ライフサイエンスコーパス: inhibitory factor

1 ular endothelial growth factor, and leukemia inhibitory factor).

2 he pleiotropic cytokine macrophage migration inhibitory factor.

3 igand (APRIL), IL-6, or macrophage migration inhibitory factor.

4 ains pluripotency in the absence of leukemia inhibitory factor.

5 ceptor for the cytokine macrophage migration inhibitory factor.

6 chemokines Ccl3/4/5 and macrophage migration inhibitory factor.

7 on but also secretion of known hair follicle inhibitory factors.

8 istones H3 and H4 as concentration-dependent inhibitory factors.

9 low-progesterone periods, we found more HIV inhibitory factors.

10 ontribute to their ability to overcome these inhibitory factors.

11 cs of a new cell identity without removal of inhibitory factors.

12 ulin resistance, suggesting the existence of inhibitory factors.

13 xtrinsic environment composed of a milieu of inhibitory factors.

14 restricted at early postentry steps by host inhibitory factors.

15 egative sera a purified fraction enriched in inhibitory factors.

16 lated by a complex network of excitatory and inhibitory factors.

17 etic screens and cloned mitochondrial ATPase inhibitory factor 1 (atpif1) from a zebrafish mutant wit

18 Last, the ATPase inhibitory factor 1 (IF(1)) binds in a mode that is diff

19 ATPase inhibitory factor 1 (IF1) is a nuclear-encoded, ATP synt

20 ATPase inhibitory factor 1 (IF1) is an ATP synthase-interacting

21 ATP synthase inhibitory factor 1 (IF1), a novel myokine, regulates gl

22 nd spheroid growth in vitro and elevated Wnt-inhibitory factor 1 (WIF1) activity.

23 reted protein Shifted (Shf), a member of Wnt inhibitory factor 1 (WIF1) family.

24 ethylation in the promoter CpG island of Wnt inhibitory factor 1 (WIF1) has been observed in differen

25 cDNA microarray with ChIP-chip analyses, Wnt inhibitory factor 1 (Wif1) was identified as a novel tar

26 The WNT inhibitory factor 1 (WIF1), a secreted inhibitor of WNTs

27 Here, we demonstrate that the Wnt inhibitory factor 1 (WIF1), a secreted Wnt antagonist, i

28 che by expressing the pan Wnt inhibitor, Wnt inhibitory factor 1 (Wif1), specifically in osteoblasts.

29 s secreted frizzled-related protein 2 or Wnt inhibitory factor 1 enhanced regeneration of the central

30 ptor frizzled family receptor 3, and the Wnt inhibitory factor 1 were differentially expressed along

31 d EZH2 and H3K27me3's occupancy on WIF1 (Wnt inhibitory factor 1) promoter resulting in reduced WIF1

32 Promoters from the chitinase 3-like 3, Wnt inhibitory factor 1, and fms-related tyrosine kinase 1/s

33 ed frizzled-related protein 3] and WIF1 [Wnt inhibitory factor 1]).

34 Strongly downregulated genes included Wnt-inhibitory factor-1 (WIF1), beta-cellulin (BTC), and CCL

35 ntained, in part, by local production of Wnt inhibitory factor-1.

36 Cytokine macrophage migration inhibitory factor-2 (MIF-2 or D-dopachrome tautomerase)

37 ein 5 and antiapoptotic macrophage migration inhibitory factor accumulated in the infected-explant sp

38 ific deletion of genes encoding ATGL or ATGL inhibitory factors altered neutrophil lipid profiles and

39 tion but opposite effects regarding leukemia inhibitory factor and insulin-like growth factor 1.

40 se, and is regulated by macrophage migration inhibitory factor and its receptor, CD74.

41 y, HIF-1alpha regulated macrophage migration inhibitory factor and promoted macrophage infiltration t

42 -DR(+) NK cells produce macrophage migration inhibitory factor and provide costimulatory signaling du

43 newal of mESCs in combination with leukaemia inhibitory factor and regulates the formation of the mou

44 iesterase-4 and -10 and macrophage migration inhibitory factor and was recently found to reduce alcoh

45 onsisting of oxygen, glucose, hydrogen ions, inhibitory factors and growth factors.

