ライフサイエンスコーパス: armadillo

1 ion with Shaggy and two for interaction with Armadillo.

2 ough interactions with Drosophila Shaggy and Armadillo.

3 adherin does not accumulate with its partner Armadillo.

4 acts downstream of wingless and upstream of armadillo.

5 d by Axin, resulting in nuclear signaling by Armadillo.

6 ree genes: neuroglian (nrg), erect wing, and armadillo.

7 ssary for E-APC to function in destabilising Armadillo.

8 stabilization of beta-catenin and Drosophila Armadillo.

9 gmental patterning of the larval cuticle via Armadillo.

10 hort-term passage of strains in nude mice or armadillos.

11 was more common after long-term expansion in armadillos.

12 ation, the beta-catenin-related protein Worm armadillo 1 (WRM-1) also plays a role in controlling EMS

13 beta-catenin and its fruitfly counterpart Armadillo act as a coactivator in the canonical Wnt/Wing

14 we show that two gain-of-function alleles of Armadillo activate Wingless signaling by different mecha

15 covered a branch of the Wnt pathway in which Armadillo activity is regulated concomitantly with the l

16 ctors have been implicated in modulating TCF/Armadillo activity, their importance remains poorly unde

17 iating Wnt signals by promoting beta-catenin/Armadillo activity.

18 show that the levels of the adhesion protein Armadillo affect competition.

19 ilis, Cyprinius carpio), and osteoderms from armadillos, alligators, and leatherback turtles.

20 s signal causes stabilization of cytoplasmic Armadillo allowing it to enter the nucleus where it can

21 ion, can be mimicked by an activated form of armadillo and blocked by a dominant negative form of pan

22 n their own cause increased stabilization of Armadillo and cuticle pattern disruptions that include r

23 ed behind the furrow, and all cells show low Armadillo and DE-cadherin levels, although in the case o

24 ctin and ZO-1 in between, and a reduction of Armadillo and Discs lost within, mutant cells, indicativ

25 We report a conserved armadillo and pleckstrin homology (PH) domain-containing

26 'glmgraph' is implemented in R and C++ Armadillo and publicly available under CRAN.

27 y transcriptional co-activators beta-catenin/Armadillo and T-cell factor (TCF).

28 nd Apc allows GSK3 (Shaggy) to phosphorylate Armadillo and target it for degradation.

29 y transcriptional co-activators beta-catenin/Armadillo and TCF to facilitate context-dependent Wnt si

30 p a threshold for the amount of this form of Armadillo and therefore for Wnt signalling.

31 nome resequencing of M. leprae from one wild armadillo and three U.S. patients with leprosy revealed

32 ype (3I-2-v1) was found in 28 of the 33 wild armadillos and 25 of the 39 U.S. patients who resided in

33 o, and the Philippines, as well as from wild armadillos and a sooty mangabey monkey.

34 Wild armadillos and many patients with leprosy in the souther

35 ir natural group, the cingulate xenarthrans (armadillos and their allies).

36 e pathway, beta-catenin (betacat, Drosophila Armadillo), and helps to target it for degradation.

37 such as Drosophila E-cadherin, beta-catenin/Armadillo, and alpha-spectrin, and the disruption of epi

38 endently lost three times in carnivores, the armadillo, and lagomorphs.

39 ental mammals, mouse, guinea pig, rabbit and armadillo, and one marsupial, opossum.

40 oprecipitated with anti-DE-cadherin and anti-Armadillo antibodies from embryonic protein extracts.

41 that Akt regulates a complex containing Zw3, Armadillo, APC2, and EB1 and that this complex has a rol

42 Human beta-catenin and its fly homolog Armadillo are best known for their roles in cadherin-bas

43 Armadillos are a large natural reservoir for M. leprae,

44 the same region, as well as in Mexico, wild armadillos are infected with Mycobacterium leprae.

