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1 ors (ELISA) and virus quantity (quantitative reverse-transcriptase polymerase chain reaction).
2 , and gene profiling (quantitative real-time reverse-transcriptase polymerase chain reaction).
3 ndidate miRNAs were verified by quantitative reverse transcriptase polymerase chain reaction.
4 muscle and myoblast cultures was analyzed by reverse transcriptase polymerase chain reaction.
5 espiratory illnesses and tested by real-time reverse transcriptase polymerase chain reaction.
6 re selected for verification by quantitative reverse transcriptase polymerase chain reaction.
7 ray hybridization and quantitative real-time reverse transcriptase polymerase chain reaction.
8 oxyribonucleic acid microarray and real-time reverse transcriptase polymerase chain reaction.
9 sing Western blot, immunohistochemistry, and reverse transcriptase polymerase chain reaction.
10 s was assayed by microarray and quantitative reverse transcriptase polymerase chain reaction.
11 C1 gene expression by real-time quantitative reverse transcriptase polymerase chain reaction.
12 evaluated for ERG expression by quantitative reverse transcriptase polymerase chain reaction.
13 AMBA internalization assays and quantitative reverse transcriptase polymerase chain reaction.
14 ed for FXN transcript levels by quantitative reverse transcriptase polymerase chain reaction.
15 ure microdissection followed by quantitative reverse transcriptase polymerase chain reaction.
16 2); and villin were measured by quantitative reverse transcriptase-polymerase chain reaction.
17 ssion of iNOS was quantified by quantitative reverse transcriptase-polymerase chain reaction.
18 tilage explants was assessed by quantitative reverse transcriptase-polymerase chain reaction.
19 se and throat samples for influenza virus by reverse transcriptase-polymerase chain reaction.
20 isoforms in mouse retina was established by reverse transcriptase-polymerase chain reaction.
21 endogenous LH2(long) mRNA was determined by reverse transcriptase-polymerase chain reaction.
22 of chemokines was confirmed by quantitative reverse transcriptase-polymerase chain reaction.
23 d by using laser capture microdissection and reverse transcriptase-polymerase chain reaction.
24 rphometry, nanoindentation, and quantitative reverse transcriptase-polymerase chain reaction.
25 ctin, and collagen 1 expression by real-time reverse transcriptase-polymerase chain reaction.
26 tissues, and IGF-II mRNA was measured using reverse transcriptase-polymerase chain reaction.
27 ssion was measured by quantitative real-time reverse transcriptase-polymerase chain reaction.
28 on was measured using quantitative real-time reverse transcriptase-polymerase chain reaction.
29 microarray data with quantitative real-time reverse transcriptase-polymerase chain reaction.
30 imary chondrocyte monolayers was assessed by reverse transcriptase-polymerase chain reaction.
31 sured by histology, Western blot, ELISA, and reverse transcriptase-polymerase chain reaction.
32 0A messenger RNA expression was confirmed by reverse transcriptase-polymerase chain reaction.
33 22 countries and screened for MERS-CoV using reverse transcriptase-polymerase chain reaction.
34 idate gene in ocular tissues was analyzed by reverse transcriptase-polymerase chain reaction.
35 MMP7, and MMP28 was assessed by quantitative reverse-transcriptase polymerase chain reaction.
36 itu hybridization and quantitative real-time reverse-transcriptase polymerase chain reaction.
37 fficile was also compared using quantitative reverse-transcriptase polymerase chain reaction.
38 ere tested for influenza, RSV, and HMPV with reverse-transcriptase polymerase chain reaction.
39 and dermal fibroblasts were tested by using reverse-transcriptase polymerase chain reaction.
40 l RNA was attempted on a subset of 20 DBS by reverse-transcriptase polymerase chain reaction.
41 and the data were confirmed by quantitative reverse-transcriptase polymerase chain reaction.
42 elative to levels of GAPDH mRNA by real-time reverse-transcriptase polymerase chain reaction.
43 tochemisty, flow cytometry, and quantitative reverse-transcriptase polymerase chain reaction.
