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1 -MYC promoter functions as a transcriptional repressor element.
2 omoter region functions as a transcriptional repressor element.
3 e deacetylase HDAC1 when bound to the HLA-B7 repressor element.
4 demonstrating that CDP/cut binds the HLA-B7 repressor element.
5 may be partially mediated through a G/C-rich repressor element.
6 truct containing multiple copies of the VIPR repressor element.
7 t, possibly as a DNA-binding transcriptional repressor element.
8 activator element while helix II serves as a repressor element.
9 t the CpG resides within a putative internal repressor element.
10 otein complex dependent on the SM22alpha G/C Repressor element.
11 ecause it is repressed by an upstream distal repressor element.
12 lex (G4) that functions as a transcriptional repressor element.
13 ored Pur alpha protein and binding to the AR repressor element.
14 of the previously identified In100 splicing repressor element.
15 ter of UBX sites that can also function as a repressor element.
16 omoter activity, suggesting that CACCC was a repressor element.
17 -MYC promoter functions as a transcriptional repressor element.
18 transcription of the hAT1R gene through the repressor element.
19 RNA by promoting the removal of a cis-acting repressor element.
20 GLD-1 binds directly and specifically to the repressor element.
21 nce of removing the downstream translational repressor element.
22 accompanied by increased AP-1 binding to the repressor elements.
23 nd defined regions that contain enhancer and repressor elements.
24 '-flanking region suggesting the presence of repressor elements.
25 t and does not require upstream activator or repressor elements.
26 for genes in which the E2F sites function as repressor elements.
27 sting interaction between the activators and repressor elements.
28 inding to RelB for optimal repression at DNA repressor elements.
29 reakpoint, which may involve inactivation of repressor elements.
30 sequential binding of pELK-1 and KLF4 to G/C Repressor elements.
31 ledge of TFs bound to promoter, enhancer and repressor elements.
32 so contains a variety of known activator and repressor elements.
33 ession in neurons, whereas Sp1/Sp3 bound the repressor elements.
34 cells, resulting in deletion of translation repressor elements.
35 he TATA box of the PTP-oc contains potential repressor elements.
36 zed to a neuron-restrictive silencer element/repressor element 1 (NRSE/RE-1) sequence within the chol
37 on is repressed in non-neuronal cells by the repressor element 1 (RE-1)-silencing transcription facto
38 has been proposed to restrict expression of repressor element 1 (RE1) bearing genes to differentiate
42 analyses, we show that the binding of REST (repressor element 1 (RE1) silencing transcription factor
45 report the light-mediated regulation of the repressor element 1 (RE1)-silencing transcription factor
47 ough the cis-regulatory element known as the repressor element 1 or neural restrictive silencer (RE1/
48 so stabilized binding of the Corepressor for Repressor Element 1 Silencing Transcription Factor (CoRE
51 single master transcriptional regulator, the Repressor Element 1 Silencing Transcription factor (REST
52 f SCF(betaTrCP)-dependent destruction of the repressor element 1 silencing transcription factor (REST
53 we show that the transcriptional repressor, repressor element 1 silencing transcription factor (REST
55 s study, the transcriptional repressor REST (Repressor Element 1 Silencing Transcription factor) was
56 he gene silencing transcription factor REST (repressor element 1 silencing transcription factor), whi
57 udy, we reported that aberrant expression of repressor element 1 silencing transcription factor/neuro
58 he gene silencing transcription factor REST [repressor element 1 silencing transcription factor]/NRSF
59 r miR-124a promoters despite the presence of repressor element 1 sites, indicating REST target specif
60 demonstrate that nuclear localization of the Repressor Element 1-Silencing Transcription factor (REST
62 e show that the master epigenetic regulator, Repressor Element 1-Silencing Transcription factor (REST
66 promoter was effectively counteracted by the repressor element 1-silencing transcription factor (REST
67 racts with the master neuronal gene-silencer repressor element 1-silencing transcription factor (REST
69 nes mediated by the interaction of TRF2 with repressor element 1-silencing transcription factor (REST
70 r that recruits BRG1 as a corepressor is the repressor element 1-silencing transcription factor (REST
72 whereas the transcriptional repressor REST (repressor element 1-silencing transcription factor) repr
74 arget of hypoxia through the transcriptional repressor element 1-silencing transcription factor, link
75 ons may be linked to increased levels of the repressor element 1-silencing transcription factor, whic
76 tors implicated in vertebrate development is repressor element 1-silencing transcription/neuron-restr
77 in sequence and position dependence from the repressor element 1/neuron-restrictive silencer element
79 on factor neuron-restrictive silencer factor/repressor element-1 (RE-1) silencing transcription facto
83 tection by inducing the transcription factor repressor element-1 silencing transcription factor (REST
90 that NED of PCa requires down-regulation of repressor element-1 silencing transcription factor (REST
91 gene silencing transcription factor neuronal repressor element-1 silencing transcription factor (REST
92 w that the lysine-specific demethylase 1 and repressor element-1 silencing transcription factor corep
94 ilencer factor (NRSF; also known as REST for repressor element-1 silencing transcription factor) is a
95 lencer factor (NRSF; also known as REST, for repressor element-1 silencing transcription factor) to 1
96 he gene silencing transcription factor REST (repressor element-1 silencing transcription factor)/NRSF
97 recruitment of the transcriptional repressor repressor element-1 silencing transcription factor/neuro
100 that miR-9* and miR-124 are repressed by the repressor-element-1-silencing transcription factor (REST
103 nd K562 cells demonstrated the presence of a repressor element 650 base pairs upstream of the first e
104 is mediated through KLF4 binding to the G/C Repressor element and (2) the transcriptional repressor
105 sults in destabilization of the G-quadruplex repressor element and an increase in basal transcription
106 n requires integration of typical CDE/CHR G1 repressor elements and basal transcriptional activity by
107 hift assays indicate that the activation and repressor elements are bound by AP1 and an LBP1-related
110 , suggesting that additional HSF-1-dependent repressor elements are present upstream of the minimal -
111 protein specifically interacts with the VIPR repressor element as demonstrated by gel shift assays.
