<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Kara B</submitter><pubmed_abstract>Soluble tau oligomeric assemblies display neurotoxic properties and may provide a pathogenic link between neurofibrillary tangle evolution and selective neuronal vulnerability in Alzheimer's disease (AD). However, the precise molecular and cellular pathways mediating tau oligomer toxicity are unclear. We combined single-neuron laser capture microdissection with custom microarrays to investigate differences in the molecular signatures of basal forebrain neurons within the nucleus basalis of Meynert (nbM) labeled for p75&lt;sup>NTR&lt;/sup>, a cholinergic cell marker, or dual-labeled for p75&lt;sup>NTR&lt;/sup> and TOC1, a tau oligomer marker. Tissue was obtained postmortem from Rush Religious Orders Study participants who died with an antemortem clinical diagnosis of no cognitive impairment (NCI), mild</pubmed_abstract><journal>Acta neuropathologica communications</journal><pagination>218</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12557935</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Neuronal gene profiling of tau oligomer-bearing cholinergic nucleus basalis neurons during the onset of Alzheimer's disease.</pubmed_title><pmcid>PMC12557935</pmcid><pubmed_authors>Kara B</pubmed_authors><pubmed_authors>Kanaan NM</pubmed_authors><pubmed_authors>Beck JS</pubmed_authors><pubmed_authors>Mufson EJ</pubmed_authors><pubmed_authors>Fu Z</pubmed_authors><pubmed_authors>Hickey SL</pubmed_authors><pubmed_authors>Ginsberg SD</pubmed_authors><pubmed_authors>Counts SE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neuronal gene profiling of tau oligomer-bearing cholinergic nucleus basalis neurons during the onset of Alzheimer's disease.</name><description>Soluble tau oligomeric assemblies display neurotoxic properties and may provide a pathogenic link between neurofibrillary tangle evolution and selective neuronal vulnerability in Alzheimer's disease (AD). However, the precise molecular and cellular pathways mediating tau oligomer toxicity are unclear. We combined single-neuron laser capture microdissection with custom microarrays to investigate differences in the molecular signatures of basal forebrain neurons within the nucleus basalis of Meynert (nbM) labeled for p75&lt;sup>NTR&lt;/sup>, a cholinergic cell marker, or dual-labeled for p75&lt;sup>NTR&lt;/sup> and TOC1, a tau oligomer marker. Tissue was obtained postmortem from Rush Religious Orders Study participants who died with an antemortem clinical diagnosis of no cognitive impairment (NCI), mild</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-05-14T03:25:13.745Z</modification><creation>2026-05-14T03:12:40.994Z</creation></dates><accession>S-EPMC12557935</accession><cross_references><pubmed>41146342</pubmed><doi>10.1186/s40478-025-02080-2</doi></cross_references></HashMap>