ライフサイエンスコーパス: qRT-PCR

1 qRT-PCR analyses revealed that GPC1 mRNA abundance is re

2 qRT-PCR analyses revealed the expression profiles of the

3 qRT-PCR analysis confirmed the expression pattern of 11

4 qRT-PCR analysis confirmed the microarray results, that

5 qRT-PCR analysis indicated the expression of G-protein-c

6 qRT-PCR analysis of GmSNAPs indicates a co-regulation fo

7 qRT-PCR analysis of total calvariae versus isolated oste

8 qRT-PCR analysis performed on hMSCs (isolated from femor

9 qRT-PCR analysis revealed that only expression of acid c

10 qRT-PCR analysis revealed tissue-specific and hormone-re

11 qRT-PCR analysis was performed to verify the expression

12 qRT-PCR and protease activity assays demonstrated that u

13 qRT-PCR assay detected higher miR-214 expression in the

14 qRT-PCR assay indicated that compound 1 and DBL exposure

15 qRT-PCR experiments revealed that TcSOD2 was present thr

16 qRT-PCR indicated that all DR subtypes were expressed by

17 qRT-PCR of intact RNA showed that the amount of phytoene

18 qRT-PCR of pathogen miRNAs isolated from extracellular v

19 qRT-PCR results on 25 multi-isoform genes in a stem cell

20 qRT-PCR results were consistent with the motility phenot

21 qRT-PCR revealed expression of P2X(1-6), and P2Y(1-2), P

22 qRT-PCR showed 4- to 10-fold overexpression of NT3 from

23 qRT-PCR studies on the expression of genes known to be i

24 qRT-PCR validation statistics (PPV and AUC) were high an

25 qRT-PCR was performed to validate the expression of the

26 qRT-PCR, Western blotting, and enzymatic assays were per

27 qRT-PCR-based measurements revealed multifold inaccuraci

28 Here, we have used microarrays and a qRT-PCR primer platform covering 1,880 genes encoding tr

29 authorization for the test, which excluded a qRT-PCR reference method threshold cutoff, were a PPA of

30 d from serum samples of 156 patients using a qRT-PCR array for 22 miRNAs.

31 Accordingly, qRT-PCR analysis on a panel of cytokines shows that cell

32 quantitative reverse transcription analysis (qRT-PCR), and semiquantitative methods, such as microarr

33 xyresorufin-O-deethylase (EROD) activity and qRT-PCR, and cell cycle was measured by flow cytometry.

34 xpression based on fundus image analysis and qRT-PCR.

35 ated using the TaqMan low-density arrays and qRT-PCR.

36 Immunohistochemistry, Western blot, and qRT-PCR were performed on the outflow vein at 7 and 21 d

37 ive in vitro assays using flow cytometry and qRT-PCR analyses and in vivo assays to determine acute t

38 xpression was assessed by flow cytometry and qRT-PCR in brain tumor cell lines and patient tumor-deri

39 stimulated cells by using flow cytometry and qRT-PCR, respectively.

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

41 ssection of autopsy human hippocampus DG and qRT-PCR miRNA analyses were combined with immunofluoresc

42 tern blotting, immunofluorescence, ELISA and qRT-PCR, we investigated the production of transthyretin

43 eatment conditions was measured by ELISA and qRT-PCR.

44 The limit of detection for FilmArray and qRT-PCR assays with inactivated ZEBOV, based on duplicat

45 Rates of agreement between FilmArray and qRT-PCR results for clinical specimens from patients wit

46 Cell fractionation and qRT-PCR analysis indicated that LINC00152 is found mainl

47 or live-cell fluorescent calcium imaging and qRT-PCR to determine the expression profile of P2X and P

48 ing flow cytometry, immunocytochemistry, and qRT-PCR showed high neuralization efficiency.

49 nce (kappa of >/=0.723) with the RT-LAMP and qRT-PCR assays in detecting the dengue viremic samples.

