ライフサイエンスコーパス: repressor

1 x repressor CzrA (chromosomal zinc-regulated repressor).

2 e known to be repressed by a transcriptional repressor.

3 for PRMT5's proposed role as a transcription repressor.

4 ng the formation of the GLI3 transcriptional repressor.

5 Notch signal, RBPJ acts as a transcriptional repressor.

6 s (SaPIs) by binding to the SaPI-encoded Stl repressor.

7 ed one such protein, Zfp36, as a translation repressor.

8 the -44 region, where it acts as a splicing repressor.

9 NA-binding domain-containing transcriptional repressor.

10 RMINAL FLOWER1 (FvTFL1) as the causal floral repressor.

11 tors (TCF) and kept silent by Groucho/TLE co-repressors.

12 fic gene expression, either as activators or repressors.

13 the result of repression by transcriptional repressors.

14 r degradation of the Aux/IAA transcriptional repressors.

15 ighly conserved surface for interaction with repressors.

16 d the regulation of Gli2/Gli3 activators and repressors.

17 al novel uncharacterized MYB transcriptional repressors.

18 ly conserved, class-specific transcriptional repressors.

19 thologue Snf1 and downstream transcriptional repressors.

20 tion as either transcriptional activators or repressors.

21 protein interactions with co-activators and -repressors.

22 tes, and also by mRNA-specific translational repressors.

23 ression, while OsCPP5 and OsNIN-like2 act as repressors.

24 the specific deletion of nuclear receptor co-repressor 1 (NCoR1) in T cells causes excessive negative

25 gene silencing, as a member of the polycomb repressor 2 (PRC2) complex.

26 ttranslational regulation of the translation repressor, 4E-BP (eukaryotic translation initiation fact

27 plants must rapidly remove photomorphogenic repressors accumulated in the dark.

28 e interaction of Int3 with the transcription repressor/activator Rbpj.

29 ns in blood stages, and identify AP2-G2 as a repressor active in both asexual and sexual stages.

30 hr of immature INP birth, downregulation of repressor activities alleviates Rpd3-mediated repression

31 nd revealed that these have both inducer and repressor activities, possibly due to competitive bindin

32 FPs that inhibit ABA response have intrinsic repressor activity in a heterologous system, which does

33 We investigated AhR and AhR repressor (AhRR) expression and functional consequences

34 methylation of the aryl hydrocarbon-receptor repressor (AHRR) locus, which is observed in blood and s

35 DNA methylation in aryl-hydrocarbon receptor repressor (AHRR), a sentinel epigenetic biomarker of exp

36 action of LIMR and aryl-hydrocarbon receptor repressor (AHRR), and promoted protein expression as wel

37 on enhancing induction of Cyp1b1/CYP1B1, AhR repressor (Ahrr/AhRR) and TCDD-inducible poly(ADP-ribose

38 ne response in the lung epithelium and whose repressor, AHRR, has recently been implicated in smoking

39 coactivator proteins, functioning as both a repressor and activator, respectively.

40 YY1 acts both as a repressor and as an activator of gene expression.

41 Using dCas9(KRAB) repressor and dCas9(p300) activator constructs and lenti

42 CSL, a transcriptional repressor and Notch mediator, suppresses CAF activation.

43 matin at DSBs, limits binding of the L3MBTL1 repressor and promotes 53BP1 binding, while limiting end

44 antagonistic activities of the Tup1-Cyc8 co-repressor and Swi-Snf co-activator complexes.

45 henotypes in line with TgTFL1 being a floral repressor and TgSOC1-like2 being a floral activator in t

46 ions in turn reduce the affinity for the Stl repressor and the capacity to induce the SaPI cycle.

47 ays, indicating that the balance between GLI repressors and activators is altered in affected subject

48 through cryptochromes (CRYs)-transcriptional repressors and components of the circadian clock.

