k Human prion protein, molecular model Human prion protein, molecular model. Prions are abnormal proteins that cause a group of fatal neurodegenerative diseases including BSE in cows and CJD in humans. Prions do not have a nucleic acid RNA or DNA genome for replication. Abnormal infectious prions directly change normal prions found in the brain to the abnormal form. The altered prion structure is extremely stable and accumulates as amyloid plaques that lead to neurodegeneration. Stock Photo - Afloimages
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Human prion protein, molecular model Human prion protein, molecular model. Prions are abnormal proteins that cause a group of fatal neurodegenerative diseases including BSE in cows and CJD in humans. Prions do not have a nucleic acid RNA or DNA genome for replication. Abnormal infectious prions directly change normal prions found in the brain to the abnormal form. The altered prion structure is extremely stable and accumulates as amyloid plaques that lead to neurodegeneration.
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Human prion protein, molecular model

Human prion protein, molecular model. Prions are abnormal proteins that cause a group of fatal neurodegenerative diseases including BSE in cows and CJD in humans. Prions do not have a nucleic acid (RNA or DNA) genome for replication. Abnormal infectious prions directly change normal prions found in the brain to the abnormal form. The altered prion structure is extremely stable and accumulates as amyloid plaques that lead to neurodegeneration.

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