ライフサイエンスコーパス: double-stranded DNA

1 charomyces cerevisiae Pif1 can unwind dsDNA (double-stranded DNA).

2 e of introducing sequence specific breaks in double stranded DNA.

3 H1 association with mononucleosomes or bare double stranded DNA.

4 breaks or alkali-labile lesions in single or double stranded DNA.

5 by ATP, which allows efficient processing of double-stranded DNA.

6 les that are mixtures of single-stranded and double-stranded DNA.

7 on the transition of single-stranded DNA to double-stranded DNA.

8 53, which binds to specific DNA sequences on double-stranded DNA.

9 n guanine bases in either single-stranded or double-stranded DNA.

10 helicase domains bind tightly to single- and double-stranded DNA.

11 ng CMGs pass one another and dissociate from double-stranded DNA.

12 rate single-stranded DNA but largely exclude double-stranded DNA.

13 d on non-specific Rad51 binding to undamaged double-stranded DNA.

14 its of Cascade that are critical for binding double-stranded DNA.

15 on of viral core DNA and, in particular, the double-stranded DNA.

16 coherent and incoherent processes coexist in double-stranded DNA.

17 enables the translocation and processing of double-stranded DNA.

18 4) complex formation immediately adjacent to double-stranded DNA.

19 ate hydrolysis-dependent translocation along double-stranded DNA.

20 ble an Mcm2-7 double-hexamer around adjacent double-stranded DNA.

21 f potato is further able to bind and distort double-stranded DNA.

22 y structure which appears capable of binding double-stranded DNA.

23 y displaced one nucleotide when encountering double-stranded DNA after filling a gap or nicked DNA.

24 hed amphiphilic peptides that associate with double stranded DNA and promote in vitro transfection of

25 In comparison with conventional double stranded DNA and with antiparallel DNA double cro

26 oprotein C1/C2 (hnRNPC1/C2) can also bind to double-stranded DNA and function in trans as a vitamin D

27 e CTM domain) that binds efficiently to both double-stranded DNA and G-quadruplex (G4) DNA.

28 ether CMG translocation occurs on single- or double-stranded DNA and how ATP hydrolysis drives DNA un

29 dro-2'-deoxyguanine (8-oxoG) often occurs in double-stranded DNA and poses a threat to genomic integr

30 d by immunofluorescence antibody staining in double-stranded DNA and positive-strand RNA virus infect

31 psid shell, must be reverse transcribed into double-stranded DNA and released from the capsid (in a p

32 Double-stranded DNA and RNA adopt different helical conf

33 tor domains are specifically adapted to bind double-stranded DNA and to facilitate DNA sliding via a

34 facilitation of primer strand invasion into double-stranded DNA, and a suppression of non-homologous

35 lanoma 2 (AIM2) inflammasome is activated by double-stranded DNA, and AIM2 expression is reduced in s

36 igher in single-stranded DNA (ssDNA) than in double-stranded DNA, and copying the resulting uracils c

37 ystal structures of cyclic GMP-AMP synthase, double-stranded DNA, and inhibitors within the enzymatic

38 n of our method using the known structure of double-stranded DNA as a benchmark, resolve 10-base-pair

39 ting such models have been reported that use double-stranded DNA as donors, but their efficiency is t

40 The assay utilized a dually labeled double-stranded DNA as the reporter probe.

41 Genome editing by Cas9, which cleaves double-stranded DNA at a sequence programmed by a short

42 sent a method that can be used to solubilize double-stranded DNA at high concentrations in organic me

43 assembly of head-to-head CMGs that encircle double-stranded DNA at the origin, the two CMGs must pas

44 Importantly, it renders the labeled double-stranded DNA available in long intact stretches f

45 hermore, our data indicate that the entry of double-stranded DNA beyond a short threshold distance fr

46 Specifically, the N-terminal double-stranded DNA binding functions of Hop2 and Mnd1 c

47 that provides insight into the mechanism of double-stranded DNA binding.

