<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Andries V</submitter><funding>Stichting Tegen Kanker</funding><funding>Federaal Wetenschapsbeleid</funding><funding>Fonds Wetenschappelijk Onderzoek</funding><funding>Universiteit Gent</funding><funding>Federaal Wetenschapsbeleid (BE)</funding><pagination>598</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6580527</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>19(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>NANOS3 is a gene conserved throughout evolution. Despite the quite low conservation of Nanos sequences between different organisms and even between Nanos paralogs, their role in germ cell development is remarkably universal. Human Nanos3 expression is normally restricted to the gonads and the brain. However, ectopic activation of this gene has been detected in various human cancers. Until now, Nanos3 and other Nanos proteins have been studied almost exclusively in germ cell development.&lt;h4>Methods&lt;/h4>Transgenic mice were generated by targeted insertion of a human Nanos3 cDNA into the ROSA26 locus. The transgene could be spatiotemporally induced by Cre recombinase activity removing an upstream floxed STOP cassette. A lung tumor model with ectopic Nanos3 expression was ba</pubmed_abstract><journal>BMC cancer</journal><pubmed_title>A new mouse model to study the role of ectopic Nanos3 expression in cancer.</pubmed_title><pmcid>PMC6580527</pmcid><funding_grant_id>2012-191</funding_grant_id><funding_grant_id>B/13590</funding_grant_id><funding_grant_id>IAP7/07</funding_grant_id><funding_grant_id>G.0235.10N</funding_grant_id><funding_grant_id>Concerted Research Actions BOF08/GOA/019</funding_grant_id><pubmed_authors>Andries V</pubmed_authors><pubmed_authors>Hochepied T</pubmed_authors><pubmed_authors>Lemeire K</pubmed_authors><pubmed_authors>Staes K</pubmed_authors><pubmed_authors>Birembaut P</pubmed_authors><pubmed_authors>Berx G</pubmed_authors><pubmed_authors>Taminau J</pubmed_authors><pubmed_authors>van Roy F</pubmed_authors><pubmed_authors>De Keuckelaere E</pubmed_authors></additional><is_claimable>false</is_claimable><name>A new mouse model to study the role of ectopic Nanos3 expression in cancer.</name><description>&lt;h4>Background&lt;/h4>NANOS3 is a gene conserved throughout evolution. Despite the quite low conservation of Nanos sequences between different organisms and even between Nanos paralogs, their role in germ cell development is remarkably universal. Human Nanos3 expression is normally restricted to the gonads and the brain. However, ectopic activation of this gene has been detected in various human cancers. Until now, Nanos3 and other Nanos proteins have been studied almost exclusively in germ cell development.&lt;h4>Methods&lt;/h4>Transgenic mice were generated by targeted insertion of a human Nanos3 cDNA into the ROSA26 locus. The transgene could be spatiotemporally induced by Cre recombinase activity removing an upstream floxed STOP cassette. A lung tumor model with ectopic Nanos3 expression was ba</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2025-04-18T13:30:40.975Z</modification><creation>2019-07-24T07:20:37Z</creation></dates><accession>S-EPMC6580527</accession><cross_references><pubmed>31208373</pubmed><doi>10.1186/s12885-019-5807-x</doi></cross_references></HashMap>