ライフサイエンスコーパス: homeodomain protein

1 ription factors including Prox1, an atypical homeodomain protein.

2 direct interaction with the UNC-86/Brn3 POU homeodomain protein.

3 opment requires the REDUCED COMPLEXITY (RCO) homeodomain protein.

4 nteraction with Extradenticle (Exd), another homeodomain protein.

5 by the cooperative actions of an ncRNA and a homeodomain protein.

6 also regulated by interaction with a partner homeodomain protein.

7 FD neurons and is regulated by the TTX-1 OTX homeodomain protein.

8 rform a structure/function analysis for this homeodomain protein.

9 epression and activation domains of vnd/NK-2 homeodomain protein.

10 nt disorder caused by mutations in the PITX2 homeodomain protein.

11 -1, which encodes a deltaEF1/ZFH-1 Zn-finger-homeodomain protein.

12 fferential expression of the Nkx6-type COG-1 homeodomain protein.

13 important decision is regulated by the UNC-4 homeodomain protein.

14 tetranucleotide ATTA commonly recognized by homeodomain proteins.

15 anocortin is potentiated by lineage-specific homeodomain proteins.

16 es of TALE (Three Amino acid Loop Extension) homeodomain proteins.

17 ural homology with the DNA-binding domain of homeodomain proteins.

18 many of which are developmentally important homeodomain proteins.

19 with each other as well as the PBX family of homeodomain proteins.

20 unctions in part as a cofactor for Hox class homeodomain proteins.

21 e consensus site for Antennapedia superclass homeodomain proteins.

22 lular subtypes in conjunction with other LIM/homeodomain proteins.

23 to the Cart1/Alx3/Alx4 family of vertebrate homeodomain proteins.

24 uence identified previously for paired class homeodomain proteins.

25 inguishes HNF-1alpha from other flexible POU-homeodomain proteins.

26 y at positions 24 and 25 compared to related homeodomain proteins.

27 bers of the Pitx gene family of bicoid-class homeodomain proteins.

28 sequence distinct from those of other fungal homeodomain proteins.

29 (CREB) and can interact with cofactor of LIM homeodomain protein 1 (CLIM1) and CLIM2.

30 Here, we show that zinc-finger and homeodomain protein 2 (ZHX2) is specifically expressed i

31 he product of the C15 gene, which is another homeodomain protein, a homolog of the human Hox11 oncoge

32 s were enriched in alpha cells; in contrast, homeodomain proteins accounted for 51% of a total of 45

33 controls large micromere specification, the homeodomain protein Alx1.

34 s identified near the N terminus of vnd/NK-2 homeodomain protein (amino acid residues 154-193), which

35 NKX3.1 transcription factor is an NK family homeodomain protein and a tumor suppressor gene that is

36 ftz encodes a DNA-binding homeodomain protein and is known to regulate genes of th

37 n the 5' leader of the mRNA encoding the Gtx homeodomain protein and showed that shorter nonoverlappi

38 include Oct4, a member of the POU family of homeodomain proteins and a second recently identified ho

39 pped to 8p21, is a member of the NK class of homeodomain proteins and is expressed primarily in the p

40 uggesting that the associations between TALE homeodomain proteins and Oct-1 regulate neuron-specific

41 y of transcriptional complexes involving LIM-homeodomain proteins and other transcription factors tha

42 Several transcription factors, including homeodomain proteins and T-box proteins, are essential f

43 direct transcriptional targets of clustered homeodomain proteins and that different homeodomain prot

44 nalogous to the N-terminal arm of eukaryotic homeodomain proteins and the "wings" of winged-helix pro

45 The regulatory functions of individual homeodomain proteins and the networks in which they act

46 KNOX proteins interact with BEL1-like (BELL) homeodomain proteins and together bind a target sequence

47 XSEs (nuclear receptors and homeodomain proteins) and ASEs (T-box and zinc finger pr

48 ely half of the NUP98 fusion partners encode homeodomain proteins, and at least 5 NUP98 fusions invol

49 ing development through interaction of WDR5, homeodomain proteins, and chromatin remodeling enzymes.