44 nrolled asymptomatic controls with real-time reverse-transcriptase polymerase chain reaction.
45 ML adults younger than 60 years by real-time reverse-transcriptase polymerase chain reaction.
46 RSV was detected by culture and reverse-transcriptase polymerase chain reaction.
47 uction cascades in the liver by quantitative reverse-transcriptase polymerase chain reaction.
48 luenza infection was confirmed by culture or reverse-transcriptase polymerase chain reaction.
49 bead separation followed by strand-specific reverse-transcriptase polymerase chain reaction.
50 pressions were studied by flow cytometry and reverse-transcriptase polymerase chain reaction.
51 by chromatin immunoprecipitation followed by reverse-transcriptase polymerase chain reaction.
52 nd ICC (n = 80) using real-time quantitative reverse-transcriptase polymerase chain reaction.
53 ere analyzed by ELISA, Western blotting, and reverse-transcriptase polymerase chain reaction.
54 tested for A/California/7/2009(H1N1), using reverse-transcriptase polymerase chain reaction.
55 opontin expression were detected by means of reverse-transcriptase polymerase chain reaction.
56 were positive for a respiratory pathogen by reverse-transcriptase polymerase chain reaction.
57 lected and tested for influenza by real-time reverse-transcriptase polymerase chain reaction.
58 es was measured using quantitative real-time reverse transcriptase polymerase chain reaction (2) in d
59 s evaluated using the quantitative real-time reverse-transcriptase polymerase chain reaction (2(-Delt
60 Gene expression was assessed by real-time reverse-transcriptase polymerase chain reaction after 6-
61 Histologic, immunohistochemical, and reverse transcriptase-polymerase chain reaction analyses
62 roteins, and verified the microarray data by reverse transcriptase-polymerase chain reaction analyses
63 histochemistry, immunoblot, and quantitative reverse-transcriptase polymerase chain reaction analyses
64 Reverse transcriptase-polymerase chain reaction analysis
65 Reverse-transcriptase polymerase chain reaction analysis
66 ine VEGF-A gene and protein expression using reverse transcriptase polymerase chain reaction and ELIS
67 angiogenic genes on microarray and real-time reverse transcriptase polymerase chain reaction and gene
69 Ingenuity) were confirmed using quantitative reverse transcriptase polymerase chain reaction and immu
70 ignaling and was confirmed with quantitative reverse transcriptase polymerase chain reaction and immu
71 stochemistry, western blotting, quantitative reverse transcriptase polymerase chain reaction and term
72 letion strain was constructed, and real-time reverse transcriptase polymerase chain reaction and West
73 human CD45 antigen by quantitative real-time reverse transcriptase-polymerase chain reaction and flow
74 sion patterns were validated by quantitative reverse transcriptase-polymerase chain reaction and immu
79 lopmental stages as measured by quantitative reverse transcriptase-polymerase chain reaction and in s
81 RNA and protein expression were analyzed by reverse transcriptase-polymerase chain reaction and West
83 ession on CDH1 transcription was analyzed by reverse transcriptase-polymerase chain reaction and West
84 itical expression patterns were validated by reverse transcriptase-polymerase chain reaction and West
85 the expression of CD39 and CD73 by means of reverse-transcriptase polymerase chain reaction and flow
87 expression of the 5-HT(4)R was evaluated by reverse-transcriptase polymerase chain reaction and immu
89 proliferation were analyzed by quantitative reverse-transcriptase polymerase chain reaction and immu
90 level was assessed in tumors by quantitative reverse-transcriptase polymerase chain reaction and immu
