Excitatory neuron-prone prion propagation and excitatory neuronal loss in prion-infected mice
The accumulation of a disease-specific isoform of prion protein (PrPSc) and histopathological lesions, such as neuronal loss, are unevenly distributed in the brains of humans and animals affected with prion Cocktail Table with 2 Stools diseases.This distribution varies depending on the diseases and/or the combinations of prion strain and experiment