<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bodofsky S</submitter><funding>Muhlenberg College</funding><funding>NIH Office of Research Infrastructure Programs</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><funding>NIGMS</funding><pagination>71-81</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6373727</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30</volume><pubmed_abstract>The nhr-67 nuclear receptor gene of Caenorhabditis elegans encodes the ortholog of the Drosophila tailless and vertebrate Tlx genes. In C. elegans, nhr-67 plays multiple roles in the development of the uterus during L2 and L3 larval stages. Four pre-VU cells are born in the L2 stage and form the precursor complement for the ventral surface of the mature uterus. One of the four pre-VU cells becomes the anchor cell (AC), which exits the cell cycle and differentiates, while the remaining three VU cells serve as stem cells that populate the ventral uterus. The nhr-67 gene functions in the development of both VU cell lineages and AC differentiation. Hypomorphic mutations in nhr-67 identify a 276bp region of the distal promoter that is sufficient to activate nhr-67 expression in pre-VU cells and</pubmed_abstract><journal>Gene expression patterns : GEP</journal><pubmed_title>A tissue-specific enhancer of the C. elegans nhr-67/tailless gene drives coordinated expression in uterine stem cells and the differentiated anchor cell.</pubmed_title><pmcid>PMC6373727</pmcid><funding_grant_id>1R15GM107799</funding_grant_id><funding_grant_id>R15 GM107799</funding_grant_id><funding_grant_id>P40 OD010440</funding_grant_id><pubmed_authors>Pioppo L</pubmed_authors><pubmed_authors>Birnbaum S</pubmed_authors><pubmed_authors>Lapadula D</pubmed_authors><pubmed_authors>Liberatore K</pubmed_authors><pubmed_authors>Thompson L</pubmed_authors><pubmed_authors>Kartik A</pubmed_authors><pubmed_authors>McClung G</pubmed_authors><pubmed_authors>Wightman B</pubmed_authors><pubmed_authors>Clever S</pubmed_authors><pubmed_authors>Bodofsky S</pubmed_authors></additional><is_claimable>false</is_claimable><name>A tissue-specific enhancer of the C. elegans nhr-67/tailless gene drives coordinated expression in uterine stem cells and the differentiated anchor cell.</name><description>The nhr-67 nuclear receptor gene of Caenorhabditis elegans encodes the ortholog of the Drosophila tailless and vertebrate Tlx genes. In C. elegans, nhr-67 plays multiple roles in the development of the uterus during L2 and L3 larval stages. Four pre-VU cells are born in the L2 stage and form the precursor complement for the ventral surface of the mature uterus. One of the four pre-VU cells becomes the anchor cell (AC), which exits the cell cycle and differentiates, while the remaining three VU cells serve as stem cells that populate the ventral uterus. The nhr-67 gene functions in the development of both VU cell lineages and AC differentiation. Hypomorphic mutations in nhr-67 identify a 276bp region of the distal promoter that is sufficient to activate nhr-67 expression in pre-VU cells and</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Dec</publication><modification>2025-04-19T01:49:39.99Z</modification><creation>2020-10-29T10:19:57Z</creation></dates><accession>S-EPMC6373727</accession><cross_references><pubmed>30404043</pubmed><doi>10.1016/j.gep.2018.10.003</doi></cross_references></HashMap>