92 infiltration of leukocytes, and quantitative reverse-transcriptase polymerase chain reaction and inte
93 on levels were quantified using quantitative reverse-transcriptase polymerase chain reaction and prom
94 and homing of GAS were followed by real-time reverse-transcriptase polymerase chain reaction and quan
96 winters were tested for RSV and influenza by reverse-transcriptase polymerase chain reaction and sero
97 and relapse-free survival using quantitative reverse-transcriptase polymerase chain reaction and spec
98 re investigated using real-time quantitative reverse-transcriptase polymerase chain reaction and vali
100 all of the samples evaluated by quantitative reverse-transcriptase polymerase chain reaction and West
101 l fluid were tested for ZIKV using real-time reverse-transcriptase-polymerase chain reaction and an I
103 ion levels of the receptor were evaluated by reverse transcriptase polymerase chain reaction, and inf
104 enty-one genes were assessed by quantitative reverse transcriptase polymerase chain reaction, and the
105 performed immunocytochemistry, quantitative reverse transcriptase polymerase chain reaction, and Wes
106 et SFRP1 was also quantified by quantitative reverse transcriptase-polymerase chain reaction, and DNA
107 er capture microdissection-coupled real-time reverse transcriptase-polymerase chain reaction, and imm
108 t-1 mRNA levels, as measured by quantitative reverse transcriptase-polymerase chain reaction, and lev
109 RNA (mRNA) levels were analyzed by real-time reverse transcriptase-polymerase chain reaction, and pro
110 (mRNA) levels were monitored by quantitative reverse transcriptase-polymerase chain reaction, and sol
111 antibody specificity by immunoprecipitation, reverse transcriptase-polymerase chain reaction, and Sou
113 VEGF signaling (n=20 per group) using ELISA, reverse transcriptase-polymerase chain reaction, and Wes
114 orphologic, immunofluorescence, quantitative reverse-transcriptase polymerase chain reaction, and imm
115 ith Affymetrix Rat Expression Array 230 2.0, reverse-transcriptase polymerase chain reaction, and imm
116 iation process and used differential display reverse transcriptase polymerase chain reaction as a fir
118 vity of BCR-ABL transcript in a quantitative reverse transcriptase polymerase chain reaction assay co
119 mbedded breast cancer tumors, a quantitative reverse transcriptase polymerase chain reaction assay wa
120 90 elite controllers with use of a real time reverse-transcriptase polymerase chain reaction assay wi
121 cal records, HMPV was detected by means of a reverse-transcriptase polymerase-chain-reaction assay, a
122 7N9 virus was verified by means of real-time reverse-transcriptase-polymerase-chain-reaction assay (R
123 ns were confirmed by means of a quantitative reverse-transcriptase-polymerase-chain-reaction assay an
125 ncer from 111 patients, using a quantitative reverse-transcriptase-polymerase-chain-reaction assay, a
126 noglobulin heavy-chain gene rearrangement by reverse-transcriptase-polymerase-chain-reaction assay, w
127 2009 H1N1 virus with the use of a real-time reverse-transcriptase-polymerase-chain-reaction assay.
128 with AMI and 198 controls using quantitative reverse transcriptase polymerase chain reaction assays a
129 d-type littermates by real-time quantitative reverse-transcriptase polymerase chain reaction assays.
130 ssed and monitored in plasma using real-time reverse-transcriptase polymerase chain reaction assays.
131 validate our findings, we used quantitative reverse-transcriptase-polymerase-chain-reaction assays t
133 structural protein 1 antigen immunoassay and reverse-transcriptase-polymerase-chain-reaction assays.
134 tested blood and urine specimens for ZIKV by reverse-transcriptase-polymerase-chain-reaction assays.
