コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 cis-element TGGGGA located in the -6/-1 Mtor promoter region.
2 herapeutic target, via interactions with its promoter region.
3 two XBP-response elements (XRE) on the ORF21 promoter region.
4 l co-activation effect of Dube3a on the lola promoter region.
5 ription via HIF-binding sites in the RASSF1A promoter region.
6 ivation regulatory element identified in the promoter region.
7 , promoting its association with the miR-571 promoter region.
8 druplex DNA forming sequence in the upstream promoter region.
9 the intrinsic kinetic properties of a given promoter region.
10 increased histone acetylation levels at this promoter region.
11 epresses miR-223 expression by occupying its promoter region.
12 ines presented hypermethylation of the BRCA1 promoter region.
13 tein 1 (AP1), STAT, and Smad DBS in the TSLP promoter region.
14 ze three different binding sites within this promoter region.
15 ated histone 3 lysine 9 (H3K9ac) at the HER2 promoter region.
16 nding of the phosphorylated OmpR to the mcpM promoter region.
17 also revealed DNA methylation changes at its promoter region.
18 response and had methylation sites in their promoter region.
19 883 lies in a PAX2 binding site in the EPHA2 promoter region.
20 fferences reside in the "so called JP2" ltxA promoter region.
21 dant changes in DNA methylation at the Fgf21 promoter region.
22 5% CI 12.7%-16.8%) in both katG and the inhA promoter region.
23 7 and histone 3 lysine 18) flanking the ATF3 promoter region.
24 through association with the 5' replication promoter region.
25 s in the latency-associated transcript (LAT) promoter region.
26 ain containing 4 (BRD4) in the NRP1 proximal promoter region.
27 ight isolates with no mutation in tox or the promoter region.
28 helices, preventing AimR binding to the aimX promoter region.
29 9 (H3K9ac) enrichment at TNF-alpha and IL-6 promoter regions.
30 ntioxidant-response elements (AREs) in their promoter regions.
31 n predicted NF-kappaB binding sites in their promoter regions.
32 ed with increased H3K4me2 levels at proximal promoter regions.
33 , TYMS and TK1 expression and binds to their promoter regions.
34 h the liver lineage by acting at euchromatic promoter regions.
35 thylation in adipose tissue, particularly in promoter regions.
36 ut genomes, and are especially found in gene promoter regions.
37 nctional categories, such as coding SNPs and promoter regions.
38 bidirectional at newly evolved enhancers and promoter regions.
39 ased against accessible chromatin located at promoter regions.
40 s to 18S and 28S rRNAs and localizes to rDNA promoter regions.
41 oxidant gene expression by direct binding to promoter regions.
42 were analyzed for methylation alterations at promoter regions.
43 serum response factor binding sites in their promoter regions.
44 redict the nucleosome positioning signals in promoter regions.
45 mark peaks in relevant tissue types and gene promoter regions.
46 As induces 'elongation marks' on histones in promoter regions.
47 ained by DNA methylation within the proximal promoter regions.
48 with these variants falling in enhancer and promoter regions.
49 ere suppressed with increased methylation in promoter regions.
50 e correlated with chromatin accessibility in promoter regions.
51 with X-escape is reduced DNA methylation in promoter regions.
52 tion with USF-1 for recruitment to lipogenic promoter regions.
53 creased acetylation at the BTK, SYK, and LAT promoter regions.
54 by a potential transcriptional terminator in promoter region 298 to 397 with a DeltaG = -7.9 kcal/mol
56 tion of the G-rich sequence factor 1 (GRSF1) promoter region, a mitochondrial RNA binding protein, in
57 factor M1BP, which associates with the core promoter region, activates transcription of RP genes.
58 Ps, rs7905446 (T/G), which is located at the promoter region, also showed nominal significance (P < 0
59 e that strain-specific sequences in the cagA promoter region and CagA expression levels influence int
60 one deacetylation and CpG methylation of the promoter region and can be re-activated with Trichostati
61 lly modulated by both DNA methylation at the promoter region and chromatin accessibility of an upstre
62 pendent potassium (Kv) channel subunit Kcna2 promoter region and rescues Kcna2 expression in the inju
63 ear translocation that could bind to the KIT promoter region and subsequently reduced KIT transcripti
64 re, we found enrichment of KLF4 at the S18-2 promoter region and that the S18-2 expression is positiv
65 Furthermore, KDM5A bound directly to MPC-1 promoter region and transcriptionally suppressed the exp
66 elated with increased DNA methylation in its promoter region and upregulation of DNA methyltransferas
68 preference for transcription start site and promoter regions and a large number of active enhancers
70 stly alters the CpG methylation landscape of promoter regions and activates methylation-silenced gene
72 Bmal1 protein bound to Atm, Brca1, and Brca2 promoter regions and its expression level was inversely
73 tivates their expression by binding to their promoter regions and recruiting the histone demethylase
74 he DNA methylation levels (especially in the promoter regions) and the transcript abundances of the r
75 tance related genes including mdr1, the gch1 promoter region, and a putative novel duplication of crt
76 nding sites within the LIF (stemness factor) promoter region, and demonstrate LIF repression by ZEB1.
