ライフサイエンスコーパス: double-stranded DNA

1 termined positions on the backbone of native double-stranded DNA.

2 racellular innate immune sensor that detects double-stranded DNA.

3 ICP4 is a viral nucleoprotein which binds double-stranded DNA.

4 echanisms operate only when the damage is in double-stranded DNA.

5 n transfer through (or from) electrode-bound double-stranded DNA.

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

7 logously to the nucleosome's organization of double-stranded DNA.

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

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

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

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

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

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

14 omote extensive and reversible compaction of double-stranded DNA.

15 sult in the formation of physical defects in double-stranded DNA.

16 le at joint molecule structures and adjacent double-stranded DNA.

17 uclease to introduce site-specific breaks in double-stranded DNA.

18 bqp)(2)](2+) with i-motif, G-quadruplex, and double-stranded DNA.

19 olocalizing with cGAS, which is activated by double-stranded DNA.

20 scence quenching to detect unpaired bases in double-stranded DNA.

21 ith similar efficiencies in both single- and double-stranded DNA, 1-methyladenine is preferentially r

22 iotic recombination intermediates by nicking double-stranded DNA adjacent to the junction points(9).

23 r the cytoplasm by electrostatically linking double-stranded DNA and 70S-polysomes.

24 oacervate droplets prepared from mixtures of double-stranded DNA and an azobenzene cation.

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

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

27 Alpha-synuclein binds double-stranded DNA and helps to facilitate the non-homo

28 terminal domain displays strong affinity for double-stranded DNA and is sufficient for the accumulati

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

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

31 Double-stranded DNA and RNA adopt different helical conf

32 stinguishable fluorescence upon binding with double-stranded DNA and single-stranded RNA in live cell

33 shishijimicin A binds to the minor groove of double-stranded DNA and that its beta-carboline moiety p

34 king and unstacking reactions in single- and double-stranded DNA and thus may help to define the mole

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

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 with the presence of pathogenic anti-dsDNA (double-stranded DNA) antibodies, and provided spontaneou

39 Formation of TLS was found in anti-double-stranded DNA antibody-positive mice, and the stru

40 Double-stranded DNAs are usually present in the form of

41 n remodelers are ATP-driven motors that pump double-stranded DNA around the histone core of the nucle

42 fluorescence which was slightly enhanced in double-stranded DNA as compared to single-stranded oligo

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

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

45 Tailed, double-stranded DNA bacteriophages provide a well-charac

46 During morphogenesis of double-stranded DNA bacteriophages, a molecular motor dr

47 for the capsid shell assembly of many tailed double-stranded DNA bacteriophages, some archaeal viruse

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

49 hich uses unique structures for programmable double-stranded DNA binding and cleavage.

50 High-affinity nucleosome binding blocks double-stranded DNA binding and maintains cGAS in an ina

51 ed that both affect the dynamic features and double-stranded DNA binding properties of Mre11, but in

52 with RNA (coacervates) to avid and specific double-stranded DNA binding.

53 t, independently of its nucleotide sequence, double-stranded DNA binds to a specific helix of the vWF

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

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

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

57 method, which predicts the extent to which a double-stranded DNA break site will utilize the microhom

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

59 ubiquitin ligase is activated in response to double stranded DNA breaks (DSBs) where it mono-ubiquiti

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

61 In mammalian cells, double-stranded DNA breaks (DSBs) are preferentially rep

62 are particularly susceptible to formation of double-stranded DNA breaks (DSBs) arising from physiolog

63 and acceptor genomic sequences subjected to double-stranded DNA breaks (DSBs) made by programmable n

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

65 predictably and independent of Cas9-induced double-stranded DNA breaks (which causes substantial ind

66 esulted from nuclear entry by Dox, promoting double-stranded DNA breaks and apoptosis.

67 Depletion of WRN induced double-stranded DNA breaks and promoted apoptosis and ce

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

69 tumours are often deficient in the repair of double-stranded DNA breaks by homologous recombination(8

70 of linked loci is limited as multiple nearby double-stranded DNA breaks created by Cas9 routinely res

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

72 Although Cas9 efficiently induces double-stranded DNA breaks in the early embryo and male

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

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

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

76 CRISPR/Cas9 causes double-stranded DNA breaks that can undergo DNA repair e

77 gly, CSR induced by staggered but not blunt, double-stranded DNA breaks was impaired by SAMHD1 deplet

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

79 parallel with CRISPRi/a, which do not induce double-stranded DNA breaks, revealed that a distinct set

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

81 maternally or paternally derived and display double-stranded DNA breaks.

