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1 and 2 up-regulated genes) were validated by real time quantitative PCR.
2 iral vector to other organs was evaluated by real time quantitative PCR.
3 PTGS2, CXCR1, and PTK2 were determined using real-time quantitative PCR.
4 ication in human beta-cells was performed by real-time quantitative PCR.
5 1), differential expression was confirmed by real-time quantitative PCR.
6 (promote N-glycan branching) as detected by real-time quantitative PCR.
7 as in CD4+CD8- single-positive thymocytes by real-time quantitative PCR.
8 were confirmed in microdissected samples by real-time quantitative PCR.
9 t and 3 and 7 days later, was analyzed using real-time quantitative PCR.
10 east 10-fold more than the other isoforms by real-time quantitative PCR.
11 individual infection load then estimated by real-time quantitative PCR.
12 of these two methods were then validated by real-time quantitative PCR.
13 remodeling, respectively) was quantified by real-time quantitative PCR.
14 ded the peak levels of CCL17, as measured by real-time quantitative PCR.
15 e blood recall assays, HLA-A2 tetramers, and real-time quantitative PCR.
16 in lung tissue of bleomycin-treated mice by real-time quantitative PCR.
17 expression were subsequently confirmed using real-time quantitative PCR.
18 The load of infection was then estimated by real-time quantitative PCR.
19 communities in Tanzania and The Gambia with real-time quantitative PCR.
20 ome fetuses and five independent controls by real-time quantitative PCR.
21 sion of some of these genes was confirmed by real-time quantitative PCR.
22 anglia, as demonstrated by virus culture and real-time quantitative PCR.
23 CCDC134, UBD, and ZIC2 were validated using real-time quantitative PCR.
24 wing abnormal expression were validated with real-time quantitative PCR.
25 All patients were monitored by real-time quantitative PCR.
26 ormances and reaching similar sensitivity as real-time quantitative PCR.
27 ntification of the repaired, CPD-free DNA by real-time quantitative PCR.
28 an innate, immune response was quantified by real-time quantitative PCR.
29 Relative MCP-1 mRNA was measured by real-time quantitative PCR.
30 tern blot or harboring HDV RNA detectable by real-time quantitative PCR.
31 MRD was measured by using standardized real-time quantitative PCR.
32 elongs to the same cluster, was confirmed by real-time quantitative PCR.
33 e different cultured cells was validated via real-time quantitative-PCR.
34 cycling, making this method well suited for real-time quantitative PCRs.
41 at are impaired in the resistant cell lines, real-time quantitative PCR analyses were employed and tw
50 enome hybridization (aCGH) followed by rapid real-time quantitative PCR analysis to identify, confirm
53 as carried out on a subset of 66 clones with real time quantitative PCR and 40 clones were positive.
55 seI and Trap1 mRNA levels were determined by real-time quantitative PCR and compared with protein exp
57 sion varied considerably as measured by both real-time quantitative PCR and flow cytometry analysis.
59 re highly upregulated or downregulated using real-time quantitative PCR and found a strong correlatio
63 vo gene expression profiles were verified by real-time quantitative PCR and immunohistochemistry.
70 of candidate genes by reverse transcriptase real-time quantitative PCR and subsequent testing for ak
71 expression patterns of mouse macrophages by real-time quantitative PCR and tested the functional eff
74 irmed in splenocytes and total thymocytes by real-time quantitative PCR and Western blot as well as i
75 human epidermal keratinocytes (n = 11) with real-time quantitative PCR and Western blotting revealed
76 genes in the region was carried out by using real-time quantitative PCR and/or oligo-microarray profi
77 n and gene transcript levels (gene array and real-time quantitative PCR) and compared with insulin-tr
78 n of IL-13Ralpha2 mRNA was measured by using real-time quantitative PCR, and cell-surface IL-13Ralpha
79 ds for islet expansion using immunostaining, real-time quantitative PCR, and microarrays at the follo
81 mutant TIP30, by Affymetrix GeneChip array, real-time quantitative PCR, and Western blotting assays
82 cts has been utilized extensively in various real-time quantitative PCR applications, including post-
83 g conventional reverse transcriptase-PCR and real-time quantitative PCR, as well as whole-mount in si
84 bjects from 3 independent cohorts by using a real-time quantitative PCR assay to detect a noninherite
85 growth factor (EGF) mRNA were measured using real-time quantitative PCR assay, and levels were correl
91 estimate infection prevalence, we developed real-time quantitative PCR assays for each virus and scr
97 using traditional plaque assays, as well as real-time quantitative PCR-based genome quantification a
98 sured by a highly sensitive and quantitative real-time quantitative-PCR-based telomeric repeat amplif
100 istry, Western blotting, DNA binding assays, real-time quantitative PCR, coimmunoprecipitation, and E
109 principle, we demonstrate an electrochemical real-time quantitative PCR (e-PCR) measurement in the to
110 microscopy, cocultures, suppression assays, real-time quantitative PCR, ELISAs, and ELISpot assays w
111 portions were subjected to mRNA extraction, real-time quantitative PCR, enzyme-linked immunosorbent
112 "Minimum Information for the publication of real-time Quantitative PCR Experiments" (MIQE) guideline
114 pression of candidate genes was confirmed by real-time quantitative PCR, fluorescence, and immunohist