114 and its serial deletions identified a 15-bp repressor element at the 3'-UTR of CDKN1A, which contain
119 of reporter constructs containing the HLA-B7 repressor element but not the corresponding region of th
120 show that the Z-DNA forming transcriptional repressor element, by interacting with these putative Z-
123 tential activator protein 1 (AP1) site and a repressor element containing a potential binding site fo
124 oteins; association of the proteins with the repressor elements correlated negatively with FR-beta ex
125 shift assays that Sp1 binding to the GC-rich repressor element did not prevent SRF binding to the adj
127 rgenic region functions as a tissue-specific repressor element, forming an integral part of the compl
128 R4 promoter identified a seven-base pair p53-repressor element homologous to cyclic AMP/AP-1 response
129 bstitution mutations identified a functional repressor element I RE1-like silencer and functional Sp1
130 We have reported the presence of another repressor element in exon 1 that interacted with a prote
132 ncreased DNA binding activity to the labeled repressor element in nuclear extracts treated with high
133 Targeting a newly discovered y-globin gene repressor element in SCD donor CD34(+) hematopoietic pro
136 s-acting factor(s) binding to the cis-acting repressor element in the hAT1R promoter, which may parti
137 ctor that interacts with the tissue-specific repressor element in the rat serum amyloid A1 (SAA1) pro
139 mming gene expression by releasing circadian repressor elements in the transcriptional regulatory pat
142 ssor complex that binds a specific sequence (repressor element) in the AR gene 5'-untranslated region
143 estern blot analysis indicated that the VIPR repressor element interacts specifically with a nuclear
146 5 promoter is regulated by a silencer (Kv1.5 repressor element; KRE) containing a dinucleotide-repeti
149 romoter also reveals a novel transcriptional repressor element located approximately 60 bp 5' of the
150 29-bp (5'-AACTGATTTTTGTATATTGATCTTGTATT-3') repressor element located between -1582 and -1610 bp was
151 gnificant sequence homology with an intronic repressor element located downstream of the alpha-exon.
152 ols Pax6 transcription by interacting with a repressor element located in the 5'-flanking region upst
154 o begin to assess mechanisms whereby the G/C repressor element mediates suppression of SM22alpha in a
158 ed to be under negative control, mediated by repressor elements present in the promoters of stalk cel
159 we report that the zinc-finger gene-specific repressor element RE-1 silencing transcription factor/ne
160 covery of an element designated H1t promoter repressor element (RE) located between -130 and -106 bp
162 ' elements of AS1 are competed by a putative repressor element 'RE1' defined previously in the oat ph
163 regions of neuron-specific genes possess the repressor element repressor element 1/neuron-restrictive
164 These studies suggest that transcriptional repressor element(s) located in PLP intron 1 are importa
165 factors, and the action of tissue-selective repressor element(s) may combine to enable a wide variet
166 cells, and suggest that there is a secondary repressor element(s) that is located in the terminal reg
167 ) mediates transcriptional repression by the repressor element silencing transcription factor/neuron-
169 0 kb from the proximal tethering sequence, a repressor element that excludes activation of Scr by ina
170 ikingly, mutations in a previously described repressor element that overlaps the TATA box restored pr
171 PA-dependent binding of USF1 and USF2 to the repressor element that required nucleotides within the E
172 however, is limited due to the presence of a repressor element that shows similarity to a non-canonic
173 s expression in dorsolateral epidermis; 2) a repressor element that suppresses expression in the epid
174 hus consists of closely linked activator and repressor elements that function collectively to cause e
175 (IRE) that shares sequence homology with the repressor element, the cardiac specific sequence, in the
176 3' intergenic loop formations competed with repressor elements to access promoter-proximal sequences
179 Gel-shift analysis showed that this GC-rich repressor element was recognized by both Sp1 and Sp3.
181 y-old mouse brain nuclear extracts bound the repressor elements, whereas both dephosphorylated and ph
182 are similar to those of the adenovirus IIIa repressor element, which has been shown to inhibit use o
183 egulate Pax6 transcription by binding to the repressor element, which in turn blocks the effect of th
184 ATA-less promoters predominantly function as repressor elements, while in other genes constitutively
185 e of the MOR gene is a functionally synergic repressor element with NRSE in NS20Y cells, but not in t
187 these results support a model whereby a G/C repressor element within the SM22alpha promoter mediates
189 gs indicate that the combination of enhancer/repressor elements within the proximal 5'-flanking regio
190 The data indicate that there are additional repressor elements within the vWf promoter region suppre