50 y by E1A, Twist, Pu.1, and the Hox family of homeodomain proteins-and suggest that E47 and EBF play d

51 y of complexes comprised of Chip and the LIM-homeodomain protein Apterous.

52 The Six3 and Rx3 homeodomain proteins are essential for the specification

53 Homeodomain proteins are key regulators of patterning du

54 LIM homeodomain proteins are known to regulate several aspec

55 Bar homeodomain proteins are required for transcriptional re

56 echanism by which the activities of bHLH and homeodomain proteins are temporally and spatially integr

57 genes, and prep, which encodes a TALE-family homeodomain protein, are expressed at the anterior pole.

58 We show that two LIM-homeodomain proteins, Arrowhead and Lim1, are expressed

59 s in the highly conserved Aristaless-related homeodomain protein ARX have been shown to underlie mult

60 Aristaless related homeodomain protein (Arx) specifies the formation of the

61 vations, we suggest that the function of Bar homeodomain proteins as cell-type-specific inhibitors of

62 that successfully predicts binding sites for homeodomain proteins as distant from mouse as Drosophila

63 We have identified a homeodomain protein, AtNDX, that regulates COOLAIR, a se

64 ne products: the silkworm orthologues of LIM homeodomain protein Awh, LIM domain-binding protein (Ldb

65 y by a combination of factors, including the homeodomain protein Bar.

66 imers containing Pbx/Prep1 or Pbx/Meis1 TALE homeodomain proteins bind to four functional elements wi

67 r reporter genes demonstrated that the three homeodomain protein binding sites located between -80 an

68 observed between the R2 site and an adjacent homeodomain protein-binding site previously characterize

69 lity shift assay, we report that Lhx2, a LIM-homeodomain protein, binds to the homeodomain site in th

70 mber of studies that HOX11, similar to other homeodomain proteins, binds DNA and transactivates trans

71 The zinc finger protein Klf7 and POU homeodomain protein Brn3a are each required for efficien

72 he interactions between Clone A and vnd/NK-2 homeodomain protein by mobility-shift assay, DNase I foo

73 w that the Caenorhabditis elegans Six family homeodomain protein C. elegans homeobox (CEH-34) and the

74 ristem and interact with another subclass of homeodomain proteins called the BELL family.

75 This is the first report that a homeodomain protein can modify the activity of Topo I an

76 This is the first demonstration that a homeodomain protein can oligomerise in vivo.

77 We show that the MEC-3 LIM homeodomain protein can outcompete the execution of a ne

78 st-muscle gene expression, thus showing that homeodomain proteins can direct bHLH proteins to establi

79 have demonstrated that in RCC, the Cut-like homeodomain protein (CDP/Cut) is involved in FIH transcr

80 The caudal-type homeodomain protein Cdx2 is implicated in the formation

81 The homeodomain protein CDX2 specifies the embryonic intesti

82 ha (HNF-1 alpha), GATA-4, and caudal related homeodomain proteins Cdx2 and Cdx1 are the primary trans

83 de operating in DVC was defined from the LIM-homeodomain protein CEH-14 through CEH-63 to the helix-t

84 Here we report that the Six homeodomain protein CEH-34 and its cofactor Eyes Absent,

85 ivates the CC specification factor, the Six2 homeodomain protein CEH-34, and functions cooperatively

86 al bHLH proteins NGN-1 and HLH-2 and the Otx homeodomain protein CEH-36.

87 We identified a new XSE, the ONECUT homeodomain protein CEH-39, and showed that it acts as a

88 nd and activated by the Paired- and LIM-type homeodomain proteins CEH-10 and TTX-3.

