ライフサイエンスコーパス: PCR analyses

1 whole-genome microarray and confirmed by RT-PCR analyses.

2 transgene was confirmed by Southern blot and PCR analyses.

3 66 have been validated by RNA blot and/or RT-PCR analyses.

4 sgene was confirmed by Southern blotting and PCR analyses.

5 HIV-p24 production and reverse transcription-PCR analyses.

6 spermatogenic cells using semi-quantitative PCR analyses.

7 n blot analysis, immunocytochemistry, and RT-PCR analyses.

8 were compared by microarray and quantitative PCR analyses.

9 vident by transgene expression and real-time PCR analyses.

10 ts transcription was confirmed by PCR and RT-PCR analyses.

11 ciliary body (CB) cells was determined by RT-PCR analyses.

12 acenta as determined by Northern blot and RT-PCR analyses.

13 ied by RT-qPCR, RNA gel blot, and in situ RT-PCR analyses.

14 Northern and real-time reverse transcription-PCR analyses.

15 rn or semiquantitative reverse transcription-PCR analyses.

16 d using Taqman and energy-transfer real-time PCR analyses.

17 orthern blot, eDNA microarray, and real-time PCR analyses.

18 imulated, and analyzed by flow cytometry and PCR analyses.

19 as determined by both restriction enzyme and PCR analyses.

20 via quantitative reverse transcription (RT)-PCR analyses.

21 A amplification and multiplexed quantitative PCR analyses.

22 yed by microarray and quantitative real-time-PCR analyses.

23 NA, as observed with western blotting and RT-PCR analyses.

24 ic, immunohistochemical, and quantitative RT-PCR analyses.

25 and quantitative polymerase chain reaction (PCR) analyses.

26 quantitative reverse transcriptase PCR (qRT-PCR) analyses.

27 filter paper for polymerase chain reaction (PCR) analyses.

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

29 By real-time PCR analyses, ALS treatment of CD4-deficient mice adopti

30 Finally, cecal quantitative PCR analyses also revealed a significant reduction in ba

31 DNA microarray analyses and confirmed by RT-PCR analyses and biological assays.

32 in vitro assays using flow cytometry and qRT-PCR analyses and in vivo assays to determine acute toxic

33 Here we show both by DNA PCR analyses and infectivity assays, using live sorted C

34 eased both expression (reverse transcription-PCR analyses) and function (high-performance liquid chro

35 in, using has deletion mutants, quantitative PCR analyses, and immunoblotting, we show that the activ

36 ere identified by reverse transcription (RT)-PCR analyses, and the encoded proteins were predicted to

37 The results of RT-PCR analyses are consistent with this prediction.

38 We carried out quantitative PCR analyses as an independent test of transcript abunda

39 Repetitive PCR analyses at the single DNA template molecule level e

40 lts from bioinformatic and nested degenerate PCR analyses collectively suggest that HYD1 and HYD2 may

41 Further quantitative reverse transcription-PCR analyses comparing 3B(-)/3C(low) LCLs to a previousl

42 quantitative reverse transcription-PCR (qRT-PCR) analyses confirm that HSV-1 latently infects neuron

43 uantitative, real time reverse transcriptase PCR analyses confirmed altered expression in 14 of 16 ge

44 Northern blot and RT-PCR analyses confirmed an operon structure of tfsAB, sug

45 Southern blotting and PCR analyses confirmed deletion of hbhA in the DeltahbhA

46 Semiquantitative RT-PCR analyses confirmed loss of or reduced transcription

47 Further reverse-transcription PCR analyses confirmed SBEM expression in most of establ

48 Northern blot and quantitative real-time PCR analyses confirmed that alphaA-crystallin expression

49 PCR analyses confirmed that HP0217 (encoding a lipopolys

50 Microarray and PCR analyses confirmed that the mutations were caused by

51 Quantitative RT-PCR analyses confirmed the decreased expression of diffe

52 Quantitative-PCR analyses confirmed the microarray data for 21 of 22

53 qRT-PCR analyses confirmed the predicted expression patterns

54 on, quantitative real-time PCR, and standard PCR analyses confirmed the presence of m(6)A-modified FA