45 l-autonomously, downstream or in parallel to Armadillo (Arm) and upstream of Wg-dependent target gene

46 and it regulates cell fate decisions through Armadillo (Arm) by acting as a receptor for the Wnt prot

47 Vid28p contains an Armadillo (ARM) domain required for FBPase degradation.

48 eviously hypothesized to involve the central Armadillo (Arm) domain.

49 hanisms of missense mutations located in the armadillo (ARM) domains of PKP2, as well as their conseq

50 interacts with the adherens junction protein Armadillo (Arm) during morphogenesis.

51 tructural homology to beta-catenin and other armadillo (arm) family proteins.

52 hich attenuates the activity of beta-catenin/Armadillo (Arm) in immature INPs.

53 ARABIDILLO proteins are F-box-Armadillo (ARM) proteins that regulate root branching in

54 A local unfolding of importin alpha5 Armadillo (ARM) repeat 10 accompanies high-affinity bind

55 Armadillo (Arm) repeat 10 to the COOH terminus of beta-c

56 tide can compete binding of the beta-catenin armadillo (arm) repeat domain to axin in vitro, indicati

57 protein contains both a U-box domain and an armadillo (ARM) repeat domain, which were demonstrated i

58 tional activation in vitro requires both the armadillo (ARM) repeats and the C terminus of beta-caten

59 tify a novel set of evolutionarily conserved Armadillo (ARM) repeats within CED-12/ELMO that mediate

60 f Huntingtin, EF3, PP2A, and TOR1 (HEAT) and Armadillo (ARM) repeats.

61 he activity of the transcriptional activator Armadillo (Arm) to elicit precise, concentration-depende

62 o activation, repression required binding of Armadillo (Arm) to the N terminus of TCF.

63 beta-catenins, including Drosophila Armadillo (Arm), link activation of Fz at the cell surfa

64 rmines how efficiently Wnt signals stabilize Armadillo (Arm)/beta-catenin and activate downstream gen

65 Armadillo (Arm)/beta-catenin and Dishevelled (Dsh) are k

66 t activity, Pbl/ECT2 functions downstream of Armadillo (Arm)/beta-catenin stabilization.

67 CBP binds directly to the C-terminus of Armadillo (Arm, the fly beta-cat) and is recruited to a

68 We demonstrate that miR-310/13 can modulate Armadillo (Arm; Drosophila beta-catenin) expression and

69 developmental processes through a complex of Armadillo(Arm)/beta-catenin and the HMG-box transcriptio

70 lular accumulation of Actin, DE-cadherin and Armadillo associated with apical constriction of the cen

71 terminal kinase signaling pathway suppresses armadillo-associated defects.

72 lacking the entire Shaggy (AxinDeltaSgg) or Armadillo (AxinDeltaArm) binding domain.

73 spatial distribution of organ blood flow in armadillos because they have genetically identical litte

74 GSK3beta, and CK1 that targets beta-catenin/Armadillo (beta-cat/Arm) for proteosomal degradation.

75 recycling endosomes (REs) and E-cadherin and Armadillo (beta-catenin) are both found in reduced amoun

76 Arc protein colocalizes with Armadillo (beta-catenin) to the apical (luminal) surface

77 is required for Cubitus interruptus (Ci) and Armadillo/beta-catenin (Arm) proteolysis, Roc1a mutant c

78 /E-cadherin (DE-cad) and its binding partner Armadillo/beta-catenin (beta-cat) are expressed in newly

79 DE-cadherin and Armadillo/beta-catenin accumulate in the junctions betwe

80 Armadillo/beta-catenin and related proteins have importa

81 enes that show greatest sequence homology to Armadillo/beta-catenin are called ARABIDILLO-1 and -2.

82 tivation of Armadillo/beta-catenin, and that Armadillo/beta-catenin does not play a general role in i

83 xpression of alphaPS integrin, inhibitors of Armadillo/beta-catenin nuclear activity and baculovirus

84 Hyd/UBR5 is a key prerequisite that enables Armadillo/beta-catenin to activate transcription.

85 development by promoting the association of Armadillo/beta-catenin with TCFs on Wg-regulated enhance

86 ts of this adhesion process, DE-cadherin and Armadillo/beta-catenin, accumulate at high levels in the

87 certain cells are affected by activation of Armadillo/beta-catenin, and that Armadillo/beta-catenin

88 ossesses an importin-beta-binding domain and armadillo/beta-catenin-like repeats.

