ライフサイエンスコーパス: inducible protein

1 ylation, suggesting that MLCK is a TNF-alpha-inducible protein.

2 and is modulated (suppressed) by early song-inducible proteins.

3 yanobacterial homologs designated high-light-inducible proteins.

4 t on the role of hexamethylene-bis-acetamide-inducible protein 1 (HEXIM1) as an inhibitor of metastas

5 nscription factor hexamethylene bisacetamide-inducible protein 1 (HEXIM1) in mice leads to abnormalit

6 ly reported that hexamethylene bis-acetamide-inducible protein 1 (HEXIM1) inhibits ERalpha activity b

7 sly reported that hexamethylene bisacetamide inducible protein 1 (HEXIM1) inhibits the activity of li

8 scription factor Hexamethylene-bis-acetamide-inducible protein 1 (HEXIM1) is a tumor suppressor and c

9 Hexamethylene bisacetamide-inducible protein 1 (HEXIM1) is best known as the inhibi

10 nuclear RNA, and hexamethylene bisacetamide-inducible protein 1 (Hexim1).

11 c antioxidant (TSA), Leishmania major stress-inducible protein 1 (LmSTI1), and Leishmania elongation

12 cGMP-AMP synthase, ritinoic acid-inducible protein 1 (RIG-I)-like receptors, and Toll-lik

13 at the TPR domain-containing Hop-like stress-inducible protein 1 (Sti1p) cochaperone selectively inhi

14 r, the authors find that the Hop-like stress-inducible protein 1 (Sti1p) cochaperone selectively inhi

15 ressing the NKG2D ligand retinoic acid early-inducible protein 1-gamma (RAE-1gamma) dramatically enha

16 rom latently infected cells, via a CDK9/HMBA inducible protein-1 dependent process.

17 e transcription elongation factor b and HMBA inducible protein-1.

18 STAT)-1 activation triggers interferon (IFN)-inducible protein 10 (CXCL-10), one of major products of

19 IL-17, IL-4, IFN-gamma, and IFN-gamma-inducible protein 10 (CXCL10 or IP-10) remained statisti

20 tant protein 1 (MCP-1), and gamma interferon-inducible protein 10 (gammaIP-10) mRNA transcription in

21 ntly stimulated gene expression of IFN-gamma-inducible protein 10 (gammaIP-10), MHC class II beta-cha

22 eta (CCL-4), lymphotactin (XCL-1), IFN-gamma-inducible protein 10 (IP-10) (CXCL-10), MCP-1 (CCL-2), a

23 xamined the roles of CXCL10/gamma interferon-inducible protein 10 (IP-10) and CCL2/monocyte chemoattr

24 gamma interferon (IFN-gamma), and IFN-gamma-inducible protein 10 (IP-10) from the arrays for further

25 0.75 mg/kg CPG 10101, interferon (IFN)-gamma-inducible protein 10 (IP-10) had a mean increase over ba

26 e show that induction of IL28B and IFN-gamma-inducible protein 10 (IP-10) mRNA relies on TT/-G, but n

27 d measures of CD3epsilon mRNA and interferon-inducible protein 10 (IP-10) mRNA, and 18S rRNA discrimi

28 n IL28B and serum levels of interferon gamma inducible protein 10 (IP-10) predict outcomes of antivir

29 timulation (P = .037), and reduced IFN-gamma-inducible protein 10 (IP-10) response to TLR2 stimulatio

30 In addition, interferon-inducible protein 10 (IP-10) was identified as playing a

31 Nasal and serum IFN-inducible protein 10 (IP-10) were measured after doses 1

32 Plasma levels of interferon-gamma-inducible protein 10 (IP-10) were quantified by enzyme-l

33 hesion molecule 1 (ICAM-1), interferon-gamma-inducible protein 10 (IP-10), and the signaling intermed

34 duced beta interferon (IFN-beta), interferon-inducible protein 10 (IP-10), chemokine ligand 5 (CCL-5)

35 t measured serial plasma levels of IFN-gamma-inducible protein 10 (IP-10), monocyte chemoattractant p

36 ecretion of interleukin 8 (IL-8), interferon-inducible protein 10 (IP-10), monocyte chemotactic prote

37 a, hepatocyte growth factor (HGF), IFN-gamma-inducible protein 10 (IP-10), monokine induced by IFN-ga

38 (IFN-beta), interleukin 6 (IL-6), interferon-inducible protein 10 (IP-10), RANTES, and IL-1beta.

