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1 terized this transcription factor, flowering basic helix-loop-helix 1 (FBH1) that binds in vivo to th
2 th the three closest homologs of ILR3 (i.e., basic-helix-loop-helix 34 [bHLH34], bHLH104, and bHLH115
5 nslocator (ARNT) subunit, which dimerize via basic helix-loop-helix and PAS domains, and recruit coac
6 -like 3), bZIP (basic-leucine zipper), bHLH (basic helix-loop-helix) and SBP (SQUAMOSA promoter bindi
7 transcription factors composed of R2R3 MYB, basic helix-loop-helix, and WD40 proteins that activate
8 orylation and degradation of phy-interacting basic Helix Loop Helix (bHLH) transcription factors (PIF
9 rted to be activated by a triad of R2R3-MYB, basic helix-loop helix (bHLH) and WD40 transcription fac
10 ing protein (SSBP) cofactors and DNA-binding basic helix-loop-helix (bHLH) and GATA transcription fac
11 G1) from Arabidopsis thaliana and associated basic helix-loop-helix (bHLH) and MYB transcription fact
12 in enhanced mRNA and protein expression of a basic helix-loop-helix (bHLH) class myogenic determinati
13 roteins constitute a subclass (VIIIc) of the basic helix-loop-helix (bHLH) class VIII transcription f
14 g specificities of 19 Caenorhabditis elegans basic helix-loop-helix (bHLH) dimers using protein bindi
15 ansporter 1 is actually a membrane-localized basic helix-loop-helix (bHLH) DNA-binding transcription
16 lar to other species' HIF-1, HdHIF-1 has one basic helix-loop-helix (bHLH) domain and two Per-Arnt-Si
17 thermore, Gsx2 physically interacts with the basic helix-loop-helix (bHLH) domain of Ascl1, and DNA-b
18 ze R2R3-MYB regulator C1 cooperates with the basic helix-loop-helix (bHLH) factor R to activate the e
22 ment, proneural transcription factors of the basic helix-loop-helix (bHLH) family are required to com
26 NTERACTING FACTORs (PIFs) are members of the basic helix-loop-helix (bHLH) family of transcription fa
28 re identified as homologs of the subgroup lb basic helix-loop-helix (bHLH) genes that are known to re
30 binds DNA as a homo- or heterodimer via its basic helix-loop-helix (bHLH) motif, little is known abo
32 ferentiation is largely under the control of basic Helix-Loop-Helix (bHLH) proneural transcription fa
33 tor 4 (TCF4 also known as ITF2 or E2-2) is a basic helix-loop-helix (bHLH) protein associated with Pi
36 ctional characterization of a plant-specific basic helix-loop-helix (bHLH) protein, FEHLSTART (FST),
37 Phytochrome Interacting Factor 1 (PIF1), a basic helix-loop-helix (bHLH) protein, functions as a ne
38 H1 interacts with and inhibits a DNA binding basic helix-loop-helix (bHLH) protein, HBI1, in Arabidop
41 ging to a family of atypical non-DNA binding basic helix-loop-helix (bHLH) proteins that heterodimeri
44 or both proneural activator (P) proteins and basic helix-loop-helix (bHLH) repressor (R) factors (a "
47 r of Id proteins in pluripotent cells as the basic helix-loop-helix (bHLH) transcription factor (TF)
49 CIENCY-INDUCED TRANSCRIPTION FACTOR (FIT), a basic helix-loop-helix (bHLH) transcription factor (TF),
50 We have identified Noemi, which encodes a basic helix-loop-helix (bHLH) transcription factor and w
52 production depends on the expression of the basic helix-loop-helix (bHLH) transcription factor Atoh1
54 e we demonstrate that mice deficient for the basic helix-loop-helix (bHLH) transcription factor Bhlhe
56 Neurog1 (Ngn1, Neurod3, neurogenin1) is a basic helix-loop-helix (bHLH) transcription factor essen
57 lastine, we identified a jasmonate-regulated basic helix-loop-helix (bHLH) transcription factor from
59 ence of SPARC, as well as the Notch effector basic helix-loop-helix (bHLH) transcription factor hairy
62 , and gibberellin, that inhibit the atypical basic helix-loop-helix (bHLH) transcription factor INCRE
67 Ms23), encoding an anther-specific predicted basic helix-loop-helix (bHLH) transcription factor requi
68 dopsis thaliana) require the function of the basic helix-loop-helix (bHLH) transcription factor SPEEC
71 ikely candidate for Rf4 was GRMZM2G021276, a basic helix-loop-helix (bHLH) transcription factor with
72 utations of TWIST1, which encodes a class II basic helix-loop-helix (bHLH) transcription factor, and
73 end to arise from progenitors expressing the basic helix-loop-helix (bHLH) transcription factor, Atoh
74 show that mutations in lin-22, a Hes-related basic helix-loop-helix (bHLH) transcription factor, incr
76 maize gene male sterility32 (ms32) encodes a basic helix-loop-helix (bHLH) transcription factor, whic
