ライフサイエンスコーパス: duplex

1 ic scaffold to recognize the shape of an RNA duplex.

2 gh covalent attachment of each strand of the duplex.

3 lty of separating the strands of the product duplex.

4 L2 loop, which inserts into and opens up the duplex.

5 ntroduction of mismatches within the initial duplex.

6 he C3'-endo conformation formed in canonical duplexes.

7 trands in the context of 3'-OH/5'-PO4 nicked duplexes.

8 oint the locations of the spin labels on the duplexes.

9 plexes are more stable than Cgamma(R)-bm-PNA duplexes.

10 s the canonical conformations of DNA and RNA duplexes.

11 NA, such structures were not observed in RNA duplexes.

12 HG base pairs for both naked B-DNA and A-RNA duplexes.

13 verted to parallel-stranded homo-base paired duplexes.

14 able in the polymerase relative to these DNA duplexes.

15 alters the hybridization kinetics in two RNA duplexes.

16 ymerase than in aqueous solution and the DNA duplexes.

17 ed, with few exceptions, in low stability of duplexes.

18 x reporter appended onto electrode-bound DNA duplexes.

19 ns while protecting the remainder in DNA-RNA duplexes.

20 ing honeycomb edges composed of six parallel duplexes.

21 bes and to construct closely packed parallel duplexes.

22 e edges that are composed only of one or two duplexes.

23 striction endonucleases naturally target DNA duplexes.

24 e stable than the corresponding DNA/RNA self-duplexes.

25 entary RNA relative to the canonical DNA/RNA duplex (~10 degrees C).

26 nces with 100% AT content, a poly(A)-poly(T) duplex (AA-TT) and a poly(AT)-poly(TA) duplex (AT-TA).

27 hermodynamically different modes at a single duplexed AATT site.

28 rithmic improvements in a new version of the duplex analysis software, Du Novo 2.0.

29 that introduces site-specific nicks into the duplex and a dynamic motor complex that rapidly transloc

30 the melting temperature of both an 8-mer DNA duplex and a hairpin with a stem of 6-nt depending on th

31 n between parallel-stranded homo-base paired duplex and antiparallel unimolecular hairpin in a pH-dep

32 study the kinetics and thermodynamics of DNA duplex and hairpin formation in crowded environments.

33 ns a regular C:G base pairing pattern in RNA duplex and has a relatively small effect on its base pai

34 including the influenza viral RNA panhandle duplex and HIV-1-1 ribosomal frameshift-inducing RNA hai

35 hate bond is relatively stable within an RNA duplex and in the presence of chelated magnesium.

36 ptor but also promotes the remodeling of RNA duplex and quadruplex structures.

37 Subsequently, we established single, duplex and triplex TaqMan MGB probe-based fluorescence q

38 circRNAs tend to form 16-26 bp imperfect RNA duplexes and act as inhibitors of double-stranded RNA (d

39 NS5B in ternary complex with template-primer duplexes and nucleotides, to address the question of rib

40 The methodology was validated on two DNA duplexes and then applied to examine how a single m(6)A

41 endent reductive charge transfer through RNA duplexes and through the non-Watson-Crick base-paired re

42 and expels fewer anions compared to the DNA duplex, and the RNA duplex interacts significantly stron

43 nstriction site, its complete unzip from the duplex, and translocation.

44 steen (HG) base pairing pattern in naked DNA duplexes, and estimated its relative stability and lifet

45 t better thermal stability than the isolated duplexes, and the Cgamma(S)-bm-PNA duplexes are more sta

46 n aqueous solution, in A-form and B-form DNA duplexes, and within the active site of a DNA polymerase

47 icular, the presence or absence of short RNA duplexes-and suggests that the equilibrium size of the c

48 ~1-fold but significantly slows the rate of duplex annealing, decreasing k(on) by ~7-fold.

49 of the most common aptasensor formats is the duplexed aptamer (DA).

50 zing both the flipped base and the distorted duplex are poorly conserved among McrB homologs, suggest

51 ch oligonucleotides, the resulting C-Ag(+)-C duplexes are able to conduct charge efficiently.

52 RNA duplexes are destabilized, on average, 1.02 kcal/mol in

53 isolated duplexes, and the Cgamma(S)-bm-PNA duplexes are more stable than Cgamma(R)-bm-PNA duplexes.

