<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Meas SJ</submitter><funding>NIA NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>National Aeronautics and Space Administration</funding><funding>UBC CIHR SRTC</funding><funding>National Institutes of Health</funding><funding>NASA Goddard Space Flight Center</funding><funding>NIAMS NIH HHS</funding><funding>Canadian Institutes of Health Research</funding><pagination>116973</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11651238</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>179</volume><pubmed_abstract>Age- and disuse-related bone loss both result in decreases in bone mineral density, cortical thickness, and trabecular thickness and connectivity. Disuse induces changes in the balance of bone formation and bone resorption like those seen with aging. There is a need to experimentally compare these two mechanisms at a structural and transcriptomic level to better understand how they may be similar or different. Bone microarchitecture and biomechanical properties were compared between 6- and 22-month-old C57BL/6 J male control mice and 6-month-old mice that were hindlimb unloaded (HLU) for 3 weeks. Epiphyseal trabecular bone was the compartment most affected by HLU and demonstrated an intermediate bone phenotype between age-matched controls and aged controls. RNA extracted from whole-bone ma</pubmed_abstract><journal>Bone</journal><pubmed_title>A comparison of bone microarchitectural and transcriptomic changes in murine long bones in response to hindlimb unloading and aging.</pubmed_title><pmcid>PMC11651238</pmcid><funding_grant_id>R01 AR068132</funding_grant_id><funding_grant_id>DFSA 454761</funding_grant_id><funding_grant_id>80NSSC18K1473</funding_grant_id><funding_grant_id>R01 AG013087</funding_grant_id><funding_grant_id>R01 DK128552</funding_grant_id><pubmed_authors>DeNapoli R</pubmed_authors><pubmed_authors>Ghosh P</pubmed_authors><pubmed_authors>Friedman MA</pubmed_authors><pubmed_authors>Meas SJ</pubmed_authors><pubmed_authors>Daire GM</pubmed_authors><pubmed_authors>Donahue HJ</pubmed_authors><pubmed_authors>Farr JN</pubmed_authors></additional><is_claimable>false</is_claimable><name>A comparison of bone microarchitectural and transcriptomic changes in murine long bones in response to hindlimb unloading and aging.</name><description>Age- and disuse-related bone loss both result in decreases in bone mineral density, cortical thickness, and trabecular thickness and connectivity. Disuse induces changes in the balance of bone formation and bone resorption like those seen with aging. There is a need to experimentally compare these two mechanisms at a structural and transcriptomic level to better understand how they may be similar or different. Bone microarchitecture and biomechanical properties were compared between 6- and 22-month-old C57BL/6 J male control mice and 6-month-old mice that were hindlimb unloaded (HLU) for 3 weeks. Epiphyseal trabecular bone was the compartment most affected by HLU and demonstrated an intermediate bone phenotype between age-matched controls and aged controls. RNA extracted from whole-bone ma</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-06-01T05:46:03.164Z</modification><creation>2025-04-05T10:19:13.303Z</creation></dates><accession>S-EPMC11651238</accession><cross_references><pubmed>37996046</pubmed><doi>10.1016/j.bone.2023.116973</doi></cross_references></HashMap>