ライフサイエンスコーパス: helix-loop-helix

1 d this transcription factor, flowering basic helix-loop-helix 1 (FBH1) that binds in vivo to the prom

2 at protein and transcript levels of nescient helix loop helix 2 (NHLH2) and the prohormone convertase

3 ow that the Caenorhabditis elegans E-protein helix-loop-helix-2 (HLH-2) functions as a homodimer in d

4 three closest homologs of ILR3 (i.e., basic-helix-loop-helix 34 [bHLH34], bHLH104, and bHLH115).

5 As demonstrated for the basic helix-loop-helix and homeodomain TF families, our TFBSsh

6 Interestingly, the basic helix-loop-helix and NAC proteins showed developmental p

7 3), bZIP (basic-leucine zipper), bHLH (basic helix-loop-helix) and SBP (SQUAMOSA promoter binding pro

8 cription factors composed of R2R3 MYB, basic helix-loop-helix, and WD40 proteins that activate the pr

9 The PRE-IBH1-HBI1 tripartite helix-loop-helix/basic helix-loop-helix module is part o

10 ion and degradation of phy-interacting basic Helix Loop Helix (bHLH) transcription factors (PIFs), su

11 o be activated by a triad of R2R3-MYB, basic helix-loop helix (bHLH) and WD40 transcription factors (

12 otein (SSBP) cofactors and DNA-binding basic helix-loop-helix (bHLH) and GATA transcription factors.

13 om Arabidopsis thaliana and associated basic helix-loop-helix (bHLH) and MYB transcription factors ac

14 both the anthocyanin pathway genes and basic-helix-loop-helix (bHLH) ANTHOCYANIN1 (AN1), itself an es

15 s constitute a subclass (VIIIc) of the basic helix-loop-helix (bHLH) class VIII transcription factor

16 TCF4 contains a C-terminal basic-helix-loop-helix (bHLH) DNA binding domain which recogni

17 ter 1 is actually a membrane-localized basic helix-loop-helix (bHLH) DNA-binding transcription factor

18 other species' HIF-1, HdHIF-1 has one basic helix-loop-helix (bHLH) domain and two Per-Arnt-Sim (PAS

19 re, Gsx2 physically interacts with the basic helix-loop-helix (bHLH) domain of Ascl1, and DNA-binding

20 Notch signaling regulates basic helix-loop-helix (bHLH) factors as an evolutionarily con

21 It is unclear how these two basic helix-loop-helix (bHLH) factors mediate such fundamental

22 proneural transcription factors of the basic helix-loop-helix (bHLH) family are required to commit ce

23 The basic helix-loop-helix (bHLH) family of transcription factors

24 TING FACTORs (PIFs) are members of the basic helix-loop-helix (bHLH) family of transcription factors

25 We analyzed the basic helix-loop-helix (bHLH) family of transcription factors,

26 MXD family transcription factor of the basic helix-loop-helix (bHLH) family.

27 ntified as homologs of the subgroup lb basic helix-loop-helix (bHLH) genes that are known to regulate

28 The transcription factor (TF) basic/Helix-Loop-Helix (bHLH) is important for plant growth, d

29 We hypothesized that basic helix-loop-helix (bHLH) MIST1 (BHLHA15) is a "scaling fa

30 DNA as a homo- or heterodimer via its basic helix-loop-helix (bHLH) motif, little is known about the

31 We show here that the Ascl1 and Neurog basic helix-loop-helix (bHLH) proneural factors are expressed

32 iation is largely under the control of basic Helix-Loop-Helix (bHLH) proneural transcription factors

33 (TCF4 also known as ITF2 or E2-2) is a basic helix-loop-helix (bHLH) protein associated with Pitt-Hop

34 Expression of the basic helix-loop-helix (bHLH) protein NeuroD1 is restricted to

35 Functional analysis of the basic helix-loop-helix (bHLH) protein SPEECHLESS, one of three

36 l characterization of a plant-specific basic helix-loop-helix (bHLH) protein, FEHLSTART (FST), a defe

37 eracts with and inhibits a DNA binding basic helix-loop-helix (bHLH) protein, HBI1, in Arabidopsis th

38 Its expression is induced by the basic helix-loop-helix (bHLH) protein, Pho4p, in response to p

39 The basic Helix-Loop-Helix (bHLH) proteins represent a well-known

40 Basic helix-loop-helix (bHLH) proteins, which are characterize

41 h proneural activator (P) proteins and basic helix-loop-helix (bHLH) repressor (R) factors (a "P+R" r

42 of chromatin binding of members of the basic helix-loop-helix (bHLH) TF family.

