<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Niu L</submitter><funding>The Dunhill Medical Trust</funding><pagination>ziaf007</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11831985</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(3)</volume><pubmed_abstract>A wide range of specific microRNAs have been shown to have either positive or negative effects on osteoblast differentiation and function, with consequent changes in postnatal bone mass. A number of specific targets have been identified. We previously used CrispR-Cas9 to make a miR-455 null mouse, characterizing a behavioral phenotype with age. The current study identifies a bone phenotype, starting in younger animals. At 3 weeks of age, the miR-455 null mice (both male and female) display increased length of both long bones and vertebrae and, while this difference diminishes across 1 year, it remains significant. Increased bone formation in vivo is mirrored by an increase in osteogenesis from bone marrow-derived stem cells in vitro. This is accompanied by a decrease in osteoclastogenesis </pubmed_abstract><journal>JBMR plus</journal><pubmed_title>The microRNA-455 null mouse shows dysregulated bone turnover.</pubmed_title><pmcid>PMC11831985</pmcid><funding_grant_id>R476/0516</funding_grant_id><pubmed_authors>Hayman DJ</pubmed_authors><pubmed_authors>Young DA</pubmed_authors><pubmed_authors>Ersek A</pubmed_authors><pubmed_authors>Suelzu C</pubmed_authors><pubmed_authors>Niu L</pubmed_authors><pubmed_authors>Swingler TE</pubmed_authors><pubmed_authors>Barter MJ</pubmed_authors><pubmed_authors>Horwood N</pubmed_authors><pubmed_authors>Clark IM</pubmed_authors><pubmed_authors>Orriss IR</pubmed_authors></additional><is_claimable>false</is_claimable><name>The microRNA-455 null mouse shows dysregulated bone turnover.</name><description>A wide range of specific microRNAs have been shown to have either positive or negative effects on osteoblast differentiation and function, with consequent changes in postnatal bone mass. A number of specific targets have been identified. We previously used CrispR-Cas9 to make a miR-455 null mouse, characterizing a behavioral phenotype with age. The current study identifies a bone phenotype, starting in younger animals. At 3 weeks of age, the miR-455 null mice (both male and female) display increased length of both long bones and vertebrae and, while this difference diminishes across 1 year, it remains significant. Increased bone formation in vivo is mirrored by an increase in osteogenesis from bone marrow-derived stem cells in vitro. This is accompanied by a decrease in osteoclastogenesis </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-04-18T12:53:23.853Z</modification><creation>2025-04-04T00:51:45.677Z</creation></dates><accession>S-EPMC11831985</accession><cross_references><pubmed>39963339</pubmed><doi>10.1093/jbmrpl/ziaf007</doi></cross_references></HashMap>