ライフサイエンスコーパス: nuclear DNA

1 r of indels made during replication of yeast nuclear DNA.

2 year, an order of magnitude higher than for nuclear DNA.

3 ut shared many haplotypes with the latter at nuclear DNA.

4 polymorphism is linked to differences in the nuclear DNA.

5 ation from organellar DNA in preparations of nuclear DNA.

6 , precluding their use on most alignments of nuclear DNA.

7 3 subunits encoded by both mitochondrial and nuclear DNA.

8 us, whereas APOBEC3A alone efficiently edits nuclear DNA.

9 ferent subunits encoded by mitochondrial and nuclear DNA.

10 different cells possess variable amounts of nuclear DNA.

11 ithful replication of both mitochondrial and nuclear DNA.

12 nstrating the inaccessibility of most of the nuclear DNA.

13 include components that are not specified by nuclear DNA.

14 n be caused by mutations in mitochondrial or nuclear DNA.

15 ch is thought to prevent cGAS from accessing nuclear DNA.

16 on and from contamination of cell debris and nuclear DNA.

17 H 3) 2} 1,2-intrastrand d(GpG) cross-link in nuclear DNA.

18 reactive oxygen species and fragmentation of nuclear DNA.

19 d Chk1/Chk2 phosphorylation and release from nuclear DNA.

20 mount of the triphosphate form (L-OddCTP) in nuclear DNA.

21 ation, and oligonucleosomal fragmentation of nuclear DNA.

22 II trials; however, all of these target only nuclear DNA.

23 ove approximately 20 muM, the complex images nuclear DNA.

24 D4-PLAG1; a fusion between mitochondrial and nuclear DNA.

25 thelia is associated with the degradation of nuclear DNA.

26 ften enriched in the cytoplasm away from the nuclear DNA.

27 -characterized function is repair of damaged nuclear DNA.

28 ell explored in central Europe using ancient nuclear DNA [1, 2], its genetic impact on northern and e

29 was found in 5 cases (mean ratio of mtDNA to nuclear DNA: 239 [95% CI, 217-239] vs 179 [95% CI, 165-1

30 Nuclear DNA abnormalities in individual glands were iden

31 and cytochrome c oxidase subunit I (COI)] or nuclear DNA [adenine nucleotide translocator 1 (ANT1) an

32 Finally, enzymatic degradation of nuclear DNA allows us to recover 45% of tight nuclear-bo

33 ntimicrobial strategy comprising decondensed nuclear DNA and associated histones that are extruded in

34 iminate invading microorganisms by expelling nuclear DNA and histones to form extracellular web-like

35 essential to prevent uracil accumulation in nuclear DNA and indicate that SHMT1-mediated nuclear de

36 TMZ methylates nuclear DNA and induces cell death; however, the impact

37 ukaryotes (polymerases delta and epsilon for nuclear DNA and polymerase gamma for mitochondrial) are

38 d on the newly synthesized leading strand of nuclear DNA and were present upstream of (G+C)-rich trac

39 Although iPSCs and nt-ESCs shared the same nuclear DNA and yet carried different sources of mitocho

40 liced and unspliced RNA, (b) cytoplasmic and nuclear DNA, and (c) Gag.

41 dependent manner, increased uracil levels in nuclear DNA, and increased genome instability.

42 The amplicon curves for mitochondrial and nuclear DNA, and the correlations among the curves, were

43 FUS is a predominantly nuclear DNA- and RNA-binding protein that is involved in

44 anism by which Ty1 integrase gains access to nuclear DNA as a model for how other retroelements, incl

45 nters the nucleus and reacts with its target nuclear DNA, as determined by platinum atomic absorption

46 ophil extracellular traps (NETs) composed of nuclear DNA associated with histones and granule protein

47 t dendritic cells (DCs) can uptake and sense nuclear DNA-associated entities released by dying cells

48 entional SR probes, it can provide images of nuclear DNA at unprecedented resolution.