49 geting mRNA, and zinc finger transcriptional repressors and CRISPR-Cas9 methods aiming to reduce tran

50 ndent of the Snail family of transcriptional repressors and down-regulation of Drosophila E-cadherin

51 protein interactions; for instance, between repressors and PcG proteins.

52 1, falls into a class of MYB transcriptional repressors and, accordingly, higher expression of this g

53 This C-terminus binds to the Groucho/TLE co-repressor, and also to the Chip/LDB1-SSDP enhanceosome c

54 These repressors are continuously required in postmitotic neur

55 present together in an approximately 1.9-MDa repressor assembly that quantitatively incorporates its

56 response results from saturation of the LacI repressor at low inducer concentrations and dilution of

57 ely mimic those of deleting the fetal globin repressor BCL11A, implicating BCL11A in the function of

58 In Drosophila, the translational repressor Bgcn is required for spermatogonia to stop mit

59 vivo and showed that TPL tetramerization and repressor binding are interdependent.

60 ntire MeCP2 protein sequence, the DNA and co-repressor binding domains alone are sufficient to avoid

61 consisting of overlapping RNA polymerase and repressor binding sites.

62 BldO now joins pleiotropic repressor BldD to exert a multi-layer control of the tem

63 lic diguanylic acid (c-di-GMP) to the master repressor, BldD.

64 ously unidentified role that transcriptional repressor Blimp1 plays in the control of breast cancer i

65 xpression of the zinc finger transcriptional repressor Blimp1/PRDM1 is essential for the establishmen

66 The Polycomb group transcriptional repressor Bmi-1 often overexpressed and participated in

67 iors that are well-suited to transcriptional repressors but perhaps incompatible with precise activat

68 can be converted into an As(III)-responsive repressor by introduction of an additional cysteine that

69 In Arabidopsis, a key flowering repressor called FLOWERING LOCUS C (FLC) quantitatively

70 he developmentally regulated transcriptional repressor Capicua (CIC) suppresses invasion and metastas

71 -domain transcription factor Pointed and the repressor Capicua.

72 Here we show the transcriptional repressor Capicua/CIC maintains peripheral immune tolera

73 ependent photoreceptors, the transcriptional repressor CarH, is widespread in bacteria and mediates l

74 Recruitment of the transcriptional repressor CCCTC-binding factor (CTCF) to the MSMP enhanc

75 Carbon catabolite repressor (CCR)4 and CCR4-associated factor (CAF)1 in th

76 erating mice in which both Apc and ER stress repressor chaperone Grp78 can be conditionally deleted f

77 Polycomb repressor complex 2 (PRC2) places the histone mark H3K27

78 Jarid2 is a component of the Polycomb Repressor complex 2 (PRC2), which is responsible for gen

79 ZIC2 interacts with and maintains polycomb repressor complex 2 at the K-Rta promoter.

80 Our results implicate DAF-3 repressor complex activity as a key molecular mechanism

81 s through engagement of the REST-coREST-LSD1-repressor complex and altered histone marks at the p21 p

82 ine-specific histone demethylase 1 (LSD1) co-repressor complex associates with the hTERT promoter in

83 eal for the first time role of TRF2 in REST- repressor complex mediated transcription repression.

84 chment of the OGT-containing transcriptional repressor complex mSin3A-HDAC1 at the proximal promoter

85 essential for occupancy of NME2 and the REST repressor complex on the hTERT promoter.

86 TRalpha1PV to recruit NCOR1DeltaID to form a repressor complex relieved the deleterious actions of TR

87 omoter and recruits the NuRD transcriptional repressor complex to de-acetylate H3K9 and repress RNA p

88 active transcription mark and recruits a co-repressor complex to regulate gluconeogenic gene express

89 xin 1 (ATXN1), which forms a transcriptional repressor complex with capicua (CIC).

90 We show that the SETDB1 repressor complex, which involves multiple KRAB zinc fin

91 DING REPRESSOR FACTOR1 (HBF1) and HBF2, form repressor complexes that reduce Hd3a and RFT1 expression

92 a promiscuous transactivator, and it blocks repressor complexes to enable viral gene transcription.

