ライフサイエンスコーパス: PCR analysis

1 A extracted from the neurons was used in qRT-PCR analysis.

2 id response genes were analysed by real time PCR analysis.

3 The results were validated by real-time RT-PCR analysis.

4 termined by Western blot and quantitative RT-PCR analysis.

5 sue samples from 93 patients using real-time PCR analysis.

6 ing 27 eyes were negative for all viruses on PCR analysis.

7 Tissue bacterial burdens were examined by PCR analysis.

8 A synthesis, and then underwent quantitative PCR analysis.

9 n mESCs and validated this observation by RT-PCR analysis.

10 om array studies with quantitative real-time PCR analysis.

11 cted GC-C+/+ and GC-C-/- mice using 16S rRNA PCR analysis.

12 a significant increase of sensitivity during PCR analysis.

13 situ remove contaminants that interfere with PCR analysis.

14 n the mule deer genome based on quantitative PCR analysis.

15 s of glioblastoma stem cells by real-time RT-PCR analysis.

16 o a riboflavin transporter is revealed in RT-PCR analysis.

17 further validated by quantitative real-time PCR analysis.

18 uencing (RNA-Seq) combined with extensive RT-PCR analysis.

19 ly identified following RNA isolation and RT-PCR analysis.

20 cted DNA was amplified using IS6110-targeted PCR analysis.

21 espectively, both compatible with downstream PCR analysis.

22 racil treatment as assessed by real-time qRT-PCR analysis.

23 nfirmed by both DNA microarray and real-time PCR analysis.

24 f ECM, as measured by quantitative real-time PCR analysis.

25 ning, gene expression, and ChIP-quantitative PCR analysis.

26 resh and processed seafood, suitable for any PCR analysis.

27 istologic, flow cytometric, and quantitative PCR analysis.

28 rom the remaining tissue for quantitative RT-PCR analysis.

29 on in isolated platelets was confirmed by RT-PCR analysis.

30 in all the other 23 samples by individual RT-PCR analysis.

31 -transcription polymerase chain reaction (RT-PCR) analysis.

32 ive real-time reverse transcriptase PCR (qRT-PCR) analysis.

33 transcription polymerase chain reaction (qRT-PCR) analysis.

34 time quantitative polymerase chain reaction (PCR) analysis.

35 okine levels, and polymerase chain reaction (PCR) analysis.

36 RT-PCR analysis also identified that OR2W3 gene was express

37 RT-PCR analysis also revealed reduced mRNA levels of IL-1be

38 qRT-PCR analysis also showed lowered levels of expression of

39 Both RT-PCR analysis and crossing into Rosa26-lacZ reporter mice

40 ession pattern was confirmed by quantitative PCR analysis and ELISA.

41 Using RT-quantitative PCR analysis and gene promoter::GUS fusions, we first sh

42 Quantitative PCR analysis and GUS activity measurements revealed that

43 By using RT-PCR analysis and immunofluorescence microscopy, we descr

44 Using RT-PCR analysis and pharmacological interventions, we demon

45 Real time PCR analysis and reporter gene assay revealed that PMA i

46 tion of Minos was also seen by site-specific PCR analysis and sequence validation.

47 xA, bexB, and capsule type-specific genes by PCR analysis and thus likely represent false-positive se

48 We examined MSI by PCR analysis and tolerance to methylating or thiopurine

49 metry and immunohistochemistry, quantitative PCR analysis and Western blot techniques.

50 ized by real-time polymerase chain reaction (PCR) analysis and in situ hybridization histochemistry.

51 her DNA repair genes (quantitative real-time PCR analysis) and resulted in an increased nuclear local

52 assays, confocal microscopy, flow cytometry, PCR analysis, and proteome array.

53 tive quantitative polymerase chain reaction (PCR) analysis, and gametocytes were quantified by revers

54 itative real-time polymerase chain reaction (PCR) analysis, and PMR was modeled from these data.

55 rse transcription polymerase chain reaction (PCR) analysis as well as Western blot analysis.

56 PCR analysis at the single-cell level revealed that RORC

57 liitis may benefit from preoperative aqueous PCR analysis before corneal transplantation.

