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

1 and ovary expressed basic helix-loop-helix (bHLH) transcription factor).

2 MAX also dimerizes with MYC, an oncogenic bHLH transcription factor.

3 The C. elegans genome encodes a single Hand bHLH transcription factor.

4 epends on Olig2, one of the five Olig family bHLH transcription factors.

5 forms homodimers and heterodimers with other bHLH transcription factors.

6 ication is achieved through few well-defined bHLH transcription factors.

7 aling by Notch and Sox2 on the expression of bHLH transcription factors.

8 vation of NvHes genes, a conserved family of bHLH transcription factors.

9 heterodimerize with and negatively regulate bHLH transcription factors.

10 roviding new insight into gene regulation by bHLH transcription factors.

11 ic gene expression and activation by Myb and bHLH transcription factors.

12 yase and pectinesterase, are targets of both bHLH transcription factors.

13 in its capacity as a basic helix-loop-helix (bHLH) transcription factor.

14 hogenesis is HFR1, a basic helix-loop-helix (bHLH) transcription factor.

15 FACTORs, a group of basic helix-loop-helix (bHLH) transcription factors.

16 tivity of neurogenic basic helix-loop-helix (bHLH) transcription factors.

17 ly activate myogenic basic helix-loop-helix (bHLH) transcription factors.

18 ompromises the onset of achaete-scute family bHLH transcription factor 1 (Ascl-1)(+) vomeronasal prog

19 Although Achaete-scute family bHLH transcription factor 1 (Ascl1) plays important role

20 n of sT and the cell fate-determinant atonal bHLH transcription factor 1 (ATOH1) leads to development

21 a complex with the Notch effector hes family bHLH transcription factor 1 (HES1) and the protein deace

22 nding factor 1 (LEF1) and mesoderm posterior BHLH transcription factor 1 (MESP1; from mesoderm to car

23 tivation protein Ascl1 (achaete-scute family bHLH transcription factor 1) in proliferating hippocampa

24 Cleaved NOTCH1, HES1 (Hes family BHLH transcription factor 1), and c-MYC protein expressi

25 sion of either Twist1 (encoding twist family bHLH transcription factor 1, known as Twist) or Snai1 (e

26 iscovered that the gene single minded family bHLH transcription factor 1a (sim1a) is dynamically expr

27 which encodes a photomorphogenesis-promoting bHLH transcription factor, acts downstream of SPA1 and i

28 maize R gene has been used to suggest that a bHLH transcription factor also participates in this proc

29 DYT1 encodes a putative bHLH transcription factor and is strongly expressed in t

30 s deduced where targets, such as AP2/ERF and bHLH transcription factors and chromatin remodelers form

31 lators of neurogenesis, including neurogenic bHLH transcription factors and dorsal interneuron progen

32 Designer TALEs (dTALEs) for the bHLH transcription factors and the pectate lyase, but no

33 ed genes that could be direct targets of the bHLH transcription factors and therefore indirect target

34 rabidopsis, a ternary complex formed by MYB, bHLH transcription factors and TTG1 modulates unicellula

35 emi, which encodes a basic helix-loop-helix (bHLH) transcription factor and which controls these appa

36 development through basic-helix-loop-helix (bHLH) transcription factors and promotes astrocytosis.

37 ered that it encodes a PAS-domain-containing bHLH transcription factor, and that it is expressed in a

38 h encodes a class II basic helix-loop-helix (bHLH) transcription factor, and causes Saethre-Chotzen s

39 cell cycle proteins, basic helix-loop-helix (bHLH) transcription factors, and other retinal cell mark

40 Instead, our results suggest that bHLH transcription factors are regulated by a previously

41 ut the Hey family of basic helix-loop-helix (bHLH) transcription factors are candidates for mediating

42 Proneural basic helix-loop-helix (bHLH) transcription factors are critical positive regula

43 Neural basic helix-loop-helix (bHLH) transcription factors are crucial in regulating th

44 Basic helix-loop-helix (bHLH) transcription factors are key regulators of neurog

45 rl), a Hairy-related basic helix-loop-helix (bHLH) transcription factor, as a negative regulator of c

46 ediated overexpression of a single gene, the bHLH transcription factor Ascl1, redirected the fate of

47 tube depends on the basic helix-loop-helix (bHLH) transcription factors Ascl1 (Mash1) and Neurog2 (N

48 We identified a basic helix-loop-helix (bHLH) transcription factor at chickpea's B locus that co

49 In a wide range of vertebrate species, the bHLH transcription factor Ath5 is tightly associated wit

50 retinoblasts, and functions upstream of the bHLH transcription factors ath5/atoh7 and neurod, and th

51 on resulted from an increase in the level of bHLH transcription factor Atoh1 in response to inhibitio

52 ns share a developmental requirement for the bHLH transcription factor Atoh1.

