions of osteoprotegerin and beta-defensins than group EP (P <0.0
24 vels of biomarkers of vascular inflammation (osteoprotegerin and C-terminal proendothelin-1, adjusted
26 al fibroblasts, increasing the expression of osteoprotegerin and decreasing receptor activator of nuc
27 ow that muscle cells can produce and secrete osteoprotegerin and pharmacologic treatment of dystrophi
29 cently been identified: the secreted protein osteoprotegerin and the cell-surface ligand to which it
30 ys a unique role in osteocytes, up-regulates osteoprotegerin and Wnt signaling, and differentially re
31 -polymerase chain reaction (RT-PCR) for OPG (osteoprotegerin); and RANKL (receptor activator of NF-ka
32 Some of these, including oxidized lipids, osteoprotegerin, and bisphosphonates, appear to regulate
33 rcarboxylated osteocalcin (%ucOC)] and IL-6, osteoprotegerin, and C-reactive protein (CRP) concentrat
35 ces were observed in the 3-y change in IL-6, osteoprotegerin, and CRP concentrations between particip
37 g regulators of vascular calcification (OPN, osteoprotegerin, and leptin), PTH(1-34) regulated only s
38 lis infection, while mRNA for interleukin-1, osteoprotegerin, and STAT6 all increased in the suscepti
39 -H+-ATPase inhibitor SB 242784, the cytokine osteoprotegerin, and the amino bisphosphonates alendrona
40 tivator of nuclear factor-kappaB ligand, and osteoprotegerin; and up-regulate osteoclast formation.
41 igand (RANKL) and variable downregulation of osteoprotegerin are implicated, and bone health may impr
42 aB ligand (RANKL) and its receptors RANK and osteoprotegerin are key regulators of bone remodeling bu
43 e investigated whether circulating levels of osteoprotegerin are related to features of CMV disease a
44 ligand RANKL, and the soluble decoy receptor osteoprotegerin are the key regulators of osteoclast dif
46 ctivator of NF kappa B ligand and suppresses osteoprotegerin at concentrations two logs lower than th
47 h the receptor activator of NF-kappaB ligand/osteoprotegerin axis was unaffected, expression of tumor
48 of a distinct program of genes that included osteoprotegerin, BCL-2, and IAP-1 (inhibitor of apoptosi
51 vary biomarkers (especially MMP-8 and -9 and osteoprotegerin) combined with red-complex anaerobic per
53 The association observed between increased osteoprotegerin concentrations and periodontitis was los
56 appaB ligand (RANKL) coupled with decline in osteoprotegerin correlate with decreased bone mineral de
58 Juvenile Paget's disease can result from osteoprotegerin deficiency caused by homozygous deletion
62 nate zoledronic acid and the RANKL inhibitor osteoprotegerin, each blocked GM-CSF-induced tumor growt
63 of the osteoclastogenesis inhibitory factor osteoprotegerin enabled early growth of SS18-SSX2-transf
64 hematical model based on type I collagen and osteoprotegerin expression that predicts the bone-formin
65 aB ligand (RANKL) production, an increase in osteoprotegerin expression, and a decrease in serum tart
66 ANKL and M-CSF, saturating concentrations of osteoprotegerin failed to inhibit approximately 40% of t
69 AT/enhancer-binding protein-beta and -delta, osteoprotegerin, FOXC2 and FOXF2, BMP-2, p75 neurotrophi
70 eceived an injection of anti-RANKL antibody, osteoprotegerin fusion protein (OPG-Fc), or a control fu
71 This effect was antagonized by injection of osteoprotegerin fusion protein into the local gingival t
73 showed that Smad1 activates osteopontin and osteoprotegerin gene expression by dislodging Hoxc-8 fro
74 801, on chromosome 8, near to the TNFRSF11B (osteoprotegerin) gene, and rs3736228, on chromosome 11 i
78 ppa B ligand at day 7 post-treatment, strong osteoprotegerin immunoreactivity was observed at day 15
80 shed novel roles for tumor-derived CCL20 and osteoprotegerin in inducing CCL2 production from macroph
82 ace membrane fibroblasts expressed RANKL and osteoprotegerin in response to stimulation with conditio
86 conjunction with their shared decoy receptor osteoprotegerin, in the bone marrow of infected IFrag(-/
88 (3)-mediated endothelial survival depends on osteoprotegerin induction by NF-kappaB and indicate a ne
92 on SLA and modSLA [e.g., prostaglandin E(2), osteoprotegerin, latent and active TGF-beta1, and stimul
93 osis factor (TNF)-alpha, C-reactive protein, osteoprotegerin, leptin, and adiponectin were determined