39 ransferred Tc1 via induction of an IFN-gamma-inducible protein 10 (IP-10).

40 MRP8/MRP14 expressed the chemokine IFN-gamma inducible protein 10 (IP-10)/CXCL10.

41 significantly increased levels of IFN-gamma-inducible protein 10 (IP-10/CXCL), IL-8, and MCP-1, all

42 erferon (IFN-gamma; Mig/CXCL9) and IFN-gamma-inducible protein 10 (IP-10/CXCL10) in liver leukocytes

43 els of the IFN-inducible chemokines IFNgamma-inducible protein 10 (IP-10/CXCL10), IFN-inducible T cel

44 ted chemokines, interferon-gamma (IFN-gamma)-inducible protein 10 (IP-10/CXCL10), monokine induced by

45 Serum interferon gamma inducible protein 10 (IP10; CXCL10) and endothelin 1 wer

46 wth factor (P = 0.032), and interferon-gamma inducible protein 10 (P = 0.010).

47 hat lack the ELR motif, including interferon-inducible protein 10 [IP-10 (CXCL10)] and monokine induc

48 ma [Mig]) and CXCL10 (interferon [IFN] gamma-inducible protein 10 [IP-10]) have been associated with

49 C chemokines (particularly CXCL10/interferon-inducible protein 10 and CXCL8/interleukin-8) were found

50 urthermore, vasopressin decreased interferon-inducible protein 10 and granulocyte colony-stimulating

51 struct repressed the iNOS, COX-2, interferon-inducible protein 10 and interferon-gamma mRNA levels in

52 sL interaction reduces the expression of IFN-inducible protein 10 and monokine induced by IFN-gamma a

53 as accompanied by a dramatic increase in IFN-inducible protein 10 and monokine induced by IFN-gamma p

54 d secretion of IL-1beta, IL-6, and IFN-gamma-inducible protein 10 but had no significant effects on I

55 IFN-gamma and clones that produce IFN-gamma-inducible protein 10 but not Mig.

56 uced by IFN-gamma (Mig) and CXCL10/IFN-gamma-inducible protein 10 following stimulation with IFN-gamm

57 factor, interleukin-6, and interferon-gamma-inducible protein 10 in human RA synovial membrane cultu

58 chemokines CCL5/RANTES and CXCL10/interferon-inducible protein 10 in vitro.

59 ression of CCL5/RANTES and CXCL10/interferon-inducible protein 10 in vivo.

60 Interferon gamma-inducible protein 10 may be an important chemokine that

61 cting IL-2, IL-12, IFN-gamma, and interferon-inducible protein 10 production in CD3/CD28-stimulated h

62 on of IL-12, IFN-gamma, MIP-2, and IFN-gamma-inducible protein 10 than males.

63 served, with alpha interferon and interferon-inducible protein 10 undergoing significant elevations f

64 gamma-inducible chemokines MIG and IFN-gamma-inducible protein 10 were decreased in irradiated tumors

65 nds (CXCLs), such as IP-10 (interferon [IFN]-inducible protein 10) (CXCL10), I-TAC (IFN-inducible T-c

66 ivation, resulting in high IP-10 (interferon-inducible protein 10), tumor necrosis factor alpha, and

67 (iNOS), cyclooxygenase-2 (COX-2), interferon-inducible protein 10, and interferon-gamma in response t

68 1, interleukin-12p40, interferon (IFN)-gamma-inducible protein 10, and macrophage inflammatory protei

69 elevated interleukin (IL) 12p40, interferon-inducible protein 10, and monocyte chemoattractant prote

