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

1 mber of the ETHYLENE-INSENSITIVE3-LIKE (EIL) transcription factor family.

2 ral regulator PHYTOCHROME-INTERACTING FACTOR transcription factor family.

3 TS-related gene (ERG) is a member of the ETS transcription factor family.

4 and is a putative member of the winged helix transcription factor family.

5 sions between TMPRSS2 and members of the ETS transcription factor family.

6 ne (IRX3), a member of the Iroquois homeobox transcription factor family.

7 ith TLX, a repressor protein in the tailless transcription factor family.

8 the basic helix-loop-helix (bHLH) class VIII transcription factor family.

9 l cycle regulatory member of the zinc finger transcription factor family.

10 xp3 is a member of the forkhead/winged helix transcription factor family.

11 st two distinct roles for members of the ETS transcription factor family.

12 Ets1 is a member of the Ets transcription factor family.

13 ne 1 (TIEG1) is a member of the Kruppel-like transcription factor family.

14 regulated genes including members of the myb transcription factor family.

15 Lame duck and is likely a member of the ETS transcription factor family.

16 ncodes a member of the forkhead/winged-helix transcription factor family.

17 member of the Rel/nuclear factor (NF)-kappaB transcription factor family.

18 usly characterized binding site for the AP-1 transcription factor family.

19 evolutionarily conserved subgroup of the SOX transcription factor family.

20 ngly stimulated by Elf3, a member of the Ets transcription factor family.

21 ism for functional specificity within the Sp transcription factor family.

22 ors of the nuclear factor-kappaB (NF-kappaB) transcription factor family.

23 nsensus-binding site for a member of the ets transcription factor family.

24 nduction of downstream signaling by the Stat transcription factor family.

25 e genes with FKHR, a member of the fork head transcription factor family.

26 rs of the basic region leucine zipper (bZIP) transcription factor family.

27 is transcriptionally regulated by the HSFA1 transcription factor family.

28 encodes a member of the basic leucine zipper transcription factor family.

29 idopsis AINTEGUMENTA-LIKE/PLETHORA (AIL/PLT) transcription factor family.

30 ption of several genes belonging to the AP-1 transcription factor family.

31 quence identity with members of the Ros/MucR transcription factor family.

32 The affected genes include the E2F transcription factor family.

33 by binding and inhibiting members of the E2F transcription factor family.

34 ily and tulip, with special focus on the TCP transcription factor family.

35 tors (LXRs), members of the nuclear receptor transcription factor family.

36 e Wnt-signaling pathway and the Iroquois/IRX transcription factor family.

37 rm, including Geminin and members of the Zic transcription factor family.

38 e sole member of an evolutionarily conserved transcription factor family.

39 o the specificity proteins (Sp)/Kruppel-like transcription factor family.

40 f the TEOSINTE BRANCHED1/CYCLOIDEA/PCF (TCP) transcription factor family.

41 further subclassification criterion for this transcription factor family.

42 s the third member of the neural zinc finger transcription factor family.

43 tions for the future study of this important transcription factor family.

44 pointed to a regulatory hierarchy among the transcription factor families.

45 inding sites for members of the Ets and Runx transcription factor families.

46 confirmed contributions from three distinct transcription factor families.

47 atures of overlapping cis regulation by four transcription factor families.

48 mASH-1, but not by members of several other transcription factor families.

49 rmination of recognition codes for different transcription factor families.

50 ascades, using molecules from well-conserved transcription factor families.

51 TA or CCAAT/enhancer binding protein (C/EBP) transcription factor families.

52 itative binding specificity models across 27 transcription factor families.

53 ng pathways, and increased diversity in some transcription factor families.

54 -tunes the DNA binding specificities of some transcription factor families.

55 rns of expression and phosphorylation within transcription factor families.

56 uced in vivo with reporters for 46 inducible transcription factor families and found that along with

57 sical cooperativity between the bZIP and IRF transcription factor families and illustrate the critica

58 genetic pathways involving several distinct transcription factor families and small regulatory RNAs.

