ライフサイエンスコーパス: single-stranded 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 e that informs a multistep model for binding single-stranded DNA.

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

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

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

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

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

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

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

26 ys revealed that MtRecD binds efficiently to single-stranded DNA and linear duplexes containing 5' ov

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

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

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

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

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

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

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

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

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

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

37 Single-stranded DNA aptamers are oligonucleotides of app

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

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

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

41 We propose secondary structures within single-stranded DNA are potent instigators of genome ins

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

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

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

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

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

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

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

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

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

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

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

53 ibria of cooperatively-bound clusters of the single-stranded DNA binding protein (gp32) of the T4 DNA

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

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

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

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

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

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

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

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

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

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

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

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

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

67 Single-stranded DNA binding proteins (SSBs) are ubiquito

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 ressing cells also have higher levels of the single-stranded DNA-binding protein SSB1, which has a cr

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

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

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

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

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

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

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

82 ication forks with topoisomerase I-generated single-stranded DNA breaks resulted in the generation of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

115 When RecA is activated by single-stranded DNA in the presence of a nucleotide trip

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

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

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

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

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

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

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

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

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

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

126 enzymatically synthesize a micrometer-sized, single-stranded DNA molecule with only boranephosphonate

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

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

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

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

131 A1-RFA3) function as a complex that can bind single-stranded DNA molecules, promoting the repair of g

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

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

134 The circular single-stranded DNA of phytopathogenic geminiviruses is

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

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

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

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

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

140 n shown that MRN activity can generate short single-stranded DNA oligonucleotides (ssO) that may also

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

142 Single-stranded DNA oligonucleotides can achieve targete

143 Single-stranded DNA oligonucleotides have unique, and in

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

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

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

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

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

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

150 tightly to the parallel quadruplex DNA than single-stranded DNA or tailed duplexes.

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

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

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

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

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

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

157 Single-stranded DNA probes labeled with fluorescein amid

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

190 SIRV2 gp17 was found to be a single-stranded DNA (ssDNA) binding protein different in

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

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

193 n protein A (RPA) is a ubiquitous eukaryotic single-stranded DNA (ssDNA) binding protein that serves

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

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

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

197 the stripping peak currents and logarithm of single-stranded DNA (ssDNA) concentrations in the range

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

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

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

201 DNA stretches, as in stem-loop structures of single-stranded DNA (ssDNA) derived from human immunodef

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

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

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

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

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

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

208 n of Sld3 that is specifically defective for single-stranded DNA (ssDNA) interaction (sld3-m9).

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

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

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

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

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

214 nanowire biosensor for detection of specific single-stranded DNA (ssDNA) molecules.

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

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

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

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

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

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

221 RNA virus, and minute virus of mice (MVM), a single-stranded DNA (ssDNA) parvovirus, but not hepatiti

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

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

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

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

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

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

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

229 d here shows how the C-terminal domains bind single-stranded DNA (ssDNA) to recognize the accumulatio

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

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

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

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

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

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

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

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

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

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

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

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

242 ing the ATR-dependent phosphorylation of the single-stranded DNA (ssDNA)-binding complex replication

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 ide/oligopeptide) binding motif to recognize single-stranded DNA (ssDNA).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

268 is a robust assembly technique that folds a single-stranded DNA template into a target structure by

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

298 ocedure, subsets of hundreds or thousands of single-stranded DNAs with different lengths can selectiv

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