46 kine (C-C motif) ligands 2 and 3, macrophage inhibitory factor, and chemokines mediating neutrophil a

47 pluripotent cells in the absence of leukemia inhibitory factor, and directly regulated mouse Nanog ta

48 ositide 3-kinase delta, macrophage migration inhibitory factor, and glucocorticoid receptor beta expr

49 okines ciliary neurotrophic factor, leukemia inhibitory factor, and IL-11 have been identified as oli

50 ctors insulin-like growth factor 1, leukemia inhibitory factor, and urokinase-type plasminogen activa

51 onization and addition of stimulating and/or inhibitory factors, and they may not have demonstrated t

52 of the dorsal aortae occurs as the result of inhibitory factors (antagonists of BMP signaling) secret

53 , inflammatory mediator macrophage migration inhibitory factor, antioxidant SOD3, ion channel voltage

54 Oncostatin M (OSM) and leukemia inhibitory factor are pleiotropic cytokines that belong

55 t with each hair cycle, overall levels of SC-inhibitory factors are reduced, further lowering the thr

56 ative endogenous ligand macrophage migration inhibitory factor behaves opposite to CXCL12 in each ass

57 Macrophage migration inhibitory factor binding to CD74 induces its intramembr

58 crosis factor-alpha and macrophage migration inhibitory factor (both neurotoxic cytokines) and elevat

59 differentiation-associated cytokine leukemia inhibitory factor by atopic fibroblasts.

60 as due to both blockade of the release of NK-inhibitory factors by AML cells and prevention of RANK s

61 eir expression of CTGF, suggesting that this inhibitory factor can be positively regulated in astrocy

62 ulation of NK HLA-DR(+) macrophage migration inhibitory factor(+) cells in inflammatory human appendi

63 rosis) and influences on longevity (leukemia inhibitory factor, ceramides).

64 Pseudomonas aeruginosa secretes the CFTR inhibitory factor Cif and thus triggers loss of CFTR, an

65 s transmembrane conductance regulator (CFTR) inhibitory factor (Cif) is a virulence factor secreted b

66 s transmembrane conductance regulator (CFTR) inhibitory factor (Cif) is secreted by Pseudomonas aerug

67 ) and CF transmembrane conductance regulator inhibitory factor (Cif) show that P. aeruginosa also per

68 fibrosis transmembrane conductance regulator inhibitory factor (Cif), can disrupt 15-epi LXA4 transce

69 This virulence factor, named CFTR inhibitory factor (Cif), is regulated by a TetR-family,

70 ance regulator (CFTR) is blocked by the CFTR inhibitory factor (Cif).

71 olipases, alkaline phosphatase, and the CFTR inhibitory factor (Cif).

72 nd 5], CCL7, CCL4, MIF [macrophage migration inhibitory factor]), cluster 3 (n=77; IL [interleukin]-1

73 increased secretion of macrophage migration inhibitory factor; competition with the transcription fa

74 Macrophage migration inhibitory factor contains 3 cysteine (Cys) residues; us

75 f immunosuppressive cells and the release of inhibitory factors contribute to the development of a tu

76 Here we report the production of leukemia inhibitory factor-dependent, so-called naive type, pluri

77 In vitro analysis showed that the Wnt inhibitory factor domain of Ryk was necessary for Wnt bi

78 tical models: 1) parallel activation of Fshb inhibitory factors (e.g. inhibin alpha and VGF nerve gro

79 Supplementation of KM with leukemia inhibitory factor elicited lineage restriction to rHBs.

80 Plasmodium ortholog of macrophage migration inhibitory factor enhanced inflammatory cytokine product

81 Macrophage migration inhibitory factor enhances Pseudomonas aeruginosa biofil

82 indicated that KCC2 function was a critical inhibitory factor ex vivo and in vivo.

83 entiation through the withdrawal of leukemia-inhibitory factor for 6 or more days.

84 of the target cell membrane as an important inhibitory factor for ADCC.

