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1 ts as a negative regulator of RANKL-mediated osteoclast differentiation.
2 mechanisms employed by BMP signaling during osteoclast differentiation.
3 p family protein that is up-regulated during osteoclast differentiation.
4 t miR-29 controls the tempo and amplitude of osteoclast differentiation.
5 n and function of different FcgammaRs during osteoclast differentiation.
6 egative regulatory factors in RANKL-mediated osteoclast differentiation.
7 oblasts that can control both osteoblast and osteoclast differentiation.
8 itrullination of vimentin was induced during osteoclast differentiation.
9 role of A(2A) receptor in the regulation of osteoclast differentiation.
10 r LTB4R1 (BLT1) in synovial inflammation and osteoclast differentiation.
11 iptional repressors such as IRF-8 that block osteoclast differentiation.
12 tf, a transcription factor, is necessary for osteoclast differentiation.
13 ectin-induced inhibition in RANKL-stimulated osteoclast differentiation.
14 aB ligand) expression, which then stimulates osteoclast differentiation.
15 xpression program leading to cell fusion and osteoclast differentiation.
16 little is known about the role HDACs play in osteoclast differentiation.
17 loid differentiation factor 88 in modulating osteoclast differentiation.
18 gnaling, and an increase in apoptosis during osteoclast differentiation.
19 a direct and novel role of Tie2 signaling in osteoclast differentiation.
20 ctional disruption of Notch signaling during osteoclast differentiation.
21 tion in promoting macrophage recruitment and osteoclast differentiation.
22 axis to drive metabolic reprogramming during osteoclast differentiation.
23 ovide a new mechanism of inhibition of human osteoclast differentiation.
24 ) in osteoblasts and subsequently potentiate osteoclast differentiation.
25 ng, which, in turn, inhibited RANKL-mediated osteoclast differentiation.
26 cts as a negative regulator of RANKL-induced osteoclast differentiation.
27 ds to defective lymph node organogenesis and osteoclast differentiation.
28 lusively demonstrate that osteoblasts direct osteoclast differentiation.
29 ited myeloma cell-induced tube formation and osteoclast differentiation.
30 r, member 2 (SLC4A2), is up-regulated during osteoclast differentiation.
31 AMPs for the NLRP3 inflammasome and regulate osteoclast differentiation.
32 ed that MYO10 is also expressed early during osteoclast differentiation.
33 exhibited severe osteopetrosis and impaired osteoclast differentiation.
34 d the critical interaction of these genes in osteoclast differentiation.
35 nflammation, angiogenesis, tumor growth, and osteoclast differentiation.
36 (Ctsk) and acid phosphatase 5 (Acp5) during osteoclast differentiation.
37 s at the promoters during terminal stages of osteoclast differentiation.
38 of NF-kappaB ligand (RANKL) signaling during osteoclast differentiation.
39 ed kinase 1 and IKK and to cause spontaneous osteoclast differentiation.
40 like cells were treated with RANKL to induce osteoclast differentiation.
41 eoclastogenic cytokine, causes the increased osteoclast differentiation.
42 ed by Flt-1, which was down-regulated during osteoclast differentiation.
43 NFATc1 in human beta3 integrin expression in osteoclast differentiation.
44 ress from inflamed sites and is required for osteoclast differentiation.
45 ice are osteopenic with evidence of enhanced osteoclast differentiation.
46 oth in vivo and in vitro and plays a role in osteoclast differentiation.
47 appaB (RANK) and TNF receptor (TNFR) promote osteoclast differentiation.
48 ion of bone matrix remodeling enzymes during osteoclast differentiation.
49 ay and provide a mechanism for BMP-2-induced osteoclast differentiation.
50 the expression or activation of STAT5 during osteoclast differentiation.
51 al role in transducing signals from RANKL in osteoclast differentiation.
52 MITF in the absence of signals required for osteoclast differentiation.
53 H) receptor (TSHR), TSH negatively regulates osteoclast differentiation.
54 one microenvironment to promote specifically osteoclast differentiation.
55 ession of the CaR plays an important role in osteoclast differentiation.
