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1 inducing ligand (APRIL), IL-6, or macrophage migration inhibitory factor.
2 matory and direct HIF target gene macrophage migration inhibitory factor.
3 0 mol wt, the same fraction containing human migration inhibitory factor.
4 n with its only known ligand, the macrophage migration inhibitory factor.
5 surface receptor for the cytokine macrophage migration inhibitory factor.
6 ion of CC chemokines Ccl3/4/5 and macrophage migration inhibitory factor.
7 ified as the pleiotropic cytokine macrophage migration inhibitory factor.
9 identify D-dopachrome tautomerase/macrophage migration-inhibitory factor-2 (MIF-2), a paralog of the
10 death protein 5 and antiapoptotic macrophage migration inhibitory factor accumulated in the infected-
11 tified in lung tumor specimens as macrophage migration inhibitory factor and cyclophilin A, respectiv
12 CTH in the pm decreased as plasma macrophage migration inhibitory factor and IL-6 increased after CLP
15 Conversely, HIF-1alpha regulated macrophage migration inhibitory factor and promoted macrophage infi
16 agated HLA-DR(+) NK cells produce macrophage migration inhibitory factor and provide costimulatory si
17 s phosphodiesterase-4 and -10 and macrophage migration inhibitory factor and was recently found to re
18 L-18, gamma interferon, IL-6, and macrophage migration inhibitory factor) and chemokines (eotaxin, ma
19 cell expressed presumed secreted, macrophage migration inhibitory factor, and CD40 ligand, that promo
20 phosphoinositide 3-kinase delta, macrophage migration inhibitory factor, and glucocorticoid receptor
21 lase-2 (HDAC2) expression, raised macrophage migration inhibitory factor, and increased P-glycoprotei
22 portive macrophage activities (IL-10, MCP-1, migration inhibitory factor, and TGFbeta production) and
23 39 (RBM39), inflammatory mediator macrophage migration inhibitory factor, antioxidant SOD3, ion chann
24 The alternative endogenous ligand macrophage migration inhibitory factor behaves opposite to CXCL12 i
26 f tumor necrosis factor-alpha and macrophage migration inhibitory factor (both neurotoxic cytokines)
27 d this population of NK HLA-DR(+) macrophage migration inhibitory factor(+) cells in inflammatory hum
28 okine ligand 5], CCL7, CCL4, MIF [macrophage migration inhibitory factor]), cluster 3 (n=77; IL [inte
29 d GRalpha; increased secretion of macrophage migration inhibitory factor; competition with the transc
31 d that the Plasmodium ortholog of macrophage migration inhibitory factor enhanced inflammatory cytoki
33 ntercellular adhesion molecule 1, macrophage migration-inhibitory factor/glycosylation-inhibiting fac
35 peat at position 794 of the human macrophage migration inhibitory factor (hMIF) gene has been associa
36 IF), that is 47% similar to human macrophage migration inhibitory factor (HuMIF), a proinflammatory c
37 if) ligand 22, interleukin-3, and macrophage migration inhibitory factor improved the model significa
38 regulation of the expression of the cytokine migration inhibitory factor in the T cells and augmented
40 ally, we found that NSCLC-derived macrophage migration-inhibitory factor is responsible for the incre
41 -1ralpha, CXC motif chemokine 10, macrophage migration inhibitory factor, macrophage inflammatory pro
48 , were positively correlated with macrophage migration inhibitory factor (MIF) and 37 lipids were pos
50 eased during H. pylori infection, macrophage migration inhibitory factor (MIF) and interleukin-8 (IL-
53 ants of the gene for the cytokine macrophage migration inhibitory factor (MIF) are defined by a 4-nuc
57 the present study, we identified macrophage migration inhibitory factor (MIF) as an intracellular in
58 udy, we discover a novel role for macrophage migration inhibitory factor (MIF) as the key director of
59 ed genes (ISGs) and proinflammatory cytokine migration inhibitory factor (MIF) at viral rebound in pa
61 There is evidence that C5a and macrophage migration inhibitory factor (MIF) both play important ro
62 his study shows that the cytokine macrophage migration inhibitory factor (MIF) can induce pain-like b
63 eishmania secrete an inflammatory macrophage migration inhibitory factor (MIF) cytokine homolog, a vi
64 Targeted deletion of the gene for macrophage migration inhibitory factor (MIF) delays development of
67 , potentially reflecting the outcome of high Migration Inhibitory Factor (MIF) expression in those tu
