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1 ion sequencing of the 16S rRNA gene as well as quantitative PCR was performed.
2 For both tests, DNA was extracted and real-time PCR was performed according to manufacturer's instructions.
3 incubated with recombinant IL-13 and gene expression by qRT-PCR was performed for collagen1A1 and TGF-beta1.
6 Antibiotic susceptibility was determined, and multiplex PCR was performed for OXA-23-like, -24-like, -51-like, and -5
14 of the epidemiology of IDV, real-time reverse transcription-PCR was performed on a set of 208 samples from bovines with r
19 upon elution on the MagNA Pure LC instrument, and real-time PCR was performed on the Applied Biosystems 7500 Fast platfor
25 ion was measured by using ELISA, and real-time quantitative PCR was performed to detect PGE2 receptor expression.
32 by enzyme-linked immunosorbent assay, whereas quantitative PCR was performed to measure interleukin-6 (IL-6, a pro-infla
37 ies were taken and total RNA extraction, cDNA synthesis and PCR was performed using 10 candidate HKG.
41 at code identified protein, quantitative real time PCR (qRT-PCR) was performed.
42 acterial repetitive intergenic consensus sequence PCR (ERIC-PCR) was performed.
43 (MFC) and real-time quantitative polymerase chain reaction (PCR) was performed at the end of induction and at ~3-month in
44 tative reverse transcription polymerase chain reaction (qRT-PCR) was performed in 2 groups of BE patients who either deve
45 One-step reverse transcriptase PCR (RT-PCR) was performed in picoliter drops with primers that ident
46 Polymerase chain reaction for respiratory viruses (PCR) was performed on 1021 specimens obtained from 898 childr
48 tative reverse transcription-polymerase chain reaction (qRT-PCR) was performed to assess the messenger RNA (mRNA) express
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