77 sion of achaete-scute homologue 2 (Ascl2)--a basic helix-loop-helix (bHLH) transcription factor--is s
78 terized three genes (NtMYC2a, b, c) encoding basic helix-loop-helix (bHLH) transcription factors (TFs
84 s depends upon the function of the proneural basic helix-loop-helix (bHLH) transcription factors NEUR
85 el, we find that expression of the proneural basic helix-loop-helix (bHLH) transcription factors Neur
89 s, geminin antagonized the ability of neural basic helix-loop-helix (bHLH) transcription factors to a
91 vealed the differential up-regulation of two basic helix-loop-helix (bHLH) transcription factors with
92 e mediated at least partly by regulating two basic helix-loop-helix (bHLH) transcription factors, Neu
95 ate the expression of BARREN STALK1 (BA1), a basic helix-loop-helix (bHLH) transcriptional regulator
97 ell specific genes Sohlh1 and Sohlh2, encode basic helix-loop-helix (bHLH) transcriptional regulators
98 At the core of the network are TFs of the basic helix-loop-helix (bHLH), nuclear factor I (NFI), S
99 The insect juvenile hormone receptor is a basic helix-loop-helix (bHLH), Per-Arnt-Sim (PAS) domain
101 or nuclear translocator (ARNT) belong to the basic helix-loop-helix (bHLH)-PER-ARNT-SIM (PAS) family
102 ility of ARNT itself is modulated by another basic helix-loop-helix (bHLH)-Per-ARNT-SIM (PAS) protein
104 ptor (AhR), a ligand-activated member of the basic helix-loop-helix (bHLH)/PER-ARNT-SIM (PAS) transcr
105 rgets both the anthocyanin pathway genes and basic-helix-loop-helix (bHLH) ANTHOCYANIN1 (AN1), itself
107 regulatory cells in both sexes requires the basic-helix-loop-helix (bHLH) transcription factor HLH-2
108 y the ROOT HAIR DEFECTIVE SIX-LIKE1 (MpRSL1) basic-helix-loop-helix (bHLH) transcription factor, whic
109 eport characterization of two genes encoding basic-helix-loop-helix (bHLH) transcription factors (TFs
110 ppresses oligodendrocyte development through basic-helix-loop-helix (bHLH) transcription factors and
111 e sequential activation of master regulatory basic-helix-loop-helix (bHLH) transcription factors cont
112 Spatial and temporal expression of specific basic-helix-loop-helix (bHLH) transcription factors defi
113 ratio, by controlling the activity of three basic-helix-loop-helix (bHLH) transcription factors of t
115 Inhibitors of DNA binding (IDs) antagonize basic-helix-loop-helix (bHLH) transcription factors to i
116 , in the absence of synaptic excitation, the basic-helix-loop-helix (bHLH)-PAS family transcription f
119 criptional activation by MYB134 and that the basic helix-loop-helix-binding motif of MYB182 was essen
120 scription factor families (zinc finger GATA, basic helix-loop-helix, BTF3/NAC [for basic transcriptio
122 n of transcripts of a MYB PA activator and a basic helix-loop-helix cofactor was observed in MYB182-o
125 cally interact on the MIC-1 promoter via the basic helix-loop-helix domain in DEC1 and the tetrameriz
126 ing specificities, conferred by a C-terminal basic helix-loop-helix domain, which mediates heterodime
133 examine the roles of Phytochrome-Interacting basic helix-loop-helix Factors, PIF1, 3, 4, and 5, in re
134 In addition, we analyzed the expression of basic helix-loop-helix factors, WD40 repeat proteins, an
135 IFs) are members of the Arabidopsis thaliana basic helix-loop-helix family of transcriptional regulat
136 ormed microarray analyses and identified the basic helix-loop-helix family transcription factor Bhlhe
137 PC7 to the Os07g11020 or Rc locus encoding a basic helix-loop-helix family transcription factor by in
138 tissue-specific transcription factor of the basic helix-loop-helix family, and c-Kit, a tyrosine kin
139 Twist transcription factors, members of the basic helix-loop-helix family, play crucial roles in mes
140 onate-inducible transcription factors of the basic helix-loop-helix family, TRITERPENE SAPONIN BIOSYN
141 which encodes a transcription factor of the basic/helix-loop-helix family sufficient to cause hyperp
142 llogenin gene-binding protein (VBP)] and two basic helix-loop-helix leucine zipper (B-HLH-ZIP) [USF (
143 yc homology box II (MBII) and the C-terminal basic helix-loop-helix leucine zipper (bHLH-LZ) domains
144 rophthalmia transcription factor (MITF) is a basic helix-loop-helix leucine zipper (bHLH-Zip) DNA-bin
145 d its obligate transcription partner Mlx are basic helix-loop-helix leucine zipper (bHLHZip) transcri
146 -associated transcription factor (MITF) is a basic helix-loop-helix leucine zipper protein that plays
