ライフサイエンスコーパス: DNA sequence analysis

1 potential to replace gel electrophoresis for DNA sequence analysis.

2 road range of vertebrate poikilotherms using DNA sequence analysis.

3 etry, accurate mass measurements, and direct DNA sequence analysis.

4 eteroduplex mobility and tracking assays and DNA sequence analysis.

5 , and characterization of point mutations by DNA sequence analysis.

6 Bw4 expression was confirmed by DNA sequence analysis.

7 the heteroduplex mobility assay (HMA) and by DNA sequence analysis.

8 are not sufficiently similar to identify by DNA sequence analysis.

9 DNAs, and locating primer binding sites for DNA sequence analysis.

10 oaches, 71 by microarray and 63 by gel-based DNA sequence analysis.

11 olated the tumor cells and subjected them to DNA sequence analysis.

12 12 genes in four operons were identified by DNA sequence analysis.

13 hin slab gel electrophoresis-based automated DNA sequence analysis.

14 K-ras mutations were determined by DNA sequence analysis.

15 omes and is an economic tool for comparative DNA sequence analysis.

16 other nanopore devices for implementation of DNA sequence analysis.

17 Discrepant results were resolved by DNA sequence analysis.

18 Identification was based on morphology and DNA sequence analysis.

19 finally to mutant allele characterization by DNA sequence analysis.

20 and greater genetic diversity as assessed by DNA sequence analysis.

21 F MS for automated high-throughput microbial DNA sequence analysis.

22 Length of the products was confirmed by DNA sequence analysis.

23 qacA or qacB gene was determined by PCR and DNA sequence analysis.

24 solutions were used as sieving matrixes for DNA sequencing analysis.

25 es with positive H. pylori were subjected to DNA sequencing analysis.

26 arget site was estimated to be 20% by direct DNA sequencing analysis.

27 sults were consistent with those obtained by DNA sequencing analysis.

28 ytes and macrophages, which was confirmed by DNA sequencing analysis.

29 olled to achieve high performance and rugged DNA sequencing analysis.

30 d MLL-AF4-encoded proteins based on previous DNA sequencing analysis.

31 anis using PCR, multiplex real-time PCR, and DNA sequencing analysis.

32 Based upon DNA sequence analysis, a Mycoplasma ovis-like species wa

33 ations of these mutations were determined by DNA sequence analysis after PCR amplification of the pho

34 Furthermore, DNA sequence analysis allowed the determination of the p

35 l language processing (NLP), (ii) predictive DNA sequence analysis and (iii) Human activity recogniti

36 utated by microarray but not by conventional DNA sequence analysis and 6 cases identified as mutated

37 roteins and synthetic peptides based on this DNA sequence analysis and examined their reactivity with

38 luated in 108 ovarian tumors by conventional DNA sequence analysis and oligonucleotide microarray (p5

39 DNA sequence analysis and restriction mapping of one par

40 DNA sequence analysis and site-directed mutagenesis stud

41 have been validated by gel electrophoresis, DNA sequence analysis and thermal denaturation profile.

42 al samples is a bottleneck in genotyping and DNA sequencing analysis and is frequently limited by the

43 ing STS-content mapping, comparative genomic DNA sequence analysis, and cDNA cloning, we found that t

44 upted genes in 51 mutants were identified by DNA sequence analysis, and the mutations included interr

45 sed unambiguously, comparative mitochondrial-DNA-sequence analysis appears to be a reliable and power

46 AMOS project has released several innovative DNA sequence analysis applications including: Hawkeye, a

47 ng compared with methods that do not require DNA sequencing analysis as an additional step and that h

48 Cosmids are annotated by DNA sequence analysis at the transposon insertion sites,

49 odology of earlier studies relied largely on DNA sequence analysis but lacked functional assays of du

50 cases identified as mutated by conventional DNA sequence analysis but not by microarray.

