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1 ld be confirmed by in situ hybridization and Real Time quantitative polymerase chain reaction.
2 ifferentiation and function were analyzed by real-time quantitative polymerase chain reaction.
3 cytometry or allele-specific oligonucleotide real-time quantitative polymerase chain reaction.
4 e and EGR1 gene expression was quantified by real-time quantitative polymerase chain reaction.
5 s were measured by reverse transcription and real-time quantitative polymerase chain reaction.
6 SMN2 gene copy numbers were determined using real-time quantitative polymerase chain reaction.
7 ranscripts of MMP-2/MMP-9 were measured with real-time quantitative polymerase chain reaction.
8 and the degree of viremia was determined by real-time quantitative polymerase chain reaction.
9 d for analysis of pulmonary fungal burden by real-time quantitative polymerase chain reaction.
10 genes RRM1, PTEN, and RRM2 was determined by real-time quantitative polymerase chain reaction.
11 s in ovarian theca and granulosa cells using real-time quantitative polymerase chain reaction.
12 eic acid (mRNA) abundance was measured using real-time quantitative polymerase chain reaction.
13 tively expressed 18S ribosomal RNA (rRNA) by real-time quantitative polymerase chain reaction.
14 al DNA and mRNA production was assayed using real-time quantitative polymerase chain reaction.
15 tor accessory protein) were also measured by real-time quantitative polymerase chain reaction.
16 (NF)-kappa B mRNA levels were analyzed using real-time quantitative polymerase chain reaction.
17 reened for TBK1 copy number variations using real-time quantitative polymerase chain reaction.
18 Viral load was measured by real-time quantitative polymerase chain reaction.
19 d age-matched healthy female controls, using real-time quantitative polymerase chain reaction.
20 uman papillomavirus status was determined by real-time quantitative polymerase chain reaction.
21 and fluid were assessed by Luminex assay and real-time quantitative polymerase chain reaction.
22 V load in peripheral blood was determined by real-time quantitative polymerase chain reaction.
23 and possible alternative mechanoreceptors by real-time quantitative polymerase chain reaction.
24 ion were assessed by immunohistochemistry or real-time quantitative polymerase chain reaction.
25 odulated animals by immunohistochemistry and real-time quantitative polymerase chain reaction.
26 get genes in the amygdala was measured using real-time quantitative polymerase chain reaction.
27 for immunohistochemistry, Western blots and real-time quantitative polymerase chain reaction.
28 ic macrophage functions was quantified using real-time quantitative polymerase chain reaction.
29 messenger RNA expressions were determined by real-time quantitative polymerase chain reaction.
30 ses 3 and 13 gene expression was analyzed by real-time quantitative polymerase chain reaction.
31 nd TF messenger RNA (mRNA) was determined by real-time quantitative polymerase chain reaction.
32 rine and blood) were assessed for JCV DNA by real time quantitative polymerase chain reaction 6 to 47
33 Real-time quantitative polymerase chain reaction analyse
34 Real-time quantitative polymerase chain reaction analysi
35 By Northern analysis, EST distribution and real-time quantitative polymerase chain reaction analysi
36 osition of nine MITE families was studied by real-time quantitative polymerase chain reaction analysi
37 a (ALL), we assessed the clinical utility of real-time quantitative polymerase chain reaction analysi
39 otein biomarkers was also demonstrated using real-time quantitative polymerase chain reaction and imm
40 ycobacterium smegmatis (MSMEG_6042) and used real-time quantitative polymerase chain reaction and mic
41 genes from the profile were validated using real-time quantitative polymerase chain reaction and pro
42 e X, gene 1 messenger RNAs and protein using real-time quantitative polymerase chain reaction and Wes
43 pha-induced IRF-1 expression was assessed by real-time quantitative polymerase chain reaction and Wes
45 transfected cells using immunofluorescence, real-time quantitative polymerase chain reaction, and im
46 nohistochemistry, immunoblotting proteomics, real-time quantitative polymerase chain reaction, and la
47 ressed 18S rRNA was measured with the use of real-time quantitative polymerase chain reaction assay,
49 wabs were tested for HSV-2 shedding, using a real-time quantitative polymerase chain reaction assay.
50 xpression in the islets was determined using real-time quantitative polymerase chain reaction assay.
51 g BKV specific primers and TaqMan probe in a real-time quantitative polymerase chain reaction assay.
