Prion diseases are chronic and fatal neurodegenerative diseases characterized by the accumula-tion of disease-specific prion protein (PrPSc), spongiform changes, neuronal loss, and gliosis. Growing evidence shows that the neuroinflammatory response is a key component of prion diseases and contributes to neurodegeneration. Toll-like receptors (TLRs) have been proposed as important mediators of innate immune responses triggered in the central nervous system in other human neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis. However, little is known about the role of TLRs in prion dis-eases, and their involvement in the neuropathology of natural scrapie has not been studied. We asse...
Prion diseases affect both animals and humans. Research in the natural animal model of the disease c...
AbstractAccumulation of the misfolded prion protein, PrPSc in the central nervous system (CNS) is st...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
Prion diseases are chronic and fatal neurodegenerative diseases characterized by the accumulation of...
The molecular pathogenic mechanisms of prion diseases are far from clear. Genomic analyses have reve...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
Neuroinflammation and neurodegeneration are common during prion infection, but the mechanisms that u...
Neuroinflammation and neurodegeneration are common during prion infection, but the mechanisms that u...
Neurotrophins constitute a group of growth factor that exerts important functions in the nervous sys...
Autophagy is a dynamic cellular mechanism involved in protein and organelle turnover through lysosom...
Prion diseases are a group of progressive and fatal neurodegenerative disorders characterized by dep...
Background: Prion diseases are characterized by the accumulation of the pathogenic PrPSc protein, m...
Neurotrophins constitute a group of growth factor that exerts important functions in the nervous sys...
Prion diseases affect both animals and humans. Research in the natural animal model of the disease c...
Neurodegeneration and gliosis are the main neuropathological features of prion diseases. However, th...
Prion diseases affect both animals and humans. Research in the natural animal model of the disease c...
AbstractAccumulation of the misfolded prion protein, PrPSc in the central nervous system (CNS) is st...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
Prion diseases are chronic and fatal neurodegenerative diseases characterized by the accumulation of...
The molecular pathogenic mechanisms of prion diseases are far from clear. Genomic analyses have reve...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
Neuroinflammation and neurodegeneration are common during prion infection, but the mechanisms that u...
Neuroinflammation and neurodegeneration are common during prion infection, but the mechanisms that u...
Neurotrophins constitute a group of growth factor that exerts important functions in the nervous sys...
Autophagy is a dynamic cellular mechanism involved in protein and organelle turnover through lysosom...
Prion diseases are a group of progressive and fatal neurodegenerative disorders characterized by dep...
Background: Prion diseases are characterized by the accumulation of the pathogenic PrPSc protein, m...
Neurotrophins constitute a group of growth factor that exerts important functions in the nervous sys...
Prion diseases affect both animals and humans. Research in the natural animal model of the disease c...
Neurodegeneration and gliosis are the main neuropathological features of prion diseases. However, th...
Prion diseases affect both animals and humans. Research in the natural animal model of the disease c...
AbstractAccumulation of the misfolded prion protein, PrPSc in the central nervous system (CNS) is st...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...