69 Recent studies have revealed that macrophage migration inhibitory factor (MIF) expression is increase
71 signaling to macrophages through macrophage migration inhibitory factor (MIF) family proteins in sev
76 orthologue of the human cytokine, Macrophage Migration Inhibitory Factor (MIF) has been cloned from t
77 ne, the protein mediator known as macrophage migration inhibitory factor (MIF) has been found recentl
88 ated with decreased expression of macrophage migration inhibitory factor (MIF) have been linked to th
89 d and expanded the involvement of macrophage migration inhibitory factor (MIF) in a number of disease
90 s to investigate the mechanism of macrophage migration inhibitory factor (MIF) in antagonizing antime
92 recently described a role for the macrophage migration inhibitory factor (MIF) in ccRCC as an autocri
93 trate a novel role for EC-derived macrophage migration inhibitory factor (MIF) in inhibiting PC contr
94 we demonstrate a central role for macrophage migration inhibitory factor (MIF) in lung maturation at
95 is study investigated the role of macrophage migration inhibitory factor (MIF) in modulating pregnanc
96 al role of the versatile cytokine macrophage migration inhibitory factor (MIF) in regulating a metabo
98 We describe an intrinsic role for macrophage migration inhibitory factor (MIF) in the development of
99 for the pro-inflammatory cytokine macrophage migration inhibitory factor (MIF) in the presence or abs
120 Produced by many cell types, macrophage migration inhibitory factor (MIF) is a pleiotropic cytok
156 The immunoregulatory cytokine macrophage migration inhibitory factor (MIF) is encoded in a functi
162 The pro-inflammatory mediator macrophage migration inhibitory factor (MIF) is produced by immune
166 y homologous recombination of the macrophage migration inhibitory factor (Mif) locus in mouse embryon
168 Mounting evidence suggests that macrophage migration inhibitory factor (MIF) may serve as an import
171 wth factor beta1 (TGF-beta1), and macrophage migration inhibitory factor (MIF) mRNA/protein than matu
173 ogress in the characterization of macrophage migration inhibitory factor (MIF) orthologs from parasit
176 The proinflammatory cytokine macrophage migration inhibitory factor (MIF) plays a role in the ma
181 by using a study on the impact of macrophage migration inhibitory factor (MIF) reduction in neuroblas
182 evaluated for their inhibition of macrophage migration inhibitory factor (MIF) tautomerase activity.
183 he human proinflammatory cytokine macrophage migration inhibitory factor (MIF) that has the capabilit
184 analysis suggested downregulated macrophage migration inhibitory factor (MIF) to be the most pertine
185 Previously, we have shown that macrophage migration inhibitory factor (MIF) was highly elevated in
186 tured with BM-MSCs and found that macrophage migration inhibitory factor (MIF) was highly expressed b
190 that has been historically called macrophage migration inhibitory factor (MIF) was one of the first c
194 s of the proinflammatory cytokine macrophage migration inhibitory factor (MIF) were associated with m
195 of RA-FLSs identified a distinct macrophage migration inhibitory factor (MIF)(high) subset with mito
196 acrophage formation by inhibiting macrophage migration inhibitory factor (MIF), a cytokine critically
197 levation of circulating levels of macrophage migration inhibitory factor (MIF), a cytokine implicated
198 ly, the LrS induced production of macrophage migration inhibitory factor (MIF), a cytokine involved i
199 estigated the interaction between macrophage migration inhibitory factor (MIF), a major pro-inflammat
204 We found that plasma levels of macrophage migration inhibitory factor (MIF), a proinflammatory and
206 the tautomerase activity of human macrophage migration inhibitory factor (MIF), a proinflammatory cyt
209 Remarkably, circulating levels of macrophage migration inhibitory factor (MIF), a proinflammatory imm
210 carbonyloxime (OXIM) scaffold for macrophage migration inhibitory factor (MIF), a protein involved in
212 o-inflammatory mediators, such as macrophage migration inhibitory factor (MIF), also promote tumorige
213 is the first to demonstrate that macrophage migration inhibitory factor (MIF), an immune system 'inf
220 hemoattractant protein-1 (MCP-1), macrophage migration inhibitory factor (MIF), and fractalkine are c
221 surface receptor for the cytokine macrophage migration inhibitory factor (MIF), and its mRNA is known
