ライフサイエンスコーパス: homeodomain

1 d the Ssn6 (Cyc8) binding site in the alpha2 homeodomain.

2 PAX3 loads on mitotic chromosomes using its homeodomain.

3 g motifs for an independent set of divergent homeodomains.

4 ne of the strongest screen hits, zinc finger homeodomain 2 (Zfh2; mammalian orthologs ZFHX3/ATBF1 and

5 Recent data suggested that paired like homeodomain-2 transcription factor (PITX2) might play an

6 early hormone responses in potato include: a homeodomain 20 transcription factor (DMG400000248) for a

7 egulated by transcription factor paired-like homeodomain 3 (PITX3).

8 amino acid (Asn to Ile) substitution in the homeodomain abolished the repression of Mt-AS2 and STF's

9 It harbors both a plant homeodomain and a forkhead-associated domain implicated

10 th the G9a histone methyltransferase via the homeodomain and are mediated by activation of target gen

11 Homeodomain and basic helix-loop-helix transcription fac

12 Dsx interact through their highly conserved homeodomain and DM domain, respectively.

13 igenetic regulator ubiquitin-like with plant homeodomain and RING finger domains 1 (Uhrf1) is essenti

14 Furthermore, the region containing both the homeodomain and the C terminus of Caudal was sufficient

15 a structural core of Nanog encompassing the homeodomain and the tryptophan repeat can support LIF-in

16 overed functional domains in addition to the homeodomain and the WUS-box are necessary for this funct

17 show that a DUX4 minigene, bearing only the homeodomains and C-terminus, is transcriptionally functi

18 Although the homeodomains are interchangeable between WUS and WOX9 cl

19 s demonstrated that CUT domains, but not the homeodomain, are responsible for the stimulation of OGG1

20 targeted protein mutations that destabilize homeodomain binding both in vitro and in vivo in a compl

21 ISL1 binds in vitro and in vivo to critical homeodomain binding DNA motifs present in the neuronal P

22 ses of OR promoters revealed the presence of homeodomain binding sites in their sequences.

23 latory grammars, marked by enrichment of K50 homeodomain binding sites.

24 In primary mouse islets, LDB1 and its LIM homeodomain-binding partner islet 1 (ISL1) were coenrich

25 2-5 mutants, including those with a crippled homeodomain, bound hundreds of targets including NKX2-5

26 partite motif 24 protein (TRIM24) is a plant homeodomain/bromodomain histone reader, recently associa

27 Our characterization of a Dlx5 homeodomain:(CGACTAATTAGTCG)2 complex by NMR spectroscop

28 ons often depend on the presence of the TALE-homeodomain class cofactors, which form cooperative DNA-

29 we identify key centrosome-related genes and homeodomain classes previously reported as absent in fre

30 Members of the Iroquois B (IrxB) homeodomain cluster genes, specifically Irx3 and Irx5, a

31 NKXDeltaHD, which lacks the homeodomain completely, could heterodimerize with NKX2-5

32 here that VAB-3, a C. elegans homolog of the homeodomain-containing protein Pax6, has opposing functi

33 Hmx proteins are a subfamily of NK homeodomain-containing proteins that have fundamental ro

34 In Paracentrotus lividus, the Hbox12 homeodomain-containing repressor is expressed by prospec

35 of the HNF1B gene, encoding a member of the homeodomain-containing superfamily of transcription fact

36 romosomal region 2qB, which contains the LIM-homeodomain-containing transcription factor 1B (Lmx1b) g

37 e hypothalamus the developmentally regulated homeodomain-containing transcription factor Dbx1 is requ

38 HOXA1 is a member of the homeodomain-containing transcription factor family and p

39 In addition to Oct4 and Sox2, the homeodomain-containing transcription factor Nanog is an

40 We now show that the homeodomain-containing transcription factor Prep1 is a r

41 Hb9 is a homeodomain-containing transcription factor that acts in

42 HOXA9 is a homeodomain-containing transcription factor that has an

43 Engrailed-2 (EN2) is a homeodomain-containing transcription factor that has rol

44 Homeobox A9 (HOXA9) is a homeodomain-containing transcription factor that plays a

45 re highly conserved across metazoans, encode homeodomain-containing transcription factors that provid

46 To better understand homeodomain control of fungal development, we determined

47 ters, whereas divergence of the DUX4 and DUX homeodomains correlates with retrotransposon specificity

48 CsAChBP and a glia-specific homeodomain CsREPO were both expressed in glial cells th

49 lyses suggest that Hmx3a may not require its homeodomain DNA-binding domain for its roles in viabilit

50 Transcription factors that contain a homeodomain DNA-binding domain have crucial functions in

51 Heterozygous human NKX2-5 homeodomain (DNA-binding domain) missense mutations are

52 terized this phenomenon for the Antennapedia homeodomain-DNA complex by integrated use of fluorescenc

53 ains an open reading frame encoding a double homeodomain (DUX) family transcription factor.

