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1 e proinflammatory and direct HIF target gene macrophage migration inhibitory factor.
2 oted secretion of CC chemokines Ccl3/4/5 and macrophage migration inhibitory factor.
3 ne is identified as the pleiotropic cytokine macrophage migration inhibitory factor.
4 is a cell-surface receptor for the cytokine macrophage migration inhibitory factor.
5 liferation-inducing ligand (APRIL), IL-6, or macrophage migration inhibitory factor.
6 ammed cell death protein 5 and antiapoptotic macrophage migration inhibitory factor accumulated in th
7 a were identified in lung tumor specimens as macrophage migration inhibitory factor and cyclophilin A
8 10 ng/kg ACTH in the pm decreased as plasma macrophage migration inhibitory factor and IL-6 increase
9 y stages of the disease, and is regulated by macrophage migration inhibitory factor and its receptor,
10 3-kinase-delta inhibitors, and inhibition of macrophage migration inhibitory factor and P-glycoprotei
12 IL-21-propagated HLA-DR(+) NK cells produce macrophage migration inhibitory factor and provide costi
13 hat inhibits phosphodiesterase-4 and -10 and macrophage migration inhibitory factor and was recently
14 ha/beta], IL-18, gamma interferon, IL-6, and macrophage migration inhibitory factor) and chemokines (
15 n normal T cell expressed presumed secreted, macrophage migration inhibitory factor, and CD40 ligand,
16 increase in phosphoinositide 3-kinase delta, macrophage migration inhibitory factor, and glucocortico
17 one deacetylase-2 (HDAC2) expression, raised macrophage migration inhibitory factor, and increased P-
18 if protein 39 (RBM39), inflammatory mediator macrophage migration inhibitory factor, antioxidant SOD3
20 xpression of tumor necrosis factor-alpha and macrophage migration inhibitory factor (both neurotoxic
21 e identified this population of NK HLA-DR(+) macrophage migration inhibitory factor(+) cells in infla
22 ts activated GRalpha; increased secretion of macrophage migration inhibitory factor; competition with
24 we observed that the Plasmodium ortholog of macrophage migration inhibitory factor enhanced inflamma
26 , soluble intercellular adhesion molecule 1, macrophage migration-inhibitory factor/glycosylation-inh
28 factor (TvMIF), that is 47% similar to human macrophage migration inhibitory factor (HuMIF), a proinf
29 ne (C-C motif) ligand 22, interleukin-3, and macrophage migration inhibitory factor improved the mode
32 L-1beta, IL-1ralpha, CXC motif chemokine 10, macrophage migration inhibitory factor, macrophage infla
38 tokines released during H. pylori infection, macrophage migration inhibitory factor (MIF) and interle
44 In this study, we discover a novel role for macrophage migration inhibitory factor (MIF) as the key
45 ious immune-mediated diseases as part of the macrophage migration inhibitory factor (MIF) binding com
52 al pigment (hemozoin) induces the release of macrophage migration inhibitory factor (MIF) from macrop
55 a secreted orthologue of the human cytokine, Macrophage Migration Inhibitory Factor (MIF) has been cl
56 cell cytokine, the protein mediator known as macrophage migration inhibitory factor (MIF) has been fo
66 isms associated with decreased expression of macrophage migration inhibitory factor (MIF) have been l
67 ve confirmed and expanded the involvement of macrophage migration inhibitory factor (MIF) in a number
68 cent efforts to investigate the mechanism of macrophage migration inhibitory factor (MIF) in antagoni
70 ome (RDS), we demonstrate a central role for macrophage migration inhibitory factor (MIF) in lung mat
73 pe or null for the pro-inflammatory cytokine macrophage migration inhibitory factor (MIF) in the pres
125 isruption by homologous recombination of the macrophage migration inhibitory factor (Mif) locus in mo
130 forming growth factor beta1 (TGF-beta1), and macrophage migration inhibitory factor (MIF) mRNA/protei
132 s recent progress in the characterization of macrophage migration inhibitory factor (MIF) orthologs f
139 monstrated by using a study on the impact of macrophage migration inhibitory factor (MIF) reduction i
