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1 trates (e.g. O-glycan, N-glycan or the DELLA transcriptional repressors).
2  RASSF1A promoter in a complex with the ZEB1 transcriptional repressor.
3  where it binds chromatin and functions as a transcriptional repressor.
4 sion, suggesting that CarD can also act as a transcriptional repressor.
5 lymphoid cells depends on MNT, a MYC-related transcriptional repressor.
6 he SUMO-modified form of TRIM28/KAP1, a host transcriptional repressor.
7 P, rs7594852, alters the binding of the HIC1 transcriptional repressor.
8 igher expression levels and activity of this transcriptional repressor.
9 nhancers that are known to be repressed by a transcriptional repressor.
10  expressed Ets DNA-binding domain-containing transcriptional repressor.
11 ion and inhibiting the formation of the GLI3 transcriptional repressor.
12 he absence of a Notch signal, RBPJ acts as a transcriptional repressor.
13 h EAR motifs which putatively functions as a transcriptional repressor.
14  density predominantly as a cell-autonomous, transcriptional repressor.
15 inase2 (HIPK2) phosphorylates MeCP2, a known transcriptional repressor.
16  changes consistent with loss of a classical transcriptional repressor.
17 ngs suggest that CRF6 functions largely as a transcriptional repressor.
18  induction of SPIC, a hematopoietic-specific transcriptional repressor.
19 n dynamics of Her6, a basic helix-loop-helix transcriptional repressor.
20 MAD3) and SMAD4 were identified as potential transcriptional repressors.
21 BMAL1 transcriptional activators and CRY-PER transcriptional repressors.
22 s more generally the result of repression by transcriptional repressors.
23 e responsible for degradation of the Aux/IAA transcriptional repressors.
24  almost exclusively used naturally occurring transcriptional repressors.
25 nzymes and several novel uncharacterized MYB transcriptional repressors.
26 f phylogenetically conserved, class-specific transcriptional repressors.
27 ough the AMPK orthologue Snf1 and downstream transcriptional repressors.
28 n through the auxin-dependent degradation of transcriptional repressors.
29 ondary metabolites by binding to TetR family transcriptional repressors.
30 t characteristics including association with transcriptional repressors.
31 ased on de-repression via the degradation of transcriptional repressors.
32 introduction of either WISP1 or snail family transcriptional repressor 1 (SNAI1).
33 tors that regulate EMT, such as snail family transcriptional repressor 2 (SNAI2), are well characteri
34 een extensively studied, less is known about transcriptional repressors acting directly on IFN-I regu
35 ulatory complex Sin3A as a mediator of STAT3 transcriptional repressor activity and identifies the ST
36 t stimulate proteolytic cleavage of the LexA transcriptional repressor, allowing expression of > 40 g
37             Thus, Etv6's dual function, as a transcriptional repressor and activator, controls a majo
38                          ERF12 is a putative transcriptional repressor and genetically opposes the fu
39 reciated aspect of YAP nuclear function as a transcriptional repressor and highlights how loss of con
40 polymerase II interactor that functions as a transcriptional repressor and is part of a larger nuclea
41  dominant mutations in the gene encoding the transcriptional repressor and MeCP2 interactor switch-in
42                                       CSL, a transcriptional repressor and Notch mediator, suppresses
43 esponse DNA-binding protein 43 (TDP-43) is a transcriptional repressor and splicing factor.
44 inated action of the auxin-sensitive Aux/IAA transcriptional repressors and ARF transcription factors
45                                  PRRs act as transcriptional repressors and associate with chromatin
46 hila Ci or mammalian Gli proteins to nuclear transcriptional repressors and by activating the full-le
47 hromatin complexes revealed association with transcriptional repressors and coactivators including TL
48  control occurs through cryptochromes (CRYs)-transcriptional repressors and components of the circadi
49 interference targeting mRNA, and zinc finger transcriptional repressors and CRISPR-Cas9 methods aimin
50 ession is independent of the Snail family of transcriptional repressors and down-regulation of Drosop