70 coding for the chemokines RANTES, IFN-gamma-inducible protein 10, and monocyte chemoattractant prote

71 regulation of the chemokine 10-kDa IFN-gamma-inducible protein 10, and preferential upregulation of 2

72 as IL-12, IFN-gamma, IL-8, MCP-1, IFN-gamma-inducible protein 10, and RANTES, and altered expression

73 Both types of compounds induced IFN-gamma-inducible protein 10, but only the 7-deazaguanosine-cont

74 lony-stimulating factor, eotaxin, interferon-inducible protein 10, cytokine-induced neutrophil chemoa

75 ukin 1 receptor antagonist, interferon gamma-inducible protein 10, hepatocyte growth factor, soluble

76 n associated with increased interferon-gamma-inducible protein 10, interleukin (IL)-6, IL-8, vascular

77 y cytokines (interleukin 6, interferon gamma-inducible protein 10, interleukin 18, and tumor necrosis

78 anced levels of gamma interferon (IFN-gamma)-inducible protein 10, interleukin-12 (IL-12), IFN-gamma,

79 CXCL10, or IFN-gamma-inducible protein 10, is a biomarker associated with inc

80 d elevated levels of IL-8, RANTES, IFN-gamma inducible protein 10, monokine induced by IFN-gamma, and

81 se, inducing IFN-gamma, IL-12, and IFN-gamma-inducible protein 10, whereas the type 2 cytokines IL-4,

82 d high levels of interferon-gamma (IFNgamma)-inducible protein 10.

83 encoding tumor necrosis factor and IFN-gamma-inducible protein 10.

84 survival cytokines, such as interferon-gamma-inducible protein 10/CXC chemokine ligand 10, interleuki

85 hemokine CXC ligand (CXCL) 1, and interferon inducible protein 10/CXCL10.

86 egulatory factor 7, CXCL10 [gamma interferon-inducible protein 10], gamma interferon, and lambda inte

87 n, we show that serum interferon (IFN)-gamma inducible-protein 10, interleukin (IL)-12p40, and IL-18

88 that the expression of both IFN-beta and IFN-inducible protein-10 (CXCL-10) is significantly up-regul

89 The observed decreases in IL-8, IFN-gamma-inducible protein-10 (CXCL10), and MIP-3alpha (CCL20) mR

90 in their serum IL-12, interferon-gamma, and inducible protein-10 (IP-10) after the first dose, and i

91 -) mice have higher lung levels of IFN-gamma-inducible protein-10 (IP-10) and MIP-1alpha.

92 ours demonstrated higher levels of IFN-gamma-inducible protein-10 (IP-10) and tumor necrosis factor-r

93 Systemic levels of interferon-gamma-inducible protein-10 (IP-10) are predictive of treatment

94 onse to the inflammatory chemokine IFN-gamma-inducible protein-10 (IP-10) in a process contingent upo

95 Quantitation of interferon-gamma-inducible protein-10 (IP-10) may also differentiate anti

96 reases in serum IL-12, interferon gamma, and inducible protein-10 (IP-10), and these remained increas

97 motactic protein 2 (MCP-2), interferon gamma inducible protein-10 (IP-10), interferon gamma (IFN-gamm

98 TNF receptor 1, interferon (IFN)-gamma, IFN-inducible protein-10 (IP-10), interleukin (IL)-6, and ti

99 IFN-gamma, interferon-inducible protein-10 (IP-10), tumor necrosis factor (TNF

100 interferon-gamma (MIG, CXCL9) and interferon inducible protein-10 (IP-10, CXCL10) during HSV infectio

101 ding IL-12 (p40), MIP-1alpha (CCL3), and IFN inducible protein-10 (IP-10, CXCL10) were also elevated.

102 Interferongamma inducible protein-10 (IP10 or CXCL10), a Th-1 affiliated

103 Serum levels of interferon-gamma-inducible protein-10 (IP10), monokine induced by interfe

104 ecrosis factor-alpha, IL-8, interferon-gamma inducible protein-10 [IP-10], monocyte chemoattractant p

105 rtant T cell-related genes, such as IFNgamma-inducible protein-10 and I-A(b), and lower plasma trigly

106 interleukin (IL)-10 (twofold) and decreased inducible protein-10 and IL-4 (threefold) in luminex.

