ライフサイエンスコーパス: DNA array

1 bind the 2.6-kb promoter fragment by protein/DNA array.

2 riers in the spacer regions of the ribosomal DNA array.

3 ted from the microbe Escherichia coli onto a DNA array.

4 protein array can be obtained from a single DNA array.

5 rm within a two-dimensional (2D) crystalline DNA array.

6 o form a randomized multiplexed high-density DNA array.

7 ic behavior of every gene represented on the DNA array.

8 performed to confirm the results of protein-DNA array.

9 NAPI and enforces the stability of ribosomal DNA arrays.

10 tone octamer and linker histone onto the 601 DNA arrays.

11 or increased sensitivity of DNA detection on DNA arrays.

12 rces on coated glass slides with and without DNA arrays.

13 analyzed bacterial gene transcription using DNA arrays.

14 tures representing steps towards multiplexed DNA arrays.

15 germline to form multicopy extrachromosomal DNA arrays.

16 towards all-electrical multiplexed graphene DNA arrays.

17 l crosslinker, permitting the preparation of DNA arrays.

18 nterstitial space in spontaneously condensed DNA arrays.

19 bution of Rap1 monomers on defined telomeric DNA arrays.

20 lso contribute to the integrity of ribosomal DNA arrays.

21 t-directed synthetic methods for fabricating DNA arrays.

22 he standard substrate for the preparation of DNA arrays.

23 ediated signaling pathways and complementary DNA arrays.

24 scope slides were used as substrates for MEF DNA arrays.

25 igonucleotide arrays to double-stranded (ds) DNA arrays.

26 of long genome sequences, e.g. obtained from DNA arrays.

27 meres, interspersed in centromeric satellite DNA arrays [4,5].

28 By equilibrating condensed DNA arrays against reservoirs of known osmotic stress an

29 We show that human gamma-satellite DNA arrays allow a transcriptionally permissive chromati

30 oach, but also to investigate the utility of DNA array alternatives.

31 H. pylori DNA array analyses and transcriptional reporter assays i

32 DNA array analyses identified genes that may inhibit res

33 Subsequently, protein/DNA array analyses identified numerous other transcripti

34 rved from uPAR-ChIP, TF protein, and protein/DNA array analyses that uPAR associates with activating

35 Here we show, using DNA array analyses, that nicotinamide N-methyltransferas

36 Although DNA array analysis can monitor large numbers of genes, t

37 Recent studies using DNA array analysis challenge this hypothesis and suggest

38 MEFs; yet, host cell reactivation assays and DNA array analysis indicate that the nucleotide excision

39 A critical step for DNA array analysis is data filtration, which can reduce

40 DNA array analysis of 205 apoptosis-related genes indica

41 Complementary DNA array analysis of Lyn-deficient DT40 cells shows tha

42 ed at least 15,000 unique cDNAs, as shown by DNA array analysis of PCR-amplified cDNA inserts, repres

43 ownstream target gene of DeltaFosB by use of DNA array analysis of striatal material from inducible t

44 Furthermore, DNA array analysis showed that infection with a pp65-def

45 DNA array analysis showed that of 114 genes regulated by

46 DNA array analysis showed that unlike the A. niger oah g

47 spotted with genomic DNA fragments (genomic DNA array analysis).

48 In the protein-DNA array analysis, 12 transcription factors were up-reg

49 re subjected to transcription factor protein-DNA array analysis.

50 f differences and/or ratios), should improve DNA array analysis.

51 DNA-array analysis also identified known markers of card

52 Results of DNA-array analysis of over 6,000 genes from hearts expre

53 ies: genotyping high-density oligonucleotide DNA array and denaturing high-performance liquid chromat

54 for both spatial resolution of the patterned DNA array and optimization of detection through DNA-medi

55 ols examined are excluded from the condensed DNA array and strongly affect the osmotic stress force c

56 New technologies, including DNA arrays and automated sequencing, have improved detec

57 DNA arrays and chips are powerful new tools for gene exp

58 DNA arrays and chips will be key in understanding how ge

59 obertsonian chromosomes have two centromeric DNA arrays and have lost all ribosomal DNA.