89 Further, we found that 199 homeodomain proteins contain potential eIF4E-binding sit

90 d is the founding member of the K50 class of homeodomain proteins, containing a lysine residue at the

91 ctions are established, in part, through LIM homeodomain protein control of EphA receptors and ephrin

92 Now, Lee et al. report that two TALE homeodomain proteins control zygote development of the u

93 The HOX/HOM superfamily of homeodomain proteins controls cell fate and segmental em

94 y with other transcription factors (e.g. the homeodomain protein CRX).

95 hances its activity synergistically with the homeodomain protein CRX.

96 Ab and the homeodomain protein Cut are expressed in distinct but co

97 zinc finger protein Hindsight and suppresses homeodomain protein Cut to regulate the mitotic/endocycl

98 Lz causes transcriptional activation of the homeodomain protein Cut, which can then stabilize a Lz r

99 The homeodomain protein Cux1 is highly expressed in the neph

100 bdomains, we characterized expression of the homeodomain protein Dbx1 and the bHLH protein Olig2.

101 Homeodomain proteins, described 30 years ago, exert esse

102 The homeodomain protein Distal-less-3 (Dlx3) plays a crucial

103 Furthermore, the homeodomain proteins distal-less homeobox 5 (DLX5) and D

104 y shift assays identified AP-2 gamma and the homeodomain protein, Dlx 3, as the transcription factors

105 fy a and alpha cell identity, whereas the a1 homeodomain protein drives meiosis and sporulation and f

106 l of regulation to the activity of the PITX2 homeodomain protein during development.

107 In outer PRs, the K(50) homeodomain protein Dve is a key repressor that acts to

108 The mouse homeodomain protein, Engrailed-1, is generally viewed as

109 We show that LIM homeodomain proteins establish motor neuron topography b

110 ssential transcriptional regulators: Otx2, a homeodomain protein expressed broadly in head ectoderm i

111 Vsx2 (formerly Chx10), a homeodomain protein expressed in RPCs, is required for s

112 We now provide genetic evidence that Vax2, a homeodomain protein expressed in the ventral retina, is

113 Here we identify a key role for the homeodomain proteins Extradenticle (Exd) and Homothorax

114 e, curated collection of information for the homeodomain protein family.

115 Nanog is a divergent homeodomain protein found in mammalian pluripotent cells

116 TALE-homeodomain proteins function as components of heteromer

117 Most homeodomain proteins function as transcription factors,

118 Homeodomain proteins function in fungi to specify cell t

119 ardment, we show that TTG1, GL3, GL1 and the homeodomain protein GL2 do not move between adjacent epi

120 rsal expansion of ventral markers (e.g., the homeodomain protein GSH2) into the ventralmost pallial r

121 Knotted1-like TALE homeodomain proteins have been found to play important r

122 ered homeodomain proteins and that different homeodomain proteins have distinct effects on the promot

123 Nkx6 collaborates with the homeodomain protein Hb9 to specify ventrally projecting

124 he VB gene ceh-12 (encoding a homolog of the homeodomain protein HB9) in unc-4 mutants results in the

125 The homeodomain protein Hex, an early marker of anterior pos

126 xpressed homeodomain protein or proline-rich homeodomain protein (HHEX/PRH), which thereby lose their

127 , but is nuclear when complexed with another homeodomain protein, Homothorax (Hth).

128 Unlike other homeodomain proteins, Hop does not bind DNA.

129 The homeodomain protein HoxA10 interacts with negative cis e

130 to cDNA library screening we identified two homeodomain proteins, Hoxa10 and Hoxb8, which are expres

131 The homeodomain proteins, HoxA10 and Pbx1a, interact with ne

132 nce have established a critical role for the homeodomain protein HOXB7 in cancer.

133 ns, 84 homeodomain DNA-binding sites and 114 homeodomain proteins implicated in human genetic disorde

134 We demonstrate that a BELL1 related homeodomain protein in Arabidopsis, BELLRINGER, maintain

135 ttern of HOXB13, we studied the role of this homeodomain protein in prostate cells.

