ライフサイエンスコーパス: single-strand DNA

1 First, we modified a glass surface with single-stranded DNA.

2 ish this task, RAD51 must be loaded onto the single-stranded DNA.

3 yed as the redox indicator binding better to single-stranded DNA.

4 as the experimental approaches used to pull single-stranded DNA.

5 een the unwinding substrate and a homologous single-stranded DNA.

6 of the MCM work in concert to translocate on single-stranded DNA.

7 mplex that is required for loading DnaB onto single-stranded DNA.

8 ' oriented laying out of hRPA subunits along single-stranded DNA.

9 ated NPH I acts as a 5' to 3' translocase on single-stranded DNA.

10 ction, via its BRCT2 domain, with RPA-coated single-stranded DNA.

11 asize the lesser-known elastic properties of single-stranded DNA.

12 igh levels of hyperphosphorylated RPA-loaded single-stranded DNA.

13 1 protease is accelerated in the presence of single-stranded DNA.

14 d magnetic beads and macromolecular coils of single-stranded DNA.

15 ATPase activity of MtRecD was stimulated by single-stranded DNA.

16 rameters resembling enzymes translocating on single-stranded DNA.

17 bound to a parallel quadruplex compared with single-stranded DNA.

18 s comprise an RNA/DNA hybrid and a displaced single-stranded DNA.

19 ation of transcription from both double- and single-stranded DNA.

20 on associated with increased accumulation of single-stranded DNA, a substrate of APOBEC3A, triggering

21 The microbial target, single-stranded DNA amplified with asymmetric PCR, was q

22 CNA-related trimer is loaded onto RPA-coated single stranded DNA and interacts with ATR kinase to med

23 ed through pH-assisted thiol-gold bonding of single stranded DNA and salt aging, with preconjugated b

24 telomeric G-quadruplex DNA to complementary single stranded DNA and to telomere binding protein POT1

25 lyzed, radical reaction process that cleaves single-stranded DNA and requires only redox-inactive met

26 nzymes, dimerization enables processivity on single-stranded DNA and results in higher levels of muta

27 e selectivity of such a system in binding to single-stranded DNA and RNA is quadratically better than

28 e and reveals new interactions between short single-stranded DNA and the vestibule of a biological po

29 orts as to whether the enzyme also possesses single-stranded DNA and/or RNA 3'-5' exonuclease activit

30 tional R-loops (RNA/DNA duplex and displaced single-stranded DNA) and DNA double-strand breaks (DSBs)

31 H, which fills the Pol II active center with single-stranded DNA, and subsequent scanning downstream,

32 bustly with specific sequences of unmodified single-stranded DNA, and we have identified five tags th

33 binding of the human thrombin and its 15-mer single stranded DNA aptamer, under the application of ex

34 , and high-affinity PET radioligand based on single-stranded DNA aptamer to address this challenge.

35 Single-stranded DNA aptamers are oligonucleotides of app

36 exed, expanded proteomic technique that uses single-stranded DNA aptamers to assay 4783 human protein

37 RNA or single-stranded DNA aptamers with 2'-F pyrimidines have

38 eve accurate annealing when large regions of single-strand DNA are unpaired has remained unclear desp

39 hods for autonomously synthesizing arbitrary single-stranded DNA are limited.

40 iring lesions using double-stranded, but not single-stranded DNA as a template.

41 Here the authors show that APOBEC3G binds single-stranded DNA as an active deaminase monomer, subs

42 We have investigated the dynamics of single-stranded DNA as it translocates through charge-mu

43 We use short single-stranded DNAs as imaging labels that are linked t

44 DNA-end resection, the generation of single-stranded DNA at DNA double strand break (DSB) end

45 nthetic sequence that mimics freshly unwound single-stranded DNA at replication fork showed that RPA

46 reducing potentially detrimental breaks and single-stranded DNA at these loci.

47 over 30 years, the sequence specificity for single-strand DNA binding has remained unknown.