107 IFN-gamma-inducible protein-10 and MCP-1 genes, also regulated by

108 nd interferon-gamma), chemokines (interferon-inducible protein-10 and monocyte chemoattractant protei

109 pinal cord injury, suggesting a key role for inducible protein-10 in driving systemic interleukin-10

110 chemotactic protein-1, and interferon-gamma inducible protein-10 in mouse T lymphocytes stimulated i

111 ammatory protein-1beta, and interferon-gamma-inducible protein-10 in PICF.

112 ctant protein (MCP)-1, MCP-2, and interferon-inducible protein-10 in the pancreas.

113 us T cells producing the chemokine IFN-gamma-inducible protein-10 in vivo.

114 nical ventilator versus patients with plasma inducible protein-10 level less than 730 pg/mL.

115 ord injury patients, individuals with plasma inducible protein-10 levels more than or equal to 730 pg

116 inal fluid levels of IFN-alpha and IFN-gamma-inducible protein-10 levels were elevated and strongly c

117 bosomal RNA, CD3epsilon mRNA, and interferon-inducible protein-10 mRNA outperformed the metabolite si

118 B p65 to the kappaB element of the IFN-gamma-inducible protein-10 promoter.

119 s (TNF, IL-1beta, IL-6, IL-10, and IFN-gamma-inducible protein-10), chemokines (IL-8), and intracellu

120 induced by IFN-gamma) and CXCL10 (IFN-gamma-inducible protein-10), were expressed after stimulation

121 re M. leprae exposure using IFN-gamma or IFN-inducible protein-10, and also shows that MCP-1, MIP-1be

122 chemoattractant protein-1, interferon-gamma-inducible protein-10, and cyclooxygenase-2 in a dose-dep

123 a, monocyte chemotactic protein-1, IFN-gamma inducible protein-10, and IFN-alpha/beta expression in t

124 okines including IFN-alpha, IL-6, TNF-alpha, inducible protein-10, and IL-12.

125 (IFN-gamma) and chemokines (IL-8, IFN-gamma-inducible protein-10, and MCP-1) were significantly redu

126 els of interleukin (IL)-1 beta , IFN- gamma -inducible protein-10, and RANTES (regulated on activatio

127 date proinflammatory genes, interferon-gamma-inducible protein-10, beta1- and beta2-integrins, cycloo

128 n of cytokine transcripts (RANTES, IFN-gamma-inducible protein-10, IL-1alpha, IL-1-beta, IL-1Ralpha,

129 y whereby the CD8+ T cell product, IFN-gamma-inducible protein-10, induces production of macrophage e

130 ta in patients compared with EC, whereas IFN-inducible protein-10, like IFN-gamma, differed between E

131 as well as IFN-beta, IRF5, IRF7, RANTES, IFN-inducible protein-10, MCP-1, and MIP1alpha gene expressi

132 day 4, had higher levels of MCP-1, IFN-gamma-inducible protein-10, MIP-1alpha, and MIP-1beta mRNA tra

133 agonist, IL-4, IL-6, IL-8, IL-10, interferon-inducible protein-10, monocyte chemoattractant protein-1

134 or, interleukin-6, interleukin-8, interferon-inducible protein-10, monocyte chemotactic protein-1, an

135 ncreased production of IL-6, IL-8, IFN-gamma-inducible protein-10, RANTES, and platelet-derived growt

136 ma, monokine induced by IFN-gamma, IFN-gamma-inducible protein-10, RANTES, and TGF-beta1 was also dem

137 inal cord injury interleukin-10 is driven by inducible protein-10, whereas monocyte chemotactic prote

138 growth factor, IL-13, IL-17, IL-1alpha, and inducible protein-10.

