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1 terized this transcription factor, flowering basic helix-loop-helix 1 (FBH1) that binds in vivo to th
2 melanogaster, achaete (ac) and m8 are model basic helix-loop-helix activator (bHLH A) and repressor
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
9 orylation and degradation of phy-interacting basic Helix Loop Helix (bHLH) transcription factors (PIF
10 G1) from Arabidopsis thaliana and associated basic helix-loop-helix (bHLH) and MYB transcription fact
11 in enhanced mRNA and protein expression of a basic helix-loop-helix (bHLH) class myogenic determinati
12 g specificities of 19 Caenorhabditis elegans basic helix-loop-helix (bHLH) dimers using protein bindi
13 ansporter 1 is actually a membrane-localized basic helix-loop-helix (bHLH) DNA-binding transcription
14 lar to other species' HIF-1, HdHIF-1 has one basic helix-loop-helix (bHLH) domain and two Per-Arnt-Si
15 ze R2R3-MYB regulator C1 cooperates with the basic helix-loop-helix (bHLH) factor R to activate the e
19 ment, proneural transcription factors of the basic helix-loop-helix (bHLH) family are required to com
20 reventing DNA binding of activators from the basic helix-loop-helix (bHLH) family of TFs to CAGGTG E-
21 NTERACTING FACTORs (PIFs) are members of the basic helix-loop-helix (bHLH) family of transcription fa
25 s that are expressed within PCs, such as the basic helix-loop-helix (bHLH) gene mouse atonal homolog
26 re identified as homologs of the subgroup lb basic helix-loop-helix (bHLH) genes that are known to re
28 binds DNA as a homo- or heterodimer via its basic helix-loop-helix (bHLH) motif, little is known abo
30 ferentiation is largely under the control of basic Helix-Loop-Helix (bHLH) proneural transcription fa
31 tor 4 (TCF4 also known as ITF2 or E2-2) is a basic helix-loop-helix (bHLH) protein associated with Pi
34 ctional characterization of a plant-specific basic helix-loop-helix (bHLH) protein, FEHLSTART (FST),
35 Phytochrome Interacting Factor 1 (PIF1), a basic helix-loop-helix (bHLH) protein, functions as a ne
36 H1 interacts with and inhibits a DNA binding basic helix-loop-helix (bHLH) protein, HBI1, in Arabidop
39 ms of seed pod shattering has shown that the basic helix-loop-helix (bHLH) proteins INDEHISCENT and A
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 "
48 production depends on the expression of the basic helix-loop-helix (bHLH) transcription factor Atoh1
50 e we demonstrate that mice deficient for the basic helix-loop-helix (bHLH) transcription factor Bhlhe
51 Neurog1 (Ngn1, Neurod3, neurogenin1) is a basic helix-loop-helix (bHLH) transcription factor essen
52 lastine, we identified a jasmonate-regulated basic helix-loop-helix (bHLH) transcription factor from
54 ence of SPARC, as well as the Notch effector basic helix-loop-helix (bHLH) transcription factor hairy
58 , and gibberellin, that inhibit the atypical basic helix-loop-helix (bHLH) transcription factor INCRE
63 Ms23), encoding an anther-specific predicted basic helix-loop-helix (bHLH) transcription factor requi
64 dopsis thaliana) require the function of the basic helix-loop-helix (bHLH) transcription factor SPEEC
66 utations of TWIST1, which encodes a class II basic helix-loop-helix (bHLH) transcription factor, and
67 end to arise from progenitors expressing the basic helix-loop-helix (bHLH) transcription factor, Atoh
68 show that mutations in lin-22, a Hes-related basic helix-loop-helix (bHLH) transcription factor, incr
69 maize gene male sterility32 (ms32) encodes a basic helix-loop-helix (bHLH) transcription factor, whic
70 sion of achaete-scute homologue 2 (Ascl2)--a basic helix-loop-helix (bHLH) transcription factor--is s
72 terized three genes (NtMYC2a, b, c) encoding basic helix-loop-helix (bHLH) transcription factors (TFs