48 by the reliance of separation in DQAMmiR on single-strand DNA binding protein (SSB) whose native str

49 e the identification of RADX as an RPA-like, single-strand DNA binding protein.

50 t are unable to form t-loops or complex with single-strand DNA binding proteins, raising the question

51 when recombinantly expressed had the general single-stranded DNA binding activity of RPA complexes, u

52 Here we measure the single-stranded DNA binding and oligomerization kinetics

53 y is dependent on at least three RPA-encoded single-stranded DNA binding domains.

54 ralogous to the large subunit of the general single-stranded DNA binding heterotrimer replication pro

55 The bacterial single-stranded DNA binding protein (SSB) acts as an org

56 Escherichia coli single-stranded DNA binding protein (SSB) is an essentia

57 The single-stranded DNA binding protein (SSB) of Escherichia

58 The homotetrameric Escherichia coli single-stranded DNA binding protein (SSB) plays a centra

59 During DNA replication, the single-stranded DNA binding protein (SSB) wraps single-s

60 The nascent DNA colocalized with the VACV single-stranded DNA binding protein I3 in multiple punct

61 terize the role of filament formation by the single-stranded DNA binding protein ICP8 in the formatio

62 The T7 single-stranded DNA binding protein increases primer for

63 lymerase gamma holoenzyme, the mitochondrial single-stranded DNA binding protein mtSSB, the replicati

64 factor IIH prevented the accumulation of the single-stranded DNA binding protein replication protein

65 hairpin RNA (shRNA) screening, we identified single-stranded DNA binding protein replication protein

66 Cdc13, a single-stranded DNA binding protein that recruits telome

67 loader, the PCNA sliding clamp, and the RPA single-stranded DNA binding protein.

68 und by replication protein A (RPA) and other single-stranded DNA binding proteins (SSBs).

69 These results reveal the role of single-stranded DNA binding proteins in controlling Exo1

70 ains to distinguish the PriA interaction and single-stranded DNA binding.

71 This approach revealed a novel mode for single-stranded DNA-binding protein (SSB)-DNA binding, i

72 ethods, this amplification requires only the single-stranded DNA-binding protein gp32 from bacterioph

73 A (RPA) is a highly conserved heterotrimeric single-stranded DNA-binding protein involved in DNA repl

74 Interestingly, single-stranded DNA-binding protein suppresses the MtRec

75 nal proteins, including the telomeric repeat single-stranded DNA-binding protein Teb1 and its heterot

76 The replication protein A (RPA) is a single-stranded DNA-binding protein that plays an essent

77 Single-stranded DNA-binding proteins (SSBs) play a key r

78 We found that single-stranded DNA-binding proteins are recruited to th

79 d of telomeric sequence-specific double- and single-stranded DNA-binding proteins, Taz1 and Pot1, res

80 It has been previously reported that single-stranded DNA binds PLN with strong affinity and r

81 fferentiation was observed, due to increased single-strand DNA breaks that likely occur due to hetero

82 Moreover, a predominant binding of PARP1 to single-strand DNA breaks, occluding its Erk binding site

83 ive solvent environment that can concentrate single-stranded DNA but largely exclude double-stranded

84 However, cry-DASH can repair CPDs in single-stranded DNA, but their role in DNA repair in viv

85 Photoexcitation of single-stranded DNA can transfer an electron between sta

86 NA cleavage-religation activity and catalyze single-stranded DNA catenation.

87 pecificity of anti-lipid A antibodies toward single-stranded DNA combined with observed homology of S

88 In contrast, the sensor of single-stranded DNA complex 1-a recently identified huma

89 ion and emission shift of up to 120 nm for a single-stranded DNA construct, and (3) a sequence robust

90 s, as well as numerous circular Rep-encoding single-stranded DNA (CRESS DNA) viral genomes, were iden

91 Human APOBEC3H and homologous single-stranded DNA cytosine deaminases are unique to ma

92 APOBEC3s (A3s) are single-stranded DNA cytosine deaminases that provide inn

93 ng proteins, initiating the cell response to single-strand DNA damage, was also required for long-ter