89 d the amount of the active/oncogenic form of Armadillo/beta-catenin.

90 role for this protein in the localization of Armadillo/beta-catenin.

91 and human cell lines downstream of activated Armadillo/beta-catenin.

92 Two Axin point mutants within the Armadillo binding domain were weak alleles and retained

93 nteractions and deletion mutants missing the Armadillo binding repeats.

94 in-alpha-catenin fusion protein, which lacks Armadillo binding sites, causes similar defects as DE-ca

95 ients who resided in areas where exposure to armadillo-borne M. leprae was possible.

96 elevated levels of the beta-catenin homolog Armadillo but no alteration in Dsh abundance or distribu

97 The Apc2-Armadillo complex appears to link cap expansion to centr

98 surface, preventing steric clashes with its Armadillo-core.

99 todonts are in fact deeply nested within the armadillo crown-group, representing a distinct subfamily

100 sensitive manner both the dorsal and ventral armadillo cuticle defects.

101 ctures of complexes between the beta-catenin armadillo domain and the Lef-1 N-terminal domain show th

102 The crystal structure of the plakoglobin armadillo domain bound to phosphorylated E-cadherin show

103 addition, the expression of the beta-catenin armadillo domain disrupted the recruitment of beta-caten

104 Truncation of the armadillo domain of beta-catenin, but not the C terminus

105 The p120ctn subfamily of armadillo domain proteins has roles in modulating interc

106 We report that TbTOR4 associates with an Armadillo domain-containing protein (TbArmtor), a major

107 educed by the expression of the beta-catenin armadillo domain.

108 tol 4-phosphate (PI-4P) through a C-terminal armadillo domain.

109 get proteins and complexes, which exhibit an armadillo domain.

110 t, each containing about half of the central Armadillo domain.

111 leucine-rich repeats, tetratricopeptides or armadillo domains.

112 saul1) mutants, deficient in the PLANT U-BOX-ARMADILLO E3 ubiquitin ligase SAUL1.

113 zed the genome sequence assemblies of human, armadillo, elephant, and opossum to identify informative

114 Plakophilin 2 (PKP2), an armadillo family member closely related to p120 catenin

115 Plakophilins (PKPs) are armadillo family members related to the classical cadher

116 Plakoglobin (PG) is a member of the Armadillo family of adhesion/signaling proteins and has

117 Plakoglobin (PG) is a member of the Armadillo family of adhesion/signaling proteins that can

118 The Armadillo family of catenin proteins function in multipl

119 Plakophilin-1 (PKP-1) is an armadillo family protein critical for desmosomal adhesio

120 The armadillo family protein plakoglobin (Pg) is a well-char

121 p0071 is an armadillo family protein related to both the adherens ju

122 p120-catenin (p120) is an armadillo family protein that binds to the cytoplasmic d

123 embly in comparison to other closely related armadillo family proteins.

124 An armadillo-fold in its N terminus mediated a novel intera

125 the Axin complex which earmarks beta-catenin/Armadillo for degradation by the proteasome pathway.

126 To test beta-catenin function, a truncated armadillo fragment was expressed in developing chicken s

127 , in M. leprae strains obtained from 33 wild armadillos from five southern states, 50 U.S. outpatient

128 pes obtained by different ways of activating Armadillo function and provides further support for the

129 h driver and responder controls, as follows: armadillo-GAL4 (up to 38%), Tubulin-GAL4 (up to 29%), C2

130 pendent loci with either a broad expression (armadillo-GAL4, Tubulin-GAL4, C23-GAL4, and da-GAL4) or

131 moplakin was found to associate with the non-armadillo head domain of p0071.