51 B) lacking a quintet of Jasmonate ZIM-domain transcriptional repressors and the photoreceptor phyB.
52 ich we term MYBL1, falls into a class of MYB transcriptional repressors and, accordingly, higher expr
53  binds to the lytic gene promoter, acts as a transcriptional repressor, and thereby helps to maintain
54 ression or stability of JASMONATE ZIM-domain transcriptional repressors, and SA/JA cross talk did not
55  auxin, AUXIN/INDOLE-3-ACETIC ACID (AUX/IAA) transcriptional repressors are targeted for degradation
56         HB-EGF coimmunoprecipitates with the transcriptional repressor B cell lymphoma 6 (Bcl-6) in C
57                                          The transcriptional repressor B lymphocyte-induced maturatio
58 ive genes by inducing the degradation of the transcriptional repressor B2 repeat RNA.
59                 We identified a heme-binding transcriptional repressor, BACH1, as a novel regulator o
60                                          The transcriptional repressor Bcl-6 is linked to the develop
61 -21, the coinhibitory receptor TIGIT and the transcriptional repressor Bcl-6.
62 nalling leads to increased expression of the transcriptional repressor Bcl6 and that Bcl6 is required
63                          Deregulation of the transcriptional repressor BCL6 enables tumorigenesis of
64 C exit, which are also direct targets of the transcriptional repressor BCL6.
65 beta1 promotes HIV latency by upregulating a transcriptional repressor BLIMP-1.
66                                          The transcriptional repressor Blimp1 controls cell fate deci
67 e herein prove, for the first time, that the transcriptional repressor Blimp1 is a novel mediator of
68 nravel the previously unidentified role that transcriptional repressor Blimp1 plays in the control of
69 onstrated that expression of the zinc finger transcriptional repressor Blimp1/PRDM1 is essential for
70 itment of the Rpd3(L) histone deacetylase by transcriptional repressors blocks Put3 DNA binding.
71                           The Polycomb group transcriptional repressor Bmi-1 often overexpressed and
72 P, and which is essential for it to act as a transcriptional repressor but is dispensable for partiti
73                SFMBT1 was considered to be a transcriptional repressor but its role in cancer remains
74 regulatory behaviors that are well-suited to transcriptional repressors but perhaps incompatible with
75 or immunoglobulin kappa J region (RBPJ) is a transcriptional repressor, but converts into a transcrip
76                       LSD1 (KDM1A) acts as a transcriptional repressor by demethylating mono/dimethyl
77 ranscriptional activator, YAP functions as a transcriptional repressor by interacting with the multif
78  phosphorylation/inactivation of the ZKSCAN3 transcriptional repressor by JNK2/p38-MAPK.
79 , we show that the developmentally regulated transcriptional repressor Capicua (CIC) suppresses invas
80 006129.1 binds to the promoter region of the transcriptional repressor Capicua (CIC), facilitates the
81                             Here we show the transcriptional repressor Capicua/CIC maintains peripher
82 e of these B12-dependent photoreceptors, the transcriptional repressor CarH, is widespread in bacteri
83                           Recruitment of the transcriptional repressor CCCTC-binding factor (CTCF) to
84 cell cycle gene expression by formation of a transcriptional repressor complex called dimerization pa
85        Furthermore, they show that the Sin3a transcriptional repressor complex is an obligatory partn
86 observed an enrichment of the OGT-containing transcriptional repressor complex mSin3A-HDAC1 at the pr
87 scriptional activators; however, they form a transcriptional repressor complex that represses MIZ1 ta
88 oxa1 proximal promoter and recruits the NuRD transcriptional repressor complex to de-acetylate H3K9 a
89  the protein ataxin 1 (ATXN1), which forms a transcriptional repressor complex with capicua (CIC).