50 downregulation of ADAR2 both in metadata and qRT-PCR based validation.

51 Microarray and qRT-PCR analysis of human hair follicles after Nrf2 acti

52 Microarray and qRT-PCR analysis of RV confirmed effects on fibrotic pat

53 The microarrays and qRT-PCR resulted in similar gene-expression changes, con

54 Confocal microscopy and qRT-PCR were used to visualize and quantitate successful

55 rkers; immunohistochemistry, morphometry and qRT-PCR analysis were used on both kidney and intestine

56 gene expression results using NanoString and qRT-PCR for 18 genes in the same pool of RNA (RNAlater),

57 RT-PCR and qRT-PCR were performed to confirm our findings by detect

58 orescence staining, RT-PCR, and qRT-PCR, and qRT-PCR analysis revealed increased transcriptional indu

59 of immunofluorescence staining, RT-PCR, and qRT-PCR, and qRT-PCR analysis revealed increased transcr

60 st or human DBR1 enzyme prior to 5' RACE and qRT-PCR.

61 RNA-Seq and qRT-PCR analyses reveal that auxin-responsive genes and

62 RNA-seq and qRT-PCR analyses show that Mr-OPY2 is a negative regulat

63 RNA-seq and qRT-PCR analyses suggested that the expression levels of

64 RNA-seq and qRT-PCR expression analysis showed that overexpression o

65 Gene expression profiling by RNA-Seq and qRT-PCR revealed expression levels for glycan-modifying

66 in MDV-infected CD4+ T cells by RNA-Seq and qRT-PCR.

67 Single-cell RNA sequencing and qRT-PCR of sorted cells indicated that Hedgehog activati

68 RNA sequencing and qRT-PCR revealed that arginine biosynthesis genes (argR,

69 MiRNA sequencing and qRT-PCR revealed that miR-214-3p was increased in the ex

70 Next-generation sequencing and qRT-PCR were used to measure plasma microRNAs.

71 nd trans-RA16 at the grafted tumor site, and qRT-PCR showed high retention of syn-RA16 in tumor tissu

72 n-DENV RT-iiPCR, NS1 antigen rapid test, and qRT-PCR tests was 93.9%, 84.5%, and 97.4%, respectively,

73 Transcriptome and qRT-PCR analyses provide insight into the roles of PfmaF

74 microbial communities during treatment, and qRT-PCR as an indirect determination of 'Ca.

75 nnervation by the second postnatal week, and qRT-PCR shows transcripts for H(1), H(2), and H(3) hista

76 uced a pre-amplification of human RNA before qRT-PCR.

77 can and Gambian cohorts (p values <0.0001 by qRT-PCR) with a sensitivity of 53.7% (42.6-64.3) and a s

78 Validation analysis by qRT-PCR showed significant upregulation of only miR-455-

79 ndergoing bariatric surgery were analyzed by qRT-PCR for expression of WNT/PCP genes.

80 ckout mice and control mice were analyzed by qRT-PCR, immunoblot, and transepithelial electrical resi

81 ferent developmental stages were analyzed by qRT-PCR.

82 pha2 ratio was determined by SDS PAGE and by qRT-PCR in ex-vivo bone explants.

83 We tested for EBOV RNA in blood by qRT-PCR, and for anti-EBOV-specific IgM and IgG antibodi

84 nts tested negative for EBOV RNA in blood by qRT-PCR.

85 pression was confirmed in a larger cohort by qRT-PCR.

86 er variations by qPCR, RNA concentrations by qRT-PCR, and protein concentrations by immunoblotting.

87 the aforementioned stresses was confirmed by qRT-PCR analysis in distinct Arachis genotypes, whilst i

88 y of the cyclin B1/CDK1 complex confirmed by qRT-PCR and immunoblot analysis.

89 in the neonate, and adult heart confirmed by qRT-PCR and in situ hybridization.