85 e demonstrate the existence of an endogenous inhibitory factor for GnT-IX that functions as a key reg

86 LTP, and its cytoplasmic tail seems to carry inhibitory factors for LTP.

87 ar adhesion molecule 1, macrophage migration-inhibitory factor/glycosylation-inhibiting factor, inter

88 tably self-renew in the presence of leukemia inhibitory factor, GSK3 inhibitor (CHIR99021), and TGF-b

89 Macrophage migration inhibitory factor has been shown to mediate both disease

90 is 47% similar to human macrophage migration inhibitory factor (HuMIF), a proinflammatory cytokine.

91 n of SMAD 1/5/8; (ii) downregulation of SMAD inhibitory factors [i.e., noggin and SMAD6 (inhibitory S

92 22, interleukin-3, and macrophage migration inhibitory factor improved the model significantly (P <

93 e growth factor (IGF)-1, IGF-2, and leukemia inhibitory factor in medulloblastoma cells, but did not

94 small interfering (si)RNA (siGDF-8), a major inhibitory factor in the development and postnatal regen

95 t the novel idea that endogenous Gal-1 is an inhibitory factor in the development of arthritis affect

96 of the expression of the cytokine migration inhibitory factor in the T cells and augmented expressio

97 this hurdle could be due to the presence of inhibitory factors in patient serum.

98 ion of SMAD7 and IkappaBalpha, which are key inhibitory factors in renal inflammation.

99 A synthesis rates were linked to stimulatory/inhibitory factors in the culture medium, which ultimate

100 After central nervous system (CNS) injury, inhibitory factors in the lesion scar and poor axon grow

101 studies have not shown the effects of these inhibitory factors in vivo.

102 unit and confers resistance to FtsZ assembly inhibitory factors including Kil of bacteriophage lambda

103 ens, matrix metalloproteinases, and leukemia inhibitory factor, insulin-like growth factor 1, and pen

104 argeting a particular group of extracellular inhibitory factors is insufficient to trigger long-dista

105 inhibitors (2i) in the presence of leukaemia inhibitory factor (LIF) (hereafter termed 2i/L) induces

106 cells is sustained by the cytokine leukaemia inhibitory factor (LIF) acting through the transcription

107 ion factor pathway are activated by leukemia inhibitory factor (LIF) and contribute to mouse embryoni

108 he IL-6 family cytokines, including Leukemia inhibitory factor (LIF) and Interleukin 6 (IL-6), in hum

109 of cell cycle-associated genes and leukemia inhibitory factor (Lif) and revealed alterations in expr

110 ients had increased serum levels of leukemia inhibitory factor (LIF) and that higher LIF levels corre

111 Oncostatin M (OSM) and leukemia inhibitory factor (LIF) are IL-6 family members with a w

112 ication of the IL-6 family cytokine leukemia inhibitory factor (LIF) as a serum predictor of local NP

113 ated with IL-6 pointed to STAT4 and leukemia inhibitory factor (LIF) as potentially linked.

114 Expression of leukemia inhibitory factor (LIF) cytokine mRNA, but not other IL-

115 aEGFR each also express IL-6 and/or leukemia inhibitory factor (LIF) cytokines.

116 Here we show that Leukemia Inhibitory Factor (LIF) expression is induced specifical

117 Leukaemia inhibitory factor (LIF) has been recently identified as

118 Leukemia inhibitory factor (LIF) injections were given intraperit

119 pand after H-I and to determine how leukemia inhibitory factor (LIF) insufficiency affects their resp

120 lecular mechanisms, we reveal that leukaemia inhibitory factor (LIF) is a key paracrine factor from a

121 We designed a transgene in which leukemia inhibitory factor (LIF) is under control of a leukocyte-

122 11 (IL-11), oncostatin M (OSM), and leukemia inhibitory factor (LIF) levels in patients with differen

123 iation in response to withdrawal of leukemia inhibitory factor (LIF) or bone morphogenetic protein 4

124 ary neurotrophic factor (CNTF) and leukaemia inhibitory factor (LIF) potently protect axotomised reti

125 Leukaemia inhibitory factor (LIF) regulates ESCs through Stat3, in

126 increased Wnt expression, enhanced leukemia inhibitory factor (LIF) sensitivity, and reduced respons

127 ch as IL-6, oncostatin M (OSM) and leukaemia inhibitory factor (LIF) signal through receptor complexe

128 gested interaction between Tet1 and leukemia inhibitory factor (LIF) signaling.

