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1 thods, and for other respiratory viruses, by virus culture.
2 og copies higher in specimens producing live virus culture.
3 n and regulation, during noninduced (latent) virus culture.
4 correlation between antigen test results and virus culture.
5 Ct values >29.5 and were not associated with virus culture.
6     In the first year, RSV-infected infants (virus culture and antibody increase) were more likely to
7 transcription polymerase chain reaction, and virus culture and isolates were characterized.
8 d assessed their correlation with infectious virus culture and PCR cycle threshold (Ct) values.
9 e and 264 of these had been followed up with virus culture and PCR for viral DNA at least once.
10 ity to reach the ganglia, as demonstrated by virus culture and real-time quantitative PCR.
11  substrains and sequence variations in mixed virus cultures and mumps vaccines.
12                  This new method complements virus culturing and metagenomic approaches and its advan
13 ng active HHV-6 and HHV-7 infections include virus culture, antigen detection, and polymerase chain r
14 al nasal samples that had positive influenza virus cultures at the time of collection had positive re
15                Antigen-detection testing and virus culture but not real-time RT-PCR identified the en
16 eripheral blood mononuclear cells (PBMC) and virus cultures but has not been systematically evaluated
17 mental or surveillance samples are obtained, virus cultures can be generated and the presence of IAVs
18 d quantitatively in approximately 20 min, in virus cultures, combined nasal and throat swabs with add
19 is of multiple clones derived from the CF-65 virus culture demonstrated a diversity of mutations in t
20 .2 plaque-forming units/mL using a reference virus culture diluted into universal transport medium (U
21 f NNV or iridovirus infected fishes, such as virus culture, enzyme-linked immunosorbent assays and nu
22   Plasma virus matched replication-competent virus cultured from CD4+ T cells.
23  identified by clonal sequencing analyses of viruses cultured from blood cells.
24  the possibility of variant selection during virus culture in peripheral blood cells.
25 d on monitoring cytopathic effects following virus culture in vitro.
26 zees were unable to neutralize the challenge virus cultured in peripheral blood mononuclear cells (PB
27 sy, lymphoid tissues and vaginal mucosa were virus culture negative, but in 10 of 10 animals, SIV pro
28 nd 1986, and newborns were screened for CMV (virus culture of urine or saliva).
29                                              Virus cultures of conventionally processed and chlorofor
30 d by several quantitative methods, including virus cultures of PBMCs and polymerase chain reaction (P
31          A cytopathic effect was observed in virus cultures of the acute-phase serum samples and nasa
32                   Infection was confirmed by virus culture or immunoblotting.
33    Nine of the 264 children were positive by virus culture or PCR, and subsequently seroreverted.
34 tive results from polymerase chain reaction, virus culture, or serology.
35 us EBOV was detected by real-time RT-PCR and virus culture out to 290 days and 70 days, respectively,
36                 When infected with influenza virus, cultured porcine lung epithelial cells expressed
37 ople with a positive RT-PCR test result were virus culture positive was used as a proxy of infectious
38 late of viral load and for discrimination of virus culture positivity.
39 rameters and used patient samples to perform virus culture, quantitative polymerase chain reaction, a
40 asma pneumoniae infections using throat swab virus cultures, real-time PCR, DNA sequencing, immunoche
41        Two studies reported the odds of live virus culture reduced by approximately 33% for every one
42                 Although contact tracing and virus culture remained inconclusive, the health care wor
43 ect in female genital secretions by standard virus culture techniques.
44  robust, and it allows for the generation of virus cultures that can be used for downstream analyses.
45 eral blood mononuclear cells or from primary virus cultures, using serial blood samples from a Zambia
46                                     Positive virus culture was identified in 57 (40.4%) of 141 sample
47 rect fluorescent-antibody (DFA) staining and virus culture was performed on a subset of 711 respirato
48   Two studies reported that the odds of live virus culture were reduced by approximately 33% for ever
49                                              Virus cultures were negative.
50 sis of genotypic changes in nine recombinant viruses cultured with d4T, we identified a new pathway f