43 In the dorsal spinal cord, Ptf1a, a basic helix-loop-helix (bHLH) transcription activator, maintai

44 d proteins in pluripotent cells as the basic helix-loop-helix (bHLH) transcription factor (TF) E2A.

45 Atoh1, a basic helix-loop-helix (bHLH) transcription factor (TF), is es

46 -INDUCED TRANSCRIPTION FACTOR (FIT), a basic helix-loop-helix (bHLH) transcription factor (TF), regul

47 have identified Noemi, which encodes a basic helix-loop-helix (bHLH) transcription factor and which c

48 We identified a basic helix-loop-helix (bHLH) transcription factor at chickpea

49 ction depends on the expression of the basic helix-loop-helix (bHLH) transcription factor Atoh1.

50 emonstrate that mice deficient for the basic helix-loop-helix (bHLH) transcription factor Bhlhe40 (Bh

51 Here, we showed that the basic Helix-Loop-Helix (bHLH) transcription factor Cucumis sat

52 e, we identified a jasmonate-regulated basic helix-loop-helix (bHLH) transcription factor from clade

53 We show that basic helix-loop-helix (bHLH) transcription factor genes repre

54 The basic helix-loop-helix (bHLH) transcription factor Hand2 has b

55 atory cells in both sexes requires the basic-helix-loop-helix (bHLH) transcription factor HLH-2, the

56 Here, we identify the basic helix-loop-helix (bHLH) transcription factor homolog of

57 gibberellin, that inhibit the atypical basic helix-loop-helix (bHLH) transcription factor INCREASED L

58 The basic helix-loop-helix (bHLH) transcription factor Math5 (Atoh

59 The Wnt-regulated basic helix-loop-helix (bHLH) transcription factor mesogenin 1

60 encoding an anther-specific predicted basic helix-loop-helix (bHLH) transcription factor required fo

61 thaliana) require the function of the basic helix-loop-helix (bHLH) transcription factor SPEECHLESS

62 Atonal homolog 1 (Atoh1) is a basic helix-loop-helix (bHLH) transcription factor that is ess

63 We show that a basic helix-loop-helix (bHLH) transcription factor Upstream Re

64 candidate for Rf4 was GRMZM2G021276, a basic helix-loop-helix (bHLH) transcription factor with tassel

65 ns of TWIST1, which encodes a class II basic helix-loop-helix (bHLH) transcription factor, and causes

66 arise from progenitors expressing the basic helix-loop-helix (bHLH) transcription factor, Atoh7, whi

67 hat mutations in lin-22, a Hes-related basic helix-loop-helix (bHLH) transcription factor, increase s

68 Here, we show that NeuroD2, a neuronal basic helix-loop-helix (bHLH) transcription factor, promotes t

69 gene male sterility32 (ms32) encodes a basic helix-loop-helix (bHLH) transcription factor, which func

70 ROOT HAIR DEFECTIVE SIX-LIKE1 (MpRSL1) basic-helix-loop-helix (bHLH) transcription factor, which is d

71 f achaete-scute homologue 2 (Ascl2)--a basic helix-loop-helix (bHLH) transcription factor--is selecti

72 d three genes (NtMYC2a, b, c) encoding basic helix-loop-helix (bHLH) transcription factors (TFs) whos

73 characterization of two genes encoding basic-helix-loop-helix (bHLH) transcription factors (TFs), NtM

74 ential activation of master regulatory basic-helix-loop-helix (bHLH) transcription factors controls t

75 Members of the group XI basic helix-loop-helix (bHLH) transcription factors encoded by

76 Class I Basic Helix-Loop-Helix (bHLH) transcription factors form homod

77 We show that myogenic basic helix-loop-helix (bHLH) transcription factors induce myo

78 Here, we have identified basic helix-loop-helix (bHLH) transcription factors Neurod2 an

79 , by controlling the activity of three basic-helix-loop-helix (bHLH) transcription factors of the PHY