54 The daughter DNA duplexes are packaged with an equal amount of parental a

55 These duplexes are rapidly loaded into Argonaute, with <30 min

56 NA binding domain 2 (dsRBD2) bound to an RNA duplex as an asymmetric homodimer.

57 The advantage of our assay over the duplex assay is that it can specifically detect two addi

58 from n = 14 human subjects using our mobile duplex assay, and showed excellent agreement with the go

59 h the primer pair for mammalian species in a duplex assay.

60 Interactions with the unwrapped DNA duplex at the two termini of Cenp-A(Nuc) are mediated pr

61 ly(T) duplex (AA-TT) and a poly(AT)-poly(TA) duplex (AT-TA).

62 We observe that the RNA duplex attracts more cations and expels fewer anions com

63 on, triggered through the recognition of the duplex between the authentic pre-mRNA and U7 small nucle

64 ctive' state, and unveil the role of the RNA duplex beyond the seed in Ago2.

65 ting strategy by conjugating highly specific duplex-binding molecules with potent quadruplex ligands.

66 sing smFRET to study the conformation of RNA duplexes bound to the core also shows bending.

67 lex composed of two bm-Calpha-PNA-C(5):dG(5) duplexes built on a core (bm-Calpha-PNA-T(7))(2):dA(8) t

68 be endoergic in aqueous solution and the DNA duplexes but slightly exoergic in the polymerase, with A

69 ribute to stabilization of the miR-305-5p:3p duplex by 340R.

70 PNA and/or negatively charged PNA/miRNA-492 duplex by differential pulse voltammetry.

71 pha-PNA with mixed sequences can form double duplexes by simultaneous binding to two complementary DN

72 The G:G mismatch sites of the d(TTGGCGAA) duplex can also act as a hotspot for the formation of al

73 voltage across the nanopore facilitated the duplex capture inside the nanopore's vestibule against t

74 on-template DNA strand bonds with the hybrid duplex (collapsed R-loops, where the two DNA strands rem

75 hetic genetic information, relative to a DNA duplex consisting entirely of Watson-Crick base-pairs.

76 l basis of minor groove recognition of a DNA duplex containing synthetic genetic information by hairp

77 duce a higher melting stabilization of a DNA duplex containing the unnatural P.Z base-pair when an im

78 The structures of two RNA duplexes containing 5'-GPsiC/3'-CAG and 5'-CPsiG/3'-GAC

79 lved three new crystal structures of the RNA duplexes containing these two modifications.

80 ed nanopore, polyarginine-conjugated DNA-PNA duplexes dehybridize faster than their DNA-PNA counterpa

81 tility of this workflow is demonstrated with duplexed detection of bacteria in a sample imitating a c

82 nally, the defect of an exo1-K185A mutant in duplex digestion was partially rescued by longer overhan

83 e the power of this approach, we performed a duplex digital ELISA.

84 (6)A minimally impacts the rate constant for duplex dissociation, changing k(off) by ~1-fold but sign

85 is highly sensitive to mechanical motions in duplex DNA (epsilon x Phi = 150-4250 cm(-1) M(-1)).

86 er than its anisotropy decay in well-matched duplex DNA (theta = 20 ns), yet longer than the dynamic

87 strand separation, and show Csm3/Tof1 "grip" duplex DNA ahead of CMG via a network of interactions im

88 Replicative helicases generally unwind duplex DNA an order of magnitude slower compared to thei

89 gnizes the symmetric sequence 5'-GCG C-3' in duplex DNA and cleaves (' ') to produce fragments with 2

90 resis results, the abundances of hairpin and duplex DNA are unaffected by the addition of netropsin.

91 contrast, fork-bound SSB loads PriA onto the duplex DNA arms of forks, suggesting a remodeling of Pri

92 A analogues that were not excised from duplex DNA as efficiently as predicted by calculations p

93 ind and unwind several hundred base pairs of duplex DNA at an average rate of ~240 bp/min.

94 homodimer that binds, unstacks, and sculpts duplex DNA at internal unpaired regions (bubbles) into s

95 together spirally encircle 10 base pairs of duplex DNA at the double-/single-stranded (ds-ss) juncti

96 that this model intercalator interacts with duplex DNA by a "displacement insertion intercalation" m

97 Purified recombinant YaaA binds to dsDNA, duplex DNA containing bubbles of unpaired nucleotides, a

98 targeting both G-quadruplex and its flanking duplex DNA in a naturally occurring dsDNA-ssDNA telomere

99 Comparative simulations on duplex DNA in the presence of Au-carbene ligands indicat

100 structure containing the single-stranded and duplex DNA junction with the allowed extension in the 5'

101 druplexes), but did not avidly interact with duplex DNA or with other G-quadruplex structures.

