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Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease

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Cover of 'Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction and Technical Survey: Protein Aggregation and Fibrillogenesis
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    Chapter 2 Fibril Formation by Short Synthetic Peptides
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    Chapter 3 In vitro Oligomerization and Fibrillogenesis of Amyloid-beta Peptides
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    Chapter 4 Tau Fibrillogenesis
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    Chapter 5 Prion Protein Aggregation and Fibrillogenesis In Vitro
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    Chapter 6 α-Synuclein Aggregation and Modulating Factors
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    Chapter 7 Pathological Self-Aggregation ofb 2 -Microglobulin: A Challenge for Protein Biophysics
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    Chapter 8 Islet Amyloid Polypeptide: Aggregation and Fibrillogenesisin vitroand Its Inhibition.
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    Chapter 9 Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease
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    Chapter 10 Fibrillogenesis of Huntingtin and Other Glutamine Containing Proteins
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    Chapter 11 Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease
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    Chapter 12 Experimental Inhibition of Peptide Fibrillogenesis by Synthetic Peptides, Carbohydrates and Drugs
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    Chapter 13 Experimental Inhibition of Fibrillogenesis and Neurotoxicity by amyloid-beta (Aβ) and Other Disease-Related Peptides/Proteins by Plant Extracts and Herbal Compounds
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    Chapter 14 Alzheimer's disease.
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    Chapter 15 Modeling the Polyglutamine Aggregation Pathway in Huntington’s Disease: From Basic Studies to Clinical Applications
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    Chapter 16 Parkinson’s Disease
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    Chapter 17 Human prion diseases: from kuru to variant creutzfeldt-jakob disease.
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    Chapter 18 Animal prion diseases.
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    Chapter 19 β(2)-Microglobulin Amyloidosis.
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    Chapter 20 Systemic AA Amyloidosis
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    Chapter 21 Familial amyloidotic polyneuropathy and transthyretin.
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    Chapter 22 The Challenge of Systemic Immunoglobulin Light-Chain Amyloidosis (AL)
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