48 Budding yeast Rap1 is a specific double-stranded DNA-binding protein involved in repressi

49 ted T helper 17 cell differentiation through double-stranded DNA break (DSB) and ASC-mediated inflamm

50 recombination (HR) is a crucial pathway for double-stranded DNA break (DSB) repair.

51 al chromatin organization before and after a double-stranded DNA break (DSB), to estimate the level o

52 striction sites as non-self and introduces a double-stranded DNA break [3].

53 and replication fork restart, prevention of double-stranded DNA break formation, and avoidance of re

54 A-dependent protein kinase (DNA-PK) mediates double-stranded DNA break repair, V(D)J recombination an

55 is a DNA helicase/nuclease that functions in double-stranded DNA break repair.

56 ast DNAs insert into nuclear genomes through double-stranded DNA break repair.

57 nce with either event protects bacteria from double-stranded DNA breakage and TLD.

58 t during homologous recombination, repair of double stranded DNA breaks, and integron recombination.

59 Recognition and repair of double-stranded DNA breaks (DSB) involves the targeted r

60 F, XPC and AP-endonuclease-1), and repair of double-stranded DNA breaks (homologs of BRCA2, XRCC3, KU

61 Unrepaired DNA lesions, such as single- and double-stranded DNA breaks (SSBs and DSBs), and single-s

62 various stressors, such as for the repair of double-stranded DNA breaks and protein quality control,

63 CD complex, which acts in both the repair of double-stranded DNA breaks and the degradation of bacter

64 pyogenes (SpCas9) is more active in creating double-stranded DNA breaks at 37 degrees C than at 22 de

65 gous recombination compete for the repair of double-stranded DNA breaks during the cell cycle.

66 In bacterial cells, processing of double-stranded DNA breaks for repair by homologous reco

67 non-homologous end-joining (NHEJ) repair of double-stranded DNA breaks generated by Cas9 are much le

68 Cas9 can be reprogrammed to create specific double-stranded DNA breaks in the genomes of a variety o

69 Here we introduced double-stranded DNA breaks into the nuclear genome of to

70 In bacteria, the repair of double-stranded DNA breaks is modulated by Chi sequences

71 cycle progression through mitosis following double-stranded DNA breaks leads to the formation of mic

72 antage that it does not require formation of double-stranded DNA breaks or provision of a donor DNA t

73 hat the two regions differ in the density of double-stranded DNA breaks that are generated.

74 aks resulted in the generation of persistent double-stranded DNA breaks was found to be a primary cau

75 the BNP-based sunblock significantly reduced double-stranded DNA breaks when compared with a commerci

76 r growth by causing apoptotic cell death via double-stranded DNA breaks while causing a remodeling of

77 colibactin, a genotoxic molecule(s) causing double-stranded DNA breaks(4) and enhanced colorectal ca

78 ed replication forks, insufficient repair of double-stranded DNA breaks, and improper segregation of

79 etabolism, archazolid caused S-phase arrest, double-stranded DNA breaks, and p53 stabilization, leadi

80 et (UV)-C radiation and reagents that induce double-stranded DNA breaks, but exhibit normal responses

81 g cellular metabolism; these lesions include double-stranded DNA breaks, daughter-strand gaps, and DN

82 BRCA1 has no equivalent role at chromosomal double-stranded DNA breaks, indicating that tandem dupli

83 Although fluoroquinolones stabilize double-stranded DNA breaks, the antibacterial thiophenes

84 ls by inhibiting topoisomerases and inducing double-stranded DNA breaks.

85 gether with experimentally induced telomeric double-stranded DNA breaks.

86 on, and is a major pathway for the repair of double-stranded DNA breaks.

87 sions, small duplications, and generation of double-stranded DNA breaks.

88 Cas9 as an RNA-guided nuclease that creates double-stranded DNA breaks.

89 , suggests sequence capture during repair of double-stranded DNA breaks.

90 converting single-stranded DNA lesions into double-stranded DNA breaks.