49 ing phenotypes also in mice with a wild-type nuclear DNA background.

50 t that ribonucleotides are incorporated into nuclear DNA beyond their role in priming Okazaki fragmen

51 Here we show that HMGB1, a nuclear DNA-binding protein released from necrotic cells

52 otein (HMGB1), originally characterized as a nuclear DNA-binding protein, has also been described to

53 cted into wild-type and MNX mice (i.e., same nuclear DNA but different mitochondrial DNA), we showed

54 rison of cells with identical oocyte-derived nuclear DNA but different mtDNA shows that either mtDNA

55 tion of the lncRNA RMRP, which is encoded by nuclear DNA but has key functions in mitochondria.

56 not only are ribonucleotides present in the nuclear DNA, but that they can be incorporated by at lea

57 long noncoding RNAs (lncRNAs) are encoded by nuclear DNA, but the mechanisms that mediate their trans

58 ion between protein and transcript levels of nuclear DNA- but not mtDNA-encoded ETC complex subunits

59 jects, one of their strategies is to release nuclear DNA by the formation of extracellular web-like t

60 esults showed that the copy numbers of viral nuclear DNA can vary by as much as 1.8 orders of magnitu

61 en species (ROS) and the decondensing of the nuclear DNA catalyzed by peptidyl arginine deiminase-4.

62 gress in the study of circulating, cell-free nuclear DNA (ccf-nDNA) in cancer detection has led to th

63 ransferred gene has integrated into sea slug nuclear DNA comes from the finding of a highly diverged

64 In eukaryotes, a first step towards the nuclear DNA compaction process is the formation of a nuc

65 l triggering of endocycles results in higher nuclear DNA content (C value) that in some cases has bee

66 The detection of changes in nuclear DNA content by correlating color recovery of H2B

67 use mutants to show that a 16-fold change in nuclear DNA content does not influence the relative size

68 on, as a link in coordinating cell shape and nuclear DNA content in endoreplicated Arabidopsis tricho

69 yed budbreak compared with those with larger nuclear DNA content.

70 n based on both cellular DNA replication and nuclear DNA content.

71 ll size increases are not caused by a higher nuclear DNA content.

72 t visualization and estimation of changes in nuclear-DNA content in live cells during their developme

73 While the first provides information on nuclear DNA contents across land plants and some algal g

74 Measurement of nuclear DNA contents showed that PL cells were haploid r

75 er reconstructions of chromosome numbers and nuclear DNA contents.

76 s for a 519 bp region of the 18S RNA gene on nuclear DNA correlated appropriately.

77 ed by extracellular neurotrophic factors and nuclear DNA damage are integrated by the AKT-mTORC1 path

78 espond to age-related increases in oxidative nuclear DNA damage by forming DNA damage repair foci; ho

79 ased nuclear localization of cDDP, increased nuclear DNA damage by platination, and increased apoptos

80 drial ROS, however, did not cause detectable nuclear DNA damage even when base excision repair was bl

81 Nuclear DNA damage foci were detected in the endothelium

82 in the cell nucleus (K125L), suggesting that nuclear DNA damage is required for toxicity.

83 Nuclear DNA damage occurred later in EAU at day 12.

84 ered as a stereotypic response to unrepaired nuclear DNA damage or to uncapped telomeres.

85 merase in plants and plays a crucial role in nuclear DNA damage repair.

86 find that low doses of RHPS4 do not induce a nuclear DNA damage response but do cause an acute inhibi

87 ngiectasia mutated (ATM) kinase orchestrates nuclear DNA damage responses but is proposed to be invol

88 Neither mitochondrial nor nuclear DNA damage was detected in the controls.

89 ron's protective effect against H2O2-induced nuclear DNA damage was greater than the cellular antioxi

90 We examined nuclear DNA damage, micronuclei (MN), intracellular ROS

91 PCR-based measurements of mitochondrial and nuclear DNA damage, mtDNA damage was preferentially note

92 ial protein oxidation, and mitochondrial and nuclear DNA damage, without interfering with mitochondri

93 Furthermore, PPL2 accumulates at sites of nuclear DNA damage.

94 rf176; EXO5) that functions in the repair of nuclear DNA damage.