77 AT2R transcription start site contain a core promoter region, and regions upstream of 70 bp to 3 kbp
78 n the postmortem brains that map to the CPG2 promoter region, and show that they negatively affect ge
79 oximal part of a partner gene, including its promoter region, and the distal part of ALK, including t
80 f1 expression by directly binding to the Sf1 promoter region, and the repressive function was complet
81 resent at multiple loci, including the Cdca7 promoter region, and ZBTB24 binding is mostly associated
82 ces that influence nucleosome positioning in promoter regions, and their relation to gene regulation,
83 cription factors and DBS present in the TSLP promoter region are differentially used in intestinal ep
89 hromatin marks (acetylation) at its proximal promoter region as well as increased cyclic adenosine mo
91 ed acetylation of histones in the respective promoter regions but also re-expression of APM component
92 eptible, share the identical coding/proximal promoter regions, but vary in the upstream regulatory re
94 at by targeting 5hmC repressive marks in the promoter regions, C35-mediated TET inhibition activates
95 nce and show that loss of methylation within promoter regions causes a decrease in reporter expressio
96 Additionally, the analysis of the HvPAPhy_a promoter region containing the GCN4/Skn1/RY motif highli
100 ion occurs at different positions within the promoter region, depending on promoter sequence and init
101 ased on methylation discordance within their promoter regions, determined by centering a window of fi
104 ense transcribing polymerase upstream of the promoter region exhibited an increase in the absence of
105 n and identified a terminator located in the promoter region extending from 298-397 that alters ltxA
109 regions showing associations with autism in promoter regions, functional categories related to autis
110 ion and H3K27me3 modification in the miR-101 promoter region further inhibited the transcription of m
112 geneity at the Helicobacter pylori cagA gene promoter region has been linked to variation in CagA exp
114 ver, we find that 22% of common SNPs in core promoter regions have significant regulatory effects.
115 ads to a considerable increase in H3K4me3 at promoter regions; however, these changes in H3K4me3 have
118 CTCF-binding site interacted with the ORMDL3 promoter region in CD4(+) T cells exclusively from subje
119 ulated by AP-2gamma through binding with its promoter region in luminal breast cancer cell lines and
120 discovery of prevalent mutations in the TERT promoter region in many cancers and recent advances in t
122 nds to a highly conserved region in the Ngn3 promoter region in vivo, indicating that Ngn3 is a direc
123 nding sites were highly enriched in proximal promoter regions in close proximity to H3K27ac-modified
126 that pCREB enrichment on the C/EBPbeta gene promoter regions in rats with gp120 was higher than that
127 m detected 5-hmC at the regional level (MGMT promoter region) in just 10 ng of genomic DNA (gDNA, ~27
128 several responsive elements detected in the promoter region including that for different hormones as
129 ling views, they co-occurred within the same promoter region: initiation originating from a focused P
130 allele of the 5-HTTLPR serotonin transporter promoter region is associated with increased risk of dep
131 novel AP-1 site at -1363 bp of the human TF promoter region is highly conserved across multiple spec
132 cture and regulatory elements interacting at promoter regions, is a key step in plant responses to en
135 egulator proteins ArcA and Fnr binded to the promoter region localized between the citAB and citCDEFX
136 st that epigenetic dysregulation outside the promoter region may be more closely associated with tran
137 genes, such as sites of insulation near the promoter regions, may contribute to adaptation of genes
138 al oncogenes, forms a DNA G4 in its proximal promoter region (MycG4) that functions as a transcriptio
139 integration and -124G>A mutation in the TERT promoter region, occurring in a mutually exclusive manne
141 med an increase in the H3K27me3 level at the promoter region of a quarter of these genes in PRMT5-inh
142 we examine the nucleotide variations in the promoter region of a transcription factor (Ghd8) that co
146 owed an increase in acetylation in the Kr-h1 promoter region of cells exposed to JH III or dsHDAC1.
