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

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

2 The affected genes include the E2F transcription factor family.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

17 evolutionarily conserved subgroup of the SOX transcription factor family.

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

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

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

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

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

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

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

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

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

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

28 gulon that binds members of a plant-specific transcription factor family.

29 influence of the IFN regulatory factor (IRF) transcription factor family.

30 Pax6 is a member of the mammalian Pax transcription factor family.

31 in a new consensus binding site for the GATA transcription factor family.

32 show that the Y gene is a member of the MYB-transcription factor family.

33 tein, which is a member of the Rel/NF-kappaB transcription factor family.

34 if recognized by members of the AML/CBFalpha transcription factor family.

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

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

37 is transcriptionally regulated by the HSFA1 transcription factor family.

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

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

40 further subclassification criterion for this transcription factor family.

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

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

43 ral regulator PHYTOCHROME-INTERACTING FACTOR transcription factor family.

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

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

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

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

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

49 confirmed contributions from three distinct transcription factor families.

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

51 itative binding specificity models across 27 transcription factor families.

52 rmination of recognition codes for different transcription factor families.

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

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

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

56 rns of expression and phosphorylation within transcription factor families.

57 el homologues of the ptxR and tetR bacterial transcription-factor families.

58 ducers and activator of transcription (STAT) transcription factor family, a process that requires the

59 s, but the detailed mechanisms by which this transcription factor family activates embryo maturation

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

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

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

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

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

65 2I and GTF2IRD1 encode members of the TFII-I transcription factor family and are prime candidates in

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

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

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

69 -1 protein belongs to the Pit-Oct-Unc domain transcription factor family and is constitutively expres

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

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

72 is a pleiotropic regulator of the NF-kappaB transcription factor family and may be responsible for a

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

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

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

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

77 ry functions of two members of the AP1/NF-E2 transcription factor family and their stable binding in

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

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

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

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

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

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

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

85 that members of the GATA and HNF3/fork head transcription factor families are essential for the form

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

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

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

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

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

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

92 hway, including those from the GATA and Nkx2 transcription factor families, are not well defined.

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

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

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

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

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

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

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

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

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

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

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

104 Most transcription factor families contain highly related par

105 The Ets and IRF transcription factor families contain structurally diver

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

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

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

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

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

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

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

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

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

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

116 The NFkappaB transcription factor family facilitates the activation o

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

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

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

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

121 Dimers of the Rel/NFkappaB transcription factor family form with differential stabi

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

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

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

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

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

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

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

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

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

131 n beta (C/EBP beta), from two different bZIP transcription factor families, has been determined and r

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

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

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

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

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

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

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

139 Members of the NF-kappa B/Rel transcription factor family have been shown recently to

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

167 The AP2 transcription factor family is a set of developmentally

168 The ETS transcription factor family is characterized by a conser

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

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

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

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

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

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

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

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

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

178 ivity of RelA, a member of the Rel/NF-kappaB transcription factor family, is constitutively activated

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

180 1a, a member of the LIM-homeodomain (LIM-HD) transcription factor family, is expressed in the roof pl

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

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

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

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

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

186 ediate-early response, growth-promoting AP-1 transcription factor family, JunD, c-Jun, and c-Fos, to

187 The transcription factor family known as myocyte enhancer fa

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

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

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

191 rs was a big step forward in the analysis of transcription factor family member specificity, allowing

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

193 1 may function in concert with LIN-1, an Ets transcription factor family member that is one of the ta

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

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

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

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

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

199 own by this laboratory to be a 3-zinc finger transcription factor family member; its expression is ra

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

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

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

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

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

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

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

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

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

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

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

211 cations fuse the EWS gene to a subset of ets transcription factor family members, most commonly the F

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

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

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

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

216 The transcription factor family, nuclear factor of activated

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

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

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

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

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

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

223 Because members of transcription factor families often exhibit similar sequ

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

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

226 that the binding sites of the two different transcription factor families overlap.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

246 ally, HBx activates members of the NF-kappaB transcription factor family, some of which are antiapopt

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

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

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

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

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

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

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

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

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

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

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

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

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

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

261 One transcription factor family that has several members inv

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

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

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

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

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

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

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

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

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

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

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

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

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

275 lection is achieved in this large eukaryotic transcription factor family through discrete protein-pro

276 Members of transcription factor families typically have similar DNA

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

278 However, several transcription factor families varied in vascular express

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

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

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

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

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

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

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

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

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

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

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