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1 1 and proteoglycan 4 (PRG4) was evaluated by real time polymerase chain reaction.
2 t are detectable in the Ce with quantitative real time polymerase chain reaction.
3 otting, immunohistochemistry, histology, and real-time polymerase chain reaction.
4 NAT(+) samples were confirmed by real-time polymerase chain reaction.
5 filing approach on the basis of quantitative real-time polymerase chain reaction.
6 IL-8, and CXCL5 were monitored by ELISA and real-time polymerase chain reaction.
7 transcription factors were quantified using real-time polymerase chain reaction.
8 dide accumulation, immunohistochemistry, and real-time polymerase chain reaction.
9 enger RNA (mRNA) expression was measured via real-time polymerase chain reaction.
10 were evaluated with immunocytochemistry and real-time polymerase chain reaction.
11 Omni5M, and results were validated by using real-time polymerase chain reaction.
12 a range of respiratory viruses by multiplex real-time polymerase chain reaction.
13 y, pRCC and mRCC by immunohistochemistry and real-time polymerase chain reaction.
14 ha, IL-1beta, and IL-6 were quantified using real-time polymerase chain reaction.
15 7A5) and glutamine transporter (SLC38A2), by real-time polymerase chain reaction.
16 in the condylar cartilage was quantified by real-time polymerase chain reaction.
17 ulating mitochondrial DNA were quantified by real-time polymerase chain reaction.
18 miRNA expression was determined by real-time polymerase chain reaction.
19 ingival plaque were analyzed by quantitative real-time polymerase chain reaction.
20 carcinogenesis of de novo UC by quantitative real-time polymerase chain reaction.
21 ene expression determined using quantitative real-time polymerase chain reaction.
22 cific Bacteroides spp. were quantified using real-time polymerase chain reaction.
23 hage phenotype markers was investigated with real-time polymerase chain reaction.
24 ed by locked nucleic acid-based quantitative real-time polymerase chain reaction.
25 e seen in mRNA expression using quantitative real-time polymerase chain reaction.
26 -related gene transcripts using quantitative real-time polymerase chain reaction.
27 tory viruses and Streptococcus pneumoniae by real-time polymerase chain reaction.
28 e expression in skin samples was assessed by real-time polymerase chain reaction.
29 ere analyzed for the presence of pCMV, using real-time polymerase chain reaction.
30 ynthase (iNOS) were analyzed by quantitative real-time polymerase chain reaction.
31 DH1A expression was measured by quantitative real-time polymerase chain reaction.
32 uenza virus and other respiratory viruses by real-time polymerase chain reaction.
33 unohistochemistry, immunofluorescence, and a real-time polymerase chain reaction.
34 RPC1 expression analysis was performed using real-time polymerase chain reaction.
35 h-throughput pyrosequencing and quantitative real-time polymerase chain reaction.
36 789 and rs3817655 CCL5 gene polymorphisms by real-time polymerase chain reaction.
37 expression was evaluated using quantitative real-time polymerase chain reaction.
38 id peptides and receptors was measured using real-time polymerase chain reaction.
39 length (RTL) was measured using quantitative real-time polymerase chain reaction.
40 human herpesviruses (HHVs) were measured by real-time polymerase chain reaction.
41 atients were investigated by immunoassay and real-time polymerase chain reaction.
42 12 months after the infusion by quantitative real-time polymerase chain reaction.
43 and decorin was determined with quantitative real-time polymerase chain reaction.
44 L) was measured with the use of quantitative real-time polymerase chain reaction.
45 fected) cell quantification and quantitative real-time polymerase chain reaction.
46 conducted using whole-genome microarrays and real-time polymerase chain reaction.
47 ned and quantified in plasma by quantitative real-time polymerase chain reaction.
48 r RNA levels were determined by quantitative real-time polymerase chain reaction.
49 Cs at different time points were measured by real-time polymerase chain reaction.
50 expression of PPAR-gamma and NF-kappaB using real-time polymerase chain reaction.
51 I, BsmI, ApaI, and TaqI) was performed using real-time polymerase chain reaction.
52 rLTL was determined by real-time polymerase chain reaction.
53 yi at 3 sites were genotyped for SNPs, using real-time polymerase chain reaction.
54 1) and hexokinase-2 measured by quantitative real-time polymerase chain reaction.
55 sion of CD4, CCR5, and CXCR4 was measured by real-time polymerase chain reaction.
56 ed by western blot, RNA-seq and quantitative real-time polymerase chain reaction.
57 croorganisms were obtained with quantitative real-time polymerase chain reaction.
58 on and tested for Bordetella pertussis using real-time polymerase chain reaction.