80 Basic-helix-loop-helix (bHLH) transcription factors play an im

81 Basic helix-loop-helix (bHLH) transcription factors recognize

82 Core basic helix-loop-helix (bHLH) transcription factors regulating

83 This includes the basic helix-loop-helix (bHLH) transcription factors SPEECHLESS

84 inin antagonized the ability of neural basic helix-loop-helix (bHLH) transcription factors to activat

85 Basic helix-loop-helix (bHLH) transcription factors were reduc

86 the differential up-regulation of two basic helix-loop-helix (bHLH) transcription factors with predi

87 ated at least partly by regulating two basic helix-loop-helix (bHLH) transcription factors, Neurog1 a

88 CHROME INTERACTING FACTORs, a group of basic helix-loop-helix (bHLH) transcription factors.

89 Here we report interactions between basic helix-loop-helix (bHLH) transcriptional activators and t

90 e expression of BARREN STALK1 (BA1), a basic helix-loop-helix (bHLH) transcriptional regulator necess

91 The proneural basic helix-loop-helix (bHLH) transcriptional regulators are k

92 the core of the network are TFs of the basic helix-loop-helix (bHLH), nuclear factor I (NFI), SOX, an

93 insect juvenile hormone receptor is a basic helix-loop-helix (bHLH), Per-Arnt-Sim (PAS) domain prote

94 he absence of synaptic excitation, the basic-helix-loop-helix (bHLH)-PAS family transcription factor

95 lear translocator (ARNT) belong to the basic helix-loop-helix (bHLH)-PER-ARNT-SIM (PAS) family of tra

96 of ARNT itself is modulated by another basic helix-loop-helix (bHLH)-Per-ARNT-SIM (PAS) protein, the

97 The MYB- basic helix-loop-helix (bHLH)-WD40 complexes regulating anthoc

98 AhR), a ligand-activated member of the basic helix-loop-helix (bHLH)/PER-ARNT-SIM (PAS) transcription

99 The MBW (for R2R3MYB, basic helix-loop-helix [bHLH], and WD40) genes comprise an evo

100 onal activation by MYB134 and that the basic helix-loop-helix-binding motif of MYB182 was essential f

101 ion factor families (zinc finger GATA, basic helix-loop-helix, BTF3/NAC [for basic transcription fact

102 hrome 2 (Cry2)/cryptochrome-interacting beta helix-loop-helix (CIB), a blue light-activated protein-p

103 nal domain of cryptochrome-interacting basic-helix-loop-helix (CIBN).

104 ranscripts of a MYB PA activator and a basic helix-loop-helix cofactor was observed in MYB182-overexp

105 omoters, but only in the presence of a basic helix-loop-helix cofactor.

106 factor belonging to the superfamily of basic-helix-loop-helix DNA-binding proteins.

107 mapped the interaction interface to the MYC helix-loop-helix domain and a novel 15-residue MYC-bindi

108 toplasmatic structural triad composed by the Helix-Loop-Helix domain, the S2-S3 linker, and the TRP d

109 ecificities, conferred by a C-terminal basic helix-loop-helix domain, which mediates heterodimerizati

110 The basic helix-loop-helix domain-containing transcription factors

111 regions, either side of the conserved basic Helix-Loop-Helix domain.

112 Shared usage of basic helix-loop-helix E proteins as transcriptional drivers u

113 ionally and computationally designed site II helix-loop-helix epitope-scaffold vaccines distinguished

114 ges at the ligand-binding site to the remote helix-loop-helix extension.

115 to DNA by binding to the hematopoietic basic helix-loop-helix factors Scl/Tal1 or Lyl1.

116 Recently, we revealed that basic helix-loop-helix factors, HECATEs (HECs), function as po

117 e the roles of Phytochrome-Interacting basic helix-loop-helix Factors, PIF1, 3, 4, and 5, in relaying

118 ddition, we analyzed the expression of basic helix-loop-helix factors, WD40 repeat proteins, and MYB2

119 re members of the Arabidopsis thaliana basic helix-loop-helix family of transcriptional regulators th

120 encodes a transcription factor of the basic/helix-loop-helix family sufficient to cause hyperplasia.

