ライフサイエンスコーパス: single-stranded DNA

1 DNA helicase), or RPA2 (a protein that binds single-stranded DNA).

2 rogression, resulting in the accumulation of single stranded DNA.

3 cific (HMCES) as a sensor of abasic sites in single-stranded DNA.

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

5 hnique centered around the directionality of single-stranded DNA.

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

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

8 TPase that forms a nucleoprotein filament on single-stranded DNA.

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

10 by facilitating RAD51 filament formation on single-stranded DNA.

11 -methyladenine is preferentially repaired in single-stranded DNA.

12 omoting error-free repair of abasic sites in single-stranded DNA.

13 NA efficiently integrates into the genome as single-stranded DNA, (2) that the resulting heteroduplex

14 Alternatively, single-stranded DNA, a naturally occurring biological po

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

16 Furthermore, single-stranded DNA accumulated preferentially at 6-4PPs

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

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

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

20 le-stranded DNA-binding proteins (SSBs) bind single-stranded DNA and help to recruit heterologous pro

21 tructure of an archaeal MCM hexamer bound to single-stranded DNA and nucleotide cofactors.

22 e Pif1, which tracks in a 5'-3' direction on single-stranded DNA and plays a role in genome maintenan

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

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

25 f iminosulfur oxydifluorides to amine-tagged single-stranded DNA and to BSA protein demonstrate the p

26 BV DNA polymerase inhibitor, at the stage of single-stranded DNA and was followed by removal of PFA t

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

28 ES acts at replication forks, binds PCNA and single-stranded DNA, and generates a DNA-protein crossli

29 NA) could be used as a magnified analogue of single-stranded DNA, and that two meta-DNAs that contain

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

31 ted to a handful of microorganisms for which single-stranded DNA-annealing proteins (SSAPs) that prom

32 ombin is shown to be reversed by addition of single-stranded DNA antidotes.

33 A single-stranded DNA aptamer is used to bind with high af

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

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

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

37 es comprising a DNA:RNA hybrid and displaced single-stranded DNA, are important drivers of damage ari

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

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

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

41 in DNA, with some members having activity on single-stranded DNA as well as RNA.

42 We propose that the presence of persistent single-stranded DNA, as a consequence of transcription-r

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

44 Hence, a reduction in single-stranded DNA at replication forks may explain the

45 can covalently cross-link to abasic sites in single-stranded DNA at stalled replication forks to prev

46 ving deoxyribozymes (DNAzymes) are synthetic single-stranded DNA-based catalytic molecules that can b

47 semipermeable membrane allow trafficking of single-stranded DNA between neighboring protocells.

48 facilitates bypass, apparently by generating single-stranded DNA beyond the DPC.

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 hannel in hPIF1 that we show is critical for single-stranded DNA binding during unwinding, but not th

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

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

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

55 lambda Orf, a protein that binds to E. coli single-stranded DNA binding protein (SSB) to function as

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

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

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

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

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

61 with the in vivo occupancy of mitochondrial single-stranded DNA binding protein reported previously

62 n replication protein A and Escherichia coli single-stranded DNA binding protein that the magnitude o

63 ivity, which is alleviated by binding of the single-stranded DNA binding protein, RPA, to the exclude

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

65 However, while single-stranded DNA binding proteins (SSBs) readily prom

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

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

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

69 intermediates that are rapidly protected by single-stranded DNA-binding (SSB) proteins.

70 CST (CTC1-STN1-TEN1) proteins, which form a single-stranded DNA-binding complex, localize at stalled

71 on between Escherichia coli RNase HI and the single-stranded DNA-binding protein (SSB) in this proces

72 Single-stranded DNA-binding protein (SSB) is typically p

73 o investigate the prion-forming potential of single-stranded DNA-binding protein (SSB) of Campylobact

74 of core subunits of LMO2 and LDB1 as well as single-stranded DNA-binding protein (SSBP) cofactors and

75 The Chip/LIM-domain binding protein (LDB)-single-stranded DNA-binding protein (SSDP) (ChiLS) compl

76 1) transcription factor and the co-regulator single-stranded DNA-binding protein 3 (SSBP3) regulates

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

78 overcome by the DNA-binding activity of the single-stranded DNA-binding protein RPA, efficient DNA r

