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http://purl.uniprot.org/citations/24604355http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/24604355http://www.w3.org/2000/01/rdf-schema#comment"The cellular prion protein (PrPC) is a highly conserved protein whose exact physiological role remains elusive. In the present study, we investigated age-dependent behavioral abnormalities in PrPC-knockout (Prnp0/0) mice and wild-type (WT) controls. Prnp0/0 mice showed age-dependent behavioral deficits in memory performance, associative learning, basal anxiety, and nest building behavior. Using a hypothesis-free quantitative proteomic investigation, we found that loss of PrPC affected the levels of neurofilament proteins in an age-dependent manner. In order to understand the biochemical basis of these observations, we analyzed the phosphorylation status of neurofilament heavy chain (NF-H). We found a reduction in NF-H phosphorylation in both Prnp0/0 mice and in PrPC-deficient cells. The expression of Fyn and phospho-Fyn, a potential regulator for NF phosphorylation, was associated with PrPC ablation. The number of β-tubulin III-positive neurons in the hippocampus was diminished in Prnp0/0 mice relative to WT mice. These data indicate that PrPC plays an important role in cytoskeletal organization, brain function, and age-related neuroprotection. Our work represents the first direct biochemical link between these proteins and the observed behavioral phenotypes."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.org/dc/terms/identifier"doi:10.1007/s12035-014-8655-3"xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Fischer A."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Schmitz M."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Requena J.R."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Silva C.J."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Wrede A."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Zerr I."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Korth C."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Govindarajan N."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Schulz-Schaeffer W.J."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Onisko B."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Ottis P."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Greis C."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/author"Koppe K."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/date"2014"xsd:gYear
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/name"Mol Neurobiol"xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/pages"923-936"xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/title"Loss of prion protein leads to age-dependent behavioral abnormalities and changes in cytoskeletal protein expression."xsd:string
http://purl.uniprot.org/citations/24604355http://purl.uniprot.org/core/volume"50"xsd:string
http://purl.uniprot.org/citations/24604355http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/24604355
http://purl.uniprot.org/citations/24604355http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/24604355
http://purl.uniprot.org/uniprot/#_Q3TZI7-mappedCitation-24604355http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24604355
http://purl.uniprot.org/uniprot/#_Q3UG89-mappedCitation-24604355http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24604355