102 e has a quantum yield in single-stranded and duplex DNA ranging from 10% to 44% and 22% to 32%, respe

103 a185 facilitates its preferential binding to duplex DNA rather than RNA.

104 talytic sites, and cleave the two strands of duplex DNA simultaneously, in a single binding event.

105 g lesion-containing gap must be converted to duplex DNA to permit repair.

106 nism, netropsin binding induces a hairpin-to-duplex DNA transition.

107 Duplex DNA was not detected using conventional MS with l

108 rpin probes hybridized with T-DNAs to form a duplex DNA, and the ring of hairpin DNA was opened to ma

109 DNA processes that require the separation of duplex DNA, such as replication and transcription.

110 minimal activation was observed with 80-mer duplex DNA, the optimal effector for Tel1 activation is

111 ions that can migrate over long distances in duplex DNA, ultimately generating 8-oxo-7,8-dihydroguani

112 ntage of anti-parallel strand orientation of duplex DNA, within a given set of plausible premises.

113 lels the specificity of these complexes with duplex DNA.

114 ssociated with the over- or under-winding of duplex DNA.

115 ivity toward G-quadruplex telomeric DNA over duplex DNA.

116 volved in the formation of pseudo-continuous duplex DNA.

117 ly and sequentially bind to both hairpin and duplex DNA.

118 und, UvrC forms high affinity complexes with duplexed DNA substrates; the apparent dissociation const

119 enine in a single-stranded region flanked by duplexed DNA.

120 stalled due to interaction with the parental duplex, DNA rezipping-induced helicase backtracking rees

121 he absence of DNA and in complex with forked duplex DNAs before and after cleavage of the 5' single-s

122 igher affinity (>50-fold) for junctions over duplex DNAs.

123 utY excision rates with different A analogue duplexes do not correlate with the impact on overall Mut

124 Four duplexes: double-stranded DNA (dsDNA), PNA/DNA, dsRNA (m

125 ratively in the oriC to locally melt the DNA duplex during replication initiation.

126 To gain insight into the effect of Psi on duplex dynamics and hydration, we performed molecular dy

127 MicroRNA duplexes, each comprising a mature miRNA and its passeng

128 amic studies showed that AP destabilizes the duplex, enabling a structural transition of the sequence

129 By placing mismatches away from duplex ends, the thermodynamic drive for a strand-displa

130 Furthermore, every duplex experiment produces a substantial proportion of s

131 oduce periodic kinks in the crRNA-target RNA duplex, facilitating cleavage of the target RNA with 6-n

132 d not to bind to genomic DNA, resulting in a duplex flanked by single stranded binding primers.

133 Woods, which solves these challenges using a duplex-focused precursor detection method and stacked ra

134 more, the stability of the parallel-stranded duplex form can be altered by changing the 5'-nucleobase

135 , we study the hybridization kinetics of DNA duplex formation and the formation of hairpin stems, fin

136 e used to control the stereochemistry of the duplex formed in the templated oligomerization reaction

137 (11-CN-dppz)](2+) bound to d(TCGGCGCCGA), a duplex-forming sequence, and use both structural models

138 the DNA, a locally unwound and unpaired DNA duplex forms a zipper via alternating interstrand base s

139 shows that Dicer cleaves the modified siRNA duplex from the surface of the nanoparticle, and the lib

140 nd two different complementary DNAs, to form duplexes from both tert-amide side and Cgamma side.

141 se experimental results suggest that the RNA duplex generates a stronger electrostatic field than DNA

142 DNA replication requires that the duplex genomic DNA strands be separated; a function that

143 50 kbp can be readily induced using pairs of duplex guide RNPs targeted to a single chromosome.

144 lex units, while another features an unusual duplex hairpin structure adjoined to two stacked paralle

145 ectly from synthetic RNA template/DNA primer duplexes having either a blunt end or a 3'-DNA overhang

146 Such a crosstalk-free duplex imaging capability of CFR enables longitudinal me

147 ides a general molecular design strategy for duplex imaging.

148 Duplex immunofluorescence slides stained for E-cadherin

149 anges induced by ATP binding unwinds the RNA duplex in a cooperative manner.

150 d DNA in a head-to-head orientation melt the duplex in an Mcm10-dependent reaction.

