ライフサイエンスコーパス: inhibitory factor

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

2 ceptor for the 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 reasing production of IFN-gamma and leukemia inhibitory factor.

6 to differentiation upon removal of leukemia inhibitory factor.

7 least in part, to decreased binding of this inhibitory factor.

8 diated infection or express an HVEM-specific inhibitory factor.

9 for fusion and cholesterol may relieve this inhibitory factor.

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

11 he pleiotropic cytokine macrophage migration inhibitory factor.

12 restricted at early postentry steps by host inhibitory factors.

13 ontribute to their ability to overcome these inhibitory factors.

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

15 egative sera a purified fraction enriched in inhibitory factors.

16 ulin resistance, suggesting the existence of inhibitory factors.

17 xtrinsic environment composed of a milieu of inhibitory factors.

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

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

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

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

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

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

24 similarities between beta-thymosins and the inhibitory factor 1 (IF1), an inhibitor of ATP synthase

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

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

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

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

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

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

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

32 JCI, Kansara and colleagues reveal that Wnt inhibitory factor 1 is epigenetically silenced in human

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

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

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

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

37 Wnt inhibitory factor-1 (WIF-1) has been identified as one o

38 study, we investigated the mechanism of Wnt inhibitory factor-1 (WIF-1) silencing.

39 d Frizzled-related proteins (sFRPs), and Wnt inhibitory factor-1 (WIF-1).

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

41 the Wnt antagonist and tumor suppressor Wnt inhibitory factor-1 decreased, as compared with fully de

42 Furthermore, BMP signaling stimulated Wnt inhibitory factor-1 expression and promoter activity in

43 ecrosis factor alpha), chemokine (macrophage inhibitory factor 1beta), or cytotoxic degranulation mar

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

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

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

47 tors, and inhibition of macrophage migration inhibitory factor and P-glycoprotein.

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

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

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

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

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

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

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

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

56 AC2) expression, raised macrophage migration inhibitory factor, and increased P-glycoprotein-mediated

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

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

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

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

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

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

63 s within the CNS is the presence of multiple inhibitory factors associated with myelin.

64 Macrophage migration inhibitory factor binding to CD74 induces its intramembr

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

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

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

68 eta), but did augment expression of the mito-inhibitory factors C/EBPalpha, p21(Waf1/Cip1), and p27(K

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

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

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

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

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

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

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

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

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

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

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

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

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

82 We provide direct evidence that levels of an inhibitory factor control the rate of liver regeneration

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

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

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

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

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

88 Macrophage migration inhibitory factor enhances Pseudomonas aeruginosa biofil

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

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

91 We found no evidence for the existence of an inhibitory factor for avian virus polymerase in human ce

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

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

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

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

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

97 Leukemia inhibitory factor has been utilized to maintain the symm

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

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

100 her leads to a dramatic induction of the E2A inhibitory factors, Id2 and Id3.

101 22, interleukin-3, and macrophage migration inhibitory factor improved the model significantly (P <

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

124 PROK1 induces expression of leukemia inhibitory factor (LIF) in endometrial epithelial cells

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

126 11 (IL-11), oncostatin M (OSM), and leukemia inhibitory factor (LIF) levels in patients with differen

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

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

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

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

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

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

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

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

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

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

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

138 rough transcriptional regulation of leukemia inhibitory factor (LIF), a cytokine crucial for blastocy

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

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

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

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

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

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

145 -11, IL-27, oncostatin M (OSM), and leukemia inhibitory factor (LIF), signal via the common GP130 cyt

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

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

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

149 Epiblast cells are refractory to leukaemia inhibitory factor (LIF)-STAT3 signalling, but they respo

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

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

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

153 i in combination with the cytokine leukaemia inhibitory factor (LIF).

154 at Thr308, in NRVMs stimulated with leukemia inhibitory factor (LIF).

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

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

157 h may occur in conjunction with the leukemia inhibitory factor (LIF)/Stat3 pathway.

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

159 Both cell types secreted leukemia inhibitory factor (Lif); however, whereas Stat3 activati

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

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

162 Mammalian macrophage migration inhibitory factor (MIF) (mMIF) is an immune mediator tha

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

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

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

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

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

168 Antibodies to macrophage inhibitory factor (MIF) attenuate macrophage Tie-2 expre

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

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

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

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

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

174 roinflammatory cytokine macrophage migration inhibitory factor (MIF) has been shown to be elevated in

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

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

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

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

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

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

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

182 Macrophage migration inhibitory factor (MIF) is a leaderless protein that is

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

184 Macrophage migration inhibitory factor (MIF) is a multifunctional cytokine th

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

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

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

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

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

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

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

192 Macrophage migration inhibitory factor (MIF) is a proinflammatory cytokine th

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

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

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

196 Macrophage migration inhibitory factor (MIF) is a proinflammatory mediator in

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

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

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

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

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

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

203 Macrophage migration inhibitory factor (MIF) is an upstream activator of the

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

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

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

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

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

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

210 innate immune mediator macrophage migration inhibitory factor (MIF) plays a critical role in the pat

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

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

213 Macrophage migration inhibitory factor (MIF) promotes cardiomyocyte survival

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

237 The cytokine, macrophage migration inhibitory factor (MIF), is encoded in a functionally po

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

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

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

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

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

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

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

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

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

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 roinflammatory protein, macrophage migration inhibitory factor (MIF).

251 erleukin-17 (IL-17) and macrophage migration inhibitory factor (MIF).

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

253 roinflammatory cytokine macrophage migration inhibitory factor (MIF).

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

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

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

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

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

259 onservation of parasite macrophage migration inhibitory factor orthologs.

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

261 ir former territories, suggesting that local inhibitory factors persist in these regions.

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

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

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

265 Macrophage migration inhibitory factor protects from nonmelanoma epidermal tu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

283 Surgery promotes inhibitory factors that allow lingering immunosuppressiv

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

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

286 Because Smad7, a known inhibitory factor to both Nodal and BMP signaling, was d

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

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

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

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

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

292 ttractant protein-1 and macrophage migration inhibitory factor was significantly attenuated in LPA2-/

293 s were lost, RNA polymerase II was lost, and inhibitory factors were bound to the promoter in a kinas

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

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

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

297 K/AKT1 signaling declines following leukemia inhibitory factor withdrawal, active GSK3beta accumulate

298 in mESCs resulted in abrogation of leukemia inhibitory factor withdrawal-induced differentiation, al

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