132 clinical isolates of M. leprae propagated in armadillo hosts were screened by PCR.

133 ived from leprosy patients and propagated in armadillo hosts.

134 ith missense mutations in the LYST ARM/HEAT (armadillo/huntingtin, elongation factor 3, protein phosp

135 rews); (II) Xenarthra (sloths, anteaters and armadillos); (III) Glires (rodents and lagomorphs), as a

136 h releases cadherin-associated beta-catenin (Armadillo in Drosophila) and p120-catenin to induce rhom

137 through a shared component: beta-catenin, or Armadillo in Drosophila.

138 the transcriptional activity of beta-catenin/Armadillo in normal and malignant cells.

139 As a consequence, Armadillo is no longer bound by Axin, resulting in nucle

140 ls, suggesting that modulated degradation of Armadillo is not required for Wnt signaling.

141 We argue that nuclear localization of Armadillo is required for transcriptional pathway activi

142 an armadillo stabilization assay, increasing armadillo level at low concentrations but reducing it at

143 rmally required for controlling beta-catenin/Armadillo levels, suggesting that modulated degradation

144 Vertebrates have two Armadillo-like proteins, beta-catenin and plakoglobin.

145 ngated shape consisting of several irregular Armadillo-like repeats with two helical hairpins protrud

146 VHis a member of a gene family that contains Armadillo-like repeats, and NAPE-PLD encodes a phospholi

147 lpha-solenoid architecture constructed of 12 armadillo-like, tether-repeat, alpha-helical tripod moti

148 sults support the model where Axin regulates Armadillo localization and activity in the cytoplasm.

149 Sterile alpha and HEAT/Armadillo motif (SARM) is a highly conserved Toll/interl

150 d Toll/IL-1R adaptor, sterile alpha and HEAT/Armadillo motif-containing protein (SARM), has remained

151 m1 [SARM (sterile alpha-motif-containing and armadillo-motif containing protein)].

152 tenin is a neuronal protein that contains 10 Armadillo motifs and binds to the juxtamembrane segment

153 wingless or armadillo mutant embryos secrete a lawn of ventral denti

154 embryos secrete a lawn of ventral denticles; armadillo mutants also exhibit dorsal closure defects.

155 By using an allelic series of Armadillo mutations, we show that there is a threshold a

156 nts indicate that Pygopus acts downstream of Armadillo nuclear import, consistent with the nuclear lo

157 alian lineage, namely, horse, dog, elephant, armadillo, opossum, and platypus.

158 f 2 other Wnt signaling components, beta-cat/armadillo or TCF/pangolin, had relatively milder effects

159 rupt Wingless signaling through titration of Armadillo out of the cytoplasm to the membrane.

160 Drosophila melanogaster Armadillo plays two distinct roles during development.

161 The study used samples of peanuts (cultivar armadillo), produced and marketed in Maringa, PR.

162 p120 catenin (p120ctn), an armadillo protein and component of the cadherin adhesion

163 p0071, a member of the armadillo protein family, localizes to both adherens jun

164 We observed that p120 catenin (p120ctn), an Armadillo protein known to modulate cell motility, is co

165 delta-Catenin is an Armadillo protein of the p120-catenin subfamily capable

166 t depend on cytodomain interactions with the armadillo protein plakoglobin or coexpression of its com

167 as 3 min; (2) the coalescence of DP and the armadillo protein plakophilin 2 into discrete cytoplasmi

168 Here we show that the Armadillo protein plakophilin 3 (Pkp3) mediates both des

169 provide evidence that loss of the desmosomal armadillo protein Plakophilin-2 (PKP2) in cardiomyocytes

170 The armadillo protein SmgGDS promotes guanine nucleotide exc

171 an the control of ZW3 phosphorylation of the Armadillo protein, is the key step in signaling.

172 espite these apparently paradoxical results, Armadillo protein, the transducer of Wnt signaling, does

173 bstantiating redundancy between PG and other armadillo proteins (e.g. beta-catenin).

