ライフサイエンスコーパス: early response gene

1 vascular endothelial cells, verge (vascular early response gene).

2 ssociated with increased expression of c-jun early response gene.

3 , the protein product of c-fos, an immediate early response gene.

4 alpha I.1 gene is expressed as an immediate early response gene.

5 CR6, originally cloned as an IL-2 immediate-early response gene.

6 s correlated with induction of the immediate-early response genes.

7 ic hierarchy that begins with a small set of early response genes.

8 owth factor induced BiP and GRP94 as delayed-early response genes.

9 ulation of certain transcription factors and early response genes.

10 potential through modulating the activity of early response genes.

11 through the induction of a set of immediate-early response genes.

12 tor substrate-2, and STAT3 and expression of early response genes.

13 ns, which are critical for the expression of early response genes.

14 c agents and belongs to a class of "delayed" early response genes.

15 e-specific genes but not SRF/MRTFA-dependent early response genes.

16 ers of smooth muscle-specific genes, but not early response genes.

17 F3 and other undefined signaling partners to early response genes.

18 ls, and induced expression of many immediate-early response genes.

19 with the attenuated expression of immediate-early response genes.

20 increase in the mRNA of the c-myc and egr-1 early-response genes.

21 ms involved with auxin regulation of primary/early-response genes.

22 egradation of the stress-inducible immediate-early response gene 1 and other up-regulated mRNAs are a

23 TR3, an immediate-early response gene and an orphan member of the steroid-

24 so known as NGFI-B or nur77, is an immediate-early response gene and an orphan member of the steroid/

25 of TR3 (mouse homologue Nur77), an immediate-early response gene and orphan nuclear receptor transcri

26 the nucleus is associated with activation of early response genes and transcription factors, laser sc

27 e in its ability to induce the expression of early response genes as well as induce resistance to vir

28 revealed within 15 min, including immediate-early response genes as well as those specific to iron a

29 Transcripts encoding early response genes associated with the JA pathway were

30 rare, highly labile RNA species that display early response gene behavior in human neural (HN) cells

31 nhibits activation of IFN-alpha/B-stimulated early response genes but by a mechanism which does not i

32 tion, indicating positive regulation of this early response gene by Akt.

33 th factors induce transcription of immediate early response genes by activating members of the Signal

34 Auxin may regulate transcription on early response genes by influencing the types of interac

35 ed for maximal transcriptional activation of early response genes by interferon gamma (IFNgamma) as w

36 Activation of early response genes by interferons (IFNs) and other cyt

37 Activation of early response genes by interferons (IFNs) requires tyro

38 Interferons (IFNs) induce early response genes by stimulating Janus family (Jak) t

39 rsion to JA-Ile, activates the expression of early response genes by the SCF(COI1)/JAZ pathway.

40 uated the variation in the expression of the early response gene c-fos as a distal effect of EGFR inh

41 Comparison with the immediate early response gene c-fos demonstrated that the increase

42 H2O2 also induced expression of the early response gene c-FOS, and G1- to S-phase transition

43 One target for this inhibition is the early response gene c-fos.

44 ell growth and transformation, including the early response gene c-fos.

45 stimulate growth-promoting pathways and the early response gene c-fos.

46 associated with increased expression of the early response gene c-jun.

47 etics of necl-5 expression and the immediate-early response gene c-myc.

48 xpressing cells induced transcription of the early response genes c-fos and c-jun, indicating that th

49 Deformation rapidly induced the immediate early response genes c-fos and c-jun.

50 pocalin, and doses>/=0.005 mg/kg induced the early response genes c-fos and junb.

51 of TrkA protein, increased expression of the early response genes c-fos and NGF1-A, and activation of

52 a significant up-regulation of mRNA for the early response genes c-jun and c-fos on HMC.

53 of ERK1/2 and JNK and the expression of the early response genes c-jun, c-fos, ATF3 and egr-1 induce

54 als an increase in transcription of both the early response gene, c-fos, and the late response gene,

55 The early response genes, c-Fos and c-Jun, are induced by en

56 ated region AREs including a large number of early response gene cDNAs.

57 s accompanied by the selective expression of early response genes coding for transcription factors.

58 ranscriptional activation of several hundred early response genes common to both glucose and insulin

59 We detected 220 early response genes (day 14 posttreatment) that were do

60 induced, thus implicating Bcl-x as a delayed early response gene during liver regeneration.

