Global ETD Search

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Showing 1 to 3 of 3 for “"human tauopathies"”.

  1. Synaptic dysfunction, tau spreading, and cognitive resilience through the lens of tau oligomers in Alzheimer’s disease and related dementias

    … to elucidate the molecular mechanisms underlying human tauopathies, with an emphasis on Alzheimer’s disease (AD)—the most prevalent and well-characterized tauopathy. Pathological tau species are among the earliest inclusions observed in post-mortem brains of individuals with dementia and strongly …

    utmb Repository record for Synaptic dysfunction, tau spreading, and cognitive resilience through the lens of tau oligomers in Alzheimer’s disease and related dementias (opens in a new tab)

  2. Analysis of axonal transport and molecular chaperones during neurodegeneration in drosophila

    … neurodegeneration. Animal models that express human disease genes and show neurodegenerative-like pathologies are widely used to study particular molecular systems in early neurodegenerative changes. Axonal transport (AT) is perturbed in several prevalent neurodegenerative diseases. The …

    soton Repository record for Analysis of axonal transport and molecular chaperones during neurodegeneration in drosophila (opens in a new tab)

  3. Autophagy gridlock in tauopathy

    Tauopathies are a group of neurodegenerative diseases characterized by the presence of intracellular aggregates containing the microtubule associated protein tau. Bulk degradation of aggregation-prone proteins can occur via autophagy. Here, we utilized the previously developed model of human

    utmb Repository record for Autophagy gridlock in tauopathy (opens in a new tab)