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Showing 1 to 7 of 7 for “"protein inclusions"”.

  1. Topographical Differences in Stress Vulnerability in Experimental Parkinson's Disease

    … is characterized by the progressive spread of protein misfolding stress, or proteotoxicity, across the brain. During this protracted process, the allocortex of the temporal lobe develops protein inclusions before the neocortex in the frontal and parietal lobes. In the present study we tested …

    duquesne Repository record for Topographical Differences in Stress Vulnerability in Experimental Parkinson's Disease (opens in a new tab)

  2. Folding, stability and aggregation of the long-lived eye lens protein human gamma D crystallin

    … is a monomeric, two domain, primarily P-sheet protein found in high concentrations in the human eye lens. H[gamma]D-Crys and other crystallins are found in insoluble protein inclusions associated with the eye disease cataract. H[gamma]D-Crys is expressed in utero and does not regenerate during …

    mit Repository record for Folding, stability and aggregation of the long-lived eye lens protein human gamma D crystallin (opens in a new tab)

  3. Protein misfolding toxicity and inclusion formation in cellular models of neurodegeneration

    Protein misfolding characterizes most neurodegenerative diseases. Protein misfolding is the conversion of specific proteins from their normal, often soluble, and native three-dimensional conformation into an aberrant, often insoluble, non-functional conformation. Protein inclusions and aggregates …

    uwo Repository record for Protein misfolding toxicity and inclusion formation in cellular models of neurodegeneration (opens in a new tab)

  4. Blood Biomarkers of Presymptomatic Frontotemporal Dementia

    … characterised by neuronal loss and pathological protein inclusions in the frontal and/or temporal lobes of the brain. The presymptomatic stage, marked by molecular changes years before symptom onset, offers a critical window for early detection, intervention, targeted monitoring, and tracking of …

    auckland-ms Repository record for Blood Biomarkers of Presymptomatic Frontotemporal Dementia (opens in a new tab)

  5. TDP-43 and its role in neurodegeneration

    Ubiquitinated TDP-43 (TAR DNA Binding Protein) inclusions are a hallmark of ALS (amyotrophic lateral sclerosis) and FTLD-TDP-43 (frontotemporal lobar degeneration with ubiquitin inclusions). These diseases share a similar pathology of cytoplasmic ubiquitinated TDP-43 inclusions, which contain …

    utmb Repository record for TDP-43 and its role in neurodegeneration (opens in a new tab)

  6. A Study of alpha-Synuclein, Parkin and TDP-43 ; Proteins Implicated in Neurodegenerative Disease.

    alpha-Synuclein (alphaS) is a 14.5 kDa neuronal protein associated with Parkinson's disease (PD) and related disorders. Aggregated protein inclusions called Lewy bodies found in the brain in PD contain alphaS. Rare inherited forms of early-onset PD are caused by autosomal dominant mutations in …

    lancaster Repository record for A Study of alpha-Synuclein, Parkin and TDP-43 ; Proteins Implicated in Neurodegenerative Disease. (opens in a new tab)

  7. Using yeast to study neurodegenerative diseases : amyloid formation as a protective mechanism and a new Alzheimer's disease model

    … pathologically characterized by idiosyncratic protein amyloid inclusions. Not surprisingly amyloid fibrils have long been proposed to be the toxic protein species in these neurodegenerative diseases. However, more recent work has begun to suggest that the formation of ordered inclusions serves …

    mit Repository record for Using yeast to study neurodegenerative diseases : amyloid formation as a protective mechanism and a new Alzheimer's disease model (opens in a new tab)