Aslanzadeh, J. (1993). Application of hydroxylamine hydrochloride for post-PCR sterilization. Mol Cell Probes, 7, 145-150.

Belak, S., & Ballagi-Pordany, A. (1993). Experiences on the application of the polymerase chain reaction in a diagnostic laboratory. Mol Cell Probes, 7, 241-248.

Bottger, E.C. (1990). Frequent contamination of Taq Polymerase with DNA. Clin Chem, 36(6), 1258-1259.

Cimino, G.D., Metchette, K.C., Tessman, J.W., Hearst, J.E., & Isaacs, S.T. (1991). Post-PCR sterilization: a method to control carryover contamination for the polymerase chain reaction. Nucleic Acids Res, 19, 99-107.

Corless, C.E., Guiver, M., Borrow, R., Edwards-Jones, V., Kaczmarski, E.B., & Fox, J. (2000). Contamination and sensitivity issues with a real-time universal 16S rRNA PCR. J Clin Microbiol, 38(5), 1747-1752.

De la Viuda, M., Fille, M., Ruiz, J., & Aslanzadeh, J. (1996). Use of AmpliWax to optimize amplicon sterilization by isopsoralen. J Clin Microbiol, 34(12), 3115-3119.

DeFilippes, F.M. (1991). Decontaminating the polymerase chain reaction. Biotechniques, 10(1), 26-30.

Espy, M.J., Smith, T.F., & Persing, D.H. (1993). Dependence of polymerase chain reaction product inactivation protocols on amplicon length and sequence composition. J Clin Microbiol, 31(9), 2361-2365.

Fahle, G.A., Gill, V.J., & Fischer, S.H. (1999). Optimal activation of isopsoralen to prevent amplicon carryover. J Clin Microbiol, 37(1), 261-262.

Gobet P., Buisson, J.C., Vagner, O., Naciri, M., Grappin, M., Comparot, S., Harly, G., Aubert, D., Varga, I.,Camerlynck, P., & Bonnin, A. (1997). Detection of Cryptosporidium parvum DNA in formed human feces by a sensitive PCR-based assay including uracil-N-glycosylase inactivation. J Clin Microbiol, 35(1), 254-256.

Hughes, M.S., Beck, L.A., & Skuce, R.A. (1994). Identification and elimination of DNA sequences in Taq DNA Polymerase. J Clin Microbiol, 32(8), 2007-2008.

Isaacs, S.T., Tessman, J.W., Metchette, K.C., Hearst, J.E., & Cimino, G.D. (1991). Post-PCR sterilization: development and application to an HIV-1 diagnostic assay. Nucleic Acids Res, 19(1), 109-116.

Kao, S.Y., Niemiec, T.M., Loeffelholz, M.J., Dale, B. & Rotbart, H.A. (1995). Direct and uninterrupted RNA amplification of enteroviruses with colorimetric microwell detection. Clin Diagn Virol, 3, 247-257.

Kaul, K., Luke, S., McGurn, C., Snowden, N., Monti, C., & Willard W.A. (1996). Amplification of residual DNA sequences in sterile bronchoscopes leading to false-positive PCR results. J Clin Microbiol, 34(8), 1949-1951.

Kitchin, P.A., Szotyori, Z., Fromholc, C., & Almond, N. (1990). Avoidance of false positives. Nature, 344, 201.

Kwok, S., & Higuchi, R. (1989). Avoiding false positives with PCR. Nature, 339, 237-238.

Loewy, Z.G., Mecca, J., & Diaco, R. (1994). Enhancement of Borrelia burgdorferi PCR by uracil N-glycosylase. J Clin Microbiol, 32(1), 135-138.

Longo, M.C., Berninger, M.S., & Hartley, J.L. (1990). Use of uracil DNA glycosylase to control carry-over contamination in polymerase chain reaction. Gene, 93, 125-128.

Ou, C.Y., Moore, J.L., & Schochetman, G. (1991). Use of UV irradiation to reduce false positivity in polymerase chain reaction. Biotechniques, 10(4), 442-445.

Martin, T.B., Hillyard, D.R., Litwin, C.M., Taggart, E.W., Jaskowski T.D., & Hill, H.R. (2000). Evaluation of a PCR probe capture assay for the detection of Toxoplasma gondii. Microbiol Infect Dis, 113, 714-721.

Mohamed, N., Elfaitouri, A., Fohlman, J., Friman, G., & Blomberg, J. (2004). A sensitive and quantitative single-tube real-time reverse transcriptase-PCR for detection of enteroviral RNA. J Clin Virol, 30, 150-156.

Patel, R., Grogg, K.L., Edwards, W.D., Wright, A.J., & Schwenk, N.M. (2000). Death from inappropriate therapy for Lyme disease. Clin Infect Dis, 31, 1107-1109.

Persing, D.H. (1991). Polymerase chain reaction: trenches to benches. J Clin Microbiol, 29(7), 1281-1285.

Persing, D.H., & Cimino, G.D. (1993). Amplification product inactivation methods. In: Persing, D.H., Smith, T.F., Tenover F.C., et al. eds. Diagnostic Molecular Microbiology: Principles and Applications. ASM Press, Washington, DC, pp. 105-121.

Pierce, K.E., & Wangh, L.J. (2004). Effectiveness and limitations of uracil-DNA glycosy-lases in sensitive real-time PCR assays. Biotechniques, 36(1), 44-48.

Poddar, S.K., Sawyer, M.H., & Connor, J.D. (1997). Optimized PCR amplification of influenza A virus RNA using the Tth DNA polymerase, incorporating uracil N glycosylase (UNG) in a single tube reaction. J Clin Lab Anal, 11(6), 323-327.

Prince, A.M., &AndrusL. (1992). PCR: How to kill unwanted DNA. Biotechniques, 12(3), 358-360.

Ramzan, N.N., Loftus, E., Burgart, L.J., Rooney, M., Batts, K.P., Wiesner, R.H., Fredricks, D.N., Relman, D.A., & Persing, D.H. (1997). Diagnosis and monitoring of Whipple disease by polymerase chain reaction. Ann Int Med, 126(7), 520-527.

Rys, P.N., & Persing, D.H. (1993). Preventing false positives: quantitative evaluation of three protocols for inactivation of polymerase chain reaction amplification products. J Clin Microbiol, 31(9), 2356-2360.

Sarmiento, O.L., Weigle, K.A., Alexander, J., Weber, D.J., & Miller, W.C. (2003). Assessment by meta-analysis of PCR for diagnosis of smear-negative pulmonary tuberculosis. J Clin Microbiol, 41(7), 3233-3240.

Sarkar, G., & Sommer, S.S. (1990). Shedding light on PCR contamination. Nature, 343, 27.

Sefers, S. Pei, Z., & Tang, Y. W. (2005). False positives and false negatives encountered in the diagnostic molecular microbiology. Rev Med Microbiol, 16, 59-67.

Shim, T.S., Chi, H.S., Do Lee, S., Koh, Y., Kim, W.S., Kim, D.S., & Kim, W.D. (2002). Adequately washed bronchoscope does not induce false-positive amplification tests on bronchial aspirates in the diagnosis of pulmonary tuberculosis. Chest, 121(3), 774-781.

Taggart, E.W., Carroll, K.C., Byington C.L., Crist, G.A., & Hillyard, D.R. (2002). Use of heat labile UNG in an RT-PCR assay for enterovirus detection. J Virol Methods, 105, 57-65.

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