ライフサイエンスコーパス: deoxyribonucleic acid

1 enome sequencing was performed from proviral deoxyribonucleic acid.

2 ationships in proteins, ribonucleic acid and deoxyribonucleic acid.

3 ormed with cationic microbubbles and plasmid deoxyribonucleic acid.

4 e-specific cutting on target double-stranded deoxyribonucleic acids.

5 Associated with technological progress in deoxyribonucleic acid and messenger ribonucleic acid pro

6 results were confirmed using TaqMan DBS HIV-deoxyribonucleic acid and/or plasma HIV-ribonucleic acid

7 n of surface circumsporozoite protein (CSP), deoxyribonucleic acid, and 18S RNA labeling proved that

8 In this investigation, we used deoxyribonucleic acid array expression profiling to dete

9 From a deoxyribonucleic acid bank of 10,020 individuals, nondia

10 acid (RNA) levels of >55,000 copies/mL (by b-deoxyribonucleic acid [bDNA] or reverse transcriptase-po

11 Nuclear factor-kappaB deoxyribonucleic acid binding activity was significantly

12 ochondrial components, such as mitochondrial deoxyribonucleic acid, can be released by neutrophils to

13 nship to circulating cell-free mitochondrial deoxyribonucleic acid (ccf-mtDNA) in HIV-infected patien

14 an assay and rapid analysis of complementary deoxyribonucleic acid (cDNA) ends (5'-RACE).

15 al RNA extraction, followed by complementary deoxyribonucleic acid (cDNA) synthesis.

16 as reverse-transcribed and the complementary deoxyribonucleic acid (cDNA) was amplified with the poly

17 Cell-free deoxyribonucleic acid (cfDNA) released from either dead

18 = 27) were dried, dissolved, and assayed for deoxyribonucleic acid, collagen, and total GAGs.

19 Deoxyribonucleic acid containing the region of interest

20 fects mammary epithelial cells and inserts a deoxyribonucleic acid copy(ies) of its genome during rep

21 h bovine serum albumin (BSA) and calf thymus deoxyribonucleic acid (ctDNA).

22 presented in the functional pathways such as deoxyribonucleic acid damage repair.

23 factor receptor 2 inhibitor], and CC-115 [a deoxyribonucleic acid-dependent protein kinase/mammalian

24 rotein A (RPA), the eukaryotic single-strand deoxyribonucleic acid (DNA [ss-DNA])-binding protein, is

25 rs old with RR CMV infections and plasma CMV deoxyribonucleic acid (DNA) >=1000 copies/mL were random

26 (0.060 +/- 0.005 mumol/mg), and Sat-PC/lung deoxyribonucleic acid (DNA) (0.23 +/- 0.01 mumol/mg) did

27 s not only improves speed and sensitivity of deoxyribonucleic acid (DNA) amplification but also achie

28 encode histone proteins that package genomic deoxyribonucleic acid (DNA) and regulate its accessibili

29 Environmental deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) f

30 ng and transport of liquids, manipulation of deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) m

31 by hybridization studies with complementary deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) w

32 ic acids are intracellular, trace amounts of deoxyribonucleic acid (DNA) and ribonucleic acid (RNA),

33 conventional measures such as pharyngeal Mp deoxyribonucleic acid (DNA) and serum antibodies.

34 adable polycations as promising carriers for deoxyribonucleic acid (DNA) and small interfering RNA (s

35 ification of the fragmentation mechanisms of deoxyribonucleic acid (DNA) and the molecules surroundin

36 s required for the interference with foreign deoxyribonucleic acid (DNA) are concentrated in a single

37 XR5944, a deoxyribonucleic acid (DNA) bis-intercalator with potent

38 RNA) strand initiated cleavage of hybridized deoxyribonucleic acid (DNA) capture probes (CPs) by a du

39 employ magnetic beads conjugated with viral deoxyribonucleic acid (DNA) capturing probes and fluores

40 s demonstrated that an adenovirus-polylysine-deoxyribonucleic acid (DNA) complex can be used to inser

41 dependent restriction endonucleases, cleaves deoxyribonucleic acid (DNA) containing 5-hydroxymethylct

42 acteroids, regardless of the host plant, had deoxyribonucleic acid (DNA) contents, cellular sizes and

43 Aberrant deoxyribonucleic acid (DNA) contributes to inflammasome

44 on together in the Fanconi anemia network of deoxyribonucleic acid (DNA) crosslink repair.

