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1 F-alpha, IFN-gamma, IL-6, CCL2, CCL3, G-CSF, osteopontin).
2 lactoferrin, lysozyme, antitrypsin, IgA, and osteopontin).
3 C) signal sequence with that of prolactin or osteopontin.
4 in the pleural space by elaborating CCL2 and osteopontin.
5 his was reversed by neutralizing antibody to osteopontin.
6 iators, like Calgranulin A, Cathepsin S, and Osteopontin.
7 peptidase-9 (MMP-9), a protease that cleaves osteopontin.
8 sporter 1 (encoded by the SLC20A1 gene), and osteopontin.
9 cantly associated, aside from that of plasma osteopontin.
10 tion and reduction in the retentive molecule osteopontin.
11 tory mediators, such as C5a, bradykinin, and osteopontin.
12 olecule-1, vascular adhesion molecule-1, and osteopontin.
13 stimulates colon carcinoma tumor growth via osteopontin.
14 ceptor (VDR)-regulated genes osteocalcin and osteopontin.
15 eral density through candidate genes such as osteopontin.
16 ralization inhibitors matrix Gla protein and osteopontin.
17 of even a highly disordered protein such as osteopontin.
18 on in fibroblasts plated on fibrotic matrix, osteopontin.
19 tion and expression of p65, TLR4, MCP-1, and osteopontin.
20 d extracellular matrix genes fibronectin and osteopontin.
21 3 are the major integrins for this effect on osteopontin.
23 quantify the putative ovarian cancer markers osteopontin (38 mum diameter sphere), CA-125 (53 mum dia
25 pressed, also in a CD44-dependent manner, by osteopontin, a component of chronically inflamed ECM, in
26 owth factors, such as IL1beta, IL6 and SPP1 (osteopontin, a key biomarker for PCa), were upregulated
27 r volume, as well as the expression level of osteopontin, a known factor of bone remodeling and osteo
29 breast cancer cells, and tumor cell-secreted osteopontin activated a CAF phenotypes in normal mammary
30 might be a biomarker for incident ACS, using osteopontin adds moderately to traditional cardiovascula
31 AE (P = .033) and the mean percent change in osteopontin after TAE (P = .024) were significantly grea
32 he expression of osteogenic related markers (osteopontin, alkaline phosphatase activity, Alizarin red
34 Finally, our experiments have revealed that osteopontin, an important immunomodulator, contributes t
35 of (18)F-fluoride uptake are associated with osteopontin, an inflammation-associated glycophosphoprot
36 ) was 1.29 (1.06-1.57) per 1-SD increase for osteopontin and 1.30 (1.02-1.66) for CRP, respectively.
37 nalysis of cytoskeleton, Ki67, expression of osteopontin and alkaline phosphatase, and formation of m
38 extracellular matrix phosphoproteins such as osteopontin and bone sialoprotein have yielded important
41 the Dongfeng-Tongji cohort, and found plasma osteopontin and CRP concentrations were associated with
45 known regulators of mineralization, such as osteopontin and matrix Gla protein, but not osteocalcin,
48 ith hypertrophy, increased oxidative stress (osteopontin and NOX4 gene expression), and normal systol
49 n of many osteoblast-related genes including osteopontin and osteocalcin, whilst the DN subset presen
51 he nucleus where it led to the expression of osteopontin and other FN-type matrix in both mouse embry
52 ng theme in these diseases is a link between osteopontin and pathogenic T cells, particularly T helpe
53 ese mice also had pronounced upregulation of osteopontin and RUNX2 (osteogenic markers), CD63, AnX2 (
54 pression of the WNT-pathway surrogate marker osteopontin and the metastasis-associated genes SASH1 an
57 line phosphatase, secreted phosphoprotein 1 (osteopontin), and bone gamma-carboxyglutamate protein (o
58 mation (high-sensitivity C-reactive protein, osteopontin), and leukocyte adhesion (soluble vascular c
60 associated with mineralized differentiation, osteopontin, and alkaline phosphatase in DPSCs cultured
61 f bone morphogenetic protein (BMP)-2, BMP-7, osteopontin, and bone sialoprotein were evaluated in alv
62 glycoproteins (SIBLINGs): bone sialoprotein, osteopontin, and dentin matrix protein 1, respectively.
