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. 2022 May 19;42(7):839–856. doi: 10.1161/ATVBAHA.122.317790

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© 2022 The Authors.

Arteriosclerosis, Thrombosis, and Vascular Biology is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.

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Figure 7. — Functional enrichment of differentially expressed genes in the axillary lymph nodes of apoE/apoA-I double deficient (DKO) and DKO mice overexpressing human apoA-I (DKO/hA-I) mice. The most relevant KEGG and reactome pathways enriched in DKO (A and B, respectively) and in DKO/hA-I (C and D, respectively) are reported. PPAR indicates peroxisome proliferator-activated receptor.