45 Deoxyribonucleic acid (DNA) damage and triggering of pro

46 tions of these kinases in DSB repair and the deoxyribonucleic acid (DNA) damage checkpoint are unclea

47 The Chk2-mediated deoxyribonucleic acid (DNA) damage checkpoint pathway is

48 ncipal pathway that removes helix-distorting deoxyribonucleic acid (DNA) damage from the mammalian ge

49 odothyronine) to THRB induces senescence and deoxyribonucleic acid (DNA) damage in cultured cells and

50 yguanosine (8-OHdG) as a marker of oxidative deoxyribonucleic acid (DNA) damage in patients with chro

51 langiectasia and Rad3 related (ATR)-mediated deoxyribonucleic acid (DNA) damage response (DDR) pathwa

52 asia (A-T) mutated (ATM) kinase orchestrates deoxyribonucleic acid (DNA) damage responses by phosphor

53 telangiectasia (A-T) mutated (ATM) is a key deoxyribonucleic acid (DNA) damage signaling kinase that

54 s lacking Cdh1 have been shown to accumulate deoxyribonucleic acid (DNA) damage, suggesting that it m

55 tic, organisms are exposed to a multitude of deoxyribonucleic acid (DNA) damaging agents ranging from

56 te with in vivo efficacy as a potentiator of deoxyribonucleic acid (DNA) damaging chemotherapy and as

57 n (Tet) family of proteins as part of active deoxyribonucleic acid (DNA) demethylation pathway.

58 cular gate control has been demonstrated for Deoxyribonucleic acid (DNA) detection related to dengue

59 Nonhomologous end joining is the primary deoxyribonucleic acid (DNA) double-strand break repair p

60 ytic ubiquitylation of chromatin surrounding deoxyribonucleic acid (DNA) double-strand breaks (DSBs)

61 in kinase regulates the cellular response to deoxyribonucleic acid (DNA) double-strand breaks by phos

62 in PC9 and A549 cells led to an increase in deoxyribonucleic acid (DNA) double-strand breaks with in

63 fect of breast shielding on blood lymphocyte deoxyribonucleic acid (DNA) double-strand-break levels r

64 g the mechanisms that influence this choice, deoxyribonucleic acid (DNA) end resection plays a critic

65 A sequence-specific catalytic deoxyribonucleic acid (DNA) enzyme was used to reduce PA

66 ptamer with their more degradation-resistant deoxyribonucleic acid (DNA) equivalents.

67 No evidence of deoxyribonucleic acid (DNA) fragmentation, however, was

68 netic beads, (2) amplification of the target deoxyribonucleic acid (DNA) fragments by using single-nu

69 Enhancers are deoxyribonucleic acid (DNA) fragments which when bound b

70 The system analyzed proviral deoxyribonucleic acid (DNA) from an HIV-infected Jurkat

71 Effective microchip extraction of deoxyribonucleic acid (DNA) from crude biological matrix

72 Deoxyribonucleic acid (DNA) has been hypothesized to act

73 Deoxyribonucleic acid (DNA) has shown great promise in e

74 ulated recruitment of PALB2 to single-strand deoxyribonucleic acid (DNA) in a cell-free system.

75 nucleosides from ribonucleic acid (RNA) and deoxyribonucleic acid (DNA) in suitably designed isotopi

76 protein-protein interfaces, active sites or deoxyribonucleic acid (DNA) interfaces, and predicting t

77 Deoxyribonucleic acid (DNA) is emerging as an alternativ

78 The measurement of Epstein-Barr virus (EBV) deoxyribonucleic acid (DNA) is key to diagnosing and man

79 Deoxyribonucleic acid (DNA) is the blueprint of life, an

80 Deoxyribonucleic acid (DNA) is the blueprint on which li

81 roparticles in a microfluidic chip for rapid deoxyribonucleic acid (DNA) isolation.

82 h was determined by trypan blue staining and deoxyribonucleic acid (DNA) ladder electrophoresis.