78 s depends upon the function of the proneural basic helix-loop-helix (bHLH) transcription factors NEUR
79 el, we find that expression of the proneural basic helix-loop-helix (bHLH) transcription factors Neur
83 s, geminin antagonized the ability of neural basic helix-loop-helix (bHLH) transcription factors to a
85 vealed the differential up-regulation of two basic helix-loop-helix (bHLH) transcription factors with
86 e mediated at least partly by regulating two basic helix-loop-helix (bHLH) transcription factors, Neu
88 ate the expression of BARREN STALK1 (BA1), a basic helix-loop-helix (bHLH) transcriptional regulator
90 ell specific genes Sohlh1 and Sohlh2, encode basic helix-loop-helix (bHLH) transcriptional regulators
91 At the core of the network are TFs of the basic helix-loop-helix (bHLH), nuclear factor I (NFI), S
92 The insect juvenile hormone receptor is a basic helix-loop-helix (bHLH), Per-Arnt-Sim (PAS) domain
94 or nuclear translocator (ARNT) belong to the basic helix-loop-helix (bHLH)-PER-ARNT-SIM (PAS) family
96 ility of ARNT itself is modulated by another basic helix-loop-helix (bHLH)-Per-ARNT-SIM (PAS) protein
98 ptor (AhR), a ligand-activated member of the basic helix-loop-helix (bHLH)/PER-ARNT-SIM (PAS) transcr
99 rgets both the anthocyanin pathway genes and basic-helix-loop-helix (bHLH) ANTHOCYANIN1 (AN1), itself
100 regulatory cells in both sexes requires the basic-helix-loop-helix (bHLH) transcription factor HLH-2
102 eport characterization of two genes encoding basic-helix-loop-helix (bHLH) transcription factors (TFs
103 ppresses oligodendrocyte development through basic-helix-loop-helix (bHLH) transcription factors and
104 e sequential activation of master regulatory basic-helix-loop-helix (bHLH) transcription factors cont
105 Spatial and temporal expression of specific basic-helix-loop-helix (bHLH) transcription factors defi
106 ratio, by controlling the activity of three basic-helix-loop-helix (bHLH) transcription factors of t
107 Inhibitors of DNA binding (IDs) antagonize basic-helix-loop-helix (bHLH) transcription factors to i
110 criptional activation by MYB134 and that the basic helix-loop-helix-binding motif of MYB182 was essen
111 scription factor families (zinc finger GATA, basic helix-loop-helix, BTF3/NAC [for basic transcriptio
113 n of transcripts of a MYB PA activator and a basic helix-loop-helix cofactor was observed in MYB182-o
116 cally interact on the MIC-1 promoter via the basic helix-loop-helix domain in DEC1 and the tetrameriz
118 F, the Drosophila ortholog of the vertebrate basic helix-loop-helix domain-encoding genes capsulin an
124 examine the roles of Phytochrome-Interacting basic helix-loop-helix Factors, PIF1, 3, 4, and 5, in re
125 ptor (AhR), a ligand-activated member of the basic helix-loop-helix family of transcription factors,
126 IFs) are members of the Arabidopsis thaliana basic helix-loop-helix family of transcriptional regulat
127 ormed microarray analyses and identified the basic helix-loop-helix family transcription factor Bhlhe
128 PC7 to the Os07g11020 or Rc locus encoding a basic helix-loop-helix family transcription factor by in
129 tissue-specific transcription factor of the basic helix-loop-helix family, and c-Kit, a tyrosine kin
130 Twist transcription factors, members of the basic helix-loop-helix family, play crucial roles in mes
131 onate-inducible transcription factors of the basic helix-loop-helix family, TRITERPENE SAPONIN BIOSYN
132 which encodes a transcription factor of the basic/helix-loop-helix family sufficient to cause hyperp
133 llogenin gene-binding protein (VBP)] and two basic helix-loop-helix leucine zipper (B-HLH-ZIP) [USF (
134 yc homology box II (MBII) and the C-terminal basic helix-loop-helix leucine zipper (bHLH-LZ) domains
135 rophthalmia transcription factor (MITF) is a basic helix-loop-helix leucine zipper (bHLH-Zip) DNA-bin