90 f miR-21-5p in cancer tissue is confirmed by qRT-PCR and northern blot after oxidation/beta-eliminati

91 gets ZEB1/2, GATA2, and KDR was confirmed by qRT-PCR as being lower in obese patients with periodonti

92 The expression of hub genes confirmed by qRT-PCR, ELISA (IL-6, IL-1beta, and CXCL2), and Western

93 RNAs and their targets was also confirmed by qRT-PCR.

94 tis groups (i.e. RA and UA) and confirmed by qRT-PCR.

95 We demonstrate by qRT-PCR and confocal imaging that mouse Abcg4 is express

96 fferential emrB expression, as determined by qRT-PCR analysis.

97 tory cytokines/chemokines were determined by qRT-PCR, western, and immunohistochemical analyses.

98 idant enzymes MnSOD and GPx, as evaluated by qRT-PCR.

99 with chemerin and siChemR23 was examined by qRT-PCR and Western blotting.The roles of the MAPK and P

100 liable quantification of miRNA expression by qRT-PCR crucially depends on validated housekeepers for

101 Analysis of gene expression by qRT-PCR indicated that the aphid mortality rates and the

102 ith recombinant IL-13 and gene expression by qRT-PCR was performed for collagen1A1 and TGF-beta1.

103 trophoresis-based size-selection followed by qRT-PCR validated the top six up-regulated tRFs in a sep

104 etric quantification and sorting followed by qRT-PCR, and to DNA methylation analyses of the Treg-spe

105 We found by qRT-PCR that AtxA1 and AtxA2 function as positive regula

106 ssed the RNA expression of dehydrin genes by qRT-PCR.

107 us at term, and tested 86 candidate genes by qRT-PCR.

108 ssion was analyzed 4 weeks post-injection by qRT-PCR and histology.

109 otential in an independent cohort of LUAD by qRT-PCR.

110 fold higher in ATII cells than whole lung by qRT-PCR, and was undetectable in other viscera.

111 appaB targets, including IL8, as measured by qRT-PCR and cytokine array.

112 d class switch recombination was measured by qRT-PCR.

113 and lymphocyte sublineages were measured by qRT-PCR.

114 was confirmed for eight of these networks by qRT-PCR in an independent set of term and pre-term subje

115 mArray testing in four specimens and only by qRT-PCR testing in the remaining four specimens.

116 ession of 29 candidate miRNAs in placenta by qRT-PCR.

117 ected miRNAs were validated in the plasma by qRT-PCR and at tissue level by ISH.

118 s from three patients were found positive by qRT-PCR for ZIKAV and the viral RNA copy numbers detecte

119 d to the 3'-UTR of mouse MR were profiled by qRT-PCR after aldosterone stimulation.

120 evels of VEGF and VEGFR-2 were quantified by qRT-PCR and showed significant reduction in message expr

121 ed genes in these T cells were quantified by qRT-PCR.

122 NA-150-5p and miRNA-26a-5p was quantified by qRT-PCR.

123 ted in mouse PNFs versus normal mouse SCs by qRT-PCR.

124 for the expression of the oxytocin system by qRT-PCR, in situ hybridization, receptor autoradiography

125 ) and transcription factor T-Box 3 (TBX3) by qRT-PCR for selective expression in the serum samples.

126 Nasal and/or throat swabs were tested by qRT-PCR for common respiratory viruses, including RSV.

127 sting and matched plasma specimens tested by qRT-PCR testing, and 85% (11/13 specimens) for urine spe

128 35 hepatocellular carcinoma (HCC) tissues by qRT-PCR.

129 y below 1 female and 1 male gametocyte/uL by qRT-PCR.

130 xpression of selected genes was validated by qRT-PCR analysis and localisation investigated using in

131 selected candidate miRNAs were validated by qRT-PCR analysis of cohorts of 24 T1DM and 24 control su

132 t role on altered pathways were validated by qRT-PCR analysis on 12 samples per group.