139 mmatory protein-1alpha, and interferon-gamma-inducible protein-10/CXCL10 and the cytokines interleuki

140 okines (monocyte chemotactic protein-1/CCL2, inducible protein-10/CXCL10, macrophage inflammatory pro

141 nes and chemokines, including TNF-alpha; IFN-inducible protein-10; interleukin-6; macrophage inflamma

142 type domain 1 (RC3H1), and tumor protein p53-inducible protein 11 (TP53I11) interacted with TRP32 as

143 Fibroblast growth factor-inducible protein 14 (Fn14), the cell surface receptor f

144 We have found that nuclear interferon (IFN)-inducible protein 16 (IFI16) acts as a restriction facto

145 00-kb region containing the interferon gamma-inducible protein 16 (IFI16) and absent in melanoma 2 (A

146 Interferon gamma-inducible protein 16 (IFI16) and cGMP-AMP synthase (cGAS

147 ry CD4 T cells, we identify interferon-gamma-inducible protein 16 (IFI16) as a host DNA sensor requir

148 thase (cGAS) and interferon gamma (IFNgamma)-inducible protein 16 (IFI16) as well as viral RNA recept

149 The DNA sensor IFN-inducible protein 16 (IFI16) colocalized with DNA and th

150 ttern recognition receptor, gamma interferon-inducible protein 16 (IFI16) colocalized with the KSHV g

151 Here we show that interferon-gamma inducible protein 16 (IFI16) cooperates with cGAS during

152 We found that the interferon inducible protein 16 (IFI16) DNA sensor, which is requir

153 The interferon gamma-inducible protein 16 (IFI16) has recently been linked to

154 IFN-gamma-inducible protein 16 (IFI16) is an immunological DNA sen

155 nducible gene I (RIG-I) and interferon gamma-inducible protein 16 (IFI16) were involved in the sensin

156 LRP3 and AIM2 proteins or nuclear interferon-inducible protein 16 (IFI16) with adaptor ASC protein (a

157 Interferon-inducible protein 16 (IFI16), bone morphogenetic protein

158 n the DNA structure and was dependent on IFN-inducible protein 16 (IFI16), which bound immunostimulat

159 n but not after overexpression of interferon-inducible protein 16 (IFI16).

160 h the elimination of STING and of interferon-inducible protein 16 (IFI16); (iii) a DeltaUL46 virus di

161 ng protein-1, and DDX41, as well as that IFN-inducible protein 16 is the intracellular receptor recog

162 endent interaction of Cy5-labeled interferon-inducible protein 16 with DNA and the sliding via one-di

163 (absent in melanoma 2) and IFI16 (interferon-inducible protein 16) have been identified as DNA recept

164 nt in myeloma 2) and IFI16 (gamma-interferon-inducible protein 16) inflammasomes.

165 IFI16 (interferon gamma-inducible protein 16) recognizes nuclear episomal herpes

166 various cytosolic DNA sensors, including IFN-inducible protein 16, leucine-rich repeat (in Flightless

167 as an integral mechanism by which human IFN-inducible protein-16 (IFI16) engages foreign DNA.

168 Recently we identified hypoxia-inducible protein 2 (HIG2)/hypoxia-inducible lipid dropl

169 Hypoxia-inducible protein 2 Hig2/Hilpda mediates neutral lipid a

170 se 1, interferon-alpha, and interferon-alpha-inducible protein 27 messenger RNAs of the interferon si

171 ecreased at later time points, and IFN-alpha-inducible protein 27 was not induced.

172 Gprc5a is known as retinoic acid-inducible protein 3, and its deficiency leads to impaire

173 accumulation of growth arrest and DNA damage-inducible protein 34 (GADD34), 78-kDa glucose-regulated

174 or ATF4 and the growth arrest and DNA damage-inducible protein 34 (GADD34/Ppp1r15a), a phosphatase 1

175 we recently identified the interferon (IFN)-inducible protein 35 (IFI35; also known as IFP35) as a f

176 ied a novel role for a cellular protein, IFN-inducible protein 35 (IFP35/IFI35), in negatively regula

177 CCL20/macrophage-inducible protein 3alpha was the most active mucin-induc

178 differential expression of CCL20/macrophage-inducible protein 3alpha, thymic stromal lymphopoietin,