56 role of STAT5 in IL-3-mediated inhibition of osteoclast differentiation.
57 bined with RANKL had no additional effect on osteoclast differentiation.
58 s are multifunctional cells also controlling osteoclast differentiation.
59 (RANKL), a major factor in the regulation of osteoclast differentiation.
60 ntal switch and is required for monocyte and osteoclast differentiation.
61 matrix (ECM) microenvironment remodeling and osteoclast differentiation.
62 ion of Osteoprotegerin, a major inhibitor of osteoclast differentiation.
63 d suppresses canonical RANK signaling during osteoclast differentiation.
64 ted mineralization and osteoblast support of osteoclast differentiation.
65 signaling pathways, which are essential for osteoclast differentiation.
66 aB ligand (RANKL), an essential cytokine for osteoclast differentiation.
67 on using antisense oligonucleotides, impeded osteoclast differentiation.
68 esis Irf8 by DNA methylation is required for osteoclast differentiation.
69 c gene activation concomitant with defective osteoclast differentiation.
70 the IREalpha/XBP1-mediated arm of the UPR in osteoclast differentiation.
71 lation of MITF at Ser-307 by p38 MAPK during osteoclast differentiation.
72 proteins, we determined the role of EPAC in osteoclast differentiation.
73 steoblasts, HDAC4 is a critical regulator of osteoclast differentiation.
74 miR-34a is downregulated during osteoclast differentiation.
75 (Ki16425, Debio0719, and VPC12249) inhibited osteoclast differentiation.
76 or osteoclast precursors, suggesting altered osteoclast differentiation.
77 pathways are utilized at different stages of osteoclast differentiation.
78 from NF-kappaB activated LNCaP cells induce osteoclast differentiation.
79 ich decreased ERalpha expression and induced osteoclast differentiation, 10 nm estradiol, 3 microm ge
80 actor-kappaB ligand (RANKL) is essential for osteoclast differentiation, activation, and survival.
83 defines a key regulatory node that controls osteoclast differentiation and activity downstream of RA
88 y play a pivotal role in the control of both osteoclast differentiation and apoptosis in the systems
89 t facilitates bone colonization by fostering osteoclast differentiation and bone degradation and also
90 These results indicate that RvE1 modulates osteoclast differentiation and bone remodeling by direct
93 ce with arthritis, a significant increase in osteoclast differentiation and bone resorption was obser
101 These defects are the result of impaired osteoclast differentiation and compromised receptor acti
102 rsors, we hypothesized that MDSC may undergo osteoclast differentiation and contribute to enhanced bo
103 th a genetic deficiency of CYLD had aberrant osteoclast differentiation and developed severe osteopor
105 In BMMs, spleen cells, and RAW264.7 cells, osteoclast differentiation and formation stimulated by M
106 from patients with DSS, we observed reduced osteoclast differentiation and function (demineralizatio
107 A(2A) receptor agonist, CGS21680, inhibited osteoclast differentiation and function (half maximal in
109 provide new molecular mechanisms controlling osteoclast differentiation and function by the miRNA sys
110 Elucidation of the mechanisms mediating osteoclast differentiation and function has identified n
111 a highlight SLC4A2 as a critical mediator of osteoclast differentiation and function in vitro and in
113 ti-resorptive properties, directly impairing osteoclast differentiation and function through a seroto
114 ng in maintaining bone quality by regulating osteoclast differentiation and function through cAMP/PKA
115 es was evaluated by immunoassay, while human osteoclast differentiation and function were assessed vi
116 ly of transcription factors is regulation of osteoclast differentiation and function, which in turn c
123 at MYC drives metabolic reprogramming during osteoclast differentiation and functions as a metabolic
124 tion pathway leading toward the induction of osteoclast differentiation and furthermore, indicate tha
127 mily, Limd1, is uniquely up-regulated during osteoclast differentiation and interacts with Traf6, a c
128 ption factor (MITF) is required for terminal osteoclast differentiation and is a signaling effector e
129 ption factor (MITF) is required for terminal osteoclast differentiation and is a target for signaling
130 6-deficient monocytes rescues RANKL-mediated osteoclast differentiation and LPS-stimulated interleuki
131 r factor kappa B (RANK) is required for both osteoclast differentiation and mammary gland development
132 oclast progenitor survival, but its roles in osteoclast differentiation and mature osteoclast functio
133 tor activator of NF-kappaB ligand-stimulated osteoclast differentiation and may regulate bone turnove
135 Conversely, NUMBL-null BMMs, show increased osteoclast differentiation and mRNA expression of osteoc
136 receptor activator of NF-kappaB-independent osteoclast differentiation and nuclear accumulation of t
139 steoblast differentiation sets the stage for osteoclast differentiation and overall promotes osteolys