53 n the temporal and spatial regulation of the bHLH transcription factor Atoh1.

54 n depends on the regulated expression of the bHLH transcription factor Atoh1.

55 he expression of the basic helix-loop-helix (bHLH) transcription factor Atoh1.

56 The vertebrate basic helix-loop-helix (bHLH) transcription factor ATOH7 (Math5) is specifically

57 itors expressing the basic helix-loop-helix (bHLH) transcription factor, Atoh7, which is necessary fo

58 a mouse homolog of the Drosophila proneural bHLH transcription factor Atonal, is essential in the de

59 The basic helix-loop-helix (bHLH) transcription factor Atonal (Ato) plays an essenti

60 hree closely related basic helix-loop-helix (bHLH) transcription factors, BEE1, BEE2, and BEE3, as pr

61 insect and RNAi to determine functions of 19 bHLH transcription factors belonging to PAS and HES fami

62 The basic helix-loop-helix (bHLH) transcription factor Bhlhb4 was found to be expres

63 ce deficient for the basic helix-loop-helix (bHLH) transcription factor Bhlhe40 (Bhlhe40(-/-)) are re

64 Zfp148, and Plzf, overexpress a novel Tohlh2 bHLH transcription factor, but lack LIM homeobox gene Lh

65 This activation required MYC proto-oncogene bHLH transcription factor (c-Myc) and depended on the ch

66 mentation assays, we documented that the two bHLH transcription factors can dimerize in planta.

67 first neural target of Ptf1a and revealing a bHLH transcription factor cascade functioning in the spe

68 Our results reveal that a bHLH transcription factor cascade is involved in regulat

69 ng the hairy-related basic helix-loop-helix (bHLH) transcription factor CHF1/Hey2 develop a thin-wall

70 Basic helix-loop-helix (bHLH) transcription factors control developmental decisi

71 How basic helix-loop-helix (bHLH) transcription factors control neurogenesis and neu

72 of master regulatory basic-helix-loop-helix (bHLH) transcription factors controls the initiation, pro

73 NeuroD is a basic helix-loop-helix (bHLH) transcription factor critical for determining neur

74 , we showed that the basic Helix-Loop-Helix (bHLH) transcription factor Cucumis sativus Irregular Vas

75 pression of specific basic-helix-loop-helix (bHLH) transcription factors defines many types of cellul

76 We identified a basic helix-loop-helix (bHLH) transcription factor, designated PHYTOCHROME-INTER

77 have identified two basic helix-loop-helix (bHLH) transcription factors, designated PHYTOCHROME-INTE

78 e, both display significant overlap with the bHLH transcription factor DIMM, a known neuroendocrine (

79 ate the expression and function of proneural bHLH transcription factors during the onset of mouse ret

80 as EMT inducers, among them, Snail1 and the bHLH transcription factor E47.

81 bers of the group XI basic helix-loop-helix (bHLH) transcription factors encoded by LOTUS JAPONICUS R

82 es expression of two basic helix loop helix (bHLH) transcription factor encoding genes, ash1a (achaet

83 enes in opr3 encode lipoxygenase, a putative bHLH transcription factor, epithiospecifier protein and

84 ECs express mAsh1, a basic helix-loop-helix (bHLH) transcription factor essential for NE cell differe

85 3, neurogenin1) is a basic helix-loop-helix (bHLH) transcription factor essential for neuronal differ

