ライフサイエンスコーパス: leucine zipper

1 and its C terminus is mediated by a putative leucine zipper.

2 i.e., the CA-SP1 junction region fused to a leucine zipper.

3 nstituent domains: EF-hand, coiled coil, and leucine zipper.

4 e from experimental LOT measurements for the leucine zipper.

5 only when it is tethered to FtsN(TM) or to a leucine zipper.

6 at P6981 binds both the B-ZIP domain and the leucine zipper.

7 -binding domains are linked by a coiled-coil leucine zipper.

8 involved in interhelical salt bridges in the leucine zipper.

9 de sequence attached to N-terminal of bZIP53 leucine zipper.

10 interactions, such as those between pairing leucine zippers.

11 osphotyrosine interacting with PH domain and leucine zipper 1 (APPL1) signaling endosomes and MYO6+ e

12 a regulatory pathway in which spermatogenic leucine zipper 1 (SPZ1) promotes EMT through its transac

13 has been shown previously to bind the basic leucine zipper 1 domain in the C3 promoter.

14 We temporally perturbed a master TF (Basic Leucine Zipper 1, bZIP1) and the nitrogen (N) signal it

15 brane-associated transcription factor, BASIC LEUCINE ZIPPER 17 (bZIP17), and the membrane-associated

16 he DNA binding activity of protagonist basic leucine zipper 53 (bZIP53) transcription factor and its

17 s-related host genes, including basic-region leucine zipper 60 (bZIP60), SKP1, ER luminal binding pro

18 sitol-requiring protein-1) and bZIP60 (basic leucine zipper 60), two RSRE containing unfolded protein

19 re, interdimer interactions between adjacent leucine zippers allow TbBILBO1 to form extended filament

20 Unexpectedly, the predicted leucine zipper and helix-loop-helix motifs do not form t

21 s of a coiled-coil protein based on the GCN4 leucine zipper and obtain a free-energy landscape that i

22 scription factors: ERF/AP2 class I, homeobox-leucine zipper and R2R3 MYB.

23 orm heterodimers and bind to DNA via a basic leucine zipper and regulate the cell cycle, apoptosis, d

24 switches to a helical state when fused to a leucine zipper and that these helical molecules further

25 a parallel homodimer linked by an N-terminal leucine zipper, and we show that the WT chain in WT-RQ h

26 ms an antiparallel dimer, and the C-terminal leucine zipper appears to contain targeting information.

27 Mutations in the GCN4 leucine zipper are known to change its preferred oligome

28 ent of a full-length myosin-X construct with leucine zipper at the C-terminal end of the tail (M10(Fu

29 The lower part of the leucine zipper, at the intracellular mouth of the channe

30 The basic leucine zipper ATF-like 3 (BATF3)-dependent CD103(+)CD11

31 After vaccination, both migratory basic leucine zipper ATF-like transcription factor 3 (BatF3)-d

32 rotein (VBP)] and two basic helix-loop-helix leucine zipper (B-HLH-ZIP) [USF (upstream stimulating fa

33 nd of the HTLV-1 genome encodes HTLV-1 basic leucine zipper (b-ZIP) protein (HBZ), a protein that inh

34 Several basic leucine zipper (B-ZIP) transcription factors have been i

35 ression alleles of wallenda (wnd, encoding a leucine zipper bearing kinase similar to human DLK and L

36 through injury-induced stabilization of dual leucine zipper-bearing kinase (DLK/MAP3K12).

37 Leucine Zipper-bearing Kinase (LZK/MAP3K13) is a member

38 MAPKKK dual leucine zipper-bearing kinases (DLKs) are regulators of

39 I) and the C-terminal basic helix-loop-helix leucine zipper (bHLH-LZ) domains of the oncoprotein c-My

40 on factor (MITF) is a basic helix-loop-helix leucine zipper (bHLH-Zip) DNA-binding protein.

