Amyloid, prions, and other protein aggregates, B :

목차 (Table of Contents)

• 자료제공 :
• Characterization of protein deposition in vivo and ex vivo.
  
  Chapter 1: PMCA for diagnosis and prion propagation studies.
  Chapter 2: Fractionation of prion protein aggregates by asymmetrical flow field-flow fractionation.
  Chapter 3: Analysis of Amyloid Aggregates Using Agarose Gel Electrophoresis.
  Chapter 4: Characterization of Systemic Amyloid Deposits by Mass Spectrometry.
  Chapter 5: Proteomics of Polyglutamine Aggregates.
  Chapter 6: Merger of Laser Capture Microdissection and Mass Spectrometry: A Window into the Amyloid Plaque Proteome.
  Chapter 7: MALDI MS Imaging of Amyloid.
  Chapter 8: Imaging polyglutamine deposits in brain tissue.
  Chapter 9: X-34 labeling of abnormal protein aggregates during the progression of Alzheimer’s disease.
  Chapter 10: Visualizing Pathology Deposits in the Living Brain of Alzheimer’s Disease Patients.
  Chapter 11: Micro-Imaging of Amyloid in Mice
  
  Cell and animal models of amyloid formation and toxicity
  
  Chapter 12: An efficient protein transformation protocol for introducing prions into yeast.
  Chapter 13: Screening for genetic modifiers of amyloid toxicity in yeast.
  Chapter 14: Searching for anti-prion compounds: Cell-based high-throughput in vitro assays and animal testing strategies.
  Chapter 15: A Drosophila Model of Alzheimer’s Disease.
  Chapter 16: A C. elegans model of polyglutamine disease.
  
  Computational Approaches and Theory
  
  Chapter 17: Nucleation: the Connections between Equilibrium and Kinetic Behavior.
  Chapter 18: Computational Approaches to Amyloid beta Fibril Core Structure.
  Chapter 19: Amyloid beta-protein aggregations: Ab initio discrete molecular dynamics approaches.
  Chapter 20: Computational approaches to fibril structure and formation