ライフサイエンスコーパス: bZIP transcription factor

1 The identities confirm sisA as an atypical bZIP transcription factor.

2 segmentation gene kreisler, which encodes a bZip transcription factor.

3 inase, which in turn phosphorylates the Atf1 bZIP transcription factor.

4 nfection response gene irg-1 using the zip-2 bZIP transcription factor.

5 floral genes through interaction with FD, a bZIP transcription factor.

6 the yeast two-hybrid system with a putative bZIP transcription factor.

7 les for AP2 and Sp1, in combination with the bZip transcription factors.

8 ng, and (v) members of the TGA/OBF family of bZIP transcription factors.

9 eral ways including direct interactions with bZIP transcription factors.

10 ncreases the transcriptional efficacy of the bZip transcription factors.

11 nd acidic amino acid-rich (PAR) subfamily of bZIP transcription factors.

12 erved among chlorophytes and present in some bZIP transcription factors.

13 g sites for basic/helix-loop-helix, MYB, and BZIP transcription factors.

14 te the activity of members of the G-group of bZIP transcription factors.

15 sly shown to induce Gcm1 expression by other bZip transcription factors.

16 hares resemblance with the Jun/Fos family of bZIP transcription factors.

17 ct to varying extents with many ABI5-related bZIP transcription factors.

18 des derived from GCN4, a yeast basic zipper (bZIP) transcription factor.

19 ces-2 encodes a basic region leucine-zipper (bZIP) transcription factor.

20 ands from human basic-region leucine zipper (bZIP) transcription factors.

21 the CREB/ATF family of basic-leucine zipper (bZIP) transcription factors.

22 to a subclass of plant basic leucine zipper (bZIP) transcription factors.

23 superfamily of basic region-leucine zipper (bZIP) transcription factors.

24 tners for human basic-region leucine zipper (bZIP) transcription factors.

25 sponse element binding basic leucine zipper (bZIP) transcription factors (ABF/AREB/ABI5 clade).

26 o a weak interaction between PpABI3A and the bZIP transcription factor ABI5, as assayed functionally

27 diated developmental checkpoint requires the bZIP transcription factor ABI5.

28 ty in Medicago truncatula, we identified the bZIP transcription factor ABSCISIC ACID INSENSITIVE5 (AB

29 l of oxidative stress, the expression of the bZip transcription factor activating transcription facto

30 onstrating an expanded repertoire of group F bZIP transcription factors, adding to the complexity of

31 Analyses of a bZIP transcription factor and receptor recognition of Fi

32 Hypoxia induced a disproportionate number of bZIP transcription factors and related targets involved

33 for continued in vivo functional analysis of bZIP transcription factors and their corresponding cis e

34 a model to investigate interactions between bZIP transcription factors and their target sites.

35 study demonstrates the importance of group F bZIP transcription factors and ZIP transporters in respo

36 We studied the basic region-leucine zipper (bZIP) transcription factors and quantified bZIP dimeriza

37 sely related to the vertebrate PAR family of bZIP transcription factors, and a ces-2/ces-1-like pathw

38 re mediated respectively by target sites for bZIP transcription factors, and by SMAD target sites.

39 cascades, phosphorylation of c-Jun and ATF-2 bZIP transcription factors, and finally to selective ind

40 ed Nrl, a member of the Maf-Nrl subfamily of bZIP transcription factors, and the Nrl response element

41 The eukaryotic bZIP transcription factors are critical players in organ

42 We considered four bZIP transcription factors as candidates for this putati

43 he mRNA for the basic domain leucine zipper (bZip) transcription factor ATB2/AtbZip11, translation of

44 The Arabidopsis basic leucine zipper (bZIP) transcription factor AtbZIP10 shuttles between the

45 Here we examine pX interactions with bZip transcription factors ATF3, gadd153/Chop10, ICER II

46 egulated in stressed cells, primarily by the bZIP transcription factor ATF4 through its recruitment t

47 We found expression of the bZip transcription factor ATF5 in all 29 human glioblast

48 We report that the bZIP transcription factor ATF5 plays a major regulatory

49 The basic leucine zipper (bZIP) transcription factor AtfB, a member of the bZIP/CR

50 ical producing E. coli mutant, including the bZip transcription factor atfs-1 (activating transcripti

51 erties in common with the more studied human bZIP transcription factors, but also includes novel stru

52 nergistically with the basic leucine zipper (bZIP) transcription factor bZIP10 to induce dsCYC2 trans

53 rane-associated basic domain/leucine zipper (bZIP) transcription factor, bZIP28.