86 Here, we characterize Sage, a bHLH transcription factor expressed exclusively in the D

87 MyoR and capsulin are related bHLH transcription factors expressed in specific facial

88 HAND2 (dHAND) is a basic helix-loop-helix (bHLH) transcription factor expressed in numerous tissues

89 Ngn1 is a basic helix-loop-helix (bHLH) transcription factor expressed in specific regions

90 g, which has previously been shown to induce bHLH transcription factor expression, increased beta-cat

91 cies, Arabidopsis, in which three paralogous bHLH transcription factors, FAMA, MUTE and SPCH, control

92 gested that the large-scale expansion of the bHLH transcription factor family occurred before the div

93 g the composition and diversity of the apple bHLH transcription factor family that will provide a pla

94 Members of the basic helix-loop-helix (bHLH) transcription factor family play an essential role

95 The basic helix-loop-helix (bHLH) transcription factor family regulates numerous dev

96 Class I Basic Helix-Loop-Helix (bHLH) transcription factors form homodimers or heterodim

97 e identification and characterization of 175 bHLH transcription factors from apple (Malus x domestica

98 nteracting Factors (PIFs) by releasing these bHLH transcription factors from phytochrome B-mediated i

99 jasmonate-regulated basic helix-loop-helix (bHLH) transcription factor from clade IVa inducing the m

100 ults suggest that variation in the timing of bHLH transcription factor gene expression can explain th

101 ch signaling revealed a cascade of proneural bHLH transcription factor gene expression that correlate

102 e control of the regulatory sequences of the bHLH transcription factor gene hand2.

103 Phylogenetic analysis indicates that these bHLH transcription factor genes are orthologous to Arabi

104 We show that basic helix-loop-helix (bHLH) transcription factor genes represented by Glyma04g

105 utative (a PIL5, a hypothetic protein, and a bHLH transcription factor) genes based on the annotated

106 s the Notch effector basic helix-loop-helix (bHLH) transcription factor hairy and enhancer of split 1

107 the highly conserved basic helix-loop-helix (bHLH) transcription factor Hand is expressed in cardiobl

108 The bHLH transcription factor Hand1 (Heart and neural crest-

109 The basic helix-loop-helix (bHLH) transcription factor HAND1 (also called eHAND) is

110 upregulation of the basic helix-loop-helix (bHLH) transcription factor Hand1, restricted exclusively

111 ebrafish of two edn1 downstream targets, the bHLH transcription factor Hand2 and the homeobox transcr

112 The bHLH transcription factor Hand2 is essential for cardiac

113 Here, we show that the bHLH transcription factor Hand2 limits the size of the e

114 The basic helix-loop-helix (bHLH) transcription factor Hand2 has been implicated in

115 The basic helix-loop-helix (bHLH) transcription factor Hand2 has been implicated in

116 The basic helix-loop-helix (bHLH) transcription factor Hand2 has been shown to play

117 The basic helix-loop-helix (bHLH) transcription factor Hand2 is required for growth

118 The MyoD family of basic helix-loop-helix (bHLH) transcription factors has the remarkable ability t

119 1, a phy-interacting basic helix-loop-helix (bHLH) transcription factor, has been shown to negatively

120 olecular level that neuronal differentiation bHLH transcription factors have distinct lineage-specifi

121 The genes encoding basic helix-loop-helix (bHLH) transcription factors have been implicated in many

122 (2014) describe the signals regulated by the bHLH transcription factor HEC1 during Arabidopsis stem c

123 Here, we show that the bHLH transcription factors HECATE 1 (HEC1), HEC2 and HEC

124 s for expression of Notch and the hes family bHLH transcription factor (HES1) in colon tissues from m

125 by interfering with the assembly of myogenic bHLH transcription factor heterodimers on E-box sequence

126 Here, we report that the Beta3/Olig-type bHLH transcription factor hlh-16 is L/R asymmetrically e

127 h sexes requires the basic-helix-loop-helix (bHLH) transcription factor HLH-2, the sole ortholog of t

128 ere, we identify the basic helix-loop-helix (bHLH) transcription factor homolog of brassinosteroid en

129 d degradation of the basic helix-loop-helix (bHLH) transcription factor human achaete-scute homolog 1

130 lutionally conserved basic helix-loop-helix (bHLH) transcription factors implicated in development of

131 ) demonstrate unsuspected cross-talk between bHLH transcription factors, important regulators of orga

132 olated a dominant mutation in an R/B-related bHLH transcription factor in the course of studying Arab

133 l cues in the CNS and to examine the role of bHLH transcription factors in adult tissue regeneration.

