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 ith heterozygous missense mutation in NKX2-5 homeodomain.

4 g motifs for an independent set of divergent homeodomains.

5 estions about the DNA recognition process by homeodomains.

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

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

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

9 ss the pan-autonomic determinant Paired-like homeodomain 2b (Phox2b) together with markers of Schwann

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

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

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

13 X paralogs share the conserved degron in the homeodomain and are also subject to CUL4-mediated degrad

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

15 Homeodomain and basic helix-loop-helix transcription fac

16 ecules, and reaches a maximum of 52% for the homeodomain and chignolin.

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

18 The homeodomain and the interaction through the prospero-lik

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

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

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

22 NG (really interesting new gene), PHD (plant homeodomain) and ZZ (ZZ-type zinc finger) domains, parti

23 Although the homeodomains are interchangeable between WUS and WOX9 cl

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

25 g different readout mechanisms through which homeodomains attain DNA binding specificity.

26 HAT1 and BES1 bind to a conserved homeodomain binding (HB) site and BR response element (B

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

28 cations characterized by a unique grammar of homeodomain binding motifs.

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

30 ng sites improved the prediction accuracy of homeodomain binding specificities.

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

32 A crystal structure of the Pdx1 homeodomain bound to DNA (PDB 2H1K) obtained previously

33 2-5 mutants, including those with a crippled homeodomain, bound hundreds of targets including NKX2-5

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

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

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

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

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

39 ors regulating senescence, we identified the homeodomain-containing protein HLX1 (H2.0-like homeobox

40 f master transcription factors including the homeodomain-containing protein NANOG, which has an essen

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

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

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

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

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

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

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

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

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

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

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

52 lection of transcription factor mutants, the homeodomain-containing transcription repressor Cup9 is f

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

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

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

56 Because missense mutations in the NKX2-5 homeodomain (DNA-binding domain) are the most frequently

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

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

59 oups at the molecular interface of the HoxD9 homeodomain-DNA complex.

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

61 ormational properties of chicken Engrailed 2 homeodomain (En2HD) in aqueous solution and in membrane

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

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

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

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

66 erlying mechanism by which an enhancer-bound homeodomain factor effectively activates developmental g

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

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

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

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

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

72 f OB interneurons depends on the zinc finger homeodomain factor teashirt zinc finger family member 1

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

74 ious studies have shown that loss of the LIM homeodomain factor, Lhx3, which is activated by the FGF

75 studies have thus revealed an unanticipated homeodomain factor/beta-catenin/Satb1-dependent localiza

76 LIM homeodomain factors regulate the development of many cel

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

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

79 Here we focused on the homeodomain family of TFs and analyzed the DNA shape of

80 r cells by ZEB1, a member of the zinc finger/homeodomain family of transcriptional repressors.

81 Most of these are in the extended homeodomain family.

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

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

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

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

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

87 ON INSENSITIVE3 (VIN3) and its related plant homeodomain finger proteins act together with Polycomb R

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

89 tic regions via the interaction of its plant homeodomain finger with the histone mark H3K4me3.

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

91 3 lysine 4 trimethylation through its plant homeodomain finger.

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

93 We describe a genetic interaction with HOMEODOMAIN GLABROUS11 (HDG11), previously identified as

94 to their well-known DNA-binding properties, homeodomains have the ability to efficiently translocate

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

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

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

98 maintains this delicate balance by inducing homeodomain (HD) transcription factors such as Pax2 to s

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

100 otein-interacting LIM domains, a DNA-binding homeodomain (HD), and a C-terminal region.

101 6 is comprised of the paired domain (PD) and homeodomain (HD).

102 ting we investigated the function of SAWADEE HOMEODOMAIN HOMOLOG 1 (SHH1), a Pol-IV-interacting prote

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

104 A resolution crystal structure of MLL5 plant homeodomain in complex with the H3K4me3 peptide reveals

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

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

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

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

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

110 Homeodomain-Interacting Protein Kinase 1 (HIPK1) phospho

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

112 Homeodomain-interacting protein kinase 2 (Hipk2) has pre

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

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

115 orted that DNA damage activates CREB through homeodomain-interacting protein kinase 2-dependent phosp

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

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

118 The homeodomain is composed of a 3-helix domain and a mobile

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

120 ription factor genes like OsHB4 (a class III homeodomain Leu zipper member), OsBLH1 (a BEL1-like home

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

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

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

124 Characterization of the homeodomain leucine zipper I transcription factor AtHB13

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

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

127 The class IV homeodomain leucine zipper transcription factor GLABRA2

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

129 tional redundancy between GL2 and HDG11, two homeodomain leucine zipper transcription factors previou

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

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

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

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

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

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

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

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

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

139 1a (Ptf1a), the homeobox TF-Lbx1 and the Lim-homeodomain (Lim-HD), and TF Lhx1 and Lhx5.

