ライフサイエンスコーパス: DNA motif

1 t mediates stable binding to a non-canonical DNA motif.

2 ated separately through a conserved upstream DNA motif.

3 modular domains in a 42-base single-stranded DNA motif.

4 in reduced affinity of LOB for the consensus DNA motif.

5 domain of AtERF100 in complex with a GCC box DNA motif.

6 their DNA binding domains and bind a common DNA motif.

7 ing a protein (URE3-BP) that recognized this DNA motif.

8 ected to test the recognition ability of the DNA motif.

9 methylation at loci with a highly conserved DNA motif.

10 s contained the canonical RBP-Jkappa-binding DNA motif.

11 transcription, regardless of its recognition DNA motif.

12 tiation genes that it controls at a CCNNAGGC DNA motif.

13 th two affinity ligands each conjugated to a DNA motif.

14 of the FtsK-orienting polar sequence (KOPS) DNA motifs.

15 n forms homodimers that bind canonical G-box DNA motifs.

16 exposure, thereby distinguishing particular DNA motifs.

17 ional regulators recognize and bind specific DNA motifs.

18 t are programmable for a large repertoire of DNA motifs.

19 lie common functional roles in other RNA and DNA motifs.

20 ining different approaches to discover novel DNA motifs.

21 binations are enriched for different sets of DNA motifs.

22 members of the same subset and bind-specific DNA motifs.

23 b upstream that contains cytokine-responsive DNA motifs.

24 including cell wall components and specific DNA motifs.

25 both ChIP-exo tag distribution patterns and DNA motifs.

26 of VDR.retinoid X receptor-alpha to discrete DNA motifs.

27 roplast DNA, and 15% to the seven repetitive DNA motifs.

28 mmon Pbx1 or E2a-Pbx1 partner bind different DNA motifs.

29 HLH-zip region and recognize the same CACGTG DNA motifs.

30 rs and their corresponding sequence-specific DNA motifs.

31 insertions and deletions (indels), and novel DNA motifs.

32 letely lacked binding ability at its cognate DNA motifs.

33 ery and performance evaluation on methylated DNA motifs.

34 red regions bind synergistically to adjacent DNA motifs.

35 attenuated the latter's binding to promoter DNA motifs.

36 s involving known architectural proteins and DNA motifs.

37 ubiquitously expressed, and recognize G-rich DNA motifs.

38 dification and DNA methylation patterns from DNA motifs.

39 ion of most abundant double-stranded DNA (ds-DNA) motifs.

40 ents, and the extent of their hard-wiring by DNA motifs; (3) the potential to predict gene expression

41 graphic analysis shows that a hexanucleotide DNA motif (5'-TCGGAT-3') of the aptamer fits into a posi

42 Mutations of Ets or E-box sites in either DNA motif abolished the activation and reduced or elimin

43 of dot-blot hybridizations, seven repetitive DNA motifs accounted for >13% (194 kb) of the cucumber m

44 sequences, exemplified by G quadruplex and H-DNA motifs, across the genome in both avian and human ce

45 DNA motif analyses uncover binding sites for distinct TF

46 DNA motif analysis revealed an over-representation of KL

47 Here we present a new DNA motif and a strategy that has led to the assembly of

48 peptides encoded by a 'synthetic degenerate' DNA motif and fused to Maltose Binding Protein (MBP).

49 I hypersensitivity data in conjunction with DNA motif and other genomic features.

50 s were significantly enriched in the AATAATD DNA motif and specific chromatin contexts, including H3K

51 with an overall right-handed, antiparallel B-DNA motif and Watson-Crick base pairing throughout.

52 synthesis to identify candidate NiaR-binding DNA motifs and assess the NiaR regulon content in these

53 mics approach to infer candidate Rex-binding DNA motifs and assess the Rex regulon content in 119 gen

54 ow that recurrent neural networks trained on DNA motifs and basic phenotype data can reach 70% attrib

55 ies, TF family members often bind to similar DNA motifs and can confound sequence-based approaches to

56 ically identify 194 nonredundant palindromic DNA motifs and corresponding regulons in S. oneidensis.

57 The DNA motifs and CTP-dependent riboflavin kinase activity

58 ew analysis tools enable users to search for DNA motifs and define genes based on their genomic coloc

59 the target molecule triggers assembly of the DNA motifs and initiates the subsequent DNA strand displ

60 By binding to guanosine-rich DNA motifs and interacting with the Rhino chromodomain,

61 nalis genes was searched for overrepresented DNA motifs and known eukaryotic core promoter elements.