90  with SHARP, a scaffold protein that forms a transcriptional repressor complex with RBPJ in the absen
91         STAT3 constitutively bound the Sin3A transcriptional repressor complex, and both STAT3 and Si
92 OVEL INTERACTOR OF JAZ (NINJA) to assemble a transcriptional repressor complex.
93 ependence 1B (GFI1B) coordinates assembly of transcriptional repressor complexes comprised of corepre
94 bind to E2F factors forming RB-E2F and DREAM transcriptional repressor complexes.
95 te the expression of Rev-erbalpha (Nr1d1), a transcriptional repressor component of the core clock ma
96                       Engineering allosteric transcriptional repressors containing an environmental s
97 ition, LFA-1 promoted expression of Bcl-6, a transcriptional repressor critical for Tfh cell differen
98 nd brain and muscle ARNT-like 1 (BMAL1), and transcriptional repressors cryptochrome (CRY) and period
99 clear factor 6 [HNF6], FOXA1, and FOXA2) and transcriptional repressors (CUX2 and BCL6).
100 ns of catalytically-inactive Cas9 (dCas9) to transcriptional repressors (dCas9-KRAB) and DNA methyltr
101 age of colonized mice, while deletion of the transcriptional repressor (Deltargg3) increased the perc
102 ing Kruppel-like factor 9 (KLF9), a putative transcriptional repressor, demonstrate conserved respons
103 epressor domain, which serves routinely as a transcriptional repressor domain in CRISPRi.
104                                      The SID transcriptional repressor domain is effective as a fusio
105  region of the promoter, as well as the RiBi transcriptional repressors Dot6 and Tod6.
106 involves caspase-dependent cleavage of HRK's transcriptional repressor DREAM.
107  conserved molecular function of TCF7L1 as a transcriptional repressor during HP axis development in
108 N progenitors express prdm8, which encodes a transcriptional repressor, during motor neuron and OPC f
109 ators in ENCODE ChIP-seq database identified transcriptional repressor E2F6 as a possible negative re
110 ied PRMT6 as a target of hypoxia through the transcriptional repressor element 1-silencing transcript
111 siently in the c-MYC promoter functions as a transcriptional repressor element.
112 decreased histone deacetylase 11 (HDAC11), a transcriptional repressor enriched in CA1 cells importan
113 edictive network suggests that subsequently, transcriptional repressors ensure the transition of prog
114 ding protein 1, growth factor independent 1B transcriptional repressor, ETS variant 6, ecotropic vira
115                                      The ETS transcriptional repressor ETV6 (or TEL) is autoinhibited
116 enes such as Il4, as IRF8 dimerises with the transcriptional repressor ETV6 and inhibits Il4 expressi
117 sion, leading to oncogenic dependence on the transcriptional repressor EZH2.
118                                          The transcriptional repressor Fezf1 is selectively expressed
119                 We further investigate known transcriptional repressors for terminal muscle different
120               Furthermore, inhibition of the transcriptional repressor function of BCL6 in the presen
121 and highlight the growing evidence that this transcriptional repressor functions as a key regulator i
122           Fosb-ZFPs were fused to either the transcriptional repressor, G9a, which promotes histone m
123 ecipitation, followed by MS, we identified a transcriptional repressor, GATA zinc finger domain-conta
124 ime point, possibly due to the activation of transcriptional repressor genes such as Cbfa2t3 and Jdp2
125 al activator GLI1 and a decrease in the GLI3 transcriptional repressor (GLI3R).
126                                  We identify transcriptional repressor - hairy and enhancer of split-
127 zh1 and Ezh2 triggered overexpression of the transcriptional repressor Hes-related family BHLH transc
128 endent strong reduction in the levels of the transcriptional repressor HES1.
129                In this repressor system, two transcriptional repressors-heterochromatin protein 1 (HP
130  initiates the interaction of DPF3a with the transcriptional repressors HEY, followed by the release
131 xpressed (DE) along this axis identified the transcriptional repressor histone deacetylase 4 (HDAC4)
132 a rare missense mutation in the gene for the transcriptional repressor histone deacetylase 4 (HDAC4)
133                         B3 domain-containing transcriptional repressors HSI2/VAL1 and HSL1/VAL2 silen
134 athogenic Acinetobacter and regulated by the transcriptional repressor HutC.