94 -CRISPR), a targeting strategy in which long single-stranded DNA donors are injected with pre-assembl

95 mbination of alternating double-stranded and single-stranded DNA (dsDNA and ssDNA) regions of varying

96 y-mediated end-joining requires annealing of single-strand DNA ends, we addressed the contribution of

97 RecBCD generates recombinogenic single-stranded DNA ends by unwinding DNA and cutting it

98 f TER in the TERT-TER-p65 catalytic core and single-stranded DNA exit; extensive subunit interactions

99 A double-strand breaks (DSBs) to generate 3'-single-stranded DNA facilitates DSB repair via error-fre

100 applied directional deep sequencing of short single-stranded DNA fragments enriched for RNA-primed na

101 The separation and partitioning of large single-stranded DNA fragments of the homologous chromoso

102 on of the structure of S1-15 in complex with single-stranded DNA fragments, which may provide clues a

103 ent optical properties and biocompatibility, single-strand DNA-functionalized quantum dots have been

104 By contrast, single-stranded DNA-functionalized AuNPs, while attracte

105 We demonstrated that Brca2 protein prevents single-stranded DNA gap accumulation at replication fork

106 tions arise through the aberrant repair of a single-stranded DNA gap, in a process that is dependent

107 RarA ATPase activity is stimulated by single-stranded DNA gaps and double-stranded DNA ends.

108 orporates ribonucleotides and/or accumulates single-stranded DNA gaps during replication.

109 phosphate, and also for cytosine residues in single-stranded DNA generated from a phagemid, in which

110 eminivirus family, CMBs have small, circular single-stranded DNA genomes.

111 Here we find that non-homologous single-stranded DNA greatly stimulates Cas9-mediated gen

112 determine how they contribute to duplex and single-stranded DNA handling, and test the cellular cons

113 ded binding proteins both protect and expose single-stranded DNA has important implications for our u

114 an essential replisome component that binds single-stranded DNA, has a role in replication-coupled n

115 yme that specifically modifies thymidines on single-stranded DNA in a sequence-specific manner by a n

116 nduced DSBs are efficiently resected into 3' single-stranded DNA in cells and the major nuclease for

117 uble-stranded DNA in its ATP-bound state and single-stranded DNA in its apo state.

118 Secondly, TFE binds physically to single-stranded DNA in the transcription bubble of the O

119 ic/apurinic lyase activity that introduces a single-strand DNA incision.

120 unequivocally establishes the existence of a single-stranded DNA incorporation pathway in human cells

121 zes synthesis-dependent strand annealing and single-stranded DNA incorporation pathways.

122 lesions within unusually long and persistent single-strand DNA intermediates.

123 rmation and maintenance of the double-strand/single-strand DNA junction at the upstream edge of the -

124 e adapters; subsequent PCR steps amplify the single-stranded DNA junction library in preparation for

125 gy presented by the upstream double-stranded/single-stranded DNA junction of the transcription bubble

126 Here, the interaction of single stranded DNA labeled with either fluorescein (FAM

127 ude that ROS contribute to TLD by converting single-stranded DNA lesions into double-stranded DNA bre

128 The aptamers were selected in vitro from a single-stranded DNA library of 1.8 x 10(15) oligonucleot

129 NA hybridized to the complementary DNA and a single-stranded DNA loop, are formed in switch regions o

130 cancer (PCa) that specifically binds to the single-stranded DNA molecule from a 277-nt fragment that

131 Single-strand DNA molecules are introduced into DNA@ZIF-

132 Our data suggests that single-stranded DNA molecules may influence DNA junction

133 pose that these contigs correspond to linear single-stranded DNA molecules that fold onto themselves

134 ate recombination (SPDIR), facilitates short single-stranded DNA molecules to invade and replace geno

135 eads by measuring changes in ionic flow when single-stranded DNA molecules translocate through the po