61 TNFalpha is an early response gene during the initiation of inflammatio

62 Expression of early response genes during rod outer segment phagocytos

63 This finding provides a parallel to early response genes (e.g. c-FOS and EGR1) that affect m

64 wn to involve the induction of the immediate-early response gene, early growth response factor-1 (EGR

65 response to serum is mediated in part by the early response gene Egr-1 and as such provides a signali

66 sed expression of the protein product of the early response gene egr-1, enhanced activation of Jun N-

67 along genes including the mitogen-inducible early response gene EGR-1.

68 GR2 and was first identified as an immediate-early response gene, encoding a protein that binds DNA i

69 involved in the stability and translation of early response gene (ERG) transcripts and are expressed

70 gene is a growth factor-regulated, immediate-early response gene expressed in a developmental stage-

71 scription factors implicated in cytokine and early response gene expression in activated lymphocytes.

72 e, IL-10 can directly inhibit STAT-dependent early response gene expression induced by both IFNalpha

73 striking contrast, Rc-imposed repression of early response gene expression remains quantitatively st

74 oth IL-4 and IGF-I were able to induce c-myc early response gene expression, and this expression was

75 a dominant role in P. gingivalis LPS-induced early response gene expression, suggesting that IKK/NF-k

76 ant negative effect on IFNalpha/beta-induced early response gene expression.

77 opo IIbeta attenuates both DSB formation and early-response gene expression following neuronal stimul

78 rapidly resolves topological constraints to early-response gene expression in neurons.

79 ith induction of protein kinase activity and early-response gene expression.

80 emonstrate that the B2 receptor is a delayed early response gene for PDGF in vascular smooth muscle c

81 recently has been identified as an immediate-early response gene for transforming growth factor beta

82 These data suggest that the delayed early response gene HNP36 is a truncated form of ENT2 an

83 enhanced ALK3-mediated up-regulation of the early response gene ID-1.

84 We also show that a number of immediate early response genes (IEGs) are responsible for orchestr

85 the biomechanical induction of the immediate early response gene iex-1 in vascular smooth muscle cell

86 NA encoded by the stress-inducible immediate early response gene IEX-1 was up-regulated immediately a

87 e (RAI3), the radiation-inducible, immediate-early response gene (IEX1), and the stress-induced phosp

88 can be divided into two groups: an immediate-early response gene (IFNalpha4) which is induced rapidly

89 well-characterized auxin and brassinosteroid early response gene in Arabidopsis (Arabidopsis thaliana

90 tumor necrosis factor alpha (TNF)-inducible early response gene in human umbilical vein endothelial

91 ls leads to transcriptional activation of an early response gene in insulinoma cell lines and in rat

92 ssion of TIEG is regulated by TGFbeta1 as an early response gene in pancreatic epithelial cell lines.

93 trogen treatment, indicating that these were early response genes in the ER-regulated pathway.

94 The transcription factor spalt4 is a key early-response gene in otic placode induction.

95 Differential expression of IFN early-response genes in Pr4 Delta 35 relative to Pr4 was

96 and SMAD8 and upregulation of BMP downstream early-response genes in tumor cells.

97 -specific genes, but not actin/Rho-dependent early response genes, in fibroblasts.

98 ant in regulation of expression of immediate-early response genes, in particular those involved in st

99 ossibility that p300 may negatively regulate early response genes, including c-MYC and c-JUN, thereby

100 A group of early response genes, including those encoding transcrip

101 reaks (DSBs) in the promoters of a subset of early-response genes, including Fos, Npas4, and Egr1.

102 blished or predicted functional roles of the early response genes indicates that genes encoding trans

103 We identified GADD45beta as a prominent early response gene induced by bone morphogenetic protei

104 scription factor Nr4a1 (Nur77), an immediate-early response gene induced by TCR engagement.

105 genase-2 (COX-2) is produced by an immediate early response gene induced in most cells by a variety o

106 Cyclooxygenase-2 (COX-2) is an early response gene induced in renal mesangial cells by

107 factor-alpha (TNF-alpha) gene is one of the early response genes induced by phorbol 12-myristate 13-

108 eviously identified protein, B12, one of the early response genes induced by tumor necrosis factor al

109 The inclusion of PGHS-2 among the early response genes induced in leukocytes may be releva

110 fication strategy using biases for immediate-early-response genes induced by 1,25(OH)2D3 in the myelo

111 mda-5 is an early response gene inducible by IFN and tumor necrosis

112 Interferon (IFN) induction of immediate-early response genes is mediated through the signal tran

113 them, the FGF-inducible 14 (Fn14) immediate-early response gene, is predicted to encode a novel, cel

114 genes are a subset of interferon-stimulated early response genes (ISGs) that are also induced direct

115 e genes are c-fos and nur77, two of the five early-response genes known to be induced in the SCN by l

116 A second subset of PIF-dependent, early response genes, lacking G-box motifs, are enriched

117 We report that taxol induces numerous early-response genes, not just cytokine genes.

118 ponse characteristics of two closely related early response genes, Nurr1 and Nur77.