54 is engineered onto the Drosophila Engrailed homeodomain (ENH), allowing the dimerized protein comple

55 fragment of the monomeric protein engrailed homeodomain (ENH), we had instead generated a domain-swa

56 d on the backbone structure of the Engrailed homeodomain (EnHD) and is highly thermostable (T(m) > 99

57 The Engrailed Homeodomain (EnHD) transcription factor of Drosophila me

58 We report that LIM homeodomain factor 1b (Lmx1b)-deficient 5-HT neurons fai

59 , with T-box factor 1 (Tbx1) and paired-like homeodomain factor 2 (Pitx2) as key upstream genes.

60 Recent work has identified the LIM homeodomain factor encoding gene Lhx2 as necessary for b

61 ly regulated expression of Rax, an essential homeodomain factor for tanycyte development.

62 cord development, the LIM domains of the LIM homeodomain factor Lhx3 bind to either the LIM cofactor

63 ventral zona incerta, which express the LIM homeodomain factor Lhx6 and are activated by sleep press

64 CF is required for the expression of the LIM homeodomain factor LHX6 involved in fate determination o

65 C "ground state," and functions with the LIM homeodomain factor LIM-4 to suppress this ground state a

66 nuclear LIM interactor (NLI) or another LIM homeodomain factor, Isl1, assembling the tetrameric V2 i

67 Here, we show that the POU-homeodomain factors Pou2f1/Pou2f2, the homologs of Droso

68 LIM homeodomain factors regulate the development of many cel

69 nisms underlying transcriptional activity of homeodomain factors remain poorly understood.

70 r secondary motifs used by Sox, Rfx, Pou and homeodomain factors.

71 Most of these are in the extended homeodomain family.

72 ) bring to light a functional role for plant homeodomain finger 11 (PHF11) in 5' end resection at DNA

73 Here we report that PHF11 (plant homeodomain finger 11) encodes a previously unknown DDR

74 Double plant homeodomain finger 2 (DPF2) is a highly evolutionarily c

75 Blood, McRae et al report that loss of plant homeodomain finger 6 (Phf6) increases the ability of hem

76 omatically acquired mutations in PHF6 (plant homeodomain finger 6) frequently occur in hematopoietic

77 nt the crystal structure of the tandem plant homeodomain finger domain of human DPF2 at 1.6-A resolut

78 Here, we describe the function of the plant homeodomain finger protein 6 (PHF6) in leukemia and defi

79 an oncogenic role for the bromodomain plant homeodomain finger transcription factor (BPTF) gene in m

80 The bromodomain and plant homeodomain finger-containing (BRPF) family are scaffold

81 3 lysine 4 trimethylation through its plant homeodomain finger.

82 We observe that LIM (Lin-11, Isl-1, Mec-3)-homeodomain gene Lhx2 is selectively expressed in hypoth

83 We show that a consensus-designed homeodomain (HD) sequence adopts a cooperatively folded

84 Our previous studies have identified LIM-homeodomain (HD) transcription factors (TFs), expressed

85 LIM-homeodomain (HD) transcription factors form a multimeric

86 The DLX3 homeodomain (HD) was essential for DLX3-GCM1 interaction

87 cofactors, which belong to the TALE-class of homeodomain (HD)-containing transcription factors.

88 6 is comprised of the paired domain (PD) and homeodomain (HD).

89 ANGED METHYLTRANSFERASE 2 (DRM2) and SAWADEE HOMEODOMAIN HOMOLOGUE 1 (SHH1).

90 MENT In this study, we provide evidence that homeodomain interacting protein kinase 2 (HIPK2) and its

91 Here we report the identification of homeodomain interacting protein kinase 2 (HIPK2) as the

92 Here, we show that the loss of homeodomain interacting protein kinase 2 (HIPK2) in neur

93 wth factor-beta and transcriptional cofactor homeodomain interacting protein kinase 2 regulate the su

