ライフサイエンスコーパス: PCR analysis

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

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

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

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

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

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

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

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

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

10 further validation by quantitative real-time PCR analysis.

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

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

13 Tissue bacterial burdens were examined by PCR analysis.

14 A synthesis, and then underwent quantitative PCR analysis.

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

16 CGG repeat allele size by Southern Blot and PCR analysis.

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

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

19 a significant increase of sensitivity during PCR analysis.

20 situ remove contaminants that interfere with PCR analysis.

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

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

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

24 further validated by quantitative real-time PCR analysis.

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

26 esprin2-KD cells as assessed by quantitative PCR analysis.

27 ential emrB expression, as determined by qRT-PCR analysis.

28 istologic, flow cytometric, and quantitative PCR analysis.

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

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

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

32 for real-time polymerase chain reaction (RT-PCR) analysis.

33 were detected by polymerase chain reaction (PCR) analysis.

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

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

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

37 Quantitative RT-PCR analysis also showed an increase in the expression o

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

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

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

41 Quantitative PCR analysis and GUS activity measurements revealed that

42 In contrast, digestion-circularization PCR analysis and high-throughput sequencing analyses of

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

44 ssion of selected genes was validated by qRT-PCR analysis and localisation investigated using in situ

45 UVECs) in vitro, followed by quantitative RT-PCR analysis and OLINK Proteomics.

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

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

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

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

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

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

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

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

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

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

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

57 Using RT-PCR analysis at the endogenous locus, we confirm that th

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

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

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

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

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

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

64 PCR analysis confirmed 3 (0.6%) were P. ovale infections

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

66 Quantitative RT-PCR analysis confirmed increased transcription of IL-1a,

67 Quantitative PCR analysis confirmed SH3TC2 mRNA expression in differe

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

69 Quantitative PCR analysis confirmed that most polar Thaumarchaeota ha

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

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

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

73 qRT-PCR analysis confirmed the expression pattern of 11 cons

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

75 QRT-PCR analysis confirmed the microarray data and revealed

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

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

78 qRT-PCR analysis demonstrated an increased expression of tra

79 Confirmatory qRT-PCR analysis demonstrated good correlation with SnoRNASe

80 Linear amplification-mediated-PCR analysis demonstrated random integration of 57-88% o

81 RT-PCR analysis demonstrated that cultured human pulp fibro

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

83 ts' CSF was repeatedly negative on real-time PCR analysis despite concurrent neurological disease.

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

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

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

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

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

89 in a blinded fashion as well as quantitative PCR analysis for chemokines and cytokines.

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

91 observed in the cross-validation of PLS and PCR analysis for the adulteration levels between 0% and

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

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

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

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

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

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

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

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

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

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

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

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

104 cDNA before being subjected to real-time qRT-PCR analysis in triplicate within the TaqMan gene Expres

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

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

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

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

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

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

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

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

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

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

115 qRT-PCR analysis indicated the expression of G-protein-coupl

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

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

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

119 RT-PCR analysis of 17 human tissues demonstrated ubiquitous

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

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

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

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

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

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

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

127 Moreover, RT-quantitative PCR analysis of actively translated mRNAs by sucrose cus

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

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

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

131 PCR analysis of C. jejuni isolates from different animal

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

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

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

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

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

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

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

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

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

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

142 Third, PCR analysis of fractionated gut contents demonstrated t

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

144 RT-PCR analysis of genes involved in adipocyte differentiat

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

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

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

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

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

150 quantitative real-time reverse transcription PCR analysis of human epithelial-derived cell lines reve

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

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

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

154 level was measured by real-time quantitative PCR analysis of immunoglobulin and T-cell receptor gene

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 Microarray and qRT-PCR analysis of RV confirmed effects on fibrotic pathway

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

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

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

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

177 PCR analysis of sperm DNA from healthy males indicates t

178 In the 75 patients, RT-PCR analysis of tears showed positive results in 18 pati

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

180 PCR analysis of the anterior chamber fluid is important

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

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

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

184 Quantitative RT-PCR analysis of the miR-panel confirmed these results ex

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

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

187 qRT-PCR analysis of total calvariae versus isolated osteobla

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

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

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

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

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

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

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

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

196 Principal component regression (PCR) analysis of the EEM spectra of IGFR samples correla

197 out T (porA) Real-time quantitative PCR (qRT-PCR) analysis of the porA mRNA and immunoblot detection

198 ions with digital polymerase chain reaction (PCR) analysis of tissue samples from 227 prolactinomas.

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

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

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

202 Accordingly, qRT-PCR analysis on a panel of cytokines shows that cells ex

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

204 PCR analysis on DNA extracted from the immunoprecipitate

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

206 transcription-polymerase chain reaction (RT-PCR) analysis or serological testing was used to confirm

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

208 qRT-PCR analysis performed on hMSCs (isolated from femoral h

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

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

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

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

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

214 PCR analysis revealed an increase in (mt)DNA lesions and

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

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

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

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

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

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

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

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

223 In addition, single blastomere PCR analysis revealed mosaicism in CCR5 editing within t

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

225 PCR analysis revealed presence of bacterial genomic DNA,

226 equencing and stem cell pathway real-time RT-PCR analysis revealed profound reductions in WNT1 expres

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

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

229 PCR analysis revealed that 41.7 % of the analysed transg

230 Real-time quantitative PCR analysis revealed that 5azaD/TSA-expanded cells expr

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

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

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

234 In addition, real-time PCR analysis revealed that chemokines and cytokines with

235 Real-time PCR analysis revealed that FENDRR was expressed 80-fold

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

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

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

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

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

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

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

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

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

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

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

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

248 16S rDNA PCR analysis reveals the presence of bacterial DNA in in

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

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

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

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

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

254 Finally, quantitative PCR analysis showed that expression of C. trachomatis gl

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

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

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

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

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

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

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

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

263 RT-PCR analysis showed that these stable intronic sequences

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

265 Quantitative PCR analysis showed the lack of Col10alpha1 upregulation

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

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

268 Quantitative reverse-transcriptase PCR (qRT-PCR) analysis showed that these 5 genes are expressed in

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

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

271 PCR analysis specifically detected viral DNA in all 60 u

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

273 healthy controls (n = 379) were genotyped by PCR analysis; subsequently, the PCR results were integra

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

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

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

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

278 qRT-PCR analysis using independent tissue samples confirmed

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

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

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

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

283 hput expression analysis and quantitative RT-PCR analysis was further employed to identify the family

284 Quantitative real-time PCR analysis was performed to detect and relatively quan

285 qRT-PCR analysis was performed to verify the expression patt

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

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

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

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

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

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

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

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

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

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

296 s; immunohistochemistry, morphometry and qRT-PCR analysis were used on both kidney and intestine tiss

297 RNA sequencing and quantitative real-time PCR analysis were used to assess the transcriptional res

298 h HCoV genomic loads (cycle threshold <28 in PCR analysis) were associated with RTIs (odds ratio = 3.

299 os and endosperm of germinating seeds in qRT-PCR analysis, while beta-glucuronidase (GUS) assays on O

300 Further, qRT-PCR analysis with the same serum exosomes processed for