119 We demonstrate that human eotaxin is an early response gene of cytokine-stimulated epithelial an

120 dentified as a growth factor-induced delayed early response gene of unknown function.

121 ofiles of genes responding to Rc within 1 h (early response genes) of initial exposure of dark-grown

122 ell responses to the growth factor-inducible early response gene product CCN1/Cyr61 overlap with thos

123 We conclude that IKLF encodes a delayed early response gene product that positively regulates ce

124 Polo-like kinase 3 (Plk3), an immediate early response gene product, plays an important role in

125 yr kinases have been identified as immediate early response gene products that are activated by radia

126 kappaB consensus oligonucleotide or when the early response gene prostaglandin H synthase-2 mRNA was

127 IEX-1, a recently discovered early response gene, regulates cell growth and apoptosis

128 of this subfamily have been characterized as early response genes regulating essential biological pro

129 Members of this subfamily function as early-response genes regulating key cellular processes,

130 The results demonstrate that early response genes related to NF-kappaB contribute to

131 actors, BEE1, BEE2, and BEE3, as products of early response genes required for full BR response.

132 ucine zipper containing type I IFN-inducible early response gene SARI (Suppressor of AP-1, Regulated

133 nt-8 to induce an ectopic axis or the dorsal early response genes siamois and Xnr3 is lost by the ons

134 Here we show that mouse embryos lacking the early-response gene SIL have axial midline defects, a bl

135 rs XVent2 and 3GC2, and up-regulation of the early response gene Smad6.

136 criptional activation of Mix.2, an immediate-early response gene specific to activin-like members of

137 established by its ability to display known early response genes, such as c- fos, using partially de

138 naling pathways and the induction of TGFbeta early response genes, such as the TGFbeta-inducible earl

139 inding domains in the promoters of immediate early response genes suggests that it may be characteris

140 Thus, the IFN-beta gene is an early response gene that is activated in response to L-P

141 reases the expression of Egr-1, an immediate-early response gene that is identified to be involved in

142 The plant hormone auxin activates many early response genes that are thought to be responsible

143 For prediction of early response, genes that correlated to marrow status o

144 t network of nuclear factor kappaB-dependent early-response genes that are activated by HAdv-FX compl

145 inant role in Rc-induced expression of these early response genes, that phyB has minimal detectable r

146 protein kinase C-dependent inductions of the early-response genes, the subsequent regulations of othe

147 ctivities by selectively activating distinct early response genes through different JAK-STAT signalin

148 esponse genes, such as the TGFbeta-inducible early response gene (TIEG) family of transcription facto

149 observations suggest that p170 is likely an early response gene to mimosine treatment and a mediator

150 Here we report the isolation of ERNI, an early response gene to signals from the organizer (Hense

151 ated upon NGF stimulation inducing immediate early response gene transcription (i.e. c-fos, Egr-1).

152 egative Stat5 induction on expression of IL3 early response genes was examined, and expression of sev

153 A total of 88 early response genes were found to be induced by P. ging

154 E(2)-induced changes in the expression of early-response genes were examined by real-time quantiti

155 p-regulation of mRNA for c-fos, an immediate early response gene, whereas Ab cross-linking of HLA cla

156 ivity can lead to expression of an immediate early response gene which encodes for a secreted protein

157 It is a key regulator of many cellular early response genes which are believed to be involved i

158 It is a key regulator of many cellular early response genes which are believed to be involved i

159 RhoB is an early-response gene whose expression is elevated by mult

160 We also demonstrate that c-Krox is an early response gene, whose expression is detectable as e

161 Immediate early response gene X-1 (IEX-1) is a stress-inducible ge

162 , we report an unexpected role for immediate early response gene X-1 (IEX-1), a downstream target of

163 Immediate-early response gene X-1 (IEX-1), protects T cells from a

164 d in the promoter region of IEX-1 (Immediate Early response gene X-1) gene that can either suppress o

165 IEX-1 (immediate early response gene X-1) is a stress-inducible gene.

166 NF-kappa B/rel target gene IEX-1 (Immediate Early response gene X-1) is highly expressed in T cells

167 zinc fingers and is encoded by the immediate-early response gene, Zfp-36.