Altres ajuts: MINCIETEC/EET2002-05168-C04Gene expression analysis has proven to be a very useful tool to gain knowledge of the factors involved in the pathogenesis of diseases, particularly in the initial or preclinical stages. With the aim of finding new data on the events occurring in the Central Nervous System in animals affected with Bovine Spongiform Encephalopathy, a comprehensive genome wide gene expression study was conducted at different time points of the disease on mice genetically modified to model the bovine species brain in terms of cellular prion protein. An accurate analysis of the information generated by microarray technique was the key point to assess the biological relevance of the data obtained in terms of Transmissible...
Abstract Background Prion infection results in progressive neurodegeneration of the central nervous ...
In humans, insert mutations within the repetitive octapeptide region of the prion protein gene (Prnp...
Background: Prion diseases are characterized by the accumulation of the pathogenic PrPSc protein, m...
BACKGROUND: Prion diseases are fatal neurodegenerative disorders whose pathogenesis mechanisms are ...
Prion diseases, such as bovine spongiform encephalopathies (BSE), are transmissible neurodegenerativ...
Abstract Background Transmissible spongiform encephalopathies (TSEs) or prion diseases are fatal neu...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
Bovine spongiform encephalopathy (BSE) is a fatal, transmissible, neurodegenerative disease of cattl...
Prion diseases or transmissible spongiform encephalopathies (TSEs) are infectious neurodegenerative ...
Bovine spongiform encephalopathy (BSE) is a fatal disorder in cattle characterized by progressive ne...
The most likely route of entry of infection following oral exposure to transmissible spongiform ence...
The molecular pathogenic mechanisms of prion diseases are far from clear. Genomic analyses have reve...
AbstractTransgenic (Tg) mice carrying four extra octapeptide repeats (OR) in the bovine PrP gene (10...
Prion diseases, such as bovine spongiform encephalopathies (BSE), are transmissible neurodegenerativ...
Hyeon O Kim1, Greg P Snyder1, Tyler M Blazey1, Richard E Race2, Bruce Chesebro2, Pamela J Skinner11D...
Abstract Background Prion infection results in progressive neurodegeneration of the central nervous ...
In humans, insert mutations within the repetitive octapeptide region of the prion protein gene (Prnp...
Background: Prion diseases are characterized by the accumulation of the pathogenic PrPSc protein, m...
BACKGROUND: Prion diseases are fatal neurodegenerative disorders whose pathogenesis mechanisms are ...
Prion diseases, such as bovine spongiform encephalopathies (BSE), are transmissible neurodegenerativ...
Abstract Background Transmissible spongiform encephalopathies (TSEs) or prion diseases are fatal neu...
The pathogenesis of natural scrapie and other prion diseases remains unclear. Examining transcriptom...
Bovine spongiform encephalopathy (BSE) is a fatal, transmissible, neurodegenerative disease of cattl...
Prion diseases or transmissible spongiform encephalopathies (TSEs) are infectious neurodegenerative ...
Bovine spongiform encephalopathy (BSE) is a fatal disorder in cattle characterized by progressive ne...
The most likely route of entry of infection following oral exposure to transmissible spongiform ence...
The molecular pathogenic mechanisms of prion diseases are far from clear. Genomic analyses have reve...
AbstractTransgenic (Tg) mice carrying four extra octapeptide repeats (OR) in the bovine PrP gene (10...
Prion diseases, such as bovine spongiform encephalopathies (BSE), are transmissible neurodegenerativ...
Hyeon O Kim1, Greg P Snyder1, Tyler M Blazey1, Richard E Race2, Bruce Chesebro2, Pamela J Skinner11D...
Abstract Background Prion infection results in progressive neurodegeneration of the central nervous ...
In humans, insert mutations within the repetitive octapeptide region of the prion protein gene (Prnp...
Background: Prion diseases are characterized by the accumulation of the pathogenic PrPSc protein, m...