,

The polymorphisms of the prion-like protein gene (PRND) in Korean normal population and sporadic creutzfeldt-jakob disease

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The generation of new astrocytes mediated by P-STAT3 in scrapie-infected mice brains

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Scrapie infection activates MULV replication and its replication accelerates the progression of scrapie pathogenesis

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Murine leukemia virus in senescence-prone 8 mice (SAMP8) accelerate the cell death in apoptotic stress condition

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Comparison of gene expression of profile of prion protein-deficient and wild type neuronal cell lines and mice