| Literature DB >> 11163580 |
Abstract
Quantification of human immunodeficiency virus type 1 (HIV-1) is useful in obtaining information about the prognosis of patients and monitoring of antiviral therapy. Today, commercial assays based on reverse transcription-polymerase chain reaction (RT-PCR), the branched DNA (bDNA) technology and on nucleic acid sequence-based amplification (NASBA) are available. Clinical relevance of those assays is limited because of relatively poor reproducibility, especially for low copy numbers and unequal amplification dynamics for different genotypes. Better standardisation is most important in order to improve the reliability of quantitative molecular assays.Entities:
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Year: 2001 PMID: 11163580 DOI: 10.1016/s1386-6532(00)00152-9
Source DB: PubMed Journal: J Clin Virol ISSN: 1386-6532 Impact factor: 3.168