<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mendenhall AR</submitter><funding>NIGMS NIH HHS</funding><pagination>167-78</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2646460</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(3)</volume><pubmed_abstract>Identifying genotypes and phenotypes that enhance an organism's ability to survive stress is of interest. We used Caenorhabditis elegans mutants, RNA interference (RNAi), and the chemical 5-fluorodeoxyuridine (FUDR) to test the hypothesis that a reduction in progeny would increase oxygen deprivation (anoxia) survival. In the hermaphrodite gonad, germ line processes such as spermatogenesis and oogenesis can be simultaneously as well as independently disrupted by genetic mutations. We analyzed genetic mutants [glp-1(q158), glp-4(bn2ts), plc-1(rx1), ksr-1(ku68), fog-2(q71), fem-3(q20), spe-9(hc52ts), fer-15(hc15ts)] with reduced progeny production due to various reproductive defects. Furthermore, we used RNAi to inhibit the function of gene products in the RTK/Ras/MAPK signaling pathway, whic</pubmed_abstract><journal>Physiological genomics</journal><pubmed_title>Reduction in ovulation or male sex phenotype increases long-term anoxia survival in a daf-16-independent manner in Caenorhabditis elegans.</pubmed_title><pmcid>PMC2646460</pmcid><funding_grant_id>R01-GM-069419</funding_grant_id><pubmed_authors>Mohan DP</pubmed_authors><pubmed_authors>Mendenhall AR</pubmed_authors><pubmed_authors>Padilla PA</pubmed_authors><pubmed_authors>LeBlanc MG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reduction in ovulation or male sex phenotype increases long-term anoxia survival in a daf-16-independent manner in Caenorhabditis elegans.</name><description>Identifying genotypes and phenotypes that enhance an organism's ability to survive stress is of interest. We used Caenorhabditis elegans mutants, RNA interference (RNAi), and the chemical 5-fluorodeoxyuridine (FUDR) to test the hypothesis that a reduction in progeny would increase oxygen deprivation (anoxia) survival. In the hermaphrodite gonad, germ line processes such as spermatogenesis and oogenesis can be simultaneously as well as independently disrupted by genetic mutations. We analyzed genetic mutants [glp-1(q158), glp-4(bn2ts), plc-1(rx1), ksr-1(ku68), fog-2(q71), fem-3(q20), spe-9(hc52ts), fer-15(hc15ts)] with reduced progeny production due to various reproductive defects. Furthermore, we used RNAi to inhibit the function of gene products in the RTK/Ras/MAPK signaling pathway, whic</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Feb</publication><modification>2025-04-04T07:58:04.458Z</modification><creation>2019-03-27T00:20:51Z</creation></dates><accession>S-EPMC2646460</accession><cross_references><pubmed>19050081</pubmed><doi>10.1152/physiolgenomics.90278.2008</doi></cross_references></HashMap>