ライフサイエンスコーパス: DNA analysis

1 ssfully detected through the maternal plasma DNA analysis.

2 en generally supported by more sophisticated DNA analysis.

3 r increased sensitivity on DNA arrays or for DNA analysis.

4 escein is a widely used fluorescent probe in DNA analysis.

5 ighly suitable for characterization by sperm DNA analysis.

6 ar polyacrylamide and polyethylene oxide for DNA analysis.

7 ected, portable device that allows real-time DNA analysis.

8 or leap in the efficiency of high-throughput DNA analysis.

9 ing galactosylceramidase (GALC) activity and DNA analysis.

10 y the nanoparticles may make them useful for DNA analysis.

11 e/consensus IGS sequence, as well as genomic DNA analysis.

12 esis (PFGE) and random amplified polymorphic DNA analysis.

13 st lobules or ducts in 9 cases available for DNA analysis.

14 sue DNA analyses were also negative by stool DNA analysis.

15 sequence and by random amplified polymorphic DNA analysis.

16 with FDCM underwent clinical evaluation and DNA analysis.

17 or the authentication of seafood by means of DNA analysis.

18 ilm can improve the MALDI-TOF performance in DNA analysis.

19 re examined for O. formigenes by culture and DNA analysis.

20 erase chain reaction (PCR) and Southern blot DNA analysis.

21 on include performing cyst wall cytology and DNA analysis.

22 CR/LiPA25 HPV genotyping system was used for DNA analysis.

23 ational frameshift as shown by complementary DNA analysis.

24 tedness using randomly amplified polymorphic DNA analysis.

25 and 304 nasal samples were eligible for HPV DNA analysis.

26 nd screen samples for radiocarbon dating and DNA analysis.

27 nces, which provides another means for rapid DNA analysis.

28 ies that exist in Hawaii using mitochondrial DNA analysis.

29 etection applications such as nanopore-based DNA analysis.

30 6 patients with blood available for germline DNA analysis.

31 testing procedures, either skin biopsies or DNA analysis.

32 ew designs for lab-on-a-chip devices used in DNA analysis.

33 equences may be observed after mitochondrial DNA analysis.

34 ny legal systems have developed for forensic DNA analysis.

35 r evaluation, including echocardiography and DNA analysis.

36 supporting stroma comprised, by murine Cot-1 DNA analysis, 30% of the tumor.

37 tudy who provided baseline blood samples for DNA analysis, 374 suffered first myocardial infarction a

38 rated into the microchip for high-throughput DNA analysis, a miniaturized purification process must b

39 ious studies on morphology and mitochondrial DNA analysis, a number of issues regarding the details o

40 By 16S ribosomal DNA analysis, all six permafrost isolates were identifie

41 suggested by morphological and mitochondrial DNA analysis alone.

42 mitochondrial pathology by histochemical and DNA analysis and a poor response to immunosuppressive th

43 Participants provided blood for DNA analysis and cancer family history, and cancer treat

44 ection limits for other applications such as DNA analysis and clinical diagnostics.

45 discuss 'Type II' REases, the kind used for DNA analysis and cloning.

46 each visit, a cervical cell specimen for HPV DNA analysis and cytology and a fasting blood sample to

47 network analysis, single fibre mitochondrial DNA analysis and deep re-sequencing of mitochondrial DNA

48 6-diamidino-2-phenylindole for simultaneous DNA analysis and immunophenotyping.

49 with those of randomly amplified polymorphic DNA analysis and internally transcribed spacer region se

50 , as defined by random-amplified polymorphic DNA analysis and pulsed-field gel electrophoresis.

51 A comparison of the B19 DNA analysis and the results of TAB indicated a statisti

52 tic cell death at 72 h that was supported by DNA analysis and TUNEL staining.

53 Study provided baseline blood specimens for DNA analysis and were followed prospectively for a mean

54 bivariate proliferating nuclear cell antigen/DNA analysis) and activation (percent lymphocytes expres

55 and granulocyte lineages to donor origin by DNA analysis, and (4) increased ADA activity and metabol

56 cations in biophysics, clinical diagnostics, DNA analysis, and drug discovery.

57 ctrophoresis, randomly amplified polymorphic DNA analysis, and phage typing as epidemiological tools.