135 g quantified the percentage of fibrosis, and reverse transcriptase polymerase chain reaction assessed
136 n arm) were analyzed by using a quantitative reverse transcriptase polymerase chain reaction-based as
138 fin-embedded tumor samples with quantitative reverse transcriptase polymerase chain reaction by using
139 patients with CUP were tested with a 92-gene reverse transcriptase polymerase chain reaction cancer c
140 ted and analyzed by immunohistochemistry and reverse transcriptase polymerase chain reaction; cells w
141 oforms of KLF4 in pancreatic cancer cells by reverse-transcriptase polymerase chain reaction, cloning
142 Reverse transcriptase polymerase chain reaction confirme
143 ybridization showed PRKCA rearrangement, and reverse transcriptase-polymerase chain reaction confirme
144 Measurements: The primary outcome was reverse transcriptase polymerase chain reaction-confirme
145 developed using microarray and quantitative reverse transcriptase polymerase chain reaction data fro
146 Real-time reverse transcriptase-polymerase chain reaction demonstr
147 filing followed by confirmatory quantitative reverse transcriptase-polymerase chain reaction demonstr
149 rflow obstruction, and patients with COPD by reverse transcriptase-polymerase chain reaction, ELISA,
150 D and in lungs of air- or CS-exposed mice by reverse-transcriptase polymerase chain reaction, ELISA,
151 TF induction was documented by quantitative reverse transcriptase-polymerase chain reaction, enzyme-
152 e monitored at the gene and protein level by reverse transcriptase-polymerase chain reaction, enzyme-
153 assessed allograft rejection, and real-time reverse-transcriptase polymerase chain reaction evaluate
154 ease in miR-126 expression in a quantitative reverse transcriptase polymerase chain reaction experime
155 ell cultures, followed by ELISA/quantitative reverse transcriptase-polymerase chain reaction/flow cyt
156 l gene expression analysis with quantitative reverse transcriptase polymerase chain reaction followed
157 Complementation studies and reverse transcriptase-polymerase chain reaction followed
158 reverse transcription, primer extension and reverse transcriptase-polymerase chain reaction, followi
159 essed >/= median HER2 levels by quantitative reverse transcriptase polymerase chain reaction for HER2
160 luenza-like illness were tested by real-time reverse transcriptase polymerase chain reaction for RSV.
162 hemical analyses, and real-time quantitative reverse-transcriptase polymerase chain reaction gene exp
163 It analyzed plasma A(H1N1) 2009 reverse-transcriptase polymerase chain reaction, hemaggl
164 Reverse transcriptase-polymerase chain reaction identifi
165 Oligonucleotide microarray and real-time reverse-transcriptase polymerase chain reaction identifi
166 Multiplex reverse-transcriptase polymerase chain reaction identifi
167 Quantitative reverse transcriptase-polymerase chain reaction, immunob
168 ducts in the coronary microvasculature using reverse transcriptase-polymerase chain reaction, immunob
169 two experimental COPD models by quantitative reverse transcriptase-polymerase chain reaction, immunob
170 n-1 expression was evaluated by quantitative reverse-transcriptase polymerase chain reaction, immunob
171 to 24 hours later and analyzed by real-time reverse-transcriptase polymerase chain reaction, immunob
172 e analyzed by BrdU labeling, flow cytometry, reverse transcriptase-polymerase chain reaction, immunoc
173 aine-treated mice were used for quantitative reverse-transcriptase polymerase chain reaction, immunoc
174 or (GDNF) were determined using quantitative reverse transcriptase polymerase chain reaction, immunoh
175 e-linked immunosorbent assay, Northern blot, reverse transcriptase-polymerase chain reaction, immunoh
176 F versus control subjects using quantitative reverse transcriptase-polymerase chain reaction, immunoh
177 R4 mRNA levels were measured by quantitative reverse transcriptase polymerase chain reaction in 915 p
178 sensitive genes was explored by quantitative reverse transcriptase polymerase chain reaction in rat p
179 e international scale (IS) and determined by reverse transcriptase polymerase chain reaction in two c
180 Results were validated by using quantitative reverse transcriptase-polymerase chain reaction in 350 s
181 ainings and quantified by ELISA/quantitative reverse transcriptase-polymerase chain reaction in patie