147 ast, the RTG pathway relies on Rtg1 and Rtg3 basic helix-loop-helix leucine Zipper transcription fact
148 Among ~550 identified screen hits is MLX, a basic helix-loop-helix leucine-zipper transcription fact
149 We report here for the first time that the basic helix-loop-helix-leucine-zip transcription factor
150 he PRE-IBH1-HBI1 tripartite helix-loop-helix/basic helix-loop-helix module is part of a central trans
151 oeolog containing putative binding sites for basic/helix-loop-helix, MYB, and BZIP transcription fact
152 , the zebrafish ortholog of human HES4, is a basic helix-loop-helix-orange transcriptional repressor
154 s a transcription factor that belongs to the basic helix-loop-helix PAS (Per-Arnt-Sim homology domain
156 acid-related orphan receptors (RORs) and the basic helix-loop-helix-PAS transcription factor Npas2 ha
157 transcriptional activator consisting of two basic helix-loop-helix PER-ARNT-SIM (bHLH-PAS) domain pr
158 e clock regulates the sleep-wake cycle via 2 basic helix-loop-helix PER-ARNT-SIM (bHLH-PAS) domain pr
159 endent transcription factor belonging to the basic helix-loop-helix Per-Arnt-Sim (bHLH-PAS) superfami
160 ted transcription factor and a member of the basic helix-loop-helix PER/ARNT/SIM family of chemosenso
161 proteins NPAS1 and NPAS3 are members of the basic helix-loop-helix-PER-ARNT-SIM (bHLH-PAS) family, a
163 regulator required for ear initiation is the basic helix-loop-helix protein BARREN STALK1 (BA1).
164 e interacting factoR3-like5, which encodes a basic helix-loop-helix protein coordinating hormone resp
167 tedly limited in part by binding to both the basic helix-loop-helix protein LONG HYPOCOTYL IN FAR RED
168 skeletal muscle that expresses the myogenic basic helix-loop-helix protein MyoD but fails to undergo
169 a functional 26S proteasome and involves the basic helix-loop-helix protein SPATULA as a key componen
171 beta-catenin through an interaction with the basic helix-loop-helix protein upstream stimulatory tran
172 f Arabidopsis (Arabidopsis thaliana) FAMA, a basic helix-loop-helix protein whose actions during the
175 ve and negative heterodimer partners for the basic-helix-loop-helix protein family and as such contri
176 g ROOT HAIR DEFECTIVE-SIX LIKE (RSL) class I basic helix-loop-helix proteins are expressed in future
177 Here, we show that genes encoding the two basic helix-loop-helix proteins PpSMF1 (SPEECH, MUTE and
179 1 and CEBPbeta recognition of 5mC; and bHLH (basic helix-loop-helix) proteins, exemplified by MAX and
180 ferentiation via induction of GATA-4 and the basic helix-loop-helix TAL1 and that knockdown of both f
183 ed embryos, we identified an auxin-dependent basic Helix Loop Helix transcription factor network that
184 receptors have recently been established as basic helix-loop-helix transcription factor (bHLH)/PAS p
185 erized PP2A substrates is MYC proto-oncogene basic helix-loop-helix transcription factor (MYC), whose
187 ed the C3 promoter and identified that twist basic helix-loop-helix transcription factor 1 (TWIST1) b
188 rther, our data suggest TWIST1 (twist family basic helix-loop-helix transcription factor 1) and SSPN
189 nal stem-cell regulator achaete-scute family basic helix-loop-helix transcription factor 2 (ASCL2), W
190 In this study, we subjected worms lacking basic helix-loop-helix transcription factor 30 (hlh-30),
191 Our previous data suggested that the human basic helix-loop-helix transcription factor achaete-scut
194 Additionally, we have identified Twist1, a basic helix-loop-helix transcription factor and a well-k
198 In the present study we demonstrate that the basic helix-loop-helix transcription factor Atonal homol
200 Evidence is provided that the BR-controlled basic helix-loop-helix transcription factor CESTA (CES)
203 he central regulator of this response is the basic helix-loop-helix transcription factor FER-LIKE IRO
204 novel homozygous frameshift mutation in the basic helix-loop-helix transcription factor gene ARNT2 (
205 um, restricting the expression domain of the basic helix-loop-helix transcription factor gene SPATULA
206 that progesterone-induced expression of the basic helix-loop-helix transcription factor Hand2 in the
210 ays, and 5' RACE identified the prooncogenic basic helix-loop-helix transcription factor ID1 as an IR
211 over, we show that overexpression of the GL3 basic helix-loop-helix transcription factor in A. alpina
215 direct inhibitory interaction with Twist1, a basic helix-loop-helix transcription factor known to inc