133 ors (emx2, lhx2, and hopx), was validated by qRT-PCR and immunostaining in brain sections.

134 Relevant miRNAs were validated by qRT-PCR and in situ hybridization (ISH).

135 L1, TPD52, IQCG, and ACOX2 were validated by qRT-PCR in a third cohort of 40 ER+ HER2- and ER- HER2-

136 nges identified by RNA-Seq were validated by qRT-PCR open arrays.

137 iRNAs, among which miR-200b was validated by qRT-PCR to be significantly increased in obesity.

138 different S. mussotii tissues, validated by qRT-PCR, and compared with the homologous genes from S.

139 n CPT biosynthetic pathway were validated by qRT-PCR.

140 AGL9, LRR, PKL and ARF8-1 were validated by qRT-PCR.

141 xpression of miRNA and mRNA was validated by qRT-PCR.

142 iles of these eight miRNAs were validated by qRT-PCR.

143 RNAs, tasiRNAs and targets were validated by qRT-PCR.

144 ene expression in the apples was verified by qRT-PCR.

145 ter harvest at 20 degrees C and 4 degrees C. qRT-PCR results were supported by correlation analysis w

146 Single cell qRT-PCR analysis showed that the combination of IFN-gamm

147 of colon or bladder, followed by single-cell qRT-PCR and analysis via an automated hierarchical clust

148 This efficient method that combines qRT-PCR and high resolution melting (HRM) could be appli

149 Confirmatory qRT-PCR analysis demonstrated good correlation with SnoR

150 ssion activation and chromatin conformation: qRT-PCR and mRNA in situ hybridization showed that the c

151 re analyzed by cytokine multiplex detection, qRT-PCR, and flow cytometry respectively.

152 Our findings showed that the developed qRT-PCR could detect LGTV at a titre as low as 0.1 FFU/m

153 patient's blood sample was negative by EBOV qRT-PCR testing, identification of viral reads by mNGS c

154 (p=0.018 for RNA sequencing and p=0.0095 for qRT-PCR) and in the independent South African and Gambia

155 ality (average RIN 6.7 + /- 0.8) allowed for qRT-PCR.

156 imals, unexposed cochleas were extracted for qRT-PCR.

157 optimized set of oligonucleotide primers for qRT-PCR assays and cloned cDNA plasmids corresponding to

158 Data from qRT-PCR, patch clamp, ex vivo coronary perfusion Langend

159 Gametocyte sex ratios from qRT-PCR were compared with those from immunofluorescence

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

161 Furthermore, qRT-PCR analysis of the AD postmortem brains with differ

162 Furthermore, qRT-PCR profiling of key ripening regulatory genes indic

163 as approximately 70% accurate using in-house qRT-PCR influenza A as a gold-standard comparison.

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

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

166 However, qRT-PCR does not confirm presence of infectious virus, p

167 normal parathyroid by in situ hybridization, qRT-PCR, and immunohistochemistry.

168 elial cells (MeT5A) by immunohistochemistry, qRT-PCR and ELISA.

169 In qRT-PCR of in vitro plants, secondary metabolite biosynt

170 In qRT-PCR validations, pRSEM was shown to be superior than

171 hat mRNA levels were significantly higher in qRT-PCR evaluation in septic groups than control groups

172 mbryos and endosperm of germinating seeds in qRT-PCR analysis, while beta-glucuronidase (GUS) assays

173 ion, microarray experiments, and independent qRT-PCR validation analyses revealed that the branch rep

174 chromatography (to measure creatine levels), qRT-PCR, transepithelial electrical resistance, barrier

175 proaches to simulate results from microarray/qRT-PCR platforms and a local probabilistic model to ass

176 cific pfs25 and male-specific pfmget or mssp qRT-PCR.

177 articularly recommended for normalization of qRT-PCR data.