121 microarray analyses and identified the basic helix-loop-helix family transcription factor Bhlhe40 as

122 e-specific transcription factor of the basic helix-loop-helix family, and c-Kit, a tyrosine kinase re

123 transcription factors, members of the basic helix-loop-helix family, play crucial roles in mesoderm

124 inducible transcription factors of the basic helix-loop-helix family, TRITERPENE SAPONIN BIOSYNTHESIS

125 ily of plant defense peptides that share the helix-loop-helix fold stabilized by two disulfide bridge

126 f the secondary structure topology into a CS helix-loop-helix fold.

127 ers of the inhibitor of differentiation (ID) helix-loop-helix gene family.

128 e yet to be elucidated, although a predicted helix-loop-helix (H-L-H) was suggested to form pores by

129 ocator (ARNT) protein, occurring through the Helix-Loop-Helix (HLH) and PER-ARNT-SIM (PAS) domains, i

130 We demonstrate that the helix-loop-helix (HLH) protein Extramacrochaetae (Emc) r

131 Id1, a helix-loop-helix (HLH) protein that inhibits the functio

132 We demonstrate that the helix-loop-helix (HLH) protein, HEB, directly associates

133 Helix-loop-helix (HLH) proteins are dimeric transcriptio

134 e expression and function of the Id3 and E2A helix-loop-helix (HLH) proteins.

135 Neurogenin-3 (NEUROG3) is a helix-loop-helix (HLH) transcription factor involved in

136 of extramacrochaetae (emc), which encodes a helix-loop-helix (HLH) transcription factor.

137 Here, we identify a network of helix-loop-helix (HLH) transcriptional regulators contro

138 ppress the expression of a common downstream helix-loop-helix (HLH)/bHLH network, thus forming an inc

139 ining the structure of MerFt, the 60-residue helix-loop-helix integral membrane core of the 81-residu

140 in gene-binding protein (VBP)] and two basic helix-loop-helix leucine zipper (B-HLH-ZIP) [USF (upstre

141 ology box II (MBII) and the C-terminal basic helix-loop-helix leucine zipper (bHLH-LZ) domains of the

142 almia transcription factor (MITF) is a basic helix-loop-helix leucine zipper (bHLH-Zip) DNA-binding p

143 obligate transcription partner Mlx are basic helix-loop-helix leucine zipper (bHLHZip) transcription

144 he RTG pathway relies on Rtg1 and Rtg3 basic helix-loop-helix leucine Zipper transcription factors.

145 ~550 identified screen hits is MLX, a basic helix-loop-helix leucine-zipper transcription factor tha

146 eport here for the first time that the basic helix-loop-helix-leucine-zip transcription factor upstre

147 an be generated by tandem repeating a simple helix-loop-helix-loop structural motif.

148 -IBH1-HBI1 tripartite helix-loop-helix/basic helix-loop-helix module is part of a central transcripti

149 In both cases, the dimer is stabilized by a helix-loop-helix motif at the C terminus and interaction

150 rts the first two helices and the associated helix-loop-helix motif into a continuous alpha-helix, as

151 The examination of the helix-loop-helix motif observed in the core protein stru

152 c core domain and C-terminal domain adopts a helix-loop-helix motif that is similar to the correspond

153 t both Fis1 and the second helix of the Mdv1 helix-loop-helix motif.

154 que tetrameric organization composed of four helix-loop-helix motifs.

155 y an N-terminal region including a predicted helix-loop-helix motive.

156 containing putative binding sites for basic/helix-loop-helix, MYB, and BZIP transcription factors.

157 zebrafish ortholog of human HES4, is a basic helix-loop-helix-orange transcriptional repressor that r

158 anscription factor that belongs to the basic helix-loop-helix PAS (Per-Arnt-Sim homology domain) fami

159 The basic helix-loop-helix PAS domain (bHLH-PAS) transcription fac

160 criptional activator consisting of two basic helix-loop-helix PER-ARNT-SIM (bHLH-PAS) domain protein

161 k regulates the sleep-wake cycle via 2 basic helix-loop-helix PER-ARNT-SIM (bHLH-PAS) domain proteins

162 transcription factor belonging to the basic helix-loop-helix Per-Arnt-Sim (bHLH-PAS) superfamily.

163 anscription factor and a member of the basic helix-loop-helix PER/ARNT/SIM family of chemosensors and

164 ins NPAS1 and NPAS3 are members of the basic helix-loop-helix-PER-ARNT-SIM (bHLH-PAS) family, and the

165 and interact with a family of negative basic helix-loop-helix PIF regulators.