95 enerated reactive oxygen species that caused nuclear DNA damage.

96 oint mutation of mitochondrial DNA or with a nuclear DNA defect (44% and 52%, respectively; P<0.001).

97 only independent predictor associated with a nuclear DNA defect (P=0.002; odds ratio 8.43, 95% confid

98 hat it is highly predictive of an underlying nuclear DNA defect.

99 kelihood ratio (5.87) for the diagnosis of a nuclear DNA defect.

100 l feature in mitochondrial disease caused by nuclear DNA defects and single, large-scale mitochondria

101 Eukaryotes express at least three nuclear DNA-dependent RNA polymerases (Pols) responsible

102 NETs are composed of nuclear DNA-derived web-like structures decorated with n

103 In addition to a direct role of nuclear DNA double-strand breaks as inducer of a DNA dam

104 in the Prkdc gene, which encodes a critical nuclear DNA double-stranded break repair protein.

105 for the treatment of mtDNA-driven, and some nuclear DNA-driven, mitochondrial diseases.

106 We show that GSH co-localizes with nuclear DNA during the proliferation of A. thaliana cell

107 BEC3A with a TRIB3 expression vector reduced nuclear DNA editing whereas siRNA knockdown of TRIB3 inc

108 A knockdown of TRIB3 increased the levels of nuclear DNA editing, indicating that TRIB3 functioned as

109 ervation may yield substantial quantities of nuclear DNA, enabling novel applications of ancient DNA

110 -binding factor 1), that associated with the nuclear DNA-encoded lncRNA RMRP and mobilized it to mito

111 n adipocytes similarly induced expression of nuclear DNA-encoded mitochondrial ETC genes, including t

112 d genes by regulating expression of multiple nuclear DNA-encoded mitochondrial ribosomal proteins.

113 tion, the basal expression levels of several nuclear DNA-encoded oxidative damage responsive genes wh

114 ith mutations in the gene NDUFS4, encoding a nuclear DNA-encoded subunit of CI (NADH dehydrogenase ub

115 I) and subcellular organelles (mitochondria, nuclear DNA, etc.) not known to affect either focal adhe

116 However, limited mitochondrial and nuclear DNA evidence conflicts in the timing of PB origi

117 of 2 were investigated and interactions with nuclear DNA explored.

118 sults demonstrated there were alterations in nuclear DNA expression and DNA methylation driven by mtD

119 In situ full-length Rx1 binds nuclear DNA following activation by its cognate pathogen

120 Human hair contains minimal intact nuclear DNA for human identification in forensic and arc

121 esults suggest that mitochondrial damage and nuclear DNA fragmentation are likely to be critical even

122 Peak nuclear DNA fragmentation in the abnormal LT cohort was

123 al release of apoptosis inducing factor, and nuclear DNA fragmentation resulting in centrilobular nec

124 this leads to mitochondrial dysfunction and nuclear DNA fragmentation, resulting in necrotic cell de

125 luorometric TUNEL System was used to observe nuclear DNA fragmentation.

126 ase [GDH] and mitochondrial DNA [mtDNA]) and nuclear DNA fragments were measured in plasma from APAP-

127 nd binds to the Abl interactor 1, SHP-1, and nuclear DNA fragments.

128 To address these issues, we compared nuclear DNA from 32 archaeological maize samples spannin

129 r body transfer: all involve the transfer of nuclear DNA from an egg or zygote containing defective m

130 ave focused on developing methods to recover nuclear DNA from Neanderthal remains.

131 rial Nuclear eXchange mice, that contain the nuclear DNA from one inbred mouse strain, and the mtDNA

132 The movement of nuclear DNA from one vascular plant species to another i

133 d W-linked DNA, but are indistinguishable at nuclear DNA from other common cuckoos.