91 Mre11 and Rad50 to coordinate the repair of double-stranded DNA breaks.

92 n a large set of 438 GQ forming sequences in double-stranded DNA by integrating fluorescence measurem

93 g specific sequences along the backbone of a double-stranded DNA carrier.

94 sembly and utilization of a surface-attached double-stranded DNA catenane composed of two intact inte

95 While CRISPR/Cas9 executes double-stranded DNA cleavage efficiently, closure of the

96 ersion of one base pair into another without double-stranded DNA cleavage, excess stochastic insertio

97 ion of all four transition mutations without double-stranded DNA cleavage.

98 of the single stranded viral RNA genome into double-stranded DNA, competent for host-cell integration

99 cruitment domain) pyrin domain and the IFI16-double stranded DNA complex has established that the for

100 ional and linear joints that integrate stiff double-stranded DNA components and flexible single-stran

101 e complex for telomeric quadruplex DNA and a double-stranded DNA control.

102 everse transcribe its RNA genome to create a double-stranded DNA copy and then integrate this viral D

103 Upon binding double-stranded DNA, cyclic GMP-AMP synthase synthesizes

104 This enzyme is a double-stranded DNA-dependent ATPase and chromatin remod

105 mouse cytomegalovirus (MCMV) or transfected double-stranded DNA did not require IRF1.

106 n done for the manipulation of most abundant double-stranded DNA (ds-DNA) motifs.

107 report on e.g., the conformational state of double stranded DNA (dsDNA) following its interaction wi

108 via the solid-phase hybridisation, a 144-bp double stranded DNA (dsDNA) was then detected directly u

109 hematosus (SLE), IgE antibodies specific for double-stranded DNA (dsDNA) activated plasmacytoid dendr

110 an be adapted for sequencing via ligation of double-stranded DNA (dsDNA) adapters.

111 flict with each other: i) the impact of anti-double-stranded DNA (dsDNA) antibodies that cross-react

112 ently repressed to prevent the generation of double-stranded DNA (dsDNA) breaks in cycling large pre-

113 Double-stranded DNA (dsDNA) can trigger the production o

114 Double-stranded DNA (dsDNA) cleavage by Cas9 is a hallma

115 ing via homology-directed repair (HDR) after double-stranded DNA (dsDNA) cleavage facilitates functio

116 We demonstrate that, unlike double-stranded DNA (dsDNA) donors with central heterolo

117 cant correlation between the release of host double-stranded DNA (dsDNA) following rhinovirus infecti

118 the inner core of adenovirus containing its double-stranded DNA (dsDNA) genome and associated protei

119 Each strain encodes a 9.8- to 9.9-kb linear double-stranded DNA (dsDNA) genome with large inverted t

120 Translocation of viral double-stranded DNA (dsDNA) into the icosahedral prohead

121 ection of circulating autoantibodies against double-stranded DNA (dsDNA) is used in the diagnosis of

122 that BLM localizes in the vicinity of ssDNA/double-stranded DNA (dsDNA) junction and reels in the ss

123 d to bind RNA in addition to their canonical double-stranded DNA (dsDNA) ligand.

124 the dimerized protein complex to bind to two double-stranded DNA (dsDNA) molecules.

125 So far, only double-stranded DNA (dsDNA) over 40 base pairs (bp) in l

126 e mechanism studies on spCas9-sgRNA-mediated double-stranded DNA (dsDNA) recognition and cleavage, it

127 rategies that enable recognition of specific double-stranded DNA (dsDNA) regions has been a longstand

128 olves direct interactions between homologous double-stranded DNA (dsDNA) segments.