136 mine the thermal motion of a voltage-clamped single-stranded DNA-NeutrAvidin complex in a Mycobacteri

137 olecule arrays by electrostatically adhering single-stranded DNA of gene-like length onto positively

138 The circular single-stranded DNA of phytopathogenic geminiviruses is

139 nal DNA origami, the DNR scaffold is a long, single-stranded DNA of tandem repeats, originating from

140 BAC simultaneously by co-transformation of a single-stranded DNA oligo and a double-stranded selectio

141 An amino-modified single stranded DNA oligonucleotide probe synthesised ba

142 ce receptor of interest is conjugated with a single-stranded DNA oligonucleotide, which hybridizes to

143 tutions via HDR following co-delivery with a single-stranded DNA oligonucleotide.

144 Synthetic single-stranded DNA oligonucleotides (ssODNs) can be use

145 Single-stranded DNA oligonucleotides can achieve targete

146 Single-stranded DNA oligonucleotides have unique, and in

147 ins for Proteomics) is an approach that uses single-stranded DNA oligonucleotides to capture specific

148 and diffusion constants of several different single-stranded DNA oligonucleotides trapped in an MspA

149 in the frequency of gene editing directed by single-stranded DNA oligonucleotides.

150 hydrolysis, although they both cleave simple single-stranded DNA oligonucleotides.

151 Aptamers are artificial single-stranded DNA or RNA oligonucleotides capable of b

152 Aptamers are oligonucleotides (single-stranded DNA or RNA) that can bind their targets

153 ination (HR) requires the generation of a 3' single-strand DNA overhang by exonuclease activities in

154 choice is determined by the generation of 3 single-strand DNA overhangs at the break that are initia

155 sequence, the proteinosome payload (dextran, single-stranded DNA, platinum nanoparticles) is traffick

156 and Rad52 to promote nucleation of Rad51 on single-stranded DNA pre-occupied by replication protein

157 ped AuNPs and the d-AuNPs were stabilized by single stranded DNA probe (ssDNAp).

158 which is able to detect the hybridization of single stranded DNA probe with its complementary target

159 fficient covalent immobilization of purified single-stranded DNA probe oligomers on cleaned gold micr

160 orters we conjugated it to one terminus of a single-stranded DNA "probe" that was attached by its oth

161 Single-stranded DNA probes labeled with fluorescein amid

162 ate in methylated regions involving frequent single-stranded DNA processing as part of DSB repair.

163 ine starvation leads to accumulation of both single-stranded DNA regions and intracellular ROS, and i

164 by facilitating the generation of RPA-bound single-stranded DNA regions upon replication stress in a

165 ivery of CRISPR/Cpf1 ribonucleoproteins with single-stranded DNA repair templates results in precise

166 stranded MLPA products and subsequently to a single stranded DNA reporter probe bearing a HRP molecul

167 nd resection, which generates long tracts of single-stranded DNA required for checkpoint activation a

168 hrough deaminating cytosine (C) to uracil on single-stranded DNA/RNA.

169 RPA-coated single-stranded DNA (RPA-ssDNA), a nucleoprotein structu

170 lection of high-affinity reagents based upon single-stranded DNA scaffolding of peptide fragments.

171 We have screened over 300 short single-stranded DNA sequences with palindrome symmetry,

172 High-throughput single-stranded DNA sequencing (ssDNA-seq) of cell-free

173 lity through the introduction of an unpaired single-stranded DNA spacer in the middle of each duplex.

174 Single-strand DNA-specific APOBEC cytidine deaminase(s)

175 y of S1-15 and A6 and the reports of several single-stranded DNA-specific mAbs prompted the determina

176 The successfully immobilization of the single strand DNA (ss-DNA) probe and hybridization with

177 educed graphene oxide aerogel labeled with a single strand DNA (ss-HSDNA/rGOae) modified on a rotatin

178 ions in the lattices using responsiveness of single-stranded DNA (ss-DNA), far less work has been don

179 de experimental evidence that ComFA binds to single stranded DNA (ssDNA) and has ssDNA-dependent ATPa

180 Various helicases and single stranded DNA (ssDNA) binding proteins unfold G-qu

181 fication, hybridisation between short 25-mer single stranded DNA (ssDNA) fragments and a complementar

182 ipment and facilitates the immobilization of single stranded DNA (ssDNA) probe sequences on a wide va

183 zyme which selectively digests the 3'-end of single stranded DNA (ssDNA).