140 esized and evaluated for their inhibition of macrophage migration inhibitory factor (MIF) tautomerase
141 ologue of the human proinflammatory cytokine macrophage migration inhibitory factor (MIF) that has th
142 Microarray analysis suggested downregulated macrophage migration inhibitory factor (MIF) to be the m
144 ith AML cultured with BM-MSCs and found that macrophage migration inhibitory factor (MIF) was highly
147 he protein that has been historically called macrophage migration inhibitory factor (MIF) was one of
150 olymorphisms of the proinflammatory cytokine macrophage migration inhibitory factor (MIF) were associ
151 1 reduces macrophage formation by inhibiting macrophage migration inhibitory factor (MIF), a cytokine
152 we have investigated the interaction between macrophage migration inhibitory factor (MIF), a major pr
158 ibitors of the tautomerase activity of human macrophage migration inhibitory factor (MIF), a proinfla
162 based on a carbonyloxime (OXIM) scaffold for macrophage migration inhibitory factor (MIF), a protein
164 This study is the first to demonstrate that macrophage migration inhibitory factor (MIF), an immune
172 on of CD74, which interacts with its ligand, macrophage migration inhibitory factor (MIF), and thereb
173 cells produce gamma interferon (IFN-gamma), macrophage migration inhibitory factor (MIF), and tumor
174 monstrated that the proinflammatory peptide, macrophage migration inhibitory factor (MIF), functions
175 usly found that the proinflammatory peptide, macrophage migration inhibitory factor (MIF), functions
176 oad, lipopolysaccharide (LPS), soluble CD14, macrophage migration inhibitory factor (MIF), intestinal
179 (MS), although inflammatory factors, such as macrophage migration inhibitory factor (MIF), its homolo
180 ury was associated with robust generation of macrophage migration inhibitory factor (MIF), leukotrien
181 rotectin, colony-stimulating factor (CSF)-1, macrophage migration inhibitory factor (MIF), monokine i
182 ess and secrete the chemokine-like mediator, macrophage migration inhibitory factor (MIF), more stron
184 xine (T(4)) and the proinflammatory cytokine macrophage migration inhibitory factor (MIF), together w
185 enic growth factors and proteinases, such as macrophage migration inhibitory factor (MIF), VEGF, and
186 y other solid tumors produce high amounts of macrophage migration inhibitory factor (MIF), which appe
187 tivity: a lymphocyte-derived mediator called macrophage migration inhibitory factor (MIF), which inhi
188 ted the role of the proinflammatory cytokine macrophage migration inhibitory factor (MIF), which is a
189 describe herein an ortholog of the cytokine, macrophage migration inhibitory factor (MIF), which is p
190 vation through the secretion of the cytokine macrophage migration inhibitory factor (MIF), which resu
191 ied and identified to be the multifunctional macrophage migration inhibitory factor (MIF), whose acti
192 ia major encodes 2 orthologs of the cytokine macrophage migration inhibitory factor (MIF), whose func
209 derived from tissues in the eye that produce macrophage migration-inhibitory factor (MIF), a cytokine
210 CL12, the cytokines interleukin-6 (IL-6) and macrophage migration-inhibitory factor (MIF), and the an
214 tively expressed were those for the cytokine macrophage migration inhibitory factor neurohormone rece
216 s of two inhibitors of Plasmodium falciparum macrophage migration inhibitory factor (PfMIF) with nano
217 8 and 14, natural killer cell function, and macrophage migration inhibitory factor production are un
220 p are limited to fungal species, whereas the macrophage migration inhibitory factor subgroup has wide
221 . vaginalis secretes a protein, T. vaginalis macrophage migration inhibitory factor (TvMIF), that is
222 a-globin, 6.8 kDa mitochondrial proteolipid, macrophage migration inhibitory factor, ubiquitin, beta-
223 on of monocyte chemoattractant protein-1 and macrophage migration inhibitory factor was significantly
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