129 ously, we reported that delivery of leukemia inhibitory factor (LIF) to the CNS stimulates the self-r

130 generally accepted that addition of leukemia inhibitory factor (LIF) together with either serum or bo

131 tiated normal differentiation after leukemia inhibitory factor (LIF) withdrawal but, unlike control E

132 eous onset of differentiation after leukemia inhibitory factor (LIF) withdrawal.

133 Leukemia inhibitory factor (LIF), a critical implantation factor

134 e mannose phosphorylation status of leukemia inhibitory factor (LIF), a previously identified high af

135 However, leukemia inhibitory factor (LIF), an IL-6 family cytokine, restri

136 Leukemia inhibitory factor (LIF), an interleukin-6 family neurocy

137 including IL-6, oncostatin M (OSM), leukemia inhibitory factor (LIF), and IL-11, have fibrogenic feat

138 and engineered to express zebrafish leukemia inhibitory factor (Lif), basic fibroblast growth factor

139 gnificantly lower concentrations of leukemia inhibitory factor (LIF), basic fibroblast growth factor

140 L-11, IL-6, oncostatin M (OSM), and leukemia inhibitory factor (LIF), only OSM and LIF were sufficien

141 -11, IL-27, oncostatin M (OSM), and leukemia inhibitory factor (LIF), signal via the common GP130 cyt

142 with media containing the cytokine leukemia inhibitory factor (LIF), which propagates the pluripoten

143 episomal reprogramming), which uses leukemia inhibitory factor (LIF)-expressing SNL feeders, frequent

144 (FGF)-ERK1/2 pathway, PI3K-AKT, the leukemia inhibitory factor (LIF)-JAK-STAT3 axis, Wnt-GSK3 signall

145 nocorticotropic hormone (ACTH) and leukaemia inhibitory factor (LIF).

146 pendent GE-expressed genes, such as leukemia inhibitory factor (LIF).

147 (IL6) but also the related cytokine leukemia inhibitory factor (LIF).

148 criptional up-regulation of uterine leukemia inhibitory factor (LIF).

149 nation with Fgf8b and the cytokine leukaemia inhibitory factor (Lif).

150 S) cells downstream of the cytokine leukemia inhibitory factor (LIF).

151 be maintained by activation of the leukaemia inhibitory factor (LIF)/signal transducer and activator

152 er, it provides a mechanism for how leukemia inhibitory factor (LIF)/STAT3 signaling reaches across t

153 ngth globular proteins [mCherry and leukemia inhibitory factor (LIF)].

154 CXC motif chemokine 10, macrophage migration inhibitory factor, macrophage inflammatory protein (MIP)

155 Macrophage migration inhibitory factor (MIF) affects inflammation, glucose ho

156 Because macrophage migration inhibitory factor (MIF) and its functional homolog, d-do

157 We identified macrophage migration inhibitory factor (MIF) as a PARP-1-dependent AIF-associ

158 Here, we identified macrophage migration inhibitory factor (MIF) as an important regulator of cys

159 scover a novel role for macrophage migration inhibitory factor (MIF) as the key director of MSC migra

160 diseases as part of the macrophage migration inhibitory factor (MIF) binding complex.

161 secrete an inflammatory macrophage migration inhibitory factor (MIF) cytokine homolog, a virulence fa

162 eletion of the gene for macrophage migration inhibitory factor (MIF) delays development of chronic ly

163 Macrophage migration inhibitory factor (MIF) exerts a protective effect on is

164 Macrophage migration inhibitory factor (MIF) has a cytoprotective effect on l

165 The cytokine macrophage migration inhibitory factor (MIF) has been characterized as a key

166 Macrophage migration inhibitory factor (MIF) has been recognized as a major p

167 Macrophage migration inhibitory factor (MIF) has been recognized as a potent

168 also find that D-DT and macrophage migration inhibitory factor (MIF) have additive effects in neutrop