59 teraction between the lineage-defining T-box transcription factor family and a Brg1-containing SWI/SN

60 e ELL (eleven-nineteen lysine-rich leukemia) transcription factor family and also acts as a tumor sup

61 2I and GTF2IRD1 encode members of the TFII-I transcription factor family and are prime candidates in

62 ury (T) is the founding member of this T-box transcription factor family and has been implicated in g

63 ene encodes a member of the Arabidopsis GATA transcription factor family and has been implicated in t

64 finger/Bric-a-brac Tramtrack Broad complex) transcription factor family and is a novel protein that

65 -1 protein belongs to the Pit-Oct-Unc domain transcription factor family and is constitutively expres

66 Fli-1 belongs to the Ets transcription factor family and is expressed primarily i

67 The ER71 protein belongs to the ETS transcription factor family and is testis-specifically e

68 ric-abrac/poxvirus and zinc finger (BTB/POZ) transcription factor family and master regulator of the

69 Sox10 is a member of the group E Sox transcription factor family and plays key roles in neura

70 A1 is a member of the homeodomain-containing transcription factor family and possesses pivotal roles

71 PGC-1beta coactivates the SREBP transcription factor family and stimulates lipogenic gen

72 LCA-4 reveals that it is a member of the ETS transcription factor family and that it seems to associa

73 the plant-specific NAC (NAM, ATAF1,2, CUC2) transcription factor family and we have shown previously

74 Expression of NFAT, a CN-dependent transcription factor family, and FK506 binding protein 1

75 INK ME (DKM; bZIP30) is a member of the bZIP transcription factor family, and is expressed in meriste

76 nge PAX3 and PAX7, members of the paired box transcription factor family, and juxtapose these genes w

77 Response Factors (ERFs), which belong to the transcription factor family APETALA2/ERF.

78 evidence that interactions between these two transcription factor families are crucial for the develo

79 evious work, these data reveal that distinct transcription factor families are deployed in post-mitot

80 e nine-member GRF (GROWTH REGULATORY FACTOR) transcription factor family are DELLA interactors and, a

81 ot analyses revealed that members of the AP1 transcription factor family are differentially regulated

82 Members of the MiT transcription factor family are pivotal regulators of se

83 Members of the large Arabidopsis NAC domain transcription factor family are regulators of meristem d

84 erent members of the plant-specific R2R3-MYB transcription factor family are required for mediating s

85 Members of the Stat transcription factor family are specifically activated b

86 Members of the Ets transcription factor family are widely expressed in both

87 FOXA1 and FOXA2, members of the forkhead transcription factor family, are critical for epithelial

88 led RUNX1), a DNA-binding subunit of the CBF transcription factor family, are crucial for the generat

89 that (i) PYR/RCAR ABA receptor and ABF-type transcription factor families arose during land coloniza

90 s of the Sry-related high mobility box (Sox) transcription factor family as being transcriptional reg

91 ETS-related gene (ERG), a member of the ETS transcription factor family, as the most frequently over

92 We have identified transcription factor families associated with these earl

93 bers of the myocyte enhancer factor 2 (MEF2) transcription factor family bind a regulatory element up

94 RB1 gene product, pRB, is to repress the E2F transcription factor family, but pRB also functions to r

95 d evolvability of the basic helix-loop-helix transcription factor family by creating all possible 95

96 l members of the early growth response (EGR) transcription factor family can be implicated in regulat

97 Furthermore, they reveal how a single transcription factor family can control and integrate mu

98 Different members of the same transcription factor family can follow opposite trajecto

99 The Nuclear factor I (NFI) transcription factor family consists of four genes (Nfia

100 Most transcription factor families contain highly related par

101 The Ets and IRF transcription factor families contain structurally diver

102 Transcription factors belonging to the same transcription factor families contain very similar DNA b

103 show that lambda distributions for different transcription factor families correspond with their DNA

104 n annotation we have also performed a custom transcription factor-family curation of all Pfam domains

105 ion has been how the various members of this transcription factor family distinguish identity feature

106 aling coordinates dysregulation of these two transcription factor families during oncogenesis remains

107 ling, pointing to an alternate role for this transcription factor family during retinal development.