94 , a calcium-sensing receptor related factor, osteoprotegerin, leptin, bisphosphonates and oxidized li
95 Recent observational studies show that serum osteoprotegerin levels are associated with the severity
97 essive atherosclerosis with increased plasma osteoprotegerin levels, consistent with observational st
100 ivator of NF-kappaB (RANK), the receptor for osteoprotegerin ligand (OPGL), also known as RANK ligand
101 tem is enhanced by the addition of exogenous osteoprotegerin ligand (OPGL), an essential Ocl differen
103 insic cell surface determinant that mediates osteoprotegerin ligand effects on bone resorption and re
104 nduced cytokine (TRANCE, also referred to as osteoprotegerin ligand), and kit ligand-1 (KL-1) in vitr
105 enetic interactions between osteoprotegerin, osteoprotegerin ligand, and RANK during bone resorption
106 t differentiation factor (ODF; also known as osteoprotegerin ligand, receptor activator of nuclear fa
107 01 with Bonferroni correction for both), but osteoprotegerin lost significance after age and sex adju
108 differentiation and calcification inhibitors osteoprotegerin, matrix Gla protein, and osteopontin.
109 c and treatment studies in mice suggest that osteoprotegerin may protect against vascular calcificati
110 the generation of bone cancer pain and that osteoprotegerin may provide an effective treatment for t
111 of soluble RANKL, but not its decoy receptor osteoprotegerin, measured in diseased tissue homogenates
112 ding macrophage inflammatory protein-1Delta, osteoprotegerin, monokine induced by interferon-gamma (I
120 hosphatase mRNA levels, and potently induced osteoprotegerin mRNA, whereas LiCl was ineffective alone
124 TNF-related apoptosis-inducing ligand; OPG, osteoprotegerin; Omp29, 29-kDa outer membrane protein; P
125 r of nuclear factor kappaBeta ligand (RANKL)/osteoprotegerin (OPG) (2.5 +/- 0.7-fold, p < 0.001) rati
130 o compare the activity of TSG-6 with that of osteoprotegerin (OPG) and to investigate its role as an
131 r activator of NF-kappaB) and decoy receptor osteoprotegerin (OPG) are constitutively expressed at al
132 tor for NF-kappaB (RANK)/RANK ligand (RANKL)/osteoprotegerin (OPG) axis and expression of the transcr
135 nic markers, alkaline phosphatase (ALP), and osteoprotegerin (OPG) by hMSCs and transcriptome analysi
136 ulatory factors in osteoblasts by decreasing osteoprotegerin (OPG) expression and increasing monocyte
137 ld lower RANKL expression but >2-fold higher osteoprotegerin (OPG) expression than donor-matched ABCs
138 ormone-related protein (PTHrP) down-regulate osteoprotegerin (OPG) gene expression in the dental foll
139 of nuclear factor kappa B ligand (RANKL) and osteoprotegerin (OPG) immunohistochemistry was carried o
142 from tumor cells suppress the expression of osteoprotegerin (OPG) in osteoblasts and subsequently po
144 bular molar, a decrease in the expression of osteoprotegerin (OPG) in the dental follicle at day 3 en
145 ukin (IL)-17A, IL-17E, IL-17F, IL-17A/F, and osteoprotegerin (OPG) in women with rheumatoid arthritis
146 lear factor-kappa B ligand (RANKL) inhibitor osteoprotegerin (OPG) inhibits osteoclastogenesis and su
160 of nuclear factor-kappaB ligand (RANKL) and osteoprotegerin (OPG) levels and RANKL/OPG ratios in ser
161 pressed significantly higher RANKL and lower osteoprotegerin (OPG) mRNA and increased RANKL:OPG ratio
162 uclear factor kappaB ligand (RANKL) and RANK/osteoprotegerin (OPG) plays a dominant role in osteoclas
163 of nuclear factor kappaB ligand (RANKL) with osteoprotegerin (OPG) prevents the osteolytic activity o
164 or activator of NF-kappaB ligand (RANKL) and osteoprotegerin (OPG) production by ST2 cells, despite M
166 f nuclear factor kappaB ligand) promotes and osteoprotegerin (OPG) protects against vascular calcific
167 ce with established myeloma with recombinant osteoprotegerin (OPG) protein, the soluble decoy recepto
168 e dermatomyositis (DM), to compare the RANKL:osteoprotegerin (OPG) ratio in patients with juvenile DM
169 f nuclear factor kappa-B ligand (RANKL)-RANK-osteoprotegerin (OPG) signaling associated with bone res
170 or activator of NF-kappaB ligand (RANKL) and osteoprotegerin (OPG) signaling in osteocytes was not st
171 ctor-kappaB (RANK), RANK ligand (RANKL), and osteoprotegerin (OPG) signaling pathway (RANKL/RANK/OPG
172 r activator of NF-kappaB ligand (RANKL), and osteoprotegerin (OPG) that modulate bone homeostasis.