134 y PHYTOCHROME-INTERACTING FACTOR (PIF)-class bHLH transcription factors in darkness, but light-activa

135 Two bHLH transcription factors in this network, Olig1 and Ol

136 l1), which encodes a basic helix-loop-helix (bHLH) transcription factor, in the regulation of both as

137 ibit the function of basic helix-loop-helix (bHLH) transcription factors including those that regulat

138 oteins are known to negatively regulate many bHLH transcription factors, including Math1, in a number

139 in-22, a Hes-related basic helix-loop-helix (bHLH) transcription factor, increase seam cell number va

140 inhibit the atypical basic helix-loop-helix (bHLH) transcription factor INCREASED LEAF INCLINATION1 B

141 e show that myogenic basic helix-loop-helix (bHLH) transcription factors induce myomaker expression i

142 Conversely, activation of bHLH transcription factors induces a cluster of genes wi

143 irect target of EZH2, and repression of this bHLH transcription factor is critical for neuronal diffe

144 We show that the REF-1 family of bHLH transcription factors is a major target of Notch si

145 The scleraxis (Scx) gene, encoding a bHLH transcription factor, is expressed in the progenito

146 Twist1, a class II basic-helix-loop-helix (bHLH) transcription factor, is expressed during early EC

147 report that Ptf1a, a basic-helix-loop-helix (bHLH) transcription factor, is transiently expressed by

148 mologue 2 (Ascl2)--a basic helix-loop-helix (bHLH) transcription factor--is selectively upregulated i

149 The basic helix-loop-helix (bHLH) transcription factors known as E proteins and thei

150 The Mnt gene encodes a Mad-family bHLH transcription factor located on human 17p13.3.

151 ow that expression of olig2, which encodes a bHLH transcription factor, marks a distinct subset of ne

152 Scleraxis (Scx), a bHLH transcription factor, marks this somitic tendon pro

153 The bHLH transcription factors Mash1 and Ngn2 have distinct

154 The basic helix-loop-helix (bHLH) transcription factor Math1 (also called Atoh1) is

155 mechanism that involved the upregulation of bHLH transcription factor, Math1 (mouse Atoh1), differen

156 The basic helix-loop-helix (bHLH) transcription factor Math5 (Atoh7) is transiently

157 The Wnt-regulated basic helix-loop-helix (bHLH) transcription factor mesogenin 1 (Msgn1) has been

158 al profiling of Wnt3a (-/-) embryos that the bHLH transcription factor, Mesogenin1 (Msgn1), is a dire

159 The bHLH transcription factor Mesp has an essential but ambi

160 gastric cell populations that identified the bHLH transcription factor Mist1 as a potential ZC regula

161 In mice, expression of the bHLH transcription factor MIST1, normally restricted to

162 JAZ13 interacts with the bHLH transcription factor MYC2 and the co-repressor TOPL

163 conserved E-box is a target for the myogenic bHLH transcription factors MYF5 and MYOD.

164 The basic helix-loop-helix (bHLH) transcription factor Myod directly regulates gene

165 1) and identified EAN1 as a tapetum-specific bHLH transcription factor necessary for tapetum degenera

166 BMP4 stimulation promotes Id2 binding to the bHLH transcription factor NeuroD, which is required for

167 ar expression of the basic helix-loop-helix (bHLH) transcription factor neuroD in the persistently ne

168 sient and prefigures expression of a related bHLH transcription factor, neuroD.

169 , we have identified basic helix-loop-helix (bHLH) transcription factors Neurod2 and Neurod6 as key r

170 The basic helix-loop-helix (bHLH) transcription factor, neuroD2, induces neuronal di

171 In the present work, we demonstrate that the bHLH transcription factor NeuroD6 is specifically and tr

172 The bHLH transcription factor Neurog1 (Ngn1, Neurod3, neurog

173 ion of the proneural basic helix-loop-helix (bHLH) transcription factors NEUROG1 and NEUROD1.

174 ly by regulating two basic helix-loop-helix (bHLH) transcription factors, Neurog1 and Neurog2.