58 ssed using laser capture microdissection and DNA analysis, and revealed no significant intratumor het

59 vidence for senescence; normal karyotype and DNA analysis; and expression of vimentin, CD90 (thy1.1),

60 ations of these submicrometer structures for DNA analysis are discussed.

61 n disorders, as well as in the technology of DNA analysis, are rapidly changing the landscape of mole

62 s study, young patients identified by direct DNA analysis as carriers of a RET mutation characteristi

63 ion has the potential to impact the forensic DNA analysis backlog of sexual assault cases by circumve

64 tly verified by random amplified polymorphic DNA analysis-based genotyping and by restriction enzyme

65 sequencing required for genome-wide ancient DNA analysis by a median of around 250-fold, allowing us

66 ted vaginal swab specimens were sent for HPV DNA analysis by L1 consensus polymerase chain reaction f

67 itives improve sensitivity and resolution of DNA analysis by MALDI.

68 DNA analysis by matrix-assisted laser desorption/ionizat

69 Quantitative trait locus mapping and genomic DNA analysis by microarray hybridization were used to id

70 ere collected, at 4-month intervals, for HPV-DNA analysis by polymerase chain reaction.

71 DNA analysis by this method identified two major cluster

72 e of European ancestry and were targeted for DNA analysis by use of probands with a heavy-smoking phe

73 Body fluids can easily be identified, and DNA analysis can be used to link a stain found at a crim

74 Circulating tumour DNA analysis can be used to track tumour burden and anal

75 m) surface improves the MALDI performance in DNA analysis compared to the commonly used metal surface

76 was performed in order to analyze realistic DNA analysis conditions within microdevices.

77 DNA analysis confirmed that nuclear DNA was identical to

78 The diagnostic reliability of circulating DNA analysis depends on the fractional concentration of

79 logy for the construction of high-throughput DNA analysis devices.

80 In recent years, honey has become subject of DNA analysis due to potential risks evoked by microorgan

81 DNA analysis excluded mutations in the transforming grow

82 DNA analysis failed to detect mutations in the genes enc

83 nasal potential difference measurement, and DNA analysis for additional mutations.

84 On-site DNA analysis for diagnostic or forensic purposes is much

85 ion and emphasize the importance of parental DNA analysis for establishing an etiologic relation betw

86 lood-lymphocyte karyotype and the results of DNA analysis for fragile-X syndrome and of other routine

87 med by polymerase chain reaction (PCR)-based DNA analysis for polymorphic short tandem tetrameric rep

88 Cheek swab samples were obtained for DNA analysis from 116 case/parent trios.

89 Skin swab samples were obtained for DNA analysis from 4 sites around the abscess site (herea

90 A) that we developed for this assay, genomic DNA analysis from thirteen relapsed patients revealed th

91 1) or by combining the trypsinogen test with DNA analysis (from July 1991 through June 1994).

92 Multiple target DNA analysis gave over 86% detection of total TRFs predi

93 be predominantly maternal, and mitochondrial DNA analysis has become a standard taxonomic tool.

94 Although DNA analysis has been carried out successfully in both c

95 Whilst DNA analysis has helped to combat this type of fraud som

96 During the past 10 years, DNA analysis has revolutionized the determination of ide

97 advances in the sensitivity and accuracy of DNA analysis have allowed for genotyping of cfDNA for so

98 We performed DNA analysis in 44 of these patients to search for a gen

99 DNA analysis in 47 cases (68%) revealed a significant as

100 t and simplified magnetic bead actuation for DNA analysis in a continuous flow platform with minimal

101 liable instruments may facilitate the use of DNA analysis in applications such as rapid medical diagn

102 ctional genomics, proteomics, and regulatory DNA analysis in essentially any transformed human cell t

103 Here, we demonstrate direct DNA analysis in paper-based devices, uniquely enabled by

104 s 1 and 2, which will help limit unnecessary DNA analysis in the diagnosis and management of this gen

105 diagnosis was undertaken by chorionic villus DNA analysis in two unrelated families with the inherite

106 ll 25 Cryptosporidium isolates submitted for DNA analysis, including 3 from the ill foodhandler, were

107 ement efficient sample-handling practices in DNA analysis, including DNA fragment sizing flow cytomet

108 Genomic DNA analysis indicates that the 17-amino-acid insert is

109 ration or, conversely, for low cost portable DNA analysis instruments in point-of-care medical diagno

110 Current experience suggests that DNA analysis is a better test for diagnosis as compared

111 DNA analysis is a fast and economic tool to identify pla

112 DNA analysis is essential for diagnosis and monitoring o

113 DNA analysis is making a valuable contribution to the un

114 This shows that DNA analysis is necessary to exclude emerin mutations in

115 Thus, circulating tumor DNA analysis is perhaps one of the most practical and pr

116 s microplate and scanner for high-throughput DNA analysis is presented.