136 srupt the dimeric complex formed between its basic helix-loop-helix leucine zipper (bHLHZip) domain a
137 d its obligate transcription partner Mlx are basic helix-loop-helix leucine zipper (bHLHZip) transcri
138 Myc, Mad, and Max proteins belong to the basic helix-loop-helix leucine zipper family of transcri
139 -associated transcription factor (MITF) is a basic helix-loop-helix leucine zipper protein that plays
140 ast, the RTG pathway relies on Rtg1 and Rtg3 basic helix-loop-helix leucine Zipper transcription fact
142 We report here for the first time that the basic helix-loop-helix-leucine-zip transcription factor
143 he PRE-IBH1-HBI1 tripartite helix-loop-helix/basic helix-loop-helix module is part of a central trans
144 oeolog containing putative binding sites for basic/helix-loop-helix, MYB, and BZIP transcription fact
146 s a transcription factor that belongs to the basic helix-loop-helix PAS (Per-Arnt-Sim homology domain
148 acid-related orphan receptors (RORs) and the basic helix-loop-helix-PAS transcription factor Npas2 ha
149 transcriptional activator consisting of two basic helix-loop-helix PER-ARNT-SIM (bHLH-PAS) domain pr
150 hat Singleminded-2s (SIM2s), a member of the basic helix-loop-helix Per-Arnt-Sim (bHLH/PAS) family of
151 carbon receptor (AhR) is a ligand-dependent, basic helix-loop-helix Per-Arnt-Sim (PAS)-containing tra
153 ted transcription factor and a member of the basic helix-loop-helix PER/ARNT/SIM family of chemosenso
154 proteins NPAS1 and NPAS3 are members of the basic helix-loop-helix-PER-ARNT-SIM (bHLH-PAS) family, a
155 uclear translocator (ARNT) is a promiscuous, basic helix-loop-helix Period/ARNT/Single-minded protein
156 or or xenobiotic receptor is a member of the basic helix-loop-helix/period AhR nuclear translocator s
157 regulator required for ear initiation is the basic helix-loop-helix protein BARREN STALK1 (BA1).
159 e interacting factoR3-like5, which encodes a basic helix-loop-helix protein coordinating hormone resp
162 tedly limited in part by binding to both the basic helix-loop-helix protein LONG HYPOCOTYL IN FAR RED
163 skeletal muscle that expresses the myogenic basic helix-loop-helix protein MyoD but fails to undergo
164 a functional 26S proteasome and involves the basic helix-loop-helix protein SPATULA as a key componen
166 beta-catenin through an interaction with the basic helix-loop-helix protein upstream stimulatory tran
167 f Arabidopsis (Arabidopsis thaliana) FAMA, a basic helix-loop-helix protein whose actions during the
171 ve and negative heterodimer partners for the basic-helix-loop-helix protein family and as such contri
172 g ROOT HAIR DEFECTIVE-SIX LIKE (RSL) class I basic helix-loop-helix proteins are expressed in future
173 Here, we show that genes encoding the two basic helix-loop-helix proteins PpSMF1 (SPEECH, MUTE and
174 anscription regulator complex, including the basic helix-loop-helix proteins SCL/TAL1 and E47, the zi
177 ferentiation via induction of GATA-4 and the basic helix-loop-helix TAL1 and that knockdown of both f
179 ed the C3 promoter and identified that twist basic helix-loop-helix transcription factor 1 (TWIST1) b
180 rther, our data suggest TWIST1 (twist family basic helix-loop-helix transcription factor 1) and SSPN
181 nal stem-cell regulator achaete-scute family basic helix-loop-helix transcription factor 2 (ASCL2), W
182 Our previous data suggested that the human basic helix-loop-helix transcription factor achaete-scut
185 Up-regulation of Pr specifically activated a basic helix-loop-helix transcription factor and a subset
187 Additionally, we have identified Twist1, a basic helix-loop-helix transcription factor and a well-k
192 In the present study we demonstrate that the basic helix-loop-helix transcription factor Atonal homol
194 Evidence is provided that the BR-controlled basic helix-loop-helix transcription factor CESTA (CES)
