Biochemical and biophysical research communications

[1] PrP (122-139) is a covert mitochondrial targeting signal of prion protein and it specifically triggers the perinuclear clustering of mitochondria in neuronal culture cells.

[2] prion protein and aging

[3] Prion protein glycans reduce intracerebral fibril formation and spongiosis in prion disease.

[4] a medicinal herb scutellaria lateriflora inhibits prp replication in vitro and delays the onset of prion disease in mice

[5] age and environment influences on mouse prion disease progression: behavioral changes and morphometry and stereology of hippocampal astrocytes

[6] seeking a new paradigm for alzheimer’s disease: considering the roles of inflammation, blood-brain barrier dysfunction, and prion disease

[7] prion disease risk perception in canadian medical laboratories

[8] synaptic dysfunction in prion diseases: a trafficking problem?

[9] prion diseases and the gastrointestinal tract

[10] from prion diseases to prion-like propagation mechanisms of neurodegenerative diseases