129 onjugate accumulation was dependent upon the double-stranded DNA (dsDNA) sensor cyclic GMP-AMP syntha

130 We show that dissociation of Cas9 from double-stranded DNA (dsDNA) substrates is slow (lifetime

131 e can form a nucleoprotein filament (NPF) on double-stranded DNA (dsDNA) that is capable of unwrappin

132 cryo-EM), we show that the binding of target double-stranded DNA (dsDNA) to a type I-F CRISPR system

133 tion releases granule proteins together with double-stranded DNA (dsDNA) to form extracellular fibers

134 DNA helicases are motor proteins that unwind double-stranded DNA (dsDNA) to reveal single-stranded DN

135 termination of the complete 70.8-kb circular double-stranded DNA (dsDNA) viral genome content, and id

136 related icosahedral capsids that encase the double-stranded DNA (dsDNA) viral genome.

137 Here, we use quantitative double-stranded DNA (dsDNA) viral-fraction metagenomes (

138 Bacteriophage P22, a double-stranded DNA (dsDNA) virus, has a nonconserved 12

139 ies to prevent active infection with certain double-stranded DNA (dsDNA) viruses after allogeneic hem

140 Human adenoviruses (Ad) are double-stranded DNA (dsDNA) viruses associated with infe

141 Ascoviruses are double-stranded DNA (dsDNA) viruses that attack caterpil

142 mine (T)) on single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA) with acetone, ethanol, H2S a

143 pgRNA is then reverse transcribed to double-stranded DNA (dsDNA) within the capsid.

144 The ability to directly detect double-stranded DNA (dsDNA) without sequence-preference

145 u magnetic nanoparticles functionalized with double-stranded DNA (dsDNA), a sequence of the breast ca

146 hat is initiated upon cytosolic detection of double-stranded DNA (dsDNA), but how dsDNA is detected i

147 ost lupus patients develop autoantibodies to double-stranded DNA (dsDNA), but the source of DNA antig

148 dynamics, the division between the rates of double-stranded DNA (dsDNA), single-stranded RNA (ssRNA)

149 nsible for pairing the ssDNA with homologous double-stranded DNA (dsDNA), which serves as the templat

150 nt elucidation of the mechanism of the viral double-stranded DNA (dsDNA)-packaging motor with sequent

151 ed on aqueous gold nanoparticles (AuNPs) and double-stranded DNA (dsDNA).

152 tection of human clinical samples comprising double-stranded DNA (dsDNA).

153 SWNTs with single-stranded DNA (ssDNA) than double-stranded DNA (dsDNA).

154 Once the filament is formed, it interrogates double-stranded DNA (dsDNA).

155 red by host defenses that detect cytoplasmic double-stranded DNA (dsDNA).

156 plex led to the release of the AuNPs-S2 from double-stranded DNA(dsDNA) and the recovery of the ECL s

157 robe (single stranded DNA-ssDNA) and hybrid (double stranded DNA-dsDNA) both via 3-NT reduction and g

158 At these double-stranded DNA ends, RarA couples the energy of ATP

159 genetic transfer by producing recombinogenic double-stranded DNA ends.

160 s stimulated by single-stranded DNA gaps and double-stranded DNA ends.

161 ctions, the viral genome is established as a double-stranded DNA episome.

162 ce) facilitates the crRNA-guided invasion of double-stranded DNA for complementary base-pairing with

163 g in aqueous solutions of monodisperse stiff double-stranded DNA fragments is known not to occur, des

164 nthetic DNA, through the in vivo excision of double-stranded DNA from an episomal replicon by CRISPR/

165 ination events are associated with repair of double-stranded DNA gaps and/or involve Mlh1-independent

166 Poxviridae are viruses with a large linear double-stranded DNA genome coding for up to 250 open rea

167 illus subtilis phage whose uracil-containing double-stranded DNA genome encodes distant homologs of b

168 phage, the DNA packaging nanomotor packs its double-stranded DNA genome into the virus capsid.

169 We show that the end of the phi812 double-stranded DNA genome is bound to one protein subun

170 The double-stranded DNA genome is covalently circularized at

171 The duplication of the poxvirus double-stranded DNA genome occurs in cytoplasmic membran

172 ith T=13 icosahedral geometry and encloses a double-stranded DNA genome that measures 121kbp.