41 blastosis), SFH3 (SEC14-like 3), bZIP (basic-leucine zipper), bHLH (basic helix-loop-helix) and SBP (

42 ption partner Mlx are basic helix-loop-helix leucine zipper (bHLHZip) transcription factors that sens

43 nd the TIRs identified a heterodimeric basic leucine zipper (bZIP) complex between an uncharacterized

44 The protein consists of the basic region-leucine zipper (BZip) domain of the CCAAT/enhancer-bindi

45 esign peptides that bind to the basic region leucine zipper (bZIP) domain of the viral transcription

46 T-cell leukemia virus type 1 (HTLV-1) basic leucine zipper (bZIP) factor (HBZ) could be used for imm

47 Here, a novel basic leucine zipper (bZIP) family transcription factor TubZIP

48 The basic region and leucine zipper (bZIP) of C/EBPbeta, zinc finger (ZF) mot

49 ich functions synergistically with the basic leucine zipper (bZIP) transcription factor bZIP10 to ind

50 ere, we use Hac1, a well-characterized basic leucine zipper (bZIP) transcription factor involved in t

51 ELONGATED HYPOCOTYL 5 (HY5), a basic domain/leucine zipper (bZIP) transcription factor, acts as a ma

52 ELONGATED HYPOCOTYL5 (HY5) is a basic domain/leucine zipper (bZIP) transcription factor, central for

53 components identified to date, HY5, a basic leucine zipper (bZIP) transcription factor, has been inv

54 s such as ABA-response element binding basic leucine zipper (bZIP) transcription factors (ABF/AREB/AB

55 We studied the basic region-leucine zipper (bZIP) transcription factors and quantifi

56 Basic leucine zipper (bZip) transcription factors regulate cel

57 Basic region leucine zipper (bZIP) transcription factors regulate gen

58 Flowering Locus T 1 (RFT1), OsFD-like basic leucine zipper (bZIP) transcription factors, and Gf14 pr

59 elong to the AP1 superfamily of basic region-leucine zipper (bZIP) transcription factors.

60 elease a cytosolic domain containing a basic leucine zipper (bZIP) transcriptional activator.

61 s to the G-group of Arabidopsis basic region leucine zipper (bZIP) type transcription factors.

62 -resolved ICIRD spectroscopy on basic-region leucine zipper (bZIP)-LOV of aureochrome 1a from the dia

63 Selective dimerization of the basic-region leucine-zipper (bZIP) transcription factors presents a v

64 Basic region leucine zippers (bZIPs) are modular transcription factor

65 nal domain of the protein: the coiled-coil 2-leucine zipper (CC2-LZ) domain and the zinc finger (ZF)

66 ranscription factors in hematopoiesis is the leucine zipper CCAAT-enhancer binding protein alpha (C/E

67 onse of two Arabidopsis thaliana homeodomain-leucine zipper class I genes; ATHB7 and ATHB12, both str

68 Leucine zipper coiled coils were combined with either gl

69 In the presence of the ligand, the leucine zipper conformation is completely inhibited and

70 Phosphotyrosine Interaction, PH domain, and leucine zipper containing 1 (APPL1) that were identified

71 We recently identified that vimentin, a leucine zipper-containing intermediate filament protein,

72 The MAPKKK dual leucine zipper-containing kinase (DLK, Wallenda in Droso

73 ions, the MAP3K ZAK (Sterile alpha motif and leucine zipper-containing kinase) has also been proven t

74 ption factor 4 (ATF4), a member of the basic leucine zipper-containing protein subfamily.

75 action, pleckstrin homology (PH) domain, and leucine zipper-containing protein)) are localized to the

76 rotic fibrosarcoma oncogene homolog (MAF), a leucine zipper-containing transcription factor of the AP

77 Atf4 is a leucine zipper-containing transcription factor that acti

78 VCCs when the NC domain was replaced with a leucine zipper dimerization motif that promotes Gag mult

79 interaction between the LOV and basic region leucine zipper DNA-binding domain that together with LOV

80 n and one nuclear export signal (NES) in the leucine zipper domain (named LZ-NES).

81 A leucine zipper domain can replace NC in Gag and still le

82 ucleic acid-binding domain with a dimerizing leucine zipper domain leads to the assembly of RNA-free

83 ltransferase, interacts with the octapeptide/leucine zipper domain of AF10, and this region has been

84 The ATF3-AR interaction requires the leucine zipper domain of ATF3 that independently binds t

85 Deletion of the carboxy-terminal leucine zipper domain relaxed the constraint and permitt

86 e NF-kappaB members RelB and p52 through its leucine zipper domain.