178 The results of qRT-PCR and western blot assay clearly showed that all o

179 nguishable when studied by flow cytometry or qRT-PCR.

180 receptors was evaluated by flow cytometry or qRT-PCR.

181 Our qRT-PCR and immunoblotting analysis revealed that reduce

182 or selected human and mouse candidate pairs, qRT-PCR and in vitro RNA structure probing supported bot

183 without T (porA) Real-time quantitative PCR (qRT-PCR) analysis of the porA mRNA and immunoblot detect

184 Quantitative PCR (qRT-PCR) and Western blotting confirmed changes in expre

185 and reverse transcription-quantitative PCR (qRT-PCR) in the screening cohort.

186 ng SnoRNASeq and real-time quantitative PCR (qRT-PCR) we demonstrate snoRNA expression levels in muri

187 ing, reverse transcription-quantitative PCR (qRT-PCR), and carbohydrate utilization studies.

188 via reverse transcriptase quantitative PCR (qRT-PCR).

189 the multiplex real-time quantitative RT-PCR (qRT-PCR) assay for DENV-1, -3, and -4 detection but 10-f

190 was determined by using quantitative RT-PCR (qRT-PCR) in cell pellets.

191 modulated by steroids, quantitative RT-PCR (qRT-PCR) mRNA expression, enzymatic assay aromatase acti

192 reaction (RT-PCR), and quantitative RT-PCR (qRT-PCR), and the proinflammatory cytokines interleukin

193 Quantitative real-time PCR (qRT-PCR) analysis of selected genes also validated the i

194 titative assays, quantitative real-time PCR (qRT-PCR) and droplet digital PCR (ddPCR), gave similar r

195 these findings, quantitative real-time PCR (qRT-PCR) and enzyme-linked immunosorbent assay (ELISA) a

196 rthern blotting, quantitative real time PCR (qRT-PCR) and microarray technology besides novel techniq

197 vels analyzed by quantitative real time PCR (qRT-PCR) at different time points after harvest at 20 de

198 Quantitative real-time PCR (qRT-PCR) experiment results of lncRNAs, pre-miRNAs and m

199 NA profiling and quantitative real-time PCR (qRT-PCR) in the orbitofrontal cortex (OFC) of SCZ (N = 2

200 validation using quantitative real-time PCR (qRT-PCR) indicated four promising candidate genes having

201 enes measured by quantitative real-time PCR (qRT-PCR) showed consistent results with that of transcri

202 te markers using quantitative real-time PCR (qRT-PCR) showed that two markers (arsR [NGO1562] and rps

203 ntified protein, quantitative real time PCR (qRT-PCR) was performed.

204 Using quantitative real-time PCR (qRT-PCR) we have measured the gene expression profiles o

205 Using quantitative real-time PCR (qRT-PCR), it showed that the DRELFA is very effective in

206 ion to multiplex quantitative real-time PCR (qRT-PCR), the signature was used to predict tuberculosis

207 y controls using quantitative real-time PCR (qRT-PCR).

208 validated using quantitative real-time PCR (qRT-PCR).

209 ere validated by quantitative real time-PCR (qRT-PCR) in 43 patients with different tumour stages (pT

210 Quantitative reverse-transcriptase PCR (qRT-PCR) analysis showed that these 5 genes are expresse

211 nome quantitative reverse transcriptase PCR (qRT-PCR) array and chromatin immunoprecipitation, we elu

212 try, quantitative reverse-transcriptase PCR (qRT-PCR), and RNA-Seq for PD-1 expression.

213 sing quantitative reverse-transcriptase PCR (qRT-PCR), immunofluorescence, and Luminex technology.

214 e by quantitative reverse transcriptase PCR (qRT-PCR).

215 and quantitative reverse transcriptase PCR (qRT-PCR).