63 renal macrophages that expressed Il10, MMPs, osteopontin, and growth factors, including Pdgfc and Hbe
64 kaline phosphatase, osteocalcin, osteonectin/osteopontin, and in vitro mineralized nodule formation c
66 ms (SNPs) in candidate genes (SPP1, encoding osteopontin, and LTBP4, encoding latent transforming gro
67 glycan secretion and production of aggrecan, osteopontin, and matrix extracellular phosphoglycoprotei
69 ins, such as alpha-lactalbumin, lactoferrin, osteopontin, and milk fat globule membrane proteins.
71 CD163 (sCD163), chitinase-3-like protein 1, osteopontin, and pentraxin-3, in hOE cells; however, the
72 d the specific role of alpha/beta integrins, osteopontin, and related extracellular matrix proteins;
73 vels of RANKL, osteoprotegerin, osteocalcin, osteopontin, and serum glycosylated hemoglobin A1c, insu
74 f cholangiocytes including cytokeratin 7 and osteopontin, and the transcription factors SOX9 and hepa
75 ch the staining profile for the MIPs S100A4, osteopontin, anterior gradient-2, and S100P has already
78 d (RANKL), osteoprotegerin, osteocalcin, and osteopontin as potential biomarkers of alveolar bone los
79 onal assay with physiological TRAP substrate osteopontin, AubipyOMe inhibited mouse macrophage migrat
80 beta3, but not alphaIIbbeta3 (D552A), caused osteopontin binding to alphavbeta3, but not fibrinogen b
82 gramming and neutralizing antibodies against osteopontin-blocked fibroblast activation induced by tum
84 regulated in cancer survivors while MMP9 and Osteopontin both had significant positive correlations w
85 ression of alkaline phosphatase, MMP-13, and osteopontin but decreased expression of osteocalcin, ost
86 tested for their role in Th differentiation, osteopontin, but not hyaluronic acid, promoted Th1/Th17
87 active protein by 13% (95% CI, -14% to -9%), osteopontin by 12% (95% CI, -14% to -10%), soluble vascu
88 sms, and involves the processing of elevated osteopontin by activated MMP-9, and subsequent macrophag
91 e show by in vitro experiments that secreted osteopontin can be processed by extracellular proteasome
95 Osteoprogenitor cells and endosteal-lining osteopontin(+) cells were reduced, and osteocalcin mRNA
105 c (up- and then down-regulation) of the Spp1/osteopontin-dependent network and up-regulation of mRNA
106 tions of interleukin 6, interleukin 8, VEGF, osteopontin, E-selectin, and HGF with continuous tumour
108 ort that mice deficient in the expression of osteopontin exhibit reduced numbers of the IEL subpopula
109 ited reduced mesodermal fibronectin (FN) and osteopontin expression and died during mesoderm developm
112 ogenic differentiation, but robustly induces osteopontin expression in osteoblasts through the induct
114 in D(3) -induced increase of osteocalcin and osteopontin expression was significantly decreased in th
116 AT3KO) mice are defective in alpha4beta1 and osteopontin expression, defects that correlated with ina
119 RNA sequencing analysis revealed that Spp1 (osteopontin) expression is markedly upregulated in Snai2
121 metalloproteinase (MMP)-7 > 1.75 ng/ml, and osteopontin > 6 ng/ml each significantly distinguished p
122 ally secreted form, an intracellular form of osteopontin has been identified, which participates in s
123 he calcium-regulating proteins, fetuin-A and osteopontin, have been found in the serum of patients wi
124 f this study is to produce recombinant human osteopontin (hOPN) in plants for inducing dental bone re
125 In this review, we focus on the role of osteopontin in a series of immune-related diseases, part
126 inent association for matrix Gla protein and osteopontin in ABCC6-related dystrophic cardiac calcific
128 esmon in stromal cells and the expression of osteopontin in both tumor cells and stroma were signific
129 ence the inflammatory cytokines TNF-alpha or osteopontin in epididymal ATMs of obese mice caused sign
130 ltered levels of dentin matrix protein 1 and osteopontin in Fam20C-deficient bone may be significant
131 evelopment of Sjogren's disease, the role of osteopontin in inflammatory conditions in the oral cavit
132 ole for paracrine signaling by tumor-derived osteopontin in reprograming normal fibroblasts into tumo
135 creted phosphoprotein 1 (SPP1, also known as osteopontin) increases in pulmonary fibrosis, and Spp1 t
136 te survival of different IEL populations via osteopontin, indicating an important role for iCD8alpha
137 aracterized by increased expression of COX2, osteopontin, inflammatory cytokines, and chemokines but
138 actor 2 (TRAF2) and intracellular isoform of osteopontin (iOPN) whereas TLR4 signaling provides IFN r
142 roperty of highly phosphorylated isoforms of osteopontin is their ability to sequester nanoclusters o
143 naling through the reestablished Jagged1 and osteopontin levels correlated with the rescue of the fun
145 Indeed, the detection limit falls within the osteopontin levels reported in the literature for patien
146 of inflammatory cytokines interleukin-6 and osteopontin, lowered plasma endothelin-1 and blood press
155 s (M1 macrophages) with higher expression of osteopontin (OPN) and an increase in number of prolifera
156 factors were selected for further analysis: osteopontin (OPN) and clusterin (CLU) which were upregul
157 terns of osteoblast-derived proteins such as osteopontin (OPN) and osteocalcin (OCN) modulate osteobl
158 vels among RGCs and also selectively express osteopontin (OPN) and receptors for the insulin-like gro
159 s of patients with alcoholic hepatitis (AH), osteopontin (OPN) as one of the most up-regulated genes.