55 Reverse transcription-PCR analyses confirmed the regulation of a group of apop

56 Western blotting and quantitative RT-PCR analyses confirmed these patterns of expression.

57 Initial cytogenetic and RT-PCR analyses correctly classified 95.7% and 96.1% of pat

58 Moreover, qRT-PCR analyses coupled with cycloheximide inhibition studi

59 Reverse transcription-PCR analyses, coupled with S1 nuclease protection assays

60 h reverse transcription-PCR and quantitative PCR analyses demonstrate that these variants have differ

61 hysical, pharmacological, and single-cell RT-PCR analyses demonstrate that this ability of OPCs estab

62 RNA sequencing and quantitative PCR analyses demonstrate the up-regulation of E2F1 targe

63 Northern blot and PCR analyses demonstrated a restricted expression of Alt

64 Pulsed-field gel electrophoresis and PCR analyses demonstrated genomic alterations and/or uni

65 Real-time RT-PCR analyses demonstrated higher levels of bdrF2 transcr

66 Initial RT - PCR analyses demonstrated marked discrepancies between l

67 Real time reverse transcription-PCR analyses demonstrated normal RNA transcript levels f

68 Overlapping PCR analyses demonstrated some similarity between the ia

69 Mass spectrometry and qRT-PCR analyses demonstrated that both capsid protein and g

70 Quantitative reverse transcriptase PCR analyses demonstrated that expression of feoB2 is in

71 Northern blot and qualitative PCR analyses demonstrated that IpFcRI is primarily expre

72 PCR analyses demonstrated that rats were orally colonize

73 Real-time PCR analyses demonstrated that significant accumulation

74 leotide microarray and reverse transcription-PCR analyses demonstrated that SPARC mRNA was expressed

75 Quantitative RT-PCR analyses demonstrated that the bm2 mutants accumulat

76 Additional PCR analyses demonstrated that the iap/ibp locus is loca

77 cDNA microarray and RT-PCR analyses demonstrated that transcription of the gene

78 Semiquantitative reverse transcription-PCR analyses demonstrated that transcripts for cytidine

79 All inoculated subjects died, and PCR analyses demonstrated the ability of the m2 and M fo

80 n blotting and reverse transcription-PCR (RT-PCR) analyses demonstrated that Mep72 was expressed only

81 n breast tissue, where reverse transcription-PCR analyses detected lytic Zta transcripts in 7 of 10 b

82 Laser capture microdissection coupled with PCR analyses detected the mutation only in cancerous but

83 Reverse transcriptase PCR analyses determined that tlyC and pld were transcrib

84 5'-rapid amplification of cDNA ends, and RT-PCR analyses disclosed an EP400/PHF1 fusion transcript i

85 s of this study using sensitive and specific PCR analyses do not support a role for C pneumoniae in t

86 by RLM-5'RACE PCR and reverse transcriptase PCR analyses during expression.

87 Transcriptional profiling and RT-PCR analyses during these phases enabled us to determine

88 We used two Polymerase Chain Reaction (PCR) analyses: Enterobacterial Repetitive Intergenic Con

89 as detected by immunohistochemistry, and DNA PCR analyses estimated an EBV copy number of 300 to 600

90 -specific quantitative reverse transcription-PCR analyses facilitated the assessment of target tissue

91 we performed real-time reverse transcriptase PCR analyses for a selection of the genes.

92 istological, Western blot (alpha-SMA), and q-PCR analyses for expressions of pro-inflammatory (IL-6,

93 n of toxin genes correlated with independent PCR analyses for the toxin genes.

94 Polymerase chain reaction (PCR) analyses for C pneumoniae were performed on the 180

95 RNA-1 (EBER1) and polymerase chain reaction (PCR) analyses for immunoglobulin (Ig) heavy chain and T-

96 Indirect end labeling and ligation-mediated PCR analyses further demonstrated that the occupation of

97 quantitative real-time reverse transcription-PCR analyses further revealed that NhaR affects the stea

98 DNA microarray and real-time PCR analyses identified a series of myofibroblast differ

99 RNA sequencing and quantitative RT-PCR analyses identified reduced transcript levels during

100 Sequence and PCR analyses identified the mutation responsible for the

101 and real-time reverse transcription-PCR (RT-PCR) analyses identified M. catarrhalis genes whose expr

102 mutagenesis, allelic exchange, quantitative PCR analyses, immunoblotting, and (13)C-heme uptake expe