134 at low levels of genetic capture of maternal nuclear DNA from other species occur within otherwise an

135 Host nuclear DNA further indicated unanticipated gene flow th

136 lude the possibility that some mitochondrial-nuclear DNA fusions observed in cancer occurred years ea

137 chondrial genome encompasses over a thousand nuclear DNA genes plus hundreds to thousands of copies o

138 pecific targeting of the metalloinsertors to nuclear DNA gives rise to their cell-selective cytotoxic

139 Furthermore, interplay between mtDNA and nuclear DNA has been found in cancer cells, necessitatin

140 nor nuclei into recipient oocytes, whose own nuclear DNA has been removed, can result in large number

141 a result of DNA damage, mitochondrial DNA or nuclear DNA has been shown to enter the cytoplasm where

142 nscription and nucleotide excision repair of nuclear DNA, however, whether or not XPD exerts similar

143 Nuclear DNA identified the ivory source as African fores

144 at antiviral therapy leads to a reduction in nuclear DNA in a manner consistent with symmetrical dist

145 nd apoptotic cells, but whether C1q binds to nuclear DNA in apoptotic cells remains to be investigate

146 ifetime imaging microscopy (PLIM) probes for nuclear DNA in both live and fixed cells.

147 Histones mediate dynamic packaging of nuclear DNA in chromatin, a process that is precisely co

148 duck hepatitis B virus (DHBV) cccDNA and HBV nuclear DNA in established cell lines.

149 ochondrial DNA (mtDNA), the only form of non-nuclear DNA in eukaryotic cells, is a major activator of

150 These properties enable to image nuclear DNA in fixed cells at submicromolar concentratio

151 equency of contact between mitochondrial and nuclear DNA in some somatic cells.

152 Nuclear DNA in the male gamete of sexually reproducing a

153 Genetic analysis confirmed that nuclear DNA in the three infants born so far originated

154 Deletion of DNase1L2 causes retention of nuclear DNA in the tongue epithelium but not in the skin

155 Nuclear DNA indicated Neanderthals as a sister group of

156 mice exhibited decreased levels of uracil in nuclear DNA, indicating enhanced de novo thymidylate syn

157 Insults to nuclear DNA induce multiple response pathways to mitigat

158 ced enhancement of ROS formation, attenuated nuclear DNA injury, reduced the activation of the nuclea

159 chromosomal abnormalities and the release of nuclear DNA into the cytoplasm, activating the cGAS-STIN

160 iscordance between mitochondrial (mtDNA) and nuclear DNA introgression detected in North American pop

161 Degradation and modification of nuclear DNA is a central feature of apoptosis, and DNA f

162 hysical studies and a significant portion of nuclear DNA is compacted, a unique effect different from

163 Nuclear DNA is the target responsible for anticancer act

164 Damage to nuclear DNA is thought to be its primary mechanism of ce

165 Nuclear DNA is tightly packaged into chromatin, which pr

166 Chromosomal structure of nuclear DNA is usually maintained by insertion of nucleo

167 Nuclear DNA is wrapped around histones.

168 acene (DMBA), cisplatin and etoposide induce nuclear DNA leakage into the cytosol that intrinsically

169 nt correlations were observed between plasma nuclear DNA levels and ex vivo cytokine production.

170 biosensor strategy that rewards exposure to nuclear DNA ligase.

171 The use of various kinds of nuclear DNA markers is increasing, as are multiple locus

172 Nuclear DNA markers reflect a species tree consistent wi

173 d 467 amplified fragment-length polymorphism nuclear DNA markers, we show that the introduced white s

174 strong genetic differentiation identified by nuclear DNA markers.

175 ed to uncouple the inheritance of mtDNA from nuclear DNA may enable affected women to have a genetica

176 nization of chromatin affects all aspects of nuclear DNA metabolism in eukaryotes.

