<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(1)</volume><submitter>Piechota M</submitter><funding>National Science Centre, Poland</funding><pubmed_abstract>Glucocorticoids, acting through the glucocorticoid receptor (GR), control metabolism, maintain homeostasis, and enable adaptive responses to environmental challenges. Their function has been comprehensively studied, leading to identification of numerous tissue-specific GR-dependent mechanisms. Abundant evidence shows that GR-triggered responses differ across tissues, however, the extent of this specificity was not comprehensively explored. It is also unknown how particular GR-induced molecular patterns are translated into profile of higher-level human traits. Here, we examine cross-tissue effects of GR activation on gene expression. We assessed changes induced by stimulation with GR agonist, dexamethasone in nine tissues (adrenal cortex, perigonadal adipose tissue, hypothalamus, liver, kid</pubmed_abstract><journal>BMC genomics</journal><pagination>462</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12063231</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A cross-tissue transcriptomic approach decodes glucocorticoid receptor-dependent links to human metabolic phenotypes.</pubmed_title><pmcid>PMC12063231</pmcid><pubmed_authors>Skupio U</pubmed_authors><pubmed_authors>Golda S</pubmed_authors><pubmed_authors>Hajto J</pubmed_authors><pubmed_authors>Slezak M</pubmed_authors><pubmed_authors>Piechota M</pubmed_authors><pubmed_authors>Borczyk M</pubmed_authors><pubmed_authors>Zieba M</pubmed_authors><pubmed_authors>Korostynski M</pubmed_authors><pubmed_authors>Parkitna JR</pubmed_authors></additional><is_claimable>false</is_claimable><name>A cross-tissue transcriptomic approach decodes glucocorticoid receptor-dependent links to human metabolic phenotypes.</name><description>Glucocorticoids, acting through the glucocorticoid receptor (GR), control metabolism, maintain homeostasis, and enable adaptive responses to environmental challenges. Their function has been comprehensively studied, leading to identification of numerous tissue-specific GR-dependent mechanisms. Abundant evidence shows that GR-triggered responses differ across tissues, however, the extent of this specificity was not comprehensively explored. It is also unknown how particular GR-induced molecular patterns are translated into profile of higher-level human traits. Here, we examine cross-tissue effects of GR activation on gene expression. We assessed changes induced by stimulation with GR agonist, dexamethasone in nine tissues (adrenal cortex, perigonadal adipose tissue, hypothalamus, liver, kid</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-04-15T03:25:51.648Z</modification><creation>2026-04-15T03:15:19.064Z</creation></dates><accession>S-EPMC12063231</accession><cross_references><pubmed>40346507</pubmed><doi>10.1186/s12864-025-11676-w</doi></cross_references></HashMap>