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1 in 4 h of the induction of the GLABRA3 (GL3) basic helix-loop-helix transcription factor.
2 egulator of acinar cell polarity is Mist1, a basic helix-loop-helix transcription factor.
3 the photoactivated phy molecule with PIF3, a basic helix-loop-helix transcription factor.
4 ted by hypoxia-inducible factor 1 (HIF-1), a basic helix-loop-helix transcription factor.
5 MATH1 is a neural-specific basic helix-loop-helix transcription factor.
6 by inhibiting Twist, a prominent mesenchymal basic helix-loop-helix transcription factor.
7 proteins and basic domain/leucine zipper and basic helix-loop-helix transcription factors.
8 g (ID) family, which inhibits DNA binding of basic helix-loop-helix transcription factors.
9 ly occurring dominant-negative inhibitors of basic helix-loop-helix transcription factors.
10 proteins are dominant negative regulators of basic helix-loop-helix transcription factors.
11 igodendrocyte lineage genes (Olig1/2) encode basic helix-loop-helix transcription factors.
12 patterning molecules, such as the proneural basic helix-loop-helix transcription factors.
13 yocyte enhancer factor-2 (MEF2) and myogenic basic helix-loop-helix transcription factors.
14 for neuronal migration that is regulated by basic helix-loop-helix transcription factors.
15 ed the C3 promoter and identified that twist basic helix-loop-helix transcription factor 1 (TWIST1) b
16 rther, our data suggest TWIST1 (twist family basic helix-loop-helix transcription factor 1) and SSPN
17 nal stem-cell regulator achaete-scute family basic helix-loop-helix transcription factor 2 (ASCL2), W
19 Our previous data suggested that the human basic helix-loop-helix transcription factor achaete-scut
21 Up-regulation of Pr specifically activated a basic helix-loop-helix transcription factor and a subset
23 Additionally, we have identified Twist1, a basic helix-loop-helix transcription factor and a well-k
24 Atoh1, a gene also known as Math1 encoding a basic helix-loop-helix transcription factor and key regu
26 ly by inhibiting transcriptional activity of basic helix-loop-helix transcription factors and abrogat
27 tein (BMP)-dependent growth pathway in which basic helix-loop-helix transcription factors and downstr
30 mily of genes encodes negative regulators of basic helix-loop-helix transcription factors and has bee
31 Stomata formation is induced by a set of basic helix-loop-helix transcription factors and inhibit
32 Id2 is a dominant-negative antagonist of basic helix-loop-helix transcription factors and protein
35 genes: a DNA replication control protein, a basic helix-loop-helix transcription factor, and a novel
37 ivo with the PHYTOCHROME INTERACTING FACTOR3 basic helix-loop-helix transcription factor, and this in
38 been identified as an inhibitor of myogenic basic helix-loop-helix transcription factors, and a rela
39 -helix protein Id-1 inhibits the activity of basic helix-loop-helix transcription factors, and is an
40 ein Id-1 is a dominant negative regulator of basic helix-loop-helix transcription factors, and plays
41 a(1B)-adrenergic receptor subtype, proneural basic helix-loop-helix transcription factors, and the di
47 s system, different proneural genes encoding basic helix-loop-helix transcription factors are require
49 ary epithelial cells and identified ITF-2, a basic helix-loop-helix transcription factor, as an Id-1-
51 very few olfactory sensory neurons when the basic helix-loop-helix transcription factor, ASCL1 (prev
57 In the present study we demonstrate that the basic helix-loop-helix transcription factor Atonal homol
60 s suggest that XREs, E-boxes, and PAS domain/basic helix-loop-helix transcription factors (bHLH-PAS)
61 we have determined that the two Arabidopsis basic helix-loop-helix transcription factors bHLH25 and
62 we examined whether four of the subgroup Ib basic helix-loop-helix transcription factors (bHLH38, bH
63 hyperglycemia induces the expression of the basic helix-loop-helix transcription factor c-Myc in isl
65 inner ear sensory neurons are dependent on a basic helix-loop-helix transcription factor called Neuro
67 OP1-SPA) E3 ubiquitin ligase and a subset of basic helix-loop-helix transcription factors called phyt
68 that differential expression of a ubiquitous basic helix-loop-helix transcription factor can modulate
69 Evidence is provided that the BR-controlled basic helix-loop-helix transcription factor CESTA (CES)
70 Id1 is an inhibitor of a group of basic helix-loop-helix transcription factors, collective
72 nducible factor 1 (HIF-1) is a heterodimeric basic helix-loop-helix transcription factor composed of
73 nducible factor 1 (HIF-1) is a heterodimeric basic helix-loop-helix transcription factor composed of
75 E-proteins, the widely expressed basic helix-loop-helix transcription factors, contribute
78 e cells, expression of Id-1, an inhibitor of basic helix-loop-helix transcription factors, declines p
79 A4 also interacts with the cardiac-expressed basic helix-loop-helix transcription factor dHAND (also
88 The E2A gene encodes two E protein/class I basic helix-loop-helix transcription factors, E12 and E4
92 ibited reduced ventricular expression of the basic helix-loop-helix transcription factor eHand (Hand1
97 beta-catenin interacts directly with MyoD, a basic helix-loop-helix transcription factor essential fo