83 The recognition of helix-distorting deoxyribonucleic acid (DNA) lesions by the global genome

84 Deoxyribonucleic acid (DNA) lesions encountered during r

85 may be more likely to form robust long-range deoxyribonucleic acid (DNA) loops.

86 s in MPV17 are associated with mitochondrial deoxyribonucleic acid (DNA) maintenance disorders.

87 We assessed host cell deoxyribonucleic acid (DNA) methylation markers for dete

88 Deoxyribonucleic acid (DNA) methylation plays a crucial

89 ere we demonstrate the imaging of individual deoxyribonucleic acid (DNA) molecules at the resolution

90 ine (5fC) were found to exist in the genomic deoxyribonucleic acid (DNA) of a wide range of mammalian

91 of 5-methylcytosine which is present in the deoxyribonucleic acid (DNA) of most mammalian cells.

92 Deoxyribonucleic acid (DNA) of precise length, by contra

93 of the phosphorus content of nucleotides and deoxyribonucleic acid (DNA) offers an approach to the qu

94 ents that allow the labeling and grafting of deoxyribonucleic acid (DNA) oligonucleotide probes in a

95 Representative genomic deoxyribonucleic acid (DNA) pools were created from male

96 Especially, only 2-mul usage for FISH deoxyribonucleic acid (DNA) probe was used, which is fiv

97 Deoxyribonucleic acid (DNA) replication and chromosome s

98 TopBP1-interacting protein, is necessary for deoxyribonucleic acid (DNA) replication in vertebrates.

99 origin recognition complex, is essential for deoxyribonucleic acid (DNA) replication initiation from

100 s and high-resolution imaging, we found that deoxyribonucleic acid (DNA) replication is asymmetricall

101 Deoxyribonucleic acid (DNA) samples are available for 5,

102 e complete cohort of patients with available deoxyribonucleic acid (DNA) samples.

103 low-density lipoprotein (LDL) oxidation and deoxyribonucleic acid (DNA) scission.

104 Deoxyribonucleic acid (DNA) sequencing analysis indicate

105 The cost of deoxyribonucleic acid (DNA) sequencing has gone from mil

106 challenge causes an increase in decatenated deoxyribonucleic acid (DNA) structures and late-replicat

107 scribe the intricate equilibrium among non-B deoxyribonucleic acid (DNA) structures.

108 genetics and the application of recombinant deoxyribonucleic acid (DNA) techniques.

109 eotides out of register, with respect to the deoxyribonucleic acid (DNA) template.

110 Letermovir (LET), a cytomegalovirus (CMV) deoxyribonucleic acid (DNA) terminase inhibitor, was rec

111 A new extraordinary application of deoxyribonucleic acid (DNA) thin-solid-film was experime

112 ts Cse4-H4 through a dimer intermediate onto deoxyribonucleic acid (DNA) to form a (Cse4-H4)2-DNA com

113 Deoxyribonucleic acid (DNA) topoisomerases are essential

114 Deoxyribonucleic acid (DNA) was obtained after informed

115 xpression of circadian-associated genes, HIV deoxyribonucleic acid (DNA), and cell-associated unsplic

116 extracellular polymeric substances (EPS) and deoxyribonucleic acid (DNA), and fluorescence intensitie

117 (23 dilated, 14 ischemic) were analyzed for deoxyribonucleic acid (DNA), collagen, glycosaminoglycan

118 t strain capable of expressing environmental deoxyribonucleic acid (DNA), precluding the need for pur

119 Melanoma, influenced by changes in deoxyribonucleic acid (DNA), requires early detection fo

120 i-task architecture that accurately predicts deoxyribonucleic acid (DNA)-, ribonucleic acid (RNA)- an

121 gineered (GE) plants is typically done using deoxyribonucleic acid (DNA)-based methods to detect the

122 ssues that include cross-predictions between deoxyribonucleic acid (DNA)-binding and ribonucleic acid

123 n this paper, we report that, in contrast to deoxyribonucleic acid (DNA)-dependent protein kinase cat

124 tions in detecting topological variations in deoxyribonucleic acid (DNA).

125 rus content in acid-digested nucleotides and deoxyribonucleic acid (DNA).

126 extend the method from adenoviral to plasmid deoxyribonucleic acid (DNA).

