Protein Misfolding, Aggregation, and Conformational Diseases Part A: Protein Aggregation and Conformational Diseases /
Protein Misfolding, Aggregation, and Conformational Disease, is the first book to discuss significant achievements in protein structure-function relationships in the areas of biochemistry, molecular biology and molecular medicine. This volume summarizes recent achievements in the understanding of th...
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| Other Authors: | , |
| Format: | Electronic eBook |
| Language: | English |
| Published: |
Boston, MA :
Springer US,
2006.
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| Series: | Protein Reviews ;
4 |
| Subjects: | |
| Online Access: | Full Text via HEAL-Link |
Table of Contents:
- Structural and Conformational Prerequisites of Amyloidogenesis
- Structural and Conformational Prerequisites of Amyloidogenesis
- The Generic Nature of Protein Folding and Misfolding
- The Generic Nature of Protein Folding and Misfolding
- Relative Importance of Hydrophobicity, Net Charge, and Secondary Structure Propensities in Protein Aggregation
- Relative Importance of Hydrophobicity, Net Charge, and Secondary Structure Propensities in Protein Aggregation
- Cytotoxic Intermediates in the Fibrillation Pathway: A? Oligomers in Alzheimer’s Disease as a Case Study
- Cytotoxic Intermediates in the Fibrillation Pathway: A? Oligomers in Alzheimer’s Disease as a Case Study
- Glycosaminoglycans, Proteoglycans, and Conformational Disorders
- Glycosaminoglycans, Proteoglycans, and Conformational Disorders
- Apolipoproteins in Different Amyloidoses
- Apolipoproteins in Different Amyloidoses
- Oxidative Stress and Protein Deposition Diseases
- Oxidative Stress and Protein Deposition Diseases
- Chaperone and Conformational Disorders
- Chaperone Suppression of Aggregated Protein Toxicity
- Mechanisms of Active Solubilization of Stable Protein Aggregates by Molecular Chaperones
- The Aggresome: Proteasomes, Inclusion Bodies, and Protein Aggregation
- The Aggresome: Proteasomes, Inclusion Bodies, and Protein Aggregation
- Protein Aggregation, Ion Channel Formation, and Membrane Damage
- Protein Aggregation, Ion Channel Formation, and Membrane Damage
- Visualization of Protein Deposits In Vivo
- Congo Red Staining of Amyloid: Improvements and Practical Guide for a More Precise Diagnosis of Amyloid and the Different Amyloidoses
- Immunohistological Study of Experimental Murine AA Amyloidosis
- Visualization of Protein Deposits In Vitro
- Reporters of Amyloid Structure
- Three-Dimensional Structural Analysis of Amyloid Fibrils by Electron Microscopy
- Atomic Force Microscopy
- Direct Observation of Amyloid Fibril Growth Monitored by Total Internal Reflection Fluorescence Microscopy
- Animal and Cell Models of Human Neurodegenerative Disorders
- Drosophila and C. elegans Models of Human Age-Associated Neurodegenerative Diseases
- Genetically Engineered Mouse Models of Neurodegenerative Disorders.