51 DNA sequence analysis by oligonucleotide binding is ofte

52 High-throughput DNA sequence analysis can potentially identify all sourc

53 DNA sequence analysis confirmed TCC-specific mutations i

54 The DNA sequence analysis confirmed that the polymerase chai

55 DNA sequence analysis confirmed the integration of ACME

56 Conventional DNA sequence analysis demonstrated an 87% accuracy rate,

57 DNA sequence analysis demonstrated that the RTX locus is

58 DNA sequence analysis demonstrated that this region cont

59 We performed DNA sequence analysis, differential polymerase chain rea

60 DNA sequence analysis established that all three 60A all

61 rologous expression in Escherichia coli, and DNA sequence analysis excluded cis-acting mutations as t

62 DNA sequence analysis failed, however, to identify the R

63 Based on DNA sequence analysis, fit encodes an outer membrane pro

64 In addition, DNA sequence analysis formally demonstrated a loss of di

65 PCR and DNA sequence analysis found that Spy1325 is very well co

66 DNA sequence analysis from -3.8 to -7.2 kb identified fi

67 Here we have used PCR DNA sequence analysis from multiple segments of DNA ampl

68 be grown in cell culture, but by direct PCR DNA sequence analysis from segments totaling 15 to 30% o

69 DNA sequence analysis, gel mobility shifting, chromatin

70 DNA sequence analysis grouped this orf virus isolate amo

71 The deduced proteins, based on DNA sequence analysis, have molecular masses of 13 and 2

72 DNA sequence analysis identified 38 laf genes in two loc

73 Genomic DNA sequence analysis identified conserved E2F consensus

74 DNA sequence analysis identified two different mutations

75 ola virus orthopoxviruses were positive, and DNA sequence analysis implicated a novel orthopoxvirus s

76 DNA sequence analysis, in combination with genetic compl

77 ranscriptase-dependent nested PCR, including DNA sequence analysis, in situ hybridization, and immuno

78 DNA sequence analysis indicated that most of the mutatio

79 Characterization of the sde locus by DNA sequence analysis indicated that the Omega4408 inser

80 DNA sequencing analysis indicated that this was a fusion

81 Deoxyribonucleic acid (DNA) sequencing analysis indicated that this gene contai

82 DNA-sequencing analysis indicated that the Y586F mutatio

83 DNA sequence analysis indicates that both proteins are l

84 Recent DNA sequence analysis indicates that rhesus rhadinovirus

85 DNA sequence analysis indicates that this region contain

86 One of the main tasks of DNA sequence analysis is identification of repetitive pa

87 From DNA sequence analysis, it was predicted that the transla

88 HTA findings were used to select for DNA sequence analysis maternal virus populations that we

89 e BACTEC 460TB system combined with standard DNA sequencing analysis methods for katG, inhA, and rpoB

90 ion, p16 gene inactivation was determined by DNA sequence analysis, methylation-specific PCR, and imm

91 clinical sources were evaluated by ribosomal DNA sequence analysis, multilocus sequence analysis, DNA

92 DNA sequence analysis of 130 alleles of the HRAS1 minisa

93 DNA sequence analysis of 18 GRD copies reveal 4 distinct

94 length polymorphism (RFLP) analysis of flaA, DNA sequence analysis of 582 bp of flaA that included th

95 DNA sequence analysis of 66 low-risk a1 alleles revealed

96 DNA sequence analysis of a 2.6-kb portion of the promote

97 used to design a strategy for isolation and DNA sequence analysis of a 7,886-base pair A. vinelandii

98 ogy has offered the potential for the direct DNA sequence analysis of a broad spectrum of pathogens o

99 Our DNA sequence analysis of a major fraction of eleutheroda

100 DNA sequence analysis of a region downstream of exoU ide

101 DNA sequence analysis of amplified ITS1 region DNA from

102 Ancient DNA sequence analysis of archaeological bottle gourd spe

103 DNA sequence analysis of autism subjects and controls re

104 tyrosine kinase inhibitors that would inform DNA sequence analysis of candidate tyrosine kinases.

105 DNA sequence analysis of cDNA clones for tRNA(Ser) and 1

106 DNA sequence analysis of cDNA generated by 5'RACE from C

107 DNA sequence analysis of cloned regions of classI mutant

108 During DNA sequence analysis of cosmid L373 from the Mycobacter

109 DNA sequence analysis of cosmid pLM49 revealed a cluster

110 However, DNA sequence analysis of crossover junctions indicated t

111 DNA sequence analysis of different clones identified 19

112 DNA sequence analysis of each of the Alu Yd subfamilies

113 t (Mutector; TrimGen, Sparks, MD) and direct DNA sequence analysis of exon 15 after PCR amplification

114 DNA sequence analysis of exons 2 to 9 of the neuroserpin

115 DNA sequence analysis of four independent isolates revea

116 o sort the libraries for active mutants, and DNA sequence analysis of functional BLIP mutants identif

117 Genomic DNA sequence analysis of human COX-2 revealed a silent m

118 DNA sequence analysis of intellectual disability patient

119 DNA sequence analysis of its 330, 742-bp genome leads to

120 We hypothesized that DNA sequence analysis of multiple loci is useful for rap

121 DNA sequence analysis of murA from C. trachomatis predic

122 This method relies on DNA sequence analysis of nucleotide polymorphisms in hou

123 DNA sequence analysis of one full-length 1.3-kb clone (p

124 rium nucleatum were characterized, including DNA sequence analysis of one plasmid, pFN1.