216 ion, quantitative reverse transcriptase-PCR (qRT-PCR) and immunoblot experiments demonstrated direct

217 s of quantitative reverse-transcription PCR (qRT-PCR) demonstrated that expression of the genes encod

218 and quantitative reverse transcription-PCR (qRT-PCR) analyses confirm that HSV-1 latently infects ne

219 Quantitative reverse transcription-PCR (qRT-PCR) analyses revealed that both drugs altered E1A R

220 sing quantitative reverse transcription-PCR (qRT-PCR) and microarrays have shown a significant transi

221 d by quantitative reverse transcription-PCR (qRT-PCR) subsequently confirmed QS upregulation within 1

222 ing, quantitative reverse transcription-PCR (qRT-PCR), and functional analysis.

223 with quantitative reverse transcription-PCR (qRT-PCR), to augment or potentially replace the DFA test

224 d by quantitative reverse transcription-PCR (qRT-PCR).

225 on rHSV48Y replication was assessed by PCR, qRT-PCR, Western-blot, flow-cytometry, epifluorescence a

226 fidence interval, 0.33-0.44) by pfs25/pfmget qRT-PCR; this correlated well with IFA results (Pearsons

227 gation was carried out combining proteomics, qRT-PCR mRNA transcripts analysis, and enzyme activities

228 analyzed by in-gel fluorescence, proteomics, qRT-PCR, immunofluorescence, fluorescence resonance ener

229 rse transcription polymerase chain reaction (qRT-PCR) amplification of miRNA extracted directly from

230 rse transcription polymerase chain reaction (qRT-PCR) analysis.

231 itative real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry (IHC).

232 itative real-time polymerase chain reaction (qRT-PCR) and RNA in situ hybridization.

233 rse Transcription-Polymerase Chain Reaction (qRT-PCR) and western blot analysis performed on (I) HEK2

234 rse transcription polymerase chain reaction (qRT-PCR) array on 156 samples.

235 rse transcription-polymerase chain reaction (qRT-PCR) could exceed 5 days.

236 rse-transcription-polymerase chain reaction (qRT-PCR) for rapid detection of LGTV.

237 itative real-time polymerase chain reaction (qRT-PCR) identified pro-TRH transcript in a number of di

238 rse transcription-polymerase chain reaction (qRT-PCR) in biopsy samples of 19 patients with esophagea

239 rse transcriptase polymerase chain reaction (qRT-PCR) in colonic mucosal biopsies of patients from th

240 itative real-time polymerase chain reaction (qRT-PCR) in stool collected on alternate days for 10 day

241 rse transcription polymerase chain reaction (qRT-PCR) to determine malaria positivity.

242 rse transcription-polymerase chain reaction (qRT-PCR) was performed to assess the messenger RNA (mRNA

243 rse transcription polymerase chain reaction (qRT-PCR) was performed to measure the mRNA levels of the

244 itative real time polymerase chain reaction (qRT-PCR) was used to analyse neuronal-associated gene ex

245 rse transcription-polymerase chain reaction (qRT-PCR), a sensitive method to detect viral genetic mat

246 rse transcription polymerase chain reaction (qRT-PCR), chromatin immunoprecipitation (ChIP)-PCR and E

247 rse transcriptase polymerase chain reaction (qRT-PCR)-based threshold cycle (Ct) value and the presen

248 rse transcription-polymerase chain reaction (qRT-PCR).

249 rse-transcription polymerase chain reaction (qRT-PCR).

250 rse transcription polymerase chain reaction (qRT-PCR).

251 rse transcription polymerase chain reaction (qRT-PCR).

252 rse transcription polymerase chain reaction (qRT-PCR).

253 Compared to reference qRT-PCR, LAMP had the highest sensitivity (92.6%, 95% co

254 f 70 (30.0%) EBOV-positive samples by repeat qRT-PCR (overall concordance = 87.1%).

255 xpression in single samples using repetitive qRT-PCR assays.

256 block was successful and allowed large-scale qRT-PCR and RNAseq analyses for gene expression.