147 repeat transposable element insertion in the promoter region of CitRWP that cosegregated with polyemb
148 nucleus, Pak1 via C-Fos binds to a specific promoter region of DNA repair kinase ATR (ataxia-telangi
149 rch profile of nucleosome positioning at the promoter region of each gene across all samples and make
151 on revealed that MYST3 binds to the proximal promoter region of ERalpha gene, and inactivating mutati
153 e, we find that Drosophila SIN3 binds to the promoter region of genes involved in methionine cataboli
156 he ER stress response element present in the promoter region of Grp78, the master regulator of ER str
160 egulation through directly binding to the 5' promoter region of its host gene SMG1, We showed that ER
161 ty of glucocorticoid receptor binding to the promoter region of KLF15 In three independent proteinuri
162 with its DNA-binding partner DP1 bond to the promoter region of KPNA2 and induced KPNA2 expression.
164 d to elevated H3 lysine 9 acetylation on the promoter region of miR-1185-1, which increased expressio
167 d, we subsequently found REX1 to bind to the promoter region of mitogen-activated protein kinase kina
168 ntifies the A-allele of rs1800734 within the promoter region of MLH1 as perturbing the binding of TFA
170 the PAF1-PHF5A-DDX3 sub-complex bound to the promoter region of Nanog, whose product regulates genes
172 accessions of limetta, a change in the core promoter region of Noemi is associated with reduced expr
173 pressor complex mSin3A-HDAC1 at the proximal promoter region of OGA and correspondingly decreased OGA
174 ication, and bound to the KSHV genome in the promoter region of ORF50, increasing its transactivation
176 , DNA methylation of CG and CHG sites in the promoter region of proviral PVCV decreased in aged plant
178 , in NK cells stimulated with IFN-alpha, the promoter region of Rsad2 was enriched for STAT1 binding
179 complex, and both STAT3 and Sin3A bound the promoter region of silenced TSG via a resveratrol-sensit
180 ions, we demonstrate that Med23 binds to the promoter region of Sox9 and represses Sox9 expression in
181 sis reveals that PRMT5 binds to the proximal promoter region of the AR gene and contributes mainly to
184 ctures are present using a sequence from the promoter region of the death-associated protein (DAP).
187 KLF10 occupied GC-rich sequences in the promoter region of the EMT-promoting transcription facto
188 studied bind a conserved AT-rich site in the promoter region of the exoY gene from Mesorhizobium loti
189 e, the mutations TR34 and TR46, found in the promoter region of the gene encoding the azole target cy
191 Interestingly, we find that RALY binds the promoter region of the master metabolic regulator Srebp2
192 ruct consisting of a portion of the proximal promoter region of the mouse COX-2 gene upstream of luci
193 The G-quadruplex formed in the proximal promoter region of the MYC oncogene (MycG4) has been sho
194 enes, bind to adjacent sites in the upstream promoter region of the nitrate reductase gene, NIA1, and
196 l as validating the importance of a specific promoter region of the PAPhy_a gene which contains three
197 ted that directed DNA methylation of a wider promoter region of the target loci IL6ST and BACH2 decre
200 rrant hypermethylation of CpG islands in the promoter region of tumor suppressor genes is a promising
201 factor downstream from MEK/ERK, binds to the promoter region of VE-cadherin (chip assay) and is induc
202 y techniques, we show that Etv2 binds to the promoter region of Yes1 and functions as a direct upstre
205 blood DNA methylation levels of 384 CpGs in promoter regions of 82 addiction-related genes in 256 Af
207 thylation (H3K4me3) mark frequently found at promoter regions of actively transcribed genes and is th
208 ion of gene expression enabled by tiling the promoter regions of all 969 genes that comprise the ito9
211 istone H3, including the K19/14 sites in the promoter regions of bone morphogenetic proteins (BMPs) g
213 ed methylation values of ~ 300 K CpGs in the promoter regions of chromosome 17 and identified some no
216 heterodimers bind to E box sequences in the promoter regions of genes and activate transcription.
218 elements, and AHL4 was shown to bind to the promoter regions of genes encoding the TAG lipases SDP1
219 ry specific alterations were observed to the promoter regions of genes involved with immune responsiv
222 , and KDM4C (ARID3B-complex)] that binds the promoter regions of HMGA1, c-MYC, VEGF-A, and WNT1.