60 st promising gains have come in the areas of DNA arrays and mass spectrometry, where differential seq

61 ology and show promise for future electronic DNA arrays and rapid characterization of nucleic acid sa

62 erences between stable clones as revealed by DNA arrays and sequencing.

63 kes possible the construction of genome-wide DNA arrays and the study of this organism on a global sc

64 In budding yeast, telomeres, the ribosomal DNA array, and HM loci are transcriptionally silenced by

65 ination along chromosomes carrying ribosomal DNA arrays, and (iii) an inversely proportional relation

66 chemical analysis, custom-made complementary DNA arrays, and quantitative real-time reverse transcrip

67 encing such as acrocentric p-arms, ribosomal DNA arrays, and telomeric repeats, and involved complex

68 such as transcription factors in randomized DNA arrays; and computer-generated physical trajectories

69 ially well suited for multiplexed electronic DNA array applications, since its large two-dimensional

70 , we reconstructed the centromeric satellite DNA array (approximately 3.1 Mb) and closed the 29 remai

71 Heterochromatinized repetitive DNA arrays are abundant in most eukaryotic genomes.

72 the ion contents and DNA-DNA spacings of the DNA arrays are determined by atomic emission spectroscop

73 DNA arrays are fabricated by high-speed robotics on glas

74 nd of glycerol with condensed spermidine(3+)-DNA arrays are investigated with direct force measuremen

75 Of further relevance, the DNA arrays are of tunable dimensions, and fabricated on

76 ntified genetic instability of the ribosomal DNA array as the first known cause of aging in yeast cel

77 ntal measurements on the osmotic pressure of DNA array as well as the results from the computer simul

78 iments, we measured the internal pressure of DNA arrays as a function of the DNA-DNA distance, showin

79 urface immobilization of oligonucleotides in DNA arrays as well as a route for the coupling of nuclei

80 zed the orientational correlations of DNA in DNA arrays as well as diffusive motion of DNA and cation

81 ologic and pathophysiologic conditions using DNA arrays, as well as the development and use of robust

82 X-ray scattering on highly ordered DNA arrays at high density and with the helical axis ori

83 Preliminary whole-genome DNA arrays at various time points within 1 h of incubati

84 Algorithms designed for analysis of DNA array autoradiographs incorporate 3-D peak fitting o

85 DNA array based screening approaches permit detection of

86 on of datasets generated with single-channel DNA arrays based on principal component analysis.

87 e employed an inducible cell culture system, DNA array-based and in silico transcript profiling, and

88 w tool for saponin pathway gene discovery by DNA array-based approaches.

89 In contrast to DNA array-based methods, reporter gene technology has be

90 A comparison of their respective DNA array-based transcriptional profiles identified gene

91 We describe a DNA-array-based method to infer intramolecular connectio

92 DNA arrays can be used as periodic templates to create,

93 DNA arrays can be used for many different purposes, most

94 sion of nested GBATM primers on miniaturized DNA arrays can be used to effectively scan targeted sequ

95 We report a multiplexed high-density DNA array capable of rapid, sensitive, and reliable iden

96 DNA array-cell surface interactions were visualized by f

97 in mu-total analysis systems (mu-TAS) and in DNA-array chips utilized for environmental monitoring of

98 nd evaluate the stabilities of the resultant DNA arrays compared to those fabricated on silanized gla

99 on of bpDNA oligomers into a two-dimensional DNA array comprised of tiles containing double crossover

100 ptotic effects of TRO, we screened a limited DNA array containing 23 genes involved in regulating eit

101 ected with wild type and a mutant virus to a DNA array containing probes for 588 human genes represen

102 Glass DNA arrays containing a selected set of 1,019 genes (inc

103 analysis of MHV-68 gene expression, we made DNA arrays containing nearly all of the known and predic