103 yzed by immunodot blot, Western blot, and RT-PCR analyses in cells obtained directly from human corne

104 Northern blot and RT-PCR analyses indicate that all of these genes are expres

105 Immunoblot, isoenzyme, and RT-PCR analyses indicate that AtGLR1.1 regulates the accumu

106 Single-cell PCR analyses indicate that one neuron can express multip

107 Unpredictably, confirmatory RT-PCR analyses indicated cellular expression of a splice v

108 ray and real-time reverse transcriptase (RT) PCR analyses indicated several potential regulatory targ

109 Western blot and reverse transcription-PCR analyses indicated that BFT mutants lacking seven or

110 The microarray and qRT-PCR analyses indicated that ChillPeach is rich in putati

111 array and quantitative reverse transcription-PCR analyses indicated that during stationary-phase grow

112 Reverse transcriptase-PCR analyses indicated that PRDC transcripts are widely

113 Quantitative PCR analyses indicated that RetS and LadS regulate genes

114 Northern blot and RT-PCR analyses indicated that RU5 does not increase the st

115 croarray and real-time reverse transcriptase PCR analyses indicated that several genes previously sho

116 Furthermore, FISH and PCR analyses indicated that there is aneuploidy and incr

117 Northern blot and RT-PCR analyses indicated the existence of Pitx2a and Pitx2

118 In silico as well as Northern blot and RT-PCR analyses indicated these genes were expressed in a v

119 A sequence and reverse transcription-PCR (RT-PCR) analyses now reveal the presence of an iron-repress

120 PCR analyses of 28 isolates of B. hermsii and 8 isolates

121 c expression, as assessed by quantitative RT-PCR analyses of a large panel of tissues, and conservati

122 Western blot and real-time PCR analyses of a select group of genes further confirm

123 using whole-genome microarray and real-time PCR analyses of abhd11 and wild-type plants, we noted th

124 Quantitative PCR analyses of abundance of genetic markers in size-fra

125 RT-PCR analyses of activated CD4(+) T cells and live images

126 In situ hybridization and RT-PCR analyses of affected mutant embryos at E7.5 revealed

127 was carried out using quantitative real time PCR analyses of all known genes involved in the biosynth

128 RT-PCR analyses of amelogenin mRNA between control and Mmp2

129 V chimeric virus inoculation as monitored by PCR analyses of and attempted virus isolations from plas

130 These studies, and initial RT-PCR analyses of brain CB1 and CB2 mRNAs, also support th

131 length successfully measured using real-time PCR analyses of DNA extracted from peripheral blood mono

132 Based on quantitative PCR analyses of DNA, unlike other ETS fusions described

133 we used microarray and reverse transcription-PCR analyses of E2-treated U2OS-ERalpha or -ERbeta cells

134 ne expression were confirmed by quantitative PCR analyses of each of these six genes.

135 e identified by in situ hybridization and by PCR analyses of epithelial cells immunoaffinity purified

136 RT-PCR analyses of gene expression in the peptide-treated l

137 , we have conducted microarray and real-time PCR analyses of gene expression to determine the global

138 Therefore, immunohistochemical and RT-PCR analyses of human gingival explants (HGX) and human

139 we conducted microarray and RT-quantitative PCR analyses of immortalized human podocytes and identif

140 RT-PCR analyses of iPS and ES cell-derived cardiomyocytes d

141 Real-time PCR analyses of islet RNA derived from MCH-KO revealed a

142 Microarray and quantitative PCR analyses of isolated human islets incubated with int

143 Real-time quantitative PCR analyses of Jurkat cell infections revealed that amp

144 ormal C57BL/6 corneas were harvested for qRT-PCR analyses of Langerin expression in the epithelium ve

145 RT-PCR analyses of mRNA for enzyme genes Gss and Ggt in GC-

146 RT-PCR analyses of mRNA levels from wild-type and Bsg(-/-)

147 Reverse transcriptase-PCR analyses of mRNA levels supported the Northern blot

148 Quantitative PCR analyses of mRNA obtained from differentiating eryth

149 Real-time PCR analyses of multiple chemical allergens, irritants,

150 es of subcellular fractions as well as by RT-PCR analyses of neutrophil precursors from human bone ma

151 PCR analyses of oral microbial samples demonstrated that

152 measured by luciferase assays and real-time PCR analyses of p63 target genes.

