ライフサイエンスコーパス: DNA

1 DNA adducts reflect the internal exposure to genotoxican

2 DNA binding and transcription assays demonstrated that t

3 DNA damage induced by reactive carbonyls (mainly methylg

4 DNA is a remarkably precise medium for copying and stori

5 DNA methylation aberrations have been implicated in acqu

6 DNA methylation at promoters is an important determinant

7 DNA methylation changes associated with maternal smoking

8 DNA obtained from 20 fresh OSCC biopsies (cases) and 20

9 DNA photocleavage experiments demonstrate that, upon pho

10 DNA repair protein counteracting oxidative promoter lesi

11 DNA replication depends on primase, the specialised poly

12 DNA replication results in the doubling of the genome pr

13 DNA tumor viruses such as Kaposi's sarcoma-associated he

14 ediated isothermal amplification (LAMP) is a DNA amplification approach characterized by high sensiti

15 Homologous recombination (HR) is a DNA double-strand break (DSB) repair pathway that protec

16 an apurinic/apyrimidinic endonuclease 1 is a DNA repair enzyme involved in genome stability and expre

17 R36W) or Arg35 (R35H/L) completely abolished DNA binding, mutation of Arg60 (R60Q) significantly redu

18 rackish vs. freshwaters), and nucleic acids (DNA vs. RNA), suggesting niche differentiation.

19 he dynamic phosphorylation of DNA-PKcs after DNA damage to mediate NHEJ.

20 further improve our understanding of ancient DNA breakdown dynamics.

21 Previously published ancient DNA analyses of uniparental genetic markers have shown t

22 teins involved in cellular redox balance and DNA replication, including the Mcm replicative helicases

23 Many chromatin- and DNA-modifying enzymes make use of substrates and cofacto

24 , AgNP concentration, PNA concentration, and DNA strand mismatches.

25 T1AM), on cell proliferation, cell death and DNA damage was studied in two ovarian cancer cell lines

26 on of [4Fe-4S] clusters of dehydratases, and DNA damage.

27 ivation of MutLalpha endonuclease, PCNA- and DNA-dependent activation of MutLalpha ATPase, and MutLal

28 e disorders (eg, ataxia-telangiectasia), and DNA double-strand breaks are crucial to the modulation o

29 ng mechanistic links to histone variants and DNA replication.

30 ange were determined by spiking B. anthracis DNA into individual PCR mixtures and B. anthracis CFU in

31 lysis revealed pathways including apoptosis, DNA repair and early estrogen response that were differe

32 arable in accuracy to other state-of-the-art DNA methylation prediction algorithms.

33 Targeting PARP-associated DNA repair may represent a novel therapeutic strategy fo

34 yacrylamide, unlike many currently available DNA ladders.

35 important in immunity to cytosolic bacteria, DNA viruses, or HIV.

36 ge model, but we find no correlation between DNA fragmentation and sample age over the timespans anal

37 n, which provides a mechanistic link between DNA repair and neurodegeneration.

38 ts demonstrate the potential synergy between DNA origami technology and colloidal science, in which t

39 demonstrate that the ability of Lon to bind DNA is determined by its ATPase domain, that this bindin

40 oncentrates (VCs), containing bioinformative DNA and proteins, have been used to study viral diversit

41 ed longitudinal changes of genome-wide blood DNA methylation profiles in relation to the development

42 an average ratio of 29.2% by targeting both DNA strands simultaneously with an over 98.6% coverage.

43 s (mainly methylglyoxal and glyoxal), called DNA glycation, is quantitatively as important as oxidati

44 pad and the dispensing cycles of the capture DNA probes on the test-zone), the biosensor could detect

45 vestigated the impact of genome-wide cardiac DNA methylation on global gene expression in myocardial

46 We show here that while the central DNA binding domain is essential for anchoring at parS, t

47 the interactions between negatively charged DNA and positively charged amino acid residues, the tran

48 The chimeric DNA oligomer was synthesized in a conventional DNA synth

49 Compared with temozolomide, a clinical DNA-alkylating agent against glioma, 6OTD required lower

50 , we monitored oxidatively induced clustered DNA lesions (OCDL), DNA double-strand breaks (DSB), apop

51 The proposed paper-based colorimetric DNA sensor has potential to be an alternative approach f

52 Synthetic gene circuits that combine DNA, protein, and RNA components have demonstrated a ran

53 Comparisons between eDNA, community DNA, taxonomy and UK species abundance data further show

54 ctivity is required to activate compensatory DNA synthesis during mitosis and to resolve mitotic inte

55 Complex DNA sequences are difficult to detect and profile, but a

56 namic hetero-vesicle assemblies with complex DNA nano-scaffolds.