173 enovirus (HAdV), a medium-sized virus with a double-stranded DNA genome, needs to be identified.

174 ruses, which we denote magroviruses, possess double-stranded DNA genomes of 65 to 100 kilobases in si

175 needed for expression and synthesis of their double-stranded DNA genomes.

176 Although the large-scale separation of double-stranded DNA has been studied with a variety of t

177 inner cavity, large enough to accommodate a double-stranded DNA helix, as well as a protruding Tower

178 lore melting properties for short (</=50 bp) double-stranded DNA homopolymers.

179 9 endonuclease for introducing breaks in the double-stranded DNA identified by the gRNA.

180 bulins (especially IgM, P < .0001), and anti-double-stranded DNA IgG (P < .05).

181 The interaction of single- and double-stranded DNA immobilized onto morphologically dif

182 spired by homology dependent pairing between double stranded DNA in bacteria.

183 It not only senses DNA damage, binds double-stranded DNA in a sequence-independent manner, fa

184 on) to analyze the differential stability of double-stranded DNA in complex with either cisplatin or

185 We demonstrate that RarA binds to double-stranded DNA in its ATP-bound state and single-st

186 TRIM29 is also highly induced by cytosolic double-stranded DNA in myeloid dendritic cells.

187 We apply this method to double-stranded DNA in vitro and microtubules and actin

188 complex shows reduced binding to single- and double-stranded DNA in vitro relative to wild-type MRX,

189 The latter allows MjAgo to process long double-stranded DNAs, including circular plasmid DNAs an

190 hich preferentially bind the minor groove of double-stranded DNA, inhibit vaccinia virus infection by

191 r using a custom synthesized ferrocenyl (Fc) double-stranded DNA intercalator as a redox marker is pr

192 Double-stranded DNA is a locally inflexible polymer that

193 e difference in affinity between single- and double-stranded DNA is minor.

194 To quantify ligand binding, double-stranded DNA is stretched with optical tweezers a

195 The double-stranded DNA is tightly packed in the capsid as a

196 P-AMP synthase (cGAS), a cytosolic sensor of double-stranded DNA, is activated in autoinflammatory di

197 finely designing the curvature and torsion, double-stranded DNA knots were accessed by hybridizing a

198 The final produced long nicked double-stranded DNA loses the ability to protect AgNPs f

199 tes DNA topology by transiently breaking one double-stranded DNA molecule (cleavage), allowing a seco

200 s (Cas) that utilize RNA to find and cut the double-stranded DNA molecules at specific locations.

201 Using short double-stranded DNA molecules internally labelled with t

202 ombination, in which the repair of breaks in double-stranded DNA molecules is taking place with a hel

203 f the resulting diffusion coefficients using double-stranded DNA molecules ranging in size from 20 to

204 asmid with the products annealing to produce double-stranded DNA molecules with 5'-overhangs.

205 l plastid (chloroplast) genomes are circular double-stranded DNA molecules, typically between 100 and

206 bridging, condensation, and pairing between double-stranded DNA molecules.

207 Hop1-promoted intermolecular pairing between double-stranded DNA molecules.

208 linear HCR is a hairpin-free system in which double-stranded DNA monomers could dendritically assembl

209 Due to the linear double-stranded DNA nature of the adenovirus genome, the

210 Nucleosomes, double-stranded DNA, neutrophil elastase, myeloperoxidas

211 ative DNA-binding domain, selectively senses double-stranded DNA of at least 40 base pairs in length

212 e analyze smFRET data of structurally rigid, double-stranded DNA-oligonucleotides in aqueous buffer a

213 and chromosomal gene conversion with either double-stranded DNA or single-stranded oligonucleotide d

214 y transferred in trans from ssNucs to either double-stranded DNA or ssDNA.