135                                          The transcriptional repressor Id2 is constitutively expresse
136                                    E2F4 is a transcriptional repressor implicated in cell cycle arres
137                              NACC1 encodes a transcriptional repressor implicated in gene expression
138 actor for other methyltransferases, and as a transcriptional repressor in mouse embryogenesis.
139 -1 (INSM1) is a key protein functioning as a transcriptional repressor in neuroendocrine differentiat
140 Samd7 is a recently identified Crx-regulated transcriptional repressor in retina, we hypothesize that
141 y delivered RNA interference and zinc finger transcriptional repressors in advanced testing in animal
142        Although CCA1 is targeted by multiple transcriptional repressors, including PSEUDO-RESPONSE RE
143 enced by nicotinic acid and by a NadQ family transcriptional repressor, indicating that these organis
144                                     The Rest transcriptional repressor interacts with chromatin-modif
145          Like CSL, ATF3, a stress-responsive transcriptional repressor, is down-modulated in skin can
146 tory element antagonist modulator (DREAM), a transcriptional repressor, is known to modulate pain res
147 argets of Blimp1 and potent osteoclastogenic transcriptional repressors, is increased.
148 rly repressor (ICER) has been described as a transcriptional repressor isoform of the cAMP response e
149 is effect by promoting degradation of the JA transcriptional repressor JAZs.
150  through regulation of the gene encoding the transcriptional repressor JMJD8.
151 induced expression of the well-characterized transcriptional repressor Kruppel-like factor 3 (KLF3),
152 ivation caused by decreased association with transcriptional repressors, leading to increased chromat
153 lly define a novel binding motif for the SOS transcriptional repressor LexA, and we use this motif to
154 charomyces pombe lacking the zinc-responsive transcriptional repressor Loz1 with the goal of identify
155 cluded those encoding two GH/STAT5-regulated transcriptional repressors: male-biased BCL6, which was
156                              The MAX network transcriptional repressor (MNT) is an MXD family transcr
157 rs, which all contain tetramer together with transcriptional repressor moieties.
158                           Capicua (Cic) is a transcriptional repressor mutated in the brain cancer ol
159             CIC (also known as Capicua) is a transcriptional repressor negatively regulated by RAS/MA
160                                            A transcriptional repressor network including THAP11 was i
161 terference with the chromatin binding of the transcriptional repressor neuron restrictive silencing f
162 y expressed HCMV miR-US5-2 downregulates the transcriptional repressor NGFI-A binding protein (NAB1)
163 mphiphilic repression (EAR) domain-dependent transcriptional repressors: NO abolished this activity f
164           Here we identify Snail as a strong transcriptional repressor of 4E-BP1.
165 her these findings identify FOXF1 as a novel transcriptional repressor of ATX and demonstrate that lo
166  function of LR-MSCs via its role as a novel transcriptional repressor of autocrine motility-stimulat
167 ether, our findings reveal Foxp1 as a master transcriptional repressor of brown/beige adipocyte diffe
168 ts with CCCTC-binding factor (CTCF), a known transcriptional repressor of c-Myc.
169 INOBLASTOMA RELATED (RBR), a sugar-dependent transcriptional repressor of cell proliferation, deplete
170 otic aztreonam through a mutation in NalD, a transcriptional repressor of cellular efflux.
171          It does so by protecting Capicua, a transcriptional repressor of EGFR target genes, from EGF
172                        We report here that a Transcriptional Repressor of EIN3-dependent Ethylene-res
173                                    EthR is a transcriptional repressor of EthA expression in Mycobact
174 on the downstream gene glpR, which encodes a transcriptional repressor of factors that catalyze glyce
175 cyanin biosynthesis in grapevine acting as a transcriptional repressor of flavonoid structural genes.
