<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>32(5)</volume><submitter>Park KS</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>Fast detection of β-lactamase (&lt;i>bla&lt;/i>) genes can minimize the spread of antibiotic resistance. Although several molecular diagnostic methods have been developed to detect limited &lt;i>bla&lt;/i> gene types, these methods have significant limitations, such as their failure to detect almost all clinically available &lt;i>bla&lt;/i> genes. We have evaluated a further refinement of our fast and accurate molecular method, developed to overcome these limitations, using clinical isolates.&lt;h4>Methods&lt;/h4&gt;We have recently developed the efficient large-scale &lt;i>bla&lt;/i> detection method (&lt;sub>large-scale&lt;/sub>&lt;i>bla&lt;/i>Finder) that can detect &lt;i>bla&lt;/i> gene types including almost all clinically available 1,352 &lt;i>bla&lt;/i> genes with perfect specificity and sensitivity. Using this method, w</pubmed_abstract><journal>Pakistan journal of medical sciences</journal><pagination>1309-1311</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5103155</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Why cannot a β-lactamase gene be detected using an efficient molecular diagnostic method?</pubmed_title><pmcid>PMC5103155</pmcid><pubmed_authors>Park M</pubmed_authors><pubmed_authors>Lee SH</pubmed_authors><pubmed_authors>Karim AM</pubmed_authors><pubmed_authors>Park KS</pubmed_authors><pubmed_authors>Lee JH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Why cannot a β-lactamase gene be detected using an efficient molecular diagnostic method?</name><description>&lt;h4>Objective&lt;/h4>Fast detection of β-lactamase (&lt;i>bla&lt;/i>) genes can minimize the spread of antibiotic resistance. Although several molecular diagnostic methods have been developed to detect limited &lt;i>bla&lt;/i> gene types, these methods have significant limitations, such as their failure to detect almost all clinically available &lt;i>bla&lt;/i> genes. We have evaluated a further refinement of our fast and accurate molecular method, developed to overcome these limitations, using clinical isolates.&lt;h4>Methods&lt;/h4&gt;We have recently developed the efficient large-scale &lt;i>bla&lt;/i> detection method (&lt;sub>large-scale&lt;/sub>&lt;i>bla&lt;/i>Finder) that can detect &lt;i>bla&lt;/i> gene types including almost all clinically available 1,352 &lt;i>bla&lt;/i> genes with perfect specificity and sensitivity. Using this method, w</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Sep-Oct</publication><modification>2025-05-29T20:20:37.668Z</modification><creation>2025-05-29T20:20:37.668Z</creation></dates><accession>S-EPMC5103155</accession><cross_references><pubmed>27882043</pubmed><doi>10.12669/pjms.325.9837</doi></cross_references></HashMap>