108 omine expression analysis suggested that the transcription factor family E2F played an important role

109 Drosophila contains two members of the E2F transcription factor family (E2f and E2f2), which contro

110 Members of the AP-1 transcription factor family, especially c-Jun and c-Fos,

111 e families examined, including genes in most transcription factor families, exhibited a median freque

112 The NFkappaB transcription factor family facilitates the activation o

113 rs within the CNS, and the relevance of this transcription factor family for learning and memory.

114 pensability of these two members of the Foxo transcription factor family for normal vascular developm

115 First, by screening the entire ETS transcription factor family for rearrangements, we found

116 pumps by members of the fungal zinc-cluster transcription-factor family (for example Pdr1p orthologu

117 Two members of the forkhead/winged helix transcription factor family, Foxa1 and Foxa2, have been

118 highly related members of the mammalian FoxO transcription factor family, FoxO1, FoxO3, and FoxO4, re

119 ATAs are a subfamily of the 30-membered GATA transcription factor family from Arabidopsis.

120 GCMB is a member of the small transcription factor family GCM (glial cells missing), w

121 ng to enhanced expression of a subset of E2F transcription factor family gene targets.

122 demonstrate that a member of the grainyhead transcription factor family, Grainyhead-like 1 (XGrhl1)

123 nd we implicate another member of the TFII-I transcription factor family, GTF2I, in both aspects.

124 ple lines of evidence indicate that the AP-2 transcription factor family has an important regulatory

125 The nuclear factor-kappaB (NF-kappaB) transcription factor family has been considered the cent

126 The diversified NF-kappaB transcription factor family has been extensively charact

127 a, the AT-hook motif nuclear-localized (AHL) transcription factor family has been implicated in restr

128 The NF-kappaB/Rel transcription factor family has been shown to protect ma

129 rowth response 1), a member of a zinc finger transcription factor family, has been described as tumor

130 t, a recently discovered member of the T-box transcription factor family, has been reported to play a

131 gration factor 1 (Fli1), a member of the Ets transcription factor family, has been shown to play a pi

132 Klf5, a member of the Kruppel-like transcription factor family, has essential roles during

133 here describe a novel member of the Six gene transcription factor family, Hau-Six1/2A, which contribu

134 s (BMPs) and members of the Sox and homeobox transcription factor families have been shown to have cr

135 re unclear, the STAT, Rel/NF-kappaB, and Ets transcription factor families have recently been reporte

136 Members of the POU4F/Brn3 transcription factor family have an established role in

137 Members of the well-conserved Olf/EBF (O/E) transcription factor family have been shown to play impo

138 coding genes, making this one of the largest transcription factor families in Arabidopsis.

139 The presence of transcription factor families in genomes represents a si

140 standing of the evolution of these prominent transcription factor families in the angiosperms.

141 , we studied the regulatory role of the AP-1 transcription factor family in blood development using e

142 zation and is the first to implicate the KLF transcription factor family in cardiac metabolism.

143 vide the first comprehensive analysis of any transcription factor family in Cryptosporidium, a basal-

144 ssociated domain (ZAD) family is the largest transcription factor family in dipteran insects.

145 e C(2)H(2) zinc-finger proteins, the largest transcription factor family in eukaryotic genomes.

146 ification and expression analysis of the TCP transcription factor family in Gossypium raimondii.

147 PETALA2/ethylene-responsive factor (AP2/ERF) transcription factor family in rose (Rosa hybrida), RhER

148 new function for a member of the heat-shock transcription factor family in stem cell development and

149 C2H2 zinc fingers define the largest transcription factor family in the human proteome.

150 er transcription factors compose the largest transcription factor family in the mammalian genome.