151 stinct dissociation kinetic rates for a 7 bp duplex in which one G-C basepair is mutated to an A-T ba

152 nd RNA quadruplex structures and unwinds DNA duplexes in an ATP-dependent manner.

153 roximal-face pore, whereas the remaining DNA duplexes interact with the rims and serve as bridges bet

154 ions compared to the DNA duplex, and the RNA duplex interacts significantly stronger with the divalen

155 crA proteins interact to nick and unwind the duplex is not fully understood.

156 1 garlic samples) designed by application of duplex Kennard-Stone algorithm.

157 The generated duplex L(1)L(1)' or L(2)L(2)' is designed to be nicked b

158 can be achieved by either triplex first and duplex later or vice versa.

159 gonaute, with <30 min typically required for duplex loading and silencing-complex maturation.

160 tively sequence-independent quantum yield in duplexes makes 2CNqA promising as a nucleic acid label a

161 unusual interaction with RNA wherein an RNA duplex mediates dimerization of two A3H proteins.

162 ystal structures of B-form spin-labelled DNA duplexes, molecular dynamics simulations and nuclear mag

163 s, from nanoscale optical isolators and full-duplex nanoantennas to topologically-protected networks.

164 can range from separation of strands within duplex nucleic acids to the physical remodeling or remov

165 fluorophore-labeled oligodeoxyribonucleotide duplex (ODND) probes.

166 PNA 1 forms a higher order pentameric double duplex of a triplex composed of two bm-Calpha-PNA-C(5):d

167 introduction of a base-pair mismatch in the duplex of the hairpins.

168 NA-dependent RNA polymerase (RdRp) with each duplex of their segmented genomes.

169 of force-dependent dissociation of short DNA duplexes of 7, 8, and 9 bp.

170 The conjoined duplexes of Cgamma-bimodal PNAs can be used to generate

171 tep, there is a roughly 20% probability that duplex opening will terminate and the as-yet-unopened ds

172 DNA duplex operations demonstrate the responsiveness of the

173 polymerase KOD, in complex with either a DNA duplex or an RNA-DNA hybrid.

174 ofile of the nucleotide analogues into a DNA duplex overhang using recently evolved XNA polymerases i

175 th UNA at the T(15) position and LNAs in the duplex part possess the highest value of melting tempera

176 Duplex patch clamping and Angle SICM recordings show tha

177 In this work, a duplex PCR-Enzyme Linked Oligonucleotide Assay (ELONA) i

178 tion pathway from initial recognition of the duplex promoter in a closed complex to the final RPo.

179 was determined from both types of sample by duplex qPCR, and across a range of densities.

180 led with GAA and TTC strands; the two hybrid duplexes [r(GAA):d(TTC) and d(GAA):r(UUC)] in an R-loop;

181 d and confirmed using a previously published duplex real-time PCR (capable of detecting E. histolytic

182 ty comparable with those demonstrated by the duplex real-time PCR assay.

183 he digestion strand of the substrate DNA for duplex recognition, critical for Exo1 activation on not

184 Using RNA duplexes recognized by ADARs as readout of pre-messenger

185 lomere loss, hallmarks of deficient telomere duplex replication.

186 rations during evolution responsible for the duplex retina.

187 ely during evolution to have resulted in the duplex retina.

188 at the protein DGCR8 binds primary miRNA and duplex RNA with similar affinities.

189 enzymes that convert adenosine to inosine in duplex RNA, a modification that exhibits a multitude of

190 nd a slightly lower one (average 12%) inside duplex RNA.

191 nisms in which an RNA transcript forms a DNA duplex.RNA triple helix with a gene or one of its regula

192 interface between them and a continuous DNA duplex running along a central channel.

193 -care duplex ultrasound test (podiatry ankle duplex scan; PAD-scan) against commonly used bedside tes

194 However, all of the published Duplex-seq implementations so far required pair-end sequ

195 Among them, Duplex-seq was shown to be highly effective, by leveragi

196 ation between mutation induction measured by duplex sequencing and the gold-standard transgenic roden

197 Duplex sequencing can be broadly applied to basic mutati

198 cacies of germline de novo mutagenesis using duplex sequencing directly in oocytes, which provided un

199 Duplex sequencing is the most accurate approach for iden

200 Furthermore, the duplex sequencing method we optimized for single cells o

201 e simplified workflow than existing targeted duplex sequencing methods.

202 tly diminishes coverage, making whole genome duplex sequencing prohibitively expensive.