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

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

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

143 main Leu zipper member), OsBLH1 (a BEL1-like homeodomain member), OsKANADI2, OsKANADI4, and OsETTIN2

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

145 mains of the proteins, as well as on a novel homeodomain motif in the Myf5 promoter and the essential

146 The homeodomain motif is required for direct repression of A

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

148 Certain NKX2-5 homeodomain mutations show abnormal protein degradation

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

165 ncoding plant-specific proteins with a plant homeodomain (PHD) motif, SHORT LIFE (SHL) and EARLY BOLT

166 show that the linked tandem Tudor and plant homeodomain (PHD) of UHRF1 (ubiquitin-like PHD and RING

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

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

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

170 These screens identified the plant homeodomain (PHD)-finger domain protein PHF5A as differe

171 onnX resulted in the identification of plant homeodomain (PHD)-like finger 6 (PHF6) as a potential TM

172 Plant homeodomain (PHD)-type zinc fingers play an important ro

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

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

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

176 The mutation was located at homeodomain position 52Arg-->Gly (R52G).

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

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

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

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

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

182 entiated into motoneurons expressing the LIM homeodomain protein Lhx3.

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

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

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

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

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

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

189 While the homeodomain protein vHnf1/Hnf1b directly activates Mafb

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

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

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

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

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

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

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

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

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

199 TALE-homeodomain proteins function as components of heteromer

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

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

202 Homeodomain proteins, described 30 years ago, exert esse

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

204 ygous missense mutation in the murine Nkx2-5 homeodomain (R52G) is highly penetrant and result in ple

205 We found distinct homeodomain regions that were more correlated with eithe

206 We identified specific homeodomain residues that likely play key roles in DNA r

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 The second type of homeodomain site is a Pbx-type site, which is recognized

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

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

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

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

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

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

216 t Ascl1 and Ptf1a directly regulate distinct homeodomain TFs that specify excitatory or inhibitory ne

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

218 characterized the DNA binding properties of homeodomains, the factors behind the binding specificity

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

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

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

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

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

224 e 4q25 in close proximity to the paired-like homeodomain transcription factor 2 (Pitx2) homeobox gene

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

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

227 The homeodomain transcription factor and human diabetes gene

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

229 Aberrant expression of the homeodomain transcription factor CDX2 occurs in most cas

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

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

232 s typically recessive; however, mutations in homeodomain transcription factor CRX lead to an autosoma

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

234 The homeodomain transcription factor distal-less homeobox 3

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

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

237 Hmx1 encodes a homeodomain transcription factor expressed in the develo

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

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

240 LHX6 and the PITX2 homeodomain transcription factor have overlapping expres

241 The homeodomain transcription factor HHEX (hematopoietically

242 The kinetics of translocation of the homeodomain transcription factor HoxD9 between specific

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

244 We identified that PITX2 homeodomain transcription factor interacts with and regu

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

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

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

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

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

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

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

252 The TALE homeodomain transcription factor KNOTTED ARABIDOPSIS THA

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

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

255 The homeodomain transcription factor Meis1 is required for n

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

257 cytotic regulator Shibire (Dynamin), and the homeodomain transcription factor Mirror, as TTK69 effect

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

259 The homeodomain transcription factor Nanog is a central part

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

261 Here, we show the paired-box homeodomain transcription factor Pax6 acts as a negative

262 The homeodomain transcription factor Pdx-1 has important rol

263 The homeodomain transcription factor Pdx1 controls pancreas

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

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

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

267 The homeodomain transcription factor Prrxl1/DRG11 has emerge

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

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

270 Lmx1b is a homeodomain transcription factor responsible for limb do

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

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

273 Isl1 is a LIM-homeodomain transcription factor that is critical in the

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

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

276 ing, as a starting point, the C. elegans LIM homeodomain transcription factor ttx-3, which acts as a

277 The homeodomain transcription factor WUSCHEL (WUS) promotes

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

279 Lhx6, a LIM-homeodomain transcription factor, is essential for speci

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

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

282 identified for amiRNAs targeting zinc finger homeodomain transcription factors and mitogen-activated

283 LIM homeodomain transcription factors are critical regulator

284 Irx homeodomain transcription factors are involved in the pa

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

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

287 undary of Otx2 and Gbx2, mutually repressive homeodomain transcription factors expressed in the midbr

288 ry perspective for a class of miPs targeting homeodomain transcription factors in plants and metazoan

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

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

291 Hox genes encode a conserved family of homeodomain transcription factors regulating development

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

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

294 a paralogues hnf1ba and hnf1bb, which encode homeodomain transcription factors, are essential for nor

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

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

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 function did require the shared DNA-binding homeodomain, which plays less of a role in Ftz segmentat

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