136 ive chromatin and reveals a critical role of homeodomain proteins in marking specific genes for activ

137 have investigated the role of Isl-class LIM homeodomain proteins in motor neuron diversification usi

138 -1/Oct-2 suggests an important role of these homeodomain proteins in the overall regulation of the Ig

139 hat CK2 may regulate the activity of several homeodomain proteins in this manner.

140 Hedgehog (Hh) and Fgf signals and Vax family homeodomain proteins in this patterning event.

141 Three-amino-acid-loop-extension (TALE) homeodomain proteins including Meis and Pbx families are

142 pools is governed by coordinately acting LIM-homeodomain proteins including the Islet-class factor Is

143 CNS pattern along the dorsoventral axis, the homeodomain protein Ind and the Sox-domain protein Dicha

144 e Pbx TALE (three-amino-acid loop extension) homeodomain proteins interact with class 1 Hox proteins,

145 We show that the Pbx1 and Meis2 homeodomain proteins interact with Klf4 and can be recru

146 ribe the use of 10 linked copies of the Gtx (homeodomain protein) IRES (abbreviated as SIRES) in plac

147 that one of these targets, the Iroquois-like homeodomain protein, IRX-1, functions as a key regulator

148 The Six1 homeodomain protein is a developmental transcription fac

149 The HOXA9 homeodomain protein is a key regulator of hematopoiesis

150 he pancreatic and duodenal homeobox 1 (PDX1) homeodomain protein is critical for the initiation of al

151 The PITX2 homeodomain protein is mutated in patients with Axenfeld

152 The UNC-86 POU homeodomain protein is present in CEM and URA neurons, a

153 er, a physical interaction between these two homeodomain proteins is necessary for induction of these

154 PRH/HHex (proline-rich homeodomain protein) is a transcription factor that cont

155 lisation of VAN, like that of the animal PBC homeodomain protein, is also regulated by interaction wi

156 We have previously shown that lmx1b, a LIM homeodomain protein, is expressed in the pronephric glom

157 ains two perfect consensus sites for the LIM-homeodomain protein ISL1.

158 The LIM-homeodomain protein, Isl1, plays an essential role in ce

159 Here we show that the LIM/homeodomain protein islet-1 is expressed in cells of the

160 The LIM homeodomain protein Islet1 (ISL1) is involved in the reg

161 Plant homeodomain protein Jade-1 (PHF17) is a candidate renal

162 a plant with dissected leaves, KNOTTED1-like homeodomain proteins (KNOX) are positive regulators of l

163 We show that two closely related LIM homeodomain proteins, Lhx2 and Lhx9, are expressed by a

164 entiated into motoneurons expressing the LIM homeodomain protein Lhx3.

165 ctivity by maintaining expression of the LIM homeodomain proteins Lhx3/4 in spinal motor neurons.

166 These precursors express the LIM homeodomain protein Lhx6 and have characteristics of pro

167 ate that the redundant activities of the LIM homeodomain proteins Lhx6 and Lhx7 are critical for cran

168 ted by the combinatorial activity of the LIM homeodomain proteins Lhx6, Lhx7 (Lhx8) and Isl1.

169 Here, we demonstrate that the LIM homeodomain protein Lhx9 is transiently expressed in Xen

170 lation in mice, we demonstrate here that the homeodomain protein LIM homeobox (Lhx)7 is essential for

171 on of their LIM domains with cofactor of LIM homeodomain proteins (LIM-HDs) (CLIM, also known as Ldb

172 less has been shown to function with the LIM-homeodomain protein LIM1 to regulate leg development.

