ライフサイエンスコーパス: PCR analyses

1 were compared by microarray and quantitative PCR analyses.

2 sgene was confirmed by Southern blotting and PCR analyses.

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

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

5 spermatogenic cells using semi-quantitative PCR analyses.

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

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

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

9 via quantitative reverse transcription (RT)-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 Northern and real-time reverse transcription-PCR analyses.

14 rn or semiquantitative reverse transcription-PCR analyses.

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

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

17 as determined by both restriction enzyme and PCR analyses.

18 ession was confirmed by northern blot and RT-PCR analyses.

19 tterns were confirmed by RNA dot blot and RT-PCR analyses.

20 A amplification and multiplexed quantitative PCR analyses.

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

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

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

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

25 transgene was confirmed by Southern blot and PCR analyses.

26 66 have been validated by RNA blot and/or RT-PCR analyses.

27 and quantitative polymerase chain reaction (PCR) analyses.

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

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

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

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

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

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

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

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

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 RT/PCR analyses detected dmax mRNA in multiple tissues of t

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

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

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

85 5'-rapid amplification of cDNA ends, and RT-PCR analyses disclosed an EP400/PHF1 fusion transcript i

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

87 -transcription polymerase chain reaction (RT-PCR) analyses documented efficient self-liberation of th

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

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

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

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

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

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

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

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

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

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

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

99 The RT-PCR analyses further demonstrated that up to 20% of the

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

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

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

103 Sequence and PCR analyses identified the mutation responsible for the

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

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

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

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

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

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

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

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

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

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

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

115 Quantitative PCR analyses indicated that RetS and LadS regulate genes

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

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

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

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

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

121 uld be infected with HHV-6, as determined by PCR analyses, intracellular monoclonal antibody staining

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

139 Reverse transcription-PCR analyses of fibroblasts, astrocytes, and neural prog

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

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

142 Quantitative PCR analyses of human erythroid cells should prove usefu

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

144 Northern blot and reverse transcription-PCR analyses of human mRNA samples demonstrate that RNR

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

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

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

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

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

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

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

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

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

154 Quantitative PCR analyses of mRNA obtained from differentiating eryth

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

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

157 PCR analyses of oral microbial samples demonstrated that

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

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

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

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

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

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

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

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

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

167 PCR analyses of the rats with polymicrobial infections d

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

169 Immunocytochemical and reverse transcription PCR analyses of these cells allowed determination of tra

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

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

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

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

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

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

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

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

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

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

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

181 otting and comparative reverse transcription-PCR analyses performed on borreliae cultivated in vitro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

200 Real time quantitative RT-PCR analyses revealed that a rapid upregulation of FGFR1

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

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

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

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

205 RT - PCR analyses revealed that both genes were highly expres

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

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

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

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

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

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

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

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

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

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

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

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

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

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

220 RT-PCR analyses revealed that vitronectin mRNA is expressed

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

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

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

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

225 Quantitative PCR analyses revealed the upregulation of many chemokine

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

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

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

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

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

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

232 Q-PCR analyses show significantly lower expression levels

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

258 Semiquantitative RT-PCR analyses showed that overexpression of Wnt-1 or Wnt-

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

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

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

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

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

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

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

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

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

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

269 Quantitative PCR analyses suggest that the longer qm188 deletion may

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

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

272 Overlapping PCR analyses suggested that the toxin-encoding plasmids

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

293 PCR analyses were performed on 553 consecutive biopsy sa

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