57 A comprehensive DNA microarray-based assay was performed on all isolates

58 of both RECQL5 and WRN severely compromises DNA replication, accumulates genomic instability and ult

59 opsies from CKD patients and show concordant DNA methylation changes in kidney cortex.

60 la pertussis Ptl systems support conjugative DNA transfer in E. coli and trigger P. aeruginosa T6SS k

61 s of PHF1 and MTF2 with bound CpG-containing DNAs in the presence of H3K36me3-containing histone pept

62 d with chitosan scaffolds containing control DNA or wounded controls.

63 A oligomer was synthesized in a conventional DNA synthesizer, containing neutral nucleotides with a m

64 d breaks (DSBs) represent highly deleterious DNA damage and need to be accurately repaired.

65 In vertebrates, pathogen-derived DNA is sensed in the cytosol by cGAS, which produces the

66 ning buffers, the concentration of detection DNA probe used in the preparation of FCN-DNA conjugates,

67 tigation of these DMRs revealed differential DNA methylation localized to a 600 bp region in the prom

68 s the misreplication of structurally diverse DNA lesions.

69 hree distinct monolayer double-stranded (ds) DNA-gold nanoparticles (DNA-AuNPs).

70 ect ligand binding as blocking events during DNA unzipping, allowing determination of ligand selectiv

71 ition in vitro, it is required for efficient DNA synthesis-coupled nucleosome assembly.

72 I)) as an electrocatalyst in electrochemical DNA sensing.

73 s the recent developments of electrochemical DNA methylation detection approaches.

74 H19 knockdown activates SAHH, enabling DNA methyltransferase 3B to methylate a subset of genes.

75 Accumulation of endogenous DNA damage is concomitant with defective ATM-mediated DN

76 promotes survival by suppressing endogenous DNA damage, and may control cell fate through the regula

77 biogenesis and composition of the eukaryotic DNA replication fork, with an emphasis on the enzymes th

78 Extracellular DNA (eDNA) has been identified in the matrix of many dif

79 Analysis of enriched transcription factor DNA-binding sites in the promoters of differentially exp

80 t least six (35%) alter transcription factor-DNA binding in neuroblastoma cells.

81 ion DNA probe used in the preparation of FCN-DNA conjugates, the amount of FCN-DNA dispensed on the c

82 ion of FCN-DNA conjugates, the amount of FCN-DNA dispensed on the conjugate pad and the dispensing cy

83 uld detect a minimum concentration of 0.4 fM DNA.

84 le for histone (H3-H4)2 deposition following DNA synthesis.

85 ed with full width half maxima of 417 fs for DNA and 323 fs for DNA-CTMA thin-solid-film SAs.

86 half maxima of 417 fs for DNA and 323 fs for DNA-CTMA thin-solid-film SAs.

87 t parS, this interaction is not required for DNA condensation.

88 vels of TET enzyme, which is responsible for DNA demethylation in UVB-exposed skin.

89 owerful weapons in the fight against foreign DNA, such as phages and plasmids, as well as a revolutio

90 utilizes RNA-functionalized AuNPs which form DNA-RNA heteroduplex structures through specific hybridi

91 The presence of longer nucleosome-free DNA regions can positively or negatively affect the rate

92 se of nuclear factor kappa B (NFkappaB) from DNA target sites in a process we have termed molecular s

93 Further, DNA-bound RecA protein increases the rate of ATP hydroly

94 We also mapped phage 9 g DNA packaging (pac) site containing two 21-bp direct rep

95 were randomized to receive 4 mg of PENNVAX-G DNA delivered intramuscularly by Biojector or electropor

96 he binding and ATPase-driven unwinding of G4 DNA.

97 We demonstrate that targeted next-generation DNA sequencing reactions and in situ point mutation dete

98 table labeling and monitoring of HIV genomic DNA within infected cells during cytoplasmic transit, nu

99 ration of interstrand cross-links in genomic DNA may contribute to aging, neurodegeneration, and canc

100 ensitive enough to detect changes in genomic DNA methylation levels as a function of growth phase in

101 bility to rewrite large stretches of genomic DNA enables the creation of new organisms with customize

102 organisms that lack large amounts of genomic DNA.