224 late lysine 14 of histone 3 (H3K14ac) in the promoter regions of its target genes even though GCN5 bi
225 epigenetic modifiers KDM1A and HDAC1 to the promoter regions of LAMB3 and CTNNAL1, influencing histo
227 favour histone H4K20 hypomethylation at the promoter regions of MYC regulated genes, leading to incr
229 inal neurons: 1) repressive chromatin in the promoter regions of non-photoreceptor retinal neuron gen
230 of genes they contact in 3D localize to the promoter regions of other genes, supporting the notion o
232 xperiments indicated that c-Myc bound to the promoter regions of PGC1alpha and PPARD to counteract th
233 and TIP60 proteins were co-recruited to the promoter regions of proteasome genes after proteasome in
234 ctor upstream binding factor 1 (UBF1) on the promoter regions of ribosomal DNA (rDNA) and activates r
235 t Rev-erbalpha physically interacts with the promoter regions of several NF-kappaB-related genes in p
236 several mechanisms: chromatin remodeling in promoter regions of specific genes, blockade of NF-kappa
237 rvation triggers lncRNA transcription across promoter regions of stress-responsive genes including fb
238 he methylation status of CpG loci within the promoter regions of Th1/2 lineage commitment genes (GATA
239 Mechanistically, FOXC1 bound directly to the promoter regions of the FBP1 gene and negatively regulat
240 te that endogenous Osr2 protein binds to the promoter regions of the Sema3a and Sema3d genes in the e
241 raction, Dot1l is recruited by Zc3h10 to the promoter regions of thermogenic genes to function as a c
242 ly, PRDM16 represses ISGs through binding to promoter regions of these genes and blocking the activat
246 trait loci: with 10 eQTLs involving SNPs in promoter regions or transcriptional start sites; and 12
248 the full mtrR sequence and a portion of its promoter region; portions of ponA, porB, gyrA, and parC;
250 ies were mostly restricted to CpG islands or promoter regions, recent findings indicate that many of
252 4 di-methylation (H3K4me2), to the AHR gene promoter region, resulting in repression of AHR expressi
253 on increased binding of RBP-J to its cognate promoter regions, resulting in increased downstream Notc
256 e determined the LTA4H genotype based on the promoter region single-nucleotide polymorphism rs1752549
258 ng contacts identified in certain well-known promoter regions, such as the -35 and -10 elements, do n
259 -box cis-regulatory element within the SlWUS promoter region, suggesting that ENO directly regulates
260 ICln (but not vice versa) to the AR proximal promoter region, suggesting that PRMT5 recruits pICln to
261 interacting with the putative NACbs in their promoter region, suggesting their direct role in plant s
262 sed fathers, especially at dopamine receptor promoter regions, suggesting that epigenetic modificatio
263 nd polymorphisms in the CCR5 gene as well as promoter region that alter cell surface expression have
264 Moreover, TCP15 directly binds to the SAUR63 promoter region that contains the TCP target motif in vi
265 with expansion of a GGC repeat in the XYLT1 promoter region that is not present in the reference gen
266 ation of two different mutations in the mecA promoter region that lowers mecA-encoded penicillin-bind
267 me capture, we included genome-wide proximal promoter regions that contain sequences that regulate ge
268 screen transcription factor binding sites in promoter regions that intersect DNase I hypersensitive s
271 nt for the NR4A1/Sp4 complex to bind GC-rich promoter regions to elevate transcription of the PAX3-FO
272 r accuracy short-reads and annotated GM12878 promoter regions to identify 33,984 plausible RNA isofor
273 manner to bind sequence-specific DNA within promoter regions to regulate lineage-specific gene expre
274 r envelope via interaction with translocated promoter region (TPR), a component of the nuclear pore c
275 detect TR(34) (a 34-bp tandem repeat in the promoter region), TR(46), G54W (a change of G to W at po
276 Analysis of DNA methylation at proximal promoter regions uncovered >250 genes harbouring interme
278 h analysis of the functional consequences of promoter region variation within the classical HLA class
280 thylation at multiple CpG sites in the HOXA4 promoter region was associated with height in a cohort o
283 ntegrated HBV and point mutation at the TERT promoter region was identified as a mechanism for the ma
285 itative RT-PCR, and DNA methylation of their promoter regions was analyzed by PCR and pyrosequencing.
286 DNA methylation at the INSR and IGF2 gene promoter regions was detected by the Sequenom's MassARRA
288 c were significantly increased; enhancer and promoter regions were transcribed; and GREB1 mRNA was ro
289 ivator-Like Element (TALE) locating an Ascl1 promoter region, were designed for site specific epigene
290 es ugtL transcription by binding to the ugtL promoter region, where it overcomes gene silencing by th
291 translocates to lysosomal and autophagy gene promoter regions, where ACSS2 incorporates acetate gener
292 re replaced by a point mutation in the parEC promoter region which resulted in a fivefold increase of
293 to the Androgen Response Elements on its 5' promoter region, which could then lead to suppress the h
294 y demonstrated the binding of c-Myc to KPNB1 promoter region, which indicated a positive feedback reg
295 of LanFTc1 revealed a 1.4-kb deletion in the promoter region, which was perfectly predictive of verna
296 ion is more likely to result from binding to promoter regions, which are often accessible regardless
297 ble regions of Dmp1 gene were located in the promoter region while effect of Klf5 on Dspp activity wa
298 of CTCF binding, highly enriched for gain in promoter regions, while AML in general was enriched for
299 ed by pairwise nucleotide differences in the promoter regions with estimated differences in mRNA expr