62 and a data yielded all of the four relevant DNA motifs and most of the known a- and alpha-specific g

63 comparative genomics approach, we identified DNA motifs and reconstructed regulons for 40 TunR family

64 parative genomics, we predicted SahR-binding DNA motifs and reconstructed SahR regulons in the genome

65 include transcription factors, their cognate DNA motifs and regulated genes/operons linked to the can

66 the behavior of single- and double-stranded DNA motifs and transitions between them, allowing us to

67 also distinct in their recognition of short DNA motifs and utilization of open DNA interaction inter

68 etail how CO positioning relates to genetic (DNA motifs) and epigenetic (chromatin structure) feature

69 d TRP120-bound sequences revealed a G+C-rich DNA motif, and recombinant TRP120 specifically bound syn

70 gical processes, share unique cis-regulatory DNA motifs, and are enriched for binding of specific tra

71 d binding of transcription factors, variable DNA motifs, and bursts in gene expression.

72 nding to noncoding variants, uncharacterized DNA motifs, and repetitive genomic elements has been tec

73 Metallic nanoparticles can be attached to DNA motifs, and the arrangement of these particles can b

74 These data support the hypothesis that CpG DNA motifs are a "danger signal" that activates protecti

75 We find that these DNA motifs are also present in the muscle promoters of C

76 ctions between Ap2 and Sp1 and their cognate DNA motifs are critical for basal transcription from the

77 with embryo cells indicate that the enriched DNA motifs are functional cis elements that regulate tra

78 The binding of Fpr to various DNA motifs are mediated by its flat DNA-binding surface,

79 Our data indicate that these two DNA motifs are novel cis -regulatory elements and exhibi

80 n factor binding sites (TFBSs, also known as DNA motifs) are critical activities in gene transcriptio

81 ction in the gene, reveals that these (short DNA motifs) are more prevalent in exons that encode diso

82 HOT regions harbor specific DNA motifs, are enriched for differentially expressed ge

83 Microsatellites--tandem repeats of short DNA motifs--are abundant in the human genome and have hi

84 inity of a transcription factor to different DNA motifs, as it can model complex interactions that ar

85 have been developed for mapping promoters or DNA motifs associated with promoters.

86 scripts that regulate the cell cycle and for DNA motifs associated with the transcription factor FOXP

87 This assay allows us to demonstrate G4 DNA motif-associated epigenetic instability in mutants o

88 ies demonstrates that Piwi binds a conserved DNA motif at approximately 72 genomic sites and inhibits

89 ng contrasting functional attributes of this DNA motif at different stages of myogenesis.

90 onic cell line H1, we mutated only the found DNA motifs at particular loci and the significant reduct

91 DNA motifs at several informative loci in more than 500

92 nt a method to measure the DeltaG degrees of DNA motifs at temperatures and buffer conditions of inte

93 ssociating genes frequently contain the same DNA motifs at their promoter regions, suggesting that po

94 is-regulatory sequence here corresponds to a DNA motif bound by a TF.

95 The DNA motif bound by BLIMP1 in vitro overlaps with that of

96 A DNA motif bound by CBP60g and SARD1, GAAATTT, was signif

97 ctly controlled by CviR, in part because the DNA motif bound by CviR is not well characterized.

98 wed that this T372R substitution changes the DNA motif bound by YY1.

99 pparently by disrupting interaction with the DNA motifs bound specifically by the recombinase.

100 we showed that in erythroid K562 cells these DNA motifs bound the following three transcription facto

101 controlled by Stat1/2 and Irf9 and the ISRE DNA motif, but others appeared dependent on non-canonica

102 We have thoroughly characterized such DNA motifs by polyacrylamide gel electrophoresis (PAGE)

103 res Rta to bind to multiple copies of an Rta DNA motif (called "CANT" or Rta-c) proximal to an RBP-Jk

104 zed with an ATP-binding aptamer-incorporated DNA motif can selectively release the intercalating doxo

105 Branched DNA motifs can be designed to assume a variety of shapes

106 broadly, these findings show that functional DNA motifs can be identified by machine learning analysi

107 ore, it has been speculated that these non-B DNA motifs can play regulatory roles in gene transcripti

108 The frequency of these six DNA motifs can predict housekeeping promoters as accurat

109 deoxyribozyme 8-17 is the most common small DNA motif capable of catalyzing RNA cleavage.