87 he folding behavior of the well-studied GCN4 leucine-zipper domain is more complex than was previousl

88 inositol pyrophosphate kinase and the basic leucine zipper domains of KCS1 are required for INO1 exp

89 Both FLX and FLX4 contain leucine zipper domains that facilitate interaction with

90 ors is based on the shared capacity of their leucine zipper domains to interact with non-AP1 factors

91 rm, DLK-1S, that shares identical kinase and leucine zipper domains with the previously described lon

92 These LZD (leucine zipper dual-binding) peptides were derived by fu

93 rter (MCU), uncoupling protein 2 (UCP2), and leucine zipper EF-hand-containing transmembrane protein

94 Leucine zipper-EF-hand containing transmembrane protein

95 : the novel uncoupling proteins 2 and 3, the leucine zipper-EF-hand containing transmembrane protein

96 tochondrial calcium uniporter-dependent, but leucine zipper-EF-hand containing transmembrane protein

97 ing transmembrane protein 1-independent to a leucine zipper-EF-hand containing transmembrane protein

98 X (mitochondrial Na/Ca exchanger) and LETM1 (leucine zipper-EF-hand-containing transmembrane protein

99 homology to the mitochondrial protein LETM1 (leucine zipper-EF-hand-containing transmembrane protein)

100 HTLV-1 basic leucine zipper factor (HBZ) is one of the viral proteins

101 V-1 regulatory proteins Tax and HTLV-1 basic leucine zipper factor (HBZ) play a major role in ATLL de

102 and of its proviral genome, the HTLV-1 basic leucine zipper factor (HBZ), which inhibits Tax-1-mediat

103 The neural retina leucine zipper factor (NRL) transcription factor critica

104 ription factor 2 (ATF2) belongs to the basic leucine zipper family of transcription factors.

105 eoblast-enriched transcription factor of the leucine zipper family.

106 nserved Ala-Ala in many members of the basic leucine-zipper family of transcription factors, importan

107 cted protein product, compared to the intact leucine zipper found in two YAP1 (alpha) isoforms.

108 Purified c-Jun leucine zipper fragments could also form stable homodime

109 NC domain had been replaced by a dimerizing leucine zipper [Gag(LZ)].

110 (CD2), a member of the class IV homeodomain-leucine zipper gene family, previously only associated w

111 found that it encodes a class I homeodomain leucine zipper gene that promotes lateral bud dormancy a

112 oid responsive genes [glucocorticoid-induced leucine zipper (GILZ) and FK506 binding protein-51 (FKBP

113 Induction of glucocorticoid-induced leucine zipper (GILZ) by glucocorticoids plays a key rol

114 Glucocorticoid (GC)-induced leucine zipper (GILZ) has been shown to mediate or mimic

115 at expression of glucocorticoid (GC)-induced leucine zipper (GILZ) in bone marrow mesenchymal lineage

116 Glucocorticoid-induced leucine zipper (GILZ) is a rapidly, potently, and invari

117 Glucocorticoid-induced leucine zipper (GILZ) is an anti-inflammatory protein fi

118 n at serine 211 and expression of GC-induced leucine zipper (GILZ) were significantly reduced in ASM

119 ated transcription of glucocorticoid-induced leucine zipper (GILZ).

120 ranscription factor glucocorticoid-inducible leucine zipper (GILZ).

121 Class III homeodomain-leucine zipper (HD ZIP) transcription factors have been

122 The gamma-clade of class I homeodomain-leucine zipper (HD-Zip I) transcription factors (TFs) co

123 uxin levels activating class III homeodomain leucine zipper (HD-ZIP III) transcription factors (TFs).

124 nsequent expression of CLASS III HOMEODOMAIN-LEUCINE ZIPPER (HD-ZIP III) transcription factors, promo

125 rotein 1 (HAT1), which encodes a homeodomain-leucine zipper (HD-Zip) class II transcription factor, w

126 Here we report that a homeodomain-leucine zipper (HD-ZIP) transcription factor, GhHOX3, co

127 analysis revealed that ATHB13, a homeodomain-leucine zipper (HD-Zip) transcription factor, was consti

128 The broadly conserved Class III homeodomain leucine zipper (HD-ZIPIII) and KANADI transcription fact

129 Members of the class III homeodomain-leucine zipper (HD-ZIPIII) gene family are critical play

130 on in three paralogous class III homeodomain leucine zipper (HD-ZIPIII) genes leads to aberrations in

131 ontext, members of the class III homeodomain leucine zipper (HD-ZIPIII) transcription factor family s

132 PKGIalpha (residues 1-59), which includes a leucine zipper heptad repeat motif.

133 d to tune ZF-TF response by fusing ZF-TFs to leucine zipper homodimerization domains.