177 n and can participate in distinct aspects of nuclear DNA metabolism.

178 bred mouse strain to examine the genome-wide nuclear DNA methylation and gene expression patterns of

179 tosis and micronucleus formation, by loss of nuclear DNA methylation, and by an increased fraction of

180 sial; whether DNMT2 functions primarily as a nuclear DNA methyltransferase or as a cytoplasmic tRNA m

181 We found non-coincident clines in mtDNA and nuclear DNA, mirroring directionality of premating isola

182 Hence, the cardiac phenotype of nuclear DNA mitochondrial mutations might be modulated b

183 Cellular processes mediated through nuclear DNA must contend with chromatin.

184 es, despite evidence both compounds increase nuclear DNA mutations and demonstrated B[a]P adduct form

185 luated the minimum prevalence of symptomatic nuclear DNA mutations and symptomatic and asymptomatic m

186 Results suggest that the nuclear DNA mutations that give rise to ADOA in our pati

187 hip between concentrations of cell-free (cf) nuclear DNA (ncDNA) and mitochondrial DNA (mtDNA) within

188 ernally inherited mtDNA, the more than 1,000 nuclear DNA (nDNA) bioenergetic genes, and the epigenomi

189 caused greater mitochondrial DNA (mtDNA) and nuclear DNA (nDNA) damage in female mice, indicative of

190 ) generation, mitochondrial DNA (mtDNA), and nuclear DNA (nDNA) damage).

191 e action spectra of UVR-induced erythema and nuclear DNA (nDNA) damage.

192 genase (GDH), mitochondrial DNA (mtDNA), and nuclear DNA (nDNA) fragments can be measured in circulat

193 th differences in mitochondrial function and nuclear DNA (nDNA) gene expression, which are recapitula

194 an evolve different anatomical forms through nuclear DNA (nDNA) mutations permitting exploitation of

195 The adipose tissue mtDNA/nuclear DNA (nDNA) ratio was increased in untreated HIV-

196 In contrast to nuclear DNA (nDNA), mtDNA is more exposed to oxidative d

197 mitochondrial DNA (mtDNA) and the Mendelian nuclear DNA (nDNA).

198 Replication of nuclear DNA occurs in the context of chromatin and is in

199 ries of rNMPs derived from mitochondrial and nuclear DNA of budding and fission yeast.

200 such as doxorubicin (DXR), intercalate into nuclear DNA of cancer cells, thereby inhibiting their gr

201 an epigenetic modification of thymine in the nuclear DNA of flagellated protozoa of the order Kinetop

202 l-hydroxymethyluracil) was discovered in the nuclear DNA of some pathogenic protozoa, such as trypano

203 to sequence 70 and 0.4 megabase pairs (Mbp) nuclear DNA of the Forbes' Quarry and Devil's Tower spec

204 Therefore, partial defects in either the nuclear DNA or mtDNA genes or combinations of the two ca

205 sbestos induced a dose-dependent increase in nuclear DNA oxidative damage and MN in SAE cells.

206 without mitosis, resulting in an increase in nuclear DNA ploidy.

207 Human DNA polymerase N (PolN) is an A-family nuclear DNA polymerase whose function is unknown.

208 lear antigen (PCNA), the auxiliary factor of nuclear DNA polymerases, plays an important role in regu

209 A nuclear-DNA rate calibration suggests that mohoids diver

210 used whole blood to analyze mitochondrial-to-nuclear DNA ratio (mtDNA/nDNA) using quantitative polyme

211 s, as evidenced by elevated mitochondrial-to-nuclear DNA ratio and increased expression of the mitoch

212 aded intact mtDNA and decreased the mtDNA-to-nuclear DNA ratio.

213 haromyces cerevisiae, we determined mtDNA-to-nuclear DNA ratios in 5148 strains lacking nonessential

214 ases in mitochondrial mass, mitochondrial-to-nuclear DNA ratios, and both nuclear and mitochondrial e

215 bal biological effects, that is, they damage nuclear DNA, reduce the mitochondrial membrane potential

216 al effects that it induces did not involve a nuclear DNA related mode of action.

