@prefix dcat: <http://www.w3.org/ns/dcat#> .
@prefix dct: <http://purl.org/dc/terms/> .
@prefix foaf: <http://xmlns.com/foaf/0.1/> .
@prefix vcard: <http://www.w3.org/2006/vcard/ns#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

<https://rec.harvest-normandie.data4citizen.com/dataset/oai-hal-tel-00864013v1> a dcat:Dataset ;
    dct:description """
              The overlap of neurotoxic mecanisms involved in prion diseases and synucleinopathies, and the concomitant detection of pathological forms of prion and α-synuclein in a same neurodegenerative disease, raise questions about the existence of potential relationship between α‐synuclein molecular alteration and prion diseases. First, we developed monoclonal antibodies by immunizing mice presenting a spontaneous deletion of the α-synuclein gene with human recombinant α‐synuclein. Then, we characterized the molecular alterations appearing jointly to clinical signs during the aging of a transgenic mouse model of synucleinopathies (TgM83), overexpressing human A53T α‐synuclein. Then, an approach routinely done in the field of prion was used to trigger a synucleinopathy alongside a prion disease. For this purpose, TgM83 mice were inoculated intracerebrally by three different prion strains : transmission of H-type bovine spongiform encephalopathy allows the onset of a prion disease concomitantly to the α‐synuclein pathology developed by the TgM83 mouse model. Finally, intracerebral inoculation of TgM83 mice with brain homogenates from symptomatic mice affected by a synucleinopathy triggers an important acceleration of the α‐synuclein pathology, resulting in the early onset of motor clinical signs associated with molecular alterations of α-synuclein. These data suggest that α-synuclein alterations can be experimentally transmitted from one mouse to another, supporting the idea that, far from being confined to the transmissible spongiform encephalopathies, the « prion-like » propagation of misfolded neuronal proteins might occur in synucleinopathies
            """ ;
    dct:identifier "NNT: 2011LYO10057" ;
    dct:issued "2026-05-09T16:24:37.120977"^^xsd:dateTime ;
    dct:language "fr" ;
    dct:modified "2026-05-09T16:24:37.120982"^^xsd:dateTime ;
    dct:publisher <https://rec.harvest-normandie.data4citizen.com/organization/cce9db95-46d9-4dc2-84b6-764215d0a002> ;
    dct:title "Alpha-synuclein molecular pathology : potential relationship with prion diseases" ;
    dcat:contactPoint [ a vcard:Organization ;
            vcard:fn "CCSD" ] ;
    dcat:distribution <https://rec.harvest-normandie.data4citizen.com/dataset/oai-hal-tel-00864013v1/resource/686289b4-a823-42b2-8295-592e2271edbc> ;
    dcat:keyword "encephalopathie-spongiforme-transmissible-est",
        "infoeu-reposemanticsdoctoralthesis",
        "lpha-synuclein",
        "lpha-synucleine",
        "maladie-neurodegenerative",
        "neurodegenerative-disease",
        "parkinson",
        "prion",
        "sdvsalife-sciences-q-bioagricultural-sciences",
        "synucleinopathie",
        "synucleinopathy",
        "theses",
        "transmissible-spongiform-encephalopathies-est" ;
    dcat:landingPage <https://theses.hal.science/tel-00864013> .

<https://rec.harvest-normandie.data4citizen.com/dataset/oai-hal-tel-00864013v1/resource/686289b4-a823-42b2-8295-592e2271edbc> a dcat:Distribution ;
    dct:format "HTML" ;
    dct:issued "2026-05-09T16:24:37.131090"^^xsd:dateTime ;
    dct:modified "2026-05-09T16:24:37.107665"^^xsd:dateTime ;
    dct:title "Alpha-synuclein molecular pathology : potential relationship with prion diseases" ;
    dcat:accessURL <https://theses.hal.science/tel-00864013> .

<https://rec.harvest-normandie.data4citizen.com/organization/cce9db95-46d9-4dc2-84b6-764215d0a002> a foaf:Agent ;
    foaf:name "test_moissonnage_selune" .

<https://theses.hal.science/tel-00864013> a foaf:Document .