153 PCR analyses of plasma viral RNA indicated an env gene s

154 Reverse transcriptase PCR analyses of RNA prepared from Kaposi's sarcoma-assoc

155 RT-PCR analyses of RNA purified from E2f2 mutant follicle c

156 Further RT-PCR analyses of selected genes support the microarray re

157 Chromatin immunoprecipitation PCR analyses of several regions of vector genomes reveal

158 , we report extensive real-time quantitative PCR analyses of SIX3 and SIX6 expression in many differe

159 In addition, quantitative RT-PCR analyses of ST7 mRNA expression levels in 11/13 norm

160 Microarray and real-time PCR analyses of the laser-captured hair matrix cells sho

161 PCR analyses of the rats with polymicrobial infections d

162 RT-PCR analyses of the top-27 candidate genes confirmed 5 g

163 Subsequent quantitative PCR analyses of these splenic B cells revealed that C/EB

164 Combined culture and PCR analyses of tick- and syringe-infected animals indic

165 Quantitative competitive RT-PCR analyses of type I collagen mRNA, normalized to beta

166 extraction, preamplification, and real-time PCR analyses of viral DNA (vDNA) and viral RNA (vRNA) in

167 transcriptase-polymerase chain reaction (RT-PCR) analyses of each tumor group revealed 3- to 6-fold

168 ime, quantitative polymerase chain reaction (PCR) analyses of globin messenger RNA (mRNA) levels in a

169 transcriptase-polymerase chain reaction (RT-PCR) analyses of renal cytokines and adhesion molecules

170 with real-time reverse transcriptase PCR (RT-PCR) analyses of single-neuron mRNA expression in the mo

171 transcriptase/polymerase chain reaction (RT/PCR) analyses of the mRNA from various human tissues rev

172 Quantitative reverse transcription-PCR (qRT-PCR) analyses of the sigE mutant showed lower levels of

173 Chromatin immunoprecipitation (ChIP)-PCR analyses on the chromatin of the OsMADS6 gene find t

174 Real-time RT-PCR analyses, performed to assess the expression of thes

175 n small RNA deep sequencing and quantitative PCR analyses, pilRNA expression is dynamic and displays

176 ress HBB mRNA based on reverse transcription-PCR analyses, prophylactic vaccination of BALB/c mice wi

177 sion with microarray and semiquantitative RT-PCR analyses proved to be a versatile strategy for ident

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

179 re measured by Western blot and quantitative PCR analyses, respectively, and in a subset of the parti

180 quantitative real-time reverse transcription PCR analyses, respectively.

181 Microarray and quantitative PCR analyses reveal an up-regulation of several regenera

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

183 -dependent reporter expression and real-time PCR analyses reveal that human and mouse thyrocytes and

184 Northern blot and RT-PCR analyses reveal that mouse calcyon transcripts are m

185 Real-time PCR analyses revealed a significant reduction in the lev

186 In addition, cecal quantitative PCR analyses revealed a significant suppression in the e

187 F-3-specific probe and reverse transcription-PCR analyses revealed a single transcript of 2.2 kb with

188 Northern blot and real time PCR analyses revealed an elevated VEGF transcript level

189 Quantitative RT-PCR analyses revealed an inverse correlation between hTE

190 Reverse transcription-PCR analyses revealed coordinate regulation of EHEC U-es

191 Histological and real-time RT-PCR analyses revealed differences in the nature of immun

192 Southern blot and PCR analyses revealed disruption of the homologous gene

193 Microarray and quantitative real-time PCR analyses revealed five downregulated genes in ilr3-1

194 RNA-Seq and quantitative RT-PCR analyses revealed increased expression of genes asso

195 Microarray and reverse transcriptase-PCR analyses revealed reduced expression of two retinoid

196 mistry, Western blotting and quantitative RT-PCR analyses revealed that adjudin exerted its otoprotec