94 Homeodomain interacting protein kinase-2 (HIPK2) is a me

95 Homeodomain-interacting protein kinase (HIPK) 2, a nucle

96 The homeodomain-interacting protein kinase (HIPK) family is

97 Homeodomain-interacting protein kinase (Hipk), a conserv

98 tumor model expressing oncogenic Drosophila Homeodomain-interacting protein kinase (Hipk), tumor cel

99 nd O-GlcNAc transferase (OGT) for Drosophila homeodomain-interacting protein kinase (Hipk)-induced gr

100 Homeodomain-Interacting Protein Kinase 1 (HIPK1) phospho

101 AIRE-interacting proteins and identified the homeodomain-interacting protein kinase 2 (HIPK2) as a no

102 s and bioinformatics analysis and identified Homeodomain-Interacting Protein Kinase 2 (HIPK2) as a no

103 Homeodomain-interacting protein kinase 2 (HIPK2) is a nu

104 Here, we demonstrated that homeodomain-interacting protein kinase 2 (HIPK2) was req

105 ere, we investigated c-Abl regulation of the homeodomain-interacting protein kinase 2 (HIPK2), an imp

106 ell understood, and we demonstrate here that homeodomain-interacting protein kinase 4 (HIPK4) is esse

107 Homeodomain-interacting protein kinases (HIPKs) are kina

108 The importance of BRG1/RNA and BRG1/homeodomain interactions in neurodevelopmental disorders

109 The Dlx5 homeodomain is a transcription factor related to the Dro

110 The Satb1 homeodomain is dispensable for high affinity binding but

111 eam of SlSHINE3 and possibly cooperates with homeodomain Leu zipper IV transcription factors.

112 ed by high auxin levels activating class III homeodomain leucine zipper (HD-ZIP III) transcription fa

113 Mutation in three paralogous class III homeodomain leucine zipper (HD-ZIPIII) genes leads to ab

114 In this context, members of the class III homeodomain leucine zipper (HD-ZIPIII) transcription fac

115 Characterization of the homeodomain leucine zipper I transcription factor AtHB13

116 re, we establish SiMPull in plants using the HOMEODOMAIN LEUCINE ZIPPER III (HD-ZIPIII) and LITTLE ZI

117 regulates the transcription of three related Homeodomain leucine zipper protein (HD-ZIP)-encoding gen

118 The class IV homeodomain leucine zipper transcription factor GLABRA2

119 f, implicating sterol/lipid-binding class IV homeodomain leucine zipper transcription factors as pote

120 The gamma-clade of class I homeodomain-leucine zipper (HD-Zip I) transcription fact

121 uxin, and consequent expression of CLASS III HOMEODOMAIN-LEUCINE ZIPPER (HD-ZIP III) transcription fa

122 ine zipper protein 1 (HAT1), which encodes a homeodomain-leucine zipper (HD-Zip) class II transcripti

123 Here we report that a homeodomain-leucine zipper (HD-ZIP) transcription factor

124 microarray analysis revealed that ATHB13, a homeodomain-leucine zipper (HD-Zip) transcription factor

125 Members of the class III homeodomain-leucine zipper (HD-ZIPIII) gene family are c

126 Arabodopsis thaliana homeodomain-leucine zipper protein 1 (HAT1), which encod

127 NPs) in the poplar ortholog of the class III homeodomain-leucine zipper transcription factor gene REV

128 KNAT7 function is enhanced expression of the homeodomain-leucine zipper transcription factor REVOLUTA

129 HB1 is an Arabidopsis (Arabidopsis thaliana) homeodomain-leucine zipper transcription factor that par

130 ved to control the activity of the class-III homeodomain-leucine zipper transcription factors(6-8)-an

131 form and a truncated form lacking the plant homeodomain-like domain associated with epigenetic repre

132 tify a detailed working mechanism of how the homeodomain-like transcription factor NSY-7, previously

133 l fate specification by interacting with LIM-homeodomain (LIM-HD) proteins in a tetrameric complex co

134 1a (Ptf1a), the homeobox TF-Lbx1 and the Lim-homeodomain (Lim-HD), and TF Lhx1 and Lhx5.

135 atin regulator BRPF1 (bromodomain- and plant homeodomain-linked (PHD) zinc finger-containing protein

136 PAX3 WS mutants with mutations in homeodomain lose the ability to bind mitotic chromosomes

137 of the longest polyalanine expansions on the homeodomain-mediated nuclear import, and our data clearl

138 genetic background by knocking-in an Nkx2-5 homeodomain missense mutation previously identified in h

139 The homeodomain motif is required for direct repression of A

140 nt of E-box motifs in bipolar cells, and Q50 homeodomain motifs in photoreceptors.