125 DNA sequence analysis of ORF99 from each of the existing

126 ecting the 3 family members was confirmed by DNA sequence analysis of pol, gag, and env genes.

127 DNA sequence analysis of pph1 indicates that it encodes

128 DNA sequence analysis of R. typhi tlyC revealed an open

129 DNA sequence analysis of regions flanking their transpos

130 DNA sequence analysis of representative polyphyletic mar

131 DNA sequence analysis of RRV indicates that it shares nu

132 DNA sequence analysis of spliced LRT cDNAs, poly(A)+ or

133 PCR amplification and DNA sequence analysis of SRY revealed no mutations in th

134 DNA sequence analysis of tau coding regions in affected

135 DNA sequence analysis of the 1.3-kb region predicted an

136 DNA sequence analysis of the 5.0 kb fragment revealed th

137 DNA sequence analysis of the 5.8 Mb S. arenicola circula

138 DNA sequence analysis of the 51 patients with defective

139 DNA sequence analysis of the bt2-7503 mutant allele of t

140 DNA sequence analysis of the cloned insert revealed a 30

141 This study presents DNA sequence analysis of the core promoter region for CH

142 DNA sequence analysis of the direct repeat units within

143 DNA sequence analysis of the E. coli flo gene demonstrat

144 DNA sequence analysis of the fibrinogen genes A, B, and

145 e clinical diagnosis of AROA were studied by DNA sequence analysis of the four classic OCA genes: TYR

146 on-Hispanic Caucasian patients, we performed DNA sequence analysis of the four genes associated with

147 DNA sequence analysis of the gene for IFNgammaR2 showed

148 DNA sequence analysis of the gene in these 50 isolates f

149 DNA sequence analysis of the genes encoding the MAb reve

150 DNA sequence analysis of the hrp/hrc regions in Psy 61,

151 DNA sequence analysis of the individual Alu elements rev

152 Here we provide a DNA sequence analysis of the innate immune gene STAT2 an

153 DNA sequence analysis of the internal transcribed spacer

154 ification was confirmed for most isolates by DNA sequence analysis of the internal transcribed spacer

155 DNA sequence analysis of the isolate indicated that it w

156 ms for identifying yeasts, were confirmed by DNA sequence analysis of the ITS2 region from 93 isolate

157 DNA sequence analysis of the known CCM genes in a cohort

158 Further DNA sequence analysis of the lpfA1 and lpfA2 genes from

159 DNA sequence analysis of the molecular clones revealed t

160 DNA sequence analysis of the O37 wb* region revealed tha

161 groups has been confirmed and refined by PCR DNA sequence analysis of the ORF-K1 gene encoding a high

162 Here we report the results of a comparative DNA sequence analysis of the orthologous human (750 kb)

163 DNA sequence analysis of the orthologous inserts showed

164 DNA sequence analysis of the P. syringae ES4326 rpoN gen

165 DNA sequence analysis of the pbs1-2 allele showed it to

166 Extensive DNA sequence analysis of the PCGEM1 cDNA and genomic DNA

167 of a genetic alteration, as demonstrated by DNA sequence analysis of the PCNA gene from malignant an

168 ses detected by this assay were confirmed by DNA sequence analysis of the PCR amplicons.Results.

169 Previously, we had shown that DNA sequence analysis of the protein A gene variable rep

170 the puc mRNA transcriptional start site and DNA sequence analysis of the puc upstream regulatory seq

171 rrelia species as assessed by microscopy and DNA sequence analysis of the pyrG gene.