151 nriched in granule neurons, implicating this transcription factor family in the neuronal subtype-sele

152 ining a role for selected members of the ETS transcription factor family in the regulation of vascula

153 Mei4p, a member of the forkhead transcription factor family, in turn regulates a host of

154 The paired-type homeodomain transcription factor family includes more than 20 member

155 mers corresponded to sites for several known transcription factor families (including CREB, ETS, EGR-

156 ion, Tax is known to interface with numerous transcription factor families, including activating tran

157 s accompanied by altered activity of several transcription factor families, including beta-catenin, A

158 ediated by the concerted action of different transcription factor families, including the transcripti

159 of the AINTEGUMENTA-LIKE/PLETHORA (AIL/PLT) transcription factor family, including AINTEGUMENTA (ANT

160 The members of the class O forkhead (FOXO) transcription factor family, including FOXO3a, act as se

161 way and on members of the Runx, Fox, and Sox transcription factor families, indicating that RA modula

162 The NF-kappaB transcription factor family influences breast cancer out

163 echanism via which the stress-responsive AHL transcription factor family influences growth in petiole

164 n addition to activating members of the STAT transcription factor family, interferon alpha/beta (IFNa

165 l regulatory element-binding protein (SREBP) transcription factor family is a critical regulator of l

166 The AP2 transcription factor family is a set of developmentally

167 The ETS transcription factor family is characterized by a conser

168 This transcription factor family is characterized by a DNA-bi

169 The T-box transcription factor family is important in cellular spe

170 The T-box transcription factor family is important in numerous dev

171 Our data indicate that the BPC transcription factor family is integral for a wide range

172 The Ets transcription factor family is involved in a variety of

173 The LSF/Grainyhead transcription factor family is involved in many importan

174 The E2F transcription factor family is known to play a key role

175 These results demonstrate that the NF-kappaB transcription factor family is regulated by GpI-mGluRs i

176 KLF7, a member of the Kruppel-like transcription factor family, is believed to regulate neu

177 Isl1, a member of the LIM-homeodomain transcription factor family, is expressed early in this

178 1a, a member of the LIM-homeodomain (LIM-HD) transcription factor family, is expressed in the roof pl

179 ERG, a member of the ETS transcription factor family, is frequently overexpressed

180 type A (NFI-A), a member of the NFI/CAAT-box transcription factor family, is induced in mouse neurons

181 Helios, a member of the Ikaros transcription factor family, is preferentially expressed

182 FRUITFULL (FUL), a member of the MADS-domain transcription factor family, is required for fruit growt

183 We show that Tbx1, a member of the T-box transcription factor family, is required for normal deve

184 The transcription factor family known as myocyte enhancer fa

185 Sequences for binding by other transcription factor families like MYC, AP2/ERF, bZIP, e

186 the gene for the basic leucine zipper (bZIP) transcription factor family member ATF-2.

187 l target of MK2 has been identified, the ETS transcription factor family member ER81, whose dysregula

188 further validated by the case studies of Sox transcription factor family member proteins and Zika vir

189 roblast transformation-specific domain (Ets) transcription factor family member Spi-C, and oncogene M

190 1 may function in concert with LIN-1, an Ets transcription factor family member that is one of the ta

191 r the first time that a Cut-like homeodomain transcription factor family member, Cux2 (Cutl2), regula

192 Foxp3, an X chromosome-encoded forkhead transcription factor family member, is indispensable for

193 leukemia virus integration 1 (FLI1), an Ets transcription factor family member, is linked to acute m

194 sly isolated different isoforms of a new Ets transcription factor family member, NERF/ELF-2, NERF-2,

195 NFIB (nuclear factor I B) is a NFI transcription factor family member, which is essential f

196 t, Src family kinases, NFkappaB p65, and AP1 transcription factor family members c-Jun and c-Fos, dem

197 that the unique functions of closely related transcription factor family members can be dictated by d

198 The TFII-I transcription factor family members contain multiple put

199 androgen-regulated gene TMPRSS2 and the ETS transcription factor family members ERG, ETV1, and ETV4

200 Here, we show that the Pea3 transcription factor family members Etv4 and Etv5 are ex

201 ng activity of HMG (TCF) and RHD (NF-kappaB) transcription factor family members in contrast to highe

202 ve immunity are guided by activation of STAT transcription factor family members in response to envir

203 androgen-regulated TMPRSS2 promoter with ETS transcription factor family members is found frequently

204 es disrupted the DNA binding activity of Sp1 transcription factor family members to an ERalpha minima

205 ver, putative binding sites for ETS and AP-1 transcription factor family members were identified.

