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Mammalian prions and their wider relevance in neurodegenerative diseases
by
Collinge, John
in
631/378
/ 692/699
/ Alzheimer's disease
/ Amyloid beta-Peptides - chemistry
/ Amyloid beta-Peptides - classification
/ Amyloid beta-Peptides - metabolism
/ Animals
/ Brain research
/ Creutzfeldt-Jakob disease
/ Development and progression
/ Health aspects
/ Humanities and Social Sciences
/ Humans
/ Kinetics
/ Mammals
/ multidisciplinary
/ Mutation
/ Neurodegeneration
/ Neurodegenerative diseases
/ Neurodegenerative Diseases - genetics
/ Neurodegenerative Diseases - metabolism
/ Neurodegenerative Diseases - pathology
/ Neurodegenerative Diseases - therapy
/ Neurotoxicity
/ Pathology
/ Prions
/ Prions (Proteins)
/ Prions - chemistry
/ Prions - genetics
/ Prions - metabolism
/ Prions - toxicity
/ Protein Folding
/ Proteins
/ review-article
/ Science
/ Studies
2016
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Mammalian prions and their wider relevance in neurodegenerative diseases
by
Collinge, John
in
631/378
/ 692/699
/ Alzheimer's disease
/ Amyloid beta-Peptides - chemistry
/ Amyloid beta-Peptides - classification
/ Amyloid beta-Peptides - metabolism
/ Animals
/ Brain research
/ Creutzfeldt-Jakob disease
/ Development and progression
/ Health aspects
/ Humanities and Social Sciences
/ Humans
/ Kinetics
/ Mammals
/ multidisciplinary
/ Mutation
/ Neurodegeneration
/ Neurodegenerative diseases
/ Neurodegenerative Diseases - genetics
/ Neurodegenerative Diseases - metabolism
/ Neurodegenerative Diseases - pathology
/ Neurodegenerative Diseases - therapy
/ Neurotoxicity
/ Pathology
/ Prions
/ Prions (Proteins)
/ Prions - chemistry
/ Prions - genetics
/ Prions - metabolism
/ Prions - toxicity
/ Protein Folding
/ Proteins
/ review-article
/ Science
/ Studies
2016
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Do you wish to request the book?
Mammalian prions and their wider relevance in neurodegenerative diseases
by
Collinge, John
in
631/378
/ 692/699
/ Alzheimer's disease
/ Amyloid beta-Peptides - chemistry
/ Amyloid beta-Peptides - classification
/ Amyloid beta-Peptides - metabolism
/ Animals
/ Brain research
/ Creutzfeldt-Jakob disease
/ Development and progression
/ Health aspects
/ Humanities and Social Sciences
/ Humans
/ Kinetics
/ Mammals
/ multidisciplinary
/ Mutation
/ Neurodegeneration
/ Neurodegenerative diseases
/ Neurodegenerative Diseases - genetics
/ Neurodegenerative Diseases - metabolism
/ Neurodegenerative Diseases - pathology
/ Neurodegenerative Diseases - therapy
/ Neurotoxicity
/ Pathology
/ Prions
/ Prions (Proteins)
/ Prions - chemistry
/ Prions - genetics
/ Prions - metabolism
/ Prions - toxicity
/ Protein Folding
/ Proteins
/ review-article
/ Science
/ Studies
2016
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Mammalian prions and their wider relevance in neurodegenerative diseases
Journal Article
Mammalian prions and their wider relevance in neurodegenerative diseases
2016
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Overview
Prions are notorious protein-only infectious agents that cause invariably fatal brain diseases following silent incubation periods that can span a lifetime. These diseases can arise spontaneously, through infection or be inherited. Remarkably, prions are composed of self-propagating assemblies of a misfolded cellular protein that encode information, generate neurotoxicity and evolve and adapt
in vivo
. Although parallels have been drawn with Alzheimer's disease and other neurodegenerative conditions involving the deposition of assemblies of misfolded proteins in the brain, insights are now being provided into the usefulness and limitations of prion analogies and their aetiological and therapeutic relevance.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ 692/699
/ Amyloid beta-Peptides - chemistry
/ Amyloid beta-Peptides - classification
/ Amyloid beta-Peptides - metabolism
/ Animals
/ Humanities and Social Sciences
/ Humans
/ Kinetics
/ Mammals
/ Mutation
/ Neurodegenerative Diseases - genetics
/ Neurodegenerative Diseases - metabolism
/ Neurodegenerative Diseases - pathology
/ Neurodegenerative Diseases - therapy
/ Prions
/ Proteins
/ Science
/ Studies
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