173 Pbx homeodomain proteins mark promoters of a subset of Myod

174 In the ancestral mating circuit, two homeodomain proteins, Mata1 and Matalpha2, form a hetero

175 Coexpression of the homeodomain protein Meis1 and either HoxA7 or HoxA9 is c

176 One of the downstream targets of VegT, the homeodomain protein Mixer, is expressed at high levels a

177 We have identified an HMX homeodomain protein MLS-2 in a screen for factors requir

178 Here we show that the Nkx5/HMX homeodomain protein MLS-2 is required for cellular elong

179 Here, we show that the HMX/NKX homeodomain protein MLS-2 regulates ceh-36 expression sp

180 In the chick embryo, the Mnx class homeodomain protein MNR2 is expressed selectively by mot

181 We previously showed that Pbx homeodomain proteins modulate the activity of Myod to pr

182 th two regulators of GnRH transcription, the homeodomain proteins MSX1 and OCT1.

183 We propose that the three homeodomain proteins MSX2, DLX3, and DLX5 provide a key

184 show regulation of the Runx2 gene by several homeodomain proteins: MSX2 and CDP/cut repress whereas D

185 Here we present evidence that the homeodomain protein Nanog mediates acquisition of both e

186 One candidate is the variant homeodomain protein Nanog, which has the capacity to ent

187 on somatic cells, a process promoted by the homeodomain protein Nanog, which is central to the maint

188 The homeodomain proteins Nanog and Oct4 are essential for mo

189 in proteins and a second recently identified homeodomain protein, Nanog.

190 ession and maintaining the expression of key homeodomain proteins necessary for MN identity and survi

191 nation of transcriptional programs, with the homeodomain protein NKX2-5 being one of the key transcri

192 ast in part, by associating with the cardiac homeodomain protein Nkx2-5.

193 tricle during late gestation and require the homeodomain protein Nkx2.1 for their specification.

194 The homeodomain protein Nkx2.2 (Nkx2-2) is a key regulator o

195 Within the pancreatic islet, the homeodomain protein Nkx2.2 is essential for the differen

196 tiple binding sites for the cardiac-specific homeodomain protein Nkx2.5, and its promoter activity wa

197 hin the rostral hindbrain, the Shh-activated homeodomain proteins Nkx2.2 and Nkx6.1 cooperate to indu

198 factor, was a novel downstream target of the homeodomain protein, Nkx2-5.

199 The prostate-specific homeodomain protein NKX3.1 is a tumor suppressor that is

200 The prostate-specific tumor suppressor homeodomain protein NKX3.1 is inactivated by a variety o

201 We identify the homeodomain protein Nkx3.2 as a potent sequence-specific

202 Here, we demonstrate that homeodomain protein Nkx6 is a key member of the genetic

203 NvFollistatin, and NvFollistatin-like), the homeodomain proteins NvGoosecoid (NvGsc) and NvGbx, and

204 d induction, and that interacts with the POU homeodomain protein Oct-1.

205 The POU homeodomain protein Oct-4 and the Forkhead Box protein F

206 16-residue CPP derived from the Antennapedia homeodomain protein of Drosophila, was measured in singl

207 unc-30 encodes a homeodomain protein of the Pitx family and regulates the

208 Obox1 and Obox2 transcripts encode homeodomain proteins of 204 amino acids that share 97% i

209 Homeodomain proteins of the Hox family play an important

210 h studies also document co-overexpression of homeodomain proteins of the Meis and Pbx families in poo

211 TALE (three-amino-acid loop extension) class homeodomain proteins of the Pbx and Meis families are al

212 knox genes encode homeodomain proteins of the TALE superclass of transcrip

213 scription factor hematopoietically expressed homeodomain protein or proline-rich homeodomain protein

214 The homeodomain protein, Otx2, is a critical regulator of ve

215 these amino acids are conserved between many homeodomain proteins, our results suggest that CK2 may r

216 oring of hexameric complexes of specific LIM homeodomain proteins over tetramers could dictate the ch