206 epithelia, and epithelium-specific Ets (ESE) transcription factor family members were increased durin

207 n assays were used to identify the different transcription factor family members whose DNA binding ac

208 -binding preferences of the C2H2 zinc-finger transcription factor family members.

209 IP1); GADD153; CAAT/enhancer binding protein transcription factor family members; and proteins involv

210 MITF, TFE3, TFEB, and TFEC comprise a transcription factor family (MiT) that regulates key dev

211 ated TMPRSS2 promoter to a member of the ETS transcription factor family, most commonly ERG.

212 The transcription factor family, nuclear factor of activated

213 Forkhead box transcription factor family O (FOXO) transcription facto

214 asal promoter activity by members of the NFI transcription factor family occur via multiple mechanism

215 d that the large-scale expansion of the bHLH transcription factor family occurred before the divergen

216 ed drug screening strategy targeting the p53 transcription factor family of importance in human cance

217 evel by the specificity protein/Kruppel-like transcription factor family of members, which explains t

218 The highly conserved fungal Ste12 transcription factor family of proteins play critical ro

219 Because members of transcription factor families often exhibit similar sequ

220 the expression of two members of the onecut transcription factor family, Onecut1 (Oc1) and Onecut2 (

221 and metabolic processes change, and identify transcription factor families operating at different tim

222 e suggested that members of the GATA and Nkx transcription factor families physically interact, and s

223 The SRY-related (SOX) transcription factor family pivotally contributes to det

224 CIS genes included members of a zinc finger transcription factors family, Plag1 and Plagl2, with eig

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

226 Members of the SoxB transcription factor family play critical roles in the r

227 The NF-kappaB transcription factor family plays a central role in the

228 The E2F transcription factor family plays a crucial and well est

229 e fraction of motifs examined we describe 25 transcription factor family predictions for lung.

230 HOXB4, a member of the Homeobox transcription factor family, promotes expansion of hemat

231 y disruption assays demonstrated that an Ets transcription factor family protein, GA-binding protein

232 results demonstrate that members of the NFI transcription factor family regulate CYP3A4 and CYP3A7 b

233 The auxin response factor (ARF) transcription factor family regulates auxin-responsive g

234 In developing bilaterans, the Hox transcription factor family regulates batteries of downs

235 In plants, the AUXIN RESPONSE FACTOR (ARF) transcription factor family regulates gene expression in

236 The basic helix-loop-helix (bHLH) transcription factor family regulates numerous developme

237 ne demethylases, members of a newly emerging transcription-factor family, remove methyl groups from t

238 WRKY75 is the first member of the WRKY transcription factor family reported to be involved in r

239 onents of the Cdk5 signaling pathway and Irx transcription factor family, representing genes identifi

240 proteomic breadth and complexity of the KLF transcription factor family, revealing the existence of

241 ry of the GATA binding protein (GATA factor) transcription factor family revolutionized hematology.

242 uitously expressed members of the grainyhead transcription factor family, sharing significant sequenc

243 s III homeodomain leucine zipper (HD-ZIPIII) transcription factor family specify the adaxial domain (

244 t from the most studied genes in the AP2/ERF transcription factor family such as AP2s, CBF/DREB1s, DR

245 onstitutively nuclear basic helix-loop-helix transcription factor family, such as PHYTOCHROME-INTERAC

246 Members of the T-box transcription factor family (Tbx) are associated with se

247 tative co-regulatory proteins are members of transcription factor families that all bind to the same

248 the Fox family, highlighting several key Fox transcription factor families that are important for mam

249 We identify transcription factor families that bind to these PREs, c

250 bers of the G2-like, NAC, AP2, MADS, and MYB transcription factor families that may play roles as reg

251 NF-kappaB is a transcription factor family that activates numerous gene

252 -independent, noncanonical member of the E2F transcription factor family that acts as a transcription