134 d also form stable homodimers, whereas c-Fos leucine zipper homodimers were found to be much less sta

135 Characterization of the homeodomain leucine zipper I transcription factor AtHB13, which is e

136 rylstibonic acid, NSC13778, bound to the VBP leucine zipper identified electrostatic interactions bet

137 lish SiMPull in plants using the HOMEODOMAIN LEUCINE ZIPPER III (HD-ZIPIII) and LITTLE ZIPPER (ZPR) i

138 a GFP reporter system, we defined a putative leucine zipper in the N terminus of human pro-EMAP II pr

139 We have identified a leucine zipper in the S5 segment of HCNs, regulating hyp

140 Residues of the leucine zipper interact with the adjacent S6 segment of

141 The leucine zipper interaction between MAX and c-MYC has bee

142 Thus, our data indicate that the leucine zipper is an important molecular determinant for

143 ation and functional characterization of the leucine zipper is an important step toward the understan

144 The leucine zipper is essential for HCN channel gating.

145 GILZ (glucocorticoid-induced leucine zipper) is inducible by glucocorticoids and play

146 identification of an Arabidopsis homeodomain-leucine zipper IV (HD-ZIP IV) protein, HOMEODOMAIN GLABR

147 ronal stress response controlled by the Dual Leucine Zipper Kinase (DLK) and contributes to DLK-media

148 Two convergent pathways, involving dual leucine zipper kinase (DLK) and fragile X mental retarda

149 NK activation in neurons is mediated by dual leucine zipper kinase (DLK) and JNK-interacting protein

150 The screen identified dual leucine zipper kinase (DLK) as a key neuroprotective tar

151 Dual leucine zipper kinase (DLK) has been implicated in cell

152 Dual leucine zipper kinase (DLK) has emerged as a key mediato

153 Here we show that the mixed-lineage dual leucine zipper kinase (DLK) is an essential upstream med

154 We show that dual leucine zipper kinase (DLK) is essential for excitotoxic

155 Dual leucine zipper kinase (DLK) is required for stress-induc

156 ue of Neuron, Shin et al. show that the dual leucine zipper kinase (DLK) is responsible for the retro

157 Dual leucine zipper kinase (DLK) promotes growth cone motilit

158 Here we demonstrate that the dual leucine zipper kinase (DLK) promotes robust regeneration

159 We find that the dual leucine zipper kinase (DLK) signaling pathway in Drosoph

160 The Wallenda (Wnd)/dual leucine zipper kinase (DLK)-Jnk pathway is an evolutiona

161 microtubule dynamics was independent of dual leucine zipper kinase (DLK)-mediated stress but was resc

162 The dual leucine zipper kinase (DLK)/c-Jun-N-terminal kinase (JNK

163 Dual leucine zipper kinase (DLK, MAP3K12) was recently identi

164 e family with high sequence identity to Dual Leucine Zipper Kinase (DLK/MAP3K12).

165 on is only partially protective, we identify leucine zipper kinase (LZK) as cooperating with DLK to a

166 Maternal embryonic leucine zipper kinase (MELK) belongs to the subfamily of

167 The maternal embryonic leucine zipper kinase (MELK) has been implicated in the

168 The Maternal Embryonic Leucine Zipper Kinase (MELK) has been reported to be a g

169 ment of a novel selective maternal embryonic leucine zipper kinase (MELK) inhibitor HTH-01-091, CRISP

170 The protein kinase maternal and embryonic leucine zipper kinase (MELK) is critical for mitotic pro

171 on after injury is regulated in part by dual-leucine zipper kinase 1 (DLK-1), a conserved regulator o

172 se selectivity of type II maternal embryonic leucine zipper kinase inhibitors by applying these two c

173 /Thr protein kinase MELK (maternal embryonic leucine zipper kinase) has been considered an attractive

174 conserved, retrograde DLK-1 MAPK (DLK-1/dual leucine zipper kinase) pathway, which triggered synaptic

175 K (zipper protein kinase, also known as dual leucine zipper kinase), a mitogen-activated protein kina

176 n the level of the MAPKKK Wallenda/DLK (dual leucine zipper kinase), a previously identified substrat

177 e) expression and loss of wallenda/DLK (dual leucine zipper kinase).

