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1 viruses, and parainfluenza viruses by use of nested polymerase chain reaction.
2 nd HHV-6 genomic sequences were amplified by nested polymerase chain reaction.
3 V) were identified by sensitive and specific nested polymerase chain reaction.
4 pneumoniae DNA was then checked for using a nested polymerase chain reaction.
5 and amplified VH regions from the library by nested polymerase chain reaction.
6 lations were quantified by limiting-dilution nested polymerase chain reaction.
7 immunofluorescence testing and confirmed by nested polymerase chain reaction: 50% (6/12) of men and
8 hoblasts, and specific reverse transcriptase-nested polymerase chain reactions amplified and sequence
13 samples (37.5%) by the reverse transcription-nested polymerase chain reaction, correlating with antig
17 A positivity was determined by positivity of nested polymerase chain reaction in at least two of thre
18 were assessed using direct sequencing after nested polymerase chain reaction in patients with persis
19 nd five patients with pemphigus foliaceus by nested polymerase chain reaction (lower limit of detecti
20 99-2004 were examined for Pneumocystis using nested polymerase chain reaction (nPCR) amplification of
23 ng laser capture microdissection followed by nested polymerase chain reaction or reverse-transcribed
24 for all viral markers with the exception of nested polymerase chain reaction (PCR) analysis of PBMCs
25 ons, placenta, and cord blood were tested by nested polymerase chain reaction (PCR) and reverse-trans
27 period were analyzed for OspC types by semi-nested polymerase chain reaction (PCR) and sequencing, a
28 n, 200 HBV copies per milliliter) and a semi-nested polymerase chain reaction (PCR) assay (lower limi
30 eases and from normal subjects was tested by nested polymerase chain reaction (PCR) for HRV-5 provira
32 st study, parvovirus B19 DNA was detected by nested polymerase chain reaction (PCR) in 4 of 15 livers
34 NS), and we assessed the diagnostic value of nested polymerase chain reaction (PCR) testing for Trepo
37 and liver, when available, were tested using nested polymerase chain reaction (PCR) with primers in t
38 ed them using light and electron microscopy, nested polymerase chain reaction (PCR), and quantitative
43 n liver biopsy specimens with MMAs by using "nested" polymerase chain reaction (PCR), indicating that
45 molecular bacterial identification methods (nested polymerase chain reaction [PCR] and quantitative
47 tations were identified by a mutant-enriched nested polymerase chain reaction-restriction fragment le
48 n and were screened for XMRV proviral DNA by nested polymerase chain reaction specific for the env ge
50 tested for microchimerism using a sensitive nested polymerase chain reaction technique, and for anti
54 resence of HCV RNA in the CNS as detected by nested polymerase chain reaction was associated with a h
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