253 RelB is an unusual member of the NF-kappaB transcription factor family that acts as both a transcri

254 s to mammals, and yet they belong to a large transcription factor family that bind nearly identical D

255 el-like factor 8) is a member of the Kruppel transcription factor family that binds CACCC elements in

256 ctivated by specific isoforms of the LEF/TCF transcription factor family that contain an alternative

257 E2F7 as a novel member of the mammalian E2F transcription factor family that has properties of a tra

258 One transcription factor family that has several members inv

259 gulated by and able to activate NF-kappaB, a transcription factor family that induces transcription o

260 known as TCF7L1) is a member of the TCF/LEF transcription factor family that is central in regulatin

261 a member of the Ca(2+) /calmodulin-regulated transcription factor family that is conserved in multice

262 ERG is a member of the ETS transcription factor family that is highly enriched in e

263 ototypic member of a novel subset of the ETS transcription factor family that is predominantly expres

264 CYSTEINE (BPC) proteins are a plant-specific transcription factor family that is present throughout l

265 the dominant-negative basic helix-loop-helix transcription factor family that lacks DNA binding activ

266 luences of conflicting behavioral cues and a transcription factor family that may contribute to the d

267 ore, we found that PU.1 (a member of the Ets transcription factor family that plays a crucial role in

268 GATA-1 is the founding member of a transcription factor family that regulates growth and ma

269 VIVIPAROUS1/ABI3-LIKE (VAL) clades of the B3 transcription factor family that respectively activate a

270 composition and diversity of the apple bHLH transcription factor family that will provide a platform

271 ng site of a member of the Plasmodium ApiAP2 transcription factor family, that we recently showed fun

272 e-amino acid contacting pairs for particular transcription factor families, thereby yielding structur

273 on blocked the binding of members of the E26 transcription factor family to the TERT promoter, reduce

274 mours described as microphthalmia-associated transcription factor family translocation-associated ren

275 Members of transcription factor families typically have similar DNA

276 on-helix-loop-helix-leucine-zipper (bHLH-LZ) transcription factor family, USF1 and USF2, and reporter

277 However, several transcription factor families varied in vascular express

278 ion of genes that encode members of the WRKY transcription factor family was rapidly and strongly ind

279 GATA-4, a member of a zinc finger transcription factor family, was confirmed to be amplifi

280 FOXO1, a member of forkhead transcription factor family, was phosphorylated at Ser-2

281 zinc finger, high mobility group, and other transcription factor families were enriched in alpha cel

282 ncoding proteins belonging to 39 of the main transcription factor families were examined by microarra

283 Furthermore, members of other transcription factor families were identified as interac

284 Twenty-two transcription factor families were predicted to have bin

285 n all three tissues, members of NAC and WRKY transcription factor families were up-regulated, but com

286 Phylogenetic analyses of each transcription factor family were used to identify subgro

287 AP1-motifs, which bind JUN and FOS transcription factor families, were observed in MED25-oc

288 riptional regulation is found in a different transcription factor family where two Bacillus species p

289 Lmx1b, another member of the LIM-HD transcription factor family which is highly related to L

290 inhibition of members of the forkhead (FKHR) transcription factor family, which are key regulators of

291 igated the role of the Forkhead box O (FOXO) transcription factor family, which has been shown to pot

292 an epithelially restricted member of the ETS transcription factor family, which is involved in a wide

293 Foxc1 belongs to the forkhead transcription factors family, which plays a critical rol

294 There are many examples of transcription factor families whose members control gene

295 s a ubiquitously expressed member of the Fox transcription factor family whose expression is restrict

296 during early larval development, focusing on transcription factor families with known functions in ve

297 Elf-1, a member of the E 26-specific transcription factor family with a predicted molecular m

298 solation of Tel-2, a novel member of the Ets transcription factor family, with high homology to Tel/E

299 ultiple consensus binding sites for specific transcription factor families within the BIRM are requir

300 e selected representatives of four different transcription factor families (zinc finger GATA, basic h