203 Here, we applied highly accurate duplex sequencing to detect low-frequency, de novo mutat

204 -end sequencing and in the case of combining duplex sequencing with target enrichment, lengthy hybrid

205 er-nucleotide frequencies <=1 x 10(-7) Using duplex sequencing, an extremely accurate error-corrected

206 In such PNA:DNA ternary complexes, the two duplexes share a common PNA backbone.

207 with modified small interfering RNA (siRNA) duplexes, SNAs act as single-entity transfection and gen

208 Patients should undergo routine duplex sonography after extracorporeal membrane oxygenat

209 extracorporeal membrane oxygenation weaning, duplex sonography or CT was conducted to detect cannula-

210 target sites, we evaluated three dodecameric duplexes spanning >10(3)-fold in binding affinity.

211 One DNA duplex spans the diameter of the hexamer and passes over

212 two thermostable enzymes, BST-polymerase and duplex-specific nuclease DSN.

213 y observed sequence dependent changes in the duplex stability from Psi modification.

214 fects of oligomeric state, DNA geometry, and duplex stability on wtRep and RepDelta2B unwinding activ

215 the C:G pair and significantly decreases the duplex stability through a conformational shift of nativ

216 This was attributed to high duplex stability, which maintains a steady orientation a

217 e low carbon steel by cladding it with super duplex stainless steel using laser powder bed fusion pro

218 sion resistance to rolled and annealed super duplex stainless steel.

219 merhead ribozyme sequence from its inactive, duplex state to its active, folded state.

220 he formation of a metallo-base pair within a duplexed strand and is therefore attractive for screenin

221 merases change both $K$ and $\Delta Lk$ by a duplex-strand-passage mechanism and have been shown to s

222 However, the manner in which modified siRNA duplex strands that comprise the SNA lead to gene silenc

223 labels were shown to be nonperturbing of the duplex structure.

224 e data report on charge transfer through RNA duplex structures mainly composed of homonucleotide sequ

225 s may harbor many functionally important non-duplex structures.

226 essential for remodeling RNA quadruplex and duplex structures.

227 iation constants to well-matched and damaged duplex substrates are 100 +/- 20 nM and 80 +/- 30 nM, re

228 ation of DNA and RNA polymerases along their duplex substrates results in DNA supercoiling.

229 Duplex substrates with identical thermodynamic stability

230 has not been observed for 5'- and 3'-tailed duplexes, suggesting that it is the fork structure that

231 ads contains PCR or sequencing errors within duplex tags.

232 formation transfer from both strands of long duplex templates.

233 In matched duplexes, (th)G's hypochromism was larger for flanking G

234 environments, accumulated RNA, and preserved duplexes than those formed by longer polyions.

235 tro transcribed Cas9 mRNA and crRNA:tracrRNA duplex that can effectively generate indels in four gene

236 sgRNA molecule or a synthetic crRNA:tracrRNA duplex that perfectly matches the protospacer target sit

237 bit translation of target mRNAs by forming a duplex that sequesters the Shine-Dalgarno (SD) sequence

238 The exponentially amplified DNA duplex that was intercalated with SYBR Green was designa

239 erted Alu repeats capable of forming RNA:RNA duplexes that bring splice sites together for backsplici

240 th transition in contrast to the other three duplexes that show sawtooth patterns, the latter being a

241 d (ANA) within small interfering RNA (siRNA) duplexes that were otherwise fully modified with the 2'-

242 ment of a single base pair in the miRNA-mRNA duplex-that elongates a weak five-base-pair seed to a co

243 re, and can displace the hemi-methylated DNA duplex, the native substrate of DNMT1, off the protein o

244 aphy, and the structure explains the loss in duplex thermal stability for the (R) isomer compared wit

245 o backbone ester bonds generally promote RNA duplex thermal stability to a greater magnitude than do

246 and break (DSB) in DNA and passing an intact duplex through the break.

247 A molecule and passage of another intact DNA duplex through the break.

248 e RPo, RNA polymerase (RNAP) unwinds the DNA duplex to form the transcription bubble and loads the DN

249 The dicer endonuclease DCL3 cuts resulting duplexes to generate 24- and 23-nt siRNAs.

250 production, indicating that 340R binds siRNA duplexes to prevent RNA-induced silencing complex assemb

251 lements, mitigating noise and operating full-duplex transceivers.