172 DNA sequence analysis of the region encoding the tail fi

173 DNA sequence analysis of the region flanking cobB locate

174 DNA sequence analysis of the region immediately upstream

175 Using DNA sequence analysis of the ribosomal DNA intergenic tr

176 DNA sequence analysis of the RT-encoding region of the p

177 DNA sequence analysis of the S. boydii 0-1392 island, de

178 nstraint, we developed a typing system using DNA sequence analysis of the serine-aspartate (SD) repea

179 DNA sequence analysis of the Sry ORF and a 5' 800-bp seg

180 DNA sequence analysis of the structural subunit gene afr

181 Genomic DNA sequence analysis of the uropathogenic Escherichia c

182 DNA sequence analysis of the viral DNA-target junctions

183 DNA sequence analysis of the viral genomes cloned from d

184 lates of Staphylococcus aureus were typed by DNA sequence analysis of the X region of the protein A g

185 DNA sequence analysis of the zwi-3 mutation indicated th

186 DNA sequence analysis of this Alu fragment revealed that

187 DNA sequence analysis of this clone revealed the identit

188 DNA sequence analysis of this clone, containing a 2.7-kb

189 DNA sequence analysis of this enhancer element revealed

190 DNA sequence analysis of this mutant revealed a transpos

191 DNA sequence analysis of this region identified 13 signi

192 DNA sequence analysis of this region revealed the presen

193 DNA sequence analysis of two SIRE-1 subclones revealed t

194 processed viral DNAs, we performed extensive DNA sequencing analysis of 2-LTR-circle junctions.

195 By nested methylation-specific DNA sequencing analysis of lung and breast cancer cell l

196 DNA sequencing analysis of nonfluorescent GFP clones ind

197 entiate C. hominis and C. parvum is based on DNA sequencing analysis of PCR amplicons.

198 Restriction enzyme mapping, subcloning, and DNA sequencing analysis of recombinant phage lambda and

199 DNA sequencing analysis of unselected library members re

200 Importantly, high-throughput DNA sequencing analysis on the transcriptome of ES cells

201 e rapid bacterial identification by targeted DNA sequence analysis or by whole-genome sequencing perf

202 With near full-length 16S ribosomal DNA sequence analysis, organisms cultured from the blood

203 induced mutation spectrum as established by DNA sequence analysis (p < 0.005; 95% CI, 0.002-0.009).

204 te 20 of 33 species of molds tested, and ITS DNA sequence analysis permits identification of all spec

205 on was formed by a simple terminal deletion, DNA sequence analysis, pulsed-field gel electrophoresis

206 Most existing methods for DNA sequence analysis rely on accurate sequences or geno

207 DNA sequence analysis revealed a binding motif for octam

208 ription start site for SR-BI was mapped, and DNA sequence analysis revealed a binding site for SF-1 i

209 DNA sequence analysis revealed a C to A transversion in

210 DNA sequence analysis revealed a high degree of genetic

211 DNA sequence analysis revealed a mosaic nature of the ca

212 DNA sequence analysis revealed a mutation resulting in a

213 DNA sequence analysis revealed a novel homozygous mutati

214 ence for cooperativity among the SARs, while DNA sequence analysis revealed a series of clustered A-t

215 DNA sequence analysis revealed a single missense mutatio

216 DNA sequence analysis revealed a single point mutation c

217 DNA sequence analysis revealed changes in c.545A>G, c.13

218 DNA sequence analysis revealed dominant T cell clones ob

219 DNA sequence analysis revealed multiple nucleotide subst

220 DNA sequence analysis revealed potential transcriptional

221 DNA sequence analysis revealed several widely distribute

222 DNA sequence analysis revealed that 18 isolates containe

223 DNA sequence analysis revealed that CAP60 has similarity

224 DNA sequence analysis revealed that EUs4 of the pathogen

225 DNA sequence analysis revealed that in both 91-R and ry5

226 DNA sequence analysis revealed that in six of nine delet

227 DNA sequence analysis revealed that M. smegmatis does in

228 wly synthesized strand followed by multiplex DNA sequence analysis revealed that mutation fixation at