178 This decrease was independent of the dual leucine zipper kinase-Wallenda pathway and required func

179 After axonal insult and injury, Dual leucine-zipper kinase (DLK) conveys retrograde pro-degen

180 Dual leucine-zipper kinase (DLK) is critical for axon-to-soma

181 poE binding to ApoE receptors activates dual leucine-zipper kinase (DLK), a MAP-kinase kinase kinase

182 Here we identify the Dual Leucine-zipper Kinase (DLK, Wnd in Drosophila) as a crit

183 e show here that long glucocorticoid-induced leucine zipper (L-GILZ) is highly expressed in spermatog

184 between Golgin45 and GM130, we found that a leucine zipper-like motif in the central coiled-coil reg

185 on is driven by hydrophobic interactions via leucine zipper-like motifs.

186 spectrometry, we detected a RIT1 interactor, leucine zipper-like transcription regulator 1 (LZTR1), t

187 tom caused by biallelic mutations within the leucine zipper-like transcription regulator 1 (LZTR1).

188 tients with NS harboring mutations of LZTR1 (leucine zipper-like transcription regulator 1), an adapt

189 ow that scaffold assembly requires conserved leucine zipper (LZ) and Cnn-motif 2 (CM2) domains that c

190 ted the domains of K-bZIP and found that the leucine zipper (LZ) domain is essential for the interact

191 -terminal coiled-coil domain (CC) and/or the leucine zipper (LZ) domain of the myosin light-chain pho

192 such as a C(2) H(2) -zinc finger (ZF), and a leucine zipper (LZ), whose roles in FOXP2 remain largely

193 binds to the LTCC C-terminus via a modified leucine-zipper (LZ) interaction.

194 ynthesized, along with the corresponding MAX leucine zipper (MAX-Zip residues 74-102).

195 uman retina, we used Nrl(-/-) (neural retina leucine zipper) mice, to generate Rpgr(ko)::Nrl(-/-) dou

196 n, phosphotyrosine-binding (PTB) domain, and leucine zipper motif (APPL)-positive endosomes and EEA1-

197 ain, a phosphotyrosine-binding domain, and a leucine zipper motif (APPL)1, an early endosomal protein

198 n, phosphotyrosine-binding (PTB) domain, and leucine zipper motif 1 (APPL1) in regulating cell migrat

199 23 skipped isoform coding for the C-terminal leucine zipper motif caused increased sensitivity of the

200 We have identified a highly conserved leucine zipper motif in the S5 segment of HCN family mem

201 that an evolutionarily conserved, truncated leucine zipper motif near the N terminus as well as a st

202 y domain, phosphotyrosine binding domain and leucine zipper motif) mediates rab5 overactivation in Do

203 he first 936 amino acids, followed by a GCN4 leucine zipper motif, to force dimerization.

204 A number of BASIC LEUCINE-ZIPPER MOTIF transcription factors involved in t

205 t only activated PKGIalpha binds RhoA, and a leucine zipper mutant PKGIalpha was unable to bind RhoA

206 Leucine zipper mutants traffic to the plasma membrane, b

207 Furthermore, the non-Leucine zipper N-terminal helical bundle contains severa

208 repeatedly occur at core positions a and d (leucine zipper nomenclature) in homologous and nonhomolo

209 to +33 bp) of Frmpd1 binds to neural retina leucine zipper (NRL) and cone-rod homeobox protein (CRX)

210 cantly higher in cone-dominant neural retina leucine zipper (Nrl) knock-out mouse retinas compared wi

211 tors-cone--rod homeobox (CRX), neural retina leucine zipper (NRL), and nuclear receptor subfamily 2,

212 ne zipper transcription factor neural retina leucine zipper (NRL).

