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. 2014 Feb 28;3(1):e000772. doi: 10.1161/JAHA.113.000772

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© 2014 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell.

This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

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Figure 2. — Raw data from MALDI‐MS analysis of lipid extracts of murine thrombi harvested 14 days after IVC ligation. Mass spectra of splenectomized (A) and sham‐operated mice (controls) (B) recorded in positive mode showing the composition of cationic phospholipids and of splenectomized mice (C) and controls (D) recorded in negative mode showing the composition of anionic phospholipids are displayed. The peaks of most abundant phospholipid species of the different phospholipid classes are indicated, and peaks of the synthetic phospholipid standards added for quantitative evaluation are highlighted by asterisks. IVC indicates inferior vena cava; MALDI matrix‐assisted laser desorption/ionization; PA, phosphatidic acid; PC, phosphatidylcholine; PE, phosphatidylethanolamine, PG, phosphatidylglycerol; PI, phosphatidylinositol; PS, phosphatidylserine; SM, sphingomyelin.