174 This model may be applicable to other armadillo proteins in addition to SmgGDS, because we dem

175 large insert are common to this subfamily of armadillo proteins.

176 a PBR can regulate the nuclear transport of armadillo proteins.

177 In the flowering plant Arabidopsis thaliana, Armadillo-related ARABIDILLO proteins promote multicellu

178 s describe the characterization of PHOR1, an armadillo-related protein involved in gibberellin signal

179 Armadillo-related proteins regulate development througho

180 ZIX encodes an Armadillo repeat (Arm) protein highly conserved across e

181 served caspase consensus motif (DELD) within Armadillo repeat 6 of delta-catenin, was identified thro

182 e K(+) channel's alpha-subunit and the ninth armadillo repeat and carboxyl terminus of beta-catenin a

183 The effects of armadillo repeat containing 5 (ARMC5) inactivation and o

184 Armadillo repeat containing 5 (ARMC5) is a cytosolic pro

185 otein product of the BHD gene, and p0071, an armadillo repeat containing protein that localizes to th

186 of a complex between the PLSCR1 NLS and the armadillo repeat core of vertebrate importin alpha.

187 s containing the Pkp-3 head domain and Pkp-1 armadillo repeat domain localized to the desmosome and t

188 Previous yeast 2-hybrid screens, using the armadillo repeat domain of APC as bait, identified hTID-

189 catenin-mediated transcription, bound to the armadillo repeat domain of beta-catenin, has been determ

190 ah-1 and TBL1 were found to bind to the same armadillo repeat domain of beta-catenin, suggesting that

191 complex between this region of Nup2p and the armadillo repeat domain of Kap60p.

192 he yeast two-hybrid system revealed that the armadillo repeat domain of p0071 bound directly to VE-ca

193 terminal "tails" that flank the beta-catenin armadillo repeat domain on ligand binding have also been

194 rystal structure of the importin-alpha3/MOS6 armadillo repeat domain suggests that five of the six Ar

195 go proteins interact with the importin-alpha armadillo repeat domain via nuclear localization sequenc

196 s containing the Pkp-1 head domain and Pkp-3 armadillo repeat domain were localized to the nucleus in

197 lation of beta-catenin by CK2 is the central armadillo repeat domain, where carrier proteins like axi

198 The armadillo repeat domains encoded by TTC12 and dopamine i

199 rminus of APC, involving both the heptad and armadillo repeat domains, whereas the APC binding site i

200 We identify a conserved class of U-box ARMADILLO repeat E3 ligases that are positive regulators

201 delta-catenin is a member of the Armadillo repeat family and component of the adherens ju

202 ral, handle and helical domains, display the armadillo repeat fold.

203 e addressed the requirement and functions of armadillo repeat gene deleted in velo-cardio-facial synd

204 hree-dimensional structure of a beta-catenin armadillo repeat in complex with the liver receptor homo

205 s of repeat-specific features, especially in armadillo repeat modules.

206 s a Thr653Lys substitution in the C-terminal armadillo repeat of beta-catenin and displayed a reduced

207 forms an alpha helix that binds to the first armadillo repeat of beta-catenin, which can be mutated t

208 mpetition experiments revealed that the 11th armadillo repeat of Vac8 is an important element for rec

209 -catenin binding with all other beta-catenin armadillo repeat partners.

210 The armadillo repeat protein ARVCF is a component of adheren

211 erin superfamily, the plakin family, and the armadillo repeat protein family.

212 We also show that the P. pastoris Vac8 armadillo repeat protein is not essential for macropexop

213 ae, Vac8p, a myristoylated and palmitoylated armadillo repeat protein, is required for homotypic vacu

214 Armadillo repeat proteins (ArmRPs) recognize their targe

215 -specific binding protein, based on designed armadillo repeat proteins (dArmRP), binding to peptides

216 Natural armadillo repeat proteins (nArmRP) like importin-alpha o

217 Plakoglobin and beta-catenin are homologous armadillo repeat proteins found in adherens junctions, w

218 The structural similarity of SNI1 to Armadillo repeat proteins implies that SNI1 may form a s

219 chanical unfolding pathway, the beta-catenin armadillo repeat region (ARM) displays low mechanostabil

220 catenin binding repeat from APC bound to the armadillo repeat region of beta-catenin.