160 18 cirrhosis and 17 HCC patients identified osteopontin (OPN) as significantly up-regulated in HCC c
161 Thrombin cleavage alters the function of osteopontin (OPN) by exposing an integrin binding site a
163 s), IgG anti-Helicobacter pylori (HpAb), and osteopontin (OPN) can be used as a panel for GC diagnose
165 critical mediator of the CAF phenotype, and osteopontin (OPN) expression in tumors is associated wit
169 umulation of the macrophage-derived cytokine osteopontin (OPN) in adipose tissue and induction of loc
171 he expression of the proatherogenic cytokine osteopontin (OPN) in mouse arteries via local release of
173 scular endothelial growth factor (VEGF), and osteopontin (OPN) in the DPSC + THSG group were signific
175 stimulation, we previously demonstrated that osteopontin (OPN) increased STAT1 ubiquitination and 26
195 rine asbestos inhalation model, we show that osteopontin (OPN) is up-regulated by bronchiolar epithel
197 sforming growth factor beta1 (TGF-beta1) and osteopontin (OPN) play important roles in bone remodelin
198 ion and its inhibition by the phosphoprotein osteopontin (OPN) plays a key role in COM stone-forming
200 IL-10-producing regulatory T cells, whereas osteopontin (OPN) promotes pathogenic IL-17 T cell respo
201 l adhesion with the gene Spp1, also known as osteopontin (OPN) serving as a key common node connectin
203 EAD4)-dependent transcriptional induction of osteopontin (Opn) stimulated c-Met expression in EC with
204 es, deposition of mineral-regulating protein osteopontin (OPN) was increased in alveolar bone in Phos
205 ns of phosphatidylserine (DPPS) bilayers and osteopontin (OPN) were fabricated on silica substrates t
206 tory cytokines (IL1beta, TNF-alpha, IL6, and osteopontin (OPN)) were increased in MacGHR KO AT stroma
207 orm causally implicated in autoimmunity, and osteopontin (OPN), a CD44v7 ligand implicated in chronic
209 c osteochondrogenic programs and circulating osteopontin (OPN), a matricellular regulator of arterios
210 MGB1), a sterile danger signal molecule, and osteopontin (OPN), a multifunctional phosphoprotein invo
211 s expression of the SPP1 gene, which encodes osteopontin (OPN), a pleiotropic cytokine implicated in
219 tures, immunoblotting revealed more abundant osteopontin (OPN), dentin matrix protein 1 (DMP1), and m
221 mely insulin-like growth factor 1 (IGF1) and osteopontin (OPN), in cortical neurons leads to robust C
222 ferase alpha, alpha-fetoprotein, arginase-1, osteopontin (OPN), sorbitol dehydrogenase, fatty acid bi
223 ntal chain of events by the up-regulation of osteopontin (OPN), which in turn enhances osteoclastic a
224 ion of the pro-tumorigenic secreted protein, Osteopontin (OPN), which is especially critical for meta
226 e osteoprotegerin (OPG)-RANK-RANKL system or osteopontin (OPN)-play a role in the bone abnormalities
233 d SOCS3 co-deletion, or co-overexpression of osteopontin (OPN)/insulin-like growth factor 1 (IGF1)/ci
235 he signaling kinase PI(3)K and intracellular osteopontin (OPN-i), followed by translocation of OPN-i
236 (8.2+/-4.6-fold), RANKL (21+/-5.9-fold), and osteopontin (OPN; 17+/-5.3-fold), whereas C2 had little
237 sessment at Liver Transplant [REVERSE]: high osteopontin [OPN] and tissue inhibitor of metalloprotein
239 tabolism-related markers (osteocalcin [OCN], osteopontin [OPN], bone sialoprotein [BSP], osteoprotege
240 T plasma (not urine) kidney injury proteins (osteopontin [OPN], neutrophil gelatinase-associated lipo
242 t highly upregulated upon T-cell activation, osteopontin (or Eta-1, as it was designated then) has be
243 ce had significantly higher plasma levels of osteopontin, osteocalcin, and osteoprotegerin (204%, 148