93 with its E3 ligase activity, and it disrupts repressor complexes via protein-protein interaction to e

94 es, including intracellular Notch, or within repressor complexes, including the antagonist Hairless.

95 he yeast Saccharomyces cerevisiae, the Opi1p repressor controls the expression of INO1 via the Opi1p/

96 f OR stabilization; (2) colocalizes with the repressor CoREST (also known as RCOR1) and histone deace

97 cle ARNT-like 1 (BMAL1), and transcriptional repressors cryptochrome (CRY) and period (PER).

98 and the NAD(H) sensitive transcriptional co-repressor CtBP.

99 lysine 670 is required for recruiting the co-repressor CtBP1 and transcriptional repression.

100 c inhibition of DNA binding by the Zn efflux repressor CzrA (chromosomal zinc-regulated repressor).

101 uding the E26 transformation-specific family repressors Drosophila melanogaster Yan and its human hom

102 ChIP-seq database identified transcriptional repressor E2F6 as a possible negative regulator of MDM2

103 analyses, we show that the binding of REST (repressor element 1 (RE1) silencing transcription factor

104 that NED of PCa requires down-regulation of repressor element-1 silencing transcription factor (REST

105 suggests that subsequently, transcriptional repressors ensure the transition of progenitors to matur

106 of CLOCK:BMAL1 activity by coactivators and repressors establishes the approximately 24-h periodicit

107 growth factor independent 1B transcriptional repressor, ETS variant 6, ecotropic viral integration si

108 , as IRF8 dimerises with the transcriptional repressor ETV6 and inhibits Il4 expression.

109 peculate that similar 'many-but-one' lineage repressors exist for other cell fates; such repressors,

110 Consistent with this, JAZ repressor expression was highly correlated with the seve

111 al deletions of another ETS member, the ETS2 repressor factor ERF.

112 experiments reveal increased binding of the repressor factor RE1-silencing transcription (also known

113 er, additional bZIPs, including Hd3a BINDING REPRESSOR FACTOR1 (HBF1) and HBF2, form repressor comple

114 Polycomb to mediate silencing of the floral repressor FLOWERING LOCUS C (FLC) during the process of

115 We further investigate known transcriptional repressors for terminal muscle differentiation, namely Z

116 nding partners, including transcriptional co-repressors (for example, the NCoR/SMRT complex), transcr

117 bind GLI3 and promote its cleavage into the repressor form GLI3R.

118 The mechanism by which Musashi repressor function is attenuated has not been fully esta

119 ssue development and repair however, Musashi repressor function must be dynamically regulated to allo

120 rthermore, inhibition of the transcriptional repressor function of BCL6 in the presence of IM and IFN

121 ken together, these studies define a crucial repressor function of Sf1 SUMOylation and Dax1 in the ph

122 volutionary conservation of the dopaminergic repressor function of Zic proteins and show that it is a

123 sites in FoxM1b serve as a regulator for its repressor function, and they provide insights into how F

124 myeloid cell maturation and promoted immune repressor function.

125 FPs were fused to either the transcriptional repressor, G9a, which promotes histone methylation or th

126 lowed by MS, we identified a transcriptional repressor, GATA zinc finger domain-containing 2B (GATAD2

127 1 and a decrease in the GLI3 transcriptional repressor (GLI3R).

128 rase (gp29), the endolysin (gp31), the phage repressor (gp47), and six proteins of unknown function (

129 the transcriptional control of a glucuronide repressor, GusR.

130 nism of action, whether as an activator or a repressor, has remained unclear.

131 This is accomplished because the SaPI Stl repressors have acquired different domains to interact w

132 e elements (GREs) and adjacent transcription repressor HES1 binding N-boxes.