197 RT-PCR analyses revealed that all 16 novel exons are expres

198 Microarray and quantitative RT-PCR analyses revealed that all classes of floral homeoti

199 Microarray and RT-PCR analyses revealed that basal levels of several auxin

200 Here, quantitative real-time PCR analyses revealed that brains from TBI rats displaye

201 Real-time PCR analyses revealed that endogenous levels of Hairy Re

202 Reverse transcriptase-PCR analyses revealed that exon II, containing the first

203 Quantitative real-time PCR analyses revealed that expression of dnaA, an essent

204 Microarray and reverse transcription-PCR analyses revealed that gene regulatory processes ind

205 qRT-PCR analyses revealed that GPC1 mRNA abundance is regula

206 Additionally, microarray and quantitative PCR analyses revealed that key genes of fatty acid oxida

207 situ hybridization and reverse transcription-PCR analyses revealed that Notch1 was expressed in prost

208 qRT-PCR analyses revealed that PnSERK2 was expressed at sign

209 note, our single-cell reverse transcription-PCR analyses revealed that Sirt1 mRNA is expressed in pr

210 Reverse transcription-PCR analyses revealed that the cells supported a mixture

211 Quantitative real-time RT-PCR analyses revealed that these three genes were prefer

212 Western blot and RT-PCR analyses revealed that this increase in activity in

213 Quantitative real-time RT-PCR analyses revealed that three of these sequences were

214 oblot and quantitative reverse transcription-PCR analyses revealed that unlike many well-characterize

215 RNA sequencing and quantitative real-time PCR analyses revealed that, although the expression of k

216 qRT-PCR analyses revealed the expression profiles of the neu

217 Microarray and real-time PCR analyses revealed the induction of STAT1-dependent p

218 Molecular and real-time PCR analyses revealed the presence of multiple, truncate

219 Quantitative PCR analyses revealed the upregulation of many chemokine

220 RT-PCR analyses revealed Twist-1 expression in several adul

221 ive real-time reverse-transcriptase-PCR (qRT-PCR) analyses revealed decreased expression of a number

222 Quantitative reverse transcription-PCR (qRT-PCR) analyses revealed that both drugs altered E1A RNA s

223 thern blot and reverse transcriptase PCR (RT-PCR) analyses revealed that electrogenic NBCe1B or NBCe1

224 Reverse transcription-PCR (RT-PCR) analyses revealed that these genes are cotranscribe

225 ong with gene microarray and RT-quantitative PCR analyses, revealed that UNC45A localizes to the canc

226 For RT-PCR analyses, samples from 15 subjects with diabetes wer

227 Additional PCR analyses, sequencing studies and pulsed field gel el

228 Q-PCR analyses show significantly lower expression levels

229 Single-cell PCR analyses show that both alpha- and beta-cells have N

230 Quantitative reverse transcriptase PCR analyses show that hut locus transcription is subjec

231 Reverse transcriptase PCR analyses show that hutA and tonB are divergently tra

232 RNA-seq and qRT-PCR analyses show that Mr-OPY2 is a negative regulator o

233 implantation, and real-time quantitative RT-PCR analyses show that the expression of endothelial cel

234 Results of single-male D. melanogaster PCR analyses show that the two gene size variants are al

235 Quantitative real-time reverse transcription PCR analyses show that these mRNAs are chiefly produced

236 Similarity sequence searches and PCR analyses show that this retrotransposon with LTRs (L

237 qRT-PCR analyses showed a down-regulation of neurotrophic fa

238 Southern blot and PCR analyses showed a lack of integration, irrespective

239 Quantitative PCR analyses showed an increase in Hcrtr2 mRNA levels in

240 h this, gene array and reverse transcription-PCR analyses showed down-regulation of genes encoding ke

241 Northern blot and RT-PCR analyses showed Grx1(as) mRNA was expressed in norma

242 Real-time PCR analyses showed increased PPAR mRNA and retinoid X r

243 Quantitative RT-PCR analyses showed no change in PD-L1 transcript levels

244 Quantitative real-time PCR analyses showed significantly reduced dsbD expressio

245 Northern blot and RT-PCR analyses showed that a transcript of approximately 1

246 hern hybridization and reverse transcription-PCR analyses showed that arsA, arsD, arsR, arsM, arsC, a