221 terminal beta-catenin "tails" that flank the armadillo repeat region reduces the affinity for desmoso

222 1) (PDZ) binding sites but lacks the central armadillo repeat region that binds cadherins and other p

223 ontaining protein (StBTB/POZ1) containing an Armadillo repeat region, was up-regulated in the mutant.

224 ive beta-catenin in the Wnt-on phase via the armadillo repeat region.

225 ystal structure of the PUL domain reveals an Armadillo repeat with high structural similarity to impo

226 Inactivating mutations in the Armadillo repeat-containing 5 (ARMC5) gene have recently

227 abidopsis (Arabidopsis thaliana) plant U box/armadillo repeat-containing E3 ligase9 (AtPUB9), we iden

228 ide polymorphism changing a splicing site in ARMADILLO REPEAT-CONTAINING KINESIN1.

229 Here we describe the identification of the armadillo repeat-containing protein, ARMCX3, as a Sox10-

230 bling a protein kinase, termed STRAD, and an armadillo repeat-containing protein, named mouse protein

231 bling a protein kinase, termed STRAD, and an armadillo repeat-containing protein, named mouse protein

232 ins (Pkp-1, -2, and -3) comprise a family of armadillo repeat-containing proteins first identified as

233 Plakophilins are armadillo repeat-containing proteins, initially identifi

234 a coli universal stress protein); At3g54870 (armadillo-repeat containing kinesin-related protein); At

235 ggest that Gudu and ARMC4 are a subfamily of Armadillo-repeat containing proteins that may have an ev

236 Here, we show that Arabidopsis thaliana ARMADILLO-REPEAT KINESIN1 (ARK1) plays a key role in roo

237 ghly homologous to vertebrate ARMC4, also an Armadillo-repeat-containing protein enriched in testes,

238 Armadillo-repeat-containing proteins also exist in plant

239 ), and sterile alpha motifs and beta-catenin/armadillo repeats (SARM).

240 ic analysis reveals that PLSCR1 NLS binds to armadillo repeats 1-4 of importin alpha, but its interac

241 ICAT contains a 3-helix bundle that binds armadillo repeats 10-12 and a C-terminal tail that, simi

242 -terminal fragment of beta-catenin including armadillo repeats 10-12 binds to GAC63.

243 nd E-cadherin, binds in the groove formed by armadillo repeats 5-9 of beta-catenin.

244 for the difference in signaling and that the Armadillo repeats account for the remainder of the diffe

245 mino acid protein that contains 10 predicted Armadillo repeats and a C2 domain.

246 8p may bind the fusion machinery through its armadillo repeats and that palmitoylation brings this ma

247 Most importantly, SYS-1 bears 12 armadillo repeats and the SYS-1/POP-1 interface is ancho

248 The direct binding required most of the armadillo repeats and was mutually exclusive for interac

249 ive LXXLL peptide motifs in the beta-catenin armadillo repeats did not disrupt either binding to andr

250 eats that bear unexpected resemblance to the armadillo repeats in beta-catenin and the HEAT repeats i

251 es the groove formed by the third and fourth armadillo repeats of beta-catenin and thus precludes the

252 The C-terminal armadillo repeats of beta-catenin may be an attractive t

253 e NH(2) terminus combined with the first six armadillo repeats of beta-catenin were shown to be neces

254 s PF16, an axonemal protein containing eight armadillo repeats predicted to be important for flagella

255 five motifs similar to the so-called HEAT or armadillo repeats seen in the importins.