104 DNA arrays containing up to 135,000 probes complementary

105 The MB-based DNA array could be used for DNA detection with high sens

106 Non-redundant DNA arrays could be constructed for any group of closely

107 We have constructed a DNA array covering 121 kb surrounding the DHFR locus, to

108 to reduce the multidimensional complexity of DNA array data and attempt to extract some meaningful in

109 The zone-specific DNA array data obtained from human tissue were compared

110 timates of transcript abundance suggest that DNA array data serve as adequate predictors of translati

111 oaches were used in the analysis of a sample DNA array data set derived from genome-wide gene express

112 DNA array data show that three blyA homologs were upregu

113 s (ICA) method for reducing high dimensional DNA array data to a smaller set of latent variables, eac

114 To complement DNA array data, cost-efficient high-throughput technolog

115 A DNA array detection method is reported in which the bind

116 greater potential to impact diagnostics than DNA arrays due to their potential for direct sample meas

117 Non-denatured double-stranded DNA array elements were shown to hybridize to single-str

118 F can be used to increase the sensitivity of DNA arrays, especially for far red emitting fluorophores

119 entration of Mg(2+), the Co(3+)Hex-condensed DNA array expands and eventually redissolves as a result

120 ombines bioinformatics analysis and in vitro DNA array experimentation.

121 Three independent DNA array experiments confirmed these results and showed

122 Replicate DNA array experiments identified 52 genes differentially

123 These methods differ from traditional DNA array experiments in that the readout is a direct me

124 PCR analysis of genes selected based on DNA array experiments revealed that estimation of the ra

125 DNA array experiments showed that, among other proteins,

126 sion in genome sequencing, and in subsequent DNA array experiments, has provided extensive informatio

127 otal sample volume is 500 microL; in the 2-D DNA array experiments, this volume is reduced to 1 micro

128 DNA arrays fabricated on these carbon-metal substrates a

129 gene expression with the use of high-density DNA array filters spotted with genomic DNA fragments (ge

130 aTLs measured by DNA-array-FISH predicted aTLs measured by terminal restr

131 telomere fluorescent in situ hybridization (DNA-array-FISH) approach was developed to measure the ba

132 application of this multiplexed high-density DNA array for parallel identification of target BWAs in

133 or stability enables the use of high-density DNA arrays for applications involving high temperatures,

134 a target and evaluated the use of stem-loop DNA arrays for detecting p53 mutations in the deletion s

135 gene fusions are an important alternative to DNA arrays for genomewide transcriptional analyses.

136 uce protein arrays for chip-based assays and DNA arrays for genotyping or genome sequencing.

137 The stem-loop DNA array format is simple, robust and flexible in desig

138 enotyping technology can be multiplexed in a DNA array format, permitting the parallel analysis of a

139 We report a novel method of DNA array formation that is electrochemically formed and

140 A construct with an alphoid DNA array from chromosome 22 with no detectable CENP-B m

141 New technologies using DNA arrays genotyping for a million or more SNPs promise

142 g of fluorescently tagged proteins to tandem DNA arrays has been instrumental in understanding nuclea

143 The introduction of oligonucleotide DNA arrays has resulted in much debate concerning approp

144 abases, expressed sequence tag databases and DNA arrays have been applied to find candidate genes for

145 Among these new technologies, DNA arrays have provided an important experimental appro

146 Through the use of more natural tandem DNA arrays, Hu et al. gain new insights into chromatin o

147 plication for thousands of genes in a single DNA array hybridization experiment.

148 Protein/DNA arrays identified E2F1, but not beta-catenin/Tcf, as

149 taking place upon DNA hybridization in dense DNA arrays immobilized on a layer of Au nano-particles d

150 To test the value of complement DNA arrays in identifying pathways involved in organ tra

151 try and can be applied to different types of DNA arrays, including custom arrays.