58 striction fragment length polymorphism (RFLP-PCR) analysis, but found no association between rs273538

59 s system (CNS) by polymerase chain reaction (PCR) analysis, but tissue location and cell tropism for

60 ults from quantitative reverse transcriptase PCR analysis clearly demonstrated that, during sporulati

61 ear accumulation, and data from quantitative PCR analysis closely recapitulated the EdU results.

62 Chromatin immunoprecipitation assays and PCR analysis confirmed HNF-1beta binding to the Ppargc1a

63 Quantitative real time PCR analysis confirmed microarray data for 13 of the 16

64 multiple V regions validated by quantitative PCR analysis confirmed that distinct bacterial taxa domi

65 Quantitative PCR analysis confirmed that most polar Thaumarchaeota ha

66 Moreover, RT-PCR analysis confirmed that the expression of the RNAi a

67 ted plates was observed, and quantitative RT-PCR analysis confirmed that the levels of mRNA for an as

68 A qRT-PCR analysis confirmed the dsRNA-mediated transcriptiona

69 A qRT-PCR analysis confirmed the expression profiles of select

70 QRT-PCR analysis confirmed the microarray data and revealed

71 qRT-PCR analysis confirmed the microarray results, that KIR2

72 PCR analysis confirmed the presence of pO157-2 in six ot

73 transcriptase polymerase chain reaction (qRT-PCR) analysis confirmed that Ucn 1 mRNA levels are signi

74 qRT-PCR analysis demonstrated an increased expression of tra

75 Confirmatory qRT-PCR analysis demonstrated good correlation with SnoRNASe

76 RT-PCR analysis demonstrated that cultured human pulp fibro

77 MicroRNA PCR analysis demonstrated that miR-200b expression incre

78 Nuclease protection assay and qRT-PCR analysis demonstrated transgenic mRNA expression in

79 Interestingly, quantitative PCR analysis demonstrates an increased perforin and gran

80 PCR analysis detected relatively high levels of the mRNA

81 d HIV-1 mutational loads, while quantitative PCR analysis determined that the others resulted in prem

82 Initial polymerase chain reaction (PCR) analysis documented that TCR deltaREC-psiJalpha rea

83 RT-PCR analysis exhibits a 100% correlation between Accord

84 ore, the LC-MS/MS and quantitative real-time-PCR analysis followed by inhibitor and antibody-blocking

85 RT-PCR analysis for adipokines revealed that mRNAs for TIMP

86 ed by benzidine staining and quantitative RT-PCR analysis for representative erythroid-related genes,

87 ded Periodic Acid-Schiff staining for fungi, PCR analysis for toxoplasmosis, cytomegalovirus, Epstein

88 of aqueous humor polymerase chain reaction (PCR) analysis for Herpes simplex, varicella zoster, cyto

89 -transcriptase polymerase chain reaction (RT-PCR) analysis for hSSTr2.

90 operative aqueous polymerase chain reaction (PCR) analysis for viruses, including cytomegalovirus (CM

91 Comparative studies using real time PCR analysis from cDNA samples revealed lower accumulati

92 extraction of RNA couple with direct on-chip PCR analysis from single bacterial cells could be achiev

93 RNA-immunoprecipitation and subsequent RT-PCR analysis further demonstrated that RBP-P interacts w

94 Real-time RT-PCR analysis further demonstrated that TCP1 regulates th

95 Quantitative reverse transcriptase PCR (qRT-PCR) analysis further indicated BrlR to be an activator

96 Four of the samples that failed capsid PCR analysis had low titers, which suggests that target

97 Quantitative RT-PCR analysis has been performed to determine if the IL-3

98 ansient expression employing quantitative RT-PCR analysis, histochemical GUS staining, and eGFP and R

99 ptor-mediated mechanism within follicles; RT-PCR analysis identified 3 relevant receptor genes in sca

100 PCR analysis identified deletions nested around the I-Cr

101 Gene expression array and RT-PCR analysis identified V-CAM1 and PPP1R3C as being upre

102 aforementioned stresses was confirmed by qRT-PCR analysis in distinct Arachis genotypes, whilst in si

103 gion and 5'-rapid amplification of cDNA ends PCR analysis in F9 cells identified 11 transcription sta

104 signature genes, which were validated by qRT-PCR analysis in RPE and in an independent set of 11 tiss

105 Real-time PCR analysis in tumor cells and normal human epithelial

106 was to find internal reference genes for qRT-PCR analysis in various experimental conditions for seed

107 -transcription polymerase chain reaction (RT-PCR) analysis in 17 cases and by serology in 6 cases.