175 ctor kappaB (RANK), RANK ligand (RANKL), and osteoprotegerin (OPG) were also investigated by immunohi
176 of nuclear factor-kappaB ligand (RANKL), and osteoprotegerin (OPG) were analyzed in the furcation are
177 of nuclear factor-kappaB ligand (RANKL) and osteoprotegerin (OPG) were assessed by enzyme-linked imm
178 s, RvE1 significantly enhanced expression of osteoprotegerin (OPG) without inducing change in recepto
181 teoclastogenesis by inhibiting expression of osteoprotegerin (OPG), a decoy receptor for the receptor
186 or of nuclear factor-kappaB ligand (sRANKL), osteoprotegerin (OPG), a proliferation-inducing ligand (
187 t survival, in part through the induction of osteoprotegerin (OPG), a protein known to inhibit osteoc
188 ve identified a fifth TRAIL receptor, namely osteoprotegerin (OPG), a secreted tumor necrosis factor
189 derived receptor-1 (FDCR-1), is identical to osteoprotegerin (OPG), a soluble cytokine that regulates
190 hormones or cytokines, and is neutralized by osteoprotegerin (OPG), a soluble decoy receptor also cru
191 addition to its effects on bone metabolism, osteoprotegerin (OPG), a soluble member of the tumor nec
194 nd activation, we examined the expression of osteoprotegerin (OPG), an inhibitor of osteoclast format
198 ptor activator of NF-kappa B ligand (RANKL), osteoprotegerin (OPG), and monocyte chemotactic and stim
199 r factor-kappaB (RANK), RANK-ligand (RANKL), osteoprotegerin (OPG), and osteocalcin was performed.
200 he levels and relative ratios of sclerostin, osteoprotegerin (OPG), and receptor activator of nuclear
201 or of nuclear factor-kappa B ligand (RANKL), osteoprotegerin (OPG), and tartrate-resistant acid phosp
202 tor of nuclear factor kappaB ligand (RANKL), osteoprotegerin (OPG), and tartrate-resistant acid phosp
203 ctivator of nuclear factor-kappaB (RANK) and osteoprotegerin (OPG), are known to be regulators of dev
204 r of nuclear factor-kappa B ligand (sRANKL), osteoprotegerin (OPG), B-cell activating factor (BAFF),
205 oclast numbers and activity are regulated by osteoprotegerin (OPG), bisphosphonates suppress osteocla
206 kappaB (RANK), soluble RANK ligand (sRANKL), osteoprotegerin (OPG), cathepsin-K, and sclerostin.
207 on index (ACI), fibroblast growth factor 23, osteoprotegerin (OPG), fetuin A, and clinical and bioche
209 of TRAIL, DR5 and the TRAIL decoy receptors osteoprotegerin (OPG), mDcTRAILR1, and mDcTRAILR2 were d
210 gate virus, we found that a soluble protein, osteoprotegerin (OPG), or an OPG/Fc chimeric protein inh
211 of Nuclear factor Kappa B Ligand (RANKL) and osteoprotegerin (OPG), positive and negative regulators
213 d soluble TNF receptor type I (pegTNFRI) and osteoprotegerin (OPG), respectively, affected bony spur
214 tor of nuclear factor-kappaB ligand (RANKL), osteoprotegerin (OPG), tartrate-resistant acid phosphata
215 nce with RANKL by systemic administration of osteoprotegerin (OPG), the decoy receptor for (and inhib
216 ceptor activator of NF-kappaB ligand (RANKL)/osteoprotegerin (OPG), tumor necrosis factor alpha (TNF-
217 tor of nuclear factor-kappaB ligand (RANKL), osteoprotegerin (OPG), wingless (WNT) 10b, dickkopf-rela
218 recent work showed that daily injections of osteoprotegerin (OPG)-immunoglobulin fragment complex (O
219 predictive markers of bone inflammation-the osteoprotegerin (OPG)-RANK-RANKL system or osteopontin (
230 of nuclear factor-kappa B ligand (RANKL); 2) osteoprotegerin (OPG); 3) interleukin (IL)-6; and 4) tum
231 eine chemokine receptor-5 (CCR5, 59653 C>T), osteoprotegerin (OPG, 245 T>G), and osteopontin (OPN, 70
232 mentation rate, and bone metabolism markers (osteoprotegerin [OPG], osteocalcin, procollagen type I N
233 hymic epithelial cells by using mice lacking osteoprotegerin or by adding TRANCE (RANKL, Tnfsf11).