140 We previously reported that IL-3 inhibits osteoclast differentiation and pathological bone loss.
141 ands secreted by breast cancer cells promote osteoclast differentiation and potentiate the activity o
142 , an alternative P2Y12 antagonist, inhibited osteoclast differentiation and promoted osteoblast diffe
143 on, which increases PI(4,5)P(2), also delays osteoclast differentiation and reduces cell number but i
145 in bone marrow-derived precursors disrupted osteoclast differentiation and selectively repressed tra
146 odontal pathogen Porphyromonas gingivalis on osteoclast differentiation and show that P. gingivalis d
148 eby OA/Gpnmb acts as a negative regulator of osteoclast differentiation and survival but not function
151 monstrate that Akt1/Akt2 are key elements in osteoclast differentiation and that the macrophage colon
152 r-kappa B (NF-kappa B) has a crucial role in osteoclast differentiation, and blocking NF-kappa B is a
154 F target gene promoters Acp5 and Ctsk during osteoclast differentiation, and FUS knockdown abolished
156 e in cellular proliferation, monocyte cells, osteoclast differentiation, and matrix degradation.
159 JQ1 is a potent inhibitor of osteoblast and osteoclast differentiation as well as bone tumour develo
160 icantly reduces CIA monocyte recruitment and osteoclast differentiation as well as potent joint monoc
161 d T cells c1 (NFATc1), a master regulator of osteoclast differentiation, as well as reduced expressio
162 nized role for Dim1 as a master modulator of osteoclast differentiation, as well as the molecular mec
163 the LTB4 pathway in bone loss, we performed osteoclast differentiation assays by stimulating with M-
164 , and NFATc1, suggesting that Tak1 regulates osteoclast differentiation at multiple stages via multip
165 not immediate, peaking 2 days after inducing osteoclast differentiation both in vivo and in vitro.
166 tivation sustains proliferation but prevents osteoclast differentiation, both causing osteopetrosis.
168 promote Rankl expression in osteoblasts and osteoclast differentiation by enhancing cyclic adenosine
169 osteoclastogenesis and show that MTX induces osteoclast differentiation by generating a pro-osteoclas
171 c expression of Dim1 decreases RANKL-induced osteoclast differentiation by silencing NFATc1 and its t
172 gulated during osteoclastogenesis suppresses osteoclast differentiation by targeting important osteoc
173 showed that Hh signaling indirectly induced osteoclast differentiation by upregulating osteoblast ex
175 arrow cells rendered a 5-fold lower level of osteoclast differentiation compared with Cx37(+/+) cell
176 synovial fluid-driven monocyte migration and osteoclast differentiation compared with each factor alo
177 56) in congenital hypothyroid mice activates osteoclast differentiation, confirming once again our pr
178 lear accumulation of NFATc1 and consequently osteoclast differentiation consistent with the ability o
179 s, miR-16 and miR-378, which are elevated in osteoclast differentiation, correlate with bone metastas
180 more potent in osteoblast proliferation and osteoclast differentiation culture systems, as well as i
182 Loss of Akt1 and/or Akt2 protein inhibited osteoclast differentiation due to down-regulation of Ika
183 Pharmacological activation of RXRs inhibited osteoclast differentiation due to the formation of RXR/l
184 strate that Gsalpha signaling also regulates osteoclast differentiation during bone modeling and remo
185 by mRNA expression of genes associated with osteoclast differentiation, enhanced osteoclast number,
186 minal binding protein) and Sin3A, but during osteoclast differentiation, Eos association with Ctsk an
187 gene deletion experiments in mice, that the osteoclast differentiation factor RANKL promotes lysosom
190 ear factor kappaB ligand (RANKL), a critical osteoclast differentiation factor, is expressed on T lym
191 neralization with elevated expression of the osteoclast differentiation factor, receptor activated by
192 h receptor activator of NF-kappaB ligand, an osteoclast differentiation factor, they did not complete
