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1 f. sp. carinii DNA was amplified from 98% of oral swabs.
2 reports of M. tuberculosis DNA detection in oral swabs.
6 e armored RNA concentrations spiked into the oral swab fluid specimens were stable under storage cond
7 to evaluate the use of PCR amplification of oral swabs for the antemortem detection of Pneumocystis
12 e, peak viremia, viral shedding in nasal and oral swabs, peak cytokine levels, and time to reach endp
13 tive healthy adults collected anogenital and oral swabs, respectively, 4 times per day for 60 days.
17 can detect SPPV in buffy coats, nasal swabs, oral swabs, scabs, and skin lesions as well as in lung a
18 cal blood and plasma samples and post mortem oral swabs submitted to the Liberian Institute for Biome
19 in the salivary glands and tongue and in an oral swab, suggesting that LBV is transmitted in the sal
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