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本文引用的文献
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Comparative RNA quantification of HIV-1 group M and non-M with the Roche Cobas AmpliPrep/Cobas TaqMan HIV-1 v2.0 and Abbott Real-Time HIV-1 PCR assays.
J Acquir Immune Defic Syndr. 2011 Mar 1;56(3):239-43. doi: 10.1097/QAI.0b013e3182099891.
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Comparison of the RealTime HIV-1, COBAS TaqMan 48 v1.0, Easy Q v1.2, and Versant v3.0 assays for determination of HIV-1 viral loads in a cohort of Canadian patients with diverse HIV subtype infections.
J Clin Microbiol. 2011 Jan;49(1):118-24. doi: 10.1128/JCM.00685-10. Epub 2010 Nov 17.
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Antiretroviral treatment of adult HIV infection: 2010 recommendations of the International AIDS Society-USA panel.
JAMA. 2010 Jul 21;304(3):321-33. doi: 10.1001/jama.2010.1004.
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Clinical and resistance consequences of misquantification of plasma and cerebrospinal fluid human immunodeficiency virus type 1 (HIV-1) RNA in samples from an HIV-1 subtype G-infected patient.
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Impact of discrepancies between the Abbott realtime and cobas TaqMan assays for quantification of human immunodeficiency virus type 1 group M non-B subtypes.
J Clin Microbiol. 2009 May;47(5):1543-5. doi: 10.1128/JCM.02134-08. Epub 2009 Mar 18.
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Performance of three commercial viral load assays, Versant human immunodeficiency virus type 1 (HIV-1) RNA bDNA v3.0, Cobas AmpliPrep/Cobas TaqMan HIV-1, and NucliSens HIV-1 EasyQ v1.2, testing HIV-1 non-B subtypes and recombinant variants.
J Clin Microbiol. 2008 Sep;46(9):2918-23. doi: 10.1128/JCM.02414-07. Epub 2008 Jul 2.
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Evaluation of the Roche Cobas TaqMan and Abbott RealTime extraction-quantification systems for HIV-1 subtypes.
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Comparison of four commercial quantitative HIV-1 assays for viral load monitoring in clinical daily routine.
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