103 Thus, genomic DNA DSBs act as signaling intermediates in murine macrop

104 del without fitting parameters, with genomic DNA sequence being the only input, we further validate t

105 confidence interval [CI], 6.3-21.9%) of HPV DNA detections in genital samples were attributable to v

106 table strategy to robustly re-identify human DNA called 'MinION sketching'.

107 ts, we used somatic variants in hypermutable DNA regions to reconstruct high-confidence phylogenetic

108 erdependent coupled oscillators and identify DNA replication as a critical process in the circadian m

109 Improper DNA double-strand break (DSB) repair results in complex

110 ociated with somatic variations, advances in DNA sequencing indicate that cell-specific variants affe

111 because it has a reduced net charge, and in DNA binding and protein-protein interactions because key

112 Genetic defects in DNA repair underlie other neurodegenerative disorders (e

113 ther, these data suggest that differences in DNA methylation may partly explain the enantioselectivit

114 or a ribose 8oxoG (r8oxoG) site embedded in DNA.

115 esidues in the C-terminal helix to engage in DNA binding, triggering a major reprogramming of gene ex

116 ductase (MTHFR) gene, an enzyme essential in DNA synthesis and methylation, have been associated with

117 N3-Methyladenine (3-MeA) is formed in DNA by reaction with S-adenosylmethionine, the reactive

118 ost common non-standard nucleotides found in DNA of eukaryotic cells, with over 100 million rNMPs tra

119 We sequenced exons of this gene in DNA from a total of 134 nonsyndromic cases.

120 f gene silencing, while H2AX is important in DNA damage repair.

121 junction (HJ) is a hallmark intermediate in DNA recombination and must be processed by dissolution (

122 velength UV light can cause photo-lesions in DNA origami.

123 d as an intermediate in electron transfer in DNA.

124 lly important biological processes including DNA repair and replication.

125 y, radiation therapy and chemotherapy induce DNA damage to drive cells into apoptosis or senescence a

126 PDH down-regulation potentiated H2O2-induced DNA damage and SMC apoptosis.

127 Importantly, HDM-induced DNA damage can be prevented by the antioxidants glutathi

128 ere also sufficient to mediate PGBD5-induced DNA rearrangements in rhabdoid tumor cells.

129 s on transcription recovery after UV-induced DNA damage.

130 okiol application also inhibited UVB-induced DNA hypermethylation and its elevation of the levels of

131 fragments that subsequently reintegrate into DNA breaks induced on a heterologous chromosome.

132 l comparison of holo-ScNsrR with an apo-IscR-DNA complex shows that the [4Fe-4S] cluster stabilizes a

133 plex virus type 1 (HSV-1), which has a large DNA genome, using synthetic genomics tools.

134 levels of dG-gx-dC and dG-gx-dA in leukocyte DNA were 1.94 +/- 1.20 and 2.10 +/- 1.77 in 10(8) normal

135 fic and it requires only 50 mug of leukocyte DNA isolated from 2-3 mL of blood to accurately quantify

136 plast genome that is composed only of linear DNA molecules is unprecedented among eukaryotes, and hig

137 signaling and accumulation of protein-linked DNA breaks.

138 ve in neutralizing negatively charged linker DNA because it has a reduced net charge, and in DNA bind

139 The portability and long DNA sequences of RTnS offer great potential for field-ba

140 In low-frequency AC fields, long DNA molecules form macro-ion clusters.

141 apturing fluorescent signal patterns of long DNA molecules (in the range of 0.1-1 Mbp).

142 e when free in solution or with well matched DNA but exhibits a significant luminescence increase in

143 modification coincides with the ATM-mediated DNA damage response that occurs on functional telomeres

144 We reveal that defective ATM-mediated DNA repair is a consequence of P62 accumulation, which i

145 e is concomitant with defective ATM-mediated DNA repair signaling and accumulation of protein-linked

146 ny of the three major pathways known to mend DNA DSBs, namely homologous recombination (HR), nonhomol

147 escence increase in the presence of a 27-mer DNA duplex containing a central CC mismatch.

148 tingly, 5hmC colocalized with the methylated DNA binding protein MeCP2 and with the active chromatin

149 strand breaks, or the expression of MIRAGE1 DNA transposons.

150 this gap, we analyzed ancient mitochondrial DNA (mtDNA) from Scythians of the North Pontic Region (N

151 range using microsatellite and mitochondrial DNA loci.