256 des approximately 200-kDa proteins with four Armadillo repeats similar to those in the nuclear pore p

257 encodes a large conserved protein with HEAT/Armadillo repeats that functions with sax-1, an NDR cell

258 eta-catenin physically interacts through its Armadillo repeats with the C-terminal transactivation do

259 from positions 133 to 363, which contains 4 armadillo repeats, and to the N-terminal adaptin-binding

260 Stacked armadillo repeats, each consisting of 42 aa arranged in

261 eta-catenin, a family of proteins containing armadillo repeats, suggesting similar biological functio

262 We further demonstrate that the T. gondii armadillo repeats-only protein (TgARO) mutant, which is

263 02-512 of APC, a region including 2 of the 7 armadillo repeats.

264 embly of dipeptide-specific modules based on armadillo repeats.

265 a protein of unknown function that contains armadillo repeats.

266 ditionally contains leucine-rich repeats and Armadillo repeats.

267 c domain that binds directly to beta-catenin Armadillo repeats.

268 s inhibitory domains (DIDs) composed of five armadillo repeats.

269 sactivation domain, and (3) retention of the armadillo repeats.

270 the positively charged groove formed by the armadillo repeats.

271 directly bound polymerized vimentin via its armadillo repeats.

272 ne CG5155 encodes a protein that contains 10 Armadillo-repeats and has an unknown function.

273 regulators of Wg signaling, dishevelled and armadillo, results in rapid SSC loss.

274 7 counterpart in Drosophila, is required for Armadillo stabilization and plays a positive role in reg

275 erted a biphasic effect on Wg activity in an armadillo stabilization assay, increasing armadillo leve

276 These nuclear proteins are not required for Armadillo stabilization or the recruitment of TCF and Ar

277 it ends dominant-negative acts downstream of Armadillo stabilization.

278 Ewg and Ebd1 functionally interact with the Armadillo-TCF complex and mediate the same context-depen

279 ites, coupled with its ability to facilitate Armadillo-TCF interaction and transcriptional activity,

280 r the mammalian genomes of elephant, rabbit, armadillo, tenrec, platypus, pig, cat, bush baby, common

281 in a Wnt-dependent manner, where it augments Armadillo (the fly beta-catenin) transcriptional activat

282 tations in the genes encoding DE-cadherin or Armadillo, the beta-catenin homologue.

283 hese findings, muscle-specific inhibition of Armadillo, the downstream transcriptional effector of th

284 hila have revealed that an activated form of Armadillo, the effector of Wnt signalling, interacts wit

285 Wg signaling causes nuclear translocation of Armadillo, the fly beta-catenin, which then complexes wi

286 t, PP1B, regulates stability of beta-Catenin/Armadillo: the outcome is to oppose T-cell factor (TCF)

287 applied to DNA extracts from these infected armadillo tissues (n = 21).

288 atients and from M. leprae-infected mouse or armadillo tissues infected with 14 separate strains usin

289 stabilization or the recruitment of TCF and Armadillo to a WRE.

290 Removing Axin enables Armadillo to accumulate and re-localize to the nucleus.

291 n and Nito act redundantly downstream of TCF/Armadillo to activate many Wg transcriptional targets.

292 ficient to allow a Drosophila GSK3 substrate Armadillo to be phosphorylated by BIN2 in vitro.

293 study investigated the role of sterile alpha/Armadillo/Toll-Interleukin receptor homology domain 1 pr

294 e Toll receptor adaptor Sarm1 (sterile alpha/Armadillo/Toll-Interleukin receptor homology domain prot

295 a Toll receptor adaptor dSarm (sterile alpha/Armadillo/Toll-Interleukin receptor homology domain prot

296 quench the activity of the nearby-bound dTCF/Armadillo transcription complex.

297 ests that a large portion of CFAP69 can form Armadillo-type alpha-helical repeats, which may mediate

298 cell walls of Mycobacterium leprae grown in armadillos was characterized and compared with that of M

299 In all cases, cells expressing activated Armadillo were able to migrate and extend cell processes

300 in horse and dog in contrast to elephant and armadillo, which showed high-centromeric sequence homoge