<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25(11-12)</volume><submitter>Drummond JB</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To study the beta-catenin gene in a group of Mayer-Rokitansky-Küster-Hauser patients.&lt;h4>Methods&lt;/h4>Twelve patients with the Mayer-Rokitansky-Küster-Hauser syndrome were included in this study. DNA was extracted from peripheral blood and the region codifying beta-catenin GSK-3beta phosphorylation sites on exon 3 was amplified. PCR products were purified and directly sequenced.&lt;h4>Results&lt;/h4>No mutations were found in the GSK-3beta phosphorylation sites on exon 3 of beta-catenin gene in this group of patients with the MRKH syndrome.&lt;h4>Conclusions&lt;/h4>beta-catenin gene mutations are an unlikely cause of the MRKH syndrome.</pubmed_abstract><journal>Journal of assisted reproduction and genetics</journal><pagination>511-4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2593771</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Molecular analysis of the beta-catenin gene in patients with the Mayer-Rokitansky-Kuster-Hauser syndrome.</pubmed_title><pmcid>PMC2593771</pmcid><pubmed_authors>Carvalho JS</pubmed_authors><pubmed_authors>De Marco L</pubmed_authors><pubmed_authors>Drummond JB</pubmed_authors><pubmed_authors>Rezende CF</pubmed_authors><pubmed_authors>Peixoto FC</pubmed_authors><pubmed_authors>Reis FM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular analysis of the beta-catenin gene in patients with the Mayer-Rokitansky-Kuster-Hauser syndrome.</name><description>&lt;h4>Purpose&lt;/h4>To study the beta-catenin gene in a group of Mayer-Rokitansky-Küster-Hauser patients.&lt;h4>Methods&lt;/h4>Twelve patients with the Mayer-Rokitansky-Küster-Hauser syndrome were included in this study. DNA was extracted from peripheral blood and the region codifying beta-catenin GSK-3beta phosphorylation sites on exon 3 was amplified. PCR products were purified and directly sequenced.&lt;h4>Results&lt;/h4>No mutations were found in the GSK-3beta phosphorylation sites on exon 3 of beta-catenin gene in this group of patients with the MRKH syndrome.&lt;h4>Conclusions&lt;/h4>beta-catenin gene mutations are an unlikely cause of the MRKH syndrome.</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Nov-Dec</publication><modification>2025-06-01T01:15:22.33Z</modification><creation>2025-06-01T01:15:22.33Z</creation></dates><accession>S-EPMC2593771</accession><cross_references><pubmed>18979195</pubmed><doi>10.1007/s10815-008-9261-y</doi></cross_references></HashMap>