234 this system with recombinant decoy receptor, osteoprotegerin, or soluble forms of the receptor activa
235 r for nuclear factor kappa-B ligand (RANKL), osteoprotegerin, osteocalcin, and osteopontin as potenti
237 steoblast markers bone alkaline phosphatase, osteoprotegerin, osteopontin, and matrix Gla protein.
238 e the molecular genetic interactions between osteoprotegerin, osteoprotegerin ligand, and RANK during
243 whereas no inhibition was observed by adding osteoprotegerin, RANK:Fc, TNFalpha, or interleukin-8 or
245 ppaB ligand (RANKL)), the deviation of RANKL/osteoprotegerin ratio in favor of antiosteoclastic activ
246 duced receptor activator of NF-kappaB ligand/osteoprotegerin ratio in Runx2-overexpressing osteoblast
247 l analyses for the detection of osteocalcin, osteoprotegerin, receptor activator of nuclear factor ka
248 on-gamma, toll-like receptor (TLR)-2, TLR-4, osteoprotegerin, receptor activator of nuclear factor-ka
249 pha1, osteocalcin, alkaline phosphatase, and osteoprotegerin, representative bone-regulating proteins
250 osteoblast differentiation, also stimulates osteoprotegerin secretion to attenuate bone resorption b
252 This enhanced chemotaxis can be abrogated by osteoprotegerin (soluble decoy receptor of RANKL), MIK-G
253 uld explain juvenile Paget's disease because osteoprotegerin suppresses bone turnover by functioning
254 The map locations of 25 genes including osteoprotegerin, syndecan-2, and autotaxin have been ref
255 receptor activator of nuclear factor kappa B/osteoprotegerin system involved in osteoblast-osteoclast
257 ew, we provide an overview of the RANK/RANKL/osteoprotegerin system; we describe its interaction with
259 f receptor activator of NF-kappaB ligand and osteoprotegerin through both PTH-dependent and -independ
260 t's disease for defects in the gene encoding osteoprotegerin (TNFRSF11B) using polymerase-chain-react
261 rationally designed small molecule mimic of osteoprotegerin to inhibit osteoclast formation in vitro
262 lance stemmed from a switch in production of osteoprotegerin to that of receptor activator of NF-kapp
265 Gene expression levels of soluble RANKL, osteoprotegerin, tumor necrosis factor alpha, and M-CSF
266 ator of nuclear factor kappaB ligand (RANKL)/osteoprotegerin, tumor necrosis factor-alpha, and interl
267 eptor-activated nuclear factor-kappaB ligand/osteoprotegerin/tumor necrosis factor-related apoptosis-
270 sitive to the effects of the RANKL inhibitor osteoprotegerin was identified in the activated T cell-c
271 steocalcin, and osteopontin were higher, and osteoprotegerin was lower in females than in males.
272 ctivator of nuclear factor-kappaB ligand and osteoprotegerin) was observed in the ligature group on d
273 Alterations in BM plasma levels of RANKL/osteoprotegerin were confirmed in a mouse model of posti
275 scular cell adhesion molecule 1 (VCAM-1) and osteoprotegerin were significantly associated with incid
276 d macrophage inflammatory protein-1Delta and osteoprotegerin were significantly elevated in patients
277 lasma levels of RANKL and of the ratio RANKL/osteoprotegerin were significantly elevated in patients
279 hereas other genes, such as interleukin-5 or osteoprotegerin, were initially identified as having a r
280 or Tax and the osteoclast inhibitory factor, osteoprotegerin, were protected from osteolytic bone dis
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