{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,21]],"date-time":"2026-07-21T10:47:15Z","timestamp":1784630835126,"version":"3.55.0"},"reference-count":18,"publisher":"S. Karger AG","issue":"6","license":[{"start":{"date-parts":[[2011,1,1]],"date-time":"2011-01-01T00:00:00Z","timestamp":1293840000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"},{"start":{"date-parts":[[2011,1,1]],"date-time":"2011-01-01T00:00:00Z","timestamp":1293840000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Acta Cytologica"],"published-print":{"date-parts":[[2011]]},"abstract":"<jats:p>&lt;i&gt;Objective:&lt;\/i&gt; To detect &lt;i&gt;BRAF&lt;\/i&gt; V600E mutation in thyroid fine-needle aspiration (FNA) slides and needle rinses (NR). &lt;i&gt;Study Design:&lt;\/i&gt; Tumor-enriched DNA was extracted from FNA smears, formalin-fixed paraffin-embedded (FFPE) sections, or NR specimens from 37 patients with confirmed papillary thyroid carcinoma or benign findings. An allele-specific primer selectively amplified the 1799 T&gt;A &lt;i&gt;BRAF&lt;\/i&gt; mutation while simultaneously blocking amplification of wild-type (WT) &lt;i&gt;BRAF&lt;\/i&gt; with an unlabeled probe during PCR. Mutation detection was accomplished by melting analysis of the probe. &lt;i&gt;Results:&lt;\/i&gt; Allele-specific\/blocking probe PCR confirmed the &lt;i&gt;BRAF&lt;\/i&gt; mutation status for 20 of 24 paired FNA\/FFPE samples previously tested by fluorescent probe real-time PCR. For the other 4 cases, the sensitive PCR method detected the &lt;i&gt;BRAF&lt;\/i&gt; mutation in all paired FNA\/FFPE samples. Previously, the mutation had been detected in only the FFPE samples. The &lt;i&gt;BRAF&lt;\/i&gt; mutation was also detected in some NR specimens. &lt;i&gt;Conclusion:&lt;\/i&gt; Treatment of patients with thyroid nodules is guided by FNA biopsy, which can be scantly cellular, necessitating a sensitive test that can detect low levels of &lt;i&gt;BRAF&lt;\/i&gt; V600E mutation in a WT background. We report increased detection of &lt;i&gt;BRAF&lt;\/i&gt; V600E in FNA specimens using allele-specific\/blocking probe PCR, which has an analytical sensitivity of 0.01%.<\/jats:p>","DOI":"10.1159\/000333453","type":"journal-article","created":{"date-parts":[[2011,12,9]],"date-time":"2011-12-09T08:20:51Z","timestamp":1323418851000},"page":"576-583","source":"Crossref","is-referenced-by-count":14,"title":["Allele-Specific PCR with Competitive Probe Blocking for Sensitive and Specific Detection of &lt;i&gt;BRAF&lt;\/i&gt; V600E in Thyroid Fine-Needle Aspiration Specimens"],"prefix":"10.1159","volume":"55","author":[{"given":"G. 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