184 Thiol-modified single stranded DNA (ssDNA, 20 bases, capture probe) was

185 nctionalized and codified with two different single stranded-DNA (ssDNA) chains.

186 Specifically, PtNPs are modified with a single-strand DNA (ssDNA) shell that is complementary to

187 quantities of DNA sequence to align and pair single-strand DNA (ssDNA) with a homologous double-stran

188 ultiple target DNAs causes the corresponding single-stranded DNA (ssDNA) amplicons to be generated an

189 ich forms helical nucleoprotein filaments on single-stranded DNA (ssDNA) and catalyzes strand invasio

190 ate-free synthesis of high-molecular-weight, single-stranded DNA (ssDNA) and demonstrate that it proc

191 anine (G), Cytosine (C), and Thymine (T)) on single-stranded DNA (ssDNA) and double-stranded DNA (dsD

192 nnealase, a protein that binds complementary single-stranded DNA (ssDNA) and facilitates its annealin

193 A orchestrates these processes by binding to single-stranded DNA (ssDNA) and interacting with several

194 Human RAD52 has been shown to mediate single-stranded DNA (ssDNA) and is synthetic lethal with

195 Single-stranded DNA (ssDNA) and RNA regions that include

196 or surface of hexameric helicases to protect single-stranded DNA (ssDNA) and stabilize the complex in

197 s a nucleoprotein filament that assembles on single-stranded DNA (ssDNA) at the sites of DNA damage.

198 Escherichia coli single-stranded DNA (ssDNA) binding protein (SSB) is the

199 his process is driven by the essential viral single-stranded DNA (ssDNA) binding protein ICP8, which

200 The bacterial single-stranded DNA (ssDNA) binding protein SSB is a str

201 cation protein A (RPA), the major eukaryotic single-stranded DNA (ssDNA) binding protein, is essentia

202 The 2 single-stranded DNA (ssDNA) binding proteins SSB1 and SS

203 divergent bacteria can recognize and cleave single-stranded DNA (ssDNA) by an RNA-guided, PAM-indepe

204 f a Rad51 recombinase filament that forms on single-stranded DNA (ssDNA) created at DSB ends.

205 The single-stranded DNA (ssDNA) cytidine deaminase APOBEC3F

206 The APOBEC3B (A3B) single-stranded DNA (ssDNA) cytosine deaminase has impor

207 By rationally designing single-stranded DNA (ssDNA) donors of the optimal length

208 NA repair restores the resulting 5'-Flap and single-stranded DNA (ssDNA) gap.

209 through the cell cytoplasm, and deliver the single-stranded DNA (ssDNA) genome to the nucleus, where

210 to track the population of unlabeled target single-stranded DNA (ssDNA) hybridized with probe DNA im

211 E. coli SSB can bind to long single-stranded DNA (ssDNA) in multiple binding modes us

212 search begins after RecA binds an initiating single-stranded DNA (ssDNA) in the primary DNA-binding s

213 n genome maintenance, binding and organizing single-stranded DNA (ssDNA) intermediates.

214 Single-stranded DNA (ssDNA) is notable for its interacti

215 Here we show that single-stranded DNA (ssDNA) knots and links can be creat

216 e nucleotides are removed, resulting in long single-stranded DNA (ssDNA) lesions.