152 c D2 mice manifested increased mitochondrial DNA lesions (8-oxoguanine) exclusively localized to glom

153 This was tested using a major mitochondrial DNA (mtDNA) survey and sequencing of two nuclear markers

154 excess cytosolic extrusion of mitochondrial DNA along with increased reactive oxygen species and red

155 ratory capacity and release of mitochondrial DNA into the cytosol.

156 n triggers cytosolic escape of mitochondrial DNA, which engages cGAS.

157 gation to daughter nuclei by linking mitotic DNA and NPC segregation via the mitotic specific chromat

158 ew class of site-specifically metal-modified DNA films was characterized by UV, circular dichroism (C

159 F60, represses seedling growth by modulating DNA accessibility of hypocotyl cell size regulatory gene

160 owing infection with Listeria monocytogenes, DNA-PKcs-deficient murine macrophages produce reduced le

161 to mediate the juxtaposition of two or more DNA regions on the same or different chromosomes.

162 gher levels of circulating mitochondrial (mt)DNA, soluble thrombomodulin (sCD141) and ICAM-1, reflect

163 double-stranded (ds) DNA-gold nanoparticles (DNA-AuNPs).

164 A novel DNA adenine modification, N(6)-methyladenine (6mA), has

165 Nuclear DNA indicated Neanderthals as a sister group of Denisova

166 red to female MNX mice having FVB/NJ nuclear DNA with either FVB/NJ, C57BL/6J, or BALB/cJ mtDNA.

167 hat is capable of unwrapping the nucleosomal DNA from the histone octamer (HO).

168 tively induced clustered DNA lesions (OCDL), DNA double-strand breaks (DSB), apoptosis, and the local

169 production stemmed from the accumulation of DNA in the cytoplasm of AT and Artemis-deficient cells.

170 ed liver to have a pattern of acquisition of DNA methylation targeted to candidate enhancers active i

171 he electrochemical sensing and biosensing of DNA methylation.

172 Whereas 10 bp of DNA was sufficient to support PU.1 binding as a monomer,

173 Analytical characterization of DNA microviscosity provides critical biophysical insight

174 MRN-mediated endonucleolytic cleavage of DNA at sites of protein adducts requires ATP hydrolysis

175 The details of DNA positioning on the nucleosome and the DNA conformati

176 in human populations, and the examination of DNA methylation is becoming increasingly common in psych

177 The local sequence-dependent features of DNA found in high-resolution structures introduce irregu

178 ear HCR, forming a chain-branching growth of DNA dendrimer by self-assembly.

179 re potent in uptaking tumor DNA, increase of DNA sensing by blocking the interaction of SIRPalpha wit

180 Therefore, the cooperative induction of DNA replication stress and damage by ATR inhibition and

181 The genome-wide investigation of DNA methylation levels has been limited to reference tra

182 Mechanical manipulation of DNA hairpins with an engineered sequence is used to dete

183 first quantitative human genome-wide map of DNA lesions induced by ultraviolet (UV) radiation, the u

184 The mechanics of DNA replication and cell cycling are well-characterized

185 her fine-tune the dynamic phosphorylation of DNA-PKcs after DNA damage to mediate NHEJ.

186 key factor mediating androgen protection of DNA damage via Ku70/Ku80 in prostate cancer cells.

187 d lead to fast and automated purification of DNA nanostructures of various shapes and sizes, which wo

188 tial role for EAF2 in androgen regulation of DNA repair in prostate cancer cells.

189 loprotease that is involved in the repair of DNA-protein crosslinks (DPCs).

190 no acid residues, the translocation speed of DNA can be manipulated by deliberate charge decorations

191 The sophisticated tail structures of DNA bacteriophages play essential roles in life cycles.

192 stability of the replisome once assembled on DNA.

193 Our model, which estimates age based on DNA methylation at 329 unique CpG sites, has a median ab

194 ditionally, Cu(II) chelated PyED outcompetes DNA polymerase I to successfully inhibit template strand

195 production in the spinal cord and oxidative DNA damage in dorsal horn neurons.

196 ssment of one epigenetic mark in particular, DNA methylation, in human populations, and the examinati

197 apeutics for additional infectious pathogens.DNA-delivered monoclonal antibodies (DMAbs) can be produ

198 proteins with human anelloviruses, and PCV2 DNA may be present in human food and vaccines.

199 create NGS libraries from as little as 20 pg DNA with PCR error correcting capabilities, and capture

200 were assayed for the presence of phytoplasma DNA.