166 Basic helix-loop-helix protein E2-2 is defined as an essential

167 Loss of the helix-loop-helix protein Extramacrochaetae (Emc) leads t

168 d negative regulators from the MYB and basic helix-loop-helix protein families.

169 negative heterodimer partners for the basic-helix-loop-helix protein family and as such contribute t

170 ith increased expression of the inhibitor of helix-loop-helix protein Id2.

171 tal muscle that expresses the myogenic basic helix-loop-helix protein MyoD but fails to undergo termi

172 Atonal homolog1 (Atoh1) encodes a basic helix-loop-helix protein that is the first transcription

173 The basic helix-loop-helix protein, oligodendrocyte transcription

174 HAIR DEFECTIVE-SIX LIKE (RSL) class I basic helix-loop-helix proteins are expressed in future root h

175 roaches, we discovered that the Id family of helix-loop-helix proteins is both necessary and sufficie

176 e, we show that genes encoding the two basic helix-loop-helix proteins PpSMF1 (SPEECH, MUTE and FAMA-

177 The basic helix-loop-helix proteins, Ino2p and Ino4p, mediated thi

178 CEBPbeta recognition of 5mC; and bHLH (basic helix-loop-helix) proteins, exemplified by MAX and TCF4

179 a previously undescribed fold, consisting of helix-loop-helix repeats arranged into an overall cresce

180 The spermatogenesis/oogenesis helix-loop-helix (SOHLH) proteins SOHLH1 and SOHLH2 play

181 is a well-characterized, approximately 24-aa helix-loop-helix structure on the RSV fusion (F) protein

182 omain of TbTRF, which folds into a canonical helix-loop-helix structure that is conserved to the Myb

183 internal surface of the membrane and forms a helix-loop-helix structure without crossing it.

184 l homodimer with each protomer folded into a helix-loop-helix structure.

185 Similar to PDZ2, we have identified a helix-loop-helix subdomain coupled to the canonical PDZ1

186 iation via induction of GATA-4 and the basic helix-loop-helix TAL1 and that knockdown of both factors

187 nin oxidase/dehydrogenase (CKX1) and a basic Helix-Loop-Helix TF (bHLH476).

188 elopment required interaction with the basic helix-loop-helix TF Hand2.

189 ryos, we identified an auxin-dependent basic Helix Loop Helix transcription factor network that media

190 actor 1 (cEbf1) is a member of EBF family of helix loop helix transcription factors.

191 increasing altitude is controlled by a basic/helix-loop-helix transcription factor (bHLH TF), MdbHLH3

192 tors have recently been established as basic helix-loop-helix transcription factor (bHLH)/PAS protein

193 PP2A substrates is MYC proto-oncogene basic helix-loop-helix transcription factor (MYC), whose overe

194 The basic helix-loop-helix transcription factor (TF) Bhlhe40 is em

195 liana by overexpression of a codon-optimized helix-loop-helix transcription factor (VvCEB1(opt) ) fro

196 C3 promoter and identified that twist basic helix-loop-helix transcription factor 1 (TWIST1) binds t

197 our data suggest TWIST1 (twist family basic helix-loop-helix transcription factor 1) and SSPN (sarco

198 em-cell regulator achaete-scute family basic helix-loop-helix transcription factor 2 (ASCL2), Wnt/bet

199 this study, we subjected worms lacking basic helix-loop-helix transcription factor 30 (hlh-30), the C

200 HEYL, a basic helix-loop-helix transcription factor and a direct targe

201 Previously, we showed that DEC1, a basic helix-loop-helix transcription factor and a target of p5

202 tionally, we have identified Twist1, a basic helix-loop-helix transcription factor and a well-known E

203 The basic helix-loop-helix transcription factor AP4/TFAP4/AP-4 is

204 in cells whose production requires the basic helix-loop-helix transcription factor Atoh1.

205 present study we demonstrate that the basic helix-loop-helix transcription factor Atonal homolog 8 (

206 Here, we identified a key basic helix-loop-helix transcription factor called NFL (NO FLO

207 nce is provided that the BR-controlled basic helix-loop-helix transcription factor CESTA (CES) can co

208 PTF1 is an atypical basic helix-loop-helix transcription factor complex of pancrea

209 The Scl (Tal1) gene encodes a helix-loop-helix transcription factor essential for hema

210 This work reports that the basic helix-loop-helix transcription factor FAMA that is key t

211 tral regulator of this response is the basic helix-loop-helix transcription factor FER-LIKE IRON DEFI

212 homozygous frameshift mutation in the basic helix-loop-helix transcription factor gene ARNT2 (c.1373

213 stricting the expression domain of the basic helix-loop-helix transcription factor gene SPATULA.