182 Gene expression changes were determined by reverse transcriptase-polymerase chain reaction in rat l
183 Gene expression changes were validated by reverse transcriptase-polymerase chain reaction in whole
184 of 48 genes by high-throughput quantitative reverse-transcriptase polymerase chain reaction in 1846
185 ability that a virus detected with real-time reverse-transcriptase polymerase chain reaction in patie
186 oral expression patterns of SynCAMs by using reverse transcriptase-polymerase chain reaction, in situ
187 ce were similar, as assessed by quantitative reverse transcriptase-polymerase chain reaction, indicat
188 and the locus-specific level by quantitative reverse transcriptase polymerase chain reaction of 5-hmC
191 was detected in cerebrospinal fluid (CSF) by reverse-transcriptase polymerase chain reaction of 16S r
192 ion was determined by quantitative real time reverse transcriptase-polymerase chain reaction on day 3
193 estern Blot analyses as well as quantitative reverse-transcriptase polymerase chain reaction on a hum
195 ined expression of IGF-1 mRNA and protein by reverse transcriptase-polymerase chain reaction or enzym
196 and chemokines were assayed by quantitative reverse-transcriptase polymerase chain reaction or by a
197 DAH]) were analyzed by immunohistochemistry, reverse-transcriptase polymerase chain reaction, or west
200 14) were evaluated by quantitative real-time reverse-transcriptase polymerase chain reaction (qPCR) f
203 se 10 specimens was verified by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR
205 ts receptors was analyzed using quantitative reverse transcriptase polymerase chain reaction (qRT-PCR
206 ationship between the real-time quantitative reverse transcriptase polymerase chain reaction (qRT-PCR
208 tion of a multimarker quantitative real-time reverse transcriptase-polymerase chain reaction (qRT) as
209 confirmed the results by use of quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR
210 , using dual-immunofluorescence, single-cell reverse transcriptase polymerase chain reaction, quantit
211 ditioned place preference (CPP) by real-time reverse transcriptase polymerase chain reaction (real-ti
212 t is, providing results in <30 minutes) with reverse transcriptase polymerase chain reaction referenc
213 ng immunofluorescence, Western blotting, and reverse transcriptase-polymerase chain reaction, respect
214 Quantitative reverse transcriptase polymerase chain reaction revealed
215 Real-time reverse transcriptase-polymerase chain reaction revealed
216 ker by immunohistochemistry and quantitative reverse transcriptase-polymerase chain reaction revealed
217 h is more rapid and direct than conventional reverse transcriptase polymerase chain reaction (RT-PCR)
218 systems level, and assessed using real-time reverse transcriptase polymerase chain reaction (RT-PCR)
219 ained from patients diagnosed with ESFT, and reverse transcriptase polymerase chain reaction (RT-PCR)
220 n situ hybridization (FISH) and quantitative reverse transcriptase polymerase chain reaction (RT-PCR)
221 pring were screened for transgenic status by reverse transcriptase polymerase chain reaction (RT-PCR)
222 IHC) for cytokeratin (AE1/AE3) and real-time reverse transcriptase polymerase chain reaction (RT-PCR)
223 elopment and early posthatched life by using reverse transcriptase polymerase chain reaction (RT-PCR)
224 ethods-histology, a lipid-based assay, a new reverse transcriptase polymerase chain reaction (RT-PCR)
225 istochemistry underwent molecular staging by reverse transcriptase polymerase chain reaction (RT-PCR)
226 B-NFIB fusion transcripts were studied using reverse transcriptase polymerase chain reaction (RT-PCR)
228 ecules were tested individually by real-time reverse transcriptase-polymerase chain reaction (RT-PCR)
229 These results were validated by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR)
234 vitro wound healing assays, flow cytometry, reverse transcriptase-polymerase chain reaction (RT-PCR)
236 Further, miRNA microarray and real-time reverse transcriptase-polymerase chain reaction (RT-PCR)
237 escence-activated cell sorting and real-time reverse transcriptase-polymerase chain reaction (RT-PCR)
239 f epo and epor was evaluated by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR)
240 tion, 5-HT(2B) receptor mRNA was detected by reverse transcriptase-polymerase chain reaction (RT-PCR)
241 issue culture; this finding was supported by reverse transcriptase-polymerase chain reaction (RT-PCR)