59 was independently confirmed by quantitative real-time-polymerase chain reaction.
60 retic mobility shift assays and quantitative real-time polymerase chain reactions.
61 vels and functional activity assessed by: 1) real-time polymerase chain reaction; 2) Western blotting
62 hybridization, and validated by quantitative real-time polymerase chain reaction, 71 rare de novo (n=
64 ed and mRNA transcripts were quantified with real-time polymerase chain reaction after preamplificati
65 sessed in 342 serum samples by use of TaqMan real-time polymerase chain reaction, along with TTV geno
66 ositive for EV-D68 and Epstein-Barr virus by real-time polymerase chain reaction, although the specim
67 . pallidum concentrations were determined by real-time polymerase chain reaction amplification of the
69 rformed immunohistochemical, immunoblot, and real-time polymerase chain reaction analyses of colorect
71 of-flight mass spectrometry and quantitative real-time polymerase chain reaction analyses to quantify
72 munoperoxidase staining for MMP9 and TG2 and real-time polymerase chain reaction analyses were carrie
73 and 3 and 6 months, clinical, microbiologic (real-time polymerase chain reaction analyses), cytokine
81 d1, and cd14 gene expression was detected by real-time polymerase chain reaction analysis of pancreat
82 ical effect of the tau variant by performing real-time polymerase chain reaction analysis of RNA extr
92 of 1 NPHV-positive horse using quantitative real-time polymerase chain reaction and fluorescent in s
95 and von Willebrand factor) were verified by real-time polymerase chain reaction and immunohistochemi
96 second, independent cohort and confirmed by real-time polymerase chain reaction and immunohistochemi
97 ed placental CSE expression as determined by real-time polymerase chain reaction and immunohistochemi
98 ion analysis was done with both quantitative real-time polymerase chain reaction and in situ RNA hybr
100 e amount of renal collagen was determined by real-time polymerase chain reaction and Masson staining.
101 uring autophagic progression demonstrated by real-time polymerase chain reaction and miRNA in situ hy
102 lyzed by quantitative single copy gene-based real-time polymerase chain reaction and multiserotype en
104 es related to the endocannabinoid system via real-time polymerase chain reaction and used the mitotic
105 s of 21 miRNAs were assessed by quantitative real-time polymerase chain reaction and were compared wi
106 miR-155 and miR-132, which were confirmed by real-time polymerase chain reaction and were significant
107 the arterial and lung level by quantitative real-time polymerase chain reaction and Western blot ana
108 regulations were confirmed by the subsequent real-time polymerase chain reaction and Western blot ana
110 nnel expression was analyzed by quantitative real-time polymerase chain reaction and Western blot.
111 effects on lipid metabolism were assessed by real-time polymerase chain reaction and Western blot.
112 sion analysis were performed by quantitative real-time polymerase chain reaction and Western blotting
114 27 and cell proliferation were determined by real-time polymerase chain reaction and WST-1 assay, res
115 who were recruited on the basis of positive real-time polymerase chain reaction and/or CHIK virus im
116 s at baseline and week 96 for mtDNA content (real-time polymerase chain reaction) and oxidative phosp
117 technology, (2) detection of the viruses by real-time polymerase chain reaction, and (3) presence of
118 fic MIR122 using Northern blot, quantitative real-time polymerase chain reaction, and 3' and 5' rapid
120 e analyzed by immunoblotting, mRNA levels by real-time polymerase chain reaction, and cytokine releas
121 emical, morphometric, vascular permeability, real-time polymerase chain reaction, and flow cytometry
122 alyzed by immunohistochemistry, quantitative real-time polymerase chain reaction, and flow cytometry.
123 ted and analyzed by histologic, quantitative real-time polymerase chain reaction, and immunoblot anal
124 , immunohistochemistry, luciferase activity, real-time polymerase chain reaction, and multiplex assay
125 combination of DNA microarray, quantitative real-time polymerase chain reaction, and quantitative nu
126 immunostaining, flow cytometry, quantitative real-time polymerase chain reaction, and reciprocal bone
127 alyzed in immunohistochemical, morphometric, real-time polymerase chain reaction, and western blot as
128 alyzed by immunohistochemistry, quantitative real-time polymerase chain reaction, and zymography.