175 ion of the proneural basic helix-loop-helix (bHLH) transcription factors Neurog2 or Ascl1 downregulat

176 We identified the basic helix-loop-helix (bHLH) transcription factor Neurogenic Differentiation 2

177 up-regulates transcription of the proneural bHLH transcription factor neurogenin 1 (ngn1).

178 enhancers, including basic helix-loop-helix (bHLH) transcription factor Neurogenin/Math/atonal and Ma

179 Expression of the basic helix-loop-helix (bHLH) transcription factor Neurogenin1 (Neurog1) coincid

180 Here we demonstrate that the bHLH transcription factor Neurogenin2 (Ngn2) is both nec

181 is is positively regulated by the pro-neural bHLH transcription factors Ngn1 and NeuroD, but the fact

182 ells proliferate and transiently express the bHLH transcription factor Ngn3.

183 The ability of the bHLH transcription factors Ngnr1 and NeuroD to drive neu

184 eport that proneural basic helix-loop-helix (bHLH) transcription factors not only initiate neuronal d

185 enesis and depends upon the function of both bHLH transcription factors, notably Hand2, and homeodoma

186 demonstrate that the expression of Bhlhb5, a bHLH transcription factor of the Olig family, is tightly

187 Skeletal myogenesis is controlled by bHLH transcription factors of the MyoD family that, alon

188 he activity of three basic-helix-loop-helix (bHLH) transcription factors of the PHYTOCHROME INTERACTI

189 Against this backdrop, the bHLH transcription factor Olig2 in the oligodendrocyte l

190 The bHLH transcription factor Olig2 is essential for motoneu

191 The bHLH transcription factor Olig2 is expressed in cycling

192 , Zfp488 can interact and cooperate with the bHLH transcription factor Olig2 to promote precocious an

193 oma and with more recent observations on the bHLH transcription factor Olig2.

194 ing neural tube, the basic helix-loop-helix (bHLH) transcription factor Olig2 interacts with the home

195 N) domain of the developing spinal cord, the bHLH transcription factor, Olig2, plays critical roles i

196 We show that the basic helix-loop-helix (bHLH) transcription factor Olig3 is expressed in the ent

197 TAL1/SCL is a basic helix-loop-helix (bHLH) transcription factor oncogene aberrantly expressed

198 Finally, we demonstrate that the bHLH transcription factor paraxis, which was previously

199 m by which increasing temperature causes the bHLH transcription factor PHYTOCHROME INTERACTING FACTOR

200 ncreased auxin biosynthesis, mediated by the bHLH transcription factor PHYTOCHROME-INTERACTING FACTOR

201 CCA1 regulates growth via the bHLH transcription factors PHYTOCHROME INTERACTING FACTO

202 We conclude that bHLH transcription factors PIF1, PIF3, PIF4, and PIF5 ac

203 (pifq) lacking four phytochrome-interacting bHLH transcription factors (PIF1, 3, 4, and 5) is consti

204 (phy)-interacting factor (PIF) subfamily of bHLH transcription factors (PIF1, PIF3, PIF4, and PIF5).

205 otyls, which is predominantly regulated by a bHLH transcription factor, PIF4.

206 hange and respond by directly contacting two bHLH transcription factors, PIF4 and PIF5.

207 We show that the basic helix-loop-helix (bHLH) transcription factor PIF7 (phytochrome-interacting

208 as SPA1/COP1 E3 ubiquitin ligase complex and bHLH transcription factors PIFs, would partially explain

209 family of four Phytochrome (phy)-Interacting bHLH transcription Factors (PIFs) collectively promote s

210 n of phy-interacting basic Helix Loop Helix (bHLH) transcription factors (PIFs), such as PIF3, thereb

211 Proneural basic helix-loop-helix (bHLH) transcription factors play a central role in regul

212 Basic helix-loop-helix (bHLH) transcription factors play a pivotal role in the r

213 Basic-helix-loop-helix (bHLH) transcription factors play an important role in va

214 Long Hypocotyl in Far-Red Light 1 (HFR1), a bHLH transcription factor, plays a critical role in prom

215 DYSFUNCTIONAL TAPETUM 1 (DYT1), a putative bHLH transcription factor, plays a critical role in regu

216 Twist, a basic helix-loop-helix (bHLH) transcription factor, plays an important role in m

217 ycle-specific iron deficiency response and a bHLH transcription factor, POPEYE (PYE), that may play a