169 decreased expression of macrophage migration inhibitory factor (MIF) have been linked to the risk of

170 tigate the mechanism of macrophage migration inhibitory factor (MIF) in antagonizing antimelanoma imm

171 The role of macrophage migration inhibitory factor (MIF) in autoimmunity is underscored b

172 escribed a role for the macrophage migration inhibitory factor (MIF) in ccRCC as an autocrine-signali

173 vel role for EC-derived macrophage migration inhibitory factor (MIF) in inhibiting PC contractility a

174 the versatile cytokine macrophage migration inhibitory factor (MIF) in regulating a metabolic rhythm

175 Macrophage migration inhibitory factor (MIF) is a catalytic cytokine and an u

176 Macrophage migration inhibitory factor (MIF) is a cytokine found to be associ

177 Macrophage migration inhibitory factor (MIF) is a cytokine with key roles in

178 The macrophage migration inhibitory factor (MIF) is a hypoxia regulated gene that

179 Macrophage migration inhibitory factor (MIF) is a key proinflammatory mediato

180 Mammalian macrophage migration inhibitory factor (MIF) is a multifaceted cytokine invol

181 Macrophage migration inhibitory factor (MIF) is a multipotent cytokine that i

182 Macrophage migration inhibitory factor (MIF) is a pivotal regulator of the im

183 Macrophage migration inhibitory factor (MIF) is a pleiotropic cytokine that h

184 Macrophage migration inhibitory factor (MIF) is a pleiotropic cytokine that m

185 Macrophage migration-inhibitory factor (MIF) is a pleiotropic cytokine with c

186 ced by many cell types, macrophage migration inhibitory factor (MIF) is a pleiotropic cytokine with c

187 Mammalian macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine th

188 The macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine th

189 Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine wi

190 Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine.

191 Macrophage migration inhibitory factor (MIF) is a proinflammatory mediator wi

192 Macrophage migration inhibitory factor (MIF) is a proinflammatory molecule in

193 Macrophage migration inhibitory factor (MIF) is a structurally unique inflamm

194 Macrophage migration-inhibitory factor (MIF) is an atypical chemokine that pr

195 Human macrophage migration-inhibitory factor (MIF) is an evolutionarily-conserved p

196 Macrophage migration inhibitory factor (MIF) is an immune mediator encoded in

197 The cytokine macrophage migration inhibitory factor (MIF) is an important component of the

198 Macrophage migration inhibitory factor (MIF) is an inflammatory cytokine that

199 Macrophage migration inhibitory factor (MIF) is an upstream mediator of host

200 Human macrophage migration inhibitory factor (MIF) is both a keto-enol tautomerase

201 munoregulatory cytokine macrophage migration inhibitory factor (MIF) is encoded in a functionally pol

202 Macrophage migration inhibitory factor (MIF) is released on platelet activati

203 Macrophage migration inhibitory factor (MIF) is responsible for proinflammato

204 Macrophage migration inhibitory factor (MIF) mediates inflammation and immuni

205 Intracellular macrophage migration inhibitory factor (MIF) often becomes stabilized in huma

206 roinflammatory cytokine macrophage migration inhibitory factor (MIF) plays a role in the maintenance

207 Macrophage migration inhibitory factor (MIF) plays versatile roles in the imm

208 Macrophage migration inhibitory factor (MIF) promotes cardiomyocyte survival

209 suggested downregulated macrophage migration inhibitory factor (MIF) to be the most pertinent mediato

210 stimulation identified a role for macrophage inhibitory factor (MIF) to potentiate the activation of

211 BM-MSCs and found that macrophage migration inhibitory factor (MIF) was highly expressed by primary

212 Macrophage migration inhibitory factor (MIF) was identified and evaluated for

213 Overexpression of macrophage migration inhibitory factor (MIF) was identified in human GBM spec

214 Recently, macrophage migration inhibitory factor (MIF) was shown to directly inhibit mu

215 Recently, macrophage migration inhibitory factor (MIF) was shown to directly inhibit th

216 roinflammatory cytokine macrophage migration inhibitory factor (MIF) were associated with morbidity a

