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is much older. Indeed, the symptoms of what are now known as prion diseases were first described in Europe in sheep in 1730 and called scrapie;
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The most fascinating and unique feature of prion diseases is that they are caused almost exclusively by a proteinaceous and infectious;
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Prions are best known as the agents of mad cow and related diseases, and a growing number of proteins with prion-like properties have been;
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Diseases such as Creutzfeldt-Jakob disease and kuru develop when PrP proteins form prions by misfolding, clumping together, and spreading;
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frequently used to study a group of CNS illnesses often referred to as the prion diseases. Research on prions and the disorders that they cause has;
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Prions and Neurodegenerative Diseases, Volume 172, in the Progress in Molecular Biology and Translational Science series, provides the most;
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spongiform encephalopathies (TSEs), also called prion diseases, are invariably fatal neurodegenerative infectious diseases that include bovine;
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Human Prion Diseases, Volume 153 is designed to update the reader on the latest advances and clinical aspects of prion diseases. The;
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agent-prion proteins-calls for intensive assessment of the headway gained in tracing prions, testing for transmissible neurodegenerative;
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of the transmissible spongiform encephalopathies. Transmissible spongiform encephalopathy diseases (also known as prion diseases) are caused by a;
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). Transmissible spongiform encephalopathies (TSEs), also called prion diseases, are invariably fatal neurodegenerative infectious diseases that include;
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Synthetic Prions, and Transgenic Mouse Models. As neurodegenerative diseases represent a health issue that is receiving increasing;
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The story of the revolutionary science that is unraveling the mysteries of mad cow and other fatal brain diseases Discovered and;
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fatal familial insomnia. To distinguish this pathogen from viruses and viroids, the term prion was introduced to emphasize its proteinaceous;
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Amyloids, Prions and Beta Proteins is the last volume of the three-part thematic series on Fibrous Proteins in the Advances;
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This comprehensive work, aimed at both students and researchers alike, systematically covers all aspects of prion diseases (transmissible;
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the molecular basis for antiviral drugs and vaccines. The material on the pathogenesis of AIDS, prions, emerging diseases (such as Ebola) and;
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understanding prion structure and biology. Together these chapters provide an overview of prion biology and underscore some of the challenges we face if;
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understanding prion structure and biology. Together these chapters provide an overview of prion biology and underscore some of the challenges we face if;
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in neurodegenerative disease, such as Alzheimer's, Parkinson's and prion diseases. Written by leading experts in their fields, each chapter combines elements;
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diseases, readers will learn about studies unique to each condition, including Huntington's Disease, spinocerebellar ataxia, SMA, ALS and prion;
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biochemistry and cell biology. The diseases covered in the book include Parkinsons disease, Alzheimers disease, prion disease, and ALS. The chapters;
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new insights into the pathogenic effect of E. coli, viral diseases, and protozoan parasites, as well as prions and other zoonotic diseases. It;
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