141 of structure-designed bromodomain and plant homeodomain mutants reveals that reader modules of BAZ1A

142 Here, we find that the plant homeodomain of BAZ1A, but not that of BAZ1B, has the unu

143 NA-binding activity harbored within the PBX1 homeodomain of E2A-PBX1.

144 oughput in silico screening strategy against homeodomain of MEIS proteins using the AutoDock Vina and

145 ut similar histone affinities (via the plant homeodomains of CHD3.1 and ACF1), which we suggest neces

146 study, we have investigated the role of the homeodomain-only homeobox gene, HOPX, in the pathogenesi

147 into regulatory T cells (Tregs) that require homeodomain-only protein (Hopx) to mediate T cell unresp

148 A homeodomain-only short isoform of VAB-3 is expressed in

149 usion partners include several genes bearing homeodomains or having known roles in transcriptional or

150 missense substitutions adjacent to the PBX1 homeodomain (p.Arg184Pro, p.Met224Lys, and p.Arg227Pro)

151 p.Met224Lys, and p.Arg227Pro) or within the homeodomain (p.Arg234Pro, and p.Arg235Gln), whereas p.Se

152 When trained on mouse homeodomain PBM profiles, our model correctly identifies

153 contains two histone reader modules, a plant homeodomain (PHD) and a bromodomain (BRD), linked by a l

154 The plant homeodomain (PHD) and Bromodomain cassette in ZMYND8 med

155 g proteins, including those containing plant homeodomain (PHD) and double Tudor reader domains.

156 The plant homeodomain (PHD) finger is found in many chromatin-asso

157 The plant homeodomain (PHD) finger of Set3 binds methylated lysine

158 Plant homeodomain (PHD) finger-containing proteins are implica

159 thylated histone 3 (H3K4me3) through a plant homeodomain (PHD) finger.

160 The roles of Plant Homeodomain (PHD) fingers in catalysis of histone modifi

161 Binding of H3K4me3 by a plant homeodomain (PHD) in RAG-2 induces conformational change

162 Binding of H3K4me3 by a plant homeodomain (PHD) in RAG-2 stimulates substrate binding

163 In this state the plant homeodomain (PHD) mediates interaction with the extreme

164 This modification is recognized by the plant homeodomain (PHD) present at the C-terminus of the five

165 on assays where employed to identify a plant homeodomain (PHD) protein, TaR1 in wheat that plays a cr

166 G3 tumor suppressor protein contains a plant homeodomain (PHD) that reads the epigenetic code via rec

167 se reader modules, an H3K4me3-specific plant homeodomain (PHD) within the Yng2 subunit and an H3K36me

168 tified a bromo-adjacent homology (BAH)-plant homeodomain (PHD)-containing protein, EPR-1 (effector of

169 Pf1, also known as Phf12 (plant homeodomain [PHD] zinc finger protein 12), is a member o

170 th mono-allelic mutations in the first plant homeodomain (PHD1) zinc finger of AIRE that followed dom

171 The mutation blocks nucleation of plant homeodomain-Polycomb repressive complex 2 (PHD-PRC2) and

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

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

174 Eyes Absent homolog EYA-1 and the Six-class homeodomain protein CEH-32.

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

176 entiated into motoneurons expressing the LIM homeodomain protein Lhx3.

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

178 l circuit (a-specific gene repression by the homeodomain protein Matalpha2) evolved by coding changes

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

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

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

182 mesoderm by repressing the expression of the homeodomain protein Repo, a major glial-specific target

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

184 Here we show that the absence of the homeodomain protein TG-interacting factor 1 (Tgif1) impa

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

186 While the homeodomain protein vHnf1/Hnf1b directly activates Mafb

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

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

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

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

191 Here, we show that the proline-rich homeodomain protein/hematopoietically expressed homeobox

192 NA groove geometry can affect DNA binding by homeodomain proteins and how principled modeling of ChIP

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

194 on of the expression of all of the conserved homeodomain proteins encoded by the Caenorhabditis elega

195 TALE-homeodomain proteins function as components of heteromer

196 How homeodomain proteins gain sufficient specificity to cont

197 unction analyses corroborate the notion that homeodomain proteins not only provide unique descriptors

198 The conserved Gsx homeodomain proteins regulate specific aspects of neural

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

200 Homeodomain proteins, described 30 years ago, exert esse

201 by unique combinations of the expression of homeodomain proteins, thereby providing-to our knowledge

202 ree-amino-acid loop extension) superclass of homeodomain proteins.