108 E. coli (EAEC; by polymerase chain reaction [PCR] analysis) in the stools of 254 children with diarrh

109 PCR analysis indicated that all 30 clinical A. baumannii

110 Reverse transcription PCR analysis indicated that all genes were highly expres

111 Quantitative real-time-PCR analysis indicated that CRHOEdev unexposed males exh

112 Real-time PCR analysis indicated that eroA is transcriptionally up

113 Cell fractionation and qRT-PCR analysis indicated that LINC00152 is found mainly in

114 Real-time quantitative PCR analysis indicated that several trypsin genes (OnTry

115 Microarray and PCR analysis indicated that the addition of FnIII-1c to

116 Firstly, multiplex PCR analysis indicated that the novel strain belongs to

117 Interestingly, reverse transcription PCR analysis indicated that the prostate cancer cells th

118 Our real-time PCR analysis indicated that, in contrast to our previous

119 A quantitative PCR analysis indicates that cngc16 mutant pollen have at

120 from Nrdp1/ErbB2 bigenic mice, and real time PCR analysis indicates that Nrdp1 protein levels are sup

121 DNA extraction with PCR analysis is useful for tuberculosis screening in man

122 CMV) DNA-specific polymerase chain reaction (PCR) analysis is widely used as a surveillance method fo

123 -transcriptase polymerase chain reaction (RT-PCR) analysis (n=257).

124 Quantitative RT-PCR analysis of 10 genes validated the array results.

125 RT-PCR analysis of 17 human tissues demonstrated ubiquitous

126 Highly parallel qRT-PCR analysis of 334 single neurons selected by membershi

127 n array data of 328 MIR-derived exons and RT-PCR analysis of 39 exons in 10 tissues, we identified 15

128 RT-PCR analysis of 40 exons confirmed the predicted splicin

129 ferentially expressed genes by microarray, Q-PCR analysis of a five gene-set (DUSP1, PBEF1, PSEN1, MA

130 acenta-specific expression as revealed by RT-PCR analysis of a large panel of Setifer setosus tissues

131 pecific expression, which was revealed by RT-PCR analysis of a large panel of tissues.

132 vealed by quantitative reverse transcription-PCR analysis of a large panel of tissues.

133 RT-PCR analysis of a patient lymphoblast cell line confirme

134 Real-time quantitative PCR analysis of a set of cancer-related genes (selected

135 RT-PCR analysis of a subset of these genes confirmed the mi

136 Post hoc repeat PCR analysis of all 15 tests with discrepant results res

137 RT-PCR analysis of angioplastied aortas demonstrated a sign

138 studied by performing quantitative real-time PCR analysis of blood samples obtained at admission) and

139 On admission, RT-PCR analysis of blood specimens from patients who died i

140 Furthermore, qRT-PCR analysis of breast cancer patient samples revealed t

141 PCR analysis of C. jejuni isolates from different animal

142 Real-time PCR analysis of CD150(-)Flt3(+) cells from wild-type con

143 RT-PCR analysis of CEP78 in blood leukocytes of affected in

144 ected candidate miRNAs were validated by qRT-PCR analysis of cohorts of 24 T1DM and 24 control subjec

145 ified HAEC supernatant, as well as real-time PCR analysis of CRP mRNA levels in HAECs.

146 Quantitative PCR analysis of different rat arteries found that the KC

147 Single-cell reverse transcription-PCR analysis of dissociated green fluorescent protein-la

148 were detected by blood-smear microscopy and PCR analysis of dried blood spots that had been collecte

149 genome microarray and quantitative real-time PCR analysis of endobronchial biopsies from 27 mild-to-m

150 Single-cell quantitative PCR analysis of eYFP(+) CD4 T cells confirmed their hete

151 Reverse transcriptase-PCR analysis of fetal RNA revealed, hemizygously, a sing

152 Third, PCR analysis of fractionated gut contents demonstrated t

153 Real-time quantitative PCR analysis of gene expression revealed that a signific

154 RT-PCR analysis of genes involved in adipocyte differentiat

155 RT-PCR analysis of genes involved in gluconeogenesis, lipid

156 Quantitative RT-PCR analysis of genes involved in placental development

157 monitored by real-time reverse transcription-PCR analysis of Gli1 mRNA concentration or by Gli report