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

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

81 RADX is a mammalian single-stranded DNA-binding protein that stabilizes telo

82 107Q amino acid changes in the mitochondrial single-stranded DNA-binding protein, a crucial protein i

83 Bacterial single-stranded DNA-binding proteins (SSBs) bind single-

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

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

86 ic target sites and report that simultaneous single-stranded DNA break formation at donor and accepto

87 measure the kinetics of translocation along single-stranded DNA by the helicase Hel308 from Thermoco

88 aN substrates modified with thiolated ssDNA (single stranded DNA) can be successfully used in the ana

89 By combining the single-stranded DNA cleavage ability of CRISPR-Cas12a an

90 slocates sequentially hand-over-hand along a single-stranded DNA coil, akin to the way AAA+ ATPases (

91 oligonucleotide-based FISH probes with long, single-stranded DNA concatemers that aggregate a multitu

92 nt R-loops (RNA-DNA hybrids with a displaced single-stranded DNA) create DNA damage and lead to genom

93 J and RAP80 exposed to MMC are attributed to single-stranded DNA created by Mre11 and CtIP nucleases.

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

95 e, and Iflaviridae and circular Rep-encoding single-stranded DNA (CRESS-DNA) virus, were also detecte

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

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

98 ate immune response is the APOBEC3 family of single-stranded DNA cytosine deaminases, which inhibits

99 erfacial potential changes were measured for single-stranded DNA detection with an unprecedented zept

100 When starting from single-stranded-DNA, DNA is first converted to double-st

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

102 tion checkpoint with excessive destabilizing single-stranded DNA exposure in eukaryotes.

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

104 ki2-like nucleic acid helicase that provides single-stranded DNA for alkylation damage repair by the

105 E2Ct, fail to induce RPA phosphorylation and single-stranded DNA formation, leading to defects in PCN

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

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

108 nthesis downstream of the lesion, creating a single-stranded DNA gap that is repaired primarily in an

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

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

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

112 em repaired via HJs is replication-dependent single-stranded DNA gaps, not DSBs.

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

114 whereas the non-virulent Ra strain triggered single-stranded DNA generation.

115 vely charged DNA binding protein J guide the single-stranded DNA genome into the icosahedral capsid.

116 tructures of Pf4 with and without its linear single-stranded DNA genome, and studied Pf4 assembly int

117 are structurally simple viruses with linear single-stranded DNA genomes and nonenveloped icosahedral

118 geminiviruses (plant viruses with circular, single-stranded DNA genomes) are the major group of emer

119 ack inversions were mediated by formation of single-stranded DNA hairpins.

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

121 vimetric analytical techniques, we find that single-stranded DNA has a significant flame-retardant ef

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

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

124 trol the translocation speed of helicases on single-stranded DNA, however the cause of these effects

125 They exhibit 5' exonuclease activity on single-stranded DNA, hydrolyzing it at the acidic pH ass

126 which long distance binding (25 angstrom) of single-stranded DNA in an allosteric site primes the act

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

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

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

130 nded sites and also at AT-rich regions where single-stranded DNA is exposed during origin opening.

131 sversion substitutions; results suggest that single-stranded DNA is formed during the genesis of the

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

133 o three hexanucleotide repeats resulted in a single-stranded DNA-like mechanical behavior under all c

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

135 molecular Fe(II)(4)L(4) tetrahedron binds to single stranded DNA, mismatched DNA base pairs, and thre

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

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

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

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

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

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

142 Single-stranded DNA oligonucleotides have unique, and in

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

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

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

146 -loops via the presence of long stretches of single-stranded DNA on their looped-out strand.

147 Nucleic acid aptamers are single stranded DNA or RNA sequences that specifically b

148 In this regard, aptamers, as artificial single-stranded DNA or RNA oligonucleotides with catalyt

149 Single-stranded DNA or RNA sequences rich in guanine (G)

150 nvolves introducing multiple, short pairs of single-stranded DNA overhangs to components of the struc

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

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

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

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

155 Afterward, the single-stranded DNA probe was attached to the surface of

156 nthesized oligonucleotides or amplicon-based single-stranded DNA probes and validated the technique o

157 relies on the immobilization on a surface of single-stranded DNA probes that bind complementary targe

158 or annealing activities limit the amount of single-stranded DNA product that Pif1 can generate, lead

159 nd that the Cas4-Cas1-Cas2 complex processes single-stranded DNA provided in cis or in trans with a d

160 pecifically interacts with RecA filaments on single-stranded DNA (RecA*).