203 a is paralleled by the ectopic expression of homeodomain-related oncogenes in T cell acute lymphoblas

204 3, comprising a Paired homology domain and a homeodomain, represses expression of ETS-5, a transcript

205 nary age for the KRAB domains, discover that Homeodomain repressor strength is collinear with Hox gen

206 Factor (residues Met164 to Glu231), a Plant HomeoDomain (residues Met442 to Trp495) and an ARMadillo

207 not interact with SNF2 histone linker plant homeodomain RING helicase (SHPRH) or helicase-like trans

208 ry based on a monomeric Drosophila engrailed homeodomain scaffold.

209 Structural analysis showed that homeodomain specificity for methylcytosine depends on di

210 (HD) sequence adopts a cooperatively folded homeodomain structure.

211 distinct compositions and configurations of homeodomain TF complexes.

212 For example, the homeodomain TF DACH1 and the neurofilament subunits NF-L

213 onstrated for the basic helix-loop-helix and homeodomain TF families, our TFBSshape database can be u

214 s, such as between the T-box TF TBX5 and the homeodomain TF NKX2-5, have been proposed as a mechanism

215 are believed to bind with cofactors, mainly homeodomain TFs Pbx and Meis, to select their specific t

216 velopment, particularly as key regulators of homeodomain TFs required for neuronal subtype specificat

217 ased, statistical potentials, especially for homeodomain TFs, the second largest TF family in mammals

218 ino-acid C-terminal motif (CTM) flanking the homeodomain that serves as a major determinant of ancest

219 ins) from four families (bHLH, bZIP, ETS and Homeodomain), the ADM mixture models by MODER2 being the

220 e mutations diminish the ability of the Dlx5 homeodomain to recognize and bind target DNAs, and they

221 WUS and WOX9 clade members, a WUS-compatible homeodomain together with canonical WUS-box is not suffi

222 The Cdx family of homeodomain transcript ion factors (Cdx1, Cdx2, and Cdx4

223 Mutations in the Aristaless related homeodomain transcription factor (ARX) are associated wi

224 The two major isoforms of the paired-related homeodomain transcription factor 1 (Prrx1), Prrx1a and P

225 ociation studies have shown that paired-like homeodomain transcription factor 2 (Pitx2) to be strongl

226 iption factor 1alpha) and PITX3 (paired-like homeodomain transcription factor 3) expression in the co

227 trichomes is regulated differentially by the homeodomain transcription factor AaGL2 Moreover, we show

228 ional strategy in which the UNC-30 Pitx-type homeodomain transcription factor acts together, in embry

229 The homeodomain transcription factor and human diabetes gene

230 The Repo homeodomain transcription factor and panglial direct tar

231 The class I KNOX homeodomain transcription factor ARBORKNOX1 (ARK1) is a

232 ng regulatory differences of for example the homeodomain transcription factor BELL1.

233 serve as a new paradigm for how cooperative homeodomain transcription factor binding can increase ta

234 uced polyposis following somatic loss of the homeodomain transcription factor Cdx2, alone or with a C

235 ion of the TGF-beta family gene dbl-1 by the homeodomain transcription factor CEH-28.

236 tal Cell, Dowen (2019) finds that a PBX/MEIS homeodomain transcription factor complex controls a tran

237 r Hindsight (Hnt), and downregulation of the homeodomain transcription factor Cut and the zinc-finger

238 cription factors Pdm1 (Nubbin) and Pdm2, the homeodomain transcription factor Cut, and the transcript

239 The homeodomain transcription factor distal-less homeobox 3

240 Ectopic expression of the double homeodomain transcription factor DUX4 causes facioscapul

241 s caused by the mis-expression of the double-homeodomain transcription factor DUX4 in skeletal muscle

242 Hmx1 encodes a homeodomain transcription factor expressed in the develo

243 WUSCHEL (WUS), a homeodomain transcription factor expressed in the rib me

244 ncers and find inactivating mutations in the homeodomain transcription factor gene CUX1 (cut-like hom

245 The homeodomain transcription factor HHEX (hematopoietically

246 Apterous (Ap), the best studied LIM-homeodomain transcription factor in Drosophila, cooperat

247 he present study, we demonstrate that Nkx2.2 homeodomain transcription factor is a key regulator for

248 The PBX1 homeodomain transcription factor is converted by t(1;19)

249 Here, we report that the LIM-homeodomain transcription factor Isl1 is expressed in se

250 Here, we determined that the LIM homeodomain transcription factor ISL1 plays a key role i

251 transferase neurons (ChAT(+)) or Arch in LIM-homeodomain transcription factor Isl1(+) neurons.

