Cited by 571Alzheimer's disease research and treatmentsNeuroinflammation and Neurodegeneration MechanismsDementia and Cognitive Impairment Research

The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.

CD33 Alzheimer's disease locus: altered monocyte function and amyloid biology

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Abstract

In our functional dissection of the CD33 Alzheimer's disease susceptibility locus, we found that the rs3865444(C) risk allele was associated with greater cell surface expression of CD33 in the monocytes (t50 = 10.06, P(joint) = 1.3 × 10(-13)) of young and older individuals. It was also associated with diminished internalization of amyloid-β 42 peptide, accumulation of neuritic amyloid pathology and fibrillar amyloid on in vivo imaging, and increased numbers of activated human microglia.

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  1. Wechsler, D. Wechsler Memory Scale-Revised (WMS-R) (Psychological, San Antonio, Texas, 1987).
  2. Lopresti, B.J. et al. J. Nucl. Med. 46, 1959–1972 (2005).

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Metadata

Authors
Initiative, T. A. D. N., Bradshaw, E. M., Chibnik, L. B., Keenan, B. T., Ottoboni, L., Raj, T., Tang, A., Rosenkrantz, L. L., Imboywa, S., Lee, M., Von Korff, A., Morris, M. C., Evans, D. A., Johnson, K., Sperling, R. A., Schneider, J. A., Bennett, D. A., & De Jager, P. L.
Affiliations
  • Brigham and Women's Hospital (US)
  • Broad Institute (US)
  • Rush University Medical Center (US)
  • Harvard University (US)
Venue
Nature Neuroscience
Published
2013-05-23
Volume
16
Issue
7
Pages
848-850
ISSN
  • 1097-6256 (ISSN-L)
  • 1546-1726
OpenAlex
W2074405990
Cited by
570
References
41
Citations by year
2026: 9 · 2025: 30 · 2024: 56 · 2023: 48 · 2022: 42 · 2021: 45 · 2020: 53 · 2019: 59 · 2018: 49 · 2017: 46 · 2016: 41 · 2015: 49 · 2014: 32 · 2013: 11
FWCI
30.79
Type
journal article
Language
en
Open access
Locations
  • Nature Neuroscience (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
  • eScholarship (California Digital Library) (submittedVersion, cc-by)
Funders
  • National Institute on Aging (R01AG017917, P30-AG 10161, K25AG041906, R01AG030146, R01 AG30146, R01‐AG17917, R01 AG15819, R01AG11101, P50AG005138, R01AG011101, R01AG036042, R01AG043617, R01AG015819, P30AG010161, P30AG008051, P50AG008702, P30AG013846, R01AG031553, U24AG021886)
  • National Institute of General Medical Sciences (R25GM076321, RC2GM093080)
  • National Institute of Neurological Disorders and Stroke (R10 NS067305, R01NS067305)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
Keywords
CD33, Alzheimer's disease, genetic susceptibility loci, monocytes, microglial activation, amyloid-beta, amyloid fibrils, cell surface expression
MeSH terms
Adult, Age Factors, Aged, Aged, 80 and over, Alzheimer Disease, Aniline Compounds, Brain, Dextrans, Female, Genotype, HLA-D Antigens, Humans, Male, Middle Aged, Monocytes, Peptide Fragments, Polymorphism, Genetic, Radionuclide Imaging, Thiazoles, Cohort Studies, Amyloid beta-Peptides, Microglia, Young Adult, Genetic Association Studies, Plaque, Amyloid, Cognitive Dysfunction, Sialic Acid Binding Ig-like Lectin 3

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