217 formation by inhibiting macrophage migration inhibitory factor (MIF), a cytokine critically involved

218 S induced production of macrophage migration inhibitory factor (MIF), a cytokine involved in host-mic

219 the interaction between macrophage migration inhibitory factor (MIF), a major pro-inflammatory and gr

220 Macrophage migration inhibitory factor (MIF), a multipotent protein that exhi

221 nvestigated the role of macrophage migration inhibitory factor (MIF), a pleiotropic proinflammatory c

222 d that plasma levels of macrophage migration inhibitory factor (MIF), a proinflammatory and immunoreg

223 Macrophage migration inhibitory factor (MIF), a proinflammatory cytokine and

224 erase activity of human macrophage migration inhibitory factor (MIF), a proinflammatory cytokine asso

225 Secretion of macrophage migration inhibitory factor (MIF), a proinflammatory cytokine, fro

226 , circulating levels of macrophage migration inhibitory factor (MIF), a proinflammatory immunoregulat

227 One target of ITCs is macrophage migration inhibitory factor (MIF), a widely expressed protein with

228 tory mediators, such as macrophage migration inhibitory factor (MIF), also promote tumorigenesis.

229 rst to demonstrate that macrophage migration inhibitory factor (MIF), an immune system 'inflammatory'

230 The macrophage migration inhibitory factor (MIF), an inflammatory cytokine, is ov

231 Macrophage migration inhibitory factor (MIF), an innate cytokine encoded in a

232 We demonstrate that macrophage migration inhibitory factor (MIF), an innate immune mediator, is d

233 e role of the cytokine, macrophage migration inhibitory factor (MIF), and its receptor, CD74, was ass

234 eracts with its ligand, macrophage migration inhibitory factor (MIF), and thereby activates the PI3K/

235 de (LPS), soluble CD14, macrophage migration inhibitory factor (MIF), intestinal fatty acid-binding p

236 matory factors, such as macrophage migration inhibitory factor (MIF), its homolog D-dopachrome tautom

237 ulating factor (CSF)-1, macrophage migration inhibitory factor (MIF), monokine induced by interferon-

238 hemokine-like mediator, macrophage migration inhibitory factor (MIF), more strongly than dermal fibro

239 Macrophage migration inhibitory factor (MIF), originally identified as a proi

240 roinflammatory cytokine macrophage migration inhibitory factor (MIF), together with its clinical rele

241 ne ligand (CXCL) 12 and macrophage migration inhibitory factor (MIF), using Forster resonance energy

242 nd proteinases, such as macrophage migration inhibitory factor (MIF), VEGF, and matrix metalloprotein

243 cretion of the cytokine macrophage migration inhibitory factor (MIF), which results in a M2 shift of

244 be the multifunctional macrophage migration inhibitory factor (MIF), whose activities include an ATP

245 thologs of the cytokine macrophage migration inhibitory factor (MIF), whose functions in parasite gro

246 roinflammatory cytokine macrophage migration inhibitory factor (MIF).

247 tructural homology with macrophage migration inhibitory factor (MIF).

248 uring ocular infection, macrophage migration inhibitory factor (MIF).

249 g of the human cytokine macrophage migration inhibitory factor (MIF).

250 of the pro-M2 cytokine macrophage migration inhibitory factor (MIF).

251 alloproteinase [MMP]-9, macrophage migration inhibitory factor [MIF], MIP-1alpha, and MIP-2alpha) was

252 rase Gld2, deadenylase PARN, and translation inhibitory factor neuroguidin (Ngd) as components of a d

253 Here, we determined that neonatal NET-inhibitory factor (nNIF) is an inhibitor of NET formatio

254 We also tested the ability of neonatal NET-inhibitory factor (nNIF) to block NET formation induced

255 However, claudin14 (Cldn14), an inhibitory factor of the paracellular Ca(2+) transport i

256 ling in turn triggered the secretion of some inhibitory factor (or factors) from DCs that inhibited t

257 in standard conditions (serum plus leukemia inhibitory factor) or ground-state conditions, implying

258 onservation of parasite macrophage migration inhibitory factor orthologs.