99 current chromosomal translocation, encodes a basic helix-loop-helix transcription factor essential fo
106 nce recognition code and evolvability of the basic helix-loop-helix transcription factor family by cr
107 4 (ID4) is a member of the dominant-negative basic helix-loop-helix transcription factor family that
108 lected members of the constitutively nuclear basic helix-loop-helix transcription factor family, such
109 he central regulator of this response is the basic helix-loop-helix transcription factor FER-LIKE IRO
110 rm line, alpha) encodes a germ cell-specific basic helix-loop-helix transcription factor first identi
112 novel homozygous frameshift mutation in the basic helix-loop-helix transcription factor gene ARNT2 (
113 um, restricting the expression domain of the basic helix-loop-helix transcription factor gene SPATULA
114 es in the dorsal vessel enhancer of the Hand basic helix-loop-helix transcription factor gene, with o
116 that progesterone-induced expression of the basic helix-loop-helix transcription factor Hand2 in the
120 both mouse and zebrafish illustrate that the basic-helix-loop-helix transcription factor, Hand2, is c
123 coding region of the TWIST gene (encoding a basic helix-loop-helix transcription factor) have been i
126 form of Cre under the regulation of Olig2, a basic helix-loop-helix transcription factor highly expre
127 o discover a role in innate immunity for the basic helix-loop-helix transcription factor, HLH-30.
130 product (pVHL) targets the alpha subunit of basic helix-loop-helix transcription factor hypoxia-indu
131 ays, and 5' RACE identified the prooncogenic basic helix-loop-helix transcription factor ID1 as an IR
132 may be due to a change in the regulation of basic helix-loop-helix transcription factors implicated
134 The aryl hydrocarbon receptor (AHR) is a basic helix-loop-helix transcription factor, implicated
137 that Sohlh1, a spermatogenesis and oogenesis basic helix-loop-helix transcription factor in females,
139 on of the aryl hydrocarbon receptor (AHR), a basic helix-loop-helix transcription factor, in lymphocy
140 yogenic family (I-mfa), a known inhibitor of basic helix-loop-helix transcription factors, in vitro a
141 dimerizing with and inhibiting the action of basic helix-loop-helix transcription factors including t
143 loop-helix protein that heterodimerizes with basic helix-loop-helix transcription factors inhibiting
144 PHYTOCHROME-INTERACTING FACTOR5 (PIF5), a basic helix-loop-helix transcription factor, interacts s
145 on the restriction of symplastic movement of basic helix-loop-helix transcription factors into neighb
150 EB are structurally and functionally related basic helix-loop-helix transcription factors involved in
161 direct inhibitory interaction with Twist1, a basic helix-loop-helix transcription factor known to inc
162 We previously reported that a ubiquitous basic helix-loop-helix transcription factor, known as IT
163 ecent studies demonstrate that the proneural basic helix-loop-helix transcription factor Mash1 is req
165 hestrated in part by the binding of a shared basic helix-loop-helix transcription factor MITF to the
167 onal reprogramming that does not involve the basic helix-loop-helix transcription factors MYC2 and re
168 interaction screens identified three related basic helix-loop-helix transcription factors (MYC2, MYC3
169 ysically interacts with and phosphorylates a basic helix-loop-helix transcription factor, MYC2, and i
172 erentiation, decreases, allowing the induced basic helix-loop-helix transcription factor myogenin to
174 deficiency-induced TRANSCRIPTION FACTOR1, a basic helix-loop-helix transcription factor necessary fo
176 gulated, neuron-specific genes, a neurogenic basic helix-loop-helix transcription factor, NeuroD, was
185 he ventral tegmental area that expresses the basic helix-loop-helix transcription factor, Neurogenic
186 The proneural basic helix-loop-helix transcription factors Neurogenin1
188 r, retrovirus-mediated overexpression of the basic helix-loop-helix transcription factors Neurogenin2
189 ical progenitor cell cultures, the proneural basic helix-loop-helix transcription factor Ngn1 suppres
190 interactions between BTS and PYE-like (PYEL) basic helix-loop-helix transcription factors occur withi
191 TOCHROME INTERACTING FACTOR3 (PIF3) is a key basic helix-loop-helix transcription factor of Arabidops
194 that Hey2, a hairy/enhancer-of-split-related basic helix-loop-helix transcription factor often believ
197 rein, we demonstrate the pivotal role of the basic helix-loop-helix transcription factor, Olig1, in o
198 L1CAM knockdown decreased expression of the basic helix-loop-helix transcription factor Olig2 and up
199 tors to cortical myelination, we ablated the basic helix-loop-helix transcription factor Olig2 in the
202 proneural transcription factor Ngn2 and the basic helix-loop-helix transcription factor Olig2 specif
203 Surprisingly, these cells expressed the basic helix-loop-helix transcription factor Olig2, placi
206 in stem cells, in part, by activation of the basic helix-loop-helix transcription factors, Olig2 and
208 enin 3 (ngn3), an islet- and neuron-specific basic-helix-loop-helix transcription factor, partially o
209 A basic helix-loop-helix transcription factor, PHYTOCHROME
211 titutively nucleus-localized phy-interacting basic helix-loop-helix transcription factors (PIFs).