179 e identify here growth arrest and DNA-damage-inducible protein 45 gamma (GADD45gamma) as a cold-induc

180 suggested that growth arrest and DNA damage-inducible protein 45beta (GADD45beta) prolonged the surv

181 Here, we show that interferon alpha-inducible protein 6 (IFI6) is necessary for NRASQ61K-ind

182 lu-Leu-Arg-negative CXC chemokine interferon-inducible protein 9 (IP-9; also known as CXCL11, I-TAC,

183 BPI-inducible protein A (BipA) is a member of the family of

184 osophila S2 cells stably transfected with an inducible protein A expression plasmid.

185 tors, along with elongation factor G and BPI-inducible protein A.

186 Heme oxygenase-1 (HO-1), a stress-inducible protein, also regulates IL-10 and TNF-alpha pr

187 ha- and IFN-regulated chemokines such as IFN-inducible protein and IFN-inducible T cell alpha chemoat

188 t of rontalizumab on expression of IRGs, IFN-inducible proteins, and autoantibodies.

189 ane fusion, suggesting that these interferon-inducible proteins are not involved in superinfection ex

190 Heat-shock proteins (HSPs) are abundant, inducible proteins best known for their ability to maint

191 ) generation and upregulation of the hypoxia-inducible protein BNIP3 result in mitochondrial permeabi

192 E2-inducible proteins c-Myc and E2Fs are required for optim

193 We have recently identified a type I IFN-inducible protein, CD169, as the HIV-1 attachment factor

194 ions were already in place for a majority of inducible protein-coding genes, even while the genes wer

195 expression by promoting the formation of an inducible protein complex consisting of APC and C/EBP be

196 mbda2/3, IRF7, RIG-I, MDA5, 10-kDa IFN-gamma-inducible protein/CXCL10, IL-8/CXCL8, and GM-CSF.

197 An Hlip protein, high light-inducible protein D (HliD) purified as a small complex w

198 of IL-10 was increased and that of IFN-gamma-inducible protein decreased by Alum cotreatment.

199 We engineered an inducible protein degradation system for use in Bacillus

200 nd that may provide a template for designing inducible protein-degradation systems.

201 We created a fluorescent light-inducible protein design in which Dronpa domains are fus

202 The Escherichia coli DNA damage-inducible protein DinG, a member of the superfamily 2 DN

203 press another CXCR3 ligand, CXCL10/IFN-gamma-inducible protein, does not compensate for the absent an

204 An inducible protein expression library, constructed from g

205 We demonstrate that inducible protein expression of key IFN-alpha-regulated

206 protein interaction studies, constitutive or inducible protein expression studies, gene knockdown by

207 ul for many experiments but do not allow for inducible protein expression under ambient growth condit

208 protein (CHOP)/growth arrest and DNA damage-inducible protein (GADD153) with nuclear translocation.

209 the stress, the growth arrest and DNA damage-inducible protein GADD34 associates with the broadly act

210 in DCs requires growth arrest and DNA-damage-inducible protein (Gadd45alpha).

211 ethyltransferase 1 (DNMT1) by the DNA damage inducible protein, GADD45alpha.

212 mma interferon [IFN-gamma] and the IFN-gamma-inducible protein [gamma-IP]).

213 ion of the chemokine IP-10 (interferon-gamma-inducible protein) has been documented in several inflam

214 eine-inducible, endoplasmic reticulum stress-inducible protein (HERP), and calnexin.

