<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Joshi P</submitter><funding>NIEHS NIH HHS</funding><funding>National Institutes of Health</funding><funding>Vanderbilt University</funding><pagination>148-157</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6961782</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>75</volume><pubmed_abstract>Manganese (Mn) is essential for neuronal health but neurotoxic in excess. Mn levels vary across brain regions and neurodevelopment. While Mn requirements during infanthood and childhood are significantly higher than in adulthood, the relative vulnerability to excess extracellular Mn across human neuronal developmental time and between distinct neural lineages is unknown. Neurological disease is associated with changes in brain Mn homeostasis and pathology associated with Mn neurotoxicity is not uniform across brain regions. For example, mutations associated with Huntington's disease (HD) decrease Mn bioavailability and increase resistance to Mn cytotoxicity in human and mouse striatal neuronal progenitors. Here, we sought to compare the differences in Mn cytotoxicity between control and HD</pubmed_abstract><journal>Neurotoxicology</journal><pubmed_title>Huntington's disease associated resistance to Mn neurotoxicity is neurodevelopmental stage and neuronal lineage dependent.</pubmed_title><pmcid>PMC6961782</pmcid><funding_grant_id>R01 ES016931</funding_grant_id><funding_grant_id>R01 ES010563</funding_grant_id><pubmed_authors>Joshi P</pubmed_authors><pubmed_authors>Aschner M</pubmed_authors><pubmed_authors>Bowman AB</pubmed_authors><pubmed_authors>Ilieva I</pubmed_authors><pubmed_authors>Bodnya C</pubmed_authors><pubmed_authors>Neely MD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Huntington's disease associated resistance to Mn neurotoxicity is neurodevelopmental stage and neuronal lineage dependent.</name><description>Manganese (Mn) is essential for neuronal health but neurotoxic in excess. Mn levels vary across brain regions and neurodevelopment. While Mn requirements during infanthood and childhood are significantly higher than in adulthood, the relative vulnerability to excess extracellular Mn across human neuronal developmental time and between distinct neural lineages is unknown. Neurological disease is associated with changes in brain Mn homeostasis and pathology associated with Mn neurotoxicity is not uniform across brain regions. For example, mutations associated with Huntington's disease (HD) decrease Mn bioavailability and increase resistance to Mn cytotoxicity in human and mouse striatal neuronal progenitors. Here, we sought to compare the differences in Mn cytotoxicity between control and HD</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Dec</publication><modification>2025-04-22T10:37:20.809Z</modification><creation>2021-02-20T02:07:24Z</creation></dates><accession>S-EPMC6961782</accession><cross_references><pubmed>31545971</pubmed><doi>10.1016/j.neuro.2019.09.007</doi></cross_references></HashMap>