194 inant LRRc17 protein inhibited RANKL-induced osteoclast differentiation from bone marrow precursors,
195 ; ectopic NFATc1 expression rescues impaired osteoclast differentiation from deletion of RGS10; phosp
196 tes, and have also been reported to modulate osteoclast differentiation from hemopoietic precursor ce
197 Histamine and Th17 cytokines induced the osteoclast differentiation from monocytes and JNJ7777120
200 We conclude that NF-kappaB controls early osteoclast differentiation from precursors induced direc
201 and induced a significantly higher level of osteoclast differentiation from RAW 264.7 cells than did
202 currently unknown whether, besides increased osteoclast differentiation from undifferentiated precurs
203 appaB ligand (RANKL) plays a crucial role in osteoclast differentiation, function, and survival.
206 and Jag1 in a direct manner, and influences osteoclast differentiation in a non-cell-autonomous fash
207 tor(s) shed by tumor-derived MT1-MMP enhance osteoclast differentiation in a RANKL-dependent manner.
208 n of PPAR-gamma by rosiglitazone exacerbates osteoclast differentiation in a receptor-dependent manne
209 a dominant negative TCF4 not only increases osteoclast differentiation in a tumor-bone co-culture sy
212 n the present study, effects of retinoids on osteoclast differentiation in cultured mouse bone marrow
213 AP12 appears to be primarily responsible for osteoclast differentiation in cultures directly stimulat
215 skolin treatment increased pCREB and rescued osteoclast differentiation in Gnas(+/p-) by reducing Nfa
216 ) pathway has been shown to be essential for osteoclast differentiation in inflammatory arthritis.
217 a modulator of Ca(2+)-induced NFAT-dependent osteoclast differentiation in inflammatory bone loss.
218 differentiation while concurrently enhancing osteoclast differentiation in marrow stromal cell cultur
219 eloid progenitors prior to the initiation of osteoclast differentiation in response to the appropriat
220 n IKKbeta-null osteoclast OCPs and to rescue osteoclast differentiation in the absence of IKKbeta thr
225 analysis of chemokines and receptors during osteoclast differentiation in vivo highlights the key ro
227 t all miR-29 family members increased during osteoclast differentiation, in concert with mRNAs for th
228 c1 induces Nur77 expression at late stage of osteoclast differentiation; in turn, Nur77 transcription
229 at Fzd8 and beta-catenin negatively regulate osteoclast differentiation independent of osteoblasts an
230 ovel function of PDGF-D in the regulation of osteoclast differentiation, independent of the RANKL/RAN
231 ed bone gene expression in vivo during rapid osteoclast differentiation induced by colony-stimulating
234 te target that is highly up-regulated during osteoclast differentiation induced by the cytokine recep
237 During bone homeostasis, osteoblast and osteoclast differentiation is coupled and regulated by m
238 the mechanism by which tumor cells influence osteoclast differentiation is crucial for improving trea
239 anism underlying IL-3-mediated inhibition of osteoclast differentiation is not fully understood.
241 Furthermore, IL-3 inhibited RANKL-induced osteoclast differentiation less effectively in the STAT5
242 is increased relative to the wild type, and osteoclast differentiation markers are expressed at earl
243 ession correlates with impaired induction of osteoclast differentiation markers in response to RANKL
244 strogen agonist reduced RANKL stimulation of osteoclast differentiation markers or its down-regulatio
245 Talin1-deficient precursors normally express osteoclast differentiation markers when exposed to M-CSF
246 sts and their expression of mRNA for several osteoclast differentiation markers, whereas ES significa
247 steoblast activity and concurrently impaired osteoclast differentiation, maturation and functionality
248 ine- and chemokine-related pathways but also osteoclast differentiation may be involved in the effect
251 that Fbn1(mgR/mgR) osteoblasts stimulate pre-osteoclast differentiation more than wild-type cells.
