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Non-fibrillar Amyloidogenic Protein Assemblies - Common Cytotoxins Underlying Degenerative Diseases

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Cover of 'Non-fibrillar Amyloidogenic Protein Assemblies - Common Cytotoxins Underlying Degenerative Diseases'

Table of Contents

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    Book Overview
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    Chapter 1 Overview of Fibrillar and Oligomeric Assemblies of Amyloidogenic Proteins
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    Chapter 2 Pathologic Lesions in Alzheimer Disease and Other Neurodegenerative Diseases—Cellular and Molecular Components
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    Chapter 3 Preparation and Structural Characterization of Pre-fibrillar Assemblies of Amyloidogenic Proteins
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    Chapter 4 Biological Targeting and Activity of Pre-fibrillar Aβ Assemblies
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    Chapter 5 The Role of Aβ and Tau Oligomers in the Pathogenesis of Alzheimer’s Disease
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    Chapter 6 Oligomers of α-Synuclein in the Pathogenesis of Parkinson’s Disease
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    Chapter 7 Cytotoxic Mechanisms of Islet Amyloid Polypeptide in the Pathogenesis of Type-2 Diabetes Mellitus (T2DM)
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    Chapter 8 Protein Misfolding and Toxicity in Amyotrophic Lateral Sclerosis
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    Chapter 9 Structural Studies of Prion Proteins and Prions
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    Chapter 10 Role of Prion Protein Oligomers in the Pathogenesis of Transmissible Spongiform Encephalopathies
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    Chapter 11 When More Is Not Better: Expanded Polyglutamine Domains in Neurodegenerative Disease
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    Chapter 12 Protein Misfolding and Toxicity in Dialysis-Related Amyloidosis
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    Chapter 13 Transthyretin Aggregation and Toxicity
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    Chapter 14 Strategies for Inhibiting Protein Aggregation: Therapeutic Approaches to Protein-Aggregation Diseases
Attention for Chapter 1: Overview of Fibrillar and Oligomeric Assemblies of Amyloidogenic Proteins
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