110 er activity, and mutagenesis showed that the DNA motif CCCTCCT is essential for GATA-2 promoter activ

111 omoter required a single hybrid MEF-2/GATA-4 DNA motif centered at -1256 base pairs.

112 Trans-acting factor binding to small DNA motifs (cis-elements) underlies regulatory complex a

113 We identified seven conserved DNA motifs (CM), CM1 to 7, that are present in the promo

114 re, we demonstrate how "Coordinator," a long DNA motif composed of common motifs bound by many basic

115 gomeric complex binds to a unique, bipartite DNA motif comprising an E-box, CAGGTG, followed approxim

116 involving Lmo2 which can bind to a bipartite DNA motif comprising two E-box sequences approximately 1

117 by a novel mechanism and identify a specific DNA motif conducive to strong BLM binding and cleavage.

118 based on the predicted transcription-factor-DNA-motif connections.

119 (3) certain DNA motifs conserved in regions 10 bp up- and down- stre

120 A DNA motif consisting of an inverted repeat was identifie

121 A 6-base DNA motif consisting of an unmethylated CpG dinucleotide

122 n receptor gene rearrangement is directed by DNA motifs consisting of a conserved heptamer and noname

123 ated by a pyknon, a short 20 nucleotide-long DNA motif contained in the N-BLR transcript and is targe

124 We discovered a de novo DNA motif containing a PLAG1 binding site in the promote

125 inducible hnRNP, which can recognize a novel DNA-motif, controls the expression of the CR2 gene.

126 is footprint, two unrelated 30-bp cis-acting DNA motifs (designated TOAD and FROG) function as positi

127 subflower localization of these contractile DNA motifs dictates the mode of shape change.

128 De novo DNA motif discovery revealed new putative binding sites

129 P-chip experiments followed by computational DNA motif discovery.

130 itation, followed by sequencing analysis and DNA motif discovery.

131 In contrast, REX1 binds to DNA motifs divergent from YY1, but the binding motifs of

132 The binding-induced DNA TWJ makes use of two DNA motifs each conjugated to an affinity ligand.

133 ene superfamily characterised by a conserved DNA motif encoding the homeodomain.

134 ected a protein that binds specifically to a DNA motif encompassing the cap site.

135 Three DNA motifs enriched in crossover regions and less abunda

136 olid condensates is orchestrated by specific DNA motifs enriched in OR enhancers, which are likely to

137 was incorrect; that sentence should begin: "DNA motif-enrichment analysis of the subset-specific H3K

138 These factors and their target DNA motifs exhibited a hierarchy of DNA/protein and prot

139 DNA motif finding is one of the core problems in computa

140 promoter and the omlA promoter shared a 5-bp DNA motif for their -10 promoter elements.

141 ere instead characterized by the presence of DNA motifs for AP1 or STAT.

142 h synergistic interactions between consensus DNA motifs for binding of vitamin D receptor, AP1 and EL

143 a general design principle for pH-responsive DNA motifs for general DNA sequences (not limited to tri

144 ters the ability of Ikaros complexes to bind DNA motifs found in pericentromeric heterochromatin (PC-

145 Identification of DNA motifs from ChIP-seq/ChIP-chip [chromatin immunoprec

146 e physical interaction of Myc with the E-box DNA motif has been extensively characterized, but it is

147 This DNA motif has been identified in many genes that are spe

148 hese factors, their target genes and binding DNA motifs has been linked to various neuropsychiatric d

149 the breakpoint junctions revealed no common DNA motif; however, deletions, duplications, microhomolo

150 omplex (CBC) to cooperatively bind bipartite DNA motifs; however, the mode of HapX-DNA recognition ha

151 ntrinsic biases of SHM targeting on specific DNA motifs (i.e., hot and cold spots).

152 ified TFs that bind to three uncharacterized DNA motifs identified in DNase footprinting assays.

153 cooperatively bind an evolutionary conserved DNA motif in a target promoter.

154 Unlike most TFs, NF-Y can access its target DNA motif in inactive (nonmodified) or polycomb-represse

155 TFs were shown to bind to the same GCC-like DNA motif in OsRMC promoter and to negatively regulate i

156 hree copies of a conserved 18-bp palindromic DNA motif in the promoter of each ACG family member.

157 shows that PfAP2-I interacts with a specific DNA motif in the promoters of target genes.

