ライフサイエンスコーパス: single-strand DNA

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

2 ry likely to lower the affinity of SSBP1 for single-strand DNA.

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

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

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

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

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

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

9 TPase that forms a nucleoprotein filament on 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 ed through pH-assisted thiol-gold bonding of single stranded DNA and salt aging, with preconjugated b

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

19 RPA-like complex that associates with G-rich single-strand DNA and helps resolve replication problems

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 atalyze DNA strand exchange, and it mediates single-strand DNA annealing.

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

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

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

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 The herpes simplex virus (HSV) single-strand DNA binding protein (SSB), ICP8, is the ce

50 Single-strand DNA binding protein did not affect PcrA tr

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

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

53 part of a basic patch that is essential for single-strand DNA binding.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 plementing 1 (XRCC1) are key proteins in the single-strand DNA break repair pathway.

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

88 ally deliver essential factors for repair of single-strand DNA breaks in replication regions.

89 Here, we demonstrate that single-strand DNA breaks induced by the L1 endonuclease

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

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

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

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

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

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

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

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

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

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

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

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

102 d and robust quantification of type-specific single-strand DNA damage.

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

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

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

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

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

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

109 DNA excision by Exo1, which causes increased single-strand DNA formation, RPA exhaustion, DNA breaks,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

133 DSB resection generates a single strand DNA intermediate, which is crucial for the

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

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

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

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

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

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

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

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

142 our analysis to study the kinetics of human single-strand DNA nuclease TREX2, DNA polymerases, RNA,

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

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

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

146 application for precise genome editing using single strand DNA oligonucleotides and show that an effi

147 Single-stranded DNA oligonucleotides have unique, and in

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

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

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

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

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

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

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

155 A break ends must first be processed into 3' single-strand DNA overhangs.

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

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

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

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

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

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

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

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

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

165 egrases innovated from double-strand- toward single-strand-DNA recombination through the acquisition

166 vity with various asymmetrical trade-offs in single-strand-DNA recombination.

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

168 ination with paper-based electrodes, using a single strand DNA relative to H1047R (A3140G) missense m

169 ocesses after cisplatin treatment, including single-strand DNA repair and Fanconi anemia pathways, su

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

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

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

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

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

175 nduced by CRISPR/Cas9, as well as individual single-strand DNA scissions induced by the nickase versi

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

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

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

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

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

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

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

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

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

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

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

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

188 DNA aptamers are single-strand DNA (ssDNA) capable of selectively and tig

189 red in several cancer genomes were linked to single-strand DNA (ssDNA) intermediates in various proce

190 lex DNAs before and after cleavage of the 5' single-strand DNA (ssDNA) tail by the AdnA nuclease.

191 one Zf-GRF motif mediating interaction with single-strand DNA (ssDNA), whereas the major AP endonucl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

271 site pocket suggests a binding site for the single-strand DNA substrate.

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

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

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

275 he absence of dNTPs, this leads to excessive single-strand DNA that exceeds the protective capacity o

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

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

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

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

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

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

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

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

284 the entropy associated with straightening of single-strand DNA upon nucleoprotein filament formation.

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

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

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

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

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

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

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

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

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

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

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

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

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

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