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

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

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

164 d complex thereafter nonspecifically cleaves single-stranded DNA reporter probes labeled with a fluor

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

166 ng of layered rGO and rGO/gold nanoparticles/single stranded DNA (rGO/AuNPs/ssDNA) composites over PE

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

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

169 lthough a UvrD monomer can translocate along single-stranded DNA, self-assembly or interaction with a

170 Here we describe a kethoxal-assisted single-stranded DNA sequencing (KAS-seq) approach, based

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

172 eavage can be rapidly digested by a 3' to 5' single-stranded DNA-specific exonuclease, indicating Cas

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

174 We create single stranded DNA (ssDNA) donors using PCR and add 100

175 ine nucleotides, generating deoxyuridine, in single stranded DNA (ssDNA) intermediates produced durin

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

177 becomes activated and degrades a fluorescent single stranded DNA (ssDNA) reporter present in the assa

178 hanistic understanding of Sgs1 activities on single stranded DNA (ssDNA), which is a central intermed

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

180 eation rate of ScDmc1 results from its lower single-stranded DNA (ssDNA) affinity, compared to that o

181 ATPases, which form a helical filament with single-stranded DNA (ssDNA) and ATP.

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

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

184 by hyperphosphorylation of RPA, a sensor of single-stranded DNA (ssDNA) and DNA replication stress.

185 The free-solution mobilities of small single-stranded DNA (ssDNA) and double-stranded DNA (dsD

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

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

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

189 he AID/APOBEC enzymes deaminate cytosines in single-stranded DNA (ssDNA) and play key roles in innate

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

191 replication by excising oxidized bases from single-stranded DNA (ssDNA) and unhooking interstrand cr

192 ere, three different methods that can detect single-stranded DNA (ssDNA) are utilized to identify the

193 r-SWNT hybrids with a periodically sequenced single-stranded DNA (ssDNA) as anchoring phases.

194 loading of Redbeta directly onto the initial single-stranded DNA (ssDNA) at a 3'-overhang, and second

195 The XPA protein functions together with the single-stranded DNA (ssDNA) binding protein RPA as the c

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

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

198 d-specific excision that begins at a distant single-stranded DNA (ssDNA) break and proceeds back past

199 ing that Exo1 can digest a randomly selected single-stranded DNA (ssDNA) but not a poly(dT) oligonucl

200 hemically, human RAD51 polymerises faster on single-stranded DNA (ssDNA) compared to double-stranded

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

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

203 APOBEC3G (A3G) is a single-stranded DNA (ssDNA) cytosine deaminase that can

204 atalytic polypeptide-like (APOBEC) family of single-stranded DNA (ssDNA) cytosine deaminases provides

205 iency virus type 1 (HIV-1) infectivity, is a single-stranded DNA (ssDNA) deoxycytidine deaminase with

206 luorescent sensor array made of aptamers and single-stranded DNA (ssDNA) dyes for multiplexed detecti

207 f a DSB, controlling the formation of the 3' single-stranded DNA (ssDNA) filament needed for recombin

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 about evolutionary processes in viruses with single-stranded DNA (ssDNA) genomes.

211 dimeric protein that potentially binds with single-stranded DNA (ssDNA) in a manner similar to human

212 n is a highly dynamic process that generates single-stranded DNA (ssDNA) in the genome as 'transcript

213 Accumulation of single-stranded DNA (ssDNA) in the lagging-strand templa

214 induces the generation of large stretches of single-stranded DNA (ssDNA) intermediates that are rapid

215 mportant DNA metabolic events by stabilizing single-stranded DNA (ssDNA) intermediates, activating th

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

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

218 coupled with a gold substrate can resolve a single-stranded DNA (ssDNA) molecule with a spatial reso

219 Single-stranded DNA (ssDNA) molecules in solution typica

220 There is increasing demand for single-stranded DNA (ssDNA) of lengths >200 nucleotides

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

222 nds of linear chromosomes and terminate in a single-stranded DNA (ssDNA) overhang recognized by POT1-

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

224 process (resect) the free DNA ends to expose single-stranded DNA (ssDNA) overhangs.

