ライフサイエンスコーパス: inducible protein

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

2 yanobacterial homologs designated high-light-inducible proteins.

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

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

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

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

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

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

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

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

11 x type E3 ubiquitin ligase, designated as P3-inducible protein 1 (P3IP1), which interacts with OsNRPD

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

21 0.75 mg/kg CPG 10101, interferon (IFN)-gamma-inducible protein 10 (IP-10) had a mean increase over ba

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

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

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

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

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

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

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

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

30 ing RANTES, eotaxin, interferon (IFN)-gamma- inducible protein 10 (IP-10), monocyte chemoattractant p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

52 d), RANTES (14.8-fold), and interferon gamma inducible protein 10 kDa (IP-10) (53-fold) and an increa

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

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

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

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

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

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

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

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

61 1, interleukin-12p40, interferon (IFN)-gamma-inducible protein 10, and macrophage inflammatory protei

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

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

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

65 In those with SVR, interferon-inducible protein 10, ATX, and Mac2BP levels declined by

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

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

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

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

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

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

72 Plasma HCV, soluble CD14 (sCD14), interferon-inducible protein 10, soluble CD163 (sCD163), interleuki

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

124 or 2 module expression and plasma interferon-inducible protein-10/CXCL10 negatively correlated with r

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

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

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

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

129 00-kb region containing the interferon gamma-inducible protein 16 (IFI16) and absent in melanoma 2 (A

130 hisms in inflammasome genes interferon gamma inducible protein 16 (IFI16) and absent in melanoma 2 (A

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

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

133 yclic GMP-AMP synthase (cGAS) and interferon-inducible protein 16 (IFI16) as the major DNA sensors in

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

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

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

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

138 mily member (PYHIN) protein interferon-gamma-inducible protein 16 (IFI16) detect DNA and signal via s

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

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

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

142 The interferon gamma-inducible protein 16 (IFI16) is known as immune sensor o

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

163 pharmacological inhibition of Gadd34 (damage-inducible protein 34) prolonged eukaryotic initiation fa

164 armacological inactivation of Gadd34 (damage-inducible protein 34), a subunit of the PP1 phosphatase

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

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

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

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

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

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

171 lambda 2 (IFN-lambda2) and interferon alpha-inducible protein 6 (IFI6) as genes providing high level

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

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

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

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

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

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

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

179 family of evolutionarily conserved exercise-inducible proteins, are critical mediators of exercise b

180 With an inducible protein assembly system, we further demonstrat

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

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

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

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

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

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

187 the p11/AnxA2/SMARCA3 heterohexamer, an SSRI-inducible protein complex.

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

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

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

191 was developed as a tool to achieve rapid and inducible protein degradation in nonplant systems.

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

193 Using inducible protein degradation, we show that PAR-6 and PK

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

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

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

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

198 between FeCh and a single-helix, high light-inducible protein early in the evolution of cyanobacteri

199 An inducible protein expression library, constructed from g

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

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

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

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

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

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

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

207 binding ability of cyanobacterial high-light-inducible proteins has been studied in detail.

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

209 s limited by the up-regulation of the stress-inducible protein heme-oxygenase-1.

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

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

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

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

214 0399 gene, and two members of the high-light-inducible protein (Hlip) family, HliC and HliD, which ar

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

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

217 lysis of pigment binding by plant high-light-inducible protein homologs, called ONE-HELIX PROTEINS (O

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

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

220 tiation-associated gene 5, and retinoic acid-inducible protein I in bronchial biopsy specimens from 1

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

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

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

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

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

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

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

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

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

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

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

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

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

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

235 HIV acquisition, including interferon-gamma inducible protein (IP)-10, macrophage inflammatory prote

236 (CRP), interleukin (IL)-6, interferon-gamma inducible protein (IP)-10, soluble CD14 (sCD14), soluble

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

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

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

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

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

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

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

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

245 Interferon inducible protein kinase PKR is an essential component o

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

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

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

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

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

251 covered that Cx43 interacts with the hypoxia-inducible protein N-Myc downstream-regulated gene 1 prot

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

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

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

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

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

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

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

259 o plant defence (e.g. a putative probenazole inducible protein), plant disease resistance as well as

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

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

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

263 Using degron tags for rapid inducible protein removal, we analyse how acute depletio

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

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

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

267 genetic approach for cell-type-specific drug-inducible protein synthesis inhibition that enables rapi

268 We use cell-type-specific drug-inducible protein synthesis inhibition to show that targ

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

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

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

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

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

274 c NIK, stabilized by LIGHT (lymphotoxin-like inducible protein that competes with glycoprotein D for

275 igen 6E (LY6E) is a GPI-anchored, interferon-inducible protein that has been shown to modulate viral

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

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

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

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

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

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

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

283 plore methods to achieve tight regulation of inducible proteins that are effective despite variation

284 pecific antibodies, the engineering of light-inducible proteins that can be used to recruit proteins

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

286 t shock proteins (Hsp) are a class of stress-inducible proteins that mainly act as molecular protein

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 This approach for inducible protein translation can be used for complement

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

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

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

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

294 Loss of this type-I-interferon-inducible protein, which we refer to as 'TLR adaptor int

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