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- W2124679574 abstract "Atherosclerosis and obesity-induced metabolic dysfunction are lipid-driven inflammatory pathologies responsible for a major part of cardiovascular complications. Immune cell activation as well as interactions between the different immune cells is dependent on and controlled by a variety of co-stimulatory signals. These co-stimulatory signals can either aggravate or ameliorate the disease depending on the stage of the disease, the cell-types involved and the signal transduction cascades initiated. This review focuses on the diverse roles of the most established co-stimulatory molecules of the B7 and Tumor Necrosis Factor Receptor (TNFR) families, ie the CD28/CTLA4-CD80/CD86 and CD40L/CD40 dyads in the pathogenesis of atherosclerosis and obesity. In addition, we will explore their potential as therapeutic targets in both atherosclerosis and obesity." @default.
- W2124679574 created "2016-06-24" @default.
- W2124679574 creator A5021427999 @default.
- W2124679574 creator A5069173292 @default.
- W2124679574 date "2015-01-01" @default.
- W2124679574 modified "2023-09-26" @default.
- W2124679574 title "An inflammatory link in atherosclerosis and obesity" @default.
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- W2124679574 doi "https://doi.org/10.5482/hamo-14-12-0079" @default.
- W2124679574 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26225729" @default.
- W2124679574 hasPublicationYear "2015" @default.
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