152 Studies using complementary DNA arrays indicated that the ADAM (A disintegrin and me

153 by CLOCK and/or circadian rhythms, we used a DNA array interrogating the mouse protein-encoding trans

154 By converting only part of the DNA array into a protein array, simultaneous detections

155 A high-density DNA array is fabricated by standard photolithographic me

156 ovel wireless electrochemiluminescence (ECL) DNA array is introduced for the visualized genotyping of

157 utility of these microfluidic arrays, a 2-D DNA array is used to detect a 20-fmol sample of in vitro

158 Gene expression profiling using DNA arrays is rapidly becoming an essential tool for res

159 The DNA-array is firstly converted into antibody-array using

160 Using a series of DNA array membranes, we identified a group of hypoxia-in

161 to determine spot heterogeneity in identical DNA array microspots comprising varied ratios of unlabel

162 However, realizing single-DNA arrays must tackle the challenge of capturing struct

163 Using a DNA array of 2059 genes, we analyzed cellular responses

164 n, we have constructed a partial C. albicans DNA array of 7,000 genes and used it to study the gene e

165 We used DNA arrays of 16,580 human cDNAs to identify 728 known g

166 omics data from complex tissues use barcoded DNA arrays of low- to sub-micrometer features to achieve

167 osition to specific parts of the chromosome, DNA arrays of Salmonella enterica were used to quantitat

168 DNA arrays of the entire set of Escherichia coli genes w

169 Using these MB probes, we have developed a DNA array on avidin-coated cover slips and have improved

170 nsible for the evolution of large repetitive DNA arrays on all chromosomes.

171 DNA arrays on carbon-based substrates are substantially

172 nstrated for protein adsorption onto protein/DNA arrays on gold from aqueous solution using an SPR mi

173 tify micropatterned DNA spots within printed DNA arrays on slide surfaces and quantify DNA elements w

174 can be used directly in the construction of DNA arrays or can be cloned for a large variety of funct

175 ilver particles for increased sensitivity on DNA arrays or for DNA analysis.

176 or DNA self-assembled nanostructures such as DNA arrays, origami, and designer crystals.

177 DNA arrays permit rapid, large-scale screening for patte

178 The radioactivity labeled DNA array platform is a robust and accurate way for a hi

179 to detect specific targets in the multiplex DNA array platform.

180 DNA arrays provide a broad snapshot of the state of the

181 and/or organization of centromeric satellite DNA arrays rather than a more direct involvement in cent

182 Cross-species hybridization of a DNA array representing 1628 open reading frames (ORF) of

183 We used nylon-substrate DNA arrays representing approximately 96% of the predict

184 e body or changing the position of ribosomal DNA arrays resulted in the association of Pol III-transc

185 and MUC-1, the powerful coupling of SAGE and DNA arrays resulted in the identification of genes and p

186 Comparative genome hybridization with DNA arrays revealed strain differences in S. pneumoniae

187 ates faster then the parental strain and the DNA arrays revealed that nearly every MHV-68 ORF examine

188 We analyzed with Affymetrix DNA Arrays (Santa Clara, CA) the endothelial cell transc

189 bal gene expression analysis using an MHV-68 DNA array showed that PGE(2) increased production of mul

190 Analysis of protein/DNA array showed that TCEAL7 downregulation resulted in

191 Whole genome DNA arrays showed that at 10 muM RA839 significantly reg

192 lly affect probe-target duplex formation and DNA array signal generation.

193 Moreover, protein-DNA array studies identified two novel GSK-3-regulated t

194 DNA array studies provide a nonbiased detection of netwo

195 ole-blood gene-expression profiles by use of DNA array technology and confirmed the results by use of

196 ing this invasive cleavage assay and surface DNA array technology has been developed for potentially

197 DNA array technology is still in its infancy, but many h

198 With the advent of DNA array technology it is now possible to obtain a larg

199 Here we apply DNA array technology to examine the specificity of antis

200 We have used DNA array technology to monitor the level of approximate

201 We have developed methods for using DNA array technology to probe the entire transcriptome t

202 Among these, DNA array technology, which allows one to assay thousand

203 henotype of these cells was determined using DNA array technology.

204 g kidney organogenesis by using high-density DNA array technology.