176                                    LHP1 is a transcriptional repressor of flowering-related genes, su
177 related proline domain protein 2 (ZPO2) as a transcriptional repressor of GATA3 expression and transc
178 stically, we identified FOXO1 as a bona fide transcriptional repressor of HAS2.
179 nts reveal that ZBED2 is a sequence-specific transcriptional repressor of IFN-stimulated genes, which
180 t produce IL-2, but express Blimp-1, a known transcriptional repressor of IL-2.
181 dy provides new insights into YAP as a broad transcriptional repressor of key regulators of the cell
182  in the 3' UTR of the mRNA encoding Rme1p, a transcriptional repressor of meiosis.
183  Zinc Finger and BTB Domain Containing 7C, a transcriptional repressor of membrane metalloproteases (
184              GmPRR3b(H6) appears to act as a transcriptional repressor of multiple predicted circadia
185 1 silencing transcription factor (REST) is a transcriptional repressor of neuronal genes.
186 omb-group protein PHC1, which functions as a transcriptional repressor of Notch genes.
187  our understanding of how CSL functions as a transcriptional repressor of Notch target genes.
188 escent SCs of mice and functions as a direct transcriptional repressor of p16(Ink4a).
189 zed glucagon-mediated inhibition of STAT3, a transcriptional repressor of PEPCK.
190 n required for the nuclear import of MYB4, a transcriptional repressor of phenylpropanoid metabolism.
191   Here, we demonstrate that mutations in the transcriptional repressor of purine biosynthesis, purR,
192 nhanced promoter-proximal binding of MAF1, a transcriptional repressor of RNAPIII activity, altogethe
193 h PUB25 and PUB26 poly-ubiquitinate MYB15, a transcriptional repressor of the CBF-dependent cold sign
194 hat ATF3 in conjunction with HDAC6 acts as a transcriptional repressor of the DNM3os/miR-199a2 locus.
195 and tissue growth by functioning as a direct transcriptional repressor of the master regulator of gro
196                          MexR functions as a transcriptional repressor of the mexAB-oprM operon.
197 e report that the AcrIIA1(NTD) is a critical transcriptional repressor of the strong anti-CRISPR prom
198 oduction by decreasing levels of several key transcriptional repressors of fetal globin gene expressi
199 ivity of PUMILIO proteins, which act as post-transcriptional repressors of target mRNAs to which they
200 an clock and the Cryptochromes (CRY1/2), key transcriptional repressors of this molecular apparatus,
201 ow AR and its corepressor, REST, function as transcriptional-repressors of SPINK1, and AR-antagonists
202 e protein Scs2p regulate localization of the transcriptional repressor Opi1p, which controls expressi
203                        Forkhead Box P (FOXP) transcriptional repressors play a major role in brain de
204 experiments demonstrate that the zinc finger transcriptional repressor Prdm1/Blimp1 is essential for
205 tional targets recognized by the zinc finger transcriptional repressor Prdm1/Blimp1, an essential reg
206 ix (bHLH) transcriptional activators and the transcriptional repressor PRDM13 that are critical for s
207 nctional studies to demonstrate that Bcl6, a transcriptional repressor previously reported to promote
208  SWI/SNF and Polycomb group proteins and the transcriptional repressor protein REST determined differ
209 tion caused a loss of O-GlcNAc from multiple transcriptional repressor proteins associated with TRIM2
210                                      As most transcriptional repressor proteins do not comprise tetra
211 ing complex acts as a temperature-responsive transcriptional repressor, providing rhythmicity and tem
212  B1 overexpression plants suggests a role as transcriptional repressor, putatively targeting pathways
213 of-Split Related with YRPW Motif 1 (HEY1), a transcriptional repressor, regulates germ cell different
214                            CouR, a MarR-type transcriptional repressor, regulates the cou genes, enco
215 on Crh, and this required recruitment of the transcriptional repressor repressor element-1 silencing
216 -B-INSENSITIVE4 protein and the DP-E2F-Like1 transcriptional repressor, respectively.