252 by making a double-stranded break in one DNA duplex, transporting another DNA segment through this br

253 Background Color-duplex ultrasonography (DUS) could be an alternative to

254 nous thrombosis after ICU admission with 102 duplex ultrasound examinations, with 12 cases (16.7%) of

255 Routine follow-up visits include serial duplex ultrasound for stent patency assessment.

256 Participants underwent screening duplex ultrasound postoperatively.

257 gnostic performance of a novel point-of-care duplex ultrasound test (podiatry ankle duplex scan; PAD-

258 blood gases and global cerebral blood flow (duplex ultrasound) during a 9 day ascent to 5050 m.

259 volumetric measures of cerebral blood flow (duplex ultrasound) to quantify resting cerebral metaboli

260 CA, respectively) and vertebral artery (VA) (Duplex ultrasound) was measured.

261 s (28 +/- 7 years; 23 +/- 2 kg m(-2) ), FMD (Duplex ultrasound), arterial blood gases, Hct and [Hb],

262 We measured cerebral blood flow (CBF, duplex ultrasound), cerebral oxygen delivery (CDO(2) ),

263 The reference test was a full lower limb duplex ultrasound.

264 ple protocol, which enabled the retrieval of duplex UMI in multiplex PCR based enrichment and sequenc

265 equencing method offers the benefit of using duplex UMI to remove NGS artifacts in a much more simpli

266 SNVs at 0.1-0.2% allele fractions, aided by duplex UMI.

267 t to promote the mechanical functions of DNA duplex unwinding by DnaA.

268 ides a mechanistic basis for relatively slow duplex unwinding by replicative helicases and explains h

269 f1 bound to the 3' ss/dsDNA junction impacts duplex unwinding by stabilizing the unpaired first base-

270 We demonstrate and characterize RNA duplex unwinding for DHX36 and examine the remodeling of

271 Duplex unwinding is then performed by the PcrA helicase,

272 dy identifies key particularities of DNA-PNA duplex unzipping as it takes place inside the nanopore a

273 erparts and proposed a model to describe the duplex unzipping.

274 DNA-PNA and polyarginine-conjugated DNA-PNA duplexes unzipping inside the alpha-hemolysin nanopore (

275 step toward understanding the nucleic acids duplexes unzipping kinetics variability, in confined, va

276 compared with 61 of 236 (26%) sections with duplex US (P = .01).

277 ipheral arterial disease not recognized with duplex US and was more predictive than duplex US of the

278 oxytol-enhanced MR angiography compared with duplex US for vascular mapping before upper limb AVF cre

279 Background Duplex US is performed routinely for vascular mapping pr

280 with duplex US and was more predictive than duplex US of the outcome of arteriovenous fistula surger

281 as the dependent variable and age, sex, and duplex US or ferumoxytol-enhanced MR angiography finding

282 went ferumoxytol-enhanced MR angiography and duplex US.

283 analogues that can form DNA2:PNA:DNA1 double duplexes via recognition through natural bases.

284 Sense and antisense strands of the parent duplex were synthesized with single ANA residues at each

285 e foundation for future applications, 20 DNA duplexes, where the bases facing and neighboring (th)G w

286 differences in thermal stability of the DNA duplex, which require extensive optimization of the reac

287 imers formed sequence-specific, imine-linked duplexes, which could be separated and used as templates

288 e helicases alternate between strands of the duplex-which does not require the 2B subdomain, contrary

289 n therefore replace any G residue in matched duplexes, while always maintaining similar photophysical

290 -base pairs stabilize a parallel A-form-like duplex with a 5' adenine-rich pocket, which binds a meta

291 Here, we report that SgrS forms a duplex with a uridine-rich translation-enhancing element

292 les the PCNA clamp to "waterskate" along the duplex with minimum drag.

293 d molecular dynamics (MD) simulations of RNA duplexes with 5'-GPsiC/3'-CAG, 5'-CPsiG/3'-GAC, 5'-APsiU

294 template switching are optimal from starter duplexes with a single nucleotide 3'-DNA overhang comple

295 These formed duplexes with complementary DNA and RNA as shown by UV a

296 es in this study is composed of two parallel duplexes with crossovers on both ends, and three, four,

297 The protein complex binds two short DNA duplexes with high affinity and bridges DNA molecules in

298 d as templates for the synthesis of daughter duplexes with identical sequences.

299 t is established that LC8 forms parallel IDP duplexes with some partners, such as nucleoporin Nup159

300 ur Cas2 subunits and contains two DNA ~30-bp duplexes within the channel.