127 ion (OXPHOS) system encoded by mitochondrial Deoxyribonucleic acid (DNA).

128 wo nucleic acids, ribonucleic acid (RNA) and deoxyribonucleic acid (DNA).

129 proved binding affinity toward complementary deoxyribonucleic acid (DNA)/ribonucleic acid (RNA) stran

130 Fused in sarcoma (FUS), a multifunctional deoxyribonucleic acid (DNA)/ribonucleic acid (RNA)-bindi

131 Deoxyribonucleic acids (DNA) of periodontal pathogens, P

132 mechanism, synthetic single-strand antisense deoxyribonucleic acids (DNAs) are now in clinical trials

133 ytic ubiquitylation of chromatin surrounding deoxyribonucleic acid double-strand breaks (DSBs), media

134 cence (RTP) sensor to detect double stranded deoxyribonucleic acid (ds-DNA)/drug interaction.

135 se, covalently modifies self double-stranded deoxyribonucleic acid (dsDNA) and induces apoptosis.

136 transport and separation of double-stranded deoxyribonucleic acid (dsDNA) oligonucleotides in custom

137 Chromatin structure is modulated during deoxyribonucleic acid excision repair, but how this is a

138 al postmortem examination were the source of deoxyribonucleic acid for genetic analysis.

139 Deoxyribonucleic acid for the genome was obtained from t

140 Using deoxyribonucleic acid from 389 unrelated patients with H

141 We tested genomic deoxyribonucleic acid from 608 prospectively recruited p

142 Genomic deoxyribonucleic acid from 95 healthy African Americans

143 s the profibrogenic release of mitochondrial deoxyribonucleic acid from dying hepatocytes in a p38-de

144 release of mitochondrial DAMP mitochondrial deoxyribonucleic acid from dying hepatocytes was blocked

145 Herein, an aptamer-tethered deoxyribonucleic acids-gold particle (Apt-DNA-Au) nanoma

146 ibonucleic acid (rrs), flagellin (flaB), and deoxyribonucleic acid gyrase (gyrB) genes and conducting

147 f the rate of undetectable serum Hepatitis B deoxyribonucleic acid (HBV DNA) as the sustained virolog

148 is highly toxic to dividing cells when it is deoxyribonucleic acid incorporated, but it is relatively

149 n situ end-labeling method and confirmed by "deoxyribonucleic acid laddering" on agarose-gel electrop

150 purines and pyrimidines directly from lambda-deoxyribonucleic acid (lambda-DNA) and Escherichia coli

151 Viral deoxyribonucleic acid load in salivary glands was determ

152 Genotyping of FAF 1 to 4 with deoxyribonucleic acid markers spanning the chromosome 10

153 Deoxyribonucleic acid methylation data from this cross-s

154 We investigated intratumoral deoxyribonucleic acid methylation heterogeneity by analy

155 etic or regulatory mechanisms, which include deoxyribonucleic acid methylation, histone methylation,

156 The gene expression profile was examined by deoxyribonucleic acid microarray and real-time reverse t

157 Moreover, we found that deoxyribonucleic acid microarray technology could distin

158 t allow for absolute quantification of input deoxyribonucleic acid molecules following PCR.

159 We use suspended deoxyribonucleic acid molecules or single-walled carbon

160 ic, with mutated and wild-type mitochondrial deoxyribonucleic acid (mtDNA) coexisting within the same

161 e-wide association analyses of mitochondrial deoxyribonucleic acid (mtDNA) copy number (mtDNA CN) mea

162 ne C10orf2 encoding Twinkle, a mitochondrial deoxyribonucleic acid (mtDNA)-specific helicase, and a r

163 es the level of negative supercoiling of the deoxyribonucleic acid of compensated genes, and we have

164 on of chemically synthesized single-stranded deoxyribonucleic acid (oligonucleotides) into the chromo

165 -based hydrogels are synthesized by grafting deoxyribonucleic acid onto the cellulose backbone throug

166 ensor for determination of mercury(II) using deoxyribonucleic acid/poly-L-methionine-gold nanoparticl

167 esolved the status of 5 uncharacterized UL54 deoxyribonucleic acid polymerase (G441S, A543V, F460S, R

168 tion were performed along with HIV-1 RNA and deoxyribonucleic acid quantification and measurement of

169 R adaptation, a copy of a segment of foreign deoxyribonucleic acid referred to as protospacer is adde

170 rythroid-derived) 2-like; NFE2L2) binding to deoxyribonucleic acid-regulatory sequences near stress-r

171 During meiosis, one round of deoxyribonucleic acid replication is followed by two rou

172 c proteins that are essential for processive deoxyribonucleic acid replication.