158 qRT-PCR analysis of GmSNAPs indicates a co-regulation follow

159 Microarray and quantitative real-time-PCR analysis of gonads showed elevated expression of NF-

160 Western blot and real-time PCR analysis of hairy hindpaw skin and L2/L3 DRGs after

161 Microarray and qRT-PCR analysis of human hair follicles after Nrf2 activati

162 This was corroborated with real-time PCR analysis of human prostate tumor tissue arrays that

163 GFP to identify B cells, as demonstrated by PCR analysis of IgH-mu expression in sorted cells.

164 Western blotting and quantitative PCR analysis of infected cells treated with siRNAs indic

165 Upon quantitative reverse transcription (RT)-PCR analysis of infected host cells, an lspF mutant, but

166 CD11b-based retinal flow cytometry, and qRT-PCR analysis of key microglia markers.

167 Real-time PCR analysis of laminin subunits showed that spheroids f

168 ment, which is comparable to quantitative RT-PCR analysis of liver infection.

169 Quantitative real-time PCR analysis of macrophages isolated by laser capture mi

170 We performed real-time PCR analysis of miR-31-3p expression in human colonic ep

171 RT-PCR analysis of mRNA expression for pro-osteoclastogenic

172 cells was further confirmed by quantitative PCR analysis of mRNA isolated from highly purified popul

173 Immunohistological and RT-PCR analysis of muscle biopsy specimens from anti-MDA5 a

174 For real-time quantitative RT-PCR analysis of p15, RNA was extracted from FFPE section

175 ors and small interfering RNA, as well as RT-PCR analysis of p38 isoforms, demonstrated the requireme

176 Reverse transcriptase-PCR analysis of paired human prostate samples revealed t

177 lood transfusion to naive monkeys based upon PCR analysis of PBMCs using XMRV-specific gag and env pr

178 The RT-PCR analysis of PRDM13 expression in developing retinal

179 Immunohistochemical and RT-PCR analysis of retinal pigmented epithelium (RPE)-choro

180 However, qRT-PCR analysis of RNA extracted from 200 muL of serum extr

181 icroRNAs and mRNAs by quantitative real-time PCR analysis of RNA extracted from plasma, liver, muscle

182 Quantitative real-time PCR analysis of Samd9L revealed near-ubiquitous expressi

183 The RT-PCR analysis of selected genes was performed in stem cel

184 In previously BCG-vaccinated individuals, PCR analysis of skin biopsy specimens reflected a degree

185 Microarray and quantitative RT-PCR analysis of smooth muscle from mice harboring smooth

186 PCR analysis of sperm DNA from healthy males indicates t

187 Furthermore, qRT-PCR analysis of the AD postmortem brains with different

188 We performed PCR analysis of the H. pylori vacA gene and for the pres

189 Real-time PCR analysis of the HIV-1 life cycle demonstrated that P

190 The real-time PCR analysis of the HuR gene showed a relative 4.7-fold

191 Quantitative RT-PCR analysis of the plr1 mutants showed little change in

192 yanate-dextran uptake assay, quantitative RT-PCR analysis of tight junction proteins, myosin light ch

193 Quantitative real-time reverse transcription-PCR analysis of total RNA extracted from the parental st

194 Northern blots and RT-PCR analysis of total RNA revealed truncated transcripts

195 Quantitative real-time PCR analysis of viral DNA indicated that the absence of

196 zed by antimicrobial susceptibility testing, PCR analysis of virulence genes, and Diversilab typing.

197 Quantitative reverse transcription-PCR (RT-PCR) analysis of a select set of genes (csfB, gpr, spoII

198 itative real-time polymerase chain reaction (PCR) analysis of blood samples, but these viruses are pr

199 Reverse transcription-PCR (RT-PCR) analysis of distal colonic tissue on day 10 postinf

200 transcription-polymerase chain reaction (RT-PCR) analysis of genomic DNA and total RNA extracted fro

201 ing microscopy or polymerase chain reaction (PCR) analysis of placental blood specimens.