217                                          The transcriptional repressor REST (repressor element-1 sile
218 -specific antagonistic interplay between the transcriptional repressor REST and the activator GLI1 at
219  critically depends on BRG1 and contains the transcriptional repressor REST, whereas a non-overlappin
220 res down-regulation and loss of the neuronal transcriptional repressor, REST.
221            BMAL1 regulates expression of the transcriptional repressor REV-ERBalpha, and deletion of
222 d increased stability of the haem-responsive transcriptional repressors Rev-Erbalpha and BACH1.
223  of Srebp1 expression, and engaged circadian transcriptional repressors REV-ERBalpha and beta as rhyt
224                     Here, we reveal that the transcriptional repressor role of SerRS is inactivated u
225 on and feeding initiation via the downstream transcriptional repressor Schnurri.
226 lm state is regulated by the activity of the transcriptional repressor, SinR, and its inactivation by
227 d the EMT inducers ZEB1, ZEB2, and the snail transcriptional repressor SNAI2, each crucial factors in
228 s the Wnt pathway and stabilizes the nephrin transcriptional repressor SNAIL.
229 d talin regulate the stability of E-cadherin transcriptional repressors, snail and slug, induced by t
230 have recently been identified, including the transcriptional repressor SPEN(1-3), the loss of which h
231  such as early naive pluripotency markers or transcriptional repressors such as TLE4.
232 egions are enriched for the binding sites of transcriptional repressors (such as CTCF, MECOM, SMAD4,
233        Zinc finger and BTB domain containing transcriptional repressors, such as ZBTB7A and ZBTB16, h
234  also show that mutation of Capicua (CIC), a transcriptional repressor, suppresses the effects of EGF
235 vealed that ERRalpha predominantly acts as a transcriptional repressor, targeting genes linked with a
236 ode of cell-fate specification involving the transcriptional repressors Tbr1, Fezf2, Satb2, and Ctip2
237 x transcriptional activator, Tbx5, and T-box transcriptional repressor, Tbx3, determined the molecula
238 lusions, neuritic plaques, inclusions of the transcriptional repressor TDP-43, angiopathy, neuron los
239                                    E2F8 is a transcriptional repressor that antagonizes E2F1 at the c
240 of the nuclear hormone receptor family, as a transcriptional repressor that antagonizes RORgammat fun
241     In this study, we identify Nerfin-1 as a transcriptional repressor that antagonizes the activity
242 conclusion, we have identified SPIN.DOC as a transcriptional repressor that binds SPIN1 and masks its
243 e describe an unexpected role for Blimp-1, a transcriptional repressor that constrains autoimmunity,
244                           Capicua (CIC) is a transcriptional repressor that counteracts activation of
245                                   CNOT1 is a transcriptional repressor that has been suggested as bei
246 ated in part by Rest (also known as Nrsf), a transcriptional repressor that inhibits neuroendocrine g
247 1-silencing transcription factor (Rest) is a transcriptional repressor that interacts with chromatin-
248 ther, Bap180 and Baf180 serve as a conserved transcriptional repressor that is critical for the maint
249 is revealed that SMAD4 interacts with SKI, a transcriptional repressor that is degraded upon TGFbeta
250          Capicua (CIC) is a highly conserved transcriptional repressor that is differentially regulat
251                                    REST is a transcriptional repressor that is expressed throughout t
252               B cell lymphoma-6 (Bcl-6) is a transcriptional repressor that is required for the diffe
253            The BCL6 proto-oncogene encodes a transcriptional repressor that is required for the germi
254                        The FrmR protein is a transcriptional repressor that is specifically inactivat
255 ensing loci by competing with H-NS, a global transcriptional repressor that oligomerizes on DNA to fo
256     Growth Factor Independence 1 (GFI1) is a transcriptional repressor that plays a critical role dur
257                        Gfi1 is a zinc-finger transcriptional repressor that plays an important role i
258                       Further, we identify a transcriptional repressor that preferentially binds an u
259 e-induced maturation protein 1 (Blimp1) is a transcriptional repressor that regulates cell growth and
260 man HES4, is a basic helix-loop-helix-orange transcriptional repressor that regulates neurogenesis in
261  affinity for Klumpfuss (Klu), a zinc finger transcriptional repressor that regulates ss expression.