247 In seedlings, RT-PCR analyses showed that AtDi19-1 and AtDi19-3 steady-st

248 RT-PCR analyses showed that both poly I:C and interferon co

249 Real-time PCR analyses showed that IFN-gamma suppressed gene expre

250 Real-time PCR analyses showed that in Gpr48-/- mice both adult hem

251 Reverse transcription-PCR analyses showed that mouse GPRC6A is widely expresse

252 Real-time RT-PCR analyses showed that Myc did not alter the VEGF mRNA

253 Quantitative and semiquantitative PCR analyses showed that overexpression as well as downr

254 array and quantitative reverse transcription-PCR analyses showed that TGFbeta up-regulated a host of

255 Despite these findings, quantitative RT-PCR analyses showed that the activation of the expressio

256 Quantitative PCR analyses showed that the expression level of PtACO1-

257 Real-time quantitative PCR analyses showed that the expression of bioBFDA and b

258 Whole-genome DNA microarray and quantitative PCR analyses showed that the expression of NSR is up-reg

259 roarray and quantified reverse transcription-PCR analyses showed that the expression of the Fos famil

260 ative and quantitative reverse transcription-PCR analyses showed that the promoter impairment abolish

261 Real time quantitative PCR analyses showed that unlike in liver and heart, in m

262 DNA microarray and RT-PCR analyses significantly increased CHI3L1 expression i

263 Targeted integration was verified by PCR analyses, Southern blot, and germ-line transmission.

264 EMSA, ChIP assay and real-time PCR analyses suggest CaWRKY40 binds at the promoters and

265 Results from RT-PCR analyses suggest that differential integrin sialylat

266 Quantitative PCR analyses suggest that the longer qm188 deletion may

267 RT-PCR analyses suggested little impact of caffeine on SRSF

268 Northern blot and real-time PCR analyses suggested that induction of gbpB expression

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

270 Overlapping PCR analyses suggested that the toxin-encoding plasmids

271 Quantitative real-time PCR analyses supported the results of M2H experiments.

272 transcribed, and reverse transcription (RT)-PCR analyses targeting primary transcripts from chlamydi

273 Here, we show by microarray and real-time PCR analyses that LRBA is overexpressed in several diffe

274 via immunostaining, Western blotting, and RT-PCR analyses, that TrkC, the receptor for neurotrophin-3

275 By microarray and real-time PCR analyses, the allergen 1 gene (ALL1) was found to be

276 In reverse transcription-PCR analyses, the expression of the pic and tsh genes in

277 Real-time PCR analyses to evaluate D(2) and D(4) dopamine receptor

278 array and confirmatory reverse transcription-PCR analyses to identify BRCA1-regulated gene expression

279 We performed microarray and real-time PCR analyses to identify genes involved in invasion that

280 transcription polymerase chain reaction (qRT-PCR) analyses to examine changes in gene expression patt

281 th histologic and polymerase-chain-reaction (PCR) analyses, to determine the physiological and genomi

282 RT-PCR analyses using gene-specific primers allowed us to m

283 Using quantitative RT-PCR analyses (validation set), the key components haptog

284 Histology, immunohistochemistry, and RT-PCR analyses verified the upregulation of CCR5 in the pr

285 based on chemical (LC-ESI-MS) and molecular (PCR) analyses was conducted.

286 ing both population-based and single-cell RT-PCR analyses, we found large subsets of MHC class II (MH

287 croarray and real-time reverse transcriptase PCR analyses, we found that SaeRS regulates the expressi

288 Significantly, using microarray and RT-PCR analyses, we have identified up-regulated genes such

289 and negative predictive values of multiplex PCR analyses were 87, 96, 94, and 93%, respectively.

290 resistant cell lines, real-time quantitative PCR analyses were employed and two phenotypic groups wer

291 PCR analyses were performed on 553 consecutive biopsy sa

292 Real-time PCR analyses were performed to quantify the levels of pe

293 y, Western Blotting, Zymogram, and Real-time PCR analyses were performed.

294 Southern blot and PCR analyses were used to confirm the presence of the de

295 ential display RT-PCR, Northern blot, and RT-PCR analyses were used to determine the transcript level

296 Semiquantitative reverse transcription-PCR analyses were used to determine whether transcripts

297 rn immunoblotting, and reverse transcription-PCR analyses were used to investigate LHRH receptors in

298 ot and degenerate-polymerase chain reaction (PCR) analyses were undertaken to better understand the d

299 Correlation of real-time RT-PCR analyses with disease-free survival in this patient

300 Combining quantitative PCR analyses with immunofluorescence studies revealed ex