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A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome

Journal

NATURE REVIEWS NEUROSCIENCE
Volume 16, Issue 9, Pages 564-574

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrn3983

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Funding

  1. Wellcome Trust Strategic Award [098330/Z/12/Z]
  2. Medical Research Council [U117527252]
  3. Alzheimer Research UK
  4. Alzheimer Society
  5. Bailey Thomas Trust
  6. Epilepsy Research UK
  7. Lee Kong Chian School of Medicine
  8. Nanyang Technological University Start-up Grant
  9. Singapore Ministry of Education Academic Research Fund Tier 1 [2014-T1-001-173]
  10. Wellcome Trust [098327/Z/12/Z] Funding Source: Wellcome Trust
  11. MRC [G0601056] Funding Source: UKRI
  12. Alzheimer's Society [192] Funding Source: researchfish
  13. Epilepsy Research UK [PGE1301] Funding Source: researchfish
  14. Medical Research Council [G0601056] Funding Source: researchfish
  15. The Francis Crick Institute [10194, 10197] Funding Source: researchfish
  16. Wellcome Trust [098327/Z/12/Z] Funding Source: researchfish

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Down syndrome, which arises in individuals carrying an extra copy of chromosome 21, is associated with a greatly increased risk of early-onset Alzheimer disease. It is thought that this risk is conferred by the presence of three copies of the gene encoding amyloid precursor protein (APP)-an Alzheimer disease risk factor-although the possession of extra copies of other chromosome 21 genes may also play a part. Further study of the mechanisms underlying the development of Alzheimer disease in people with Down syndrome could provide insights into the mechanisms that cause dementia in the general population.

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