133 mutation in the gene for the transcriptional repressor histone deacetylase 4 (HDAC4) is associated wi

134 th the levels and activity of the epigenetic repressor, histone methyltransferase enhancer of zeste h

135 The transcriptional repressor Id2 is constitutively expressed in all innate

136 NACC1 encodes a transcriptional repressor implicated in gene expression and has not prev

137 ing Th1 effector commitment, T-bet acts as a repressor in differentiated Th1 cells to prevent abberan

138 Constitutive expression of GLI3 repressor in Ptch1-deficient mice rescued ectopic Ptch2

139 4 (Vgll4) functions as a transcriptional co-repressor in the Hippo-Yes-associated protein (YAP) path

140 n eudicots but also functions as a flowering repressor in the vernalization pathway of Brachypodium a

141 interference and zinc finger transcriptional repressors in advanced testing in animal models.

142 The role of spatially localized repressors in supporting embryonic patterning is well ap

143 ot apical meristem, the expression of floral repressors in tulip is suppressed by increased ambient t

144 repressors exist for other cell fates; such repressors, in combination with lineage-specific activat

145 ic acid and by a NadQ family transcriptional repressor, indicating that these organisms prioritize th

146 ar, JunB limits the expression of the subset repressor IRF8, and impedes access of JunD to regulatory

147 R/NOT gates) are encoded in pools where each repressor is fused to all permutations of input promoter

148 ally stimulates the lytic promoters while CI repressor is still present, stimulating the level of Cro

149 L, ATF3, a stress-responsive transcriptional repressor, is down-modulated in skin cancer stromal cell

150 agonist modulator (DREAM), a transcriptional repressor, is known to modulate pain responses.

151 complex by connecting it to the JA signaling repressor JAZ3.

152 ion of the gene encoding the transcriptional repressor JMJD8.

153 Using a coarse-grained model of DNA and lac repressor (LacI) in the Escherichia coli nucleoid, simul

154 The lac repressor (LacI) is a well characterized transcription f

155 es can interact with the SaPIbov1 Stl master repressor, leading to derepression and mobilization.

156 structurally distinct dUTPases bind the same repressor led us to speculate that dUTPase activity may

157 ts are refractory to Nodal ligands and Nodal repressor Lefty1.

158 el binding motif for the SOS transcriptional repressor LexA, and we use this motif to characterize th

159 lacking the zinc-responsive transcriptional repressor Loz1 with the goal of identifying metabolic pa

160 oding two GH/STAT5-regulated transcriptional repressors: male-biased BCL6, which was repressed, and f

161 s, such as hyperactivation of its endogenous repressors MDM2 or MDM4.

162 and spatiotemporal dynamics of a GFP tagged repressor, Mig1, from a paradigm signaling pathway of Sa

163 its interaction with the nuclear receptor co-repressor (NCoR1), resulting in repression of Rev-erbbet

164 (also known as Capicua) is a transcriptional repressor negatively regulated by RAS/MAPK signaling.

165 A transcriptional repressor network including THAP11 was identified and ne

166 the chromatin binding of the transcriptional repressor neuron restrictive silencing factor (NRSF or R

167 l 1030 possible genetic circuits based on 10 repressors (NOR/NOT gates) are encoded in pools where ea

168 ggest that TDP-43 represents a translational repressor not only for specific mRNAs but for overall tr

169 e identify Snail as a strong transcriptional repressor of 4E-BP1.

170 ing of endogenous retroelements, as a direct repressor of a placental-specific Igf2 transcript (desig

171 we show that BldO functions as the dedicated repressor of a single key target gene, whiB, and that de

172 n-containing transcription factor Prep1 is a repressor of adipogenic differentiation since its down-r

173 helix (bHLH)-Per-ARNT-SIM (PAS) protein, the repressor of AhR function (AhRR).

174 d1 (tb1) transcription factor that acts as a repressor of axillary bud growth.