213 We observed the expression of genes like leucine zipper, ntd, nced, geraniol synthase, raffinose

214 Thus, we conclude that the leucine zipper of HCN channels is a major determinant fo

215 he proline- and acidic amino acid-rich basic leucine zipper (PAR-bZip) clock-controlled genes.

216 ng high levels of the glucocorticoid-induced leucine zipper protein (GILZ) generate antigen-specific

217 We show that the glucocorticoid-induced leucine zipper protein (GILZ), already known to regulate

218 IL-10, or TGF-beta upregulate the GC-Induced Leucine Zipper protein (GILZ).

219 e transcription of three related Homeodomain leucine zipper protein (HD-ZIP)-encoding genes: HOMEOBOX

220 Small heterodimer partner interacting leucine zipper protein (SMILE) has been identified as a

221 Arabodopsis thaliana homeodomain-leucine zipper protein 1 (HAT1), which encodes a homeodo

222 nal activation potential of the basic region leucine zipper protein ATF2.

223 dominant-negative mutant of the basic region leucine zipper protein c-Jun, a major constituent of the

224 on factor (MITF) is a basic helix-loop-helix leucine zipper protein that plays major roles in the dev

225 JLP (JNK-associated leucine zipper protein) is a scaffolding protein that in

226 rl gene, encoding for Neural retina-specific leucine zipper protein, a rod fate determinant during ph

227 mulated expression of glucocorticoid-induced leucine-zipper protein and the alpha-subunit of the epit

228 ation in human fibroblasts, we uncovered the leucine-zipper protein LUZP1 as an interactor of truncat

229 which compose a large group of basic region leucine zipper proteins whose members mediate diverse tr

230 -specific transcription factors: bZIP (basic leucine-zipper) proteins, exemplified by the AP-1 and CE

231 3, we observed that the previously described leucine zipper region at the C terminus of MSP3 may not

232 5 extension, exon 6 or both would have their leucine zipper region disrupted in the predicted protein

233 To determine the importance of the leucine zipper sequence of melittin in its neutralizatio

234 a indicated a probable important role of the leucine zipper sequence of melittin in neutralizing LPS-

235 ion of LPS aggregates with alteration in the leucine zipper sequence of melittin was observed.

236 Furthermore, with alteration in the leucine zipper sequence of melittin, these analogues fai

237 Peptides comprising the leucine zipper sequence with (c-MYC-Zip residues 402-434

238 of melittin with minor rearrangement in its leucine zipper sequence.

239 The helical leucine zipper structure previously determined from NMR

240 entral to this platform is the addition of a leucine zipper to the C terminus of the C(H)3 domain of

241 ion domain of NPM1, ATF5 binds via its basic leucine zipper to the C-terminal region of NPM1 where it

242 ATF4 is a member of the basic leucine zipper transcription factor (bZIP) superfamily.

243 imeric partner BTB and CNC homology 1, basic leucine zipper transcription factor 1 (BACH1), the chrom

244 Recently, basic leucine zipper transcription factor 2 (BACH2) has been a

245 inding that the BTB and CNC homology 1 basic leucine zipper transcription factor 2 (BACH2) induces ne

246 d differential BTB and CNC homology 1, basic leucine zipper transcription factor 2 expression.

247 ociated transcription factors, such as basic leucine zipper transcription factor 28 (bZIP28).

248 n large part by the ABA-induced basic domain/leucine zipper transcription factor ABA INSENSITIVE5 (AB

249 The basic Leucine zipper transcription factor ABSCISIC ACID INSENS

250 inding protein alpha (C/EBPalpha) is a basic leucine zipper transcription factor and is expressed in

251 poneurotic fibrosarcoma (c-Maf), Bcl6, basic leucine zipper transcription factor ATF-like (Batf), and

252 The basic leucine zipper transcription factor ATF-like 3 (BATF3) i

253 Here, we show that the basic leucine zipper transcription factor ATF-like, Batf is im

254 The basic leucine zipper transcription factor ATF6alpha functions

255 MENT-BINDING FACTOR2 (VvABF2), a grape basic leucine zipper transcription factor belonging to a phylo

256 Until recently, the basic leucine zipper transcription factor E4BP4 (also known as

257 We previously reported that the basic leucine zipper transcription factor E4BP4 (E4 binding pr

258 poplar ortholog of the class III homeodomain-leucine zipper transcription factor gene REVOLUTA (PtREV