217 Maternal and zygotic activities of the homeodomain protein PAL-1 specify the identity and maint

218 Furthermore, we report that the Caudal-like homeodomain protein PAL-1, whose role in early embryogen

219 onstrated the physical association between a homeodomain protein, pancreatic-duodenal homeobox factor

220 h an adjacent protein complex containing the homeodomain protein Pbx, which appears to be constitutiv

221 rs form multimeric complexes with TALE-class homeodomain proteins (Pbx, Meis) to regulate tissue morp

222 resent the first work demonstrating that the homeodomain proteins PBX1 and PREP1 are cellular factors

223 , we demonstrate that the beta cell-specific homeodomain protein Pdx-1 interacts with histone deacety

224 Two related BELL1-like homeodomain proteins, PENNYWISE (PNY) and POUND-FOOLISH

225 Homeodomain proteins play critical roles during developm

226 nscriptional regulations, the BarH family of homeodomain proteins play essential roles in cell fate s

227 Homeodomain proteins play important roles in normal deve

228 as found to be identical to WUSCHEL (WUS), a homeodomain protein previously shown to be involved in s

229 at a trans cription factor, the proline-rich homeodomain protein PRH, is a negative regulator of eIF4

230 The Proline Rich Homeodomain protein (PRH/Hex) is a transcription factor

231 The proline-rich homeodomain protein (PRH/Hex) regulates transcription by

232 have shown previously that the Proline-Rich Homeodomain protein (PRH/Hex) self-assembles to form oli

233 sly that phosphorylation of the Proline-Rich Homeodomain protein (PRH/Hhex) by CK2 inhibits the DNA-b

234 The proline-rich homeodomain protein, PRH/HEX, participates in the early

235 tiation by suppressing the expression of the homeodomain protein Prospero in immature INPs.

236 We found that the homeodomain protein Prox1 regulates the exit of progenit

237 ated by the orphan nuclear receptor SF-1 and homeodomain protein Ptx1.

238 ight into the molecular mechanism underlying homeodomain-protein recognition and may serve as a parad

239 TALE homeodomain proteins regulate development in many eukary

240 Homeodomain proteins regulate multiple developmental pat

241 ferentiation in vitro, whereas Prx1, another homeodomain protein, regulates SMC differentiation marke

242 s tools, which revealed that the Arabidopsis homeodomain protein REPLUMLESS (RPL) establishes distinc

243 ces upstream of nt -68, and the CDP/cut/Cux1 homeodomain protein represses transcription down-stream

244 Here, we show that expression of Otx2, a homeodomain protein required for the formation of the fo

245 through direct control of the Dlx1 and Dlx2 homeodomain proteins, required for interneuron specifica

246 Examination of mouse orthologs of these homeodomain proteins resulted in the identification of m

247 f Ldb1, which encodes a cofactor for all LIM-homeodomain proteins, resulted in a similar phenotype.

248 GhHOX3 interacts with GhHD1, another homeodomain protein, resulting in enhanced transcription

249 otprinting analysis of Clone A with vnd/NK-2 homeodomain protein revealed three strong binding sites

250 em (SAM) is maintained in Arabidopsis by the homeodomain protein SHOOT MERISTEMLESS (STM).

251 At least three homeodomain proteins, Six1, LBX1, and HoxA5, transactiva

252 Here, we report that BLH6, a BELL1-LIKE HOMEODOMAIN protein, specifically interacts with KNAT7,

253 Co-factor homeodomain proteins such as Drosophila Homothorax (Hth)

254 Mix family homeodomain proteins, such as Xenopus Mixer and zebrafis

255 The interaction of an arenavirus with a homeodomain protein suggests a mechanism for viral terat

256 Here we show that BMP2 induces DLX3, a homeodomain protein that activates Runx2 gene transcript

257 ceh-30 encodes a BarH homeodomain protein that acts downstream from the termin

258 /cut homolog (CDP/cut) is a highly conserved homeodomain protein that contains three cut repeat seque