158 ed structures self-assembled from individual DNA motifs in 1D, 2D, and finally 3D.

159 to de novo discover significant co-occurring DNA motifs in 349 human DNase I hypersensitive site data

160 d E2A-Pbx1 exhibit tight binding to specific DNA motifs in conjunction with certain other homeodomain

161 d to connect novel transcription factors and DNA motifs in E. coli.

162 We have identified 361 and 369 DNA motifs in human and mouse, respectively, that are th

163 key highlight is the successful assembly of DNA motifs in nickel-containing buffer at temperatures b

164 We found an enrichment of some non-B DNA motifs in regulatory regions, and we show that this

165 In total, we obtained 209 unique DNA motifs in S. oneidensis that cover 849 unique transc

166 dentified significant enrichment of specific DNA motifs in the 1000 bp proximal promotor, some of whi

167 matode muscle genes, we identified conserved DNA motifs in the promoter regions using computational D

168 Based on the presence of kappaB-like DNA motifs in the region upstream of the TNF gene, some

169 We compared the distributions of non-B DNA motifs in the regulatory regions of operons with tho

170 d stabilized NF-Y interaction with CCAAT-box DNA motifs in vitro.

171 e predicted regulatory regions identified 31 DNA motifs, including 57.1% of experimentally validated

172 Stimulatory CpG DNA motifs induced B, T, and natural killer cells to sec

173 he integration of noncanonical and canonical DNA motif information yields new hypotheses on cobinding

174 Previous designs have inserted pH-sensitive DNA motifs into aptamer sequences.

175 Watson-Crick base pairing rules to assemble DNA motifs into diverse arrangements of geometric shapes

176 ect inverted repeat spaced by one nucleotide DNA motif, inverted repeat-1 (5'-AGGTCAcAGACCT-3'), as a

177 Half of the DNA motifs involved are matched to the existing motif da

178 motif-based fashion, assuming that the same DNA motif is equally likely to be targeted regardless of

179 The identification of the DNA motifs is a vital task for downstream analysis.

180 Understanding the thermodynamics of DNA motifs is important for prediction and design of pro

181 range coupling information between different DNA motifs is still lacking.

182 ial for binding to the vast majority of GATA DNA motifs, is strictly required for GATA-1-mediated ery

183 use monomeric Hox proteins bind very similar DNA motifs, it is unclear how they activate diverse deve

184 s gene transcription via a sequence-specific DNA motif known as the neuron-restrictive silencer eleme

185 ecombinant PtMYB4 protein is able to bind to DNA motifs known as AC elements.

186 hts of the CNN confirmed it detects familiar DNA motifs known to correlate with real variation, like

187 ysis revealed putative Lrp-binding consensus DNA motifs located in P(hilA), P(invF), and P(ssrA).

188 a complicated arrangement of A-box and B-box DNA motifs located on opposite ends of a sharply bent pa

189 to a given list of CpGs, and generating the DNA motif logo enriched in the genomic contexts of a giv

190 that TFs that preferentially bind divergent DNA motifs may bind overlapping genomic regions due to l

191 plified product strongly suggests that local DNA motifs may have contributed to the generation of thi

192 es of relatively frequent GC-rich cis-acting DNA motifs may offer reiterated binding sites to factors

193 MDscan can be used to find DNA motifs not only in ChIP-array experiments but also i

194 Hot spot-enriched A-rich and CTT-repeat DNA motifs occurred upstream and downstream, respectivel

195 Novel DNA motifs of archaeal DtxR-TFs that have a common palin

196 ding activity to methylated and unmethylated DNA motifs of distinct sequences.

197 P1 sites with fast binding kinetics, whereas DNA motifs of ETS and homeodomain proteins are preferent

198 CaCse4p-rich regions not only lack conserved DNA motifs of point (<400 bp) centromeres and repeated e

199 he genome either by directly binding cognate DNA motifs or via protein-protein interactions with othe

200 searching genomic DNA sequences with genomic DNA motifs (or matrices) that are representative of the

201 It was determined that a 14-bp novel DNA motif (oriLyt promoter activation element), which wa

202 study set of transcription factors and their DNA motifs, our method has a prediction accuracy of 59%

203 99 novel transcription factors and 70 novel DNA motifs, our method predicted 64 transcription-factor

204 er regions were found to contain a conserved DNA motif (p2(bp) box) identical in sequence and positio

205 probability of a given transcription-factor-DNA-motif pair being a true pair.

