The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptome variations in infected versus control animals may highlight new genes potentially involved in some of the molecular mechanisms of prion-induced pathology. The aim of this work was to identify disease-associated alterations in the gene expression profiles of the caudal medulla oblongata (MO) in sheep presenting the symptomatic phase of natural scrapie. The gene expression patterns in the MO from 7 sheep that had been naturally infected with scrapie were compared with 6 controls using a Central Veterinary Institute (CVI) custom designed 4×44K microarray. The microarray consisted of a probe set on the previously sequenced ovine tissue library ...
Abstract Background Cellular prion protein expression is essential for the development of transmissi...
Autophagy is a dynamic cellular mechanism involved in protein and organelle turnover through lysosom...
The pathogenesis of scrapie infection was studied in sheep carrying the PrPVRQ/PrPVRQ genotype, whic...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
Background The pathogenesis of natural scrapie and other prion diseases is still poorly understood. ...
Background - Prion diseases are characterized by the accumulation of the pathogenic PrPSc protein, m...
The molecular pathogenic mechanisms of prion diseases are far from clear. Genomic analyses have reve...
Abstract Background Transmissible spongiform encephalopathies (TSEs) or prion diseases are fatal neu...
Susceptibility to infection by prions is highly dependent on the amino acid sequence and host expres...
Backgound In scrapie and prion diseases, the knowledge concerning genes involved in ...
Neurodegeneration and gliosis are the main neuropathological features of prion diseases. However, th...
Abstract Heat shock proteins (Hsp) perform cytoprotective functions such as apoptosis regulation and...
Prion diseases are chronic and fatal neurodegenerative diseases characterized by the accumulation of...
Abstract Background Cellular prion protein expression is essential for the development of transmissi...
Autophagy is a dynamic cellular mechanism involved in protein and organelle turnover through lysosom...
The pathogenesis of scrapie infection was studied in sheep carrying the PrPVRQ/PrPVRQ genotype, whic...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
Background The pathogenesis of natural scrapie and other prion diseases is still poorly understood. ...
Background - Prion diseases are characterized by the accumulation of the pathogenic PrPSc protein, m...
The molecular pathogenic mechanisms of prion diseases are far from clear. Genomic analyses have reve...
Abstract Background Transmissible spongiform encephalopathies (TSEs) or prion diseases are fatal neu...
Susceptibility to infection by prions is highly dependent on the amino acid sequence and host expres...
Backgound In scrapie and prion diseases, the knowledge concerning genes involved in ...
Neurodegeneration and gliosis are the main neuropathological features of prion diseases. However, th...
Abstract Heat shock proteins (Hsp) perform cytoprotective functions such as apoptosis regulation and...
Prion diseases are chronic and fatal neurodegenerative diseases characterized by the accumulation of...
Abstract Background Cellular prion protein expression is essential for the development of transmissi...
Autophagy is a dynamic cellular mechanism involved in protein and organelle turnover through lysosom...
The pathogenesis of scrapie infection was studied in sheep carrying the PrPVRQ/PrPVRQ genotype, whic...