262 PERMAN (SUP) gene encodes a C2H2 zinc-finger transcriptional repressor that regulates the floral orga
263  to the identification of a pathway-specific transcriptional repressor that silences the gene cluster
264 Far1 Related Sequence (FRS) 7 and FRS12, two transcriptional repressors that accumulate in short-day
265              The Polycomb group proteins are transcriptional repressors that are critically important
266 p (PcG) proteins function as chromatin-based transcriptional repressors that are essential for normal
267            Polycomb group (PcG) proteins are transcriptional repressors that are important regulators
268            Polycomb group proteins (PcG) are transcriptional repressors that control cell identity an
269 m-domain (JAZ) proteins comprise a family of transcriptional repressors that modulate jasmonate (JA)
270 s) are regulated by class IIa HDACs 4 and 5, transcriptional repressors that transiently enter neuron
271               Sequence-specific targeting of transcriptional repressors thus recruits the machinery f
272  Here, we introduce an enhanced CRISPR-based transcriptional repressor to reprogram immune homeostasi
273  (GH6 family cellobiohydrolase) and the CebR transcriptional repressor to the cellulolytic phenotype.
274 o link individual mutations in an allosteric transcriptional repressor to the parameters which govern
275 tudies that inhibits expression by guiding a transcriptional repressor to the transcription start-sit
276  these new STARs with themselves and CRISPRi transcriptional repressors to deliver new types of RNA-b
277 synergy between the selective recruitment of transcriptional repressors to ERalpha and FBXO45-mediate
278 c1/Rpd3 functions together with self-renewal transcriptional repressors to maintain the erm immature
279 ation of open chromatin enables a network of transcriptional repressors to regulate expression levels
280  predicted genes, including C2H2 zinc finger transcriptional repressor TraesCS5A02G542800 upregulated
281 , this work establishes a mechanism by which transcriptional repressor TREE1 interacts with EIN3 to i
282 or suppressor genes, including the GATA-like transcriptional repressor TRPS1 Down-regulation of TRPS1
283 ith cellular proteins of E. coli such as the transcriptional repressor ulaR, and the ankyrins repeat
284 300, whereas KLF3 and related members act as transcriptional repressors via recruitment of C-terminal
285                          MprA, a MarR family transcriptional repressor, was identified as the putativ
286 rain in which csoR, encoding a Cu-responsive transcriptional repressor, was mutated.
287        Although IRF2 is generally known as a transcriptional repressor, we found that it was a transc
288 scriptional activators and Rgg3 proteins are transcriptional repressors, we propose that both are cap
289                               ERF4 acts as a transcriptional repressor whose activity is modulated by
290                            Here, we identify transcriptional repressor Wilm's Tumor 1 (WT1) as a crit
291 2 occurred in tandem with suppression of its transcriptional repressor Wilm's tumor1.
292                             NKX6-2 encodes a transcriptional repressor with early high general and la
293     Growth Factor Independence 1 (GFI1) is a transcriptional repressor with key roles in haematopoies
294 de stress regulators (PerRs) are homodimeric transcriptional repressors with each monomer typically c
295 OX9 functions together with the modern clade transcriptional repressor WOX genes in embryogenesis and
296                                      The WOX transcriptional repressor WOX1/STF, the LEUNIG (LUG) tra
297 genetic screen in zebrafish, we identify the transcriptional repressor, ZBTB11, as critical for basal
298             We report that the BTB-ZF family transcriptional repressor Zbtb20 negatively regulates CD
299 RK1/2 activation, which reduces the level of transcriptional repressor ZEB1, leading to induced expre
300 ress by inhibiting ERK1/2 activation and the transcriptional repressor ZEB1, leading to induction of

 
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