115 Plaque and saliva samples were tested with real-time quantitative PCR for DNA levels of pathogens r
116 ra-1 gene silenced RPM cells were assayed by real-time quantitative PCR for the expression of possibl
118 ce and levels of male DNA were determined by real-time quantitative PCR for the Y chromosome-specific
119 Microarray findings were confirmed by using real-time quantitative PCR in 30 subjects (12 children w
120 ssion of plasma miRNAs was measured by using real-time quantitative PCR in 35 asthmatic patients, 25
121 chromosome-specific DYS14 gene, we performed real-time quantitative PCR in autopsied brain from women
122 erated, and their expression was measured by real-time quantitative PCR in blood samples from 81 meta
123 aggression testing at both time points using real-time quantitative PCR in brain regions previously i
127 We analyzed XDH1 and XDH2 gene expression by real-time quantitative PCR in tissues from sugar- and bl
132 ects of this deficiency were demonstrated by real-time quantitative PCR measurements of altered mRNA
134 immunoprecipitation, promoter mutations, and real-time quantitative PCR, NRF-1 was found to functiona
135 ipitation, promoter mutational analysis, and real-time quantitative PCR, NRF-1 was found to functiona
136 orts to standardize MRD quantification using real-time quantitative PCR of clonal immunoglobulin and
137 ical rates in cell culture, as determined by real-time quantitative PCR of viral particles released i
138 F-beta, IL-5, and IL-10 mRNA was measured by real-time quantitative PCR on tissue homogenates of pati
139 sence or absence of certain antibiotics with real-time quantitative PCR or digital PCR to determine a
140 e tissue using Western blot, flow cytometry, real-time quantitative PCR, or RNA sequencing analyses.
141 itionally, we applied a recently established real-time quantitative PCR platform to gain insight into
142 Next generation RNA sequencing of mRNAs and real time quantitative PCR profiling established that Ez
146 ta combining transcriptional lacZ fusion and real-time quantitative PCR (qPCR) analyses indicated tha
147 ive genomic hybridization (CGH) database and real-time quantitative PCR (qPCR) analyses to identify t
150 rformance of the Xpert Carba-R test, a rapid real-time quantitative PCR (qPCR) assay that detects fiv
154 riance across the lake as fluorescence based real-time quantitative PCR (qPCR) measurements of microc
161 r the molecular detection of the organism by real-time quantitative PCRs (qPCRs) targeting the uracil
162 ononuclear cells was screened by nested- and real time-quantitative PCR (QRT-PCR) for the presence of
163 chain reaction (ddPCR) is rapidly replacing real-time quantitative PCR (qRT-PCR) as an efficient met
166 nin-concentrating hormone, as revealed using real-time quantitative PCR, radiolabeled in situ hybridi
167 tification of the transcripts by RNA-Seq and real time quantitative PCR revealed that the CYP3A4 tran
169 ypothalamic peptides via radioimmunoassay or real-time quantitative PCR revealed markedly enhanced ga
172 Progress includes establishment of optimized real-time quantitative PCR (RQ-PCR) assays for WT1 (comm
173 now possible using updated methods including real-time quantitative PCR (RQ-PCR) for abnormal fusion
175 chanism of how Dam and GidA influence Act, a real-time quantitative PCR (RT-qPCR) assay was performed
177 oter cloning, and site-directed mutagenesis, real-time quantitative PCR (RT-qPCR), and Western blotti
178 expression on prostate cancer cell lines by real-time quantitative PCR (RT-qPCR), flow cytometry, an
185 ern blot data, reverse transcription-PCR and real-time quantitative PCR showed that gp340 transcripts
193 study, we demonstrate by deep sequencing and real-time quantitative PCR that hepatic levels of Foxa2
196 viral loads of exposed fish, measured using real-time quantitative PCR; the most virulent viral stra
197 to assess metabolic reactions and fluxes and real time quantitative PCR to determine gene expression.
199 robotics, multiparameter flow cytometry, and real-time quantitative PCR to analyze T cell activation
201 tions of limbal epithelium were subjected to real-time quantitative PCR to determine c-kit ligand exp
202 ne amplification with message level, we used real-time quantitative PCR to measure hTERT mRNA in 50 e
204 -denaturing gradient gel electrophoresis and real-time quantitative PCR to monitor and quantify chang
205 opy, semithin sectioning of leaf tissue, and real-time quantitative PCR to study structural and quant
207 e, 14 human bladder tumours were analysed by real-time quantitative PCR using gene-specific primers f
208 array results with the reverse transcription real-time quantitative PCR, using a larger number of non
212 production was measured by using ELISA, and real-time quantitative PCR was performed to detect PGE2
222 te and sensitive assay of parasite genotype, real-time quantitative PCR, we have investigated protect
227 , and mRNA expression levels (measured using real-time quantitative-PCR) were related to fetal and ne
228 tissue samples from lung cancer patients by real-time quantitative PCR, Western blot, and IHC and fo
229 changes of gene expression were confirmed by real-time quantitative PCR, Western blotting, and functi
231 ion of these genes, 7 of them were tested by real-time quantitative PCR, which verified that they wer
233 n reaction (PCR) enzymes were compared using real-time quantitative PCR with SYBR Green I detection.
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