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Protein Misfolding Diseases

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Cover of 'Protein Misfolding Diseases'

Table of Contents

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    Book Overview
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    Chapter 1 Biophysical and Spectroscopic Methods for Monitoring Protein Misfolding and Amyloid Aggregation
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    Chapter 2 Ultrasensitive RT-QuIC Seed Amplification Assays for Disease-Associated Tau, α-Synuclein, and Prion Aggregates
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    Chapter 3 Vesicle-Based Assays to Study Membrane Interactions of Amyloid Peptides
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    Chapter 4 Differential Scanning Fluorimetry and Hydrogen Deuterium Exchange Mass Spectrometry to Monitor the Conformational Dynamics of NBD1 in Cystic Fibrosis
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    Chapter 5 A Multipronged Method for Unveiling Subtle Structural–Functional Defects of Mutant Chaperone Molecules Causing Human Chaperonopathies
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    Chapter 6 High-Throughput Microplate-Based Fluorescence Assays for Studying Stochastic Aggregation of Superoxide Dismutase-1
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    Chapter 7 Methods for Structural Analysis of Amyloid Fibrils in Misfolding Diseases
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    Chapter 8 Assays for Light Chain Amyloidosis Formation and Cytotoxicity
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    Chapter 9 Monitoring Aggregate Clearance and Formation in Cell-Based Assays
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    Chapter 10 Monitoring Proteome Stress in Live Cells Using HaloTag-Based Fluorogenic Sensor
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    Chapter 11 Quantification of Protein Aggregates Using Bimolecular Fluorescence Complementation
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    Chapter 12 Screening Protein Aggregation in Cells Using Fluorescent Labels Coupled to Flow Cytometry
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    Chapter 13 Induction of Cu/Zn Superoxide Dismutase (SOD1) Aggregation in Living Cells
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    Chapter 14 A Cell Model for HSP60 Deficiencies: Modeling Different Levels of Chaperonopathies Leading to Oxidative Stress and Mitochondrial Dysfunction
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    Chapter 15 Superresolution Fluorescence Imaging of Mutant Huntingtin Aggregation in Cells
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    Chapter 16 Thermal Shift and Stability Assays of Disease-Related Misfolded Proteins Using Differential Scanning Fluorimetry
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    Chapter 17 Methods to Screen Compounds Against Mutant p53 Misfolding and Aggregation for Cancer Therapeutics
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    Chapter 18 Early Stage Discovery and Validation of Pharmacological Chaperones for the Correction of Protein Misfolding Diseases
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    Chapter 19 Constructing Kinetically Controlled Denaturation Isotherms of Folded Proteins Using Denaturant-Pulse Chaperonin Binding
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    Chapter 20 In Vitro Prion Amplification Methodology for Inhibitor Screening
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    Chapter 21 SolubiS: Optimizing Protein Solubility by Minimal Point Mutations
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