245 n 6 (p<0.0001), interleukin 8 (p=0.002), and osteopontin (p<0.0001) were all prognostically associate
246 ative to median) of interleukin 8 (p=0.006), osteopontin (p=0.0004), HGF (p=0.010), and TIMP-1 (p=0.0
249 Phosphorylation increased cohesion between osteopontin polymers, and adhesion of osteopontin to hyd
250 cells, particularly T helper 17 cells, where osteopontin produced by dendritic cells supports IL-17 e
252 Our findings suggest that phosphorylated osteopontin promotes fracture toughness in a dose-depend
253 ggest that in the glioma perivascular niche, osteopontin promotes stem cell-like properties and radia
256 n-inducible Cre recombinase under control of osteopontin regulatory region crossed with yelow fluores
259 proform of secreted phosphoprotein 1 (SPP1)/osteopontin, restraining proteolytic activation of SPP1,
261 stology and immunohistochemical analyses for osteopontin, runt-related transcription factor 2 (Runx2)
262 er, our results indicate a possible way that osteopontin secreted from both NFPA cells and surroundin
264 as the main receptor for hyaluronic acid and osteopontin, serving as coreceptor for growth factor pat
267 In this study, we demonstrate that secreted osteopontin (sOPN) plays a role in the T cell migration
269 osteocalcin (BGLAP), osteonectin (SPARC) and osteopontin (SPP1) were detected in NU-CD271(high)CD45(l
270 arkers, dentin matrix protein 1 (Dmp1/DMP1), osteopontin (Spp1/OPN), and bone sialoprotein (Ibsp/BSP)
272 one marker genes (alkaline phosphatase/ALPL, osteopontin/SPP1, and bone sialoprotein II/IBSP) in a su
273 collagen 4A1/COL4A1, laminin gamma 2/LAMC2, osteopontin/SPP1, KIAA0101, and TGFbeta2 genes in the st
274 es were YFP(+) lineage-labeled; positive for osteopontin, SRY (sex determining region Y)-box 9, and e
275 BMP2 was a potent inducer of osteocalcin/osteopontin (statistically significant at P <0.01) and o
276 Moreover, we show in vitro that exogenous osteopontin stimulates the survival of murine IEL subpop
277 features demonstrated that the expression of osteopontin, TGFbeta2, and laminin in the stroma of ICC
278 arkers of renal injury including Cystatin C, Osteopontin, Tissue Inhibitor of Metalloproteinases-1 (T
280 etween osteopontin polymers, and adhesion of osteopontin to hydroxyapatite, enhancing energy dissipat
281 othelial growth factor receptor 1, 2, and 3; osteopontin; transforming growth factor beta1 and beta2;
282 ansforming growth factor beta (TGF-beta)(1), osteopontin, tumor necrosis factor alpha (TNF-alpha), le
283 demonstrated that the stromal expression of osteopontin was an independent prognostic marker for ove
285 ized within areas of mineralization, whereas osteopontin was more diffusely distributed in the area o
287 The secreted proteins analysis found that osteopontin was significantly upregulated in BD-NFPAs fi
290 e phosphatase, osteocalcin, osteonectin, and osteopontin were analyzed along with in vitro mineralize
291 ry concentrations of RANKL, osteocalcin, and osteopontin were higher, and osteoprotegerin was lower i
292 ntrol group, whereas RANKL, osteocalcin, and osteopontin were not related with periodontal status.
294 (ST2, CXCL9, matrix metalloproteinase 3, and osteopontin) were necessary to compose a four-biomarker
295 bumin, beta-2-microglobulin, cystatin C, and osteopontin) were undetectable in most AASK-N samples.
297 tified the secreted proinflammatory mediator osteopontin, which has been implicated in inflammation,
298 e differences and the specific receptors for osteopontin will be a research challenge for the future.
299 a phosphoprotein has some characteristics of osteopontin with respect to amino acid composition and s
300 , respectively), and inverse associations of osteopontin with standing and walking at 12 mo (P = 0.00