242 ed immunosorbent assay (ELISA) and real-time reverse transcriptase-polymerase chain reaction (RT-PCR)
245 d tissue samples as assessed using real-time reverse-transcriptase polymerase chain reaction (RT-PCR)
246 et capture, concentration, and purification, reverse-transcriptase polymerase chain reaction (RT-PCR)
247 cell sorting (FACS), GFP visualization, and reverse-transcriptase polymerase chain reaction (RT-PCR)
248 ene expression analyses were performed using reverse-transcriptase polymerase chain reaction (RT-PCR)
249 sr39tk transgene expression by quantitative reverse-transcriptase polymerase chain reaction (RT-PCR)
251 stochemistry (IHC), central IHC, and central reverse-transcriptase polymerase chain reaction (RT-PCR)
252 h by in situ hybridization in embryos and by reverse-transcriptase polymerase chain reaction (RT-PCR)
255 e role of epithelium-derived mediators using reverse-transcriptase polymerase chain reaction (RT-PCR)
256 dual disease (MRD) positivity by qualitative reverse-transcriptase polymerase chain reaction (RT-PCR)
257 ompare the relative vaccine efficacy against reverse-transcriptase polymerase-chain-reaction (RT-PCR)
258 eline were tested by means of a quantitative reverse-transcriptase-polymerase-chain-reaction (RT-PCR)
259 ing 55 men) in whom ZIKV RNA was detected on reverse-transcriptase-polymerase-chain-reaction (RT-PCR)
262 ZIKV was found in the fetal brain tissue on reverse-transcriptase-polymerase-chain-reaction (RT-PCR)
263 f which 2485 (4%) were confirmed by means of reverse-transcriptase-polymerase-chain-reaction (RT-PCR)
264 say, and influenza was diagnosed by means of reverse-transcriptase-polymerase-chain-reaction (RT-PCR)
265 identified on the basis of reactivity in two reverse-transcriptase-polymerase-chain-reaction (RT-PCR)
267 rget genes were validated using quantitative reverse transcriptase-polymerase chain reaction, small i
268 in vitro autoradiography and by quantitative reverse transcriptase polymerase chain reaction (Spearma
270 Quantitative reverse transcriptase-polymerase chain reaction suggeste
271 he available transcriptomic data followed by reverse transcriptase-polymerase chain reaction suggeste
272 and sequencing of tissue transcripts, using reverse-transcriptase polymerase chain reaction techniqu
273 iptomic databases and showed by quantitative reverse-transcriptase polymerase chain reaction that one
276 used in situ hybridization and quantitative reverse transcriptase polymerase chain reaction to measu
277 immunohistochemistry, Western blotting, and reverse transcriptase-polymerase chain reaction to deter
278 (prespliced) insulin mRNA were quantified by reverse-transcriptase polymerase chain reaction using se
279 Reverse transcriptase polymerase chain reaction validate
280 Subsequent reverse-transcriptase polymerase chain reaction validate
284 rst, using laser capture microdissection and reverse transcriptase-polymerase chain reaction, we inve
285 n, laser-assisted microdissection and nested reverse transcriptase polymerase chain reaction were per
287 cence-activated cell sorting and single-cell reverse transcriptase polymerase chain reaction were use
288 mouse and rat retina were evaluated by using reverse transcriptase polymerase chain reaction, western
289 tase polymerase chain reaction, quantitative reverse transcriptase polymerase chain reaction, Western
290 We used quantitative reverse transcriptase polymerase chain reaction, Western
291 e and protein expression were measured using reverse transcriptase polymerase chain reaction, Western
292 Quantitative reverse transcriptase-polymerase chain reaction, Western
293 DDP and copper were measured by quantitative reverse transcriptase-polymerase chain reaction, Western
294 Reverse transcriptase-polymerase chain reaction, Western
295 ollicular and papillary thyroid carcinoma by reverse transcriptase-polymerase chain reaction, Western
296 lymerase chain reaction, gelatin zymography, reverse transcriptase-polymerase chain reaction, Western
297 d loss-of-function experiments, quantitative reverse transcriptase-polymerase chain reaction, Western
298 in-induced lung fibrosis (using quantitative reverse transcriptase-polymerase chain reaction, Western
299 Reverse-transcriptase polymerase chain reaction, Western
300 ll culture and assessed by luciferase assay, reverse-transcriptase polymerase chain reaction, Western
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