206 The coupling DNA motif pairs exhibit substantially higher DNase acces

207 to account together, we believe the coupling DNA motif pairs identified in this study can shed lights

208 -kind study, we have identified the coupling DNA motif pairs on long-range chromatin interactions in

209 our method predicted 64 transcription-factor-DNA-motif pairs.

210 i, where they associate with the TCF-4/LEF-1 DNA motif positioned in the promoters of several importa

211 We identified 17,718 PDIs between 460 DNA motifs predicted to regulate transcription and 4,191

212 n (IL)-2 promoter as well as to a homologous DNA motif present in the proximal segment of the interfe

213 and in vivo to critical homeodomain binding DNA motifs present in the neuronal Pomc enhancers nPE1 a

214 Importantly, the gene sets and associated DNA motifs provide a starting point with which to explor

215 structure predictions available, including Z-DNA motifs, quadruplex-forming motifs, inverted repeats,

216 components of heterochromatin independent of DNA motif recognition.

217 Because the DNA motif recognized by a transcription factor is typica

218 ns of endosperm cap-enriched genes contained DNA motifs recognized by ethylene response factors (ERFs

219 sults suggest that unique ligands may switch DNA motifs recognized by ligand-dependent transcription

220 from transcription start sites and contained DNA motifs recognized by regulators of cell-type identit

221 DNA motifs recognized by the CBC:HapX protein complex co

222 mmand-line tool for the scanning of known TF DNA motifs represented as Position Weight Matrices (PWMs

223 The binding-induced assembly of the DNA motifs results in the formation of a highly stable c

224 AC elements are DNA motifs rich in adenosine and cytosine that have been

225 scription factors bind a canonical consensus DNA motif, RYAAAYA (R = A/G, Y = C/T), as a monomer.

226 For eukaryotic systems, however, some DNA motif(s) are capable of binding to a family of relat

227 Branched DNA motifs serve as the basic construction elements for

228 The candidate NrtR-binding DNA motifs showed significant variability between microb

229 ulatory DNA sequences (ISS) containing a CpG DNA motif significantly inhibit airway eosinophilia and

230 n, were distinguished by clusters of a 10-bp DNA motif, suggesting a recruitment-and-spreading mechan

231 promoter region in these strains revealed a DNA motif (TAATGA) that was present in either one or two

232 ly be achieved with well-structured branched DNA motifs tailed by sticky ends.

233 ugh the upstream regulatory element 3 (URE3) DNA motif TATTCTATT.

234 pG (mCpG) sites and a specific nonmethylated DNA motif (TCCTGCNA) and represses transcription by recr

235 hFAST-1 protein was shown to bind to a novel DNA motif, TGT (G/T) (T/G)ATT, an exact copy of which wa

236 FOXC2, FOXM1, and FOXN1 to a canonical FkhP DNA motif that are greater at pH 7.0 compared with pH 7.

237 f the 100 promoters most enriched revealed a DNA motif that differs from the EBNA1 binding site in th

238 A helical sheets, and reveals a noncanonical DNA motif that has adaptive features that may be useful

239 Using PCR, we identified a specific DNA motif that is bound by Six3 and we demonstrated that

240 me-wide analysis of PGC7 reveals a consensus DNA motif that is recognized by PGC7.

241 nal analysis uncovered a novel homo-trimeric DNA motif that mediates the homo-trimeric DNA binding of

242 We used Gibbs sampling to define a CRP(Mt) DNA motif that resembles the cAMP receptor protein (CRP)

243 stness and potential utility of the many new DNA motifs that are becoming available.

244 Two DNA motifs that are conjugated to specific affinity liga

245 networks of Escherichia coli, we inferred 24 DNA motifs that are conserved in S. oneidensis.

246 sms to maintain epigenetic stability near G4 DNA motifs that are dependent on either REV1 or on the W

247 We have previously identified DNA motifs that are enriched in hot spots, particularly

248 r, TCF/Arm mediated repression by binding to DNA motifs that are markedly different from typical TCF-

249 detects and responds to hypo-methylated CpG DNA motifs that are most commonly found in microbial gen

250 ive elements, including L1 and L2 LINEs, and DNA motifs that are significantly enriched around inacti

251 plementation of a novel strategy to identify DNA motifs that bind BLM strongly.