259 Nanog is a divergent homeodomain protein that directs propagation of undiffer

260 NKX3.1 is a homeodomain protein that functions as a dosage sensitive

261 Pbx1 is a TALE-class homeodomain protein that functions in part as a cofactor

262 HOX11 encodes a homeodomain protein that is aberrantly expressed in T-ce

263 Hop is an unusual homeodomain protein that is expressed by embryonic and p

264 Dmbx1 encodes a paired-like homeodomain protein that is expressed in developing neur

265 Emx2 is a homeodomain protein that plays a critical role in inner

266 REPLUMLESS encodes a homeodomain protein that prevents replum cells from adop

267 nstrate that it regulates human Engrailed, a homeodomain protein that regulates neuronal development

268 The PRETTY FEW SEEDS2 gene encodes a homeodomain protein that regulates ovule development.

269 One of these is Vax2, a homeodomain protein that ventralizes the vertebrate eye

270 stinal barrier function, can be regulated by homeodomain proteins that control the differentiation of

271 rax Complex encodes three well-characterized homeodomain proteins that direct segment identity, as we

272 different transcription factors, 11 of them homeodomain proteins, that act in distinct combinations

273 ranscription regulatory co-factor of the LIM homeodomain proteins, the LIM domain only 4 protein Lmo4

274 cifically with the BEL1-like (BELL) class of homeodomain proteins, through a domain conserved between

275 The homeodomain protein Tinman and the GATA factors Pannier

276 s further demonstrated by the failure of the homeodomain protein to interact efficiently with two of

277 ation inactivates the ability of the vndNK-2 homeodomain protein to repress ind and msh.

278 ption factor GRD acts cooperatively with WOX homeodomain proteins to establish embryonic polarity in

279 ty acts downstream of retinoid signaling and homeodomain proteins to promote the formation of dI6, V1

280 nct co-regulatory proteins (Zelda or Sox/POU-homeodomain proteins) to control a similar pattern of ex

281 We show here that the HoxC4 and Oct-1 homeodomain proteins together with the Ku70/Ku86 heterod

282 which can mediate Wnt signaling and for Vent homeodomain proteins, transcriptional repressors that me

283 results uncover a novel mechanism whereby a homeodomain protein transduces GA signal to promote fibr

284 are binding sites for TRA-1A and a POU-type homeodomain protein UNC-86 and acts as a sensor to regul

285 hat two closely related, ventrally expressed homeodomain proteins-Vax1 and Vax2-control this neuroepi

286 tor Receptor (EGFR), in conjunction with the homeodomain proteins, Ventral nervous system defective,

287 While the homeodomain protein vHnf1/Hnf1b directly activates Mafb

288 A Xenopus homolog of the Pbx1b homeodomain protein was isolated and shown to be express

289 42, MYB43, MYB20, and KNAT7 (a Knotted1-like homeodomain protein), was developmentally associated wit

290 ctly with the N-terminal region of the PDX-1 homeodomain protein, which contains conserved amino acid

291 s regulated the pituitary homeobox 2 (PITX2) homeodomain protein, which modulates developmental gene

292 d the cloning of CD2 revealed it to encode a homeodomain protein, which we propose acts as a key regu

293 with members of the PBC family of TALE-type homeodomain proteins, which includes human Pbx1.

294 alian genes that encode closely related TALE homeodomain proteins, which serve as DNA binding partner

295 Prx1, a homeodomain protein whose expression was increased by An

296 SIX3/6 gene family in vertebrate, encodes a homeodomain protein with a SIX protein-protein interacti

297 sociation of transcriptional activators (DLX homeodomain proteins) with key DNA enhancers but repress

298 ranscription factors including Dlx and other homeodomain proteins within the evolutionarily conserved

299 expression level of the stem cell-promoting homeodomain protein WUSCHEL (WUS) in the cells beneath,

300 Two homeodomain proteins, Yox1 and Yhp1, act as repressors a