52 , immunofluorescence, electron microscopy, a real-time quantitative polymerase-chain-reaction assay,
53 primers and fluorogenic probes were used in real-time quantitative polymerase chain reaction assays
55 ary cell levels of mRNAs were measured using real-time quantitative polymerase chain reaction assays,
56 Northern blot analysis and real-time quantitative polymerase chain reaction demonst
57 ular tissues and plasma was determined using real-time quantitative polymerase chain reaction, dual-l
58 rse transcriptase-polymerase chain reaction, real-time quantitative polymerase chain reaction, ELISA,
59 noString nCounter miRNA expression assay and real-time quantitative polymerase chain reaction, follow
61 Myocardial mRNA levels were determined by real-time quantitative polymerase chain reaction in 12 r
62 ease outcomes, we examined baseline VLs with real-time quantitative polymerase chain reaction in 122
63 G7, FLOT1, c6orf48, and RASSF5) tested using real-time quantitative polymerase chain reaction in a di
65 Selected results were confirmed by real-time quantitative polymerase chain reaction, includ
66 the expression of Bax mRNA and Bcl-2 mRNA by real-time quantitative polymerase chain reaction; islet
67 otein (by immunohistochemistry) and mRNA (by real-time quantitative polymerase chain reaction) levels
68 tention was quantified by flow cytometry and real-time quantitative polymerase chain reaction methodo
69 a, but there is substantial variation in the real-time quantitative polymerase chain reaction methodo
70 Functional studies included real time quantitative polymerase chain reaction, nephel
71 ive/DNA-positive were confirmed by combining real-time quantitative polymerase chain reaction, nested
72 endent analysis by cDNA expression array and real-time quantitative polymerase chain reaction of seve
75 rate of detection of HSV DNA, by means of a real-time quantitative polymerase chain reaction (PCR) a
76 distinguish the origin of FM, we developed a real-time quantitative polymerase chain reaction (PCR) a
77 identify in vivo T-cell tropisms of HTLV-I, real-time quantitative polymerase chain reaction (PCR) a
79 negative (AC) marker genes were validated by real-time quantitative polymerase chain reaction (PCR) a
80 d using a pellet culture system, followed by real-time quantitative polymerase chain reaction (PCR) a
81 A total of 50 samples were studied by using real-time quantitative polymerase chain reaction (PCR) f
82 primary arthritis diagnosis were assayed by real-time quantitative polymerase chain reaction (PCR) u
83 g by multiparameter flow cytometry (MFC) and real-time quantitative polymerase chain reaction (PCR) w
84 nd an order of magnitude less sensitive than real-time quantitative polymerase chain reaction (PCR) w
85 were released and enumerated using benchtop real-time quantitative polymerase chain reaction (PCR),
87 olecule cDNA array analysis and confirmed by real-time quantitative polymerase chain reaction (PCR).
88 ]-gamma, interleukin [IL]-10) as detected by real-time quantitative polymerase chain reaction (PCR).
89 xperimental error and analysis procedures in real-time quantitative polymerase chain reaction (PCR).
92 We used a modified real-time quantitative polymerase chain reaction protoco
93 ription into cDNA, preamplification and then real time quantitative polymerase chain reaction (qPCR)
96 attacks have promised the future of portable real-time quantitative polymerase chain reaction (qPCR)
98 known HHVs was first studied using specific real-time quantitative Polymerase Chain Reaction (qPCR)
100 cycle (Cq) is widely used for calibration in real-time quantitative polymerase chain reaction (qPCR),
102 osol and source material samples analyzed by real-time quantitative polymerase chain reaction (qPCR).
103 investigated for the levels of COX-2 mRNA by real-time quantitative Polymerase Chain Reaction (qPCR).
104 yptdins and beta-defensins was determined by real-time quantitative polymerase chain reaction (qPCR).
105 id nodules were tested for microchimerism by real-time quantitative polymerase chain reaction (qPCR).
107 cribe a strategy that uses a novel method of real-time quantitative polymerase chain reaction, quanti
108 ent reproductive statuses were determined by real-time quantitative polymerase chain reaction (real-t
109 s be validated by some other method, such as real-time quantitative polymerase chain reaction (real-t
111 od mononuclear cells (PBMCs) as material for real-time quantitative polymerase chain reaction (RQ-PCR
112 ring minimal residual disease (MRD) by using real-time quantitative polymerase chain reaction (RQ-PCR
113 th a sensitivity of </=10(-5), comparable to real-time quantitative polymerase chain reaction (RQ-PCR
114 208; control, n = 206) were evaluated using real-time quantitative polymerase chain reaction (RQ-PCR
116 ermine response kinetics following imatinib, real-time quantitative-polymerase chain reaction (RQ-PCR
117 alysis as well as for transcript analysis by real-time quantitative polymerase chain reaction (RT-PCR
118 lular communication (GJB3) were validated by real-time quantitative polymerase chain reaction (RT-Q-P
119 Fluorescence-based reverse transcription real-time quantitative polymerase chain reaction (RT-QPC
120 assessed with luciferase reporter assays and real-time quantitative polymerase chain reaction (RT-qPC
121 ) and Fcgamma receptor 3 (FCGR3) genes using real-time quantitative polymerase chain reaction (RT-qPC
123 The real-time quantitative polymerase chain reaction (rtqPCR
125 Analyses of mRNA levels by real-time quantitative polymerase chain reactions sugges
126 /tropical spastic paraparesis patients using real-time quantitative polymerase chain reaction (TaqMan
127 Real-time quantitative polymerase chain reaction techniq
129 for quantitation of BCR-ABL translocation by real-time quantitative polymerase chain reaction was app
133 nger RNA was extracted from fixed tissue and real-time quantitative polymerase chain reaction was per
142 Using gene regulation, real-time quantitative polymerase chain reaction, wester
143 le; mean age, 63.3 years) were analyzed with real-time quantitative polymerase chain reaction with sp
144 By use of real-time quantitative polymerase chain reaction, Wolbac
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