214 The basic helix-loop-helix transcription factor Hand2, which is co

215 The basic helix-loop-helix transcription factor hASH1, encoded by

216 nd 5' RACE identified the prooncogenic basic helix-loop-helix transcription factor ID1 as an IRE1alph

217 we show that overexpression of the GL3 basic helix-loop-helix transcription factor in A. alpina leads

218 CHF1/Hey2 is a Notch-responsive basic helix-loop-helix transcription factor involved in cardia

219 Single-minded 1 (SIM1) is a basic helix-loop-helix transcription factor involved in the de

220 inhibitory interaction with Twist1, a basic helix-loop-helix transcription factor known to increase

221 the ABA receptor PYL6 (RCAR9) with the basic helix-loop-helix transcription factor MYC2.

222 iency-induced TRANSCRIPTION FACTOR1, a basic helix-loop-helix transcription factor necessary for indu

223 A role has been demonstrated for the basic helix-loop-helix transcription factor NeuroD1 in the pat

224 We show the basic helix-loop-helix transcription factor NeuroD2 promotes i

225 We show here that the basic helix-loop-helix transcription factor NeuroD2 promotes i

226 ME INTERACTING FACTOR3 (PIF3) is a key basic helix-loop-helix transcription factor of Arabidopsis tha

227 The dimmed (DIMM) basic helix-loop-helix transcription factor of Drosophila cont

228 The basic helix-loop-helix transcription factor Olig2 is required

229 THAIR DEFECTIVE SIX-LIKE (RSL) class I basic helix-loop-helix transcription factor positively regulat

230 Homozygous truncating mutations in the helix-loop-helix transcription factor PTF1A are a rare c

231 The lineage-specific basic helix-loop-helix transcription factor Ptf1a is a critica

232 Previously, it has been shown that basic helix-loop-helix transcription factor Ptf1a is required

233 Neurogenin3 (NEUROG3) is a basic helix-loop-helix transcription factor required for devel

234 Previously we demonstrated that the basic helix-loop-helix transcription factor root hair defectiv

235 recruitment followed the loss from the basic helix-loop-helix transcription factor SPATULA (SPT) of a

236 tal lineage cells is controlled by the basic helix-loop-helix transcription factor SPEECHLESS (SPCH).

237 ed a progenitor, marked by the expression of helix-loop-helix transcription factor stem cell leukemia

238 TFEB is a basic helix-loop-helix transcription factor that confers prote

239 itor of DNA-binding 2 (Id2) is an inhibitory helix-loop-helix transcription factor that is highly exp

240 p1 Inhibitor of differentiation 1 (Id1) is a helix-loop-helix transcription factor that plays an impo

241 Inhibitor of differentiation 1 (Id1) is a helix-loop-helix transcription factor that plays importa

242 demonstrate that Tal1, a Lyl1-related basic helix-loop-helix transcription factor that promotes T ac

243 TWIST2 encodes a basic helix-loop-helix transcription factor that regulates the

244 TFAP4, a basic helix-loop-helix transcription factor that regulates the

245 PK3 and MPK6 can phosphorylate ICE1, a basic-helix-loop-helix transcription factor that regulates the

246 cribed to nuclear translocation of the basic helix-loop-helix transcription factor Transcription Fact

247 ICANCE STATEMENT The importance of the basic helix-loop-helix transcription factor transcription fact

248 sion of a second regulator of EMT, the basic helix-loop-helix transcription factor Twist.

249 Notch target genes Hes-related family basic helix-loop-helix transcription factor with YRPW motif 1

250 akdown requires the endosperm-specific basic helix-loop-helix transcription factor ZHOUPI.

251 barren stalk1 (ba1), a basic helix-loop-helix transcription factor, acts downstream o

252 few olfactory sensory neurons when the basic helix-loop-helix transcription factor, ASCL1 (previously

253 Proneural basic helix-loop-helix transcription factor, Atoh1, plays a ke

254 MIST1, also a basic helix-loop-helix transcription factor, enhances the form

255 ouse and zebrafish illustrate that the basic-helix-loop-helix transcription factor, Hand2, is crucial

256 over a role in innate immunity for the basic helix-loop-helix transcription factor, HLH-30.