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

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

84 us for homology-directed DNA repair (HDR) of double-stranded DNA breaks.

85 se activity against both single-stranded and double-stranded DNA but not RNA under the conditions tes

86 Pfh1 from Schizosaccharomyces pombe, unwind double-stranded DNA by a branched mechanism with 2 modes

87 studies that reveal binding and scission of double-stranded DNA by shishijimicin A.

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

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

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

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

92 e that displays a stable product state after double-stranded-DNA cleavage.

93 how that its packaging series initiates with double-stranded DNA cleavages that are scattered across

94 -stranded DNA of various lengths and through double-stranded DNA containing oxidative damage.

95 resent the structure of CcrM in complex with double-stranded DNA containing the recognition sequence.

96 Coccolithoviruses (EhVs) are large, double-stranded DNA-containing viruses that infect the s

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

98 ranscribes its RNA genome and integrates the double-stranded DNA copy into a host cell chromosome.

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

100 a unique noncanonical role in regulating the double-stranded DNA damage response pathway through modu

101 tion of the AIM2 inflammasome in response to double-stranded DNA damage triggers the production of cy

102 To initiate replication on a double-stranded DNA de novo, all organisms require prima

103 The method relied on double stranded DNA (dsDNA) homology donors with ~1 kb h

104 nt depressants capable of rapidly denaturing double stranded DNA (dsDNA) linkers, and 8 compounds are

105 cal sensor for detection of acrylamide using double stranded DNA (dsDNA)/Hemoglobin (Hb)-modified scr

106 f single-stranded DNA (SSDNA, probe DNA) and double-stranded DNA (DSDNA) and that the ability of DSDN

107 Class-switched antibodies to double-stranded DNA (dsDNA) are prevalent and pathogenic

108 Tailed double-stranded DNA (dsDNA) bacteriophages, herpesviruse

109 uence homology, the major capsid proteins of double-stranded DNA (dsDNA) bacteriophages, some archaea

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

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

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

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

114 e-induced DNA adducts, can be converted to a double-stranded DNA (dsDNA) form by using appropriate tr

115 interferons (IFNs) and nucleosome-associated double-stranded DNA (dsDNA) fragments (nsDNA) are the ha

116 The simple 5.2-kbp double-stranded DNA (dsDNA) genome expresses just seven

117 TSPV1 packages an 18.65-kb linear double-stranded DNA (dsDNA) genome with 31 open reading

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

119 ) equal to 16-encapsidating a tightly packed double-stranded DNA (dsDNA) genome(1-3).

120 (ssDNA), in-solution- and on-chip-hybridized double-stranded DNA (dsDNA) has been studied.

121 ies of small single-stranded DNA (ssDNA) and double-stranded DNA (dsDNA) have been measured by capill

122 Cas12c, -h, and -i demonstrate RNA-guided double-stranded DNA (dsDNA) interference activity.

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

124 sport measurements through single 30-nm-long double-stranded DNA (dsDNA) molecules with an experiment

125 hannels to manipulate, stretch, sort and map double-stranded DNA (dsDNA) molecules, however nanochann

126 ectrochemical characteristics of immobilized double-stranded DNA (dsDNA) on a Au electrode were studi

127 l biosensor based on immobilized calf thymus double-stranded DNA (dsDNA) on the carbon-based screen-p

128 system to answer fundamental questions about double-stranded DNA (dsDNA) packaging by viruses that ha

129 unwound ssDNA in TECs, for immunity against double-stranded DNA (dsDNA) phages and plasmids.

130 ormation of infectious virions in the tailed double-stranded DNA (dsDNA) phages, herpesviruses, and a

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

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

133 Double-stranded DNA (dsDNA) tailed phages and herpesviru

134 tivities on an extensive class of mismatched double-stranded DNA (dsDNA) targets.

135 zole cyanine dye K21 forms dye aggregates on double-stranded DNA (dsDNA) templates.