173 e nuclear divisions follow a single round of deoxyribonucleic acid replication.

174 llograft, genetic testing from donor-derived deoxyribonucleic acid revealed a heterozygous mutation i

175 MS or nuclear magnetic resonance profiling); deoxyribonucleic acid, ribonucleic acid, protein, and me

176 Genomic deoxyribonucleic acid samples from 338 individuals among

177 nital glaucoma probands with extended family deoxyribonucleic acid samples were screened for LTBP2 an

178 ma gene, CYP1B1, was performed on 47 proband deoxyribonucleic acid samples.

179 Leukocyte deoxyribonucleic acid segments containing the genomic si

180 amplification, deletion or translocation of deoxyribonucleic acid segments in proto-oncogenes and tu

181 gorithms enhance the identification of novel deoxyribonucleic acid sequences with pivotal biological

182 ith recent reports of detection of E. dispar deoxyribonucleic acid sequences, previously considered n

183 al-derived products, in particular bacterial deoxyribonucleic acid sequences; autoreactive T cells, a

184 Deoxyribonucleic acid sequencing of affected individuals

185 high-performance liquid chromatography, and deoxyribonucleic acid sequencing on 155 unrelated patien

186 Using direct deoxyribonucleic acid sequencing, the coding exons/splic

187 erformance liquid chromatography, and direct deoxyribonucleic acid sequencing.

188 erformance liquid chromatography, and direct deoxyribonucleic acid sequencing.

189 nce liquid chromatography (DHPLC) and direct deoxyribonucleic acid sequencing.

190 able polymers with alternating single-strand deoxyribonucleic acid (ssDNA) and planar fluorescent org

191 A modified single-stranded deoxyribonucleic acid (ssDNA) aptamer was specially desi

192 ce coverage for thiol-modified single-strand deoxyribonucleic acid (ssDNA) as anchored probe and 6-Me

193 viruses (AAVs) are typically single-stranded deoxyribonucleic acid (ssDNA) encapsulated within 25-nm

194 ptamers and are either short single-stranded deoxyribonucleic acid (ssDNA) or ribonucleic acid (RNA)

195 sor is provided that detects single-stranded deoxyribonucleic acid (ssDNA) with a specific base seque

196 Thiol-terminated single-stranded deoxyribonucleic acids (ssDNA) can be immobilized onto p

197 In this study, we combined deoxyribonucleic acid-stable isotope probing (DNA-SIP) w

198 Documentation of cell cycle regulators, deoxyribonucleic acid synthesis, and mitotic images has

199 of Caco-2 cells, low-density lipoprotein and deoxyribonucleic acid than those of the spinach.

200 do not eliminate covalently closed circular deoxyribonucleic acid, the stable replication template.

201 We discover organic semiconductors from deoxyribonucleic acid topoisomerase inhibitors, featurin

202 ild-type (TG(WT)) human PRKAG2 complementary deoxyribonucleic acid under a cardiac-specific promoter.

203 Collectively, both ribonucleic acid and deoxyribonucleic acid viruses were negatively associated

204 mg b.i.d.; or placebo 10 mg b.i.d. T. cruzi deoxyribonucleic acid was detected by RT-PCR at 30, 60,

205 lymphoblastoid cell lines were immortalized, deoxyribonucleic acid was extracted, polymerase chain re

206 Genomic deoxyribonucleic acid was genotyped for the rs4680 SNP u

207 The human NIS complementary deoxyribonucleic acid was transduced into rat cardiac-de

208 ells/mm3, female sex, and lower baseline HBV deoxyribonucleic acid were associated with increased odd

209 al, 167 123 donations were screened for B19V deoxyribonucleic acid with 22 cases of viremia identifie

210 Complementary deoxyribonucleic acid with retained intron 7 failed to p

211 Z-deoxyribonucleic acid (Z-DNA) is an alternative left-han