117 The standard protocols for DNA analysis largely involve polymerase chain reaction (

118 bone marker assessment (ICTP) and microbial DNA analysis (levels and proportions of 40 bacterial spe

119 evaluated for cell survival, cell number by DNA analysis, matrix production by particle exclusion as

120 g molecular techniques such as 16S ribosomal DNA analysis may lead to interventions that shift the va

121 nostic modalities based on muscle biopsy and DNA analysis mean that diagnoses within the heterogeneou

122 ing data from the Technical Working Group on DNA Analysis Methods (TWGDAM)-sponsored "Large Fragment

123 below the sensitivity limitations of routine DNA analysis methods.

124 ers in tissues, based upon quantitative flaB DNA analysis, nor did treatment affect RNA levels of sev

125 DNA analysis of a human pituitary tumor, breast carcinom

126 was shown by immunofluorescence staining and DNA analysis of biopsied tissue.

127 DNA analysis of C57BL/6 mice from common commercial vend

128 microarray sensors was developed to perform DNA analysis of complex biological sample solutions.

129 Gilbert et al. presented DNA analysis of coprolites recovered from an Oregon cave

130 We examine this problem through ancient DNA analysis of early 16(th) century cattle bone from Se

131 DNA analysis of eight periodontal bacteria was performed

132 reports results obtained from microsatellite DNA analysis of genetic structure for populations of the

133 related disease was confirmed by comparative DNA analysis of genomic sequences from the donor liver,

134 50 years; this was later challenged based on DNA analysis of historical herbarium specimens.

135 DNA analysis of members of the extended family revealed

136 was assessed by random amplified polymorphic DNA analysis of multiple H. pylori clones from each pati

137 B and T cells, similar results were seen on DNA analysis of muscle, but these mice also demonstrated

138 ators with the immediate capacity to perform DNA analysis of normal and diseased genomes in a global

139 Forensic DNA analysis of samples obtained from sexual assault evi

140 Forensic DNA analysis of sexual assault evidence requires separat

141 DNA analysis of single blastomeres indicating whether em

142 d extinct taxa, we have conducted an ancient DNA analysis of subfossil species.

143 Checkerboard hybridization DNA analysis of subgingival plaque from ligated sextants

144 Single-molecule DNA analysis of testicular germ cells isolated by laser

145 Primate DNA analysis of the same loci revealed one human haploty

146 tact p16 and 10 lacked its protein and mRNA; DNA analysis of these 10 cell lines showed 2 homozygous

147 DNA analysis of these cell lines, whose genome is clonal

148 The RFLP markers were tested by gel blot DNA analysis of wheat group 1 nullisomic-tetrasomic line

149 have developed a highly sensitive method for DNA analysis on 3D gel element microarrays, a technique

150 42), in situ detection of DNA fragments, and DNA analysis on agarose gels indicated that apoptosis wa

151 rated by DNA fragmentation and quantified by DNA analysis on FACS, yet the majority of the cells died

152 Conclusions and Relevance: Circulating tumor DNA analysis, once sensitive and broad enough, will acce

153 Circulating tumor DNA analysis, once sensitive and broad enough, will acce

154 genotyping, and random amplified polymorphic DNA analysis, over 50% of papG-positive fecal E. coli co

155 On the basis of DNA analysis, overall prevalence of anal HPV infection w

156 Phylogenetic rRNA-encoding DNA analysis places many of the hyperthermophilic Archae

157 d to improve the sensitivity of microfluidic DNA analysis platforms.