215 ncoding photosystem II D1 (psbA), high-light inducible protein (hli), transaldolase (talC) and ribonu

216 e complex comprising ChlG and the high-light-inducible protein HliD, which associates with the Ycf39

217 ong strains, as did the number of high light inducible protein (Hlip) and DNA photolyase genes in the

218 0399 gene, and two members of the high-light-inducible protein (Hlip) family, HliC and HliD, which ar

219 ria possess a family of one-helix high light-inducible proteins (Hlips) that are homologous to light-

220 SP-16 proteins, a family of small heat shock-inducible proteins homologous to vertebrate alphaB cryst

221 yzed ligand recognition by the retinoic acid-inducible protein I (RIG-I) protein in biochemical assay

222 n (NOD)-like receptors (NLRs), retinoic acid-inducible protein I (RIG-I)-like receptors (RLRs), doubl

223 Toll-like receptor (TLR) 3 and retinoic acid-inducible protein I.

224 ng protein 1) was among the first interferon-inducible proteins identified, its function is still lar

225 , such as absent in melanoma-2 and IFN-gamma-inducible protein (IFI)16, bind dsDNA and form caspase-1

226 We establish that the interferon-inducible protein IFI16 acts as a nuclear DNA sensor fol

227 IFN-inducible protein IFI16 has emerged as a critical sensor

228 The interferon-inducible protein IFI16 was shown to bind nuclear viral

229 We hypothesized that inducible proteins impair the ability of factor H to loc

230 ator of G-protein signaling 3 (AGS3), an LPS-inducible protein in macrophages, affects both lysosomal

231 d2 phosphorylation and expression of TGFbeta-inducible proteins in cell culture.

232 Here we describe genetically encoded light-inducible protein-interaction modules based on Arabidops

233 at regulates production of Type 1 interferon-inducible proteins (interferon gamma-induced protein-10,

234 , interferon regulatory factor-1, interferon-inducible proteins (interferon gamma-induced protein-10,

235 (mRNA) expression (P<0.01) and sixfold more inducible protein (IP)-10 chemokine (CCL10) mRNA express

236 interferon (MIG)-gamma, and interferon-gamma-inducible protein (IP)-10 in the corneal epithelia and c

237 compared with Fil(-), whereas levels of IFN-inducible protein (IP)-10 were lower in Fil(+) (GM, 66.3

238 ors, and the CXC and CC chemokines IFN-gamma inducible protein (IP)-10, growth-related oncogene (GRO)

239 nalysis for IFN-gamma, IL-10, and interferon-inducible protein (IP)-10.

240 IL-2/interferon-gamma, and interferon-gamma-inducible protein (IP)-10/monocyte chemotactic protein-1

241 chemoattractant protein-1, interferon-gamma-inducible protein (IP-10), and macrophage inflammatory p

242 Here, we showed that the interferon-inducible protein IRGB10 is essential for activation of

243 , Man et al. (2016) show that the interferon-inducible protein IRGB10 liberates bacterial ligands for

244 The IFN-inducible protein Irgm1 (LRG-47) belongs to the family o

245 how that Cyclon, a newly identified cytokine-inducible protein, is induced in T cells on T-cell recep

246 t the induction of key IFNalpha- or IFNgamma-inducible proteins (ISG15 (interferon-stimulated gene 15

247 To test the hypothesis that JA-inducible proteins (JIPs) thwart attack by disrupting di

248 kt-related kinase, serum- and glucocorticoid-inducible protein kinase (SGK).

249 Expression of an inducible protein kinase Calpha (PKCalpha) translocation

250 Interferon inducible protein kinase PKR is an essential component o

251 n by SCF(beta-TRCP) depended on the activity-inducible protein kinase Polo-like kinase 2 (Plk2).

252 periencing heightened activity, the activity-inducible protein kinase Polo-like kinase 2 (Plk2, also

253 e gamma(1)34.5 gene function: evasion of IFN-inducible protein kinase R, allowing late viral protein

254 WNK1 activates the serum- and glucocorticoid-inducible protein kinase SGK1, leading to activation of

255 es the UPR in cardiac myocytes and that XBP1-inducible proteins may contribute to protecting the myoc

256 Here, we determined that ER stress inducible protein Mesencephalic Astrocyte-derived Neurot

257 ted in our genetic screening, two cold shock-inducible proteins, namely, CspA, an RNA chaperone, and

258 , interleukin (IL)-6, IL-8, interferon-gamma-inducible protein of 10 kDa (IP-10), monocyte chemoattra

259 e T cell chemoattractant chemokine IFN-gamma-inducible protein of 10 kDa (IP-10).

