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RNA病毒扩增检测的质控品和标准品研究进展 被引量:20

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作者 李金明
出处 《中华检验医学杂志》 CAS CSCD 北大核心 2004年第12期873-874,共2页 Chinese Journal of Laboratory Medicine
基金 国家自然科学研究基金资助项目 (3 0 3 713 65 ) 首都医学发展科研基金资助项目 (2 0 0 2 3 0 41)
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  • 1Fronhoffs S, Totzke G, Stier S, et al. A method for the rapid construction of cRNA standard curves in quantitative real-time reverse tanscription polymerase chain reaction. Mol Cell Probes, 2002,16:99-110.
  • 2Alms WJ, Braun-Elwert L, James SP, et al. Simultaneous quantitation of cytokine mRNAs by reverse transcription-polymerase chain reaction using multiple internal standard cRNAs. Diagn Mol Pathol, 1996,5: 88-97.
  • 3Kim K, Park J, Chung Y, et al. Use of internal standard RNA molecules for the RT-PCR amplification of the faeces-borne RNA viruses. J Virol Methods, 2002,104:107-115.
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  • 5Matthews JL, Chung M, Matyas RJ. Persistent DNA contamination in competitive RT-PCR using cRNA internal standards: identity, quantity, and control. Biotechniques, 2002,32:1412-1414, 1416-1417.
  • 6Pickett GG, Peabody DS. Encapsidation of heterologous RNAs by bacteriophage MS2 coat protein. Nucleic Acids Res, 1993,21:4621-4626.
  • 7Stockley PG, Stonehouse NJ, Murray JB, et al. Probing sequence-specific RNA recognition by the bacteriophage MS2 coat protein. Nucleic Acids Res, 1995, 23: 2512-2518.
  • 8Cartwright CP. Synthetic Viral Particles Promise to Be Valuable in the Standardization of Molecular Diagnostic Assays for Hepatitis C Virus. Clin Chem, 1999,45: 2057-2059.
  • 9Cindy R, Peach W, Winkler M, et al. Ribonuclease-resisting RNA controls (armored RNA) for reverse transcription-PCR,branched DNA, and genotyping assays for hepatitis C virus. Clin Chem, 1999,45:2079-2085.
  • 10Pasloske BL, Walkerpeach CR, Obermoeller RD, et al. Armored RNA technology for production of ribonuclease-resistant viral RNA controls and standards.J Clin Microbiol, 1998,36:3590-3594.

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