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 Nescient helix-loop-helix-2 (NHLH2) is a basic helix-loop-helix t

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 tor (ARNT) subunit, which dimerize via basic helix-loop-helix and PAS domains, and recruit coactivato

8 we have found that the previously identified helix-loop-helix and Ufd2-box domains in human Act1 have

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

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

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

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

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 anced mRNA and protein expression of a basic helix-loop-helix (bHLH) class myogenic determination fac

16 ificities of 19 Caenorhabditis elegans basic helix-loop-helix (bHLH) dimers using protein binding mic

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 3-MYB regulator C1 cooperates with the basic helix-loop-helix (bHLH) factor R to activate the express

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 ochrome Interacting Factor 1 (PIF1), a basic helix-loop-helix (bHLH) protein, functions as a negative

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 We demonstrate that two basic helix-loop-helix (bHLH) proteins-HEB and E2A-bind the SC

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

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

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

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

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

47 The vertebrate basic helix-loop-helix (bHLH) transcription factor ATOH7 (Math

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

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

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

51 f SPARC, as well as the Notch effector basic helix-loop-helix (bHLH) transcription factor hairy and e

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

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

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

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

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

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

58 Expression of the basic helix-loop-helix (bHLH) transcription factor Neurogenin1

59 We show that the basic helix-loop-helix (bHLH) transcription factor PIF7 (phyto

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

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

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

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

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

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

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

70 es oligodendrocyte development through basic-helix-loop-helix (bHLH) transcription factors and promot

71 Neural basic helix-loop-helix (bHLH) transcription factors are crucia

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

73 al and temporal expression of specific basic-helix-loop-helix (bHLH) transcription factors defines ma

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

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

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

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

78 nds upon the function of the proneural basic helix-loop-helix (bHLH) transcription factors NEUROG1 an

79 find that expression of the proneural basic helix-loop-helix (bHLH) transcription factors Neurog2 or

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

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

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

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

91 ecific genes Sohlh1 and Sohlh2, encode basic helix-loop-helix (bHLH) transcriptional regulators that

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 HIF is a basic helix-loop-helix (bHLH)-PAS (PER-ARNT-SIM) heterodimer c

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

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

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

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

106 interact on the MIC-1 promoter via the basic helix-loop-helix domain in DEC1 and the tetramerization

107 We found that Serine 147 in the helix-loop-helix domain of OLIG2 was phosphorylated duri

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

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

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

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

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

113 The basic-helix-loop helix factor Math5 (Atoh7) is required for re

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

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

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

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

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

119 the Os07g11020 or Rc locus encoding a basic helix-loop-helix family transcription factor by intragen

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

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

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

123 that the compensatory mutations increase the helix-loop-helix flexibility, allowing rescue of the cor

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

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

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

127 l structure of AS8 was solved, revealing the helix-loop-helix geometry of the unique AS8 insertion re

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

129 of the paclobutrazol-resistant (PRE) family helix-loop-helix (HLH) factors, which promote cell elong

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 play a profound role in

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

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

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

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

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

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

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

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

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

143 iated transcription factor (MITF) is a basic helix-loop-helix leucine zipper protein that plays major

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

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

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

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

148 potent neutralizing antibody that binds to a helix-loop-helix motif in the RSV fusion glycoprotein.

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

150 ture of gp6 reveals a dimeric protein with a helix-loop-helix motif similar to that of bacteriophage

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

152 studies, Mdv1 binds Fis1 through a U-shaped helix-loop-helix motif, and dimerization of the Mdv1-Fis

153 ) of the coat protein through its C-terminal helix-loop-helix motif, as well as unexpected interactio

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

155 expectedly, the predicted leucine zipper and helix-loop-helix motifs do not form these structures but

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

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

158 roteosome system, and down-regulation of the helix-loop-helix muscle regulatory factor, MyoD.

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

160 The basic helix-loop-helix PAS (Per, Arnt, Sim) domain transcripti

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

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

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

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

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

166 tor required for ear initiation is the basic helix-loop-helix protein BARREN STALK1 (BA1).

167 racting factoR3-like5, which encodes a basic helix-loop-helix protein coordinating hormone responses

168 In Drosophila, the basic-helix-loop-helix protein DIMM coordinates the molecular

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

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

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

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

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

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

175 tional 26S proteasome and involves the basic helix-loop-helix protein SPATULA as a key component.

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

177 atenin through an interaction with the basic helix-loop-helix protein upstream stimulatory transcript

178 idopsis (Arabidopsis thaliana) FAMA, a basic helix-loop-helix protein whose actions during the final

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

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

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

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

183 The ID family of helix-loop-helix proteins regulates cell proliferation a

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

185 pmental regulatory pathways that include the helix-loop-helix regulator hlh-2/daughterless and transc

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

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

188 This helix would support the helix-loop-helix structure acting as a solid "pushrod" t

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

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

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

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

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

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

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

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

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

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

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

200 previous data suggested that the human basic helix-loop-helix transcription factor achaete-scute homo

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

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

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

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

205 The proneural, basic helix-loop-helix transcription factor Atoh1 governs the

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

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

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

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

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

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

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

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

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

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

216 We show here that the basic helix-loop-helix transcription factor Hand2 plays key ro

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

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

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

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

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

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

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

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

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

226 The basic helix-loop-helix transcription factor NeuroD1 is express

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

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

229 SIRT1 deacetylates the brain-specific helix-loop-helix transcription factor NHLH2 on lysine 49

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

263 scient helix-loop-helix-2 (NHLH2) is a basic helix-loop-helix transcription factor, which has been im

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

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

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

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

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

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

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

271 ve determined that the two Arabidopsis basic helix-loop-helix transcription factors bHLH25 and bHLH27

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

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

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

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

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

277 The basic helix-loop-helix transcription factors Olig1 and Olig2 p

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

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

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

281 module is a set of "master regulator" basic helix-loop-helix transcription factors that regulate ind

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

283 E-proteins, the widely expressed basic helix-loop-helix transcription factors, contribute to HS

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

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

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

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

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

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

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

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

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

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

294 All FBH proteins are related basic helix-loop-helix-type transcription factors that prefere

295 hanges were seen in mRNA levels of conserved helix-loop-helix ubiquitous kinase, IRAK1, 2, TLR4, 9 an

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 nd RNAi-based approaches and found the basic helix-loop-helix ZIP transcription factor AP4 to have an

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