<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(12)</volume><submitter>Rodriguez-Ortiz A</submitter><pubmed_abstract>DNA methylation and histone posttranslational modifications are epigenetics processes that contribute to neurophenotype of Down Syndrome (DS). Previous reports present strong evidence that nonhistone high-mobility-group N proteins (HMGN) are epigenetic regulators. They play important functions in various process to maintain homeostasis in the brain. We aimed to analyze the differential expression of five human HMGN genes in some brain structures and age ranks from DS postmortem brain samples. Methodology: We performed a computational analysis of the expression of human HMGN from the data of a DNA microarray experiment (GEO database ID GSE59630). Using the transformed log2 data, we analyzed the differential expression of five HMGN genes in several brain areas associated with cognition in pa</pubmed_abstract><journal>Genes</journal><pagination>2000</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8700945</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Spatial and Temporal Expression of High-Mobility-Group Nucleosome-Binding (HMGN) Genes in Brain Areas Associated with Cognition in Individuals with Down Syndrome.</pubmed_title><pmcid>PMC8700945</pmcid><pubmed_authors>Mina-Paz Y</pubmed_authors><pubmed_authors>Rodriguez-Ortiz A</pubmed_authors><pubmed_authors>Montoya-Villegas JC</pubmed_authors><pubmed_authors>Garcia-Vallejo F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Spatial and Temporal Expression of High-Mobility-Group Nucleosome-Binding (HMGN) Genes in Brain Areas Associated with Cognition in Individuals with Down Syndrome.</name><description>DNA methylation and histone posttranslational modifications are epigenetics processes that contribute to neurophenotype of Down Syndrome (DS). Previous reports present strong evidence that nonhistone high-mobility-group N proteins (HMGN) are epigenetic regulators. They play important functions in various process to maintain homeostasis in the brain. We aimed to analyze the differential expression of five human HMGN genes in some brain structures and age ranks from DS postmortem brain samples. Methodology: We performed a computational analysis of the expression of human HMGN from the data of a DNA microarray experiment (GEO database ID GSE59630). Using the transformed log2 data, we analyzed the differential expression of five HMGN genes in several brain areas associated with cognition in pa</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Dec</publication><modification>2025-05-29T20:38:26.027Z</modification><creation>2022-02-11T14:32:31.786Z</creation></dates><accession>S-EPMC8700945</accession><cross_references><pubmed>34946949</pubmed><doi>10.3390/genes12122000</doi></cross_references></HashMap>