129 imide assay; gene expression was examined by real-time polymerase chain reaction; and data from The C
131 RNA (mRNA) by retrotranscription followed by real-time polymerase chain reaction as a diagnostic test
132 tudy aimed to assess the use of quantitative real-time polymerase chain reaction as an alternative to
133 measure cytokine expression by quantitative real-time polymerase chain reaction as well as tear coll
134 quantitative molecular tool using a specific real-time polymerase chain reaction assay and serial dil
136 l clinical laboratory for viral quantitative real-time polymerase chain reaction assay over a 5-year
137 n a sample of 216 European Americans using a real-time polymerase chain reaction assay, which amplifi
140 sion material with the use of a quantitative real-time polymerase-chain-reaction assay for non-variol
142 fludarabine, and FC, were screened by TaqMan real-time polymerase chain reaction assays for CYP2B6 SN
146 ng Ebola Zaire Target 1, major groove binder real-time-polymerase chain reaction assays, and original
147 and Streptococcus oralis were measured with real-time polymerase chain reaction at baseline and 90 a
148 Leukocyte TL was measured by quantitative real-time polymerase chain reaction at baseline and afte
149 opment of relapse by using a newly developed real-time polymerase chain reaction based on locked nucl
151 l of donor-derived T cells was measured with real-time polymerase chain reaction before and 1 year af
152 A on the basis of a competitive quantitative real-time polymerase chain reaction (cqPCR) was develope
153 , analysis of lipid content and quantitative real-time polymerase chain reaction data performed in qu
157 rmined from small interfering RNA knockdown, real-time polymerase chain reaction, Drosha-activity, mi
159 out pneumonia were tested using quantitative real-time polymerase chain reaction for 17 viruses.
160 issues of maxillary molars were subjected to real-time polymerase chain reaction for assessment of os
163 osis, oxidative stress, inflammation (IL-8), real-time polymerase chain reaction for epithelial-to-me
164 s measured using 1) immunohistochemistry, 2) real-time polymerase chain reaction for inflammatory mar
165 ic acid extracted from stool was analyzed by real-time polymerase chain reaction for OPV serotypes.
166 us commensal microorganisms, and analyzed by real-time polymerase chain reaction for the expression o
167 unit in Monrovia were tested by quantitative real-time polymerase chain reaction for the presence of
168 mniotic fluid, or placenta samples tested by real-time polymerase chain reaction for Zika virus.
169 qMan HIV-1 Test, version 2.0 (TaqMan 2.0), a real-time polymerase chain reaction human immunodeficien
170 aluated by microarray analysis, quantitative real-time polymerase chain reaction, immunoblotting, his
171 ealthy controls was assessed by quantitative real time polymerase chain reaction, immunohistochemistr
172 messenger RNA (mRNA) levels were measured by real time polymerase chain reaction in ethanol-treated m
174 analyzed by Western blot and/or quantitative real-time polymerase chain reaction in different cell li
175 NV isoforms were evaluated with quantitative real-time polymerase chain reaction in human postmortem
176 sses I-IV were quantified using quantitative real-time polymerase chain reaction in human postmortem
177 sses I-IV were quantified using quantitative real-time polymerase chain reaction in human postmortem
179 nd total bacterial load were determined by a real-time polymerase chain reaction in intrasulci plaque
180 rmine (1) the frequency of HAdV detection by real-time polymerase chain reaction in KD patients, (2)
181 ith nuclear DNA was measured by quantitative real-time polymerase chain reaction in peripheral blood.
185 sacrificed on day 7 after AVF placement for real-time polymerase chain reaction (n = 6 for MSC and c
186 dobronchial biopsies (n = 14) at 30 days for real-time polymerase chain reaction of hypoxia-inducible
187 ray analysis with validation by quantitative real-time polymerase chain reaction on paired tumor biop
189 d Fusobacterium nucleatum were determined by real-time polymerase chain reaction on the basis of the
193 tion is conventionally based on quantitative real-time polymerase chain reaction (PCR) analysis of bl
195 Parasitemia was monitored by quantitative real-time polymerase chain reaction (PCR) analysis, and
199 ting for N. gonorrhoeae was undertaken using real-time polymerase chain reaction (PCR) assays targeti
200 of molecular probing technologies involving real-time polymerase chain reaction (PCR) assays that fa
201 this study was to develop a method based on Real-Time Polymerase Chain Reaction (PCR) for detection
202 nd respiratory virus detection by multiplex, real-time polymerase chain reaction (PCR) from nasophary
203 lciparum DNA concentrations were measured by real-time polymerase chain reaction (PCR) in 224 African
205 ns are usually based on technologies such as real-time polymerase chain reaction (PCR) or DNA sequenc
206 Treponema denticola (Td) was performed using real-time polymerase chain reaction (PCR) procedures.
207 t RNA extraction, reverse transcription, and real-time polymerase chain reaction (PCR) to detect OPV
208 uence-specific detection of nucleic acids in real-time polymerase chain reaction (PCR) using fluoresc
210 nvironmental samples were tested by culture, real-time polymerase chain reaction (PCR), and multigene
211 Changes in TL, measured by quantitative real-time polymerase chain reaction (PCR), were assessed
220 practice and also tested with fast multiplex real-time polymerase-chain reaction (PCR) assays for 26
221 assays (AFIAs) for B. microti antibodies and real-time polymerase-chain-reaction (PCR) assays for B.