223 which interacts with its ligand, macrophage migration inhibitory factor (MIF), and thereby activates
224 uce gamma interferon (IFN-gamma), macrophage migration inhibitory factor (MIF), and tumor necrosis fa
225 that the proinflammatory peptide, macrophage migration inhibitory factor (MIF), functions as an autoc
226 that the proinflammatory peptide, macrophage migration inhibitory factor (MIF), functions as an autoc
227 lysaccharide (LPS), soluble CD14, macrophage migration inhibitory factor (MIF), intestinal fatty acid
230 ugh inflammatory factors, such as macrophage migration inhibitory factor (MIF), its homolog D-dopachr
231 ociated with robust generation of macrophage migration inhibitory factor (MIF), leukotriene B(4) (LTB
232 crophage-derived chemokine (MDC), macrophage migration inhibitory factor (MIF), monokine induced by i
233 olony-stimulating factor (CSF)-1, macrophage migration inhibitory factor (MIF), monokine induced by i
234 rete the chemokine-like mediator, macrophage migration inhibitory factor (MIF), more strongly than de
237 and the proinflammatory cytokine macrophage migration inhibitory factor (MIF), together with its cli
238 XC chemokine ligand (CXCL) 12 and macrophage migration inhibitory factor (MIF), using Forster resonan
239 factors and proteinases, such as macrophage migration inhibitory factor (MIF), VEGF, and matrix meta
240 id tumors produce high amounts of macrophage migration inhibitory factor (MIF), which appears to play
241 rthologue of the innate cytokine, Macrophage Migration Inhibitory Factor (MIF), which functions in ma
242 ymphocyte-derived mediator called macrophage migration inhibitory factor (MIF), which inhibited the r
243 e of the proinflammatory cytokine macrophage migration inhibitory factor (MIF), which is an upstream
244 rein an ortholog of the cytokine, macrophage migration inhibitory factor (MIF), which is produced by
245 ugh the secretion of the cytokine macrophage migration inhibitory factor (MIF), which results in a M2
246 ntified to be the multifunctional macrophage migration inhibitory factor (MIF), whose activities incl
247 codes 2 orthologs of the cytokine macrophage migration inhibitory factor (MIF), whose functions in pa
248 s observed only for the chemokine macrophage migration inhibitory factor (MIF), with males displaying
271 m tissues in the eye that produce macrophage migration-inhibitory factor (MIF), a cytokine that has r
272 ion is regulated by glucocorticoids, whereas migration-inhibitory factor (MIF), a pleiotropic cytokin
273 ytokines interleukin-6 (IL-6) and macrophage migration-inhibitory factor (MIF), and the angiogenic fa
274 rotein (LRP), BCL2-interacting killer (BIK), migration-inhibitory factor (MIF), matrix metalloprotein
276 matrix metalloproteinase [MMP]-9, macrophage migration inhibitory factor [MIF], MIP-1alpha, and MIP-2
277 nt studies demonstrated that proinflammatory migration inhibitory factor(MIF) blocks p53-dependent ap
278 essed were those for the cytokine macrophage migration inhibitory factor neurohormone receptors such
280 hibitors of Plasmodium falciparum macrophage migration inhibitory factor (PfMIF) with nanomolar Ki's,
281 ecreted proinflammatory cytokines, including migration inhibitory factor, plasminogen activator inhib
282 natural killer cell function, and macrophage migration inhibitory factor production are under investi
284 Leishmania-encoded orthologs of macrophage migration inhibitory factor regulate host immunity to pr
286 g of 2 individual peptide chains also called migration inhibitory factor-related protein (MRP)-8 and
287 oH, apoJ, apoL-1, apoM, alpha-1 antitrypsin, migration inhibitory factor-related protein 8, lysosome
289 ession of two S100 calcium-binding proteins, migration inhibitory factor-related proteins (MRPs) 8 an
290 stigated the novel role of recombinant human migration inhibitory factor (rhMIF) in up-regulating vas
291 n this study, we investigated the effects of migration inhibitory factor (rhMIF) on angiogenesis-rela
292 e identified cytokines, including macrophage migration inhibitory factor, secreted by the Mycn-nGEMM
293 ed to fungal species, whereas the macrophage migration inhibitory factor subgroup has wide eukaryotic
294 secretes a protein, T. vaginalis macrophage migration inhibitory factor (TvMIF), that is 47% similar
295 .8 kDa mitochondrial proteolipid, macrophage migration inhibitory factor, ubiquitin, beta-thymosin 4,
296 yte chemoattractant protein-1 and macrophage migration inhibitory factor was significantly attenuated