252 te targetting of Pbx heterodimers to related DNA motifs that differ in the sequence of their 3' half-

253 vity, in contrast to that mediated by kappaB DNA motifs that do not efficiently bind p65 homodimers,

254 e tracts of variable-length repeats of short DNA motifs that exhibit high rates of mutation in the fo

255 are the most well-characterized noncanonical DNA motifs that have been detected in vivo with either p

256 ties, and this may be useful for identifying DNA motifs that have similar functional properties that

257 (c) The architectures of the DNA motifs that lie adjacent to the G-quadruplex structu

258 network approach called GBNet to search for DNA motifs that may be cooperative in transcriptional re

259 umans and point to novel vertebrate-specific DNA motifs that might play a selective role in TATA-inde

260 do not appear to be demarcated by the usual DNA motifs that punctuate transcription in familiar euka

261 clones carried short (30-53 bp), repetitive DNA motifs that were often degenerate, overlapping, and

262 es of structurally but not textually related DNA motifs, that is, motifs whose consensus sequences ar

263 NF-Y recruits to neighboring DNA motifs the developmentally regulated, erythroid tran

264 proteins into the active ER complex with its DNA motif, the estrogen response element.

265 A new 3D-DNA motif, the ninja star, was self-assembled in quantit

266 bes and 2D arrays assembled from three novel DNA motifs, the 6-helix bundle (6HB), the 6-helix bundle

267 voring a conformation that can bind specific DNA motifs, thereby serving to either activate or repres

268 ate and high-throughput method for measuring DNA motif thermodynamics called TEEM (Toehold Exchange E

269 2s target euchromatic gene loci via specific DNA motifs, they are likely integral components of heter

270 ethylated cytosine-phosphate-guanosine (CpG) DNA motifs through toll-like receptor 9, and we found th

271 ose methods that allow virtually any desired DNA motif to be targeted in vitro.

272 AIR lncRNA preferentially occupies a GA-rich DNA motif to nucleate broad domains of Polycomb occupanc

273 TREE1 binds to the DNA motif to repress gene expression in an EIN3-dependen

274 For DNA motifs to assemble into crystals, they must be assoc

275 tiation, Twist2 competes with MyoD at shared DNA motifs to direct global gene transcription and repre

276 By mapping significant DNA motifs to the T. thermophilus HB8 genome, we identif

277 To generate a nearly complete list of human DNA motifs under given conditions, we employed a novel a

278 A conserved DNA motif upstream of many xylose-induced genes was iden

279 are attributable to variation in a specific DNA motif upstream of the cagA transcriptional start sit

280 superstructures consisting of heterogeneous DNA motifs using dsDNA in conjunction with more complex,

281 osatellites are a tract of repetitive, short DNA motifs (usually 1 to 6 bp) abundant in eukaryotic ge

282 ion factors (TFs) to short sequence-specific DNA motifs, usually located at the gene regulatory regio

283 Tn3 and Bart resolvases recognize different DNA motifs, via diverged C-terminal domains (CTDs).

284 Nuclear extract binding to kappaB DNA motifs was measured by electrophoretic mobility shif

285 Finally, a preference for some non-B DNA motifs was observed near transcription factor-bindin

286 e signaling and structural features into the DNA motifs, we envision diverse applications in biosensi

287 lthough the KSHV genome contains >100 RBP-Jk DNA motifs, we show that none of the four isoforms of ac

288 GATA factors interact with simple DNA motifs (WGATAR) to regulate critical processes, incl

289 DNA with RNA dangling-end motifs shows that DNA motifs with 5' dangling ends contribute to stability

290 te to this goal by combining stable branched DNA motifs with cohesive ends to produce programmed nano

291 For DNA motifs with exactly the same pair of sticky-end sequ

292 ant role in the assembly of nucleosomes, and DNA motifs with high specificity to nucleosomes have bee

293 ate DNA tessellations by employing multi-arm DNA motifs with low symmetry.

294 pment in mice and humans through a conserved DNA motif within Alu/B1 elements located in the promoter

295 This program searches for a given DNA motif within the entire genome of one species and us

296 Despite TFs recognizing specific DNA motifs within accessible chromatin, this information

297 howed that the distribution of several non-B DNA motifs within intergenic regions separating divergen

298 and IL-4, respectively, and bind to specific DNA motifs within the ECS.

299 on-B DNA transition-susceptible sites (non-B DNA motifs) within the context of the operon structure o

300 mapping indicates both domains bind poly(C) DNA motifs without disrupting the KH1-KH2 interaction.