ライフサイエンスコーパス: deoxyribonucleic acid

1 ationships in proteins, ribonucleic acid and deoxyribonucleic acid.

2 ormed with cationic microbubbles and plasmid deoxyribonucleic acid.

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

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

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

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

7 Nuclear factor-kappaB deoxyribonucleic acid binding activity was significantly

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

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

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

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

12 Deoxyribonucleic acid containing the region of interest

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

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

15 (0.060 +/- 0.005 mumol/mg), and Sat-PC/lung deoxyribonucleic acid (DNA) (0.23 +/- 0.01 mumol/mg) did

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

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

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

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

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

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

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

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

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

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

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

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

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

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

30 Deoxyribonucleic acid (DNA) damage and triggering of pro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 Deoxyribonucleic acid (DNA) lesions encountered during r

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

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

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

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

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

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

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

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

68 Deoxyribonucleic acid (DNA) replication and chromosome s

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

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

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

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

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

74 Deoxyribonucleic acid (DNA) sequencing analysis indicate

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

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

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

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

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

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

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

82 Deoxyribonucleic acid (DNA) topoisomerases are essential

83 Deoxyribonucleic acid (DNA) was obtained after informed

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

85 (23 dilated, 14 ischemic) were analyzed for deoxyribonucleic acid (DNA), collagen, glycosaminoglycan

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

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

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

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

90 Deoxyribonucleic acids (DNA) of periodontal pathogens, P

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

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

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

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

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

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

97 Deoxyribonucleic acid for the genome was obtained from t

98 Using deoxyribonucleic acid from 389 unrelated patients with H

99 We tested genomic deoxyribonucleic acid from 608 prospectively recruited p

100 Genomic deoxyribonucleic acid from 95 healthy African Americans

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

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

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

104 Viral deoxyribonucleic acid load in salivary glands was determ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

121 Genomic deoxyribonucleic acid samples from 338 individuals among

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

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

124 Leukocyte deoxyribonucleic acid segments containing the genomic si

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

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

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

128 Deoxyribonucleic acid sequencing of affected individuals

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

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

131 erformance liquid chromatography, and direct deoxyribonucleic acid sequencing.

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

133 erformance liquid chromatography, and direct deoxyribonucleic acid sequencing.

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

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

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

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

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

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

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

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

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

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

144 Complementary deoxyribonucleic acid with retained intron 7 failed to p