k Scrapie proteins. Coloured transmission electron micrograph TEM of scrapieassociated protein strands taken from the brain of an infected hamster. Scrapie is a transmissible spongiform encephalopathy TSE, which causes brain degeneration in some animals. The causative agent is thought to be a prion, an abnormal version of a protein naturally present in brain cells. The prion protein is not as easily degraded by cellular enzymes as the natural version and accumulates within nerve cells, destroying them. Prion proteins are also thought to cause the human TSE CreutzfeldtJakob disease CJD. Magnification x90,000 at 6x7cm size. Editorial Stock Photo - Afloimages
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Scrapie proteins. Coloured transmission electron micrograph (TEM) of scrapie-associated protein strands taken from the brain of an infected hamster. Scrapie is a transmissible spongiform encephalopathy (TSE), which causes brain degeneration in some animals. The causative agent is thought to be a prion, an abnormal version of a protein naturally present in brain cells. The prion protein is not as easily degraded by cellular enzymes as the natural version and accumulates within nerve cells, destroying them. Prion proteins are also thought to cause the human TSE Creutzfeldt-Jakob disease (CJD). Magnification: x90,000 at 6x7cm size.
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Scrapie proteins. Coloured transmission electron micrograph (TEM) of scrapie-associated protein strands taken from the brain of an infected hamster. Scrapie is a transmissible spongiform encephalopathy (TSE), which causes brain degeneration in some animals. The causative agent is thought to be a prion, an abnormal version of a protein naturally present in brain cells. The prion protein is not as easily degraded by cellular enzymes as the natural version and accumulates within nerve cells, destroying them. Prion proteins are also thought to cause the human TSE Creutzfeldt-Jakob disease (CJD). Magnification: x90,000 at 6x7cm size.

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10589622

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17-11-2010

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