215 action of cauliflower mosaic virus (CaMV), a double-stranded DNA pararetrovirus, with the model plant

216 In the double-stranded DNA phages and herpesviruses, this is ac

217 Although varphi29 differs from other double-stranded DNA phages in having an RNA motor compon

218 s for T4, we show how the energetic costs of double-stranded DNA phages scale with the capsid size, r

219 ever, the assigned viruses were dominated by double-stranded DNA phages, and sequences associated wit

220 ages from all three major families of tailed double-stranded DNA phages.

221 are studied as models for viruses containing double-stranded DNA (polymer) and condensing proteins (p

222 canonical 2'-deoxyribonucleosides) stabilize double-stranded DNA, RNA, and DNA-RNA hybrids with antip

223 As scaffold, we employed a double-stranded DNA rotaxane for its ability to undergo

224 ulator of interferon genes, a key adaptor in double-stranded DNA-sensing pathway, followed by its rap

225 Here, we show that mice deficient in the double-stranded DNA sensor AIM2 are protected from both

226 ize the replication origin (oriC) by binding double-stranded DNA sequences (DnaA-boxes); subsequently

227 as9-guide RNA complexes recognize and cleave double-stranded DNA sequences on the basis of 20-nucleot

228 PR)-associated 9 (Cas9) endonuclease cleaves double-stranded DNA sequences specified by guide RNA mol

229 We find that double-stranded DNA stimulates ATP hydrolysis by hMRN ov

230 Here we show that guanine (G) runs in double-stranded DNA support delocalization over 4-5 guan

231 es with a CRISPR RNA (crRNA) and cleaves the double-stranded DNA target complementary to the crRNA gu

232 proceed with an analytical sensitivity of 1 double-stranded DNA target copy.

233 ree proteins to achieve crRNA maturation and double-stranded DNA target recognition.

234 competent structure that is poised to engage double-stranded DNA target sequences.

235 Escherichia coli Cascade bound to a foreign double-stranded DNA target.

236 iosensor platform starting from an initially double-stranded DNA target.

237 NA guides to cleave both single stranded and double stranded DNA targets, and does not utilize RNA as

238 n bound to CRISPR RNA (crRNA), can recognize double-stranded DNA targets and recruit the Cas3 nucleas

239 The RNA-guided Cpf1 nuclease cleaves double-stranded DNA targets complementary to the CRISPR

240 The RNA-guided endonuclease Cas9 cleaves double-stranded DNA targets complementary to the guide R

241 The RNA-guided DNA endonuclease Cas9 cleaves double-stranded DNA targets with a protospacer adjacent

242 plex with a single guide RNA (sgRNA) and its double-stranded DNA targets, containing the 5'-TTGAAT-3'

243 nuclease active sites in the degradation of double-stranded DNA targets.

244 correction is more efficient when using long double-stranded DNA than single- or double-stranded olig

245 t single-stranded RNA of the viral genome to double-stranded DNA that is then integrated into the DNA

246 genome of HIV-1 is reverse transcribed into double-stranded DNA that ultimately integrates into the

247 ll lines (A375 and HCT116), interaction with double stranded DNA through in vitro assay, and molecula

248 that yeast TFIIH contains an Ssl2-dependent double-stranded DNA translocase activity.

249 unreported conductance states that occur as double-stranded DNA translocates through a 2.4 nm solid-

250 V E2.IMPORTANCE The papillomavirus (PV) is a double-stranded DNA tumor virus infecting cervix, mouth,

251 II CRISPR-Cas surveillance complexes target double-stranded DNA, type III complexes target single-st

252 ere obtained for smaller single-stranded and double-stranded DNA using the benzyltrioctylammonium bro

253 g either single-stranded oligonucleotides or double-stranded DNA vectors as repair templates yielded

254 rus (ASFV), is a highly structurally complex double stranded DNA virus.