54 The bZIP transcription factor c-Jun, which is part of the AP

55 The bZIP transcription factor C/EBPbeta is a target of Ras s

56 ng to examine the expression patterns of two bZip transcription factors, c-Fos and FosB, in the stria

57 The level of bZIP transcription factor CCAAT enhancer-binding protein

58 TYL5 (HY5) is a basic domain/leucine zipper (bZIP) transcription factor, central for the regulation o

59 ER TRUSS (SFT) and two mutations affecting a bZIP transcription factor component of the 'florigen act

60 the X box in a manner consistent with other bZIP transcription factor contact patterns.

61 LCR-F1 is a mammalian bZIP transcription factor containing a basic amino acid

62 The basic/leucine zipper (bZip) transcription factor, CREB, binds to the CRE eleme

63 is a homologue of a Saccharomyces cerevisiae bZip transcription factor designated Yap1p that is both

64 Previously, we have described a bZIP transcription factor, DimA, which is required for c

65 We have purified a novel bZIP transcription factor, DimB, by affinity chromatogra

66 escribe the identification of a DimA-related bZIP transcription factor, DimB.

67 The basic-region leucine zipper (BR-LZ or bZIP) transcription factors dimerize via their LZ domain

68 Meq, a bZIP transcription factor discovered in the 1990s, is cr

69 insight into the mechanism by which dimeric bZIP transcription factors discriminate between closely

70 Here we show that the basic leucine zipper (bZIP) transcription factor E4BP4 (also called NFIL3) is

71 The bZIP transcription factor ELONGATED HYPOCOTYL5 (HY5) act

72 of transcriptional activators, including the bZIP transcription factor encoded by the kreisler gene c

73 no (val), a zebrafish homologue of the mouse bzip transcription factor-encoding gene, kreisler, is re

74 rotein beta (C/EBP beta), from two different bZIP transcription factor families, has been determined

75 DRINK ME (DKM; bZIP30) is a member of the bZIP transcription factor family, and is expressed in me

76 Atf2, the gene for the basic leucine zipper (bZIP) transcription factor family member ATF-2.

77 members of the basic region leucine zipper (bZIP) transcription factor family.

78 atial information is mediated in part by the bZIP transcription factor FD, which is already expressed

79 pment and identifying it as a homolog of the bZIP transcription factor FD.

80 omain of MAF, a basic region leucine zipper (bZIP) transcription factor, first identified as an oncog

81 Upstream regulators including the bZIP transcription factor FlbB activate the expression o

82 ATF-2 is a bZip transcription factor for activation of cAMP respons

83 we find that the CrebA/Creb3-like family of bZip transcription factors functions to up-regulate expr

84 Arabidopsis bZIP transcription factor, GBF1, acts as a differential

85 The yeast bZIP transcription factor GCN4 does not induce DNA bendi

86 The yeast bZIP transcription factor GCN4 does not induce DNA bendi

87 derived from the yeast basic leucine zipper (bZIP) transcription factor GCN4 bound to AP-1 sites in d

88 ent of the DNA basic region (br) of the GCN4 bZIP transcription factor has been modified to include t

89 the CCAAT enhancer binding protein family of bZIP transcription factors has been linked to both growt

90 ed factor 2 (Nrf2), an oxidant-activated CNC bZip transcription factor, has been implicated in defens

91 tified to date, HY5, a basic leucine zipper (bZIP) transcription factor, has been investigated extens

92 ollar family of basic region-leucine zipper (bZIP) transcription factors, has been implicated as an e

93 ecific class of basic-region leucine zipper (bZIP) transcription factors, have been isolated in a num

94 homologous to the PAR subfamily of mammalian bZIP transcription factors HLF, DBP and VBP/TEF.