257 Sharp-1, a basic helix-loop-helix transcription factor, is a potent repre

258 Here, we report that Ascl3, a basic helix-loop-helix transcription factor, is expressed in t

259 ly interacts with and phosphorylates a basic helix-loop-helix transcription factor, MYC2, and is phos

260 tral tegmental area that expresses the basic helix-loop-helix transcription factor, Neurogenic Differ

261 subset of RPCs, those that express the basic helix-loop-helix transcription factor, Olig2.

262 E2A, a basic helix-loop-helix transcription factor, plays a crucial r

263 DNA binding of the basic helix-loop-helix transcription factor, TAL1/SCL, is requ

264 e expression of neurogenin 2 (Ngn2), a basic helix-loop-helix transcription factor, was significantly

265 ibiting Twist, a prominent mesenchymal basic helix-loop-helix transcription factor.

266 MO1 and MYCN is ASCL1, which encodes a basic helix-loop-helix transcription factor.

267 e) two-hybrid screening, we identified basic helix-loop-helix transcription factor05 (bHLH05) as an i

268 amined whether four of the subgroup Ib basic helix-loop-helix transcription factors (bHLH38, bHLH39,

269 ction screens identified three related basic helix-loop-helix transcription factors (MYC2, MYC3, and

270 Two neural basic helix-loop-helix transcription factors (TFs), Ascl1 and

271 omata formation is induced by a set of basic helix-loop-helix transcription factors and inhibited by

272 Homeodomain and basic helix-loop-helix transcription factors are required for

273 A) E3 ubiquitin ligase and a subset of basic helix-loop-helix transcription factors called phytochrom

274 NTR) is an oscillating gene regulated by the helix-loop-helix transcription factors CLOCK and BMAL1.

275 The basic helix-loop-helix transcription factors collectively call

276 The basic helix-loop-helix transcription factors E2A and Lyl1 form

277 restriction of symplastic movement of basic helix-loop-helix transcription factors into neighboring

278 eprogramming that does not involve the basic helix-loop-helix transcription factors MYC2 and related

279 ctions between BTS and PYE-like (PYEL) basic helix-loop-helix transcription factors occur within the

280 ability of MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that additively c

281 New Gene (RING) domain, interacts with basic helix-loop-helix transcription factors that are capable

282 nt lacking MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that are known to

283 ERACTING FACTORS (PIFs) are a group of basic helix-loop-helix transcription factors that can physical

284 Id proteins are helix-loop-helix transcription factors that regulate the

285 cting factors (PIFs), a small group of basic helix-loop-helix transcription factors, repress photomor

286 pid phosphorylation and degradation of basic helix-loop-helix transcription factors, such as PHYTOCHR

287 of a family of antagonistically acting basic helix-loop-helix transcription factors, the PHYTOCHROME-

288 Three basic helix-loop-helix transcription factors, UDT1 (bHLH164),

289 ID4, a dominant-negative inhibitor of basic helix-loop-helix transcription factors, up-regulated in

290 rning molecules, such as the proneural basic helix-loop-helix transcription factors.

291 euronal migration that is regulated by basic helix-loop-helix transcription factors.

292 Id1 is a helix-loop-helix transcriptional modulator that increase

293 cell factor-1 (ABF-1), which encodes a basic helix-loop-helix transcriptional repressor, participates

294 ffects the protein dynamics of Her6, a basic helix-loop-helix transcriptional repressor.

295 Overexpression of the basic helix-loop-helix type transcription factor, Mist1, induc

296 strated that proinflammatory TLRs (conserved helix-loop-helix ubiquitous kinase, IRAK1, TLR1, TLR4, T

297 n M. truncatula and a component of MYB-basic helix loop helix-WD40 (MBW) activator complexes.

298 iption factors including a central MYB-basic helix-loop-helix-WD40 complex containing WEREWOLF (WER),

299 eavage does not require the N-terminal basic helix-loop-helix zipper transcription factor domain, thu

300 The dual specificity T-box/basic-helix-loop-helix-zipper transcription factor Mga is expr