259 sion and secretion of the osteoclastogenesis inhibitory factor osteoprotegerin enabled early growth o

260 f Plasmodium falciparum macrophage migration inhibitory factor (PfMIF) with nanomolar Ki's, analyze t

261 of the human cytokine, macrophage migratory inhibitory factor (PfMIF), is produced by the parasite d

262 oinflammatory cytokines, including migration inhibitory factor, plasminogen activator inhibitor-1, an

263 more, MNP-based nanosystems are resistant to inhibitory factors present in body fluids and effectivel

264 Macrophage migration inhibitory factor protects from nonmelanoma epidermal tu

265 g heterodimers of gp130 with either leukemia inhibitory factor receptor (LIFR) (type I) or oncostatin

266 nd clinical validation, we identify leukemia inhibitory factor receptor (LIFR) as a breast cancer met

267 ermal growth factor receptor (EGFR)-leukemia inhibitory factor receptor (LIFR) signaling induced SUCL

268 ion by OSM depends on both types I [leukemia inhibitory factor receptor (LIFR)] and II [OSM receptor

269 early on by their downregulation of leukemia inhibitory factor receptor and was promoted by cell-intr

270 ffect by directly targeting p63 and leukemia inhibitory factor receptor in RMS cells, which promotes

271 cytokines and express the LIFRbeta (leukemia inhibitory factor receptor) chain on their surface.

272 iponectin, lumican, plasminogen and leukemia inhibitory factor receptor.

273 ocyte colony-stimulating factor and leukemia inhibitory factor receptors, which are normally down-reg

274 ia-encoded orthologs of macrophage migration inhibitory factor regulate host immunity to promote para

275 Macrophage migration inhibitory factor regulates innate gammadelta T-cell res

276 apoL-1, apoM, alpha-1 antitrypsin, migration inhibitory factor-related protein 8, lysosome C, prenylc

277 Little is known about the nature of the inhibitory factors released by this fungus.

278 after spinal cord injury (SCI) and are major inhibitory factors restricting the growth of fibers afte

279 They are dependent on leukemia inhibitory factor signaling for maintenance of pluripote

280 loss of CDKN2B impairs the expression of the inhibitory factor, SMAD-7, which promotes downstream TGF

281 al species, whereas the macrophage migration inhibitory factor subgroup has wide eukaryotic represent

282 s lose their pro-regenerative properties and inhibitory factors such as CSPGs accumulate in the dener

283 were accompanied by induction of key growth-inhibitory factors such as p21 and Gadd45a and reduced e

284 and called TRACHEARY ELEMENT DIFFERENTIATION INHIBITORY FACTOR (TDIF) and its cognate receptor, PHLOE

285 involving Tracheary Element Differentiation Inhibitory Factor (TDIF) and Receptor TDR/PXY (Phloem in

286 timing is controlled by a maternally loaded inhibitory factor that is titrated against the exponenti

287 of ovarian cancer-associated ascites, as an inhibitory factor that prevents innate immune activation

288 Surgery promotes inhibitory factors that allow lingering immunosuppressiv

289 Although this suppression is mediated by inhibitory factors, the mechanisms by which virus-specif

290 subsequent proteomic analysis indicated the inhibitory factor to be the heat shock protein DnaK.

291 ead to reduced gene expression by recruiting inhibitory factors to specific gene promoters following

292 a protein, T. vaginalis macrophage migration inhibitory factor (TvMIF), that is 47% similar to human

293 ochondrial proteolipid, macrophage migration inhibitory factor, ubiquitin, beta-thymosin 4, and calmo

294 amental role of fibroblast-secreted leukemia inhibitory factor was assessed by using small interferin

295 th Transwell co-culture, suggesting that the inhibitory factor was labile.

296 iprocal expression of biofilm-promoting and -inhibitory factors were observed in clinical isolates.

297 Fungal inhibitory factors were resistant to heat, acid, and pro

298 d in lesional skin, along with decreased WNT inhibitory factor (WIF)-1 immunostaining.

299 f effector T cells is critical in overcoming inhibitory factors within the tumor microenvironment and

300 stinct roles (activator, cooperative factor, inhibitory factor) within a transcriptional complex, thu