2005
DOI: 10.1016/j.jcv.2004.12.018
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Specific and quantitative detection of human polyomaviruses BKV, JCV, and SV40 by real time PCR

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Cited by 121 publications
(100 citation statements)
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References 67 publications
(64 reference statements)
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“…Absolute numbers of copies of proviral DNA copy were determined at days 1, 2, 4, and 7 postinfection. To obtain absolute proviral DNA copy numbers, a standard curve was generated using serial dilutions of a plasmid encoding HIV gag region (pHIVgag) and RNaseP gene (pRNaseP) as described (47).…”
Section: Cd4mentioning
confidence: 99%
“…Absolute numbers of copies of proviral DNA copy were determined at days 1, 2, 4, and 7 postinfection. To obtain absolute proviral DNA copy numbers, a standard curve was generated using serial dilutions of a plasmid encoding HIV gag region (pHIVgag) and RNaseP gene (pRNaseP) as described (47).…”
Section: Cd4mentioning
confidence: 99%
“…At 15 days post-infection virus was harvested from the infected cells, treated with Dnase to remove non-virion associated DNA, and then with proteinase K to expose the virion DNA. Virion associated DNA was then quantitated by real time PCR using the protocol, primers, and probes described by McNees et al on a Biorad IQ5 system (Biorad) (McNees et al, 2005). Primers and probes were designed using primer express software (Applied Biosystems).…”
Section: Quantitative Pcr Measurement Of Viral Loadmentioning
confidence: 99%
“…Primers and probe for identification of all serotypes of AdV and those for identification of BKV were designed, based on the reports described previously. [4][5] As presented in Figure 1b, the urine AdV loads at the onset of HC in the 7 patients with AdV-HC were markedly higher than the maximum values in the 8 patients with non-AdV-HC or the 54 patients without HC. There was no significant difference in the serum AdV loads among the AdV-HC, non-AdV-HC and no HC group.…”
mentioning
confidence: 90%