257 of guard cell aperture, we used large-scale qRT-PCR to compare circadian oscillator gene expression

258 Argonaute 2 immunoprecipitation sequencing, qRT-PCR, and luciferase assay identified Crem, Fn1, and

259 Combined RNA sequencing, qRT-PCR, CLIP-ADAR1, and pri-let-7 mutagenesis data sugg

260 were identified by transcriptome sequencing, qRT-PCR, immunoblotting, protein interaction studies, kn

261 Finally, during follow-up, serial qRT-PCR analyses allowed prediction of relapse in 77% of

262 cation and re-sequencing, and have a similar qRT-PCR detection ratio as their cognate canonical miRNA

263 the ReEBOV RDT, compared with EBOV-specific qRT-PCR.

264 unoblotting and immunofluorescence staining, qRT-PCR, and siRNA-mediated gene silencing, we show that

265 f two independent quantification techniques: qRT-PCR for relative quantification and ddPCR for absolu

266 The qRT-PCR results showed that 11 (91.7%) of the 12 predict

267 The qRT-PCR results showed that 3 (75.0%) of the 4 predicted

268 good correlation between the DRELFA and the qRT-PCR over a 50-fold concentration range.

269 using a DENV NS1 antigen rapid test and the qRT-PCR.

270 Additionally, we compared the qRT-PCR assay to the gold standard direct fluorescent-an

271 The detection limit of the qRT-PCR assay at 95% probability was 0.28 FFU/ml as dete

272 Consistent with this, qRT-PCR confirmed that the expression of multiple genes

273 nto cDNA before being subjected to real-time qRT-PCR analysis in triplicate within the TaqMan gene Ex

274 Real-time qRT-PCR revealed that miR-125a-3p, miR-320c were signifi

275 nohistochemistry and quantified by real-time qRT-PCR.

276 Importantly, unlike qRT-PCR, the microelectrochemical sensor offers direct a

277 We used qRT-PCR and genotyping to characterize residual circulat

278 We used qRT-PCR, Western blotting, ELISA, and ChIP (chromatin im

279 expressed and secreted) were assessed using qRT-PCR.

280 e validated differential expression by using qRT-PCR and found that genes linked to metabolism, oxida

281 and methylation changes were confirmed using qRT-PCR and qMSP methods.

282 es were further assessed and confirmed using qRT-PCR, which demonstrated reliable data and significan

283 ; a finding that was further confirmed using qRT-PCR.

284 th muscle cells (HASMCs) was evaluated using qRT-PCR, western blotting and immunofluorescent staining

285 d the expression of 29 of the 35 genes using qRT-PCR and the trend of mRNA expression is similar to t

286 idated differentially expressed miRNAs using qRT-PCR.

287 Molecular screening using qRT-PCR and Western blotting demonstrated that aldostero

288 m RNA-seq data; (v) validation studies using qRT-PCR were conducted on 26 selected representative gen

289 Validation using qRT-PCR showed significant upregulation of miR-143-3p ex

290 Key results were verified using qRT-PCR.

291 were used to treat ciGEnCs to determine via qRT-PCR potential changes in the mRNA levels of pro-infl

292 Evaluation of key neural markers via qRT-PCR demonstrated more profound differences in gene e

293 he differential expression was performed via qRT-PCR and immunoblot analysis in the defined model ner

294 These transcripts were further validated via qRT-PCR.

295 sed on multivariate regression analysis with qRT-PCR as the gold standard, for every 3.2% increase in

296 Increases were confirmed with qRT-PCR in five genes that code for proteins involved in

297 nine genes were independently confirmed with qRT-PCR.

298 UPR PCR-array analysis coupled with qRT-PCR identified and confirmed that four transcripts i

299 out microcephaly, comprising 56 infants with qRT-PCR confirmed exposure to ZIKV during gestation and

300 asion and wound healing assays together with qRT-PCR determination of epithelial-to-mesenchymal trans