259 The class IV homeodomain leucine zipper transcription factor GLABRA2 (GL2) acts i

260 homeostasis are dependent on the basic motif leucine zipper transcription factor neural retina leucin

261 The basic leucine zipper transcription factor Nfil3 (E4bp4) is ess

262 Here, we report that the basic leucine zipper transcription factor NFIL3/E4BP4 is essen

263 The Maf-family leucine zipper transcription factor NRL is essential for

264 The basic leucine zipper transcription factor nuclear factor (eryt

265 on is enhanced expression of the homeodomain-leucine zipper transcription factor REVOLUTA/INTERFASCIC

266 riptional target of NRL, the key basic motif leucine zipper transcription factor that dictates rod ve

267 5) is a photomorphogenesis promoting a basic leucine zipper transcription factor that is degraded by

268 abidopsis (Arabidopsis thaliana) homeodomain-leucine zipper transcription factor that participates in

269 factor E2-related factor 1 (Nrf1) is a basic leucine zipper transcription factor that plays important

270 ating transcription factor 4 (ATF4), a basic leucine zipper transcription factor that regulates the e

271 ors through the interaction with FD, a basic leucine zipper transcription factor which plays a critic

272 5) is an essential and conserved plant basic leucine zipper transcription factor whose level controls

273 doplasmic reticulum (ER) transmembrane basic leucine zipper transcription factor whose mRNA and prote

274 Mice without the basic leucine zipper transcription factor, ATF-like (BATF) gen

275 The AP-1 factor basic leucine zipper transcription factor, ATF-like (BATF) is

276 ression of the Bcl6 target genes Batf (basic leucine zipper transcription factor, ATF-like) and Bcl6,

277 This correlated inversely BATF (basic leucine zipper transcription factor, ATF-like) and IRF4

278 We report here that BATF (basic leucine zipper transcription factor, ATF-like), an AP-1

279 cus on a zinc deficiency B. distachyon basic leucine zipper transcription factor, BdbZIP10, and its r

280 erized in depth the NLSs of a P. sojae basic leucine zipper transcription factor, PsbZIP1.

281 revealed that the SOR1 gene encodes a basic leucine zipper transcription factor, which controls its

282 Leucine Zipper Transcription Factor-like 1 (LZTFL1) is l

283 Leucine zipper transcription factor-like 1 (LZTFL1) was

284 Using a newly developed BBS mouse model [Leucine zipper transcription factor-like 1 (Lztfl1)/Bbs1

285 is thaliana gene encoding for a basic region-leucine zipper transcription factor.

286 TF families in the supernode network, BASIC-LEUCINE ZIPPER TRANSCRIPTION FACTOR1-TGA and HYPERSENSIT

287 Here we show that basic LEUCINE ZIPPER TRANSCRIPTION FACTOR67 (bZIP67) acts down

288 ATF6 and BBF2H7 are transmembrane basic leucine zipper transcription factors and are subjected t

289 ng sterol/lipid-binding class IV homeodomain leucine zipper transcription factors as potential regula

290 oots, which revealed that the group S1 basic leucine zipper transcription factors bZIP1 and bZIP53 re

291 dancy between GL2 and HDG11, two homeodomain leucine zipper transcription factors previously thought

292 ol the activity of the class-III homeodomain-leucine zipper transcription factors(6-8)-and thereby re

293 y connected to two MtAP2/EREBP and two basic leucine zipper transcription factors.

294 lies on Rtg1 and Rtg3 basic helix-loop-helix leucine Zipper transcription factors.

295 A complex between FT and the basic leucine-zipper transcription factor FD is proposed to fo

296 screen hits is MLX, a basic helix-loop-helix leucine-zipper transcription factor that regulates metab

297 ification-dependent CpA recognition by basic leucine-zipper transcription factors.

298 The basic leucine zipper transcriptional regulator Cnc is necessar

299 tial and sequence-specific approach by basic leucine-zipper transcriptional factors.

300 M1-linked) di-ubiquitin to its coiled-coil 2-leucine zipper ubiquitin binding domain.