Title |
Genetics ignite focus on microglial inflammation in Alzheimer’s disease
|
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Published in |
Molecular Neurodegeneration, October 2015
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DOI | 10.1186/s13024-015-0048-1 |
Pubmed ID | |
Authors |
Manasi Malik, Ishita Parikh, Jared B. Vasquez, Conor Smith, Leon Tai, Guojun Bu, Mary Jo LaDu, David W. Fardo, G. William Rebeck, Steven Estus |
Abstract |
In the past five years, a series of large-scale genetic studies have revealed novel risk factors for Alzheimer's disease (AD). Analyses of these risk factors have focused attention upon the role of immune processes in AD, specifically microglial function. In this review, we discuss interpretation of genetic studies. We then focus upon six genes implicated by AD genetics that impact microglial function: TREM2, CD33, CR1, ABCA7, SHIP1, and APOE. We review the literature regarding the biological functions of these six proteins and their putative role in AD pathogenesis. We then present a model for how these factors may interact to modulate microglial function in AD. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 2 | 50% |
Unknown | 2 | 50% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 4 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
United States | 4 | 2% |
United Kingdom | 2 | <1% |
Denmark | 1 | <1% |
France | 1 | <1% |
Unknown | 258 | 97% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Researcher | 57 | 21% |
Student > Ph. D. Student | 50 | 19% |
Student > Bachelor | 30 | 11% |
Student > Master | 29 | 11% |
Student > Doctoral Student | 14 | 5% |
Other | 34 | 13% |
Unknown | 52 | 20% |
Readers by discipline | Count | As % |
---|---|---|
Neuroscience | 65 | 24% |
Biochemistry, Genetics and Molecular Biology | 42 | 16% |
Agricultural and Biological Sciences | 36 | 14% |
Medicine and Dentistry | 27 | 10% |
Immunology and Microbiology | 11 | 4% |
Other | 29 | 11% |
Unknown | 56 | 21% |