205 RNA was eluted, amplified, and analyzed with DNA array technology.

206 of replicate protein arrays directly from a DNA array template using cell-free protein synthesis.

207 The zip code master is a DNA array that defines the location of oligonucleotides

208 can be used experimentally with high-density DNA arrays that allow complex mixtures of RNA and DNA to

209 n centromeres are defined by alpha satellite DNA arrays that are distinct and chromosome specific.

210 d by megabases of homogenous alpha-satellite DNA arrays that are packaged into specialized chromatin

211 orphism changes in the respective genes, and DNA arrays that target these changes have been validated

212 Here we show, using DNA arrays, that expression of retinol binding protein-4

213 gely determined by a single parameter of the DNA array, the fraction of DNA charges neutralized by Co

214 We use a new multi-species complementary DNA array to compare steady-state messenger RNA levels i

215 We used the Panomics TransSignal protein/DNA array to identify changes in the levels of cellular

216 We describe a method, DNA array to protein array (DAPA), which allows the 'pri

217 of AtNHX1 (nhx1 plants) and Affymetrix ATH1 DNA arrays to assess differences in transcriptional prof

218 We used whole-genome DNA arrays to determine the system response in Escherich

219 elf and the organism from UV damage, we used DNA arrays to follow UV-caused gene expression changes i

220 ed on a proof-of-principle scale using small DNA arrays to genotype 6 SNP markers in the PTPN1 gene a

221 use of RNA expression arrays and CpG-island DNA arrays to identify and characterize human PRC2/3 tar

222 The use of high-density DNA arrays to monitor gene expression at a genome-wide s

223 huntingtin protein, we used oligonucleotide DNA arrays to profile approximately 6000 striatal mRNAs

224 physiology and behavior, we used RNA-seq and DNA arrays to quantify the transcriptomes of 12 mouse or

225 We used oligo-based DNA arrays to study the expression profiles of eight mat

226 two strategies for attaching self-assembled DNA arrays to the surfaces of cells.

227 erial analysis of gene expression (SAGE) and DNA arrays, to help elucidate pathways in breast cancer

228 Recent developments have applied a DNA array-type approach to immobilize proteins on a surf

229 epeats of a few hundred base pairs into long DNA arrays up to 120 kb.

230 A method for analyzing combinatorial DNA arrays using oligonucleotide-modified gold nanoparti

231 The alphoid DNA array was also isolated from the 12 Mb human mini-ch

232 A CMS-DNA array was prepared on an array of gold electrodes on

233 ried out successfully on the above-described DNA array, we then performed a sequencing reaction on th

234 Utilizing B. burgdorferi whole genome DNA arrays, we compared the transcriptomes of the spiroc

235 By analysing these cells on DNA arrays, we define a pattern of gene expression that

236 Here, by using transcription profiling via DNA arrays, we have identified genes induced by DsrA.

237 Using genomic DNA arrays, we identified genes whose expression is affe

238 Using DNA arrays, we show that Bcl-xL features as a prominent

239 Genotypes based on the 50 K SNP DNA array were available and a total of 34,874 SNPs rema

240 DNA arrays were used to analyze gene expression profiles

241 Finally, the MHV-68 DNA arrays were used to examine the gene expression prof

242 Affymetrix GeneChip 6.0 DNA arrays were used to genotype nearly 700,000 single-n

243 TranSignal Protein/DNA arrays were used to identify the hypoxia-inducing fa

244 DNA arrays were used to investigate the functional role

245 In this study, DNA arrays were utilized to monitor the transcriptional

246 a part of the long alpha-satellite (alphoid) DNA array, where it is flanked by pericentric heterochro

247 three-layer logpile (3LL), a two-dimensional DNA array which self-assembles from four synthetic oligo

248 Spotted DNA arrays, which are found to inhibit biofouling, are u

249 A method for rapidly assembling high-density DNA arrays with near-perfect order is described.

250 Hydrophobic or amphiphilic DNA arrays would be useful for the synthesis of hydropho

251 e by using ZFP819, which targets a satellite DNA array, ZP3AR.