225 In the marine environment, only a few lytic single-stranded DNA (ssDNA) phages have been isolated an

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

227 in models containing up to 1-kb inserts when single-stranded DNA (ssDNA) repair templates are supplie

228 A synthetic GAPDH single-stranded DNA (ssDNA) standard was used to calibra

229 ceeds via binding of RPA, RAD51, and DMC1 to single-stranded DNA (ssDNA) substrates created after for

230 often begins with creation of initiating 3' single-stranded DNA (ssDNA) tails on each side of a doub

231 anded break ends resection that generates 3' single-stranded DNA (ssDNA) tails.

232 The LSPR chip was functionalized with single-stranded DNA (ssDNA) template (T30), spaced with

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

234 tly, we find no evidence for BLM activity on single-stranded DNA (ssDNA) that is bound by replication

235 and lagging strands leads to accumulation of single-stranded DNA (ssDNA) that promotes mutation.

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

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

238 helicase activity, ScPif1 is also known as a single-stranded DNA (ssDNA) translocase, while how ScPif

239 Single-stranded DNA (ssDNA) viruses appear to blend both

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

241 Geminiviruses are single-stranded DNA (ssDNA) viruses that infect a wide r

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

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

244 Scalable production of kilobase single-stranded DNA (ssDNA) with sequence control has ap

245 Csm can cleave RNA and single-stranded DNA (ssDNA), but whether it targets one

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

247 t of DNA-RNA hybridization and the displaced single-stranded DNA (ssDNA), have been identified in bac

248 ) for the label-free electrical detection of single-stranded DNA (ssDNA), in-solution- and on-chip-hy

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

250 ins engineered for large-scale production of single-stranded DNA (ssDNA), we probed the substrate spe

251 py structure of human CST bound to telomeric single-stranded DNA (ssDNA), which assembles as a decame

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

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

254 Mitochondrial single-stranded DNA (ssDNA)-binding proteins (mtSSBs) ar

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

256 In this process, a single-stranded DNA (ssDNA)-RecA nucleoprotein filament

257 is a bifunctional enzyme that contains both single-stranded DNA (ssDNA)-specific nuclease and motor

258 nd processes these lesions in the context of single-stranded DNA (ssDNA).

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

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

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

262 on to GQD surfaces, with a specific focus on single-stranded DNA (ssDNA).

263 e resected in a 5'->3' direction, generating single-stranded DNA (ssDNA).

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

265 SCNT decreased in order with the binding of single-stranded DNA (SSDNA, probe DNA) and double-strand

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

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

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

269 esection of broken ends to generate long, 3' single-stranded DNA tails, annealing of complementary se

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

271 ial signal was generated by hybridization of single stranded DNA targets to immobilized recognition p

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

273 res formed by an RNA:DNA hybrid and unpaired single-stranded DNA that represent a source of genomic i

274 We show here that Pol31-Pol32 binds single-stranded DNA that we propose underlies polymerase

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

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

277 condary structure from typical B-form DNA to single-stranded DNA to G-quadruplexes.

278 OBEC3A, an enzyme that converts cytosines in single-stranded DNA to uracil, and mutations in a variet

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

280 ibute to electrical signal modulation during single-stranded DNA translocation.

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

282 s endocytose Pf, and internalization of this single-stranded DNA virus results in phage RNA productio

283 ) and Minute Virus of Mice (MVM), both T = 1 single stranded DNA viruses, and Bromo Mosaic Virus (BMV

284 Single-stranded DNA viruses are, however, highly diverse

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

286 19) uncover a previously undefined family of single-stranded DNA viruses, Redondoviridae, in human or

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

288 een classified as a family of small circular single-stranded DNA viruses.

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

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

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

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

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

294 an entry site for Exo1 in vitro to generate single-stranded DNA, which would be susceptible to both

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

296 As artificial RNA oligonucleotides or single-stranded DNA with receptor and catalytic characte

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

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

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

300 A Polymerase Cofactor), preferentially binds single-stranded DNA, yet contains a structural fold dist