95 We have found that Pap1, a bZIP transcription factor homologous to human c-Jun, can

96 The barley bZIP transcription factor HvABI5 mediates abscisic acid

97 A barley basic domain/Leu zipper (bZIP) transcription factor, HvABI5, is able to recognize

98 light receptor phytochrome A (phyA) and the bZIP transcription factor HY5 HOMOLOG (HYH) are both req

99 n the dark, COP1 directly interacts with the bZIP transcription factor HY5, a positive regulator of p

100 and interaction between the light regulatory bZip transcription factors HY5 and HYH.

101 reconstructing ancestral interactions among bZIP transcription factors, imputing missing present-day

102 reaction was used to identify three TGA-type bZIP transcription factors in an AZ cDNA library.

103 e-varying alterations in the inducibility of bZIP transcription factors in individual striatal neuron

104 uced changes in expression and activation of bZIP transcription factors in the postsynaptic motor neu

105 The relationship between PvALF and ABI5, a bZIP transcription factor, in mediating phas expression

106 hat regulates steady-state levels of Nrf2, a bZIP transcription factor, in response to oxidative stre

107 Two FT monomers and two DNA-binding bZIP transcription factors interact with a dimeric 14-3-

108 s identifies a novel mechanism through which bZip transcription factors interact.

109 Although Yap1p and Yap2p are both bZIP transcription factors involved in multiple stress r

110 , a well-characterized basic leucine zipper (bZIP) transcription factor involved in the unfolded prot

111 dimerization of basic region-leucine zipper (bZIP) transcription factors is required for their transc

112 MAF, one of a family of large Maf bZIP transcription factors, is mutated in human developm

113 at JunD, an AP1 family basic-leucine zipper (bZip) transcription factor, is one of the ferritin H ARE

114 ember of the AP-1 subfamily of basic zipper (bZIP) transcription factors, is necessary and sufficient

115 domain arrangement is like that seen in the bZIP transcription factors it has been termed the bZIP-l

116 n cellular target of the beta-propeller is a bZIP transcription factor known as LZIP or Luman.

117 These results establish Hac1 as the first bZIP transcription factor known to adopt more than one b

118 s lacking this regulation, we identified the bZIP transcription factor LONG HYPOCOTYL 5 (HY5) as a ne

119 s shown to be allelic with a knockout of the bZIP transcription factor, Maf.

120 indicates that although other typical plant bZIP transcription factors may bind ABRCs in vitro, HvAB

121 LCR-F1 and the related bZIP transcription factors NF-E2 p45 and NRF2 must compe

122 The bZIP transcription factor Nfil3 (also known as E4BP4) is

123 e identified a novel interaction between two bZIP transcription factors, Nrf1 and the CCAAT enhancer-

124 The bZIP transcription factor Nrf2 controls a genetic progra

125 The bZIP transcription factor Nrf2 controls a genetic progra

126 ion of Keap1-dependent ubiquitination of the bZIP transcription factor Nrf2 enables Nrf2 to activate

127 The bZIP transcription factor Nrf2 has emerged as a key regu

128 sion is mediated through accumulation of the bZIP transcription factor, Nrf2, in the nucleus, and tha

129 The bZIP transcription factor NRL (neural retina leucine zip

130 ell as lower synergistic activation with the bZIP transcription factor NRL.

131 The basic motif-leucine zipper (bZIP) transcription factor NRL controls the expression o

132 ion requires the basic motif-leucine zipper (bZIP) transcription factor NRL, because loss of Nrl in m

133 We recently demonstrated that the bZip transcription factor nuclear factor erythroid-deriv

134 uggest that cross-coupling between EREBP and bZIP transcription factors occurs and may therefore be i

135 NRL, a bZIP transcription factor of the Maf subfamily, interact

136 lso found in LZIP and Zhangfei, two cellular bZIP transcription factors of unknown function.