202 low cytometry and polymerase chain reaction (PCR) analysis of rearranged immunoglobulin and T-cell re

203 Quantitative real-time PCR (qRT-PCR) analysis of selected genes also validated the induc

204 rapid culture and polymerase chain reaction (PCR) analysis of urine and saliva specimens from 80 chil

205 e quantitative reverse transcriptase PCR (RT-PCR) analysis of virus titer in L1 thrips revealed a sig

206 le on altered pathways were validated by qRT-PCR analysis on 12 samples per group.

207 Single-cell PCR analysis on beta-cell-specific (HLA-B7 tetramer-posi

208 PCR analysis on DNA extracted from the immunoprecipitate

209 Quantitative RT-PCR analysis on Newcastle disease virus-infected primary

210 uent real-time reverse transcription-PCR (RT-PCR) analysis on a panel of NPC cell lines identified HP

211 sing western blot and quantitative real-time PCR analysis, our results indicated that knockdown of en

212 Immunoblot and RT-PCR analysis reveal that expression of NM II-C1C2 peaks

213 Gene expression profiling and RT-PCR analysis revealed a coordinate down-regulation of va

214 Quantitative reverse transcriptase (qRT)-PCR analysis revealed a heightened basal expression of i

215 Real-time quantitative RT-PCR analysis revealed a lower mean qDeltaCt value in mel

216 Gene expression profiling and real-time PCR analysis revealed a significant induction of type-I

217 Quantitative real-time PCR analysis revealed an intermediate expression level o

218 Quantitative reverse transcription-PCR analysis revealed decreased glut1 transcript express

219 RT-PCR analysis revealed dramatic up-regulation of the gene

220 RT-PCR analysis revealed edited forms of 5HT2C were present

221 Single-cell reverse transcription-PCR analysis revealed expression of H3 receptors in a po

222 Single-cell reverse transcription-PCR analysis revealed expression of TRPC1, TRPC5 and TRP

223 Consistent with this, real-time PCR analysis revealed fewer transcription/replication-as

224 PCR analysis revealed haptoglobin mRNA, suggesting that

225 RT-PCR analysis revealed increased levels of EDN2 and EDNRA

226 cence staining, RT-PCR, and qRT-PCR, and qRT-PCR analysis revealed increased transcriptional inductio

227 Both immunohistochemistry and RT-PCR analysis revealed markedly decreased levels of proli

228 ession validation of selected elements by RT-PCR analysis revealed multiple transcripts not seen in t

229 PCR analysis revealed presence of bacterial genomic DNA,

230 However, our real-time quantitative PCR analysis revealed significant downregulation of miR-

231 Real-time PCR analysis revealed significant increases of key remod

232 Further, qRT-PCR analysis revealed that 17beta-E(2) pretreatment upre

233 PCR analysis revealed that 41.7 % of the analysed transg

234 RT-PCR analysis revealed that a long noncoding RNA (lncRNA)

235 In addition, PCR analysis revealed that all three unique DD treponeme

236 In situ RT-PCR analysis revealed that alpha-globulin RNAs are not d

237 Quantitative PCR analysis revealed that LOX-1 expression in HCAECs is

238 Viral tiled array and quantitative PCR analysis revealed that many late transcripts sensiti

239 immunoprecipitation followed by quantitative PCR analysis revealed that NAC019 binds to the promoters

240 qRT-PCR analysis revealed that only expression of acid ceram

241 amples by quantitative reverse transcription PCR analysis revealed that overall expression of CCND1 w

242 Microarray and qRT-PCR analysis revealed that Pgp4 is a transcriptional reg

243 Quantitative RT-PCR analysis revealed that TASK mRNA was reduced by >90%

244 Quantitative real-time PCR analysis revealed that the Sc-MSTN transcript was ex

245 Single-cell PCR analysis revealed that TNF-alpha-responding neurons

246 Second, single-cell PCR analysis revealed that two different bacterial types

247 Quantitative protein and RT-PCR analysis revealed that whereas merlin protein expres

248 qRT-PCR analysis revealed tissue-specific and hormone-respon

249 estern blotting and quantitative RT-PCR (qRT-PCR) analysis revealed no differences in viral RNA or pr

