<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2</volume><submitter>Liu Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Molecular genetic alterations with prognostic significance have been described in childhood acute myeloid leukemia (AML). The aim of this study was to establish cost-effective techniques to detect mutations of FMS-like tyrosine kinase 3 (FLT3), nucleophosmin 1 (NPM1), and a partial tandem duplication within the mixed-lineage leukemia (MLL-PTD) genes in childhood AML.&lt;h4>Procedure&lt;/h4>Ninety-nine children with newly diagnosed AML were included in this study. We developed a fluorescent dye SYTO-82 based high-resolution melting (HRM) curve analysis to detect FLT3 internal tandem duplication (FLT3-ITD), FLT3 tyrosine kinase domain (FLT3-TKD), and NPM1 mutations. MLL-PTD was screened by real-time quantitative PCR.&lt;h4>Results&lt;/h4>The HRM methodology correlated well with gold s</pubmed_abstract><journal>Frontiers in pediatrics</journal><pagination>96</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4158872</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High-resolution melting curve analysis, a rapid and affordable method for mutation analysis in childhood acute myeloid leukemia.</pubmed_title><pmcid>PMC4158872</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Tang J</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Gaynon PS</pubmed_authors><pubmed_authors>Shen S</pubmed_authors><pubmed_authors>Sun W</pubmed_authors><pubmed_authors>Wakamatsu P</pubmed_authors><pubmed_authors>Xue H</pubmed_authors></additional><is_claimable>false</is_claimable><name>High-resolution melting curve analysis, a rapid and affordable method for mutation analysis in childhood acute myeloid leukemia.</name><description>&lt;h4>Background&lt;/h4>Molecular genetic alterations with prognostic significance have been described in childhood acute myeloid leukemia (AML). The aim of this study was to establish cost-effective techniques to detect mutations of FMS-like tyrosine kinase 3 (FLT3), nucleophosmin 1 (NPM1), and a partial tandem duplication within the mixed-lineage leukemia (MLL-PTD) genes in childhood AML.&lt;h4>Procedure&lt;/h4>Ninety-nine children with newly diagnosed AML were included in this study. We developed a fluorescent dye SYTO-82 based high-resolution melting (HRM) curve analysis to detect FLT3 internal tandem duplication (FLT3-ITD), FLT3 tyrosine kinase domain (FLT3-TKD), and NPM1 mutations. MLL-PTD was screened by real-time quantitative PCR.&lt;h4>Results&lt;/h4>The HRM methodology correlated well with gold s</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2025-04-04T11:20:34.13Z</modification><creation>2019-03-27T01:35:26Z</creation></dates><accession>S-EPMC4158872</accession><cross_references><pubmed>25250304</pubmed><doi>10.3389/fped.2014.00096</doi></cross_references></HashMap>