229 DNA sequence analysis revealed that the B3 genome is 38,

230 DNA sequence analysis revealed that the chromosomal inse

231 DNA sequence analysis revealed that the complementing ac

232 DNA sequence analysis revealed that the donor clone pred

233 DNA sequence analysis revealed that the majority of the

234 DNA sequence analysis revealed that the putative yhdJ DN

235 DNA sequence analysis revealed that the transposon inser

236 DNA sequence analysis revealed that there are several ka

237 However, DNA sequence analysis revealed that these were independe

238 DNA sequence analysis revealed that this clone contains

239 Subcloning, transposon mutagenesis, and DNA sequence analysis revealed that this DNA fragment co

240 DNA sequence analysis revealed that this locus is simila

241 Subsequent cloning and DNA sequence analysis revealed that transposon insertion

242 DNA sequence analysis revealed that two of the novel HAB

243 DNA sequence analysis revealed the mutation to be a sing

244 DNA sequence analysis revealed the nature of the cer6-1,

245 DNA sequence analysis revealed the presence of multiple

246 DNA sequence analysis revealed these tumors harbor an ex

247 DNA sequence analysis revealed three open reading frames

248 The DNA sequence analysis revealed two consecutive open read

249 DNA sequence analysis revealed two xenobiotic response e

250 DNA sequencing analysis revealed target-dependent mutati

251 DNA sequence analysis reveals a proteobacterial architec

252 Genomic DNA sequence analysis reveals that JMRV is a gammaherpes

253 However, DNA sequence analysis reveals that, with the exception o

254 DNA sequence analysis showed 93% identify with the rat e

255 DNA sequence analysis showed considerable divergence bet

256 PCR and DNA sequence analysis showed extensive genotypic diversi

257 DNA sequence analysis showed normal sequence for GPIbalp

258 DNA sequence analysis showed that ORF2 extended an addit

259 DNA sequence analysis showed that the affected individua

260 DNA sequence analysis showed that the frequency of in-fr

261 o human IKCa1 cDNA probes were isolated, and DNA sequence analysis showed that they were identical to

262 DNA sequence analysis shows that the methylated componen

263 DNA sequence analysis suggested that dev and cas (CRISPR

264 This DNA sequence analysis suggested that the terminal defici

265 depending on the strain, was identified, and DNA sequence analysis suggests that horizontal gene tran

266 On the other hand, DNA sequencing analysis suggests that culture and growth

267 We developed a new approach to DNA sequence analysis that uses fluorogenic reporter mol

268 Based on DNA sequence analysis, the three genes are likely to be

269 We tested the use of comparative DNA sequence analysis to aid identification of promoter

270 , all the cases of hereditary TTP studied by DNA sequence analysis to date appear to be due to mutati

271 The SQ-PCR Av assay was verified using DNA sequence analysis to demonstrate that this methodolo

272 followed by Southern blot hybridisation and DNA sequence analysis to detect DNAs of polyomaviruses a

273 We used DNA sequence analysis to determine that the element harb

274 ed by oligodeoxynucleotide hybridization and DNA sequence analysis to establish the mutation frequenc

275 r-based genome scanning, marker sorting, and DNA sequence analysis to examine their phylogenetic rela

276 mpling and a microbiopsy device coupled with DNA sequence analysis to highlight BRAF V600E heterogene

277 nd GyrB subunits of DNA gyrase, we have used DNA sequence analysis to identify a highly conserved 'Gy

278 -strand conformation polymorphism (SSCP) and DNA sequence analysis to identify mutations in the cardi

279 Combining microarray techniques with DNA sequence analysis to identify potential let-7 target

280 Here, we describe a multigenomic DNA sequence-analysis tool, evoprinter, that facilitates

281 nterconnection of the ECR Browser with other DNA sequence analysis tools creates a unique portal for

282 For some isolates, DNA sequence analysis was also performed.

283 pparent pathologic mutations in these genes, DNA sequence analysis was performed of a candidate OCA g

284 mission distortion of the marker alleles and DNA sequence analysis was performed.

285 DNA sequence analysis was used to show that the combinat

286 Based on DNA sequence analysis we propose that GGPPS5 (At3g14510)

287 osome conformation capture (Hi-C) along with DNA sequence analysis, we demonstrate that most SEs are

288 Using direct DNA sequencing analysis, we screened 13 genes for mutati

289 ll disagreements with conventional gel-based DNA sequence analysis were confirmed by re-analysis with

290 Methods of DNA sequence analysis were employed to scan herpesvirus

291 PCR-based assays and DNA sequence analysis were performed for these 34 loci i

292 PCR and DNA sequence analysis were used to characterize the alte

293 DNA extraction, rpoB gene amplification, and DNA sequencing analysis were performed.

294 y direct fluorescent antibody test (DFA) and DNA sequencing analysis were tested.

295 Analysis of the mutant strains by DNA sequence analysis, Western blot assays, and reconstr

296 of these two qPCR products was confirmed by DNA sequencing analysis, which showed 99-100% similarity

297 results lead us to conclude that comparative DNA sequence analysis will enable identification of func

298 DNA sequence analysis with other vertebrate Rb sequences

299 d by the molecular approach (PCR followed by DNA sequencing analysis) with those from the parasitolog

300 ovel transmembrane protein was identified by DNA sequence analysis within the insulin-dependent diabe