218 Here we show that Arabidopsis lacking two bHLH transcription factors produces pollen without sperm

219 NeuroD2, a neuronal basic helix-loop-helix (bHLH) transcription factor, promotes the postnatal survi

220 The basic helix-loop-helix (bHLH) transcription factor PTF1a is critical to the deve

221 The basic helix-loop-helix (bHLH) transcription factor Ptf1a is essential for the ge

222 We demonstrated that the bHLH transcription factor R1 and hexokinase HEX9 might a

223 Basic helix-loop-helix (bHLH) transcription factors recognize the canonical E-bo

224 Neural basic helix-loop-helix (bHLH) transcription factors regulate neurogenesis in ver

225 Core basic helix-loop-helix (bHLH) transcription factors regulating stomatal developm

226 the SPATULA (SPT) gene, which also encodes a bHLH transcription factor required for development of th

227 subpopulation of NCCs that expresses Ngn2, a bHLH transcription factor required for sensory neurogene

228 Mesp encodes a bHLH transcription factor required for specification of

229 lfactory-1, OLF1), a basic helix-loop-helix (bHLH) transcription factor required for B-lineage commit

230 gene that encodes a basic helix-loop-helix (bHLH) transcription factor required for proper distal ti

231 r-specific predicted basic helix-loop-helix (bHLH) transcription factor required for tapetal differen

232 oneural genes encode basic-helix-loop-helix (bHLH) transcription factors required for neural precurso

233 al sensor of mitochondrial function, and the bHLH transcription factors Rtg1p and Rtg3p.

234 The bHLH transcription factor SCL plays a central role in th

235 In summary, we conclude that the bHLH transcription factors SHARP1 and SHARP2 are involve

236 The bHLH transcription factors SHARP1 and SHARP2 are partial

237 the function of the basic helix-loop-helix (bHLH) transcription factor SPEECHLESS (SPCH).

238 This includes the basic helix-loop-helix (bHLH) transcription factors SPEECHLESS (SPCH), MUTE, FAM

239 ila retina, stochastic expression of the PAS-bHLH transcription factor Spineless (Ss) controls photor

240 ophila eye, stochastic expression of the PAS-bHLH transcription factor Spineless (Ss) determines a ra

241 A complex of R2R3-MYB and bHLH transcription factors, stabilized by WD40 repeat pr

242 Among the bHLH transcription factors studied, the steroid receptor

243 receptor family (phyA to phyE) interact with bHLH transcription factors, such as PIF3, and induce cha

244 Prior work has implicated the bHLH transcription factor Tal1 in endocardial tube forma

245 Here, we describe the role of a bHLH transcription factor, Tcf21 (epicardin/Pod1/capsuli

246 interaction of Pfr with a small subfamily of bHLH transcription factors, termed Phy-Interacting Facto

247 Two classes of JA-responsive bHLH transcription factor (TF), CrMYC2 and BIS1/BIS2, ar

248 ipotent cells as the basic helix-loop-helix (bHLH) transcription factor (TF) E2A.

249 Atoh1, a basic helix-loop-helix (bHLH) transcription factor (TF), is essential for the di

250 TION FACTOR (FIT), a basic helix-loop-helix (bHLH) transcription factor (TF), regulates root Fe acqui

251 ing nuclear localization and activity of the bHLH transcription factor Tfe3.

252 YC2a, b, c) encoding basic helix-loop-helix (bHLH) transcription factors (TFs) whose expression is ra

253 f two genes encoding basic-helix-loop-helix (bHLH) transcription factors (TFs), NtMYC2a and NtMYC2b f

254 Sohlh1 represents the first testis-specific bHLH transcription factor that is essential for spermato

255 including IAA-Leu Resistant3 (ILR3), another bHLH transcription factor that is involved in metal ion

256 trated that AmeloD is a novel tooth-specific bHLH transcription factor that may regulate tooth develo

257 endent, per ARNT-sim (PAS) domain containing bHLH transcription factor that mediates adaptive respons