175 rn, we demonstrate that the petunia AP2-type REPRESSOR OF B-FUNCTION (ROB) genes repress the B-functi

176 Loss of bioQ, the repressor of biotin biosynthesis, in the pyc::tn strain

177 PAI-1 is an essential repressor of cardiac fibrosis in mammals.

178 patocytes, indicating that Grb14 is a potent repressor of cell division.

179 ty analysis revealed a key role for IHF as a repressor of cell motility through the control of FliA s

180 n variants of the AHK2 and AHK3 genes, named repressor of cytokinin deficiency2 (rock2) and rock3, re

181 identified miR-218 as a posttranscriptional repressor of DCC and detected coexpression of DCC and mi

182 JMJ27 is a negative modulator of WRKY25 (a repressor of defense) and a positive modulator of severa

183 XND1-RBR interaction and XND1 efficacy as a repressor of differentiation, with loss of the LXCXE mot

184 so by protecting Capicua, a transcriptional repressor of EGFR target genes, from EGFR pathway-depend

185 EthR is a transcriptional repressor of EthA expression in Mycobacterium tuberculos

186 m gene glpR, which encodes a transcriptional repressor of factors that catalyze glycerol degradation.

187 Here, we identified Klf5 as an upstream repressor of Fgf4Fgf4 was markedly upregulated in Klf5 k

188 o GATA3 promoter in association with ZBTB32 (Repressor of GATA, ROG) and that ZBTB32 is essential for

189 otent guide RNA sequence-directed inducer or repressor of gene expression in mammalian cells.

190 Here, we demonstrate that G9a, an epigenetic repressor of gene expression, acting in the nucleus accu

191 JUN-dimerization protein 2 (JDP2) as a novel repressor of GNRH-mediated Fshb induction.

192 ntified FOXO1 as a bona fide transcriptional repressor of HAS2.

193 s both an IFN-stimulated response gene and a repressor of IFN-gene transcription, suggesting the exis

194 but express Blimp-1, a known transcriptional repressor of IL-2.

195 r study establishes Grb14 as a physiological repressor of insulin mitogenic action in the liver and f

196 ch complex control is achieved because a key repressor of light signaling, the Arabidopsis (Arabidops

197 apes, which can act either as an enhancer or repressor of metastasis.

198 report that a newly identified bHLH factor, Repressor of MYC2 Targets 1 (RMT1), is activated by CrMY

199 scription factor (REST) is a transcriptional repressor of neuronal genes.

200 ng of how CSL functions as a transcriptional repressor of Notch target genes.

201 bal gatekeeper of secondary metabolism and a repressor of numerous BGCs.

202 iated inhibition of STAT3, a transcriptional repressor of PEPCK.

203 MAF1 is a repressor of Pol III transcription whose activity is con

204 We previously identified c-Myb as a repressor of Rag transcription during clonal expansion u

205 -proximal binding of MAF1, a transcriptional repressor of RNAPIII activity, altogether revealing mult

206 Furthermore, the role of Xpp1 as a repressor of secondary metabolism is shown by gene expre

207 nt activator of this exon and consequently a repressor of sIL7R, and we found strong genetic associat

208 nd that this protein is a transcriptional co-repressor of STAT1.

209 activated by CrMYC2 and BIS1, and acts as a repressor of the CrMYC2 targets.

210 gene of previously unknown function, to be a repressor of the cul-6/cullin gene and other IPR gene ex

211 -dependent manner that up-regulates Id2, the repressor of the receptor activator of nuclear factor-ka

212 anscription factor T-bet acts as a selective repressor of the type I interferon (IFN) transcriptional

213 longation factor S-II domain, which we named REPRESSOR OF VERNALIZATION1 (RVR1), represses VRN1 befor

214 tors to binding sites in Tsix, the antisense repressor of XCI.

215 ma reesei Xpp1 was previously described as a repressor of xylanases.

216 the Polynucleotide Phosphorylase PNPase as a repressor of yeeJ transcription.