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

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

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

139 This filament binds to a donor double-stranded DNA (dsDNA) to form synaptic filaments,

140 ssDNA-RecA filament searches for homologous double-stranded DNA (dsDNA) to use as a template for the

141 rsaria chlorella virus-1 (PBCV-1) is a large double-stranded DNA (dsDNA) virus that infects the unice

142 fever virus (ASFV) is a complex, cytoplasmic double-stranded DNA (dsDNA) virus that is currently expa

143 aneous quantitation of 10 transplant-related double-stranded DNA (dsDNA) viruses (adenovirus [ADV], B

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

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

146 In contrast to tailed icosahedral double-stranded DNA (dsDNA) viruses infecting bacteria a

147 ntermediates and it is unclear whether large double-stranded DNA (dsDNA) viruses may be similarly sus

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

149 Some double-stranded DNA (dsDNA) viruses use an ATP-dependent

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

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

152 d that SN1-type agents preferably mutagenize double-stranded DNA (dsDNA), and the mutation signature

153 When incorporated into double-stranded DNA (dsDNA), it forms three hydrogen bon

154 Four duplexes: double-stranded DNA (dsDNA), PNA/DNA, dsRNA (modified RN

155 r on single-stranded DNA (ssDNA) compared to double-stranded DNA (dsDNA), raising a key conceptual qu

156 nsible for the sensing of aberrant cytosolic double-stranded DNA (dsDNA), which is a hallmark of canc

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

158 AcrVA4 and AcrVA5 inhibit recognition of double-stranded DNA (dsDNA), with AcrVA4 driving dimeriz

159 ng interface exclusively occupies the strong double-stranded DNA (dsDNA)-binding surface on cGAS and

160 se in base editing requires the unwinding of double-stranded DNA (dsDNA)-for example by a CRISPR-Cas9

161 We show that the double-stranded DNA (dsDNA)-induced conformational chang

162 a complementary DNA strand (cDNA) to form a double-stranded DNA (dsDNA).

163 ar-infrared) regimes could have an effect on double-stranded DNA (dsDNA).

164 inding extensive tracts (~8-10 kilobases) of double-stranded DNA (dsDNA).

165 quitinated, creating a channel that encloses double-stranded DNA (dsDNA).

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

167 e converging fork and then translocate along double-stranded DNA (dsDNA).

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

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

170 anded DNA provided in cis or in trans with a double-stranded DNA duplex.

171 NFalpha, human cytomegalovirus infection, or double-stranded DNA, eEF2 phosphorylation on Thr56, whic

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

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

174 Herpesviruses are ubiquitous, double-stranded DNA, enveloped viruses that establish li

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

176 Following the detection of cytosolic double-stranded DNA from viral or bacterial infection in

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

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

179 or dissociation and release of SP during the double-stranded DNA genome packaging step accompanying p

180 ASFV has a large, double-stranded DNA genome that encodes over 150 protein

181 BKPyV has a circular, double-stranded DNA genome that is divided genetically i

182 All herpesviruses contain a linear double-stranded DNA genome, enclosed within an icosahedr

183 edrovirus is an insect virus with a circular double-stranded DNA genome, which, among other multiple

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

185 endogenous reverse transcription to produce double-stranded DNA genomes, which sometimes looped out

186 g activities of aTFs for small molecules and double-stranded DNA, here we develop a simple, supersens

187 served mechanism of APOBEC3 evasion by large double-stranded DNA herpesviruses.

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

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

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

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

192 modified mC residues in single-stranded and double-stranded DNA in vitro, while the extent of the re

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

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

195 lization microscopy (BALM) using fluorescent double-stranded DNA intercalators and optical astigmatis

196 The topological state of covalently closed, double-stranded DNA is defined by the knot type $K$ and

197 ds, the resulting brightness of 2CNqA inside double-stranded DNA is the highest reported for a fluore

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

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

200 in which viral RNA genome is converted into double-stranded DNA, is that it is slow and non-processi

201 Ltl1 has a general affinity for double stranded DNA (Kd ~ 350 nM) and binds specifically

202 pair, is able to use NAD+ as a substrate for double-stranded DNA ligation.

203 In comparison to spCas9, miCas9 enhances double-stranded DNA mediated large size gene knock-in ra

204 's input strands and the restriction-induced double-stranded DNA melting resets the systems.

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

206 distal' face, three statistically disordered double stranded DNA molecules bind across the proximal f

207 sitive charges on the inner rim of helicoid, double-stranded DNA molecules (dsDNA) could interact wit

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

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

210 he capture rate and translocation of 1-5 kbp double-stranded DNA molecules through solid-state nanopo

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

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

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

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

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

216 ge polarization and charge transport through double-stranded DNA of various lengths and through doubl

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

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

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

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

221 ns-RNA cleavage activities to defend against double-stranded DNA phages is not understood.

