Protein Misfolding, Aggregation and Conformational Diseases Part B: Molecular Mechanisms of Conformational Diseases /
| Autor Corporativo: | |
|---|---|
| Otros Autores: | , |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
New York, NY :
Springer US : Imprint: Springer,
2007.
|
| Edición: | 1st ed. 2007. |
| Colección: | Protein Reviews ;
6 |
| Materias: | |
| Acceso en línea: | https://doi.org/10.1007/978-0-387-36534-3 |
Tabla de Contenidos:
- Altered Protein Structure and Enhanced Aggregation/Deposition
- The Pathogenesis of Alzheimer’s Disease: General Overview
- Free Radicals, Metal Ions, and A? Aggregation and Neurotoxicity
- Progress in Understanding the Mechanisms of Neuronal Dysfunction and Degeneration in Parkinson’s Disease
- ?-Synuclein Aggregation and Parkinson’s Disease
- Cell Biology of ?-Synuclein: Implications in Parkinson’s Disease and Other Lewy Body Diseases
- Pathogenesis of Prion Diseases
- Mammalian Prion Protein
- The Yeast Prion Proteins Sup35p and Ure2p
- Immunoglobulin Light Chain and Systemic Light-Chain Amyloidosis
- Pancreatic Islet Amyloid and Diabetes
- ?2-Microglobulin and Dialysis-Related Amyloidosis
- Serum Amyloid A and AA Amyloidosis
- Point Mutations and Enhanced Protein Deposition
- Transthyretin and the Transthyretin Amyloidoses
- Human Lysozyme
- Serpins and the Diversity of Conformational Diseases
- Altered Protein Structure and Impaired Function
- Human Copper-Zinc Superoxide Dismutase and Familial Amyotrophic Lateral Sclerosis
- Understanding the Effects of Cancer-Associated Mutations in the Tumor Suppressor Protein p53: Structural Consequences of Mutations and Possible Ways of Rescuing Oncogenic Mutants
- Changes in Supramolecular Structure
- Protein Aggregation in Muscle Fibers and Respective Neuromuscular Disorders
- Muscular Dystrophies and Protein Mutations
- The Functional Consequences of Dystrophin Deficiency in Skeletal Muscles
- Eye Lens Proteins and Cataracts
- Altered Protein Structure and Changes in Cellular/Nuclear Function
- Glutamine/Asparagine-Rich Regions in Proteins and Polyglutamine Diseases
- Mechanistic Insights into the Polyglutamine Ataxias
- Molecular Pathogenesis of the Polyglutamine Disease: Spinal and Bulbar Muscular Atrophy
- Post-Translational Modification and Protein Conformational Diseases
- Protein Glycation and Cataract: A Conformational Disease
- Defective Glycosylation and Muscular Dystrophies.