217 h is induced by FGF signalling and acts as a repressor of ZRS activity, interacts with the histone de

218 Among a collection of inducers and repressors of cardiac reprogramming, we discovered that

219 dy uncovered many previously uncharacterized repressors of ERVs, and defined an essential role of Rif

220 main (JAZ) proteins, which play key roles as repressors of JA signaling.

221 drenoreceptors is likely one of the upstream repressors of miR-1 as treatment with beta-blockers in p

222 Cryptochromes (CRY1/2), key transcriptional repressors of this molecular apparatus, are subject to p

223 We find the repressor operates in clusters, which upon extracellular

224 regulate localization of the transcriptional repressor Opi1p, which controls expression of phospholip

225 iptional activators (OsPCF2, OsNIN-like4) or repressors (OsCPP5, OsNIN-like2) and their encoding gene

226 e DBD-hinge helix-O-DNA module docks on core repressor, partially dehydrating phosphate oxygens and t

227 transcription of genes encoding the feedback repressors PERIOD and TIMELESS.

228 Forkhead Box P (FOXP) transcriptional repressors play a major role in brain development and th

229 ternatively, the role ubiquitously expressed repressors play in this process is not well understood.

230 ecognized by the zinc finger transcriptional repressor Prdm1/Blimp1, an essential regulator of placen

231 riptional activators and the transcriptional repressor PRDM13 that are critical for specifying dorsal

232 ons result in gain of function of the growth repressor product SAMD9.

233 bunit deadenylase complex "carbon catabolite repressor protein 4 (CCR4)-negative on TATA-less (NOT),"

234 ting expression of the developmental synapse repressor protein Ephexin5 (also known as ARHGEF15).

235 Here, we demonstrate that the co-repressor protein Sin3a is crucial for lung endoderm dev

236 ndence of the binding of a DNA triplex and a repressor protein to distal recognition sites on superco

237 ed for interaction with the TOPLESS (TPL) co-repressor protein.

238 raction of Su(H) does not associate with the repressor proteins Groucho and CtBP.

239 Here we characterize TS for lac repressor(R)-lac operator(O) binding by analyzing effect

240 required recruitment of the transcriptional repressor repressor element-1 silencing transcription fa

241 protein and the DP-E2F-Like1 transcriptional repressor, respectively.

242 igated the function of two broadly expressed repressors, Runt (Run) and Suppressor of Hairless [Su(H)

243 driven by the florigen paralog and flowering repressor SELF-PRUNING 5G (SP5G).

244 Our data show that broadly expressed repressors silence particular enhancers within cis-regul

245 rs ZEB1, ZEB2, and the snail transcriptional repressor SNAI2, each crucial factors in mediating EMT.

246 the stability of E-cadherin transcriptional repressors, snail and slug, induced by transforming grow

247 it is largely unclear how this transcription repressor specifies the TFH program.

248 under the control of the SaPI-encoded master repressor, Stl.

249 of the Aux/IAA proteins as well as the DELLA repressors, substrate of SCF(SLY)(1) We propose that the

250 R signaling network, via loss of function of repressors such as PTEN, causes epilepsy in humans and a

251 Furthermore, redundant abaxial-enriched ARF repressors suppress WOX1 and PRS expression, also throug

252 mutation of Capicua (CIC), a transcriptional repressor, suppresses the effects of EGFR inhibition by

253 specification involving the transcriptional repressors Tbr1, Fezf2, Satb2, and Ctip2 operates in neo

254 Tetracycline repressors (TetRs) modulate multidrug efflux pathways in

255 isation of BldO, an additional developmental repressor that acts to sustain vegetative growth and pre

256 ave identified SPIN.DOC as a transcriptional repressor that binds SPIN1 and masks its ability to enga

257 ng the degradation of GLD-1, a translational repressor that blocks V-ATPase synthesis.