158 uit for the delivery of a step change in the DNA analysis process: A fully integrated instrument for

159 Cloning and DNA analysis revealed 30 DNA sequences and included eigh

160 DNA analysis revealed a heterozygous CAA-->TAA mutation

161 DNA analysis revealed a homozygous 15-base pair (bp) in-

162 The patient's DNA analysis revealed a homozygous nucleotide exchange c

163 Sperm DNA analysis revealed a second class of mutation occurri

164 Genomic DNA analysis revealed a T-->G mutation at the splice don

165 Genomic DNA analysis revealed eight epidemiologically distinct g

166 Whole heart genomic DNA analysis revealed iterative oxidative cytosine modif

167 DNA analysis revealed mutations in DPM2, 1 of the subuni

168 Genomic DNA analysis revealed substantial methylation of the Ubi

169 Both immunohistochemical and genomic DNA analysis revealed that in vivo, sorted CD8 alpha+ DC

170 Genomic DNA analysis revealed that the apple PGIP probably belon

171 DNA analysis revealed that the OHSt patients have 1 of 2

172 tion to primary bile acids, was confirmed by DNA analysis revealing a missense mutation (S52P) in the

173 Radiocarbon dating and DNA analysis show that the rib is associated with the ot

174 Plasmid DNA analysis showed a high degree of heterogeneity among

175 DNA analysis showed a smear pattern characteristic of ce

176 Mitochondrial DNA analysis showed multiple deletions in 90% of muscles

177 Buffy coat DNA analysis showed that 75-85% were EBV DNA-positive in

178 s were then generated by Affymetrix GeneChip DNA Analysis Software.

179 ices may provide significant improvements in DNA analysis speed, portability, and cost.

180 Here, we present ancient DNA analysis, stable isotope data of oxygen, and radioge

181 In vitro protein/DNA analysis suggests that one of the sites is a TEF-2-l

182 olved and quantified by the high-performance DNA analysis system, a high-throughput, multichannel, mi

183 n successfully coupled to form an integrated DNA analysis system.

184 neration of low-power, portable microfluidic DNA analysis systems.

185 the possibility of more practical integrated DNA analysis systems.

186 Melt (HRM) is a versatile and rapid post-PCR DNA analysis technique primarily used to differentiate s

187 ymatic kinetics, and when coupled with other DNA analysis techniques, this could be used to construct

188 n subsequently be studied using conventional DNA analysis technologies.

189 solates appeared to be less heterogeneous by DNA analysis than isolates from other regions.

190 k genomic scanning (RLGS), a high-resolution DNA analysis that separates labeled NotI fragments in tw

191 cpzUS) and have determined, by mitochondrial DNA analysis, the subspecies identity of all known SIVcp

192 On DNA analysis there was no evidence of meiotic recombinat

193 ent of semi-automated equipment to assist in DNA analysis, there has been a volley of articles on the

194 For DNA analysis, this technique apparently produces a more

195 istory of pancreatitis and one was proven by DNA analysis to have hereditary pancreatitis.

196 tracking and moth neurophysiology with fecal DNA analysis to show that the barbastelle, Barbastella b

197 le subjects submitted one stool specimen for DNA analysis, underwent standard Hemoccult II testing, a

198 Interest in improving the speed of DNA analysis via capillary electrophoresis has led to ef

199 DNA analysis was carried out in 12 affected and 3 nonaff

200 , but a change of mutational status based on DNA analysis was found in only 4 matched tumors (3.0%).

201 enotype (with exception of families in which DNA analysis was not available).

202 DNA analysis was performed by direct automated sequencin

203 A genome-wide methylation DNA analysis was performed using microarray hybridizatio

204 present study, BOX-polymerase chain reaction DNA analysis was used to characterize nonserotypeable S.

205 t, according to random amplified polymorphic DNA analysis, was phylogenetically distant from the "J96

206 Blood specimens for genomic DNA analysis were collected before random assignment in

207 information, family histories, and blood for DNA analysis were obtained from 263 women with breast ca

208 l analogous to that used for double-stranded DNA analysis, where fluorescent intercalating dyes are s

209 alpha-hemolysin pores, are commonly used for DNA analysis, whereas synthetic solid-state nanopores ha

210 This mutation (Ser131Cys) was confirmed by DNA analysis, which identified a single-base change of c

211 s for sex determination without resorting to DNA analysis, which requires good DNA survival and is ti

212 Polymerase chain reaction DNA analysis with BOX primers demonstrated that 12 HIV-i

213 When comparing these results for DNA analysis with previously reported limits for protein

214 nica by using randomly amplified polymorphic DNA analysis with the primer DKU49.