201 t that chitosan scaffolds containing plasmid DNA encoding VEGF189 and perlecan domain I have the pote

202 Oral administration of the plasmid DNA (pDNA) encoding GLP-1 decreased diabetic glucose lev

203 ed via freeze drying and loaded with plasmid DNA encoding perlecan domain I and VEGF189 and analyzed

204 ds to the formation of a high density of PNA/DNA heteroduplexes on the electrode surface for the subs

205 assay, based on random amplified polymorphic DNA (RAPD) analysis was developed for its efficient and

206 tins) are unsaturated imines that are potent DNA damaging agents, thereby confirming an earlier mecha

207 T-IH or during recovery from LT-IH prevented DNA methylation of AOE genes, normalized the expression

208 erated by release of single-stranded product DNA.

209 eiotic recombination, a subset of programmed DNA double-strand breaks (DSBs) are repaired as crossove

210 ction between TopBP1 and Treslin and promote DNA replication despite the presence of a Cdk2 inhibitor

211 w that ectopic dATM is sufficient to promote DNA synthesis in wild-type fat body cells.

212 ragment in complex with its cognate promoter DNA, revealing the molecular details of promoter recogni

213 In recalcified PFP, purified DNA triggered contact-dependent thrombin generation (TG)

214 lines have publicly available, high-quality DNA, RNA, and drug screening data.

215 ased diagnostic (CRISPR-Dx), providing rapid DNA or RNA detection with attomolar sensitivity and sing

216 hese metal-induced alterations decrease RcnR-DNA binding affinity, leading to rcnAB expression.

217 Recent advances in long-read DNA sequencing technologies, specifically Nanopore seque

218 tation of Arg60 (R60Q) significantly reduced DNA binding, but retained a preference for the 5caC modi

219 in complexes, and that Lon may help regulate DNA replication in response to growth conditions.

220 GA motifs in the stem region of TGGAA repeat DNA act as hot spots to facilitate the transition betwee

221 cific single-molecule analysis of replicated DNA technique, we found that depletion of FANCM dramatic

222 rimers that are elongated by the replicative DNA polymerases.

223 nt-based methods, we show that the resulting DNA-wrapped carbon nanotubes can be further sorted to pr

224 duction, with high-throughput 18 S ribosomal DNA sequencing to elucidate the relationship between euk

225 sequences by proximity ligation, forming RNA-DNA chimeric sequences, which are converted to a sequenc

226 the antibody gene deaminase AID and the RNA/DNA editing enzyme APOBEC1 (A1).

227 t simplifies the preparation of roadblocking DNA templates.

228 composed of tandem arrays of alpha-satellite DNA, which spans up to several megabases.

229 for simple, rapid, sensitive, and selective DNA detection.

230 ors (TFs) are proteins that bind to specific DNA sequences and regulate expression of genes.

231 gth DNA sample reservoir induces spontaneous DNA migration against the direction of flow.

232 erials that target DNA gyrase by stabilizing DNA-cleavage complexes, but their clinical utility has b

233 tion of clean DSBs by cleaving the 5' strand DNA approximately 10-20 nucleotides away from the ends.

234 leoprotein filament (NPF) on double-stranded DNA (dsDNA) that is capable of unwrapping the nucleosoma

235 Single-stranded DNA (ssDNA) is notable for its interactions with ssDNA b

236 Single-stranded DNA oligonucleotides have unique, and in some cases sequ

237 d microcapillary into a lower ionic strength DNA sample reservoir induces spontaneous DNA migration a

238 a, Vietnam and Cambodia and after successful DNA extraction fragment of the nuclear rhodopsin gene (R

239 These studies support DNA-delivered monoclonal antibodies delivery as a potent

240 h an emphasis on the enzymes that synthesize DNA and repair discontinuities on the lagging strand of

241 pendent degradation of the newly synthesized DNA at stalled forks.

242 The MEF8 T-DNA insertion (mef8) line exhibited reduced editing at 3

243 ing chip and the unpaired fragment of target DNA works as a trigger to initiate the nonlinear HCR, fo

244 re broad-spectrum antibacterials that target DNA gyrase by stabilizing DNA-cleavage complexes, but th

245 The target DNA partly hybridizes with capture probe on the gold sen

246 s through specific hybridization with target DNA.

247 One system (type I-F) targets DNA.

248 of G-quadruplexes formed by, e.g., telomeric DNA sequences, but are also interesting targets for supr

249 y permits very efficient use of the template DNA as well as sequence reads, which are nearly all conf

250 UV-Vis spectrophotometry reveals that DNA films with surface densities up to 0.031 mg/mm(2) ca

251 of DNA positioning on the nucleosome and the DNA conformation can provide key regulatory signals.