217 advances in paleogenomics, we have applied a single-stranded DNA (ssDNA) library preparation method t

218 unwind double-stranded DNA (dsDNA) to reveal single-stranded DNA (ssDNA) needed for many biological p

219 old nanoparticles (GNPs) self-assembled with single-stranded DNA (ssDNA) of nheA gene immobilized wit

220 epsilon has greater contact with the nascent single-stranded DNA (ssDNA) of the leading strand on act

221 Human telomeres end in a short, single-stranded DNA (ssDNA) overhang that is recognized

222 nerated DSB ends are processed to yield long single-stranded DNA (ssDNA) overhangs, which are quickly

223 he Bocaparvovirus genus of the nonenveloped, single-stranded DNA (ssDNA) Parvoviridae family.

224 Thiolated single-stranded DNA (ssDNA) probe was hybridized with ap

225 her hand, BLM and RECQ5 demonstrated similar single-stranded DNA (ssDNA) reeling activities that were

226 f an archaeal MCM N-terminal domain bound to single-stranded DNA (ssDNA) revealed ssDNA associating a

227 totype hydrogel array which can analyze only single-stranded DNA (ssDNA) targets, the device is the f

228 t and the stronger interaction of SWNTs with single-stranded DNA (ssDNA) than double-stranded DNA (ds

229 te of cytosine deamination is much higher in single-stranded DNA (ssDNA) than in double-stranded DNA,

230 egy relies on the preferential adsorption of single-stranded DNA (ssDNA) to GO over aptamer-target co

231 ons or by template-directed synthesis with a single-stranded DNA (ssDNA) topological structure.

232 tion and genomic substitution rates, RNA and single-stranded DNA (ssDNA) viruses may be important con

233 gle-stranded DNA binding protein (SSB) wraps single-stranded DNA (ssDNA) with high affinity to protec

234 (AFM) to show that Ver preferentially binds single-stranded DNA (ssDNA) with no sequence specificity

235 Furthermore, Dpb11 binds directly to single-stranded DNA (ssDNA), and ssDNA inhibits the Dpb1

236 Also, the electrochemical responses of single-stranded DNA (ssDNA), DNA hybridization and DNA s

237 ate containing RNA:DNA hybrids and displaced single-stranded DNA (ssDNA), has emerged as a major sour

238 on of the DNA damage signal, accumulation of single-stranded DNA (ssDNA), sensitivity to replication

239 are factors that regulate the generation of single-stranded DNA (ssDNA), the enzymatic substrate of

240 rize the temperature-dependent elasticity of single-stranded DNA (ssDNA), where we find a significant

241 monly used recombinant AAV vectors contain a single-stranded DNA (ssDNA), which is transcriptionally

242 or the detections of metal ion, dopamine and single-stranded DNA (ssDNA), with detection limits of 1.

243 B replicative helicase onto DNA bound by the single-stranded DNA (ssDNA)-binding protein (SSB).

244 sitive coactivator of transcription (PC4), a single-stranded DNA (ssDNA)-binding protein, as a novel

245 Strikingly, the addition of the single-stranded DNA (ssDNA)-binding replication protein

246 me which specifically degrades the 3'-end of single-stranded DNA (ssDNA).

247 A3G-CD1 (rA3G-CD1) alone and in complex with single-stranded DNA (ssDNA).

248 robes for the specific recognition of target single-stranded DNA (ssDNA).

249 sive processing, producing long stretches of single-stranded DNA (ssDNA).

250 ly 2 helicase Hel308 during translocation on single-stranded DNA (ssDNA).

251 rand synthesis leads to accumulation of long single-stranded DNA (ssDNA).

252 PF and ERCC-XPF and show that the binding to single-stranded DNA (ssDNA)/dsDNA junctions is dependent

253 ch is able to detect hybridization of probe (single stranded DNA-ssDNA) and hybrid (double stranded D

254 We recently demonstrated that long single-stranded DNAs (ssDNAs) serve as very efficient do

255 rogrammability of DNA base pairing to direct single-stranded DNAs (ssDNAs) to assemble into desired 3

256 architectures of Watson-Crick complementary single-stranded DNA ("sticky end") linking strategies.

