<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Simon MJ</submitter><funding>NIA NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>12389</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6098119</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>The deposition of misfolded proteins, including amyloid beta plaques and neurofibrillary tangles is the histopathological hallmark of Alzheimer's disease (AD). The glymphatic system, a brain-wide network of perivascular pathways that supports interstitial solute clearance, is dependent upon expression of the perivascular astroglial water channel aquaporin-4 (AQP4). Impairment of glymphatic function in the aging rodent brain is associated with reduced perivascular AQP4 localization, and in human subjects, reduced perivascular AQP4 localization is associated with AD diagnosis and pathology. Using human transcriptomic data, we demonstrate that expression of perivascular astroglial gene products dystroglycan (DAG1), dystrobrevin (DTNA) and alpha-syntrophin (SNTA1), are associated with dementia</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Transcriptional network analysis of human astrocytic endfoot genes reveals region-specific associations with dementia status and tau pathology.</pubmed_title><pmcid>PMC6098119</pmcid><funding_grant_id>P30 AG008017</funding_grant_id><funding_grant_id>R01 AG054456</funding_grant_id><funding_grant_id>F31 AG054093</funding_grant_id><funding_grant_id>R01 NS089709</funding_grant_id><pubmed_authors>Boespflug EL</pubmed_authors><pubmed_authors>Iliff JJ</pubmed_authors><pubmed_authors>Simon MJ</pubmed_authors><pubmed_authors>Wang MX</pubmed_authors><pubmed_authors>Woltjer RL</pubmed_authors><pubmed_authors>Roese NE</pubmed_authors><pubmed_authors>Murchison CF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcriptional network analysis of human astrocytic endfoot genes reveals region-specific associations with dementia status and tau pathology.</name><description>The deposition of misfolded proteins, including amyloid beta plaques and neurofibrillary tangles is the histopathological hallmark of Alzheimer's disease (AD). The glymphatic system, a brain-wide network of perivascular pathways that supports interstitial solute clearance, is dependent upon expression of the perivascular astroglial water channel aquaporin-4 (AQP4). Impairment of glymphatic function in the aging rodent brain is associated with reduced perivascular AQP4 localization, and in human subjects, reduced perivascular AQP4 localization is associated with AD diagnosis and pathology. Using human transcriptomic data, we demonstrate that expression of perivascular astroglial gene products dystroglycan (DAG1), dystrobrevin (DTNA) and alpha-syntrophin (SNTA1), are associated with dementia</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2026-05-04T05:29:54.787Z</modification><creation>2025-06-01T03:57:31.442Z</creation></dates><accession>S-EPMC6098119</accession><cross_references><pubmed>30120299</pubmed><doi>10.1038/s41598-018-30779-x</doi></cross_references></HashMap>