252 ional coupling of recombination steps at the DNA level with specific organizational features of meiot

253 n photoactivation, the conjugate cleaves the DNA backbone specifically near the mismatch site on a 27

254 hat malignant transformation compromises the DNA-nuclear matrix interface.

255 has been well studied for over a decade, the DNA-binding activities and the biological functions of t

256 y p53-dependent enhancer activity during the DNA damage response.

257 ATP hydrolysis catalysed by RecN during the DNA pairing reaction.

258 not associated with causative changes in the DNA methylome, which appears relatively impervious to dr

259 d further yielded a novel association in the DNA methyltransferase gene DNMT3B.

260 meiosis share many processes, including the DNA replication, chromosome condensation and precisely r

261 ling the transcriptional levels, but not the DNA methylation, of the Peg3 domain.

262 ates, leading to reversible switching of the DNA conductance between two discrete levels.

263 o apoptosis or senescence as outcomes of the DNA damage response (DDR).

264 enable promoter opening and trapping of the DNA non-template strand.

265 epending upon the length and location of the DNA region within the chromatin fiber.

266 MJD2B silencing led to an enhancement of the DNA-damage driven induction of p21 and PIG3.

267 y solvent-exposed in the major groove of the DNA.

268 merization of Dnmt3a/Dnmt3L complexes on the DNA.

269 e set of OL maturation genes and reduces the DNA occupancy of YY1, a transcription factor required fo

270 an exogenous source of alphaKG restored the DNA demethylation cycle by promoting TDG function, TET1

271 estabilized Miz1-4(A86K) mutant bound to the DNA consensus with a 30-fold increase in affinity (100 n

272 Cys99 properly oriented to interact with the DNA backbone.

273 5i), either alone or in combination with the DNA-demethylating agent 5-aza-2'-deoxycytidine (DAC).

274 The advent of high-throughput DNA methylation profiling techniques has enabled the pos

275 High-throughput DNA sequencing of microbiota from a diverse collection o

276 With the development of new high-throughput DNA sequencing technologies and decreasing costs, large

277 DNA-binding domain that abrogates binding to DNA and leads to complete loss of canonical TH action.

278 acterize the SOS transcriptional response to DNA damage in the Patescibacteria superphylum.

279 rated knockin mice with a mutation in the TR DNA-binding domain that abrogates binding to DNA and lea

280 e enveloped viruses with reverse-transcribed DNA genomes, constitute the family Hepadnaviridae.

281 ween ATM and histone H2AX without triggering DNA damage.

282 F. tularensis DNA in buffer or CFU of F. tularensis was spiked into hu

283 crophages were more potent in uptaking tumor DNA, increase of DNA sensing by blocking the interaction

284 Upon DNA damage, p53 mRNA is released from stress granules an

285 d cytidine deaminase are processed by uracil-DNA glycosylase (UNG) and mismatch repair (MMR) pathways

286 s in estuarine and marine environments using DNA-SIP and to characterise marine isoprene-degrading ba

287 fied 265 specimens to species or genus using DNA barcodes.

288 roteins have been identified as potent viral DNA mutators and have broad antiviral activity.

289 assembled a compartment that separated viral DNA from the cytoplasm.

290 ontaining >/=105 copies herpes simplex virus DNA/ml collected a median of 5 months apart (IQR: 2-11 m

291 In the same way DNA was modeled, the tertiary structure of RNA is constr

292 Histone mRNAs are rapidly degraded when DNA replication is inhibited by a 3' to 5' pathway that

293 into the study of human genetic disease when DNA sequencing alone is not sufficient to reveal the und

294 high-throughput sequencing technology, where DNA is sheared into smaller pieces, sequenced, and then

295 Herein, we describe a mechanism whereby DNA and associated DNABII proteins transit from the bact

296 While DNA binding is not essential for H3-H4 tetrasome deposit

297 ct measurements on single nucleotides within DNA macromolecules, we demonstrate that the distance ove

298 radical cations at defined positions within DNA.

299 dapter-inducing interferon-beta (TRIF) and Z-DNA-binding protein 1 (ZBP1)/DNA-dependent activator of

300 ta (TRIF) and Z-DNA-binding protein 1 (ZBP1)/DNA-dependent activator of IFN-regulatory factors (DAI)