257 n alkaline solutions; whereas, the denatured single-stranded DNA strands readily reform duplexes at n

258 , AddAB or AdnAB) generates the requisite 3' single-strand DNA substrate for RecA-mediated strand inv

259 f neither non-compatible ends nor protruding single strand DNA sufficiently warranted the action of n

260 ese mutants compared with wild type DnaC for single-stranded DNA, suggesting that the substitutions a

261 volves resection of the break to expose a 3' single-stranded DNA tail.

262 is modulated by the nature of the 3'-ssDNA (single-stranded DNA) tail of the substrate and its effec

263 ulting in an amplicon of a duplex flanked by single stranded DNA tails.

264 in an amplicon with a duplex flanked by two single stranded DNA tails.

265 ollowed by resection to generate invasive 3' single-stranded DNA tails.

266 The detection limit for 69-base single-stranded DNA targets is 10 pM (about 10 million c

267 r displays good discrimination between three single-stranded DNA targets studied: fully complementary

268 gents, to prime second strand synthesis of a single-stranded DNA template and generate millions of pa

269 In DNA origami, single-stranded DNA template is shaped into desired nano

270 activation, overresection produces excessive single-stranded DNA that could lead to genomic instabili

271 rial strategies (1) , especially small lytic single-stranded DNA (the microviruses) and RNA phages (t

272 plification processing for the generation of single stranded DNA, thus presenting an assay that can f

273 re we report the use of intrinsically chiral single-stranded DNA to achieve simultaneous handedness a

274 d both must remodel onto opposite strands of single-stranded DNA to do so.

275 ing capability is based on the transition of single-stranded DNA to double-stranded DNA.

276 D/APOBEC family enzymes convert cytosines in single-stranded DNA to uracils, causing base substitutio

277 ultiple base pairs may occur separately from single-stranded DNA translocation.

278 hannel of the N-tier and the unwound leading single-strand DNA traverses the channel through the N-ti

279 APOBEC3G deaminates single-stranded DNAs via its C-terminal domain, whereas

280 rminal ATPase of MCM is compact and contacts single-stranded DNA, via a set of pre-sensor 1 hairpins

281 In the case of the ubiquitous human circular single-stranded DNA virus family Anelloviridae, there is

282 Circular single-stranded DNA viruses infect archaea, bacteria, an

283 Parvoviruses are single-stranded DNA viruses that use the palindromic str

284 The relatively recent emergence of single-stranded DNA viruses, such as chicken anemia viru

285 o reach up to 22 hours, whereas unconjugated single-stranded DNA was degraded within minutes.

286 ore, the measurements of thermally denatured single-stranded DNA were carried out and the value of (G

287 Elevated levels of single-stranded DNA were necessary but insufficient for

288 Single-stranded DNAs were also tested and shown to fit w

289 uble-strand breaks creates long stretches of single-stranded DNA, which are rapidly bound by replicat

290 ecombination (HR) are first resected to form single-stranded DNA, which binds replication protein A (

291 e-stranded breaks that are processed to form single-stranded DNA, which can invade a homologous chrom

292 tides, called staple strands, to fold a long single-stranded DNA, which is called a scaffold strand,

293 sion of the DSB ends from double-stranded to single-stranded DNA, which is necessary to initiate DSB

294 an intrinsic preference for 5'-TC motifs in single-stranded DNA, which is the most frequently mutate

295 t preparations lacking DNA were able to bind single-stranded DNA with high affinity (Kd approximately

296 eir destinations allows for a simple robot a single-stranded DNA with one leg and two foot domains fo

297 different nucleic acids shows that it binds single-stranded DNA with three-fold lower affinity than

298 reaction (PER) cascades, which grow nascent single-stranded DNA with user-specified sequences follow

299 for deaminating cytosine bases to uracil in single-stranded DNA, with characteristic sequence prefer

300 Here, we present a study of surfactant and single-stranded DNA-wrapped SWNTs suspended in aqueous s