198 4 (ID4) is a member of the dominant-negative basic helix-loop-helix transcription factor family that
199 he central regulator of this response is the basic helix-loop-helix transcription factor FER-LIKE IRO
200 rm line, alpha) encodes a germ cell-specific basic helix-loop-helix transcription factor first identi
201 novel homozygous frameshift mutation in the basic helix-loop-helix transcription factor gene ARNT2 (
202 um, restricting the expression domain of the basic helix-loop-helix transcription factor gene SPATULA
203 that progesterone-induced expression of the basic helix-loop-helix transcription factor Hand2 in the
207 ays, and 5' RACE identified the prooncogenic basic helix-loop-helix transcription factor ID1 as an IR
211 direct inhibitory interaction with Twist1, a basic helix-loop-helix transcription factor known to inc
212 ecent studies demonstrate that the proneural basic helix-loop-helix transcription factor Mash1 is req
214 deficiency-induced TRANSCRIPTION FACTOR1, a basic helix-loop-helix transcription factor necessary fo
221 TOCHROME INTERACTING FACTOR3 (PIF3) is a key basic helix-loop-helix transcription factor of Arabidops
223 that Hey2, a hairy/enhancer-of-split-related basic helix-loop-helix transcription factor often believ
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
233 stomatal lineage cells is controlled by the basic helix-loop-helix transcription factor SPEECHLESS (
236 advanced MDS express high levels of TWIST, a basic helix-loop-helix transcription factor that opposes
239 SIGNIFICANCE STATEMENT The importance of the basic helix-loop-helix transcription factor transcriptio
242 rm breakdown requires the endosperm-specific basic helix-loop-helix transcription factor ZHOUPI.
243 ivo with the PHYTOCHROME INTERACTING FACTOR3 basic helix-loop-helix transcription factor, and this in
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
252 ysically interacts with and phosphorylates a basic helix-loop-helix transcription factor, MYC2, and i
253 he ventral tegmental area that expresses the basic helix-loop-helix transcription factor, Neurogenic
259 hat the expression of neurogenin 2 (Ngn2), a basic helix-loop-helix transcription factor, was signifi
260 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
270 loop-helix protein that heterodimerizes with basic helix-loop-helix transcription factors inhibiting
271 on the restriction of symplastic movement of basic helix-loop-helix transcription factors into neighb
272 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
277 the stability of MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that additi
278 sting New Gene (RING) domain, interacts with basic helix-loop-helix transcription factors that are ca
279 e mutant lacking MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that are kn
280 ecific module is a set of "master regulator" basic helix-loop-helix transcription factors that regula
282 a(1B)-adrenergic receptor subtype, proneural basic helix-loop-helix transcription factors, and the di
284 interacting factors (PIFs), a small group of basic helix-loop-helix transcription factors, repress ph
285 uce rapid phosphorylation and degradation of basic helix-loop-helix transcription factors, such as PH
286 lysis of a family of antagonistically acting basic helix-loop-helix transcription factors, the PHYTOC
292 MPK3 and MPK6 can phosphorylate ICE1, a basic-helix-loop-helix transcription factor that regulat
293 both mouse and zebrafish illustrate that the basic-helix-loop-helix transcription factor, Hand2, is c
294 ted B cell factor-1 (ABF-1), which encodes a basic helix-loop-helix transcriptional repressor, partic
297 esis in M. truncatula and a component of MYB-basic helix loop helix-WD40 (MBW) activator complexes.
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
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