213 in vertebrates, the achaete-scute family of basic helix-loop-helix transcription factors plays a cri
215 a ROOTHAIR DEFECTIVE SIX-LIKE (RSL) class I basic helix-loop-helix transcription factor positively r
219 dies have implicated important roles for the basic helix-loop-helix transcription factor Ptf1a-p48 in
222 induction of Id2 and resultant inhibition of basic helix-loop-helix transcription factor-regulated ge
224 interacting factors (PIFs), a small group of basic helix-loop-helix transcription factors, repress ph
225 ediated through members of the HRT family of basic helix-loop-helix transcription factors represses s
226 (encoded by Atoh1, also known as Math1) is a basic helix-loop-helix transcription factor required for
227 bryonic and adult NG2 cells express Olig2, a basic helix-loop-helix transcription factor required for
228 z) binds to and negatively regulates Ebf1, a basic helix-loop-helix transcription factor required for
229 AZ) binds to and negatively regulates EBF, a basic helix-loop-helix transcription factor required for
232 he mouse have demonstrated key roles for the basic helix-loop-helix transcription factor SCL and the
234 This recruitment followed the loss from the basic helix-loop-helix transcription factor SPATULA (SPT
236 stomatal lineage cells is controlled by the basic helix-loop-helix transcription factor SPEECHLESS (
239 ranscription factors associate with myogenic basic helix-loop-helix transcription factors such as Myo
241 ion to the nucleus, where they interact with basic helix-loop-helix transcription factors, such as ph
242 uce rapid phosphorylation and degradation of basic helix-loop-helix transcription factors, such as PH
248 transport, and barren stalk1 (ba1) encodes a basic helix-loop-helix transcription factor that acts do
251 The SCL gene (also known as TAL-1) encodes a basic helix-loop-helix transcription factor that is esse
252 G12D into the open reading frame of Mist1, a basic helix-loop-helix transcription factor that is expr
254 are recognizable by expression of Atonal, a basic helix-loop-helix transcription factor that is requ
255 advanced MDS express high levels of TWIST, a basic helix-loop-helix transcription factor that opposes
256 ot affect the promoter activity of NeuroD, a basic helix-loop-helix transcription factor that regulat
259 the stability of MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that additi
260 sting New Gene (RING) domain, interacts with basic helix-loop-helix transcription factors that are ca
262 e mutant lacking MYC2, MYC3, and MYC4, three basic helix-loop-helix transcription factors that are kn
264 D1 acts as a dominant-negative antagonist of basic helix-loop-helix transcription factors that drive
265 er, the AHR nuclear translocator (ARNT), are basic helix-loop-helix transcription factors that mediat
268 ursor cells express Olig genes, which encode basic helix-loop-helix transcription factors that play i
270 ecific module is a set of "master regulator" basic helix-loop-helix transcription factors that regula
272 tion-factor (HRT) genes encode three related basic helix-loop-helix transcription factors that show s
273 uction of Mesp1 and Mesp2, a pair of related basic helix-loop-helix transcription factors that togeth
274 ocarbon receptor (AhR) is a ligand-activated basic-helix-loop-helix transcription factor that binds p
275 MPK3 and MPK6 can phosphorylate ICE1, a basic-helix-loop-helix transcription factor that regulat
276 lysis of a family of antagonistically acting basic helix-loop-helix transcription factors, the PHYTOC
277 SIGNIFICANCE STATEMENT The importance of the basic helix-loop-helix transcription factor transcriptio
278 We show that Ascl1, a bHLH (basic helix-loop-helix) transcription factor, transientl
282 dominant mutations in the gene encoding the basic helix-loop-helix transcription factor Twist1 are a
285 ediated cell adhesion to fibronectin and the basic helix-loop-helix transcription factor Twist1.
288 hat the expression of neurogenin 2 (Ngn2), a basic helix-loop-helix transcription factor, was signifi
289 (Id1), a dominant negative antagonist of the basic helix-loop-helix transcription factors, was found
291 Nescient helix-loop-helix-2 (NHLH2) is a basic helix-loop-helix transcription factor, which has b
292 m involves multiple gene families, including basic helix-loop-helix transcription factors, which init
293 ble factors (HIF)-1 and -2, oxygen-sensitive basic helix-loop-helix transcription factors, which medi
296 The stem cell leukaemia gene (Scl) encodes a basic helix-loop-helix transcription factor with a pivot
298 t Dif is not capable of synergizing with the basic helix-loop-helix transcription factors with which
300 rm breakdown requires the endosperm-specific basic helix-loop-helix transcription factor ZHOUPI.
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