255 Virophages are recently discovered double-stranded DNA virus satellites that prey on giant

256 Herpes simplex virus-1 (HSV-1) is a double-stranded DNA virus that causes life-long infectio

257 Human cytomegalovirus (HCMV) is an enveloped double-stranded DNA virus that causes severe disease in

258 Human cytomegalovirus (HCMV) is a large, double-stranded DNA virus that causes significant human

259 African swine fever virus, a double-stranded DNA virus that infects pigs, is the only

260 acmanvirus is a newly discovered icosahedral double-stranded DNA virus that was isolated from an envi

261 e fever virus (ASFV) is a highly pathogenic, double-stranded DNA virus with a marked tropism for cell

262 werful ATP-hydrolyzing motor, formed in many double-stranded DNA viruses by a complex of a small term

263 dataset to present a global map of abundant, double-stranded DNA viruses complete with genomic and ec

264 e complement of alpha-helical TM proteins in double-stranded DNA viruses infecting bacteria and archa

265 rtant aspect of viral particle stability for double-stranded DNA viruses is the energetically unfavor

266 and complex genomes make evolution in these double-stranded DNA viruses more efficient than that in

267 f small viruses than in the context of large double-stranded DNA viruses such as herpesviruses.

268 Polydnaviruses are large, double-stranded DNA viruses that are beneficial symbiont

269 Virophages are a unique group of circular double-stranded DNA viruses that are considered parasite

270 Papillomaviruses (PVs) are small, double-stranded DNA viruses that are responsible for cer

271 simplex virus 1 (HSV-1) and HSV-2 are large, double-stranded DNA viruses that cause lifelong persiste

272 Papillomaviruses are small, double-stranded DNA viruses that encode the E2 protein,

273 s) are an ancient and heterogeneous group of double-stranded DNA viruses that preferentially infect t

274 steric regulatory mechanism we report allows double-stranded DNA viruses to achieve rapid, high-densi

275 e that Epstein-Barr virus and possible other double-stranded DNA viruses use TRIM29 to suppress local

276 g been thought that the genetic diversity of double-stranded DNA viruses was generated over long peri

277 ighlight the emergence of previously unknown double-stranded DNA viruses which delineate and extend t

278 Many double-stranded DNA viruses which parasitize such hosts,

279 For many double-stranded DNA viruses, confinement of the large DN

280 During assembly, double-stranded DNA viruses, including bacteriophages an

281 ckaging is strongly conserved in the complex double-stranded DNA viruses, including the herpesviruses

282 Many double-stranded DNA viruses, such as Epstein-Barr virus,

283 Unlike double-stranded DNA viruses, which pump their genome int

284 jelly-roll protein that can be found in many double-stranded DNA viruses.

285 s has advanced to largely take over study of double-stranded DNA viruses.

286 e as genome packaging motors in many complex double-stranded DNA viruses.

287 conformationally constrained acpcPNA probes, double stranded DNA was detected sensitively and specifi

288 fficient fluorescent labelling of single and double-stranded DNA was carried out using dyes functiona

289 nst autoantigens, such as thyroperoxidase or double-stranded DNA, whereas other patients make IgG aut

290 n, the viral RNA is reverse transcribed into double-stranded DNA, which is then incorporated into hos

291 erase binds to the -12T base pair as part of double-stranded DNA while opening base pairs from -11A t

292 ity to telomeric DNA substrates comprised of double-stranded DNA with a 3' single-stranded extension.

293 ApoE4 undergoes nuclear translocation, binds double-stranded DNA with high affinity (low nanomolar),

294 d 3-way junction rather than with single- or double-stranded DNA with overhangs.

295 Targeting and invading double-stranded DNA with synthetic oligonucleotides unde

296 in vitro CPD lesions in single-stranded and double-stranded DNA with the same efficiency.

297 ct a single DNA-nanogold conjugate, an 84-bp double-stranded DNA with two 5-nm nanogold particles for

298 ckage the pgRNA and reverse transcribe it to double-stranded DNA within capsids.

299 SE1/NSE3/NSE4 sub-complex of SMC5/6 binds to double-stranded DNA without any preference for DNA-repli

300 ) contain large numbers of repeats that bind double-stranded DNA, wrapping around DNA to form a conti