250 16S rDNA PCR analysis reveals the presence of bacterial DNA in in

251 Additional quantitative RT-PCR analysis showed a striking increase in IL-22 mRNA ex

252 RT-PCR analysis showed strong upregulation of OsPIP1;3 and

253 Subsequent FMRP immunoprecipitation and QRT-PCR analysis showed that astroglial mGluR5 (but not GLT1

254 Quantitative real time PCR analysis showed that Bim was transcriptionally up-re

255 However, qRT-PCR analysis showed that endogenous miR-140/141/200c exp

256 Quantitative RT-PCR analysis showed that HAUSP increased the transcript

257 Quantitative PCR analysis showed that LPS raised Kir6.1 and SUR2B tra

258 Quantitative real-time PCR analysis showed that miR-23b is significantly down-r

259 anscriptase PCR (RT-PCR) and quantitative RT-PCR analysis showed that RcrR functions as an autogenous

260 Quantitative real-time PCR analysis showed that the 16S rRNA gene copies of Deh

261 Real-time PCR analysis showed that the beta-fructofuranosidase and

262 Single cell qRT-PCR analysis showed that the combination of IFN-gamma an

263 Single-cell PCR analysis showed that the delta subunit, the principa

264 Real-time PCR analysis showed that the expression of PGC markers n

265 Quantitative PCR analysis showed that the FADY genes were expressed i

266 In situ hybridization and quantitative RT-PCR analysis showed that the miR-17-92 cluster is highly

267 Real-time PCR analysis showed that the PCR amplification was not i

268 RT-PCR analysis showed that these stable intronic sequences

269 Quantitative PCR analysis showed that treatment of neurosphere-like R

270 Quantitative PCR analysis showed the lack of Col10alpha1 upregulation

271 Finally, reverse transcription-PCR analysis showed the presence of MuLV in three other

272 Reverse transcription-PCR (RT-PCR) analysis showed that cnm is cotranscribed with SMU.

273 ive real-time reverse-transcription PCR (qRT-PCR) analysis showed that Dicer deletion lead to the upr

274 Quantitative-PCR analysis shows an increase in mtDNA damage after UVB

275 Real-time PCR analysis shows that RANKL expression is mainly regul

276 PCR analysis specifically detected viral DNA in all 60 u

277 However, the accuracy of qRT-PCR analysis strongly depends on transcript normalizatio

278 me course quantitative reverse transcription-PCR analysis suggested that the coalescence of inclusion

279 al relevance to these findings, by real-time PCR analysis, there was a strong correlation between HOX

280 MtDHDPS genes were found by quantitative RT-PCR analysis to be expressed in an organ-specific manner

281 though first studies were performed using RT-PCR analysis to monitor the acute phase of the reaction,

282 Herein, we applied multiplex RT-PCR analysis to mRNA extracted from 26 trigeminal gangli

283 RT-PCR analysis using cDNA made from Ago2-immunoprecipitate

284 Flow cytometry and RT-PCR analysis using different intestinal epithelial cell

285 qRT-PCR analysis using independent tissue samples confirmed

286 RT-PCR analysis using rat- or human-specific myosin heavy c

287 Real-time polymerase chain reaction (PCR) analysis verified significant up-regulation of miR-

288 Real-time RT-PCR analysis was applied on microdissected airways.

289 The quantitative real time PCR analysis was based on a suppression subtractive hybr

290 To achieve this goal, miRNA Real-Time (RT) PCR analysis was first utilized to examine miR-10a expre

291 Quantitative RT-PCR analysis was used to test the adhesion and apoptosis

292 vagal ganglia, but when using single cell RT-PCR analysis we found only 3 out of 34 neurons expressed

293 hromatin immunoprecipitation, followed by RT-PCR analysis, we demonstrate that endogenous Osr2 protei

294 Using quantitative real-time PCR analysis, we find that 13 formins are differentially

295 Using real-time PCR analysis, we found in resolving exudates that miR-21

296 s well as quantitative reverse transcriptase-PCR analysis, we found that endogenous TIMP-2 mRNA level

297 As determined by quantitative real-time PCR analysis, we found that levels of CD22 mRNA in a pan

298 By microarray and quantitative PCR analysis, we identified trpa1 as an L cell-enriched

299 resolve allele ambiguity, and by performing PCR analysis, we infer that the deletion breakpoints wer

300 h quantitative reverse transcription-PCR (RT-PCR) analysis, we have confirmed that the same set of re