224 olecular methods (QMMs) such as quantitative real-time polymerase chain reaction (q-PCR), reverse-tra
226 or nasopharyngeal swabs for C. pneumoniae by real-time polymerase chain reaction (qPCR) and serum sam
227 ofluidic chip interfaced with a quantitative real-time polymerase chain reaction (qPCR) device previo
228 In this study, JCV DNA was quantified by real-time polymerase chain reaction (qPCR) in brain and
229 High-throughput single-cell quantitative real-time polymerase chain reaction (qPCR) is a promisin
232 m the donor, including culture, quantitative real-time polymerase chain reaction (qPCR), and whole-ge
233 e-independent analyses, namely, quantitative real-time polymerase chain reaction (qPCR), mutliplex-te
234 nome with Oligo Microarrays and quantitative real-time polymerase chain reaction (qPCR), relevant gen
237 pressions were quantified using quantitative real time polymerase chain reaction (qRT-PCR) to further
238 MT1 in the intestinal mucosa by quantitative real-time polymerase chain reaction (qRT-PCR) and immuno
239 inflorescence morphology using quantitative real-time polymerase chain reaction (qRT-PCR) and RNA in
241 DNA (EBV-DNA), as determined by quantitative real-time polymerase chain reaction (QRT-PCR), are assoc
243 ipoprotein metabolism were compared by using real-time polymerase chain reaction quantification on du
245 rcrR mutants using RNA-Seq and quantitative real-time polymerase chain reaction revealed little expr
246 Flow-cytometric analysis and quantitative real-time polymerase chain reaction revealed that GFP(hi
248 n eliminating T. cruzi parasites measured by real time polymerase chain reaction (RT-PCR) in asymptom
250 and infant urines were tested by qualitative real-time polymerase chain reaction (RT-PCR) for CMV DNA
251 valuated using culture, slide agglutination, real-time polymerase chain reaction (rt-PCR), and whole
252 ma, n = 3; uveitis, n = 3) were arrayed by a real-time polymerase chain reaction (RT-PCR)-based micro
253 Consecutive children aged <18 years with real-time polymerase chain reaction (RT-PCR)-confirmed E
259 ated for reverse transcription- quantitative real-time polymerase chain reaction (RT-qPCR) assays and
261 ting for the presence of T. cruzi DNA, using real-time polymerase-chain-reaction (rt-PCR) assays, dur
262 iscordant miRNAs were tested in quantitative real-time-polymerase chain reaction (RT-qPCR) experiment
263 symptoms and DNA-based detection techniques (real-time polymerase chain reaction, RT-PCR) and can be
268 ecipitation (ChIP)-Seq and ChIP-quantitative real-time polymerase chain reaction studies show that Am
269 The peptide nucleic acid-mediated 5 nuclease real-time polymerase chain reaction (TaqMan) assay used
270 vel peptide nucleic acid-mediated 5 nuclease real-time polymerase chain reaction (TaqMan) assay.
271 ving in rural Zanzibar, and were analyzed by real-time polymerase chain reaction targeting multiple p
272 can be detected by established quantitative real-time polymerase chain reaction technology, making t
274 ples were collected and analyzed by means of real-time polymerase chain reaction to determine the pre
275 mistry, immunofluorescence, and quantitative real-time polymerase chain reaction to examine Sertoli a
278 k candidate allele of HLA-DRB1*01 by genomic real-time polymerase chain reaction together with high-d
279 Gene expression profiles were determined by real-time polymerase chain reaction using primers specif
280 mplification of complimentary DNA-ends-based real-time polymerase chain reaction was established for
288 Finally, via single-cell RNA-sequencing and real-time -polymerase chain reaction, we show that Th1/T
289 Whole genome sequencing and quantitative real-time polymerase chain reaction were performed on lo
291 ip array (Illumina, Inc., San Diego, CA) and real-time polymerase chain reaction were used to identif
294 on and cell proliferation were determined by real-time polymerase chain reaction, Western blots, flow
295 K2 and downstream effectors were analyzed by real-time polymerase chain reaction, western blotting, i
297 neous and 48 treatment induced) using nested real-time polymerase chain reaction with a detection lim
298 hree independent cohorts and by quantitative real-time polymerase chain reaction with high prediction
300 e of BK viruria (detected using quantitative real-time polymerase chain reaction) within the first ye
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