258 Rest (also known as Nrsf), a transcriptional repressor that inhibits neuroendocrine gene expression.

259 Baf180 serve as a conserved transcriptional repressor that is critical for the maintenance of innate

260 SMAD4 interacts with SKI, a transcriptional repressor that is degraded upon TGFbeta stimulation.

261 REST is a transcriptional repressor that is expressed throughout the body; it has

262 cell lymphoma-6 (Bcl-6) is a transcriptional repressor that is required for the differentiation of T

263 o-chaperone ERdj4/DNAJB9 is a selective IRE1 repressor that promotes a complex between the luminal Hs

264 tion protein 1 (Blimp1) is a transcriptional repressor that regulates cell growth and differentiation

265 AZi functions as a flower-specific jasmonate repressor that regulates JAs, (E)-alpha-bergamotene, TPI

266 umpfuss (Klu), a zinc finger transcriptional repressor that regulates ss expression.

267 cation of a pathway-specific transcriptional repressor that silences the gene cluster under standard

268 iana) COP1/SPA ubiquitin ligase is a central repressor that suppresses light signaling in darkness by

269 ory hub for transcriptional coactivators and repressors that compete for binding and, consequently, c

270 omb group proteins (PcG) are transcriptional repressors that control cell identity and development.

271 The Aux/IAA proteins are auxin-sensitive repressors that mediate diverse physiological and develo

272 osome, long known to serve as a general gene repressor, thus also performs an important positive role

273 s during cleavage stages and recruits the co-repressor Tle/Groucho in the early blastula.

274 phosphorylation, converting Musashi2 from a repressor to an activator of target mRNA translation.

275 olving miRNA-mediated suppression of a Notch repressor to assign non-neuronal cell fate.

276 (PDP1epsilon) activator and the VRILLE (VRI) repressor to drive rhythmic transcription peaking at daw

277 nd antagonize the binding of FBP-interacting repressor to FUBP1, thereby coordinating the expression

278 with themselves and CRISPRi transcriptional repressors to deliver new types of RNA-based genetic cir

279 YC) activators and PERIOD-TIMELESS (PER-TIM) repressors to drive rhythmic transcription peaking at du

280 s together with self-renewal transcriptional repressors to maintain the erm immature INP enhancer in

281 suggested that the AFPs interact with the co-repressor TOPLESS to inhibit ABA-regulated gene expressi

282 actions with histone deacetylases and the co-repressor TOPLESS.

283 is required for the interaction with the Stl repressor, usually only those Duts with normal enzymatic

284 3 and related members act as transcriptional repressors via recruitment of C-terminal Binding Protein

285 Binding by the enhanced lac repressor was sufficiently tight to allow strong attenua

286 RshA anti-sigma factors and the Zur and NrdR repressors were identified as NaOCl-sensitive proteins a

287 N OF CONSTANS1-like1 (TgSOC1-like1) might be repressors, whereas TgSOC1-like2 likely is an activator,

288 We propose that ME31B is a global repressor whose regulatory impact changes based on its b

289 Apoptosis repressor with caspase recruitment domain (ARC) binds an

290 NKX6-2 encodes a transcriptional repressor with early high general and late focused CNS e

291 miRNA-139-5p as differentially expressed RNA repressor with highest expression in the purely phasic s

292 This is a transcriptional activator/repressor with presumed pleiotropic activities.

293 tors (PerRs) are homodimeric transcriptional repressors with each monomer typically containing both s

294 ut indicates that overexpression of the LacI repressor would drive the system into the bistable regim

295 Distinct lineage repressors would have to be induced in different donor c

296 n zebrafish, we identify the transcriptional repressor, ZBTB11, as critical for basal and emergency g

297 , which reduces the level of transcriptional repressor ZEB1, leading to induced expression of miR-183

298 ng ERK1/2 activation and the transcriptional repressor ZEB1, leading to induction of miR-183-5p and d

299 Among these, the GATA-3 repressor zinc finger protein 1 (Zfpm1) emerged as a pot

300 minus and a specific interaction with the co-repressor ZMYND11 (BS69).