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1 various intervals, and RNA was isolated and reverse transcribed.
2 d from captured tissue, DNAse I treated, and reverse transcribed.
3 strictly define which TER nucleotides can be reverse transcribed.
4 liced RNA to pgRNA that are encapsidated and reverse transcribed.
5 immediate translation template if not being reverse transcribed.
6 RNA was extracted and reverse transcribed.
7 Total RNA was isolated and reverse-transcribed.
8 is end, human reticulocyte RNA was isolated, reverse transcribed, amplified by PCR and appropriate pr
9 ease controls, and 21 healthy volunteers was reverse transcribed, amplified by polymerase chain react
10 l system for intracellular protein sorting), reverse transcribed, amplified using polymerase chain re
11 ransductance regulator (CFTR) target mRNA is reverse transcribed, amplified, detected, and quantitate
17 f the CLL B cell were detected when mRNA was reverse transcribed and amplified using c mu- and/or C a
18 RNA from human lymphoblastoid cell lines was reverse transcribed and amplified using specific "nested
20 normal donors and patients with leukemia was reverse transcribed and analyzed by polymerase chain rea
22 ssed pseudogenes are copies of cellular RNAs reverse transcribed and inserted into the nuclear genome
23 oson that replicates via an RNA copy that is reverse transcribed and integrated elsewhere in the plan
24 nct genes, and the resulting chimera is then reverse transcribed and integrated into the genome by th
26 (DM) and two polymyositis (PM) patients was reverse transcribed and reamplified by semi-quantitative
27 the cesium chloride-guanidine method and was reverse transcribed and semiquantitated with the polymer
29 RNA from KB-V1 multidrug-resistant cells was reverse-transcribed and amplified by using primers deriv
30 tein (MAVS)-dependent RNA sensing pathway or reverse-transcribed and detected via the cGAS-cGAMP-STIN
31 nd isotype-control Ab, and eluted mRNAs were reverse-transcribed and hybridized to an inflammatory-fo
35 as extracted from lenses of 12-day-old rats, reverse transcribed, and amplified using polymerase chai
37 ed children age 3 to 18 years, was purified, reverse transcribed, and biotinylated cRNA hybridized to
39 IV Env-pseudotyped lentiviral vectors fused, reverse transcribed, and integrated in resting cells.
41 i, total RNA was extracted from the thrombi, reverse transcribed, and subjected to amplification with
42 coculture, HAEC poly (A+) RNA was isolated, reverse-transcribed, and the cDNA-amplified (PCR) for a
44 m of LTR retrotransposition, in which RNA is reverse transcribed away from the chromosomal target sit
45 uential transesterification reactions and is reverse transcribed by the associated intron-encoded pro
46 one strand of a DNA target site and is then reverse transcribed by the associated intron-encoded pro
47 directly into a DNA target site and is then reverse transcribed by the associated intron-encoded pro
53 ogenous immunostimulatory nucleic acids: the reverse-transcribed cDNA of endogenous retroelements.
54 embranes and probed with temporally isolated reverse transcribed cDNAs from HIV-1-infected and TNF-al
60 f an ancestral intron-containing gene with a reverse-transcribed DNA copy of a fully spliced mRNA.
61 ses (HBVs), which are enveloped viruses with reverse-transcribed DNA genomes, constitute the family H
66 expressed during embryogenesis, VHL mRNA was reverse transcribed from 13 fetal tissues (8-10 weeks ge
67 B virus (HBV) and related hepadnaviruses is reverse transcribed from a pregenomic RNA by a viral pol
68 The devised assays can detect ERalpha cDNAs reverse transcribed from as low as 50-100 pg of total RN
70 rocessed" and "nonprocessed"; the former are reverse transcribed from mRNA (and therefore have no int
72 hybridization to complementary DNA samples, reverse-transcribed from polyadenylated RNA obtained fro
77 erum HBsAg were assessed by (PCR) for either reverse-transcribed HBV RNA, or an intact direct repeat
78 nse EPR-1 riboprobe, and by amplification of reverse-transcribed HD RNA with EPR-1-specific primers.