258 TWIST is a bHLH transcription factor that promotes epithelial-mesen

259 Twist1 is a bHLH transcription factor that regulates cell proliferat

260 his question, we focused on Atoh1 (Math1), a bHLH transcription factor that specifies distinct neuron

261 ith inhibition of the Notch effector Hey1, a bHLH transcription factor that we here characterize as a

262 , BEE1 and BEE3 genes encode closely related bHLH transcription factors that act redundantly to speci

263 MYC2, MYC3 and MYC4 are JAZ-interacting bHLH transcription factors that play a major role in con

264 The bHLH transcription factors that regulate early developme

265 nctions of Myf5 and MyoD, two highly related bHLH transcription factors that regulate skeletal muscle

266 ng analysis we identified five MYB and three bHLH transcription factors that were upregulated in the

267 is a multifunctional basic helix-loop-helix (bHLH) transcription factor that has been shown to be a p

268 molog 1 (Atoh1) is a basic helix-loop-helix (bHLH) transcription factor that is essential for the gen

269 Mist1 is a basic helix-loop-helix (bHLH) transcription factor that is important to the prop

270 S (SPCH), encoding a basic helix-loop-helix (bHLH) transcription factor that is necessary and suffici

271 PTF1a is an unusual basic helix-loop-helix (bHLH) transcription factor that is required for the deve

272 are closely related basic helix-loop-helix (bHLH) transcription factors that are expressed in myelin

273 s (PIFs) are nuclear basic helix-loop-helix (bHLH) transcription factors that negatively regulate pho

274 des highly conserved basic helix-loop-helix (bHLH) transcription factors that play crucial roles in c

275 n TWIST2 and TWIST1 encode highly homologous bHLH transcription factors, the finding that TWIST2 rece

276 hese results uncover a novel mechanism for a bHLH transcription factor to recognize a unique spatial

277 a functionally relevant target recruited by bHLH transcription factors to induce cell cycle arrest i

278 he ability of neural basic helix-loop-helix (bHLH) transcription factors to activate transcriptional

279 h the MyoD family of basic helix-loop-helix (bHLH) transcription factors to drive skeletal muscle dev

280 ing (IDs) antagonize basic-helix-loop-helix (bHLH) transcription factors to inhibit differentiation a

281 ermal subdivision requires regulation of the bHLH transcription factor Twist.

282 f the 29 candidate genes in this region, the bHLH transcription factor, TWIST2, was initially sequenc

283 STRA13 is a pVHL-dependent bHLH transcription factor up-regulated on the mRNA level

284 We show that a basic helix-loop-helix (bHLH) transcription factor Upstream Regulator of IRT1 (U

285 a nonsynonymous SNP mutation on exon 5 of a bHLH transcription factor was found to elevate the propo

286 vonol-4-reductase (DFR) in leaves, whereas a bHLH transcription factor was highly correlated with fla

287 d by specific markers, and the expression of bHLH transcription factors was assessed.

288 Basic helix-loop-helix (bHLH) transcription factors were reduced, while secondar

289 study, we identified a novel tooth-specific bHLH transcription factor, which we named AmeloD, by scr

290 The subgroup IVc bHLH transcription factors, which have previously been s

291 y32 (ms32) encodes a basic helix-loop-helix (bHLH) transcription factor, which functions as an import

292 E SIX-LIKE1 (MpRSL1) basic-helix-loop-helix (bHLH) transcription factor, which is directly repressed

293 The stem cell leukemia (SCL) gene encodes a bHLH transcription factor with a pivotal role in hematop

294 transcriptional repressor Hes-related family BHLH transcription factor with YRPW motif 1 (Hey1), down

295 anscription factor, HEY2 (hes related family bHLH transcription factor with YRPW motif 2).

296 (SCL) gene encodes a basic helix-loop-helix (bHLH) transcription factor with an essential role in spe

297 was GRMZM2G021276, a basic helix-loop-helix (bHLH) transcription factor with tassel-specific expressi

298 enes encode putative basic helix-loop-helix (bHLH) transcription factors with overlapping functionali

299 up-regulation of two basic helix-loop-helix (bHLH) transcription factors with predicted effector bind

300 We have identified a novel bHLH transcription factor, ZHOUPI (ZOU), which mediates