<?xml version="1.0"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title>Development and validation of an oligonucleotide ligation assay to detect lamivudine resistance in hepatitis B virus</dc:title>
  <dc:creator>Beck, I. A.</dc:creator>
  <dc:creator>Payant, R.</dc:creator>
  <dc:creator>/Ngo-Giang-Huong, Nicole</dc:creator>
  <dc:creator>Khamduang, W.</dc:creator>
  <dc:creator>Laomanit, L.</dc:creator>
  <dc:creator>/Jourdain, Gonzague</dc:creator>
  <dc:creator>Frenkel, L. M.</dc:creator>
  <dc:subject>HBV drug resistance</dc:subject>
  <dc:subject>Oligonucleotide ligation assay</dc:subject>
  <dc:subject>Lamivudine resistance</dc:subject>
  <dc:subject>HBV treatment</dc:subject>
  <dc:description>Treatment of chronic hepatitis B virus (HBV) infection with lamivudine-monotherapy rapidly selects mutant variants in a high proportion of individuals. Monitoring lamivudine resistance by consensus sequencing is costly and insensitive for detection of minority variants. An oligonucleotide ligation assay (OLA) for HBV lamivudine-resistance was developed and compared to consensus sequencing. Both assays detected drug resistance mutations in 35/64 (54.7%) specimens evaluated, and OLA detected minority mutants in an additional six (9.4%). OLA may offer a sensitive and inexpensive alternative to consensus sequencing for detection of HBV drug resistance in resource-limited settings.</dc:description>
  <dc:date>2016</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010066848</dc:identifier>
  <dc:identifier>fdi:010066848</dc:identifier>
  <dc:identifier>Beck I. A., Payant R., Ngo-Giang-Huong Nicole, Khamduang W., Laomanit L., Jourdain Gonzague, Frenkel L. M.. Development and validation of an oligonucleotide ligation assay to detect lamivudine resistance in hepatitis B virus. 2016, 233,  51-55</dc:identifier>
  <dc:language>EN</dc:language>
  <dc:coverage>THAILANDE</dc:coverage>
</oai_dc:dc>