137 We identified FEA4 as a bZIP transcription factor, orthologous to Arabidopsis th

138 transcriptional activation complex with the bZIP transcription factor OsFD1 to start panicle develop

139 tion system-dependent manner, one encoding a bZIP transcription factor (OsTFX1) and the other the sma

140 Specific bZIP transcription factors partially mediate primary KIN

141 precipitation assays to demonstrate that the bZIP transcription factor PERIANTHIA (PAN) plays a role

142 ear factor E2 p45-related factor 2 (Nrf2), a bZIP transcription factor, plays a central role in the r

143 rization of the basic-region leucine-zipper (bZIP) transcription factors presents a vivid example of

144 Basic leucine zipper (bZip) transcription factors regulate cellular gene expre

145 Basic region leucine zipper (bZIP) transcription factors regulate gene expression cri

146 Hepatic leukemia factor (HLF) is a bZIP transcription factor related to the CES-2 protein,

147 Of the 32 bZIP transcription factors represented on the GeneChip,

148 g atf1(+) mRNA, which encodes a subunit of a bZIP transcription factor required for gene expression d

149 e nitrogen source requires the heterodimeric bZip transcription factors Rtg1 and Rtg3 and correlates

150 ins (C/EBP) are basic region/leucine zipper (bZIP) transcription factors selectively expressed during

151 Sage and Fkh drive expression of the bZip transcription factor Senseless (Sens), which boosts

152 HY5 is a bZIP transcription factor that binds directly to the pro

153 interaction between OsTBP2 and RF2a, a rice bZIP transcription factor that bound to the box II cis e

154 sh ortholog of mafB/Kreisler (Kr), encodes a bZip transcription factor that is required cell autonomo

155 This screen identified zip-2, a bZIP transcription factor that is required for inducing

156 Keap1 is a negative regulator of Nrf2, a bZIP transcription factor that mediates adaptation to ox

157 hancer-binding protein beta (C/EBPbeta) is a bZip transcription factor that plays crucial roles in im

158 ction with and negative regulation of HY5, a bZIP transcription factor that positively regulates phot

159 Arabidopsis HY5 is a bZIP transcription factor that promotes photomorphogenes

160 RF2a is a bZIP transcription factor that regulates expression of t

161 at Arabidopsis ELONGATED HYPOCOTYL5 (HY5), a bZIP transcription factor that regulates growth in respo

162 Atf1 and Atf21 are bZIP transcription factors that are most closely related

163 f1 and Nrf2 are members of the CNC family of bZIP transcription factors that exhibit structural simil

164 erences of coiled-coil peptides derived from bZIP transcription factors that performs very well when

165 2 is a cellular basic region-leucine zipper (bZIP) transcription factor that can mediate diverse tran

166 ransactivator Zta is a basic leucine zipper (bZIP) transcription factor that causes G0/G1 cell cycle

167 PDP1 is a basic leucine zipper (bZip) transcription factor that is expressed at high lev

168 is a cap-n-collar basic leucine zipper (CNC-bZIP) transcription factor that is well established as a

169 E4BP4 is a basic leucine zipper (bZIP) transcription factor that represses or activates t

170 ode a family of basic domain-leucine zipper (bZIP) transcription factors that are conserved in higher

171 ns (C/EBPs) are basic region leucine zipper (bZIP) transcription factors that regulate cell different

172 mbers from a family of conserved Arabidopsis bZIP transcription factors, the TGA proteins, are regula

173 an enhancer of the DNA binding potential of bZip transcription factors, thereby increasing the trans

174 coli mutant may directly activate the ATFS-1/bZIP transcription factor to induce mitochondrial stress

175 is the first member of the PAR subfamily of bZIP transcription factors to be identified in Drosophil

176 sease virus, encodes a basic leucine zipper (bZIP) transcription factor which contains a large prolin

177 and mediated by NapA, a homolog of AP-1-like bZIP transcription factor, which is essential for the re

178 zipper) is a key basic motif-leucine zipper (bZIP) transcription factor, which orchestrates rod photo

179 /enhancer-binding protein (C/EBP) alpha is a bZIP transcription factor whose expression is restricted

180 pe CREB3L2 was expressed in the thyroid as a bZIP transcription factor with a transmembrane domain th

181 gene of Schizosaccharomyces pombe encodes a bZIP transcription factor with strong homology to the ma

182 n Arabidopsis thaliana basic leucine zipper (bZIP) transcription factor with a transmembrane domain,

183 on element (ARE) of the major-groove binding bZIP transcription factor yAP-1, the yeast analogue of m

184 We asked whether a viral bZIP transcription factor, Zta (BZLF1, ZEBRA, EB1), driv