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文献和实验A Function for the Prion Protein
opportunities to consider protein function in relation to the disease phenotype arose (5 ). The identification of the prion gene on chromosome 2 of the mouse (chromosome 20 in the human) (6 ), and the determination of its sequence (7 ), led to the translation
Secondary structure of prion mRNA
of structural elements in mRNA of prion protein From the EMBL data bank, 23 PrP mRNA sequences of the following species were available: three rodents (mouse, hamster, rat), two ruminants (cattle, sheep), the human and 17 non-human primates consisting
Neuropathological Diagnosis of Human Prion Disease: Morphological Studies
The neuropathology of the classical human prion diseases, Creutzfeldt-Jakob dtsease (CJD), Gerstmann-Straussler-Scheinker syndrome (GSS), and kuru, is characterized by four main features* spongiform change, neuronal loss, ghiosts, and amyloid
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