252 report that the early expression of the LIM-homeodomain transcription factor Islet 1 (ISL1) in the d

253 The palp protrusions express the LIM-homeodomain transcription factor Islet.

254 ic nociceptor precursors is dependent on the homeodomain transcription factor Islet1, which is largel

255 The deletion of the LIM-homeodomain transcription factor Lhx2 in cortical progen

256 We show that the LIM homeodomain transcription factor Lhx2 is required for th

257 , trimethyl-H3K4, at <50 loci, including the homeodomain transcription factor Meis2.

258 Here we show that the homeodomain transcription factor MSX1, which is signific

259 eviously reported that overexpression of the homeodomain transcription factor NK6 homeobox 1 (Nkx6.1)

260 The homeodomain transcription factor Pdx-1 has important rol

261 The homeodomain transcription factor Pdx1 controls pancreas

262 Here, we report that the homeodomain transcription factor Pdx1, a gene associated

263 T function and recovered a new allele of the homeodomain transcription factor PENNYWISE (PNY).

264 defined by the expression of the paired-like homeodomain transcription factor Pitx2.

265 The Gsx2 homeodomain transcription factor promotes neural progeni

266 eatic progenitors express high levels of the homeodomain transcription factor Prox1, whereas both imm

267 all RNA targeting the autosomal MeGI gene, a homeodomain transcription factor regulating anther ferti

268 vating the transcription of GLABRA2 (GL2), a homeodomain transcription factor required for trichome f

269 Lmx1b is a homeodomain transcription factor responsible for limb do

270 e, we show that in the zebrafish embryo, the homeodomain transcription factor Rx3 coordinates these p

271 des a three amino acid loop extension (TALE) homeodomain transcription factor that forms multimeric c

272 Lhx1 encodes a LIM-homeodomain transcription factor that is essential for m

273 OTX2 is a homeodomain transcription factor that is necessary for n

274 The homeodomain transcription factor WUSCHEL (WUS) promotes

275 n to activate expression of Six6, encoding a homeodomain transcription factor, in the ventral diencep

276 HOXB13, a homeodomain transcription factor, is linked to recurrenc

277 estigation of a developmentally required POU-homeodomain transcription factor, Pit1 (also known as Po

278 hree amino acid loop extension (TALE) family homeodomain transcription factor, translocates to cardio

279 ocusing on lineage-specific functions of the homeodomain transcription factor, Unc-4.

280 ive to transcript levels of the Class I KNOX homeodomain transcription factor-encoding gene ARBORKNOX

281 Three amino acid loop extension homeodomain transcription factors (TALE HD TFs) act as l

282 ched for the binding site for the TALE-class homeodomain transcription factors Achi/Vis and for a mot

283 Irx homeodomain transcription factors are involved in the pa

284 Our work advances the understanding of how homeodomain transcription factors control complex develo

285 iated putative target genes for four Populus homeodomain transcription factors expressed during secon

286 cerevisiae, the regulation of cell types by homeodomain transcription factors is a key paradigm; how

287 The LIM-homeodomain transcription factors Lmx1a and Lmx1b play c

288 fungal pathogen Cryptococcus neoformans, the homeodomain transcription factors Sxi1alpha and Sxi2a ar

289 Lhx6 and Lhx8 encode LIM homeodomain transcription factors, and inactivation of b

290 Here, I demonstrate that two conserved homeodomain transcription factors, CEH-60/PBX and UNC-62

291 cterized by increased expression of a set of homeodomain transcription factors, including homeobox A9

292 eminiscent of overexpression of Class I KNOX-homeodomain transcription factors.

293 lated genes were enriched for those encoding homeodomain transcription factors.

294 PRRX1 is a homeodomain transcriptional factor, which has two isofor

295 he dynamics of the tandem tudor domain-plant homeodomain (TTD-PHD) histone reader module, including i

296 ozygous missense variants located within the homeodomain underlie this mild phenotype.

297 an heterozygous missense mutations in NKX2-5 homeodomain was replicated in mice by knocking in a comp

298 tants (all containing the intact DNA-binding homeodomain) we discovered that the C-terminal region of

299 E2A-PBX1, through a region spanning the PBX1 homeodomain, with RUNX1.

300 The plant homeodomain zinc finger protein Jade-1 can act as an E3