Animal Models to Study the Biology of Amyloid-β Protein Misfolding in Alzheimer Disease

Research output: Chapter in Book/Report/Conference proceedingChapter

Original languageEnglish (US)
Title of host publicationProtein Misfolding Diseases
Subtitle of host publicationCurrent and Emerging Principles and Therapies
PublisherJohn Wiley and Sons
Pages213-229
Number of pages17
ISBN (Print)9780471799283
DOIs
StatePublished - Jul 2 2010

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Amyloid beta-Peptides
Alzheimer Disease
Animals
Animal Models

Keywords

  • 56 and memory loss and differentiating between - roles of Aβ and amyloid plaques in memory loss
  • Animal models, studying biology of amyloid-β protein misfolding in Alzheimer disease
  • Evidence in mice and humans - supporting hypothesis that Aβ initiates brain dysfunction, ABD Aβ and TAU, mediating brain degeneration

Cite this

Ashe, K. H. (2010). Animal Models to Study the Biology of Amyloid-β Protein Misfolding in Alzheimer Disease. In Protein Misfolding Diseases: Current and Emerging Principles and Therapies (pp. 213-229). John Wiley and Sons. https://doi.org/10.1002/9780470572702.ch11

Animal Models to Study the Biology of Amyloid-β Protein Misfolding in Alzheimer Disease. / Ashe, Karen H.

Protein Misfolding Diseases: Current and Emerging Principles and Therapies. John Wiley and Sons, 2010. p. 213-229.

Research output: Chapter in Book/Report/Conference proceedingChapter

Ashe, KH 2010, Animal Models to Study the Biology of Amyloid-β Protein Misfolding in Alzheimer Disease. in Protein Misfolding Diseases: Current and Emerging Principles and Therapies. John Wiley and Sons, pp. 213-229. https://doi.org/10.1002/9780470572702.ch11
Ashe KH. Animal Models to Study the Biology of Amyloid-β Protein Misfolding in Alzheimer Disease. In Protein Misfolding Diseases: Current and Emerging Principles and Therapies. John Wiley and Sons. 2010. p. 213-229 https://doi.org/10.1002/9780470572702.ch11
Ashe, Karen H. / Animal Models to Study the Biology of Amyloid-β Protein Misfolding in Alzheimer Disease. Protein Misfolding Diseases: Current and Emerging Principles and Therapies. John Wiley and Sons, 2010. pp. 213-229
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