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Parkinson's Disease Molecular Mechanisms Underlying Pathology

Parkinson's Disease Molecular Mechanisms Underlying Pathology
Parkinson's Disease Molecular Mechanisms Underlying Pathology
  • Συγγραφείς: Patrik Verstreken
  • ISBN: 9780128037836
  • Εκδότης: Elsevier
  • Σελίδες: 330
  • Διαστάσεις: 152 X 229 mm
  • Έτος Έκδοσης: 2017
76,00€
Χωρίς ΦΠΑ: 71,70€

Edited by Patrik Verstreken, VIB Center for the Biology of Disease, KU Leuven, Center for Human Genetics, Laboratory of Neuronal Communication, Leuven, Belgium   Features:

  • Written by experts in the field that focus on pathways and mechanisms implicated in Parkinson’s pathology
  • Draws parallels between multidisciplinary discoveries in different model organisms using an array of technologies
  • Provides a cross-methodology and cross-species approach to understanding the molecular biology of Parkinson’s disease
  • Includes approximately 25 color Illustrations and diagrams to explain concepts and models
  • Focuses on key pathways and mechanisms (as opposed to model organism or gene) to provide a multidisciplinary approach to Parkinson’s disease
Table Of Contents:
  • List of Contributors
  • Preface
  • Chapter 1: The Neurogenetics of Parkinson’s Disease and Putative Links to Other Neurodegenerative Disorders
    • Abstract
    • 1. Introduction
    • 2. Definition of (Genetic) Parkinson’s Disease
    • 3. Classification and Nomenclature of Monogenic Parkinson’s Disease
    • 4. Monogenic Forms of Parkinson’s Disease and Parkinsonism
    • 5. PARK-SNCA
    • 6. PARK-LRRK2
    • 7. PARK-VPS35
    • 8. PARK-Parkin
    • 9. PARK-PINK1
    • 10. PARK-DJ-1
    • 11. Recent Novel Parkinson’s Disease Candidate Genes
    • 12. Systematic and Regularly Updated Overview of Parkinson’s Disease Mutations
    • 13. Reduced Penetrance and Variable Expressivity of Genetic Parkinson’s Disease
    • 14. Genetic Association Studies
    • 15. Candidate Gene Studies in Parkinson’s Disease
    • 16. Genome-Wide Association Studies
    • 17. Gene-Environment Interactions in Parkinson’s Disease
    • 18. Lessons Learned From Other Monogenic Neurodegenerative Diseases
    • 19. Translational Genetics: From Animal Models to Personalized Treatments
    • 20. Most Important Questions for Future Perspectives of PD Neurogenetics
  • Chapter 2: Electron Transport Chain
    • Abstract
    • 1. Introduction
    • 2. Glycolysis in the Cytosol
    • 3. Impact of Electron Transport Chain Dysfunction on Neuronal Function
    • 4. What Have the Genetics Taught Us About Electron Transport Chain Dysfunction and the Sporadic Forms of Parkinson’s Disease?
    • 5. Correlation Between Findings Obtained Using Different Animal Models
    • 6. Therapeutic Pathways Targeting the Electron Transport Chain
    • 7. Conclusions
    • List of Abbreviations
  • Chapter 3: Mitochondrial Fission and Fusion
    • Abstract
    • 1. Introduction
    • 2. Fission and Fusion Machinery
    • 3. Functions of Fission and Fusion in Neurons
    • 4. Fission and Fusion is Linked to Neurodegeneration
    • 5. PD Genes and Mitochondrial Morphology
    • 6. Mitochondrial Dynamics and Mitochondrial Turnover
    • 7. Therapeutic Potential of Targeting Fission and Fusion
    • 8. Conclusions
  • Chapter 4: Axonal Mitochondrial Transport
    • Abstract
    • 1. Prelude
    • 2. On the Distribution of Power: Mitochondria to Match Supply and Demand
    • 3. Mitochondrial Movement is Essential for Maintaining a Healthy Mitochondrial Population in Neurons
    • 4. A Motor/Adaptor Complex Enables and Regulates Mitochondrial Trafficking
    • 5. Linking PD and Mitochondrial Transport: Mitochondrial Dysfunction Causes Mitochondrial Arrest
    • 6. Do Other Forms of PD Involve Defects in Mitochondrial Movement?
    • 7. Summary: The Virtuous and Vicious Cycles that Link Mitochondrial Transport and Mitochondrial Health
  • Chapter 5: Mitophagy
    • Abstract
    • 1. Introduction
    • 2. Mitochondrial Quality Control
    • 3. PINK1 and Parkin
    • 4. PINK1-Parkin-Mediated Mitophagy
    • 5. PINK1 and/or Parkin-Independent Selective Mitophagy
    • 6. Methods to Detect Mitophagy
    • 7. Outstanding Questions
  • Chapter 6: Autophagy
    • Abstract
    • 1. Introduction
    • 2. Lessons from the Genetics of Parkinsons Disease
    • 3. Ageing and Autophagy
    • 4. Autophagy in the Nervous System: Friend or Foe?
    • 5. Autophagy Induction to Promote Neuronal Survival
    • 6. Conclusions
  • Chapter 7: Endocytosis and Synaptic Function
    • Abstract
    • 1. Introduction
    • 2. The Synaptic Vesicle Cycle and PD
    • 3. Exosome Release
    • 4. Summary
  • Chapter 8: Neuroinflammation as a Potential Mechanism Underlying Parkinsons Disease
    • Abstract
    • 1. Introduction
    • 2. The Role of Glial Cells in PD
    • 3. Involvement of Proinflammatory Substances and Oxidative Stress in PD
    • 4. Infiltration of Lymphocytes in PD
    • 5. Involvement of PD-related Genes in Neuroinflammation
    • 6. Potential Antiinflammatory Treatments for PD
    • 7. Summary and Conclusions
    • Acknowledgments
  • Chapter 9: Protein Translation in Parkinson’s Disease
    • Abstract
    • 1. Protein Translation and its Regulation in Neurons
    • 2. PD-Linked Mutations and Their Impact on Protein Translation
    • 3. Protein Translation and Neurotoxicity in Parkinson’s Disease
    • 4. Future Directions
    • Acknowledgments
  • Index

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