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Volumn 22, Issue 12, 2003, Pages 764-767

Preliminary Comparison of Three LightCycler PCR Assays for the Detection of Herpes Simplex Virus in Swab Specimens

Author keywords

[No Author keywords available]

Indexed keywords

VIRUS DNA;

EID: 0346992049     PISSN: 09349723     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10096-003-1031-2     Document Type: Article
Times cited : (20)

References (10)
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    • Madhavan HN, Priya K, Anand AR, Therese KL (1999) Detection of herpes simplex virus (HSV) genome using polymerase chain reaction (PCR) in clinical samples: comparison of PCR with standard laboratory methods for the detection of HSV. J Clin Virol 14:145-151
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  • 2
    • 19044386827 scopus 로고    scopus 로고
    • Detection and subtyping of herpes simplex virus in clinical samples by LightCycler PCR, enzyme immunoassay and cell culture
    • Burrows J, Nitsche A, Bayly B, Walker E, Higgins G, Kok T (2002) Detection and subtyping of herpes simplex virus in clinical samples by LightCycler PCR, enzyme immunoassay and cell culture. BMC Microbiol 9:12
    • (2002) BMC Microbiol , vol.9 , pp. 12
    • Burrows, J.1    Nitsche, A.2    Bayly, B.3    Walker, E.4    Higgins, G.5    Kok, T.6
  • 4
    • 0034027659 scopus 로고    scopus 로고
    • Fast and type-specific analysis of herpes simplex virus types 1 and 2 by rapid PCR and fluorescence melting curve analysis
    • Schalasta G, Arents A, Schmid M, Braun RW, Enders G (2000) Fast and type-specific analysis of herpes simplex virus types 1 and 2 by rapid PCR and fluorescence melting curve analysis. Infection 28:85-91
    • (2000) Infection , vol.28 , pp. 85-91
    • Schalasta, G.1    Arents, A.2    Schmid, M.3    Braun, R.W.4    Enders, G.5
  • 5
    • 0034788151 scopus 로고    scopus 로고
    • Detection of cytomegalovirus DNA in human specimens by LightCycler PCR: Melting point analysis is mandatory to detect virus strains with point mutations in the target sequence of the hybridization probes
    • Schaade L, Kockelkorn P, Ritter K, Kleines M (2001) Detection of cytomegalovirus DNA in human specimens by LightCycler PCR: melting point analysis is mandatory to detect virus strains with point mutations in the target sequence of the hybridization probes. J Clin Microbiol 39:3809
    • (2001) J Clin Microbiol , vol.39 , pp. 3809
    • Schaade, L.1    Kockelkorn, P.2    Ritter, K.3    Kleines, M.4
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    • A quantification of human cells using an ERV-3 real time PCR assay
    • Yuan CC, Miley W, Waters D (2001) A quantification of human cells using an ERV-3 real time PCR assay. J Virol Methods 91:109-117
    • (2001) J Virol Methods , vol.91 , pp. 109-117
    • Yuan, C.C.1    Miley, W.2    Waters, D.3
  • 7
    • 0031044820 scopus 로고    scopus 로고
    • Aseptic meningitis and encephalitis: The role of PCR in the diagnostic laboratory
    • Read SJ, Jeffery KJ, Bangham CR (1997) Aseptic meningitis and encephalitis: the role of PCR in the diagnostic laboratory. J Clin Microbiol 35:691-696
    • (1997) J Clin Microbiol , vol.35 , pp. 691-696
    • Read, S.J.1    Jeffery, K.J.2    Bangham, C.R.3
  • 8
    • 0034984547 scopus 로고    scopus 로고
    • Quantitative PCR-ELAHA for the determination of retroviral vector transduction efficiency
    • Mackay IM, Metharom P, Sloots TP, Wei MQ (2001) Quantitative PCR-ELAHA for the determination of retroviral vector transduction efficiency. Mol Ther 3:801-808
    • (2001) Mol Ther , vol.3 , pp. 801-808
    • Mackay, I.M.1    Metharom, P.2    Sloots, T.P.3    Wei, M.Q.4
  • 9
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    • Development of a high-throughput quantitative assay for detecting herpes simplex virus DNA in clinical samples
    • Ryncarz AJ, Goddard J, Wald A, Huang ML, Roizman B, Corey L (1999) Development of a high-throughput quantitative assay for detecting herpes simplex virus DNA in clinical samples. J Clin Microbiol 37:1941-1947
    • (1999) J Clin Microbiol , vol.37 , pp. 1941-1947
    • Ryncarz, A.J.1    Goddard, J.2    Wald, A.3    Huang, M.L.4    Roizman, B.5    Corey, L.6
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    • A convenient approach to the generation of multiple internal control DNA for a panel of real-time PCR assays
    • Stocher M, Leb V, Berg J (2003) A convenient approach to the generation of multiple internal control DNA for a panel of real-time PCR assays. J Virol Methods 108:1-8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.