252 ctivator of NF-kappaB ligand (RANKL)-induced osteoclast differentiation occurred via the inhibition o
253 (A1R, A2AR, A2BR, and A3R) on osteoblast and osteoclast differentiation of cells derived from patient
254 ofylline and A2BR agonist BAY60-6583 inhibit osteoclast differentiation of cells from patients with M
256 r of NF-kappaB ligand (RANKL) and can induce osteoclast differentiation of myeloid cells expressing R
258 a2 but not PLCgamma1 restores RANKL-mediated osteoclast differentiation of PLCgamma2-deficient bone m
259 es on these and other molecules that mediate osteoclast differentiation or function and thus serve as
261 the action of transcriptional regulators of osteoclast differentiation or is under the control of a
262 paB) ligand (RANKL), a critical activator of osteoclast differentiation, plays a pivotal role in tart
264 osteoclastogenesis in D2J mice and increased osteoclast differentiation rates ex vivo, marked by incr
265 ation abilities of patDp/+ osteoblasts while osteoclast differentiation remained unchanged compared t
268 tion in the bone microenvironment stimulates osteoclast differentiation, resulting in uncoupling of r
269 pid progress has been made in characterizing osteoclast differentiation signaling pathways, how recep
271 t amino acid 536 (p65*(536)) plays a role in osteoclast differentiation stimulated by receptor activa
272 We conclude that SR-A plays a role in normal osteoclast differentiation, suggesting a novel role for
273 ator of NF-kappa B ligand (RANKL)-stimulated osteoclast differentiation, survival, and activation.
274 binding of Cbl to PI3K negatively regulates osteoclast differentiation, survival, and signaling even
275 oped when TIEG(-/-) OBs were used to support osteoclast differentiation than when TIEG(+/+) OBs were
276 PAC2 are critical signaling intermediates in osteoclast differentiation that permit RANKL-stimulated
277 ulated a concentration-dependent increase in osteoclast differentiation that was receptor activator o
279 To characterize the OBs' ability to support osteoclast differentiation, the OBs from TIEG(+/+) and T
280 acting in concert to promote RANKL-dependent osteoclast differentiation, thereby creating an imbalanc
281 myeloid differentiation, which orchestrates osteoclast differentiation through activation of DNAX ac
282 cellular pathway that integrates the UPR and osteoclast differentiation through activation of the IRE
283 thought to be the major player in regulating osteoclast differentiation through expressing RANKL/OPG
284 trichostatin A and sodium butyrate, suppress osteoclast differentiation through multiple mechanisms.
285 ity of differentiated osteoblasts to inhibit osteoclast differentiation; thus, they broaden our knowl
286 rs that integrate CSF-1/RANKL signals during osteoclast differentiation to initiate expression of tar
287 10 dramatically increased the sensitivity of osteoclast differentiation to RANKL signaling; the defic
289 eripheral blood B and T cells did not induce osteoclast differentiation, unless they were activated i
291 e, indicate that cellular stress can enhance osteoclast differentiation via Hsf1-dependent mechanisms
292 th transforming growth factor beta to induce osteoclast differentiation was dependent on IKK alpha, s
293 (ChIPac-seq) to an established cell model of osteoclast differentiation, we discovered that H3NT prot
295 EPAC1/2 stimulation significantly increased osteoclast differentiation, whereas EPAC1/2 inhibition d
296 ored the ability of TIEG(-/-) OBs to support osteoclast differentiation, whereas M-CSF alone or combi
297 pression similar to HDAC inhibitors inhibits osteoclast differentiation, whereas osteoclasts suppress
298 IL-4 is known to inhibit the RANKL-induced osteoclast differentiation while at the same time promot
299 ANs in osteoclast precursor cells attenuated osteoclast differentiation, while their overexpression i
300 acrophages from Dicer-deficient mice rescued osteoclast differentiation with up-regulation of PU.1 le
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