217 lasmic, and how and exactly when it accesses nuclear DNA remains enigmatic.

218 the mechanism by which DLAD gains access to nuclear DNA remains unknown.

219 However, Lig3 inactivation did not result in nuclear DNA repair deficiency, indicating essential DNA

220 , and rLOX-PP localized to radiation-induced nuclear DNA repair foci.

221 d in detection of a protein complex with the nuclear DNA repair regulator MRE11 in both cell lines, a

222 These results suggest that, contrary to nuclear DNA repair, mitochondrial DNA repair is not able

223 tial for mtDNA integrity but dispensable for nuclear DNA repair.

224 with HAT1 knock-down display mitosis without nuclear DNA replication and also specific de-repression

225 C6-interacting factors also act in T. brucei nuclear DNA replication and demonstrate that TbORC1/CDC6

226 2) is essential in RNA primer removal during nuclear DNA replication and is important in repairing UV

227 an DNA2, originally identified in yeast as a nuclear DNA replication and repair factor, functions exc

228 Early embryonic development features rapid nuclear DNA replication cycles, but lacks mtDNA replicat

229 n MMR in light of increasing knowledge about nuclear DNA replication enzymology and the rate and spec

230 aintain genome stability, mismatch repair of nuclear DNA replication errors must be directed to the n

231 Perhaps surprisingly, our understanding of nuclear DNA replication in kinetoplastids was limited un

232 study, we show that TbOrc1 is essential for nuclear DNA replication in mammalian-infectious bloodstr

233 Nuclear DNA replication is, arguably, the central cellul

234 liest acting components of the kinetoplastid nuclear DNA replication machinery - the factors that dem

235 cell surface receptor tyrosine kinase to the nuclear DNA replication machinery in cancer cells.

236 In eukaryotic nuclear DNA replication, one strand of DNA is synthesize

237 During nuclear DNA replication, proofreading-deficient DNA poly

238 isiae homologs, Pif1p and Rrm3p, function in nuclear DNA replication, telomere length regulation, and

239 its primase and polymerase activities during nuclear DNA replication.

240 Human UPF1 (hUPF1) is also needed for nuclear DNA replication.

241 anscript levels of mitochondrial DNA but not nuclear DNA respiratory complex subunits, suggesting act

242 Conversely, our nuclear DNA results based on 12 microsatellites detected

243 interferon-inducible protein IFI16 acts as a nuclear DNA sensor following HCMV infection, binding vir

244 reveal that KSHV utilizes the innate immune nuclear DNA sensor IFI16 to maintain its latency and rep

245 also required for stabilization of IFI16, a nuclear DNA sensor.

246 nted the standard barcoding locus (COI) with nuclear DNA sequence data (ITS2) and analyzed congruence

247 al description, as well as mitochondrial and nuclear DNA sequence data, from another molar (Denisova

248 The nuclear DNA sequence diversity among the three Denisovan

249 However, nuclear DNA sequences (n = 77 specimens) revealed extens

250 imescale derived from analyses of multilocus nuclear DNA sequences for Holarctic genera of plethodont

251 amined approximately 32 kilobases of aligned nuclear DNA sequences from 19 independent loci for 169 s

252 Here we present nuclear DNA sequences from Denisova 4 and a morphologica

253 Nuclear DNA sequences from the two molars form a clade w

254 Nuclear DNA staining revealed that ubp3 ubp4 pollen ofte

255 onal mitochondria, there was a lack of gross nuclear DNA strand breaks and apoptosis.

256 clade "Syngnathiformes" following the latest nuclear DNA studies with some revisions on the included

257 This deletion of pre-existing nuclear DNA suggests that the genetic impact of organell

258 ncient mitochondrial genomes and genome-wide nuclear DNA surveys to reveal that the wisent is the pro

259 Nuclear DNA synthesis ceased almost immediately followin

260 lopment, a large proportion of cells undergo nuclear DNA synthesis.