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

223 in resistance to 14 phylogenetically diverse double-stranded DNA phages using two model Escherichia c

224 clusively been found to match the genomes of double-stranded DNA phages(9,10), suggesting that Cas13

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

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

227 Compared to double stranded DNA, PX DNA has dramatically enhanced (s

228 pesvirus infection to increase the levels of double-stranded DNA-reactive antibodies at the peak of v

229 specifically bound to cGAS independently of double-stranded DNA, resulting in a non-competitive inhi

230 NPs finally results in the formation of long double-stranded DNA-RNA (HCR products) -AuNPs.

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

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

233 Cyclic GMP-AMP synthase (cGAS) is a double-stranded DNA sensor that catalyses the synthesis

234 Cyclic GMP-AMP synthase (cGAS) is a double-stranded DNA sensor(7,8).

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

236 Unlike double-stranded DNA, single-stranded RNA can be spontane

237 ands of individual data points per minute on double-stranded DNA standard (dsDNA) samples containing

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

239 ominantly cleaves the non-target strand of a double-stranded DNA substrate.

240 nt states of assembly with its guide RNA and double-stranded DNA substrates reveal an extensive RNA s

241 uvC active site to make RNA-guided breaks in double-stranded DNA substrates, an activity essential fo

242 orm programmable endonucleolytic cleavage of double-stranded DNA substrates, showing enhanced activit

243 transient DNA melting that may occur during double-stranded DNA surveillance by CRISPR-Cas9.

244 Double-stranded DNA tailed bacteriophages typically code

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

246 plex) from Pseudomonas aeruginosa bound to a double-stranded DNA target.

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

248 The RNA-guided DNA endonuclease Cas9 cleaves double-stranded DNA targets bearing a protospacer adjace

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

250 through single-stranded loops embedded in a double-stranded DNA template and is programmed by a set

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

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

253 Tested with 1k base-pair double-stranded DNA, the SaS nanopore enabled sensing at

254 nome exists as a covalently closed circle of double-stranded DNA, topoisomerase 1 (Topo1) is thought

255 ation where a double-hexamer idly encircling double-stranded DNA transforms to single-hexamers that e

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

257 E2 Y138.IMPORTANCE Papillomavirus (PV) is a double-stranded DNA tumor virus infecting the cutaneous

258 Merkel cell polyomavirus (MCPyV) is a human double-stranded DNA tumor virus.

259 During cell division, FtsK translocates double-stranded DNA until both dif recombination sites a

260 ngle-stranded-DNA, DNA is first converted to double-stranded-DNA via terminal-deoxynucleotidyl-transf

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

262 ties yielded seven complete or near-complete double-stranded DNA virus genomes.

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

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

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

266 of the most frequently identified drivers of double-stranded DNA viruses evolution.

267 Giant and large eukaryotic double-stranded DNA viruses from the Nucleo-Cytoplasmic

268 More recently, several oncogenic double-stranded DNA viruses have been found to encode ci

269 but recent evidence suggests that some large double-stranded DNA viruses may also endogenize into the

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

271 The capsids of double-stranded DNA viruses protect the viral genome fro

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

273 CrAss-like phages are double-stranded DNA viruses that are prevalent in human

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

275 Baculoviruses are large double-stranded DNA viruses that are virulent pathogens

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

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

278 lve the atomic structures of two filamentous double-stranded DNA viruses that infect archaeal hosts l

279 The Nudiviridae are a family of large double-stranded DNA viruses that infects the cells of th

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

281 g infection.IMPORTANCE Poxviruses are large, double-stranded DNA viruses that replicate entirely in t

282 us expression of a cloned A* gene.IMPORTANCE Double-stranded DNA viruses typically package their geno

283 Double-stranded DNA viruses use ATP-powered molecular mo

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

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

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

287 The assembly of double-stranded DNA viruses, from phages to herpesviruse

288 he portal protein is a key component of many double-stranded DNA viruses, governing capsid assembly a

289 Double-stranded DNA viruses, including bacteriophages an

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

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

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

293 of rhodopsin genes were identified in large double-stranded DNA viruses.

294 ian on solvated nucleotide, and single-, and double-stranded DNA, we mimic hydrogen transfer reaction

295 only partial ketone formation in single- and double-stranded DNA, where the orientation of the base i

296 DSN initiates random 'nicks' on double-stranded-DNA which enable BST to polymerize DNA b

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

298 igner DNA nanoparticles are constructed from double-stranded DNA with cytosine-rich stick ends (C-mon

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

300 the HRP3 PWWP domain in complex with various double-stranded DNAs with/without bound histone peptides