217 deficiency-induced TRANSCRIPTION FACTOR1, a basic helix-loop-helix transcription factor necessary fo
223 TOCHROME INTERACTING FACTOR3 (PIF3) is a key basic helix-loop-helix transcription factor of Arabidops
226 a ROOTHAIR DEFECTIVE SIX-LIKE (RSL) class I basic helix-loop-helix transcription factor positively r
231 This recruitment followed the loss from the basic helix-loop-helix transcription factor SPATULA (SPT
232 stomatal lineage cells is controlled by the basic helix-loop-helix transcription factor SPEECHLESS (
234 advanced MDS express high levels of TWIST, a basic helix-loop-helix transcription factor that opposes
235 dy, we demonstrate that Tal1, a Lyl1-related basic helix-loop-helix transcription factor that promote
238 is ascribed to nuclear translocation of the basic helix-loop-helix transcription factor Transcriptio
239 SIGNIFICANCE STATEMENT The importance of the basic helix-loop-helix transcription factor transcriptio
241 nd the Notch target genes Hes-related family basic helix-loop-helix transcription factor with YRPW mo
242 rm breakdown requires the endosperm-specific basic helix-loop-helix transcription factor ZHOUPI.
244 very few olfactory sensory neurons when the basic helix-loop-helix transcription factor, ASCL1 (prev
247 o discover a role in innate immunity for the basic helix-loop-helix transcription factor, HLH-30.
248 The aryl hydrocarbon receptor (AHR) is a basic helix-loop-helix transcription factor, implicated
251 ysically interacts with and phosphorylates a basic helix-loop-helix transcription factor, MYC2, and i
252 he ventral tegmental area that expresses the basic helix-loop-helix transcription factor, Neurogenic
258 hat the expression of neurogenin 2 (Ngn2), a basic helix-loop-helix transcription factor, was signifi
259 Nescient helix-loop-helix-2 (NHLH2) is a basic helix-loop-helix transcription factor, which has b
262 evisiae) two-hybrid screening, we identified basic helix-loop-helix transcription factor05 (bHLH05) a
263 we examined whether four of the subgroup Ib basic helix-loop-helix transcription factors (bHLH38, bH
264 interaction screens identified three related basic helix-loop-helix transcription factors (MYC2, MYC3
266 Stomata formation is induced by a set of basic helix-loop-helix transcription factors and inhibit
268 we have determined that the two Arabidopsis basic helix-loop-helix transcription factors bHLH25 and
269 OP1-SPA) E3 ubiquitin ligase and a subset of basic helix-loop-helix transcription factors called phyt
272 on the restriction of symplastic movement of basic helix-loop-helix transcription factors into neighb
273 onal reprogramming that does not involve the basic helix-loop-helix transcription factors MYC2 and re
274 interactions between BTS and PYE-like (PYEL) basic helix-loop-helix transcription factors occur withi
276 the stability of MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that additi
277 sting New Gene (RING) domain, interacts with basic helix-loop-helix transcription factors that are ca
278 e mutant lacking MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that are kn
279 ME-INTERACTING FACTORS (PIFs) are a group of basic helix-loop-helix transcription factors that can ph
280 ecific module is a set of "master regulator" basic helix-loop-helix transcription factors that regula
282 interacting factors (PIFs), a small group of basic helix-loop-helix transcription factors, repress ph
283 uce rapid phosphorylation and degradation of basic helix-loop-helix transcription factors, such as PH
284 lysis of a family of antagonistically acting basic helix-loop-helix transcription factors, the PHYTOC
289 MPK3 and MPK6 can phosphorylate ICE1, a basic-helix-loop-helix transcription factor that regulat
290 both mouse and zebrafish illustrate that the basic-helix-loop-helix transcription factor, Hand2, is c
291 with increasing altitude is controlled by a basic/helix-loop-helix transcription factor (bHLH TF), M
292 ted B cell factor-1 (ABF-1), which encodes a basic helix-loop-helix transcriptional repressor, partic
296 esis in M. truncatula and a component of MYB-basic helix loop helix-WD40 (MBW) activator complexes.
297 ranscription factors including a central MYB-basic helix-loop-helix-WD40 complex containing WEREWOLF
298 rray and RNAi-based approaches and found the basic helix-loop-helix ZIP transcription factor AP4 to h
299 re2 cleavage does not require the N-terminal basic helix-loop-helix zipper transcription factor domai