261 vision is observed in G2 after completion of nuclear DNA synthesis.

262 hmdC is a constituent of nuclear DNA that is highly abundant in the brain, sugges

263 incorporated in mitochondrial DNA, while in nuclear DNA the ribonucleotide pattern was only altered

264 In nuclear DNA, the levels of 8-oxo-dG in controls and AMD

265 learly distributes genome-wide in vertebrate nuclear DNA, the state of methylation in the vertebrate

266 These drugs bind nuclear DNA to form Pt-DNA cross-links, which arrest key

267 ted cytoplasmic population of BAF that binds nuclear DNA to rapidly and transiently localize to the s

268 re formed when neutrophils externalize their nuclear DNA together with antimicrobial granule proteins

269 itive role of PARP1 in regulation of various nuclear DNA transactions is well established.

270 iption initiation lags that of bacterial and nuclear DNA transcription.

271 osomes) with over 70 polypeptides encoded in nuclear DNA, translated on cytoplasmic ribosomes, and im

272 PPD crystal-stimulated neutrophils and their nuclear DNA undergo morphological changes characteristic

273 Plasma nuclear DNA, used as a marker for general danger-associa

274 nents were derived from ancestry-informative nuclear DNA variants.

275 plains a proportion of the mitochondrial and nuclear DNA variation among moths on different species o

276 the cytokine's activated state) and also to nuclear DNA via its N-terminal CCP module pair (CCP1/2),

277 These results suggest that a nuclear DNA virus can selectively interfere with RNA exp

278 ated herpesvirus (KSHV) is a human oncogenic nuclear DNA virus that expresses its genes using the hos

279 i's sarcoma-associated herpesvirus (KSHV), a nuclear DNA virus, inhibits mRNA export in a transcript-

280 Damage to mitochondrial DNA and nuclear DNA was assessed using a novel long quantitative

281 platin 1,2-intrastrand d(GpG) cross-links on nuclear DNA was confirmed by using a monoclonal antibody

282 in 1,2-intrastrand d(GpG) cross-links on the nuclear DNA was demonstrated by use of a monoclonal anti

283 DNA analysis confirmed that nuclear DNA was identical to donor somatic cells and tha

284 Relative mtDNA copy number as compared with nuclear DNA was measured by quantitative real-time polym

285 platin 1,2-d(GpG) intrastrand cross-links on nuclear DNA was verified.

286 Moreover, mtDNA, not nuclear DNA, was found to have higher levels of backgrou

287 drial content, measured by mitochondrial DNA/nuclear DNA, was higher in sepsis on day 1-2 than contro

288 activity of complex II, entirely encoded by nuclear DNA, was not.

289 esions per 10 kb per genome in the mtDNA and nuclear DNA were measured with long-extension polymerase

290 Levels of oxidized mitochondrial and nuclear DNA were not significantly different.

291 0-fold increase in uracil content in hepatic nuclear DNA when fed a folate- and choline-deficient die

292 This approach discards the nuclear DNA, which constitutes the vast majority of the

293 responsible for the anticancer activity, is nuclear DNA, which is packaged in nucleosomes that compr

294 e mechanism, mitaplatin thereby attacks both nuclear DNA with cisplatin and mitochondria with DCA sel

295 e were bred to female MNX mice having FVB/NJ nuclear DNA with either FVB/NJ, C57BL/6J, or BALB/cJ mtD

296 il extracellular traps (NETs), consisting of nuclear DNA with histones and microbicidal proteins, are

297 The association of nuclear DNA with histones to form chromatin is essential

298 n addition, unlike MNase, MPE-Fe(II) cleaves nuclear DNA with little sequence bias.

299 only of the nupt itself but also of flanking nuclear DNA within one generation of transfer.

300 Nuclear DNA wraps around core histones to form nucleosom