79 induction by the virus, suggesting that the reverse-transcribed HIV DNA triggers the innate immune r
82 NA template of known secondary structure was reverse transcribed in the presence of 8-oxo-dGTP, dPTP
83 nucleotide of the "donor" RNA are frequently reverse transcribed in these jumps, indicating that the
84 with the viral core structures and could be reverse-transcribed in HIV-1 virions and in virus-infect
85 lly, using a novel PCR approach, we detected reverse-transcribed, integrated proviral sequences in TA
91 RNA enclosed inside a capsid shell, must be reverse transcribed into double-stranded DNA and release
92 shorter species of spliced RNA, which can be reverse transcribed into double-stranded DNA before viri
93 s type 1 (HIV-1) requires that its genome be reverse transcribed into double-stranded DNA for product
94 owing cell entry, the RNA genome of HIV-1 is reverse transcribed into double-stranded DNA that ultima
97 directly into DNA target sites and are then reverse-transcribed into genomic DNA by the associated i
98 PolyA+ mRNA from the TGs of each group was reverse transcribed, labeled with 32P, incubated on a 11
99 ese cells of different confluence states was reverse transcribed, labeled, and used to hybridize 10K
100 For DNA microarray analysis, total RNA is reverse-transcribed, labeled by incorporating fluorescen
107 Polymerase chain reaction amplification of reverse-transcribed mRNA using murine CYP2C-specific pri
112 ells with rigorous quantitative, competitive reverse transcribed PCR (QC-RT-PCR) that enabled the com
113 els of CD40L-specific mRNA, as determined by reverse transcribed PCR analysis (RT-PCR) using CD40L-ho
114 Comparison of the genomic sequence to a reverse transcribed PCR product and tomato cDNA confirme
116 (TNF-alpha) gene expression, as detected by reverse-transcribed PCR and by enzyme-linked immunosorbe
120 imeric full-length HIV-1 clones derived from reverse-transcribed plasma viral RNA and proviral LTRs.
121 MDR1 gene, a single product was detected by reverse-transcribed polymerase chain reaction (RT-PCR) f
122 ses of lymphoblast mRNAs from 2 patients and reverse-transcribed polymerase chain reaction (RT-PCR) o
129 fibroblast cells using the semi-quantitative reverse transcribed-polymerase chain reaction (RT-PCR) a
130 d for TCR Vbeta usage by mAb staining and/or reverse transcribed-polymerase chain reaction analysis,
131 is enzyme is required for the integration of reverse transcribed proviral DNA into the host cell's ge
133 ding a P450 monooxygenase was amplified from reverse transcribed rat heart and liver total RNA by pol
134 essary and sufficient for the integration of reverse-transcribed retroviral DNA into the host cell DN
136 nts directly from genomic DNA, as opposed to reverse transcribed RNA from muscle biopsies, we have de
137 rom several granuloma CD4+ T cell lines; yet reverse transcribed RNA from T cell-depleted, dispersed
142 ker of recent nuclear import of full-length, reverse-transcribed RNA, was detected in the biopsies, s
146 dermal keratinocytes, and normal human skin, reverse transcribed to cDNA and amplified by the polymer
147 otal RNA was extracted from single utricles, reverse transcribed to cDNA and the cDNA amplified by PC
148 RNA was extracted from renal biopsies and reverse transcribed to cDNA which was used as template f
152 elements produce an RNA intermediate that is reverse transcribed to DNA and inserted in a new genomic
154 fter infection, the retroviral RNA genome is reverse transcribed to generate a linear cDNA copy, then
158 arallels mammalian adaptive immunity through reverse-transcribed vDNA circles and the systemic dissem
159 iral replication requires the integration of reverse-transcribed viral cDNA into a cell chromosome.
164 en B-cell mRNA from these five patients were reverse transcribed with C gamma-specific primers and th
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