260 The chemokine interferon (IFN)-gamma-inducible protein of 10 kDa (IP-10; CXCL10) has been imp

261 The chemokine IFN-gamma-inducible protein of 10 kDa (IP-10; CXCL10) plays an imp

262 The chemokines CXCL10/interferon-gamma-inducible protein of 10 kDa, CCL3/macrophage inflammator

263 endothelial growth factor, interferon gamma-inducible protein of 10 kDa, monocyte chemoattractant pr

264 Ro52 is an IFN-inducible protein of the tripartite motif (TRIM) family

265 was no apparent decline in the levels of IFN-inducible proteins or levels of anti-double-stranded DNA

266 uals, here we show that rare PTVs in the p53-inducible protein phosphatase PPM1D are associated with

267 ex known as the PIDDosome comprising the p53-inducible protein PIDD, the adapter protein RAIDD and ca

268 The discovery of light-inducible protein-protein interactions has allowed for t

269 ns of photosystems I and II, the early-light-inducible proteins, PsbS involved in nonphotochemical qu

270 factors (ARF) and auxin/indole 3-acetic acid inducible proteins regulate transcriptional events modul

271 The stress-inducible protein Sestrin2 (Sesn2) plays an important ro

272 A novel stress-inducible protein, Sestrin2 (Sesn2), declines in the hea

273 regulating H2A.Z deposition using a steroid-inducible protein splicing strategy, we show that NFR es

274 midine, is activated by dimerization with an inducible protein termed prozyme.

275 We report that a localized inducible protein tether between the chromosome and cell

276 c protein 6, transforming growth factor beta-inducible protein (Tgfbi or betaig-h3), and periostin] s

277 t in melanoma gene-2 (AIM2) is an interferon-inducible protein that can form an alternative inflammas

278 LIGHT (lymphotoxin-like inducible protein that competes with glycoprotein D for

279 p204, an interferon-inducible protein that interacts with both Cbfa1 and Id2

280 Viperin is an interferon-inducible protein that is directly induced in cells by h

281 clude that Mfn2 but not Mfn1 is an ER stress-inducible protein that is required for the proper tempor

282 in is an evolutionarily conserved interferon-inducible protein that localizes to the endoplasmic reti

283 HIF-1alpha is a hypoxia-inducible protein that regulates many cell and molecular

284 a glycosylphosphatidylinositol-anchored, IFN-inducible protein that regulates T lymphocytes prolifera

285 BST-2/tetherin is an interferon-inducible protein that restricts the release of envelope

286 o proteins identified were several jasmonate-inducible proteins that have a known or proposed role in

287 m target of ATM-p53 signaling - TIGAR, a p53-inducible protein, the activation of which can regulate

288 The p53-inducible protein TIGAR (Tp53-induced Glycolysis and Apo

289 ctor GDF15, ferrodoxin reductase (FDXR), p53-inducible protein TP53I3, transcription factor ATF3, DNA

290 This approach for inducible protein translation can be used for complement

291 We show that the DNA damage-inducible proteins UmuD(2) and RecA act in concert to mo

292 l increase in the levels of the neurotrophin-inducible protein VGF (nonacronymic), a putative neurope

293 Selected IFNalpha/beta-inducible proteins were analyzed by immunohistochemistry

294 SFTSV and antiviral interferon (IFN) and IFN-inducible proteins were induced upon infection.

295 p-regulation of key IFN-alpha- and IFN-gamma-inducible proteins, which have important functional cons

296 ll cycle arrest-related genes, including p53-inducible protein with a death domain (Pidd).

297 dsRNA-dependent kinase PKR is an interferon-inducible protein with ability to phosphorylate the alph

298 e-inducible ER stress protein), an ER stress-inducible protein with an ubiquitin-like (UBL) domain, a

299 Moreover, interferon-inducible protein with tetratricopeptide repeats 1, cyst

300 eptide repeats 1, cystatin 1, and interferon-inducible protein with tetratricopeptide repeats 3 were